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Details

Stereochemistry RACEMIC
Molecular Formula C19H24N2O4
Molecular Weight 344.4049
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIPRATECOL

SMILES

COC1=C(C=CC=C1)N2CCN(CC(O)C3=CC(O)=C(O)C=C3)CC2

InChI

InChIKey=QESTYTNSJJTQCI-UHFFFAOYSA-N
InChI=1S/C19H24N2O4/c1-25-19-5-3-2-4-15(19)21-10-8-20(9-11-21)13-18(24)14-6-7-16(22)17(23)12-14/h2-7,12,18,22-24H,8-11,13H2,1H3

HIDE SMILES / InChI
Pipratecol is substituted thienoimidazole. It is the H+/K(+)-ATPase inhibitor. In a high concentration of 10(-4) g/ml, pipratecol increased the amplitude of isolated guinea-pig atrial contractions while decreased the rate. But, in a low concentration of 10(-8) g/ml, the drug decrease the amplitude and increased the rate slightly. The effects of adrenaline and noradrenaline were suppressed by the preceding addition of pipratecol, while that of isoproterenol was scarcely. The effect of pipratecol on atrial contractions was hardly influenced by reserpine with which the animal had been pretreated 24 hours before the sacrifice of animal. The augmentative effect of nicotine on atrial contractions was slightly suppressed by the preceding addition of pipratecol. From these results, it was assumed that pipratecol has some affinity with the adrenergic receptor of atria. As a peripheral vasodilator it has been used in conjunction with raubasine in the treatment of cerebrovascular disorders. Pipratecol was used as antiulcerative agent also.

Approval Year

PubMed

PubMed

TitleDatePubMed
[Pharmacological study of pipratecol (JP 711) and of a pharmaceutical combination raubasine-JP 711].
1969 Nov
Effect of a Raubasine-Pipratecol association (Isosarpan) on the sympathetic control of cerebral circulation.
1979 Feb
[Effect of raubasine and pipratecol on platelet aggregation and on the platelet release reaction].
1980 Feb 29
Substituted thieno[3,4-d]imidazoles, a novel group of H+/K(+)-ATPase inhibitors. Differentiation of their inhibition characteristics from those of omeprazole.
1990 Oct 23
Name Type Language
PIPRATECOL
INN   MART.   WHO-DD  
INN  
Official Name English
.ALPHA.-(3,4-DIHYDROXYPHENYL)-4-(2-METHOXYPHENYL)-1-PIPERAZINEETHANOL.
Common Name English
S-4216
Code English
Pipratecol [WHO-DD]
Common Name English
711-SE
Code English
1-PIPERAZINEETHANOL, .ALPHA.-(3,4-DIHYDROXYPHENYL)-4-(O-METHOXYPHENYL)-
Common Name English
711 SE
Code English
PIPRATECOL [MART.]
Common Name English
ISOSARPAN
Common Name English
711SE
Code English
pipratecol [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29707
Created by admin on Sat Dec 16 15:51:24 GMT 2023 , Edited by admin on Sat Dec 16 15:51:24 GMT 2023
Code System Code Type Description
PUBCHEM
71684
Created by admin on Sat Dec 16 15:51:24 GMT 2023 , Edited by admin on Sat Dec 16 15:51:24 GMT 2023
PRIMARY
SMS_ID
100000082199
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NCI_THESAURUS
C66407
Created by admin on Sat Dec 16 15:51:24 GMT 2023 , Edited by admin on Sat Dec 16 15:51:24 GMT 2023
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INN
2541
Created by admin on Sat Dec 16 15:51:24 GMT 2023 , Edited by admin on Sat Dec 16 15:51:24 GMT 2023
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EPA CompTox
DTXSID30864596
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ECHA (EC/EINECS)
239-578-6
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CAS
15534-05-1
Created by admin on Sat Dec 16 15:51:24 GMT 2023 , Edited by admin on Sat Dec 16 15:51:24 GMT 2023
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EVMPD
SUB09885MIG
Created by admin on Sat Dec 16 15:51:24 GMT 2023 , Edited by admin on Sat Dec 16 15:51:24 GMT 2023
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FDA UNII
E33L6C08A5
Created by admin on Sat Dec 16 15:51:24 GMT 2023 , Edited by admin on Sat Dec 16 15:51:24 GMT 2023
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ChEMBL
CHEMBL2105227
Created by admin on Sat Dec 16 15:51:24 GMT 2023 , Edited by admin on Sat Dec 16 15:51:24 GMT 2023
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