Abstract
The mechanism of biological activity of various sulfur-containing compounds and sulfur fragments of both natural and synthetic origins is presented. Unique characteristics of organosulfur compounds that are present in natural plant products are considered to reveal the most efficient sulfur components of the natural origin. An insufficient efficiency of the pharmacological action of plant raw materials and undesirable effects indisputably confirm the topical character of research on the preparation of modified analogs of natural biologically active sulfur-containing compounds. The modern data on the development of new polytopic organosulfur compounds combining different redox-active functional groups in the structure, which should favor their efficiency and a decrease in side manifestations, are reviewed. Sulfur-containing metal complexes with antimicrobial, antiviral, and anticancer properties are among the most promising pharmacologically active compounds. In spite of the success achieved in this field of chemistry, the preparation of new target-oriented biodrugs based on bioessential metals (Cu, Zn, Se) and biomimetic organosulfur fragments remains to be an urgent problem. The developments in this direction should favor to understand mechanisms of the therapeutic action of new drugs and to prepare drugs of the new generation followed by their implementation in clinical practice.
REFERENCES
Liu, Y., Guo, Ch., Zang, E., et al., Journal of Future Foods, 2023, vol. 3, no. 3, p. 206.
Mohammadhosseini, M., Frezza, C., Venditti, A., et al., Nat. Prod. Res., 2022, vol. 36, p. 5091.
Akullo, J.O., Kiage, B., Nakimbugwe, D., et al., Heliyon, 2022, vol. 8, p. e10457.
Romeiras, M.M., Essoh, A.P., Catarino, S., et al., Heliyon, 2023, vol. 9, no. 4, p. e14651.
Haile, T., Cardoso, S.M., De Oliveira Raphaelli, C., et al., Ex Benth. Front. Pharmacol., 2021, vol. 12, p. 621536.
Amalraj, A. and Gopi, S., J. Tradit. Complement. Med., 2016, vol. 7, p. 347.
Anyasor, G.N., Ogunbiyi, B., and Akinlusin, I.A., Oxid. Antioxid. Med. Sci., 2017, vol. 6, no. 2, p. 25.
Morales-López, J., Centeno-Álvarez, M., Nieto-Camacho, A., et al., Pharm. Biol., 2016, vol. 55, no. 1, p. 233.
Block, E., Garlic and the Other Alliums. The Lore and the Science, Cambridge: RSC, 2010.
Foe, M.-Ch.N., Tchinang, T.F.K. Nyegue, A.M., et al., BMC Complement. Altern. Med., 2016, vol. 19, p. 117.
Sharma, D., Rani, R., Chaturvedi, M., et al., Int. J. Pharm. Pharm. Sci., 2018, vol. 10, no. 2, p. 116.
Pradeep, S.R. and Srinivasan, K., J. Basic Clin. Physiol. Pharmacol., 2017, p. 140.
Farag, M.A., Ali, S.E., Hodaya, R.H., et al., Molecules, 2017, vol. 22, no. 5, p. 761.
Colín-González, A.L. and Santamaría, A., Gastrointestinal Tissue, 2017, p. 275.
Martins, N., Petropoulos, S., and Ferreira, I.C.F.R., Food Chem., 2016, vol. 211, p. 41.
Ryu, J.H. and Kang, D., Molecules, 2017, vol. 22, no. 6, p. 919.
Krstin, S., Sobeh, M., Braun, M.S., et al., Medicines, 2018, vol. 5, p. 37.
Mellado-García, P., Maisanaba, S., Puerto, M., et al., Food Chem. Toxicol., 2017, vol. 99, p. 231.
DeLeon, E.R., Gao, Y., Huang, E., et al., Am. J. Physiol. Regul. Integr. Comp. Physiol., 2016, vol. 310, p. 1212.
Karunanidhi, A., Ghaznavi-Rad, E., Nathan, J.J., et al., Molecules, 2019, vol. 24, p. 1003.
Leontiev, R., Hohaus, N., Jacob, C., et al., Scientific RePortS, 2018, vol. 8, p. 6763.
Al-Malki, A.L., Complementary and Alternative Medicine, 2016, vol. 2016, p. 7687915.
Curtis, H., Noll, U., Störmann, J., et al., Physiol. Mol. Plant Pathol., 2004, vol. 65, p. 79.
