Zobrazeno 1 - 10
of 277
pro vyhledávání: '"G, Ronsisvalle"'
Autor:
Lorella Giuseppina Pasquinucci, M. S. Pappalardo, Santi Spampinato, Orazio Prezzavento, G. Ronsisvalle, Lucia Carboni, F. Vittorio, Agostino Marrazzo
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f564af189aceb64d91486976dc8536e
https://doi.org/10.1002/chin.199809207
https://doi.org/10.1002/chin.199809207
Autor:
L, Pasquinucci, M, Iadanza, A, Marrazzo, O, Prezzavento, S, Ronsisvalle, G M, Scoto, C, Parenti, L, De Luca, G, Ronsisvalle
There is considerable interest in developing KOP Opioid receptor ligands as clinically useful analgesics. Moreover, compounds with mixed KOP receptor and mu-opioid peptide (MOP) receptor agonist/antagonist properties could have a better therapeutic p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::9e5a82ba4065baf644f6bc69b5ea001e
http://hdl.handle.net/11570/1669541
http://hdl.handle.net/11570/1669541
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 56(1-2)
The results of studies on the design of a heterocyclic scaffold for the dynorphin A pharmacophore and on structure-affinity relationships in the MPCB/CCB series are described. The representative ligands provide insights to binding modes of benzomorph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::83595d09e1fe89fdae2dcdff18bd79f2
https://pubmed.ncbi.nlm.nih.gov/11347952
https://pubmed.ncbi.nlm.nih.gov/11347952
Autor:
G, Ronsisvalle, O, Prezzavento, L, Pasquinucci, M S, Pappalardo, A, Marrazzo, F, Vittorio, L, Carboni, S, Spampinato
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 52(6-7)
The synthesis and the in vitro receptor affinity for sigma 1 and opiod receptors of the two diastereoisomers of (+)-cis-MPCB namely, (+)-cis-(1'S,2'R)-6,11-Dimethyl-1,2,3,4,5,6 -hexahydro-3-[[2'-(methoxycarbonyl)-2'-phenylcyclopropyl]methyl]-2 ,6 -me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::74bcfd330200e97a4ae52bff177ffa0a
https://pubmed.ncbi.nlm.nih.gov/9372600
https://pubmed.ncbi.nlm.nih.gov/9372600
Autor:
Agostino Marrazzo, Santi Spampinato, M. S. Pappalardo, S. Caccamese, Orazio Prezzavento, Lucia Carboni, G. Ronsisvalle
Publikováno v:
ChemInform. 26
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee6aaeaadac6bd2c93ff9df148bc6f8e
https://doi.org/10.1002/chin.199516276
https://doi.org/10.1002/chin.199516276
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 50(4)
2-Methyl-1-oxo-1,2-dihydro-3-carbazoyl-4-phenylisoquinoline 2, 1-methoxy-7 and 1-chloro-3-carbazoyl-4-phenylisoquinoline 12 as well as a series of their 2-hydrazono-derivatives 3 a-i, 8 a-i and 14 a-i were synthesized and evaluated for their antibact
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1a85863fdecaa759bbea3f11905b54c5
https://pubmed.ncbi.nlm.nih.gov/7669171
https://pubmed.ncbi.nlm.nih.gov/7669171
Publikováno v:
Farmaco (Societa chimica italiana : 1989). 49(4)
The dialkylamino-alkylation of 3H-pyridazino[4,5-b][1,4]benzothiazin-4(10H)-one-5,5-dioxide 5 produced the 3-dialkylaminoalkyl-derivatives 6. To the same compounds we arrived by selective reduction of the corresponding N-oxides 4, derived from the ox
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c340d6c445a114003aea0d7c425f8dbd
https://pubmed.ncbi.nlm.nih.gov/8049003
https://pubmed.ncbi.nlm.nih.gov/8049003
Autor:
P, Pothen, P, Maglio, G, Scanavacca, G, Ronsisvalle, V, Castellani, R, Pigato, A C, Pessina, C, Dal Palù
Publikováno v:
Cardiologia (Rome, Italy). 37(12)
In order to compare the ST segment changes recorded simultaneously on Holter (Del Mar Avionics 445B recorder and DCG VII Scanner) and standard electrocardiogram, 22 patients with chest discomfort and normal resting ECG were evaluated during exercise
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ccc197fafeb95460290ecc0d52fd84c0
https://pubmed.ncbi.nlm.nih.gov/1303304
https://pubmed.ncbi.nlm.nih.gov/1303304