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Details

Stereochemistry RACEMIC
Molecular Formula C20H30N2O2
Molecular Weight 330.4644
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIPIPROVERINE

SMILES

O=C(OCCN1CCCCC1)C(N2CCCCC2)C3=CC=CC=C3

InChI

InChIKey=CGYQGGSMYNXXIV-UHFFFAOYSA-N
InChI=1S/C20H30N2O2/c23-20(24-17-16-21-12-6-2-7-13-21)19(18-10-4-1-5-11-18)22-14-8-3-9-15-22/h1,4-5,10-11,19H,2-3,6-9,12-17H2

HIDE SMILES / InChI

Molecular Formula C20H30N2O2
Molecular Weight 330.4644
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

PubMed

PubMed

TitleDatePubMed
[Clinical study of an antispasmodic with a predominantly musculotropic action: 2-piperidinoethyl alpha-phenyl-alpha-piperidinoacetate dihydrochloride (dipiproverine hydrochloride)].
1959
[Study, in digestive pathology, of a new spasmolytic drug with predominatly musculotropic action: dihydrochloride of di-dipiproverine (L.D. 935)].
1960 Feb 28
[THE USE OF DIPIPROVERINE DURING THE VICHY THERMAL CURE IN THE TREATMENT OF BILIARY DYSKINESIA AND SPASMODIC COLOPATHIES. (DOCUMENTARY AND STATISTICAL STUDY APROPOS OF 98 CASES)].
1964 Jun-Jul
[CLINICAL TRIAL OF LEVOSPASM IN CANCER PATIENTS].
1964 Sep
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:21:45 GMT 2023
Edited
by admin
on Fri Dec 15 16:21:45 GMT 2023
Record UNII
4XV7PTW3FZ
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIPIPROVERINE
INN   MI  
INN  
Official Name English
1-PIPERIDINE-ETHANOL .ALPHA.-PHENYL-1-PIPERIDINEACETATE ESTER
Common Name English
1-PIPERIDINEETHANOL, .ALPHA.-PHENYL-1-PIPERIDINEACETATE
Systematic Name English
1-PIPERIDINEETHANOL, .ALPHA.-PHENYL-1-PIPERIDINEACETATE (ESTER)
Common Name English
PIPERIDINOETHYL .ALPHA.-PIPERIDINOPHENYLACETATE
Systematic Name English
dipiproverine [INN]
Common Name English
DIPIPROVERINE [MI]
Common Name English
.ALPHA.-PHENYL-1-PIPERIDINEACETIC ACID 2-(1-PIPERIDINYL)ETHYL ESTER
Systematic Name English
Classification Tree Code System Code
NCI_THESAURUS C29698
Created by admin on Fri Dec 15 16:21:45 GMT 2023 , Edited by admin on Fri Dec 15 16:21:45 GMT 2023
Code System Code Type Description
MERCK INDEX
m152
Created by admin on Fri Dec 15 16:21:45 GMT 2023 , Edited by admin on Fri Dec 15 16:21:45 GMT 2023
PRIMARY Merck Index
SMS_ID
100000082330
Created by admin on Fri Dec 15 16:21:45 GMT 2023 , Edited by admin on Fri Dec 15 16:21:45 GMT 2023
PRIMARY
NCI_THESAURUS
C65427
Created by admin on Fri Dec 15 16:21:45 GMT 2023 , Edited by admin on Fri Dec 15 16:21:45 GMT 2023
PRIMARY
INN
866
Created by admin on Fri Dec 15 16:21:45 GMT 2023 , Edited by admin on Fri Dec 15 16:21:45 GMT 2023
PRIMARY
EPA CompTox
DTXSID30861747
Created by admin on Fri Dec 15 16:21:45 GMT 2023 , Edited by admin on Fri Dec 15 16:21:45 GMT 2023
PRIMARY
ChEMBL
CHEMBL2110899
Created by admin on Fri Dec 15 16:21:45 GMT 2023 , Edited by admin on Fri Dec 15 16:21:45 GMT 2023
PRIMARY
FDA UNII
4XV7PTW3FZ
Created by admin on Fri Dec 15 16:21:45 GMT 2023 , Edited by admin on Fri Dec 15 16:21:45 GMT 2023
PRIMARY
DRUG CENTRAL
3737
Created by admin on Fri Dec 15 16:21:45 GMT 2023 , Edited by admin on Fri Dec 15 16:21:45 GMT 2023
PRIMARY
CAS
117-30-6
Created by admin on Fri Dec 15 16:21:45 GMT 2023 , Edited by admin on Fri Dec 15 16:21:45 GMT 2023
PRIMARY
PUBCHEM
72072
Created by admin on Fri Dec 15 16:21:45 GMT 2023 , Edited by admin on Fri Dec 15 16:21:45 GMT 2023
PRIMARY
EVMPD
SUB07216MIG
Created by admin on Fri Dec 15 16:21:45 GMT 2023 , Edited by admin on Fri Dec 15 16:21:45 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY