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2D-QSAR and 3D-QSAR/CoMFA analyses of the N-terminal substituted anthranilic acid based CCK1 receptor antagonists: ‘Hic Rhodus, hic saltus’

DIMITRA HADJIPAVLOU LITINA
•
PAOLO BRAIUCA
•
LASSIANI, LUCIA
altro
VARNAVAS, ANTONIOS
2009
  • journal article

Periodico
BIOORGANIC & MEDICINAL CHEMISTRY
Abstract
A research is presented on quantitative structure–activity relationship (QSAR) studies on the more recent class of non-peptidic CCK1 receptor antagonists. Our results suggest that the balance of hydrophobicity and volume dependent polarizability term plays a key role in the antagonism of CCK1 receptor.
DOI
10.1016/j.bmc.2009.05.067
Archivio
http://hdl.handle.net/11368/2264104
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-67650087483
Diritti
metadata only access
Soggetti
  • QSAR

Scopus© citazioni
2
Data di acquisizione
Jun 14, 2022
Vedi dettagli
Web of Science© citazioni
2
Data di acquisizione
Mar 16, 2024
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