Binding of organic anions to a macrocyclic alkaloid d-tubocurarine

dc.contributor.author	Alcantar, CG
dc.contributor.author	Eliseev, AV
dc.contributor.author	Yatsimirsky, AK
dc.date.accessioned	2011-01-22T10:28:26Z
dc.date.available	2011-01-22T10:28:26Z
dc.date.issued	1995
dc.identifier.issn	0960-894X
dc.identifier.uri	http://hdl.handle.net/11154/3009
dc.description.abstract	An alkaloid d-tubocurarine in aqueous solution binds 8-anilino-1-naphthalenesulfonate and anions of substituted benzoic, aliphatic dicarboxylic, and N-acetyl-alpha-amino acids. The binding constants vary from ca. 50 to 3300 M(-1) depending on the anion structure, charge and hydrophobicity. The binding of N-acetyl-alpha-amino acids is enantiospecific.	en_US
dc.language.iso	en	en_US
dc.title	Binding of organic anions to a macrocyclic alkaloid d-tubocurarine	en_US
dc.type	Article	en_US
dc.identifier.idprometeo	3135
dc.source.novolpages	5(24):2993-2998
dc.subject.wos	Chemistry, Medicinal
dc.subject.wos	Chemistry, Organic
dc.description.index	WoS: SCI, SSCI o AHCI
dc.relation.journal	Bioorganic & Medicinal Chemistry Letters