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1.
The antioxidant activity of flavonoids // Pharm. World and Sci., 1995. Vol. 17, N 3 Suppl. G.-С.4

2.
Schulz William G. Pyrrolo[1,2-'альфа']benzimidazole-based quinones and iminoquinones. The role of the 3-substituent on cytotoxicity // J. Med. Chem., 1995. Vol. 38, N 1.-С.109-118

3.
Structure-activity relationships in risk assessment of carcinogens // Hum. and Exp. Toxicol., 1995. Vol. 14, N 6.-С.521

4.
Saas Ph. Structure-activity relationships and immunosuppression // Hum. and Exp. Toxicol., 1995. Vol. 14, N 6.-С.524

5.
Эритрогеноцитостатики на основе трансформированных стероидов с гормональными и антигормональными свойствами // 2 Рос. нац. конгр. "Человек и лекарство", Москва, 10-15 апр., 1995. -М., 1995.-С.204

6.
Saas Ph. Structure-activity relationships and immunosuppression // Hum. and Exp. Toxicol., 1995. Vol. 14, N 6.-С.524

7.
Fountain K.R. Quantification of the three point receptor hypothesis of cheng and Zee-Cheng // J. Theor. Biol., 1995. Vol. 173, N 4.-С.329-337

8.
Antitumorigenic activities of chalcones I: Inhibitory effects of chalcone derivatives on {32}Pi-incorporation into phospholipids of HeLa cells promoted by 12-O-tetradecanoyl-phorbol 13-acetate (TPA) // Biol. and Pharm. Bull., 1995. Vol. 18, N 12.-С.1710-1713

9.
Structure-activity relationships of anew family of steroidal aromatase inhibitors 1: Synthesis and evaluation of a series of analogs related to 19-[(methylthio)methyl]androstenedione (RU54115) // J. Med. Chem., 1996. Vol. 39, N 3.-С.757-772

10.
Possible functional groups responsible for inhibition of in vivo angiogenesis by herbimycin A // Biol. and Pharm. Bull., 1994. Vol. 17, N 10.-С.1430-1432

11.
Aplyronine A, a potent antitumor substance of marine origin, aplyronines B and C, and artificial analogues: Total synthesis and structure - cytotoxicity relationships // J. Org. Chem., 1996. Vol. 61, N 16.-С.5326-5351

12.
The essential role of the functional group in alkyl isothiocyanates for inhibition of tobacco nitrosamine-induced lung tumorigenesis // Carcinogenesis, 1996. Vol. 17, N 4.-С.755-759

13.
Possible functional groups responsible for inhibition of in vivo angiogenesis by herbimycin A // Biol. and Pharm. Bull., 1994. Vol. 17, N 10.-С.1430-1432

14.
The essential role of the functional group in alkyl isothiocyanates for inhibition of tobacco nitrosamine-induced lung tumorigenesis // Carcinogenesis, 1996. Vol. 17, N 4.-С.755-759

15.
Поиск противоопухолевых соединений в ряду производных актиноцина // Хим.-фармац. ж., 1996. Т. 30, N 12.-С.22-26

16.
Site of action of two novel pyrimidine biosynthesis inhibitors accurately predicted by the compare program // Biochem. Pharmacol., 1995. Vol. 49, N 7.-С.947-954

17.
Correlations between topological resonance energy of methyl-substituted benz[c]acridines, benzo [a] phenothiazines and chrysenes, and their carcinogenic or antitumor activities // Anticancer Res., 1996. Vol. 16, N 5a.-С.2757-2765

18.
Correlations between topological resonance energy of methyl-substituted benz[c]acridines, benzo [a] phenothiazines and chrysenes, and their carcinogenic or antitumor activities // Anticancer Res., 1996. Vol. 16, N 5a.-С.2757-2765

19.
Antiproliferative and angiostatic activity of suramin analogues // Cancer Res., 1995. Vol. 55, N 21.-С.4957-4961

20.
Correlations between topological resonance energy of methyl-substituted benz[c]acridines, benzo [a] phenothiazines and chrysenes, and their carcinogenic or antitumor activities // Anticancer Res., 1996. Vol. 16, N 5a.-С.2757-2765

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