Novel Tdp1 Inhibitors Based on Adamantane Connected with Monoterpene Moieties via Heterocyclic Fragments

Abstract

Tyrosyl-DNA phosphodiesterase 1 (Tdp1) is a promising target for anticancer therapy due to its ability to counter the effects topoisomerase 1 (Top1) poison, such as topotecan, thus, decreasing their efficacy. Compounds containing adamantane and monoterpenoid residues connected via 1,2,4-triazole or 1,3,4-thiadiazole linkers were synthesized and tested against Tdp1. All the derivatives exhibited inhibition at low micromolar or nanomolar concentrations with the most potent inhibitors having IC₅₀ values in the 0.35–0.57 µM range. The cytotoxicity was determined in the HeLa, HCT-116 and SW837 cancer cell lines; moderate CC₅₀ (µM) values were seen from the mid-teens to no effect at 100 µM. Furthermore, citral derivative 20c, α-pinene-derived compounds 20f, 20g and 25c, and the citronellic acid derivative 25b were found to have a sensitizing effect in conjunction with topotecan in the HeLa cervical cancer and colon adenocarcinoma HCT-116 cell lines. The ligands are predicted to bind in the catalytic pocket of Tdp1 and have favorable physicochemical properties for further development as a potential adjunct therapy with Top1 poisons.

1. Introduction

Cancer is one of the leading causes of death worldwide; according to the International Agency for Research on Cancer (IARC), in 2018 new cancer cases were estimated to be approximately 18.1 million, with the number of fatal outcomes being almost 10 million worldwide [1].

The camptothecin derivatives irinotecan and topotecan are frontline cancer drugs used for the treatment of breast, small-cell lung, lymphomas, cervical, colorectal and ovarian cancers [2,3,4,5]. Their target is Topoisomerase 1 (Top1), an enzyme that catalyzes the process of relieving the torsional DNA strain during replication, transcription and chromatin remodeling [6] by generating a reversible single-stranded break and covalently attaching to the 3′-end, followed by religation and releasing of DNA. The camptothecins, or Top1 poisons, stabilize the Top1−DNA complex [7,8], thereby inhibiting the religation process that eventually leads to cell death [6]. A major disadvantage of Top1 poisons-based therapy is the ability of the cancer cells’ DNA repair systems to remove the lesions, preventing cell death. One of the DNA repair enzymes is tyrosyl-DNA-phosphodiesterase 1 (Tdp1), which is capable of cleaving different adducts from the DNA 3′-end restoring its integrity [9]. On the one hand, Tdp1 is overexpressed in some types of cancer, such as non-small lung cancer [10] and glioblastoma [11]. On the other hand, it has been shown that Tdp1 knockout mice and Tdp1-deficient cells are hypersensitive to Top1 inhibitors [12,13,14]. Therefore, the inhibition of Tdp1 could increase the efficacy of Top1 poisons, making it a promising anticancer target [15].

Monoterpenoid is a useful moiety in potent Tdp1 inhibitors. e.g., the aniline derivative 1 with a myrtenal moiety has inhibitory activity at submicromolar concentrations (Figure 1) [16]; coumarin-based (-)-myrtenal derivative 2 potentiated the cytotoxicity of camptothecin in cancer cells [17]; it has also been shown that 3, comprising diazaadamantane and citronellal residues, inhibits Tdp1 with IC₅₀ (half maximal inhibitory concentration) values of ~15 µM [18]; geranyl derivative 4 enhances the topotecan antitumor effect in in vitro and in vivo tumor models [19]; octahydro-2H-chromene-derived compound 5 was found to be an effective Tdp1 inhibitor with an IC₅₀ value of 2 µM [20]. Finally, isobenzofuran 6, containing a thiophene fragment, has a synergistic effect with topotecan in wild type cells, but not in Tdp1 knockout cells [21].

Adamantane derivatives enact many types of biological activity, including antiviral, actoprotective, antituberculosis and cannabimimetic properties, with some in clinical use [22]. Furthermore, the adamantane moiety is associated with the enhanced lipophilicity and stability of the drugs [22].

Terpenoids linked to an adamantane moiety were also found to exhibit Tdp1 activity; the dehydroabietyl amine derivative with a 1-adamantyl fragment 7 (Figure 2) not only had inhibitory activity against Tdp1, but also enhanced the antitumor effect of temozolomid in glioblastoma cells [23]; adamantyl-derived compounds containing citronellyl 8 and (+)-myrtenyl 9 fragments inhibited Tdp1 activity in the low micromolar range and citronellol derivative 8 potentiated the cytotoxicity of topotecan in the human colorectal carcinoma cell line HCT-116 [24]; moderate activity against Tdp1 was found for thioamides having adamantane and 3,7-dimethyloctyl 10 and citronellyl 11 moieties, with compound 10 showing synergetic effect with topotecan [25].

1,2,4-Triazole derivatives are broadly used as antifungal, antimigraine and antiviral agents (see Figure S1 in the Supplementary Materials). Additionally, drugs with a 1,3,4-thiadiazole fragment are used mainly as antibacterial agents, such as acetazolamide, a carbonic anhydrase inhibitor, which is used for the treatment of glaucoma [26] and high-altitude illness [27].

There are few examples of Tdp1 inhibitors having a five-membered heterocyclic core. The 1,3-thiazole moiety is as a linker between a geranyl fragment and usnic acid moiety in compound 12 (Figure 3), with the hybrid molecule demonstrating synergetic effects in combination with topotecan [28]. Another example of using a heterocyclic core as a linker is compound 13, where a thiophene residue connects an octahydro-2H-chromen-4-ol scaffold with an adamantyl residue with an IC₅₀ value of 1.2 µM [29].

In this study, we aimed at synthesizing several conjugates linking adamantane and monoterpenoid residues via 1,2,4-triazole and 1,3,4-thiadiazole linkers, to derive their structure–activity relationship for Tdp1 activity. This study is a continuation of our previous work on adamantyl conjugates with monoterpenoid residues capable of inhibiting Tdp1 to expand and improve the chemical matter of potent Tdp1 inhibitors.

2. Results and Discussion

2.1. Chemistry

According to Scheme 1, we synthesized starting compound 15 by reacting commercially available adamantane-1-carbonyl chloride 14 with thiosemicarbazide, which was used in a double excess for capturing HCl. This method allows the synthesis of the desired compound at an excellent yield. Synthesis of 1,2,4-triazole 16 was performed by the cyclocondensation of compound 15 in an aqueous solution of sodium hydroxide under refluxing conditions with 80% yield, as described previously [30]. 2-Amino-1,3,4-thiadiazole 17 was synthesized with a 71% yield after recrystallization from EtOH following a procedure previously described [31], which involved the treatment of starting compound 15 with concentrated sulfuric acid at room temperature.

For the attachment of monoterpenoid residues to compound 16, we obtained bromides 19a–g using the previously reported methods [32,33,34]. The treatment of alcohols 18c–f with PBr₃ in Et₂O or THF resulted in the bromides 19c–f. The reaction of monoterpene alcohols 18a, 18b and 18g with NBS and PPh₃ resulted in compounds 19a, 19b and 19g (Scheme 2).

The further alkylation of compound 16 with bromides in the presence of MeONa in MeOH led to the formation of the desired adamantane derivatives of 1,2,4-triazole bearing monoterpenoid fragments 20a–g. All the reactions proceeded smoothly with moderate to very good yields. Interestingly, the interaction of 15 with geranyl bromide 19c, with the formation of 20c, led to its (Z)-isomer 20d as an admixture with a ratio of 9:1 (20c:20d), as assessed by NMR. A similar situation was observed for the reaction of 15 with bromide 19d; in this case the ratio between 20d and 20c was 9.5:0.5 (Scheme 2). This ratio can be explained by a partial isomerization process of bromides or target products as described previously [35].

In order to modify amine 17, carboxylic acids 23a,c,d were obtained by applying previously reported procedures [36,37,38]. 3,7-Dimethyloctan-1-ol 18a was oxidized by Jones reagent to obtain carboxylic acid 23a [36]. Acids 23c and 23d were synthesized using Pinnick oxidation [37,38], which involved the treatment of aldehydes 21 and 22 with sodium chlorite at mild acidic conditions. The yields of compounds 23c and 23d were 85% and 50%, respectively (Scheme 3).

One of the most common methods to activate a carboxylic acid functional group is converting it to the corresponding carbonyl chloride. Utilizing this protocol, we synthesized acid chlorides 24a–d from acids 23a, 23c and 23d and commercially available citronellic acid 23b using SOCl₂, which were all used in further reactions without purification. The reaction of acid chlorides with amine 17 resulted in 1,3,4-thiadiazole derivatives 25a–d containing 1-adamantyl moiety and monoterpenoid residues at acceptable yields.

