Zobrazeno 1 - 10
of 15
pro vyhledávání: '"M. L. Kakhabrishvili"'
Publikováno v:
Chemistry of Natural Compounds. 58:178-180
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ead97463b71c2bced0ae49d2a5916a7
https://doi.org/10.1007/s10600-022-03628-7
https://doi.org/10.1007/s10600-022-03628-7
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f89fff5bb794ae43318283398c7e577f
https://doi.org/10.1007/s10600-021-03370-6
https://doi.org/10.1007/s10600-021-03370-6
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::37998f5a5d4680e22224389f5e72f26d
https://doi.org/10.1007/s10600-018-2514-9
https://doi.org/10.1007/s10600-018-2514-9
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77259a2b9d29d26b927f82269074e007
https://doi.org/10.1007/s10600-018-2330-2
https://doi.org/10.1007/s10600-018-2330-2
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,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6eb26e19f6ed2f67337b470b78068f74
https://doi.org/10.1007/s10600-016-1795-0
https://doi.org/10.1007/s10600-016-1795-0
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.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::13dc198c2b4845021b51dbf0565871c8
https://doi.org/10.1007/s10600-016-1669-5
https://doi.org/10.1007/s10600-016-1669-5
Publikováno v:
Chemistry of Natural Compounds. 48:423-425
The semicarbazone and isonicotinoylhydrazone of 5α-pregn-2-en-20-one, which was prepared from 3β-acetoxy-5α-pregn-16-en-20-one, were synthesized for the first time. The antituberculosis activity of these and semicarbazones and isonicotinoylhydrazo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::24e49f9c05c1a591dba47eaa7ca27e49
https://doi.org/10.1007/s10600-012-0265-6
https://doi.org/10.1007/s10600-012-0265-6
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6a57fded153ad489594c9e82987f6fff
https://doi.org/10.1007/s10600-014-1151-1
https://doi.org/10.1007/s10600-014-1151-1
Publikováno v:
Chemistry of Natural Compounds. 43:753-755
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f98e7ba526129f9085592e0e6c5a86ba
https://doi.org/10.1007/s10600-007-0258-z
https://doi.org/10.1007/s10600-007-0258-z
Autor:
Nana N. Barbakadze, M. L. Kakhabrishvili, M. I. Sikharulidze, K. G. Mulkidzhanyan, N. Sh. Nadaraia
Publikováno v:
Chemistry of Natural Compounds. 46:493-494
Steroidal oximes and their derivatives are known to exhibit anti-inflammatory, anticancer, and other types of physiological activity [1, 2]. In continuation of structure–activity relationship studies of 5 -steroids [3], we synthesized steroidal oxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::286311af6dfb4e443a8cce0dc3e6befd
https://doi.org/10.1007/s10600-010-9657-7
https://doi.org/10.1007/s10600-010-9657-7