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Details

Stereochemistry RACEMIC
Molecular Formula C19H24N2O4.2ClH
Molecular Weight 417.327
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIPRATECOL DIHYDROCHLORIDE

SMILES

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

InChI

InChIKey=PZQYPHRFNJMIQO-UHFFFAOYSA-N
InChI=1S/C19H24N2O4.2ClH/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;2*1H

HIDE SMILES / InChI

Molecular Formula C19H24N2O4
Molecular Weight 344.4049
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

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
Effect of a Raubasine-Pipratecol association (Isosarpan) on the sympathetic control of cerebral circulation.
1979 Feb
Substance Class Chemical
Created
by admin
on Sat Dec 16 08:45:17 GMT 2023
Edited
by admin
on Sat Dec 16 08:45:17 GMT 2023
Record UNII
QM4158R9RL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PIPRATECOL DIHYDROCHLORIDE
Common Name English
PIPRATECOL, DIHYDROCHLORIDE
Common Name English
PIPRATECOL HYDROCHLORIDE
WHO-DD  
Common Name English
1,2-BENZENEDIOL, 4-(1-HYDROXY-2-(4-(2-METHOXYPHENYL)-1-PIPERAZINYL)ETHYL)-, HYDROCHLORIDE (1:2)
Systematic Name English
1-PIPERAZINEETHANOL, .ALPHA.-(3,4-DIHYDROXYPHENYL)-4-(O-METHOXYPHENYL)-, DIHYDROCHLORIDE
Systematic Name English
Pipratecol hydrochloride [WHO-DD]
Common Name English
1,2-BENZENEDIOL, 4-(1-HYDROXY-2-(4-(2-METHOXYPHENYL)-1-PIPERAZINYL)ETHYL)-, DIHYDROCHLORIDE
Systematic Name English
Code System Code Type Description
CAS
15622-04-5
Created by admin on Sat Dec 16 08:45:17 GMT 2023 , Edited by admin on Sat Dec 16 08:45:17 GMT 2023
PRIMARY
EVMPD
SUB03865MIG
Created by admin on Sat Dec 16 08:45:17 GMT 2023 , Edited by admin on Sat Dec 16 08:45:17 GMT 2023
PRIMARY
EPA CompTox
DTXSID20935401
Created by admin on Sat Dec 16 08:45:17 GMT 2023 , Edited by admin on Sat Dec 16 08:45:17 GMT 2023
PRIMARY
FDA UNII
QM4158R9RL
Created by admin on Sat Dec 16 08:45:17 GMT 2023 , Edited by admin on Sat Dec 16 08:45:17 GMT 2023
PRIMARY
SMS_ID
100000085292
Created by admin on Sat Dec 16 08:45:17 GMT 2023 , Edited by admin on Sat Dec 16 08:45:17 GMT 2023
PRIMARY
ECHA (EC/EINECS)
239-696-8
Created by admin on Sat Dec 16 08:45:17 GMT 2023 , Edited by admin on Sat Dec 16 08:45:17 GMT 2023
PRIMARY
PUBCHEM
3014901
Created by admin on Sat Dec 16 08:45:17 GMT 2023 , Edited by admin on Sat Dec 16 08:45:17 GMT 2023
PRIMARY
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