Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Maria Panoussopoulou"'
Autor:
Maria Panoussopoulou, Andrew Tsotinis, Li-Kuan Yeh, Rüdiger Faust, Muy-Teck Teh, Robert W. Jones, Peter J. Garratt, Theodora Calogeropoulou, David Sugden
Publikováno v:
Journal of Medicinal Chemistry. 43:1050-1061
6H-Isoindolo[2,1-a]indoles (5, 7, 10, 13), 5,6-dihydroindolo[2,1-a]isoquinolines (20, 21), and 6,7-dihydro-5H-benzo[c]azepino[2,1-a]indoles (23, 25, 27, 30) have been prepared as melatonin analogues to investigate the nature of the binding site of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58a14987db28de4c5cb9bda50f9dd5f0
https://doi.org/10.1021/jm980684+
https://doi.org/10.1021/jm980684+
Publikováno v:
ChemInform. 33
We report the synthesis and biological evaluation of a series of new tricyclic analogs of the hormone melatonin, which act as probes of the constraints at the hormone's receptor site with regard to the lower N1-C2 region of the indole moiety of melat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9166c425e453e02e5c72b13ad23f6cb5
https://doi.org/10.1002/chin.200206161
https://doi.org/10.1002/chin.200206161
Publikováno v:
European journal of medicinal chemistry. 42(7)
A series of new 2,3-dihydro-1H-pyrrolo[3,2,1-ij]quinolin-6-alkanamides, with and without alkyl and cycloalkyl moieties in the beta-position of the alkanamido side chain, have been prepared and tested for their ability to activate pigment granule aggr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac8099afb7d291787486008b83dc523f
https://pubmed.ncbi.nlm.nih.gov/17346859
https://pubmed.ncbi.nlm.nih.gov/17346859
Publikováno v:
European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences. 18(5)
Tricyclic analogs of melatonin with alkyl and cycloalkyl moieties in the beta position of the ethylamido chain have been prepared and tested for their ability to activate pigment granule aggregation in Xenopus laevis melanophores. The introduction of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc48f374bd0b203e7fb8bc900ebd171e
https://pubmed.ncbi.nlm.nih.gov/12694881
https://pubmed.ncbi.nlm.nih.gov/12694881
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 56(9)
We report the synthesis and biological evaluation of a series of new tricyclic analogs of the hormone melatonin, which act as probes of the constraints at the hormone's receptor site with regard to the lower N1-C2 region of the indole moiety of melat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21ff08905dd913666d2c1f984530e997
https://pubmed.ncbi.nlm.nih.gov/11680819
https://pubmed.ncbi.nlm.nih.gov/11680819