Zobrazeno 1 - 10
of 12
pro vyhledávání: '"N N, Barbakadze"'
Publikováno v:
Chemistry of Natural Compounds. 58:178-180
Autor:
Jean Legault, N. Sh. Nadaraia, N. N. Barbakadze, André Pichette, Vakhtang Mshvildadze, B. Sylla
Publikováno v:
Chemistry of Natural Compounds. 56:274-277
Two series of hydrazones were synthesized from 3β-hydroxy- and 3β-(1-adamantoate)-5α-androstan-17- one, respectively, to study the structure–activity relationship. Cytotoxicity studies showed that 5α-androstan- 3β-ol-17-one m-nitrobenzoylhydra
Autor:
M. L. Kakhabrishvili, Vakhtang Mshvildadze, N. N. Barbakadze, N. Sh. Nadaraia, André Pichette, K. G. Mulkidzhanyan
Publikováno v:
Chemistry of Natural Compounds. 57:395-397
Autor:
N. N. Barbakadze, B. Sylla, M. L. Kakhabrishvili, N. Sh. Nadaraia, André Pichette, Vakhtang Mshvildadze, Jean Legault
Publikováno v:
Chemistry of Natural Compounds. 54:926-929
Steroidal hydrazones and pyrazolines were synthesized via condensation of a series of 5α-steroidal ketones with several hydrazines. Their cytotoxic activity against cancer cultures (A549 lung cancer, DLD-1 colorectal cancer, and WS1 normal skin fibr
Autor:
B. Sylla, N. N. Barbakadze, André Pichette, N. Sh. Nadaraia, M. L. Kakhabrishvili, U. S. Makhmudov
Publikováno v:
Chemistry of Natural Compounds
Several new N-containing epiandrosterone derivatives modified by phenylacetic acid chloride were synthesized for biological activity studies. Compounds with antiviral activity were discovered among them and 3β-hydroxy-1'-aryl-3'-methyl-5'-androstano
Autor:
N. Sh. Nadaraia, André Pichette, N. N. Barbakadze, M. L. Kakhabrishvili, B. Sylla, E. O. Onashvili
Publikováno v:
Chemistry of Natural Compounds
A study of the antiviral activity of several new hydrazones and amines and amides of 5α-steroids that were synthesized by us earlier found highly and moderately active compounds. The structures of the synthesized compounds were proven using IR, PMR,
Publikováno v:
Chemistry of Natural Compounds. 52:445-447
New peptide derivatives of 17β-amino-5α-androstan-3β-ol were synthesized. Their structures were elucidated using PMR and 13C NMR spectra and elemental analyses.
Autor:
N. N. Barbakadze, M. Z. Getia, E. O. Onashvili, M. I. Sikharulidze, André Pichette, M. L. Kakhabrishvili, N. Sh. Nadaraia, U. S. Makhmudov
Publikováno v:
Chemistry of Natural Compounds.
New androstanopyrazolines and hydrazones were synthesized via acid-catalyzed condensation of the tigogenin transformation product 5α-pregnenolone with several hydrazines. Their structures were proved using IR and NMR spectroscopy and mass spectromet
Autor:
N. O. Narimanidze, I. Sh. Chikvaidze, D. O. Kadzhrishvili, Sh. A. Samsoniya, N. N. Barbakadze
Publikováno v:
Chemistry of Heterocyclic Compounds. 46:765-767
Autor:
Merlani M; TSMU I, Kutateladze Institute of Pharmacochemistry, Tbilisi, Georgia., Nadaraia N; TSMU I, Kutateladze Institute of Pharmacochemistry, Tbilisi, Georgia., Barbakadze N; TSMU I, Kutateladze Institute of Pharmacochemistry, Tbilisi, Georgia., Amiranashvili L; TSMU I, Kutateladze Institute of Pharmacochemistry, Tbilisi, Georgia., Kakhabrishvili M; TSMU I, Kutateladze Institute of Pharmacochemistry, Tbilisi, Georgia., Petrou A; School of Pharmacy, Aristotle University of Thessaloniki, Thessaloniki, Greece., Carević T; Department of Plant Physiology, Institute for Biological Research 'Siniša Stanković' - National Institute of Republic of Serbia, University of Belgrade, Belgrade, Serbia., Glamočlija J; Department of Plant Physiology, Institute for Biological Research 'Siniša Stanković' - National Institute of Republic of Serbia, University of Belgrade, Belgrade, Serbia., Geronikaki A; School of Pharmacy, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Publikováno v:
SAR and QSAR in environmental research [SAR QSAR Environ Res] 2024 Feb; Vol. 35 (2), pp. 137-155. Date of Electronic Publication: 2024 Feb 05.