Albrecht, F., Leontiev, R., Jacob, C., et al., Molecules, 2017, vol. 22, no. 5, p. 770.
Reiter, J., Levina, N., Linden, M., et al., Molecules, 2017, vol. 22, no. 10, p. 1711.
Ilić, D.P., Nikolić, V.D., Nikoli’ć, L.B., et al., FU Phys. Chem. Technol., 2011, vol. 9, p. 9.
Gruhlke, M.C.H., Antelmann, H., Bernhardt, J., et al., Free Radical Biol. Med., 2019, vol. 131, p. 144.
Ko, J.-W., Shin, J.-Y., Kim, J.-W., et al., Food Chem. Toxicol., 2017, vol. 102, p. 156.
Ko, J.-W., Jeong, S.-H., Kwon, H.-J., et al., Nutrients, 2018, vol. 10, p. 1659.
Somade, O.T., Adedokun, A.H., Adeleke, I.K., et al., Clin. Nutr. Exp., 2019, vol. 23, p. 44.
Chu, Ch.-Ch., Wu, W.-Sh., Shieh, J.-P., et al., J. Funct. Biomater., 2017, vol. 8, p. 5.
Asdaq, S.M.B. and Avula, P.R., J. Pharm. Biol., 2015, vol. 5, no. 1, p. 44.
Sujithraa, K., Srinivasana, S., Indumathia, D., et al., Biomed. Pharmacother., 2018, vol. 107, p. 292.
Kodera, Y., Ushijima, M., Amano, H., et al., Molecules, 2017, vol. 22, no. 4, p. 570.
Tsukioka, T., Takemura, Sh., Minamiyama, Y., et al., Molecules, 2017, vol. 22, no. 4, p. 543.
Sajitha, G.R., Augusti, K.T., and Jose, R., Ind. J. Clin. Biochem., 2016, vol. 31, no. 3, p. 260.
Feng, M., Tang, B., Liang, S.H., et al., Curr. Top. Med. Chem., 2016, vol. 16, no. 11, p. 1200.
Gilgunsherki, Y., Rosenbaum, Z., Melamed, E., et al., Pharmacol. Rev., 2002, vol. 54, p. 271.
Cressier, D., Prouillac, C., Hernandez, P., et al., Bioorg. Med. Chem., 2009, vol. 17, p. 5275.
Shi, F., Li, Ch., Xia, M., et al., Bioorg. Med. Chem., 2009, vol. 19, p. 5565.
Kumar, S., Engman, L., Valgimigli, L., et al., J. Org. Chem., 2007, vol. 72, p. 6046.
Djukic, M., Fesatidou, M., Xenikakis, I., et al., Chem.-Biol. Interact., 2018, vol. 286, p. 119.
Kovacic, P. and Weston, W., Nov. Appro. Drug. Des. Dev., 2018, vol. 3, no. 3, p. 555612.
Stvolinsky, S.L., Antonova, N.A., Kulikova, OI., et al., Biochem. Moscow Suppl. Ser., 2018, vol. 12, p. 308.
Izmest’ev, E.S., Sudarikov, D.V., Shevchenko, O.G., et al., Russ. J. Bioorg. Chem., 2015, vol. 41, no. 1, p. 77.
Akhmedov, O.R., Shomurotov, Sh.A., Rakhmanova, G.G., et al., Russ. J. Bioorg. Chem., 2017, vol. 43, no. 7, p. 716.
Abbasi, M.A., Tariq, S., Aziz-ur-Rehman, et al., Russ. J. Bioorg. Chem., 2016, vol. 42, no. 2, p. 198.
AlMousawi, S.M., Moustafa, M.Sh., and Saleh, E.A., Russ. J. Bioorg. Chem., 2016, vol. 42, no. 4, p. 428.
Ghoraba, M.M. and Alsaid, M.S., Russ. J. Bioorg. Chem., 2016, vol. 42, no. 4, p. 441.
Empel, A., Kisiel, E., Wojtyczka, R.D., et al., Molecules, 2018, vol. 23, no. 1, p. 218.
Lubenets, V.I., Havryliak, V.V., Pylypets, A.Z., et al., Regulatory Mechanisms in Biosystems, 2018, vol. 9, no. 4, p. 495.
Gyrdymova, Yu.V., Izmest’ev, E.S., Rubtsova, S.A., et al., Russ. J.Org. Chem., 2016, vol. 52, no. 3, p. 332.