Propylphosphonic acid anhydride T3P is a useful coupling reagent that generates water-soluble by-products easily separated from reaction mixtures [39]. Applying T3P allowed us to synthesize amides 25a–d at good yields and with high purity. Full conversion was observed after 24 h at room temperature. α,β-Unsaturated acids 23c and 23d were found to react too slowly with amine 17 at room temperature. Carrying out the reaction under refluxing conditions for 24 h in EtOAc followed by silica gel column chromatography gave compounds 25c and 25d in very good yields (Scheme 3). Compound 26a was obtained at a good yield using the same procedure. The rest of the amides containing citronellic and (-)-myrtenic acid moieties were synthesized as previously reported [40].

Thus, starting from compound 15, we synthesized a series of conjugates, with 1,2,4-triazole and 1,3,4-thiadiazole as linkers. 1,2,4-Triazol-2-thione 16 was modified by alkylation with the corresponding bromides in good yields. To obtain 1,3,4-thiadiazole amides 25a–d, two methods were utilized: (1) converting carboxylic acids into corresponding acid chlorides followed by the acylation of amine 17; (2) direct interaction of carboxylic acids with 1,3,4-thiadiazole 17 in the presence of coupling reagent T3P. The second approach proved to be more convenient due to the expedient work-up of the reaction mixtures, the high target compound yields, and the high purity of the amides.

2.2. Biological Assays

In order to assess the inhibitory activity of the synthesized compounds, a fluorophore quencher-coupled DNA-biosensor for the real-time measurement of Tdp1 cleavage activity was used [41]. Furamidine was used as a positive control, which is a commercially available Tdp1 inhibitor (IC₅₀ 1.23 µM) [42], and the results are presented in Table 1. 25d could not be measured due to its poor solubility.

According to Table 1, of the triazoles 20a–d with aliphatic chains, the saturated 3,7-dimethyloctane derivative 20a was the most active as compared to its unsaturated counterparts. The thio-derivatives 20c and 20d, cis-trans isomers, showed practically the same IC₅₀ values (~5 μM). Interestingly, the bicyclic derivative 20f had an IC₅₀ value of 7.50 μM, whilst 20g substituted with a (-)-nopol moiety was in the submicromolar range (0.57 μM). The same pattern of saturated and unsaturated derivatives could be observed for the amides 25a and 25b as for the triazoles. Additionally, 25c with a (-)-myrtenic moiety had activity comparable to 20g, but much better activity than 20f, its triazole counterpart.

The 1,3,4-thiadiazole ring plays an important role in the inhibition of Tdp1, i.e., the amide derivatives 26 (see Scheme 4), composed of a monoterpenoid and 1-aminoadamantane [25,40], were less active, whereas their structural analogues, the thiadiazoles (25), showed good activity. Furthermore, by comparing 20a–g with the previously reported amides 28a–g [40] and thioamide 29a [25] (Scheme 4), also made up by 1-adamantane and monoterpenoid fragments, we see that the replacement of the amide or thioamide functional groups with a 1,2,4-triazole linker increased the potency for Tdp1.

The cytotoxicity of compounds was investigated using HeLa (cervical cancer), SW837 and HCT-116 (colon cancers) cell lines, and the results are shown in Table 1 and Figure S2 in the Supplementary Materials. The 1,3,4-thiadiazole derivatives (25) had a minor effect on the viability of the cell lines, with only two measured CC₅₀ values under 100 µM, whereas the triazole series (20) had a considerable impact, with CC₅₀ values as low as 15 µM. In general, the HeLa cell line was less sensitive to the inhibitors than the HCT-116 and SW837 cells. Leading compounds 20c and 20g were also tested on the noncancerous cell line HEK293A; they had no effect on cell viability (data not shown) at concentrations up to 30 μM.

The potential for sensitizing the cancer cell lines to topotecan using the Tdp1 inhibitors was investigated using the MTT assay. Neutralizing the enzymatic activity of Tdp1 by blocking access to its catalytic site using a small molecule should sensitize the cytotoxic potential of topotecan, since the complex of Top1 with DNA cannot be unraveled. Interestingly, other repair mechanisms than Tdp1 may also be at play in the cancer cells mitigating the cytotoxicity of topotecan. Nontoxic concentrations of the adamantane derivatives (5 μM) were used for the HeLa cell line; the dose response for topotecan was measured and the corresponding CC₅₀ values were derived, and the results are shown in Figure 4 for 20c and in Table 2 for all the derivatives.

For HeLa cells, increased cytotoxicity was seen when the adamantanes and topotecan were combined. The most effective sensitizer was 20c, followed by all the derivatives containing bicyclic fragments. Compound 25b, with an acyclic substituent, exhibited a moderate sensitizing effect, but due to its poor solubility it was not considered further. The combination index (CI) for different concentrations of topotecan and 20c at 5 μM was in the range 0.49–0.82, and at 10 μM of 20c, it was 0.23–0.78. This indicates a synergistic effect of topotecan and 20c. The CI values were calculated with the CompuSyn version 1.0 software. For the HCT-116 cells, the synergistic effects of the compounds were different than for the HeLa cells. The most potent compound was 20g, followed by 20c, 20e, 25a and 25c. 20b and 25b also showed moderate sensitization. The CI plot at a different fraction affected (Fa) was determined for topotecan (5, 15, 150, 500 and 1500 nM) and 20g (1, 3, 10, 20 μM). The CI values for most of the combinations correspond to a synergistic effect (CI < 1, see Figure S3 in the Supplementary Materials).

2.3. Molecular Modeling

Thirteen adamantane–monoterpene derivatives were docked into the binding site of the Tdp1 structure (PDB ID: 6DIE, resolution 1.78 Å) [43] with three water molecules retained (HOH814, 821 and 1078). It has been shown that keeping these crystalline water molecules improves the prediction quality of the docking scaffold (see the Methodology section for further information) [44]. The binding predictions of the four scoring functions used are given in Table S1 in the Supplementary Materials; all the ligands show reasonable scores, but no linear correlation was observed with the measured IC₅₀ values. Nevertheless, when the scores of the ligands with IC₅₀ values >15 µM were calculated, a clear statistical difference was seen between their average and that of the active compounds, with the exception of ChemScore (CS) (see Table S1). When the docked poses were analyzed, it emerged that the adamantane and monoterpene moieties were driving the binding, i.e., adamantane occupied the pocket containing both the catalytic histidine amino acid residues (His263 and 493) and the monoterpene fit into a lipophilic cleft. No hydrogen bonding interactions were predicted, indicating that the interaction was dominated by lipophilic contacts. The predicted configuration of 20a is shown in Figure 5 as an example of the dominant binding mode.

A subset of ligands with varied affinity to Tdp1 is 20a (0.54 µM), 20b (1.5 µM) and 20c (5.30 µM). These have similar structures; only the saturation state of the aliphatic chain is different, and thus an interesting trend is seen. The binding of a ligand to an enzyme is governed by Equation (1).

(1)$\Delta G_{Bind}=\Delta G_{Dehydration}+\Delta G_{Configuration}+\Delta G_{Intramol. binding}$

The three ligands were all predicted to bind to Tdp1 in the same manner, i.e., the configuration and intramolecular binding terms would be the same. When the log p values are considered, since log P correlates with ΔG_Dehydration [45], an excellent negative correlation is seen (R²—0.894, see Figure S4A). It is therefore clear that the interaction of these ligands is governed by an entropic push from the water phase and lipophilic contacts with the binding pocket’s surface.

The same trend was seen when structurally near-identical ligands 20f (7.50 µM) and 20g (0.57 µM) were compared; they had the same predicted binding, but 20g had a higher log p value than 20f (6.1 vs. 5.8). This trend was repeated for the 20a (0.54 µM) and 28a (>15 µM) pair, with the same binding pose but substantially different log p values (6.6 vs. 5.1). For 20g (0.57 µM) and 28g (>15 µM), a structurally similar pair, the latter was not docked into the catalytic binding pocket, i.e., it did not fit into it and therefore did not fulfill the ΔG_{Configuration} term in Equation (1). Interestingly, 28g docked into the same site as our previously reported adamantine–monoterpene series [25]. Finally, the difference in the 25a (0.45 µM) and 26a (>15 µM) pair can be explained by the low molecular weight of the latter (383.6 vs. 299.5 g mol⁻¹), as relatively small ligands have decreased binding affinity compared to their much bigger counterparts (see Chemical Space section and Figure S4B). This can be explained in terms of the smaller molecules having relatively few intramolecular interactions with the enzyme, leading to the third term in Equation (1) being small. In conclusion, the activity, or inactivity, of the ligands depends on their lipophilicity, as well as their fitting into the binding pocket (configuration) and finally having sufficient intramolecular interactions with the enzyme.

