Zobrazeno 1 - 10
of 489
pro vyhledávání: '"BARLOCCO, D."'
Autor:
Rimoldi, I., Porta, F., Villa, S., Gelain, A., Meneghetti, F., Barlocco, D., nicola ferri, Asai, A., Facchetti, G.
Publikováno v:
Università degli Studi di Padova-IRIS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2f1f20a3198d3e68537e6e6a9c036ece
http://hdl.handle.net/11577/3177840
http://hdl.handle.net/11577/3177840
Autor:
Rastelli, Giulio, Vianello, P., Barlocco, D., Costantino, Luca, Cignarella, G., DEL CORSO, A., Mura, U.
This study presents the first successful example of structure-based drug design on aldose reductase in the extant literature. Starting from the structure of the modeled complex of aldose reductase with a pyridazinone acetic acid inhibitor that we pre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27a3f3dfa2773a9ff0487d4b1479336a
https://hdl.handle.net/11380/304619
https://hdl.handle.net/11380/304619
1H-NMR conformational studies of some phtalein derivatives acting as thymidylate synthase inhibitors
Autor:
Ghelli, S., Maria Paola Costi, Barlocco, D., Rinaldi, M., Tondi, D., Pecorari, P., Rastelli, G.
Publikováno v:
Scopus-Elsevier
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::1afb2a1eaec5ebbd7c6798e892a1d951
https://hdl.handle.net/11380/458201
https://hdl.handle.net/11380/458201
Publikováno v:
Scopus-Elsevier
A series of thienocycloheptapyridazines (3aa-dd), structurally related to Minaprine, was synthesized and compounds tested for their affinity towards muscarinic receptors. All of them showed Ki values in the micromolar range towards both the antagonis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f8cc1ad03dc9c3dfa636692a5bdfb02c
https://hdl.handle.net/11380/584290
https://hdl.handle.net/11380/584290
Autor:
Barlocco, D., Francesca Fanelli, Cignarella, G., Villa, S., Cattabeni, F., Balduini, W., Cimino, M., Benedetti, P. G.
Publikováno v:
Scopus-Elsevier
A series of 2-(acyl)amino-8-substituted-2,8-diazaspiro[4,5]decan-1,3-diones (5a-j), structurally related to the muscarinic agonist RS-86, was synthesized and compounds tested for their affinity towards muscarinic receptors. Though all compounds prove
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ddcd2052eb3d5390742a44d554008850
https://hdl.handle.net/11380/584295
https://hdl.handle.net/11380/584295