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udenafil
Known as:
3-(1-methyl-7-oxo-3-propyl-4,7-dihydro-1H-pyrazolo[4,3-d]pyrimidin-5-yl)-N-{2-[(2RS)-1-methylpyrrolidin-2-yl]ethyl}-4-propoxybenzenesulfonamide
, 5-(2-propyloxy-5-(1-methyl-2-pyrollidinylethylamidosulfonyl)phenyl)-1-methyl-3-propyl-1,6-dihydro-7H-pyrazolo (4,3-d) pyrimidine-7-one
, Benzenesulfonamide, 3-(6,7-dihydro-1-methyl-7-oxo-3-propyl-1H-pyrazolo[4,3-d]pyrimidin-5-yl)-N-[2-(1-methyl-2-pyrrolidinyl)ethyl]-4-propoxy-
A benzenesulfonamide derivative with vasodilatory activity. Udenafil selectively inhibits phosphodiesterase type 5 (PDE5), thus inhibiting the…
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National Institutes of Health
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Related topics
Related topics
5 relations
Narrower (2)
DA-8159
Zydena
Broader (3)
Phosphodiesterase 5 inhibitor
Pyrimidines
Sulfonamides
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Review
2015
Review
2015
Phosphodiesterase 5 inhibitors for the treatment of erectile dysfunction: a trade-off network meta-analysis.
Liang Chen
,
Sergej E L Staubli
,
+4 authors
T. Kessler
European Urology
2015
Corpus ID: 39824864
Highly Cited
2015
Highly Cited
2015
Synthesis and biological evaluation of pyrazolo-triazole hybrids as cytotoxic and apoptosis inducing agents.
T. Srinivasa Reddy
,
H. Kulhari
,
+4 authors
R. Shukla
Organic and biomolecular chemistry
2015
Corpus ID: 205989624
A series of pyrazolo-triazole hybrids were designed and synthesized by combining the 1,3-diphenyl pyrazole and triazole scaffolds…
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Highly Cited
2004
Highly Cited
2004
Synthesis of 4,5-diaryl-1H-pyrazole-3-ol derivatives as potential COX-2 inhibitors.
Meena V Patel
,
R. Bell
,
S. Majest
,
R. Henry
,
T. Kolasa
Journal of Organic Chemistry
2004
Corpus ID: 1801924
4,5-Diaryl-1H-pyrazole-3-ol was utilized as a versatile template to synthesize several classes of compounds such as pyrazolo…
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Highly Cited
2004
Highly Cited
2004
Synthesis of some new annulated pyrazolo-pyrido (or pyrano) pyrimidine, pyrazolopyridine and pyranopyrazole derivatives.
Saied Abdullah El-Assiery
,
Galal Abdullah Sayed
,
A. Fouda
Acta Pharmaceutica
2004
Corpus ID: 551791
The bifunctional pyrazolopyridine (2) and pyrano-pyrazole (3) derivatives were prepared by the reaction of 2-(2,4-dinitrophenyl…
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Highly Cited
2002
Highly Cited
2002
1H and 13C NMR Study of 1-Hydrazino-2,3-dihydro-1H-pyrazolo[1,2-a]pyridazine-5,8-diones and -1H-pyrazolo[1,2-b]phthalazine-5,10-diones and Their Ring-Chain Tautomerism
J. Sinkkonen
,
V. Ovcharenko
,
+4 authors
K. Pihlaja
2002
Corpus ID: 55134700
Treatment of 1-hydroxy-2,3-dihydro-1H-pyrazolo[1,2-a]pyridazine-5,8-diones and -1H-pyrazolo[1,2-b]phthalazine-5,10-diones with…
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Highly Cited
2000
Highly Cited
2000
[(3)H]MRE 3008F20: a novel antagonist radioligand for the pharmacological and biochemical characterization of human A(3) adenosine receptors.
K. Varani
,
S. Merighi
,
+7 authors
P. Borea
Molecular Pharmacology
2000
Corpus ID: 425593
The lack of a radiolabeled selective A(3) adenosine receptor antagonist is a major drawback for an adequate characterization of…
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Highly Cited
2000
Highly Cited
2000
Pyrazolo-triazoles as light activable DNA cleaving agents.
S. Manfredini
,
C. B. Vicentini
,
+4 authors
R. Gambari
Bioorganic & Medicinal Chemistry
2000
Corpus ID: 33687322
Review
1998
Review
1998
Safety and efficacy of sildenafil citrate in the treatment of male erectile dysfunction.
M. Goldenberg
Clinical Therapeutics
1998
Corpus ID: 31726087
Highly Cited
1996
Highly Cited
1996
Effects of cyclic GMP elevation on isoprenaline‐induced increase in cyclic AMP and relaxation in rat aortic smooth muscle: role of phosphodiesterase 3
E. Delpy
,
H. Coste
,
Anne‐Charlotte le Monnier Gouville
British Journal of Pharmacology
1996
Corpus ID: 9174070
1 In rat aortic rings precontracted with phenylephrine, the β‐adrenoceptor agonist isoprenaline (10 nM to 30 μm) produces greater…
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1994
1994
Synthesis and analgesic properties of 5-acyl-arylhydrazone 1-H pyrazolo [3,4-b] pyridine derivatives.
L. Dias
,
M. Alvim
,
A. Freitas
,
E. Barreiro
,
A. Miranda
Pharmaceutica Acta Helvetiae
1994
Corpus ID: 1431046
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