Zobrazeno 1 - 9
of 9
pro vyhledávání: '"MEENAKSHI DEODHAR"'
Publikováno v:
Journal of Research in Pharmacy. 26:1703-1712
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::893fc644fbd49e72f841e2e8fb907f33
https://doi.org/10.29228/jrp.261
https://doi.org/10.29228/jrp.261
Publikováno v:
Medicinal Chemistry Research. 22:4316-4321
A series of substituted benzo[d]thiazol-2-ylcarbamates 4a–g and 5a–g were synthesized and evaluated for anticonvulsant activity. The structures of the synthesized compounds were confirmed on the basis of their physical and spectral data. The comp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::506cab55b5c66fd42ae369e6a810dc29
https://doi.org/10.1007/s00044-012-0434-y
https://doi.org/10.1007/s00044-012-0434-y
Autor:
Meenakshi Deodhar, Vishakha Bansode
Publikováno v:
E-Journal of Chemistry, Vol 9, Iss 4, Pp 2079-2088 (2012)
A series of the title compounds 3-(4-(4, 5-dihydro-5-(substituted phenyl)-1H-3-pyrazolyl) phenylimino) methyl)-4-chloro-2H-chromen-2-one 5(a-g) have been synthesized. These compounds were characterized on the basis of their spectral (IR,1H NMR) data
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e572f33881b0b092043602ab5c41c33a
https://doaj.org/article/559a6628180d4213814b4486a23a493e
https://doaj.org/article/559a6628180d4213814b4486a23a493e
Autor:
Sayali D. Kudale, Meenakshi Deodhar
Publikováno v:
E-Journal of Chemistry, Vol 9, Iss 4, Pp 2493-2500 (2012)
A series of the Schiff’s bases incorporating coumarin and chalcone moeities, 3-(4-(4-(substituted phenyl)prop-1-ene-3-one) phenylimino) methyl)-4-chloro-2h-chromen-2-one 4(a-g) were synthesized as potential antimicrobial agents. These compounds wer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fde8b68e7d4eb4e1e278e63e7bb0da2
https://doaj.org/article/32179f03a7c64fde85ee672225411cad
https://doaj.org/article/32179f03a7c64fde85ee672225411cad
Publikováno v:
Medicinal Chemistry Research. 21:27-37
A series of new heterocyclic derivatives having a pyridine nucleus were synthesized. 4-(5-(2-Chlorophenyl)-4H-1,2,4-triazol-3-yl)pyridine (7c) and 4-(5-(2-Nitrophenyl)-4H-1,2,4-triazol-3-yl)pyridine (7d) presented the best analgesic profie of this se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fd929d61ff1c347261f7b2d25a504444
https://doi.org/10.1007/s00044-010-9489-9
https://doi.org/10.1007/s00044-010-9489-9
Publikováno v:
International Journal of Pharmacy and Pharmaceutical Sciences. 10:57
Objective : A new series 2-phenyl-3-(substituted benzo[ d ] thiazol-2-ylamino)-quinazoline-4(3 H )-one was prepared by the fusion method by reacting 2-phenyl benzoxazine with 2-hydrazino benzothiazole and it was evaluated for their antimicrobial acti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8e096ccb395c06d4aae53d02c91cff4d
https://doi.org/10.22159/ijpps.2018v10i10.28480
https://doi.org/10.22159/ijpps.2018v10i10.28480
Publikováno v:
Medicinal Chemistry Research. 18:421-432
From the earlier quantitative structure–activity relationship (QSAR) and molecular modeling studies, a series of quinoline derivatives 5a–h mimicking terbinafine and containing different bulky aromatic rings in the side chain were designed using
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68e7150fc33513132b11d2a41df4f578
https://doi.org/10.1007/s00044-008-9138-8
https://doi.org/10.1007/s00044-008-9138-8
Publikováno v:
E-Journal of Chemistry, Vol 6, Iss 3, Pp 759-762 (2009)
4-Chloro-2-oxo-2H-chromene-3-carbaldehyde(2)was reacted with different anilines in rectified spirit as solvent to yield a series of the title compoundsi.e. 4-chloro-3-((substituted-phenylimino) methyl)-2H-chromen-2-one(3a-i). These compounds were cha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f21825ea47c7d464676fb29d75fc5a5c
Publikováno v:
Turkish Journal of Chemistry.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0db28c74c28229b1303e118e5cf119e9
https://doi.org/10.3906/kim-0711-18
https://doi.org/10.3906/kim-0711-18