Gyrdymova, Yu.V., Demakova, M.Ya., Shevchenko, O.G., et al., Chem. Nat. Compd., 2017, vol. 53, p. 5.
Shefa, U., Kim, M.-S., Jeong, N.Y., et al., Oxid. Med. Cell. Longev., 2018, vol. 2018, p. 17.
Bolton, S.G., Cerda, M.M., Gilbert, A.K., et al., Free Radical Biol. Med., 2019, vol. 131, p. 393.
Chauvin, J.-Ph.R., Griesser, M., and Pratt, D.A., Chem. Sci., 2019, vol. 10, no. 19, p. 4999.
Bhattacherjee, D., Basu, C., Bhardwaj, Q., et al., ChemistrySelect, 2017, vol. 2, no. 24, p. 7399.
Siyo, V., Schäfer, G., Hunter, R., et al., Molecules, 2017, vol. 22, no. 6, p. 892.
Block, E., Bechand, B., Gundala, S., et al., Molecules, 2017, vol. 22, no. 12, p. 2081.
Saini, V., Manral, A., Arora, R., et al., Pharmaco. Rep., 2017, vol. 69, p. 813.
Gyrdymova, Yu.V., Sudarikov, D.V., Shev-chenko, O.G., et al., Chem. Biodiversity, 2017, vol. 14, p. e1700296.
Jacob, C., Giles, G.I., Giles, N.M., et al., Angew. Chem., 2003, vol. 115, p. 4890.
Pestova, S.V., Izmest’ev, E.S., Shevchenko, O.G., et al., Russ. J. Bioorg. Chem., 2017, vol. 43, no. 3, p. 302.
Prosenko, A.E., Terakh, E.I., Gorokh, E.A., et al., Russ. J. Appl. Chem., 2003, vol. 76, no. 2, p. 248.
Osipova, V., Polovinkina, M., Osipova, A., et al., Turk. J. Chem., 2019, vol. 43, p. 1336.
Osipova, V., Polovinkina, M., Gracheva, Yu., et al., A-rab. J. Chem., 2021, vol. 14, p. 103068.
Osipova, V., Gracheva, Yu., Polovinkina, M., et al., Molecules, 2022, vol. 27, p. 3961.
Chukicheva, I.Y., Buravlev, E.V., Fedorova, I.V., et al., Russ. Chem. Bull., 2010, vol. 59, no. 12, p. 2276.
Chukicheva, I.Yu., Fedorova, I.V., Buravlev, E.V., et al., Chem. Nat. Comp., 2010, no. 3, p. 478.
Buravlev, E.V., Chukicheva, I.Y., Kutchin, A.V., et al., Lett. Org. Chem., 2011, vol. 8, no. 5, p. 301.
Chukicheva, I.Yu., Shumova, O.A., Shev-chenko, O.G., et al., Russ. Chem. Bull., 2016, vol. 65, no. 3, p. 721.
Pestova, S.V., Izmest’ev, E.S., Shevchenko, O.G., et al., Russ. Chem. Bull., 2015, vol. 64, no. 3, p. 723.
Peng, Ch., Wu, K., Chen, X., et al., Clinical Breast Cancer, 2023, vol. 23, no. 3, p. 122.
Bodewes, F.T.H., van Asselt, A.A., Dorrius, M.D., et al., The Breast, 2022, vol. 66, p. 62.
Global Burden of Disease 2019 Cancer Collaboration, JAMA Oncol., 2022, vol. 8, no. 3, p. 420.
Bray, F., Ferlay, J., Soerjomataram, I., et al., CA. A. Cancer J. Clin., 2018, vol. 68, no. 6, p. 394.
Siegel, R.L., Miller, K.D., and Jemal, A., CA. A. Cancer J. Clin., 2019, vol. 69, p. 7.
Jardim, B.V., Moschetta, M.G., Leonel, C., et al., Oncol. Rep., 2013, vol. 30, no. 3, p. 1119.
Wong, E. and Giandornenico, C.M., Chem. Rev., 1999, vol. 99, p. 2451.
Dilruba, S. and Kalayda, G.V., Cancer Chemother. Pharmacol., 2016, vol. 77, p. 1103.
Fanelli, M., Formica, M., Fusi, V., et al., Coord. Chem. Rev., 2016, vol. 310, p. 41.
