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Volumn 44, Issue 13, 2001, Pages 2204-2218
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Novel, potent, and selective phosphodiesterase 5 inhibitors: Synthesis and biological activities of a series of 4-aryl-1-isoquinolinone derivatives
a,b a,b a,b a,b a,b a,b a,b a,b a,b a,b a,b
b
NONE
(Japan)
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Author keywords
[No Author keywords available]
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Indexed keywords
2 (4 AMINOPHENYL) 1,2 DIHYDRO 1 OXO 7 (2 PYRIDINYLMETHOXY) 4 (3,4,5 TRIMETHOXYPHENYL) 3 ISOQUINOLINECARBOXYLIC ACID METHYL ESTER;
ISOENZYME;
ISOQUINOLINE DERIVATIVE;
METHYL 2 (4 AMINOPHENYL) 1,2 DIHYDRO 1 OXO 7 (2 PYRIDINYLMETHOXY) 4 (3,4,5 TRIMETHOXYPHENYL) 3 ISOQUINOLINE CARBOXYLATE;
METHYL 2 (4 AMINOPHENYL) 1,2 DIHYDRO 1 OXO 7 (2 PYRIDINYLMETHOXY) 4 (3,4,5 TRIMETHOXYPHENYL) 3 ISOQUINOLINE CARBOXYLATE SULFATE;
PHOSPHODIESTERASE INHIBITOR;
UNCLASSIFIED DRUG;
ANIMAL TISSUE;
ARTICLE;
CORPUS CAVERNOSUM;
DRUG POTENCY;
DRUG SELECTIVITY;
DRUG STRUCTURE;
DRUG SYNTHESIS;
ENZYME ACTIVITY;
ENZYME INHIBITION;
ERECTILE DYSFUNCTION;
IC 50;
MALE;
MUSCLE RELAXATION;
NONHUMAN;
RABBIT;
STRUCTURE ACTIVITY RELATION;
3',5'-CYCLIC-GMP PHOSPHODIESTERASE;
ANIMALS;
CATTLE;
DOGS;
ENZYME INHIBITORS;
ISOQUINOLINES;
LUNG;
MALE;
MUSCLE RELAXATION;
MUSCLE, SMOOTH;
MYOCARDIUM;
PHOSPHODIESTERASE INHIBITORS;
PHOSPHORIC DIESTER HYDROLASES;
PIPERAZINES;
RABBITS;
RATS;
STRUCTURE-ACTIVITY RELATIONSHIP;
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EID: 0035927445
PISSN: 00222623
EISSN: None
Source Type: Journal
DOI: 10.1021/jm000558h Document Type: Article |
Times cited : (75)
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References (29)
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