2.4. Chemical Space

The calculated molecular descriptors MW (molecular weight), log P (water–octanol partition coefficient), HD (hydrogen bond donors), HA (hydrogen bond acceptors), PSA (polar surface area) and RB (rotatable bonds) are given in Table S2 in the Supplementary Materials. Interestingly, when the molecular descriptor numbers were correlated with the IC₅₀ values, MW showed good correlation with R²—0.5638, and HA (R²—0.2267) and PSA (R²—0.2242) also had reasonable correlations (see Figure S4 in the Supplementary Materials). A correlation between the molecular descriptor values and their corresponding binding efficacy to Tdp1 has been previously seen for deoxycholic acid derivatives, with MW having an R² of 0.452, and 0.316 for RB [46]. The values of the molecular descriptors all lie within the lead- and drug-like chemical space, except for log P, which ranged from 4.7 to 6.6, thus reaching into the known drug space (for the definition of lead-like, drug-like and known drug space regions, see [47] and Table S3).

The known drug indexes (KDIs) for the ligands were calculated to gauge the balance of the molecular descriptors (MW, log P, HD, HA, PSA and RB). This method is based on the analysis of drugs in clinical use, i.e., the statistical distribution of each descriptor is fitted to a Gaussian function and normalized to 1, resulting in a weighted index. Both the summation of the indexes (KDI_2a) and multiplication (KDI_2b) methods were used [48], as shown for KDI_2a in Equation (2) and for KDI_2b in Equation (3); the numerical results are given in Table S2 in the Supplementary Materials.

KDI_2a = I_MW + I_{log P} + I_HD + I_HA + I_RB + I_PSA(2)

KDI_2b = I_MW × I_{log P} × I_HD × I_HA × I_RB × I_PSA(3)

The KDI_2a values for the ligands range from 4.82 to 5.59, with a theoretical maximum of 6 and an average of 4.08 (±1.27) for known drugs. These values are very good, since most of the descriptors lie within the lead- and drug-like boundaries of chemical space, except log P. The KDI_2b ranges from 0.23 to 0.64, with a theoretical maximum of 1 and with a KDS average of 0.18 (±0.20). Again, good values were obtained for the ligands even though the KDI_2b index is more sensitive than KDI_2a to outliers, since the multiplication of small numbers leads to smaller numbers. It can be concluded that the ligands are biocompatible as compared to drugs in clinical use.

3. Materials and Methods

3.1. Chemistry

All chemicals were purchased from commercial sources (Sigma Aldrich, Acros Organics) and used without further purification. ¹H and ¹³C NMR spectra were recorded on a Bruker AV-300 spectrometer (300.13 MHz and 75.46 MHz, respectively), a Bruker AV-400 (400.13 MHz and 100.61 MHz), a Bruker DRX-500 (500.13 MHz and 125.76 MHz) and on a Bruker Advance—III 600 (600.30 MHz and 150.95 MHz). Residual chloroform signals were used as references (δ_H 7.24, δ_C 76.90 ppm). Compound structures were determined by analyzing the ¹H-NMR spectra and ¹H–¹H 2D homonuclear correlation (COSY, NOESY), J-modulated ¹³C NMR spectra (JMOD), and ¹³C–¹H 2D heteronuclear correlation with one-bond (HSQC, ¹J = 145 Hz) and long-range spin–spin coupling constants (HMBC, ^2,3J = 7 Hz). Mass spectra (70 eV) were recorded on a DFS Thermo Scientific high-resolution mass spectrometer. The conversion of starting materials was analyzed by thin-layer chromatography, which was performed on Merck plates (UV-254). A PolAAr 3005 polarimeter was used to measure optical rotations ([α]_D). Target compounds were isolated by column chromatography (SiO₂; 63–200 µm; Macherey-Nagel). Melting points were measured on a Mettler Toledo FP900 Thermosystem apparatus. Spectral and analytical measurements were carried out at the Multi-Access Chemical Service Center of Siberian Branch of Russian Academy of Sciences (SB RAS). The atom numeration of the substances is provided for the assignment of signals into the NMR spectra, and differs from that in IUPAC. The spectra are shown in the Supplementary Materials, Figures S5–S40.

• Synthesis of 2-(adamantane-1-carbonyl)hydrazine-1-carbothioamide 15

A solution of adamantane-1-carbonyl chloride (10.0 g, 50.4 mmol) in 30 mL of THF was added to a 0 °C suspension of thiosemicarbazide (10.08 g, 110.8 mmol) in 200 mL of THF while stirring. The resulting mixture was stirred at room temperature overnight followed by evaporating the solvent on a rotary evaporator. To the reaction mixture was added water; the solid mass was filtered off, washed with water thoroughly and dried. The yield of the compound 15 was 11.48 g (90%); the product was isolated as a white solid.

• Synthesis of 5-(adamantan-1-yl)-2,4-dihydro-3H-1,2,4-triazole-3-thione 16

A mixture containing 5.0 g (8.0 mmol) of 2-(adamantane-1-carbonyl) hydrazine-1-carbothioamide 15 and 1 M solution of NaOH (25 mL) was refluxed for 3 h. After cooling to room temperature, the mixture was neutralized using concentrated HCl. The precipitate was collected by filtration, washed with water, and recrystallized from MeOH to give the product as a white solid (1.5 g, 80%).

• General procedure for obtaining 1,2,4-triazole derivatives 20a–20g

To a suspension of compound 16 (0.25 g, 1.06 mmol) in 1 mL of MeOH was added 0.304 mL of a 3.5 M solution of MeONa in MeOH. The solution obtained was stirred at room temperature for 30 min, and then corresponding bromide was added. The reaction mixture was stirred at 60 °C for 12 h and then the solvent was evaporated under reduced pressure. The product was extracted with Et₂O. The desired compound was purified using column chromatography using a n-hexane to ethyl acetate gradient.

• 5-(Adamantan-1-yl)-3-((3,7-dimethyloctyl)thio)-1H-1,2,4-triazole 20a

Colorless oil, yield 75%.

¹H-NMR (600 MHz, CDCl₃) (ppm) δ: 0.82 (d, J(23, 22) = J(24, 22) = 6.7 Hz, 6Н, 3Н-23, 3Н-24), 0.84 (d, J(25, 18) = 6.5 Hz, 3Н, Н-25), 1.03–1.12 (m, 3Н, Н-19b, 2Н-21), 1.15–1.29 (m, 3Н, Н-19a, 2Н-20), 1.42–1.55 (m, 3Н, Н-17b, Н-18, Н-22), 1.62–1.69 (m, 1Н, Н-17a), 1.70–1.77 (m, 6Н, 2Н-4, 2Н-6, 2Н-10), 1.96 (d, ³J = 3.0 Hz, 6Н, 2Н-2, 2Н-8, 2Н-9), 2.02–2.06 (m, 3Н, Н-3, Н-5, Н-7), 3.02 (ddd, J(16b, 16a) = 12.5 Hz, J(16b, 17b) = 9.5 Hz, J(16b, 17a) = 6.3 Hz, 1Н, Н-16b), 3.10 (ddd, J(16a, 16b) = 12.5 Hz, J(16a, 17a) = 9.8 Hz, J(16a, 17b) = 5.4 Hz, 1Н, H-16a). ¹³C-NMR (150 MHz, CDCl₃) (ppm) δ: 34.12 (s, С-1), 40.68 (t, С-2, С-8,С-9), 27.91 (d, С-3, С-5, С-7), 36.25 (t, С-4, С-6, С-10), 166.49 (s, С-11), 159.05 (s, С-13), 30.24 (t, С-16), 36.58 (t, С-17), 32.10 (d, С-18) 36.76 (t, С-19), 24.49 (t, С-20), 39.08 (t, С-21), 27.81 (d, С-22), 22.45, 22.55 (2q, С-23, С-24), 19.17 (q, С-25). HR MS: 375.2705 (M⁺, C₂₂H₃₇N₃S₁⁺; calc. 375.2703).

• 5-(Adamantan-1-yl)-3-(((S)-3,7-dimethyloct-6-en-1-yl)thio)-1H-1,2,4-triazole 20b

Colorless oil, yield 77%.