Omondi, R.O., Ojwach, S.O., and Jaganyi, D., Inorg. Chim. Acta, 2020, vol. 512, p. 119883.
Rahiminezhad, A., Moghadam, M.E., Divsalar, A., et al., J. Mol. Model., 2022, vol. 28, p. 2.
Wheate, N.J., Walker, S., Craig, G.E., et al., Dalton Trans., 2010, vol. 39, p. 8113.
Jia, Ch., Deacon, GB., Zhang, Y., et al., Coord. Chem. Rev., 2021, vol. 429, p. 213640.
Paprocka, R., Wiese-Szadkowska, M., Janciauskiene, S., et al., Coord. Chem. Rev., 2022, vol. 452, p. 214307.
Ndagi, U., Mhlongo, N., and Soliman, M.E., Drug Des. Devel. Ther., 2017, vol. 11, p. 599.
Khanfar, M.A., Jaber, A.M., AlDamen, M.A., et al., Molecules, 2018, vol. 23, p. 701.
Barry, N.P.E. and Sadler, P.J., Chem. Commun., 2013, vol. 49, p. 5106.
Perontsis, S., Geromichalou, E., Perdih, F., et al., J. Inorg. Biochem., 2020, p. 111213.
Lutsenko, I.A., Nikiforova, M.E., Koshenskova, K.A., et al., Russ. J. Coord. Chem., 2021, vol. 47, p. 881.
Ngwane, A.H., Petersen, R.-D., Baker, B., et al., IUBMB Life, 2019, vol. 71, no. 5, p. 523.
Jovanović, S., Obrenčević, K., Bugarčić, Ž.D., et al., Dalton Trans., 2016, vol. 45, p. 12444.
Banerjee, S. and Mukherjee, A.K., Comput. Theor. Chem., 2012, vol. 991, p. 116.
Ortega, A.L., Mena, S., and Estrela, J.M., Cancers, 2011, vol. 3, no. 1, p. 1285.
Wehr-Candler, T. and Henderson, W., Coord. Chem. Rev., 2016, vol. 313, p. 111.
Moosun, S.B., Blair, L.H., Coles, S.J., et al., Z. Anorg. Allg. Chem., 2015, vol. 641, p. 890.
Vivekananda, K.V., Dey, S., Wadawale, A., et al., Eur. J. Inorg. Chem., 2014, vol. 12, p. 2153.
Dai, C., Xu, Z., Huang, F., et al., Org. Chem., 2012, vol. 77, p. 4414.
Gilbert, J.G., Addison, A.W., Nazarenko, A.Y., et al., Inorg. Chim. Acta, 2001, vol. 324, nos 1-2, p. 123.
Jin, M., Li, C., Zhang, Q., et al., Oncol. Lett., 2018, vol. 15, no. 6, p. 8454.
Sun, J., Chen, Y., Li, K., et al., Acta Biomater., 2016, vol. 43, p. 282.
Bhaduri, R., Mandal, S., Tarai, S.K., et al., J. Mol. Liq., 2022, vol. 360, p. 119529.
Mukherjee, S., Reddy, V.P., Mitra, I., et al., Polyhedron, 2017, vol. 124, p. 251.
Gao, E.J., Guan, F., Gao, X.N., et al., J. Biol. Inorg. Chem., 2012, vol. 17, p. 263.
Beloglazkina, E.K., Manzheliy, E.A., Moiseeva, A.A., et al., Polyhedron, 2016, vol. 107, p. 27.
Furrer, J. and Süss-Fink, G., Coord. Chem. Rev., 2016, vol. 309, p. 36.
Liu, S.-H., Xu, H.-H., Zhu, J.-W., et al., Polyhedron, 2016, vol. 105, p. 12.
Beloglazkina, E.K., Majouga, A.G., Manzheliy, E.A., et al., Polyhedron, 2015, vol. 85, p. 800.
Majouga, A.G., Zvereva, M.I., Rubtsova, M.P., et al., J. Med. Chem., 2011, vol. 57, no. 14, p. 6252.
Gasser, G., Ott, I., and Metzler-Nolte, N., J. Med. Chem., 2011, vol. 54, no. 1, p. 3.
Dougan, S.J. and Sadler, P.J., CHIMIA Intern. J. Chem., 2007, vol. 61, no. 11, p. 704.
