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Bioorganic and Medicinal Chemistry Letters

Volumn 11, Issue 14, 2001, Pages 1931-1934

Introduction of alkynyl chains on C-8 of adenosine led to very selective antagonists of the A3 adenosine receptor

(7) Volpini, Rosaria a Costanzi, Stefano a Lambertucci, Catia a Vittori, Sauro a Klotz, K N b Lorenzen, Anna c Cristalli, Gloria a

a UNIVERSITY OF CAMERINO (Italy)

b UNIVERSITY OF WÜRZBURG (Germany)

c UNIVERSITY OF HEIDELBERG (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

8 ALKYNYLADENOSINE DERIVATIVE; ADENOSINE 5' (N ETHYLCARBOXAMIDE); ADENOSINE A3 RECEPTOR; ADENOSINE DERIVATIVE; ADENOSINE RECEPTOR BLOCKING AGENT; ADENYLATE CYCLASE; GUANINE NUCLEOTIDE BINDING PROTEIN; GUANOSINE 5' O (3 THIOTRIPHOSPHATE); NUCLEOSIDE DERIVATIVE; RECEPTOR SUBTYPE; RIBOSE; SULFUR 35; UNCLASSIFIED DRUG;

ANIMAL CELL; ARTICLE; BINDING AFFINITY; CHO CELL; DRUG ACTIVITY; DRUG SCREENING; DRUG STRUCTURE; DRUG SYNTHESIS; ENZYME ACTIVITY; ENZYME ASSAY; LIGAND BINDING; NONHUMAN; PROTEIN BINDING;

ADENOSINE; ADENOSINE-5'-(N-ETHYLCARBOXAMIDE); ADENYLATE CYCLASE; ANIMALS; BINDING SITES; CHO CELLS; CRICETINAE; GTP-BINDING PROTEINS; GUANOSINE 5'-O-(3-THIOTRIPHOSPHATE); HUMANS; PROTEIN BINDING; RADIOLIGAND ASSAY; RECEPTORS, PURINERGIC P1; SENSITIVITY AND SPECIFICITY;

EID: 0035939345 PISSN: 0960894X EISSN: None Source Type: Journal
DOI: 10.1016/S0960-894X(01)00347-X Document Type: Article

Times cited : (64)

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- note

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