¹H-NMR (600 MHz, CDCl₃) (ppm) δ: 0.84 (d, J(25, 18) = 6.5 Hz, 3Н, Н-25), 1.07–1.14 (m, 1Н, Н-19b), 1.25–1.32 (m, 1Н, Н-19a), 1.42–1.55 (m, 2Н, Н-17b, Н-18), 1.54 (br.s, 3Н, Н-24), 1.62 (m, 3Н, Н-23), 1.61–1.68 (m, 1Н, Н-17a), 1.68–1.75 (m, 6Н, 2Н-4. 2Н-6, 2Н-10), 1.84–1.98 (m, 2Н, Н-20), 1.94 (d, ³J = 3.0 Hz, 6Н, 2Н-2, 2Н-8, 2Н-9), 2.00–2.04 (m, 3Н, Н-3, Н-5, Н-7), 3.01 (ddd, J(16b, 16a) = 12.4 Hz, J(16b, 17) = 9.4 Hz, J(16b, 17a) = 6.2 Hz, 1Н, Н-16b), 3.08 (1Н, ddd, J(16a, 16b) = 12.4 Hz, J(16a, 17a) = 9.8 Hz, J(16a, 17b) = 5.4 Hz, H-16a), 5.03 (t.m, J(21, 20) = 7.1 Hz, 1Н, Н-21). ¹³C-NMR (150 MHz, CDCl₃) (ppm) δ: 34.11 (s, С-1), 40.65 (t, С-2, С-8, С-9), 27.90 (d, С-3, С-5, С-7), 36.22 (t, С-4, С-6, С-10), 166.45 (s, С-11), 158.99 (s, С-13), 30.15 (t, С-16), 36.47 (t, С-17), 31.73 (d, С-18), 36.54 (t, С-19), 25.23 (t, С-20), 124.47 (d, С-21), 131.02 (s, С-22), 25.52 (q, С-23), 17.47 (q, С-24), 19.02 (q, С-25). HR MS: 373.2542 (M⁺, C₂₂H₃₅N₃S₁⁺; calc. 373.2546). ${\left[\mathsf{\alpha }\right]}_{\mathrm{D}}^{24.5}$ = +7 (c 0.48 in МеОН).

• 5-(Adamantan-1-yl)-3-(((E)-3,7-dimethylocta-2,6-dien-1-yl)thio)-1H-1,2,4-triazole 20c

White solid, mp = 106.6–109.8 °С, yield 67%.

¹H-NMR (600 MHz, CDCl₃) (ppm) δ: 1.56 (br.s, 3Н, Н-24), 1.62 (m, 3Н, Н-25), 1.64 (m, 3Н, Н-23), 1.71–1.79 (m, 6Н, 2Н-4, 2Н-6, 2Н-10), 1.93–2.05 (m, 4Н, 2Н-19, 2Н-20), 1.99 (d, ³J = 3.0 Hz, 6Н, 2Н-2, 2Н-8, 2Н-9), 2.04–2.08 (m, 3Н, Н-3, Н-5, Н-7), 3.72 (d, J(16, 17) = 7.8 Hz, 2Н, Н-16), 5.02 (t.m, J(20, 21) = 6.9 Hz, 1Н, Н-21), 5.33 (t.m, J(17, 16) = 7.8 Hz, 1Н, Н-17). ¹³C-NMR (150 MHz, CDCl₃) (ppm) δ: 34.18 (s, С-1), 40.78 (t, С-2, С-8, С-9), 27.95 (d, С-3, С-5, С-7), 36.30 (t, С-4, С-6, С-10), 167.05 (s, С-11), 158.32 (s, С-13), 30.69 (t, С-16), 118.91 (d, С-17), 140.41 (s, С-18), 39.43 (t, С-19), 26.27 (t, С-20), 123.74 (d, С-21), 131.64 (s, С-22), 25.55 (q, С-23), 17.59 (q, С-24), 15.98 (q, С-25). HR MS: 371.2389 (M⁺, C₂₂H₃₃N₃S₁⁺; calc. 371.2390).

• 5-(Adamantan-1-yl)-3-(((Z)-3,7-dimethylocta-2,6-dien-1-yl)thio)-1H-1,2,4-triazole 20d

White solid, mp = 110.9–113.5 °С, yield 60%.

¹H-NMR (600 MHz, CDCl₃) (ppm) δ: 1.56 (m, 3Н, Н-24), 1.64 (br.s, 3Н, Н-23), 1.67 (m, 3Н, Н-25), 1.70–1.77 (m, 6Н, 2Н-4, 2Н-6, 2Н-10), 1.96 (d, ³J = 3.0 Hz, 6Н, 2Н-2, 2Н-8, 2Н-9), 1.98–2.06 (m, 7Н, Н-3, Н-5, Н-7, 2Н-19, 2Н-20), 3.70 (d.m, J(16, 17) = 8.0 Hz, 2Н, Н-16), 5.06 (t.m, J(21, 20) = 6.7 Hz, 1Н, Н-21), 5.32 (t.m, J(17, 16) = 8.0 Hz, 1Н, Н-17). ¹³C-NMR (150 MHz, CDCl₃) (ppm) δ: 34.14 (s, С-1), 40.71 (t, С-2, С-8, С-9), 27.93 (d, С-3, С-5, С-7), 36.26 (t, С-4, С-6, С-10), 166.70 (s, С-11), 158.63 (s, С-13), 30.40 (t, С-16), 119.60 (d, С-17), 140.32 (s, С-18), 31.71 (t, С-19), 26.48 (t, С-20), 123.72 (d, С-21), 131.79 (s, С-22), 25.53 (q, С-23), 17.54 (q, С-24), 23.27 (q, С-25). HR MS: 371.2393 (M⁺, C₂₂H₃₃N₃S₁⁺; calc. 371.2390).

• 5-(Adamantan-1-yl)-3-((((S)-4-(prop-1-en-2-yl)cyclohex-1-en-1-yl)methyl)thio)-1H-1,2,4-triazole 20e

Colorless oil, yield 65%.

¹H-NMR (600 MHz, CDCl₃) (ppm) δ: 1.38–1.47 (m, 1Н, Н-21b), 1.68 (br.s, 3Н, Н-25), 1.71–1.81 (m, 7Н, 2Н-4, 2Н-6, 2Н-10, Н-21a), 1.82–1.90 (m, 1Н, Н-19b), 1.99 (d, ³J = 3.0 Hz, 6Н, 2Н-2, 2Н-8, 2Н-9), 2.01–2.10 (m, 5Н, Н-3, Н-5, Н-7, Н-19a, Н-20), 2.13–2.18 (m, 2Н, Н-22), 3.65 (br.d, J(16b, 16a) = 12.9 Hz, 1Н, Н-16b), 3.69 (br.d, J(16a, 16b) = 12.9 Hz, 1Н, Н-16a), 4.64 (m, 1Н, Н-24b), 4.67 (m, 1Н, Н-24a), 5.61–5.65 (m, 1Н, Н-18). ¹³C-NMR (150 MHz, CDCl₃) (ppm) δ: 34.18 (s, С-1), 40.77 (t, С-2, С-8, С-9), 27.94 (d, С-3, С-5, С-7), 36.28 (t, С-4, С-6, С-10), 166.96 (s, С-11), 158.19 (s, С-13), 39.90 (t, С-16), 133.01 (s, С-17), 125.29 (d, С-18), 30.63 (t, С-19), 40.56 (d, С-20), 27.38, 27.43 (2t, С-21, С-22), 149.50 (s, С-23), 108.56 (t, С-24), 20.64 (q, С-25). HR MS: 369.2235 (M⁺, C₂₂H₃₃N₃S₁⁺; calc. 369.2233). ${\left[\mathsf{\alpha }\right]}_{\mathrm{D}}^{24}$ = ȡ243 (c 0.24 in МеОН).

• 5-(Adamantan-1-yl)-3-((((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)methyl)thio)-1H-1,2,4-triazole 20f

White solid, mp = 121.1–121.5 °С, yield 70%.

¹H-NMR (600 MHz, CDCl₃) (ppm) δ: 0.72 (s, 3Н, Н-25), 1.07 (d, J(23b, 23a) = 8.7 Hz, 1Н, Н-23b), 1.23 (s, 3Н, Н-24), 1.70–1.78 (m, 6Н, 2Н-4, 2Н-6, 2Н-10), 1.97 (d, ³J = 3.0 Hz, 6Н, 2Н-2, 2Н-8, 2Н-9), 2.00–2.09 (m, 4Н, Н-3, Н-5,Н-7, Н-20), 2.14 (d.m, J(19b, 19a) = 17.8 Hz, 1Н, Н-19b), 2.17–2.23 (m, 2Н, Н-19a, H-22), 2.34 (1Н, ddd, J(23a, 23b) = 8.7 Hz, J(23a, 20) = J(23a, 22) = 5.6 Hz, Н-23a), 3.66–3.72 (m, 2Н, Н-16), 5.45–5.48 (m, 1Н, Н-18). ¹³C-NMR (150 MHz, CDCl₃) (ppm) δ: 34.17 (s, С-1), 40.73 (t, С-2, С-8, С-9), 21.93 (d, С-3, С-5, С-7), 36.29 (t, С-4, С-6, С-10), 166.83 (s, С-11), 158.17 (s, С-13), 38.88 (t, С-16), 142.70 (s, С-17), 121.11 (d, С-18), 31.20 (t, С-19), 40.31 (d, С-20), 37.97 (s, С-21), 44.97 (d, С-22), 31.56 (t, С-23), 25.96 (q, С-24), 20.95 (q, С-25). HR MS: 369.2233 (M⁺, C₂₂H₃₁N₃S₁⁺; calc. 369.2234). ${\left[\mathsf{\alpha }\right]}_{\mathrm{D}}^{24.5}$ = −14 (c 0.53 in МеОН).