Aird, R.E., Cumkings, J., Ritchie, A.A., et al., Br. J. Cancer, 2002, vol. 86, no. 10, p. 1652.
Camm, K.D., El-Sokkary, A., Gott, A.L., et al., Dalton Trans., 2009, vol. 48, p. 10914.
Rilak, A., Puchta, R., and Bugarčic, Z.D., Polyhedron, 2015, vol. 91, p. 73.
Peacock, A.F.A., Melchart, M., Deeth, R.J., et al., Chem.-Eur. J., 2007, vol. 13, p. 2601.
Kandioller, W., Hartinger, C.G., Nazarov, A.A., et al., Chem.-Eur. J., 2009, vol. 28, p. 4249.
Kandioller, W., Hartinger, C.G., Nazarov, A.A., et al., Chem.-Eur. J., 2009, vol. 15, p. 12283.
Enyedy, É.A., Sija, É., Jakusch, T., et al., J. Inorg. Biochem., 2013, vol. 127, p. 161.
Trondl, R., Heffeter, P., Kowol, C.R., et al., Chem. Sci., 2014, vol. 5, p. 2925.
Ramachandran, R., Prakash, G., Selvamurugan, S., et al., Dalton Trans., 2014, vol. 43, no. 21, p. 7889.
Saswati, Chakraborty, A. Dash, S.P., et al., Dalton Trans., 2015, vol. 44, p. 6140.
Vijayan, P., Viswanathamurthi, P., Sugumar, P., et al., Inorg. Chim. Acta, 2016, vol. 453, p. 596.
Dimitrijević, J., Arsenijević, A.N., Milovanović, M.Z., et al., J. Inorg. Biochem., 2020, vol. 208, p. 111078.
Deng, J., Yu, P., Zhang, Z., et al., Eur. J. Med. Chem., 2018, vol. 158, p. 442.
Denoyer, D., Masaldan, S., La Fontaine, S., et al., Metallomics, 2015, vol. 7, p. 1459.
Zivanović, A.S., Bukonjić, A.M., Jovanović-Stević, S., et al., J. Inorg. Biochem., 2022, vol. 233, p. 111861.
Ali, M.H., Zaghloul, I., and Khalid, M.W., Org. Med. Chem. IJ, 2020, vol. 9, no. 4, p. 555767.
Mishra, N., Gound, S.S., Mondal, R., et al., Res. Chem., 2019, vol. 1, p. 100006.
Lobana,T.S., Sharma, R., Bawa, G., et al., Coord. Chem. Rev., 2009, vol. 253, p. 977.
Easmon, J., Pürstinger, G., Heinisch, G., et al., J. Med. Chem., 2001, vol. 44, no. 13, p. 2164.
Raja, D.S., Bhuvanesh, N.S.P., and Natarajan, K., Eur. J. Med. Chem., 2011, vol. 46, p. 4584.
Al-Khodir, F.A. and Refat, M.S., J. Mol. Struct., 2016, vol. 1119, p. 157.
Sahyon, H., El-Bindary, A., Shoair, A., et al., J. Mol. Liq., 2018, vol. 255, p. 122.
Santini, C., Pellei, M., Gandin, V., et al., Chem. Rev., 2013, vol. 114, no. 1, p. 815.
Sharfalddina, A. and Hussien, M.A., J. Mol. Struct., 2021, vol. 1228, p. 129725.
Das, D., Roy, G., and Mugesh, G., J. Med. Chem., 2008, vol. 51, no. 22, p. 7313.
López-Saucedo, F., Flores-Rojas, G.G., González-Sebastián, L., et al., Inorg. Chim. Acta, 2018, vol. 473, p. 83.
Čorić, I. and Holland, P.L., J. Am. Chem. Soc., 2016, vol. 138, no. 23, p. 7200.
Chohan, Z.H., Rauf, A., Noreen, S., et al., J. Enzyme Inhib. Med. Chem., 2002, vol. 17, p. 101.
Chandra, S., Jain, D., Sharma, A.K., et al., Molecules, 2009, vol. 14, p. 174.
Soltani, B., Ghorbanpour, M., and Ziegler, C.J., et al., Polyhedron, 2020, vol. 180, p. 114423.
Ozturk, I.-I., Urgut, O.-S., Banti, C.-N., et al., Polyhedron, 2014, vol. 70, p. 172.
Mjos, K.-D. and Orvig, C., Chem. Rev., 2014, vol. 114, p. 4540.
