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Volumn 17, Issue 1, 2003, Pages 39-51
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Exploring the molecular basis of selectivity in A1 adenosine receptors agonists: A case study
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Author keywords
Adenosine receptor: AR; Adenylate cyclase: AC; G protein coupled receptors: GPCRs; Transmembrane domain: TM
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Indexed keywords
ACTIVATION ANALYSIS;
BIOMOLECULES;
HYDROGEN BONDS;
HYDROPHOBICITY;
ADENOSINE RECEPTOR;
ADENOSINE RECEPTOR: AR;
ADENYLATE CYCLASE;
ADENYLATE CYCLASE: AC;
G PROTEIN COUPLED RECEPTORS;
G-PROTEIN-COUPLED RECEPTOR: GPCR;
MOLECULAR BASIS;
TRANS-MEMBRANE DOMAINS;
TRANSMEMBRANE DOMAIN;
TRANSMEMBRANE DOMAIN: TM;
LIGANDS;
2 CHLORO 6 N CYCLOPENTYLADENOSINE;
4 [7 [[1 [(3 CHLORO 2 THIENYL)METHYL]PROPYL]AMINO] 3H IMIDAZO[4,5 B]PYRIDIN 3 YL] N ETHYL 2,3 DIHYDROXYCYCLOPENTANECARBOXAMIDE;
6 N CYCLOHEXYL 2' O METHYLADENOSINE;
ADENOSINE;
ADENOSINE 5' (N ETHYLCARBOXAMIDE);
ADENOSINE A1 RECEPTOR;
ADENOSINE DERIVATIVE;
ADENOSINE RECEPTOR AFFECTING AGENT;
ADENOSINE RECEPTOR BLOCKING AGENT;
ADENOSINE RECEPTOR STIMULATING AGENT;
ALANINE;
AMIDE;
AMINO ACID;
AZ 1081;
BN 063;
DORIDOSINE;
DRUG RECEPTOR;
GUANOSINE DERIVATIVE;
NITROGEN;
NNC 210136;
NNC 210147;
NNC 901515;
PURINE NUCLEOSIDE;
RECEPTOR SUBTYPE;
RG 14178;
RG 14202;
RHODOPSIN;
RIBOSE;
UNCLASSIFIED DRUG;
UNINDEXED DRUG;
UP 202 32;
ANALYTIC METHOD;
ARTICLE;
BIOCHEMISTRY;
CARDIOVASCULAR DISEASE;
CASE STUDY;
CATTLE;
CONTROLLED STUDY;
DRUG DESIGN;
DRUG EFFECT;
DRUG RESEARCH;
DRUG SELECTIVITY;
DRUG STRUCTURE;
GENE MUTATION;
HUMAN;
HYDROGEN BOND;
HYDROPHOBICITY;
MOLECULAR INTERACTION;
MOLECULAR MODEL;
NEUROLOGIC DISEASE;
NONHUMAN;
PRIORITY JOURNAL;
REGULATORY MECHANISM;
STRUCTURE ACTIVITY RELATION;
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EID: 0041695555
PISSN: 0920654X
EISSN: None
Source Type: Journal
DOI: 10.1023/A:1024530029922 Document Type: Article |
Times cited : (15)
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References (31)
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