• 5-(Adamantan-1-yl)-3-((2-((1R,5S)-6,6-dimethylbicyclo[3.1.1]hept-2-en-2-yl)ethyl)thio)-1H-1,2,4-triazole 20g

Colorless oil, yield 85%.

¹H-NMR (600 MHz, CDCl₃) (ppm) δ: 0.78 (s, 3Н, Н-26), 1.10 (d, J(24b, 24a) = 8.6 Hz, 1Н, Н-24b), 1.22 (s, 3Н, Н-25), 1.69–1.76 (m, 6Н, 2Н-4, 2Н-6, 2Н-10), 1.95 (d, ³J = 3.0 Hz, 6Н, 2Н-2, 2Н-8, 2Н-9), 1.99–2.05 (m, 5Н, Н-3, Н-5, Н-7, Н-21, Н-23), 2.14 (dm, J(20b, 20a) = 17.6 Hz, 1H, H-20b), 2.20 (dm, J(20a, 20b) = 17.6 Hz, 1H, H-20a), 2.25–2.32 (m, 3Н, 2Н-17, Н-24a), 3.02–3.11 (m, 2Н, Н-16), 5.19–5.22 (m, 1Н, Н-19). ¹³C-NMR (150 MHz, CDCl₃) (ppm) δ: 34.12 (s, С-1), 40.67 (t, С-2, С-8, С-9), 27.90 (d, С-3, С-5, С-7), 36.24 (t, С-4, С-6, С-10), 166.45 (s, С-11), 159.01 (s, С-13), 30.25 (t, С-16), 36.89 (t, С-17), 146.03 (s, С-18), 117.65 (d, С-19), 31.11 (t, С-20), 40.58 (d, С-21), 37.83 (s, С-22), 45.39 (d, С-23), 31.47 (t, С-24), 26.12 (q, С-25), 21.03 (q, С-26). HR MS: 383.2388 (M⁺, C₂₃H₃₃N₃S₁⁺; calc. 383.2390). ${\left[\mathsf{\alpha }\right]}_{\mathrm{D}}^{24.5}$ = −21 (c 0.51 in МеОН).

• General procedure for synthesis of bromides

To a solution of the corresponding monoterpenoid alcohol (6.5 mmol) in 30 mL of Et₂O cooled to 0 °C was added 0.3 mL (3.1 mmol) of PBr₃ dropwise. The resulting mixture was stirred at the same temperature for 4 h. After the reaction was completed, the solution was poured onto crushed ice and extracted with Et₂O. The combined organic layer was washed with saturated aqueous NaHCO₃ then brine and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure; the resulting crude was used without further purification. ¹H NMR spectra were consistent with previously reported data.

(E)-1-Bromo-3,7-dimethylocta-2,6-diene 19c, yield 84%. The spectral data were consistent with those in the literature [49].

(S)-1-(Bromomethyl)-4-(prop-1-en-2-yl)cyclohex-1-ene 19e, yield 77%. The spectral data were consistent with those in the literature [50].

2-(Bromomethyl)-6,6-dimethylbicyclo[3.1.1]hept-2-ene 19f, yield 72%. The spectral data were consistent with those in the literature [51].

A solution of PBr₃ (0.247 mL, 2.6 mmol) in 4 mL of dry THF was added dropwise to a solution of nerol (1.0 g, 6.5 mmol) in 7 mL of THF under argon at −10 °C. The reaction mixture was stirred for 1.5 h and the solvent was evaporated under reduced pressure. The residue was dissolved in a mixture of n-hexane/diethyl ether (1:1). The solution was washed with a saturated aqueous solution of NaHCO₃, then with water and brine. The organic phase was dried over sodium sulfate, and the solvent was evaporated. The product was used directly without further purification.

(Z)-1-Bromo-3,7-dimethylocta-2,6-diene 19d, yield 68%. The spectral data were consistent with those in the literature [33].

To a solution of PPh₃ (12.2 g, 46 mmol) in dry DCM (46 mL) was added N-bromosuccinimide (NBS) (8.4 g, 46 mmol) in small portions under an ice-water bath. The mixture was cooled to r.t. and was stirred for 30 min. Then, pyridine (2 mL) was added, followed by the corresponding alcohol (24 mmol). The reaction mixture was stirred overnight at room temperature. Then, the mixture was diluted with n-hexane (60 mL) and filtered through a silica gel plug. The reaction flask was stirred three times with EtOAc: n-hexane (6:6 mL) for around 1 h and filtered through the silica gel plug. The solution was concentrated in vacuo. The crude residue was purified by flash chromatography (n-hexane) to obtain the corresponding bromide as a colorless oil. The ¹H NMR spectra were consistent with previously reported data.

1-Bromo-3,7-dimethyloctane 19a, yield 90%. The spectral data were consistent with those in the literature [52].

(S)-8-Bromo-2,6-dimethyloct-2-ene 19b, yield 85%. The spectral data were consistent with those in the literature [53].

2-(2-Bromoethyl)-6,6-dimethylbicyclo[3.1.1]hept-2-ene 19g, yield 88%. The spectral data were consistent with those in the literature [34].

• Synthesis of 5-(adamantan-1-yl)-1,3,4-thiadiazol-2-amine 17

A solution of 2.2 g (8.7 mmol) of 2-(adamantane-1-carbonyl) hydrazine-1-carbothioamide in 20 mL of concentrated sulfuric acid was kept at room temperature overnight, and then the solution was neutralized with aqueous ammonia solution while cooling with ice until pH 7 was reached. The resulting solid was filtered off, washed with water, dried and recrystallized from EtOH to yield 5-(adamantan-1-yl)-1,3,4-thiadiazol-2-amine as a pale yellow solid (1.46 g, 71%).

• Synthesis of 3,7-dimethyloctanoic acid 23a

A solution of 3,7-dimethyloctan-1-ol (5.0 g, 31.6 mmol) in acetone (17 mL) was added dropwise to a stirred solution of chromium trioxide (7.0 g, 70 mmol) in water (11 mL) and concentrated sulfuric acid (2 mL) cooled to 0 °C for 30 min. The mixture was then diluted with water and extracted with ether. The organic layer was washed with 10% sodium hydroxide solution and the water fraction was separated followed by acidification of the alkaline solution by 10% HCl. The product was extracted with ether to afford 3,7-dimethyloctanoic acid (3.06 g, 55%) as a colorless oil.

• Synthesis of (-)-myrtenic acid 23c

A solution of NaClO₂ (8.0 g, 70 mmol) in H₂O (70 mL) was added slowly for 2 h to a stirred mixture of (-)-myrtenal (7.7 g, 51 mmol) in CH₃CN (50 mL), KH₂PO₄ (1.8 g) in water (20 mL), H₂O₂ (37%, 5 mL, 52 mmol) and polyethylene glycol (PEG-400, 3.0 g) at 10 °C with ice-water cooling. The reaction was stirred overnight at room temperature. Then, Na₂SO₃ (0.5 g) was added. The resulting mixture was acidified with 10% aqueous HCl to pH 3 and extracted several times with diethyl ether. The separated organic phase was washed with saturated sodium bisulfite and water, respectively, and then dried over anhydrous sodium sulfate. Evaporation of the solvent gave (-)-myrtenic acid as a yellow solid (7.67 g, 90%).

• Synthesis of (S)-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxylic acid 23d

A solution of 1.12 g (10 mmol) of 80% sodium chlorite in 10 mL of distilled water was added dropwise over 30 min at ambient temperature to a stirred mixture of 1.0 g (6.7 mmol) of (S)-(-)-perillaldehyde in 7 mL of DMSO and 0.28 g of KH₂PO₄ in 3 mL of water. The mixture was stirred at ambient temperature overnight. The reaction mixture was quenched with 30 mL of 10% sodium hydroxide solution followed by extraction of non-acidic compounds with 80 mL of diethyl ether three times. After acidifying the aqueous phase with concentrated HCl, the acid was extracted with 30 mL of diethyl ether three times. The ether layers were combined and dried over sodium sulfate. The evaporation of the solvent under reduced pressure gave 0.5 g (50%) of a slightly yellow solid.