Hadjikakou, S.-K., Ozturk, I.-I., Banti, C.-N., et al., J. Inorg. Biochem., 2015, vol. 153, p. 293.
Sharma, P., Perez, D., Cabrera, A., et al., Acta Pharmacol. Sin., 2008, vol. 29, p. 881.
Rani, P.J., Thirumaran, S., and Ciattini, S., Phosphorus Sulfur Silicon Relat. Elem., 2013, vol. 188, p. 778.
Beniwal, S., Kumar, A., Chhimpa, S., et al., Phosphorus Sulfur Silicon Relat. Elem., 2019, vol. 194, no. 9, p. 879.
Awang, N., Kamaludin, N.F., and Ghazali, A.R., Pak. J. Biol. Sci., 2011, vol. 14, no. 15, p. 768.
Verginadis, I.I., Karkabounas, S., Simos, Y., et al., Eur. J. Pharm. Sci., 2011, vol. 42, no. 3, p. 253.
Balas, V.I., Verginadis, I.I., Geromichalos, G.D., et al., Eur. J. Med. Chem., 2011, vol. 46, no. 7, p. 2835.
Fakhar, I., Yamin, B.M., and Hasbullah, S.A., Chem. Cent. J., 2017, vol. 11, p. 76.
Ghorab, M.M., Alsaid, M.S., Al-Dosary, M.S., et al., Chem. Cent. J., 2016, vol. 10, p. 19.
Hassan, S.S., Shallan, R.N., and Salama, M.M., J. Organomet. Chem., 2020, vol. 911, p. 121115.
Eweis, M., Elkholy, S.S., and Elsabee, M.Z., Int. J. B-iol. Macromol., 2006, vol. 38, no. 1, p. 1.
Shpakovsky, D.B., Banti, C.N., Beaulieu-Houle, G., et al., Dalton Trans., 2012, vol. 41, p. 14568.
Shpakovsky, D.B., Banti, C.N., and Mukhatova, E.M., et al., Dalton Trans., 2014, vol. 43, p. 6880.
Ahrweiler-Sawaryn, M.-C., Biswas, A., Frias, C., et al., Biomed. Harmacother., 2023, vol. 161, p. 114507.
Ott, I., Coord. Chem. Rev., 2009, vol. 253, nos. 11–12, p. 1670.
Madeira, J.M., Gibson, D.L., Kean, W.F., et al., Inflammopharmacology, 2012, vol. 20, p. 297.
Shpakovsky, D.B., Shtil, A.A., Kharitonashvili, E.V., et al., Metallomics, 2018, vol. 10, p. 406.
Bormio Nunes, J.H., Simoni, D.A., Braga, Lü, E.O., et al., J. Mol. Struct., 2019, vol. 1178, p. 169.
Milacic, V., Fregona, D., and Dou, Q.P., Histol. Histopathol., 2008, vol. 23, no. 1, p. 101.
Zou, T., Lum, C.T., Lok, C.-N., et al., Chem. Soc. Rev., 2015, vol. 44, no. 24, p. 8786.
González-Barcia, L.M., Fernández-Fariña, S., Rodríguez-Silva, L., et al., J. Inorg. Biochem., 2020, vol. 203, p. 110931.
Schleser, S.W., Ghosh, H., Hörner, G., et al., Int. J. Mol. Sci., 2023, vol. 24, no. 6, p. 5738.
Oliveira, L.B., Favarin, L.R.V., Araújo, V.O., et al., Polyhedron, 2022, vol. 213, p. 115626.
Funding
This work was supported by the Research, Design, and Engineering Developments (state registration no. 123031400121-0) in the framework of the state assignment approved by FAR (section “Most Important Biologically Active Organosulfur Compounds of Plant Raw Materials”) and Russian Science Foundation (grant no. 23-13-00201) (sections “Pharmacologically Active Modified Analogs of Natural Organosulfur Compounds” and “Sulfur-Containing Metal Complexes as Promising Anticancer Agents”).
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Osipova, V.P., Berberova, N.T. Organic Sulfur Derivatives and Their Metal Complexes as Promising Pharmacologically Active Compounds. Russ J Coord Chem 49 (Suppl 2), S196–S232 (2023). https://doi.org/10.1134/S1070328423600894
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DOI: https://doi.org/10.1134/S1070328423600894