Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Ch Camoutsis"'
Publikováno v:
Journal of Heterocyclic Chemistry; September 1997, Vol. 34 Issue: 5 p1597-1601, 5p
Publikováno v:
Journal of Heterocyclic Chemistry. 35:731-759
The present review considers new useful heterocyclosteroids which contain five-membered heterocyclic systems, namely, isoxazoles, isoxazolines and isoxazolidines, condensed to the cyclopentanoperhy-drophenanthrene skeleton, in different positions of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::92eb782030afe7656e22f06db697def4
https://doi.org/10.1002/jhet.5570350401
https://doi.org/10.1002/jhet.5570350401
Publikováno v:
Anti-Cancer Drugs. 8:73-79
The alkylating agent m-N,N-bis(2-chloroethyl)aminocinnamic acid (m-ACA) and four new homo-aza-steroidal esters were studied for their ability to induce chromosomal abnormalities and to affect protein synthesis in human lymphocytes in vitro. A mitotic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::884a6b2b1923e306cb9f90bacafda231
https://doi.org/10.1097/00001813-199701000-00010
https://doi.org/10.1097/00001813-199701000-00010
Autor:
Marina Soković, Constantinos Potamitis, Panagiotis Zoumpoulakis, A. Pitsas, George Pairas, Ch. Camoutsis, Jasmina Glamočlija
Publikováno v:
Bioorganicmedicinal chemistry. 20(4)
The significant antifungal activity of a series of sulfonamide-1,2,4-triazole and 1,3,4-thiazole derivatives against a series of micromycetes, compared to the commercial fungicide bifonazole has been reported. These compounds have also shown a compar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d9f9c1fe873dbf5e1394dd94564bb4c
https://pubmed.ncbi.nlm.nih.gov/22264752
https://pubmed.ncbi.nlm.nih.gov/22264752
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b34838d70dda214a9d31c8a1d5171ab
https://doi.org/10.1002/chin.199204254
https://doi.org/10.1002/chin.199204254
Publikováno v:
ChemInform. 23
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5c91c37c28c4adc5c4e8f384732eb1c5
https://doi.org/10.1002/chin.199204088
https://doi.org/10.1002/chin.199204088
Publikováno v:
ChemInform. 29
The present review considers new useful heterocyclosteroids which contain five-membered heterocyclic systems, namely, isoxazoles, isoxazolines and isoxazolidines, condensed to the cyclopentanoperhy-drophenanthrene skeleton, in different positions of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6dd23d821b1fdf1186e595ba25725ce
https://doi.org/10.1002/chin.199852329
https://doi.org/10.1002/chin.199852329
Autor:
A, Papageorgiou, Th, Lialiaris, E, Stergiou, I, Stergiou, C, Tsigris, A, Kourti, G, Geromichalos, P, Stravoravdi, D, Trafalis, A E, Athanassiou, A, Pitsas, Ch, Camoutsis
Publikováno v:
Journal of B.U.ON. : official journal of the Balkan Union of Oncology. 13(2)
In earlier studies, this laboratory carried out research on the synthesis and anticancer evaluation of hybrid compounds, which combine two molecules in one such as homo-aza-steroidal esters (HASE) of carboxylic derivatives of N, N-bis (2-chloroethyl)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5f7361ed1e4c2f2b309b324b180a65e5
https://pubmed.ncbi.nlm.nih.gov/18555471
https://pubmed.ncbi.nlm.nih.gov/18555471
Publikováno v:
European Journal of Medicinal Chemistry. 26:659-661
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9b5f757c303526e6a209f81aa190a1c
https://doi.org/10.1016/0223-5234(91)90203-y
https://doi.org/10.1016/0223-5234(91)90203-y
Autor:
Panayotis Catsoulacos, N. Demopoulos, K. Psaraki, A. Papageorgiou, E. Margariti, Ch. Camoutsis
Publikováno v:
Journal of pharmaceutical sciences. 82(2)
Four steroidal lactams of the A- and D-rings were used for the esterification in the C-3 or C-17 positions, respectively, of their nuclei with the W,N-bis(2-chloroethyl)aminocinnamic acid isomers. The con-densation reaction of the hydroxylic group of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e92f5f5e11bc055979d30b7c9fad46f0
https://pubmed.ncbi.nlm.nih.gov/8445536
https://pubmed.ncbi.nlm.nih.gov/8445536