• General procedure for acid chloride synthesis

To a solution of carboxylic acid (1.8 mmol) in 10 mL of benzene was added SOCl₂ (5.4 mmol). The solution was refluxed for 3 h and the solvent was evaporated under reduced pressure. The crude material was used with no further purification.

• General procedure for obtaining 25a–d and 26a

Method A. A solution of corresponding carboxylic acid chloride (1.2 mmol) in dry toluene (1 mL) was added to a suspension of amine 17 (1.06 mmol) and triethylamine (0.177 mL, 1.2 mmol) in 10 mL of dry toluene. The reaction mixture was stirred overnight at room temperature and the solvent was evaporated under reduced pressure. To the residue was added the aqueous solution of KOH, followed by extraction with EtOAc. The product was purified using silica gel column chromatography using an n-hexane to ethyl acetate gradient.

Method B. To a mixture of a carboxylic acid (0.9 mmol), amine 17 (1.06 mmol), pyridine (0.264 mL) and EtOAc (0.528 mL) were added T3P (50 wt. % in EtOAc, 2 mmol) while stirring. The reaction mixture was stirred overnight, then water was added. The precipitate formed was washed with water and dried. The product obtained was purified using silica gel column chromatography using an n-hexane to ethyl acetate gradient.

• N-(5-(Adamantan-1-yl)-1,3,4-thiadiazol-2-yl)-3,7-dimethyloctanamide 25a

White solid, mp = 148.6 °С followed by decomposition, yield 61% (method A), 81% (method B).

¹H-NMR (600 MHz, CDCl₃) (ppm) δ: 0.81 (d, J(23, 22) = J(24, 22) = 6.7 Hz, 6Н, Н-23, Н-24), 0.97 (d, J(25, 18) = 6.7 Hz, 3Н, Н-25), 1.08–1.16 (m, 2Н, Н-21), 1.20–1.43 (m, 4Н, 2Н-19, 2Н-20), 1.43–1.51 (m, 1Н, Н-22), 1.73–1.82 (m, 6Н, 2Н-4, 2Н-6, 2Н-10), 2.06 (d, ³J = 2.8 Hz, 6Н, 2Н-2, 2Н-8, 2Н-9), 2.07–2.15 (m, 4Н, Н-3, Н-5, Н-7, Н-18), 2.58 (dd, ²J = 14.1 Hz, J(17b, 18) = 8.5 Hz, 1Н, Н-17b), 2.72 (dd, ²J = 14.1 Hz, J(17a, 18) = 6.1 Hz, 1Н, Н-17a). ¹³C-NMR (150 MHz, CDCl₃) (ppm) δ: 37.71 (s, С-1), 43.07 (t, С-2, С-8, С-9), 28.29 (d, С-3, С-5, С-7), 36.29 (t, С-4, С-6, С-10), 174.22 (s, С-11), 159.87 (s, С-14), 171.69 (s, С-16), 43.72 (t, С-17), 30.95 (d, С-18), 36.88 (t, С-19), 24.37 (t, С-20), 39.04 (t, С-21), 27.76 (d, С-22), 22.41 (q, С-23), 22.56 (q, С-24), 19.28 (q, С-25). HR MS: 389.2495 (M⁺, C₂₂H₃₅О₁N₃S₁⁺; calc. 389.2496).

• N-(5-(Adamantan-1-yl)-1,3,4-thiadiazol-2-yl)-3,7-dimethyloct-6-enamide 25b

White solid, mp = 136.7 °С followed by decomposition, yield 52% (method A), 85% (method B).

¹H-NMR (600 MHz, CDCl₃) (ppm) δ: 0.99 (d, J(25, 18) = 6.8 Hz, 3Н, Н-25), 1.26–1.33 (m, 1Н, Н-19b), 1.43–1.50 (m, 1Н, Н-19a), 1.55 (s, 3Н, Н-24), 1.63 (m, 3Н, Н-23), 1.73–1.82 (m, 6Н, 2Н-4, 2Н-6, 2Н-10), 1.92–2.07 (m, 2Н, Н-20), 2.05 (d, ³J = 2.8 Hz, 6Н, 2Н-2, 2Н-8, 2Н-9), 2.07–2.17 (m, 4Н, Н-3, Н-5, Н-7, Н-18), 2.59 (dd, ²J = 14.0 Hz, J(17b, 18) = 8.5 Hz, 1Н, Н-17b), 2.73 (dd, ²J = 14.0 Hz, J(17a, 18) = 6.1 Hz, 1Н, Н-17a), 5.06 (t.m, J(21, 20) = 7.0 Hz, 1Н, Н-21). ¹³C-NMR (150 MHz, CDCl₃) (ppm) δ: 37.74 (s, С-1), 43.04 (t, С-2, С-8, С-9), 28.29 (d, С-3, С-5, С-7), 36.26 (t, С-4, С-6, С-10), 174.27 (s, С-11), 159.90 (s, С-14), 171.59 (s, С-16), 43.58 (t, С-17), 30.66 (d, С-18), 36.68 (t, С-19), 25.20 (t, С-20), 124.27 (d, С-21), 131.25 (s, С-22), 25.56 (q, С-23), 17.50 (q, С-24), 19.21 (q, С-25). HR MS: 387.2339 (M⁺, C₂₂H₃₃О₁N₃S₁⁺; calc. 387.2337).

• (1R,5S)-N-(5-(Adamantan-1-yl)-1,3,4-thiadiazol-2-yl)-6,6-dimethylbicyclo[3.1.1]hept-2-ene-2-carboxamide 25c

White solid, mp = 240.2 °С followed by decomposition, yield 50% (method A), 70% (method B).

¹H-NMR (600 MHz, CDCl₃) (ppm) δ: 0.84 (s, 3Н, Н-25), 1.21 (d, J(23b, 23a) = 9.2 Hz, 1Н, Н-23b), 1.34 (s, 3Н, Н-24), 1.72–1.81 (m, 6Н, 2Н-4, 2Н-6, 2Н-10), 2.05 (d, ³J = 2.7 Hz, 6Н, 2Н-2, 2Н-8, 2Н-9), 2.07–2.11 (m, 3Н, Н-3, Н-5, Н-7), 2.14–2.19 (m, 1Н, Н-20), 2.47–2.53 (2Н, m, Н-19b, Н-23a), 2.56 (ddd, ²J = 19.7 Hz, J(19a, 18) = J(19a, 20) = 3.0 Hz, 1Н, Н-19a), 2.91 (ddd, J(22, 20) = J(22, 23a) = 5.6 Hz, J(22, 18) = 1.5 Hz, 1Н, Н-22), 7.13–7.16 (m, 1Н, Н-18). ¹³C-NMR (150 MHz, CDCl₃) (ppm) δ: 37.68 (s, С-1), 43.07 (t, С-2, С-8, С-9), 28.28 (d, С-3, С-5, С-7), 36.29 (t, С-4, С-6, С-10), 173.99 (s, С-11), 160.51 (s, С-14), 164.92 (s, С-16), 140.86 (s, С-17), 136.01 (d, С-18), 32.33 (t, С-19), 40.16 (d, С-20), 37.83 (s, С-21), 41.17 (d, С-22), 31.23 (t, С-23), 25.76 (q, С-24), 20.93 (q, С-25). HR MS: 383.2026 (M⁺, C₂₂H₂₉О₁N₃S₁⁺; calc. 383.2024). ${\left[\mathsf{\alpha }\right]}_{\mathrm{D}}^{26}$ = −11 (c 0.84 in CHCl₃).

• (S)-N-(5-(adamantan-1-yl)-1,3,4-thiadiazol-2-yl)-4-(prop-1-en-2-yl)cyclohex-1-ene-1-carboxamide 25d

White solid, mp = 265.6 °С followed by decomposition, yield 55% (method A), 75% (method B).

