Zobrazeno 1 - 10
of 83
pro vyhledávání: '"U. Gulini"'
Autor:
Elena Poggesi, Amedeo Leonardi, Gabriella Marucci, Carlo Melchiorre, Dario Giardinà, Gianni Sagratini, U. Gulini, Piero Angeli, O. Polimanti
Publikováno v:
Il Farmaco. 58:477-487
A series of quinazoline derivatives, 2-20, structurally related to the racemic alpha(1)-adrenoceptor antagonist cyclazosin (1), were synthesized and evaluated for their functional antagonism at alpha(1)- and alpha(2)-adrenoceptors and for their bindi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef473c0a04e59618f8b416017b019fce
https://doi.org/10.1016/s0014-827x(02)00025-3
https://doi.org/10.1016/s0014-827x(02)00025-3
Autor:
C. Melchiorre, P. Angeli, M.L. Bolognesi, A. Chiarini, D. Giardinà, U. Gulini, A. Leonardi, G. Marucci, A. Minarini, M. Pigini, W. Quaglia, M. Rosini, V. Tumiatti
Publikováno v:
Receptor Chemistry towards the Third Millennium, Proceedings of the 12th Camerino-Noordwijkerhout Symposium ISBN: 9780444504241
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0334ecbd8611d4249b82d50b746a899c
https://doi.org/10.1016/s0165-7208(00)80016-1
https://doi.org/10.1016/s0165-7208(00)80016-1
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 45(12)
Several WB4101 (1)-related compounds were synthesized. Their alpha-adrenoreceptor blocking properties were evaluated in order to understand the kind of interaction occurring between the amine function of (1)-related compounds and the alpha-adrenorece
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c26554407b0f5ea3363f040cb1c6fba
https://pubmed.ncbi.nlm.nih.gov/1982488
https://pubmed.ncbi.nlm.nih.gov/1982488
Publikováno v:
Pharmacological Research. 31:50
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e3bf9832d187eb217d7bcc9262e5e574
https://doi.org/10.1016/1043-6618(95)86461-x
https://doi.org/10.1016/1043-6618(95)86461-x
Receptor Chemistry Towards the Third Millennium is the result of papers presented at the 12th Camerino-Noordwijkerhout Symposium, held in Camerino, Italy in September 1999. Although much is known about the way ligands interact with receptors, which h
Publikováno v:
Il Farmaco; edizione scientifica. 31(11)
On the basis of an hypothesis according to which suitable nucleophilic agents may convert adenosine diphosphate (ADP) into adenosine monophosphate (AMP) and adenosine, well known inhibitors of ADP-induced platelet aggregation, some N-heterocyclic ald
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c2aa1e75d4c5f7be7155eaef354a218c
https://pubmed.ncbi.nlm.nih.gov/1010032
https://pubmed.ncbi.nlm.nih.gov/1010032
Publikováno v:
Chemischer Informationsdienst. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a488a1ec54654274a13abcb028aeaf6e
https://doi.org/10.1002/chin.197929268
https://doi.org/10.1002/chin.197929268
Publikováno v:
Trends in pharmacological sciences.
The possibility that polymethylene tetraamines act as divalent ligands has been explored. Structure-activity relationship studies among polymethylene tetraamines have shown that four nitrogens are necessary for high affinity binding to M2 receptors w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ef90d4c7665fdb83c8f487ce80030e64
https://pubmed.ncbi.nlm.nih.gov/2694524
https://pubmed.ncbi.nlm.nih.gov/2694524
Publikováno v:
Chemischer Informationsdienst. 8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce75c1a63560d3f53458f173afc52d2e
https://doi.org/10.1002/chin.197735224
https://doi.org/10.1002/chin.197735224
Publikováno v:
Chemischer Informationsdienst. 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b2d3c34fc30a06045f303b8c5997196
https://doi.org/10.1002/chin.197914208
https://doi.org/10.1002/chin.197914208