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etoperidone
Known as:
Clopradone
, (1,3-(4-m-chlorophenyl-1-piperazinyl)propyl)-3,4-diethyl-delta(2)-1,2,4-triazolin-5-one
, 2-(3-(4-(m-chlorophenyl)-1-piperazinyl)propyl)-4,5-diethyl-2,4-dihydro-3H-1,2,4- triazolo-3-one.HCl
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National Institutes of Health
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Related topics
Related topics
2 relations
Broader (1)
Trazodone
analogs & derivatives
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2010
2010
Molecular docking and 3D-QSAR studies on triazolinone and pyridazinone, non-nucleoside inhibitor of HIV-1 reverse transcriptase
S. Sivan
,
V. Manga
Journal of Molecular Modeling
2010
Corpus ID: 24443265
AbstractNonnucleoside reverse transcriptase inhibitors (NNRTIs) are allosteric inhibitors of the HIV-1 reverse transcriptase…
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Highly Cited
2009
Highly Cited
2009
Amicarbazone, a New Photosystem II Inhibitor
F. Dayan
,
M.L.B. Trindade
,
E. D. Velini
Weed science
2009
Corpus ID: 59398999
Abstract Amicarbazone is a new triazolinone herbicide with a broad spectrum of weed control. The phenotypic responses of…
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2008
2008
Discovery of triazolinone non-nucleoside inhibitors of HIV reverse transcriptase.
Z. Sweeney
,
S. Acharya
,
+16 authors
K. Klumpp
Bioorganic & Medicinal Chemistry Letters
2008
Corpus ID: 41332905
2004
2004
A comparative solid-phase extraction study for the simultaneous determination of fluvoxamine, mianserin, doxepin, citalopram, paroxetine, and etoperidone in whole blood by capillary gas-liquid…
M. A. Martínez
,
C. Sánchez de la Torre
,
E. Almarza
Journal of Analytical Toxicology
2004
Corpus ID: 24338356
This paper reports a simple and reliable gas chromatographic method with nitrogen-phosphorus detection without derivatization for…
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2001
2001
Degradation of [(14)C]carfentrazone-ethyl under aerobic aquatic conditions.
S. Elmarakby
,
D. Supplee
,
R. Cook
Journal of Agricultural and Food Chemistry
2001
Corpus ID: 30883309
Carfentrazone-ethyl (CF-E) is an aryl triazolinone reduced-risk herbicide for use on corn, wheat, and soybean. As part of the…
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2001
2001
3-D QSAR studies of triazolinone based balanced AT1/AT2 receptor antagonists.
T. Pandya
,
S. Pandey
,
M. Tiwari
,
S. C. Chaturved
,
A. Saxena
Bioorganic & Medicinal Chemistry
2001
Corpus ID: 30380233
1995
1995
Potent and orally active angiotensin II receptor antagonists with equal affinity for human AT1 and AT2 subtypes.
L. Chang
,
W. Ashton
,
+7 authors
R. Chang
Journal of Medicinal Chemistry
1995
Corpus ID: 26094287
In order to block the effects induced by the interactions between angiotensin II (AII) and both AT1 and AT2 receptors, we have…
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1994
1994
Triazolinone biphenylsulfonamide derivatives as orally active angiotensin II antagonists with potent AT1 receptor affinity and enhanced AT2 affinity.
W. Ashton
,
L. Chang
,
+7 authors
K. A. Faust
Journal of Medicinal Chemistry
1994
Corpus ID: 12059905
Several series of 2,4-dihydro-2,4,5-trisubstituted-3H-1,2,4-triazol-3-ones with acidic sulfonamide replacements of tetrazole at…
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1994
1994
Triazolinone biphenylsulfonamides as angiotensin II receptor antagonists with high affinity for both the AT1 and AT2 subtypes.
L. Chang
,
W. Ashton
,
+7 authors
R. Chang
Journal of Medicinal Chemistry
1994
Corpus ID: 22508526
Angiotensin II (AII), the endogenous peptide ligand of the AII receptor, has equivalent high affinity for both the AT1 and AT2…
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1984
1984
A comparative pharmacological study of trazodone, etoperidone and 1-(m-chlorophenyl)piperazine.
V. Cioli
,
C. Corradino
,
D. Piccinelli
,
M. Rocchi
,
P. Valeri
Pharmacological Research Communications
1984
Corpus ID: 11670644
Since 1-(m-chlorophenyl)piperazine (mCPP) is a metabolite of trazodone (TRZ) and etoperidone (ETO), two atypical antidepressants…
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