¹H-NMR (600 MHz, CDCl₃) (ppm) δ: 1.49–1.57 (m, 1Н, Н-21b), 1.72–1.82 (m, 6Н, 2Н-4, 2Н-6, 2Н-10) 1.75 (s, 3Н, Н-25), 1.92–1.98 (m, 1Н, Н-21a), 2.06 (d, ³J = 3.0 Hz, 6Н, 2Н-2, 2Н-8, 2Н-9), 2.07–2.12 (m, 3Н, Н-3, Н-5, Н-7), 2.18–2.27 (m, 2Н, Н-19b, H-20), 2.35–2.44 (m, 1H, H-22b), 2.45–2.52 (m, 1H, H-19a), 2.58–2.65 (m, 1H, H-22a), 4.72 (br.s, 1Н, Н-24b), 4.75–4.77 (m, 1Н, Н-24a), 7.23–7.26 (m, 1Н, Н-18). ¹³C-NMR (150 MHz, CDCl₃) (ppm) δ: 37.81 (s, С-1), 42.99 (t, С-2, С-8, С-9), 28.23 (d, С-3, С-5, С-7), 36.21 (t, С-4, С-6, С-10), 174.17 (s, С-11), 160.77 (s, С-14), 166.07 (s, С-16), 130.80 (s, С-17), 139.50 (d, С-18), 31.21 (t, С-19), 39.83 (d, С-20), 26.80 (t, С-21), 24.30 (t, С-22), 148.45 (s, С-23), 109.25 (t, С-24), 20.60 (q, С-25). HR MS: 383.2026 (M⁺, C₂₂H₂₉О₁N₃S₁⁺; calc. 383.2022) ${\left[\mathsf{\alpha }\right]}_{\mathrm{D}}^{27}$ = −32 (c 0.74 in CHCl₃).

• N-(Adamantan-1-yl)-3,7-dimethyloctanamide 26a

White solid, mp = 97.9 °C followed by decomposition, yield 52% (method B).

¹H-NMR (600 MHz, CDCl₃) (ppm) δ: 0.827 and 0.829 (2d, J(19, 18) = J(20, 18) = 6.6 Hz, 3H each, H-19, H-20), 0.88 (d, J(21, 14) = 6.6 Hz, 3H, H-21), 1.05–1.16 (m, 3H, H-15b, 2H-17), 1.17–1.33 (m, 3H, H-15a, 2H-16), 1.43–1.53 (m, 1H, H-18), 1.60–1.68 (m, 6H, 2H-4, 2H-6, 2H-10), 1.78 (dd, ²J = 13.6 Hz, J(13, 14) = 8.3 Hz, 1H, H-13b), 1.84–1.93 (m, 1H, H-14), 1.94–1.99 (m, 6H, 2H-2, 2H-8, 2H-9), 2.01–2.06 (m, 3H, H-3, H-5, H-7), 2.05 (dd, ²J = 13.6 Hz, J(13a, 14) = 6.0 Hz, 1H, H-13a), 5.08 (br. s, 1H, H-11). ¹³C-NMR (150 MHz, CDCl₃) (ppm) δ: 51.65 (s, C-1), 41.60 (t, C-2, C-8, C-9), 29.33 (d, C-3, C-5, C-7), 36.27 (t, C-4, C-6, C-10), 171.69 (s, C-12), 45.56 (t, С-13), 30.72 (d, С-14), 36.90 (t, С-15), 24.57 (t, С-16), 38.99 (t, С-17), 27.81 (d, С-18), 22.45, 22.54 (2q, С-19, С-20), 19.46 (q, С-21). HR MS: 305.2715 (M⁺, C₂₀H₃₅O₁N₁⁺; calc. 305.2713).

3.2. Biology

3.2.1. Detection of Tdp1 Activity

The recombinant Tdp1 was purified to homogeneity by chromatography on Ni-chelating resin and phosphocellulose P11 as described [54], using plasmid pET 16B-Tdp1, kindly provided by Dr. K.W. Caldecott (University of Sussex, United Kingdom). Tdp1 activity was detected as described in the work [41]. Briefly, we measured the fluorescence intensity after quencher removal from a fluorophore quencher–coupled DNA oligonucleotide catalyzed by Tdp1. The reaction was carried out at different concentrations of inhibitors. The control samples contained 1% DMSO. The reaction mixtures contained Tdp1 buffer (50 mM Tris-HCl pH 8.0, 50 mM NaCl, and 7 mM β-mercaptoethanol), 50 nM biosensor, and an inhibitor being tested. The reaction was started by the addition of purified Tdp1 (1.5 nM). The biosensor (5′-[FAM] AAC GTC AGGGTC TTC C [BHQ]-3′) was synthesized in the Laboratory of Biomedical Chemistry at the Institute of Chemical Biology and Fundamental Medicine (Novosibirsk, Russia).

The reactions were incubated on a POLARstar OPTIMA fluorimeter (BMG LAB-TECH, GmbH) to measure fluorescence every 55 s (ex. 485 nm/em. 520 nm) during the linear phase (here, data are from minute 0 to minute 8). The values of IC₅₀ were determined using a six-point concentration response curve in a minimum of three independent experiments, and were calculated using MARS Data Analysis 2.0 (BMG LABTECH).

3.2.2. Cytotoxicity Assays

The human cervical cancer HeLa cells were grown in Iscove’s modified Dulbecco’s medium (IMDM) with 40 μg/mL gentamicin, 50 IU/mL penicillin, 50 μg/mL streptomycin (MP Biomedicals), and 10% of fetal bovine serum (Biolot) in a 5% CO₂ atmosphere. Human colon adenocarcinoma HCT-116, rectum adenocarcinoma SW837, and human embryo kidney HEK293A cell lines were cultured in DMEM medium (Invitrogen) supplemented with 10% fetal bovine serum (FBS) (Invitrogen), penicillin (100 units/mL), and streptomycin (100 μg/mL), at 37 °C, 5% CO₂ in a humid atmosphere. After the formation of a 30–50% monolayer, the tested compounds were added to the medium. The volume of the added reagents was 1/100 of the total volume of the culture medium, and the amount of DMSO was 1% of the final volume. Control cells were grown in the presence of 1% DMSO. The cell culture was monitored for 3 days.

The cytotoxicity of the compounds to HeLa and HEK293A cell lines was examined using the EZ4U Cell Proliferation and Cytotoxicity Assay (Biomedica, Austria), according to the manufacturer’s protocols.

The inhibition of HCT-116 and SW837 cell growth was assessed by the MTT test, based on the reduction of MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide into formazan by mitochondrial NAD(P)H-dependent oxidoreductase enzymes [55]. Cells in the exponential growth phase were seeded in 96-well plates (2000 cells per well). The cells were allowed to attach for 24 h and were treated with compounds with concentrations ranging from 1 to 100 μM for 72 h at 37 °C. MTT solution was added to each well at a final concentration of 0.5 mg/mL, and the plates were incubated at 37 °C for 2 h. The medium was removed, and the dark blue crystals of formazan were dissolved in 100 μL of isopropanol. The absorbance at 570 nm (peak) and 620 nm (baseline) was determined using a microplate reader Multiscan FC (Thermo Fisher Scientific Corporation). All concentrations were performed in triplicate. The values are given as mean ± standard deviation (S.D.) values, and all measurements were repeated three times.

3.3. Molecular Modeling and Screening

The compounds were docked against the crystal structure of Tdp1 (PDB ID: 6DIE, resolution 1.78 Å) [43], which was obtained from the Protein Data Bank (PDB) [56,57]. The Scigress version FJ 2.6 program [58] was used to prepare the crystal structure for docking, i.e., the hydrogen atoms were added, and the co-crystallized ligand benzene-1,2,4-tricarboxylic acid was removed, as well were the crystallographic water molecules except HOH 814, 821 and 1078. The waters were toggle-bound or were displaced by the ligand during docking, and spin–automatic optimization of the orientation of the hydrogen atoms was performed. The Scigress software suite was also used to build the inhibitors and the MM2 [59] force field was applied to identify the global minimum using the CONFLEX method [60] followed by structural optimization. The docking center was defined as the position of a carbon on the ring of the co-crystallized benzene-1, 2, 4-tricarboxylic acid (x = −6.052, y = −14.428, z = 33.998) with 10 Å radius. Fifty docking runs were allowed for each ligand with default search efficiency (100%). The basic amino acids lysine and arginine were defined as protonated. Furthermore, aspartic and glutamic acids were assumed to be deprotonated. The GoldScore(GS) [61] and ChemScore (CS) [62,63] ChemPLP (piecewise linear potential) [64] and ASP (Astex statistical potential) [65] scoring functions were implemented to predict the binding modes and relative energies of the ligands using the GOLD v5.4.1 software suite.

The QikProp 6.2 [66] software package was used to calculate the molecular descriptors of the molecules. The reliability was established by QikProp for the calculated descriptors [67]. The known drug indexes (KDI) were calculated from the molecular descriptors as described by Eurtivong and Reynisson [48]. For application in Excel, columns for each property were created and the following equations used to derive the KDI numbers for each descriptor: KDI MW: = EXP(−((MW − 371.76)^2)/((2 × 112.76)^2)); KDI Log P: = EXP(−((LogP − 2.82)^2)/((2 × 2.21)^2)); KDI HD: = EXP(−((HD − 1.88)^2)/((2 × 1.7)^2)); KDI HA: = EXP(−((HA − 5.72)^2)/((2 × 2.86)^2)); KDI RB = EXP(−((RB − 4.44)^2)/((2 × 3.55)^2)), and KDI PSA: = EXP(−((PSA − 79.4)^2)/((2 × 54.16)^2)). These equations could simply be copied into Excel and the descriptor name (e.g., MW) substituted with the value in the relevant column. In order to derive KDI_2A, this equation was used: = (KDI MW + KDI LogP + KDI HD + KDI HA + KDI RB + KDI PSA) and for KDI_2B we used = (KDI MW × KDI LogP × KDI HD × KDI HA × KDI RB × KDI PSA).

4. Conclusions

New hybrid molecules consisting of adamantane, monoterpene and heterocyclic fragments were synthesized and tested for their Tdp1-inhibitory properties. All the compounds were found to exhibit an inhibitory activity, and some had submicromolar potency, which was supported by the plausible binding modes in the catalytic pocket predicted by molecular modeling. The triazole and thiadiazole linkers showed marked improvement in potency as compared to the amides and thioamides previously reported [25,40]. The triazole and thiadiazole derivatives showed comparable IC₅₀ values and the saturated aliphatic chain, 3,7-dimethyloctane, was the best substituent for both series (20a, 25a). It was found that some of the new ligands potentiated the cytotoxic potential of topotecan in vitro, 20c being the most effective sensitizer, tripling (3×) the potency. The comparison of substances synthesized with structurally similar compounds 26a–c, 28a–g and 29a demonstrated that the incorporation of a 1,3,4-thiadiazole core into amides 26a–c increased Tdp1 inhibitory properties. The replacement of the amide bond in 28a–c or the thioamide bond in 29a with a 1,2,4-triazole linker also led to enhanced activity against Tdp1.

Supplementary Materials

The following are available online. Figure S1: The molecular structures of pharmaceuticals containing 1,2,4-triazole or 1,3,4-thiadiazole moieties, Figure S2: Dose-dependent impact of the Tdp1 inhibitors on the viability of HeLa (a), HCT-116 (b), and SW837 (c) cells, Figure S3: Combination index plot determined for combined action of 20g and topotecan on HCT-116 cells, Figure S4a: The correlation of the IC50 values of the ligands 20a, 20b and 20c with log P, Figure S4b: The correlation of the IC50 values of the ligands with MW, Figures S5–S40: NMR and mass spectra of the ligands, Table S1: The binding affinities as predicted by the scoring functions used, Table S2: The molecular descriptors and their corresponding Known Drug Indexes 2a and 2b (KDI2a/2b). Table S3: Definition of lead-like, drug-like and Known Drug Space (KDS) in terms of molecular descriptors.

Author Contributions

Chemistry investigation, A.A.M., E.S.M., D.V.K., E.V.S., K.P.V.; in vitro investigation, A.A.C., O.D.Z., E.S.I., N.S.D., A.L.Z.; molecular modeling, J.R.; methodology, N.F.S. and O.I.L.; project administration, K.P.V., E.V.S.; supervision, K.P.V., E.V.S.; writing—original draft preparation, A.A.M., writing—review and editing, K.P.V., J.R., N.F.S., O.I.L. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the Russian Scientific Foundation (grant 19-13-00040). Authors would like to acknowledge the Multi-Access Chemical Research Center SB RAS for spectral and analytical measurements.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The data presented in this study are available on request from the corresponding author.

Acknowledgments

Authors would like to acknowledge the Multi-Access Chemical Research Center SB RAS for spectral and analytical measurements.

Conflicts of Interest

The funders had no role in the design of the study; in the collection, analyses, or interpretation of data; in the writing of the manuscript, or in the decision to publish the results.

Sample Availability

Samples of the compounds are available from the authors.

Abbreviations

Tdp1	Tyrosyl-DNA phosphodiesterase 1
DMSO	Dimethyl sulfoxide

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Figures, Schemes and Tables

Figure 1. The molecular structures of known monoterpenoid-derived Tdp1 inhibitors.

Figure 2. The molecular structures of Tdp1 inhibitors containing adamantane and terpene moieties.

Figure 3. The molecular structures of Tdp1 inhibitors with a heterocyclic linker.

Scheme 1. Synthesis of starting heterocyclic compounds 16 and 17. Reagents and conditions: (a) THF, 0 °C, then r.t., (b) NaOH, H2O, Δ, (c) H2SO4 conc., r.t.

Scheme 2. Synthesis of bromides 19a–g and target 1,2,4-triazole derivatives 20a–g. Reagents and conditions: (a) NBS, PPh3, CH2Cl2, r.t., (b) PBr3, 0 °C, (Et2O for 18b, 18e, 18f and THF for 18d), (c) MeONa, MeOH, 60 °C.

Scheme 3. Synthesis of desired amides 25a–d and 26a. Reagents and conditions: (a) CrO3, H2SO4, acetone, H2O; (b) NaClO2, KH2PO4, DMSO, H2O, r.t.; (c) NaClO2, KH2PO4, H2O2, CH3CN, H2O, r.t.; (d) SOCl2, benzene, Δ; (e) toluene, Et3N, r.t.; (f) T3P, Py, EtOAc (r.t. for 25a,b, reflux for 25c,d); (g) 1-aminoadamantane, T3P, Py, EtOAc, r.t.

Scheme 4. The synthesis of amides 26b, 28a, 28d, and 29a was previously described [25]. Compounds 26c, 28b, 28c, and 28e–g were reported previously [40].

Figure 4. Sensitizing effect of 20c at 5 μM non-toxic concentration on the viability of HeLa cells.

Figure 5. The docked pose of 20a in the binding site of Tdp1 as predicted by the ChemPLP scoring function. (A) The predicted configuration is shown in the ball-and-stick format and the adjacent amino acid residues are depicted in the stick format; the hydrogen atoms are not shown for clarity. The amino acids forming the pocket accommodating the adamantine cage are Tyr204, His263, Lys269, Asn283, Ser399, His493 and Lys495; the lipophilic cleft occupied by the aliphatic monoterpene is made up by Pro461, Gly498 and Try590. (B) The protein surface is rendered; blue depicts regions with a partial positive charge on the surface; red depicts regions with a partial negative charge and grey shows neutral areas. The ligand occupies the catalytic binding pocket, blocking access to it.

Table 1

The results for the Tdp1 activity inhibition at 50% (IC₅₀) values of the derivatives. Additionally, the CC₅₀ (50% cytotoxic concentration) values are given for cervical cancer (HeLa) and colorectal (HCT-116, SW837) human cancer cell lines.

Structure		IC50, μM	CC50, μM HeLa	CC50, μM HCT-116	CC50, μM SW837
1,2,4-Triazole derivatives [Image omitted. Please see PDF.]
20a	[Image omitted. Please see PDF.]	0.54 ± 0.09	85 ± 23	27 ± 6	52 ± 6
20b	[Image omitted. Please see PDF.]	1.5 ± 0.3	>100	>100	41 ± 4
20c	[Image omitted. Please see PDF.]	5.3 ± 1.7	64 ± 6	16 ± 7	41 ± 6
20d	[Image omitted. Please see PDF.]	5.6 ± 0.6	31± 11	20 ± 9	17 ± 5
20e	[Image omitted. Please see PDF.]	6.2 ± 2.2	24 ± 16	15 ± 5	40 ± 4
20f	[Image omitted. Please see PDF.]	7.5 ± 1.8	15 ± 2	54 ± 5	46 ± 6
20g	[Image omitted. Please see PDF.]	0.57 ± 0.14	74 ± 17	34 ± 6	40 ± 4
1,3,4-Thiadiazole derivatives [Image omitted. Please see PDF.]
25a	[Image omitted. Please see PDF.]	0.35 ± 0.05	>100	>100	>100
25b	[Image omitted. Please see PDF.]	2.59 ± 0.48	>100	66 ± 6	83 ± 8
25c	[Image omitted. Please see PDF.]	0.45 ± 0.09	>100	>100	>100

Table 2

The effect of the Tdp1 inhibitors at 5 µM on the 50% cytotoxic concentration (CC₅₀) value of topotecan for HeLa cancer cells. The concentrations of the Tdp1 inhibitors are 5 µM for HeLa cells and ranged from 15 to 45 µM (concentration is given in parenthesis in µM) for the HCT-116 cancer cell line.

Compound	HeLa—CC50, μM	HCT116—CC50, nM
Topotecan	6.0	715.0
20a	4.5	650.0 (20)
20b	ND *	575.3 (20)
20c	1.9	460.0 (15)
20d	5.4	689.0 (15)
20e	ND	392.0 (15)
20f	2.8	715.0 (25)
20g	2.6	235.8 (20)
25a	4.9	455.7 (45)
25b	2.9	611.9 (20)
25c	3.6	486.0 (25)

* Not determined due to poor solubility.