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Details

Stereochemistry ACHIRAL
Molecular Formula C19H24N2OS
Molecular Weight 328.472
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PHENCARBAMIDE

SMILES

CCN(CC)CCSC(=O)N(C1=CC=CC=C1)C2=CC=CC=C2

InChI

InChIKey=BZGIPVGCJGXQTA-UHFFFAOYSA-N
InChI=1S/C19H24N2OS/c1-3-20(4-2)15-16-23-19(22)21(17-11-7-5-8-12-17)18-13-9-6-10-14-18/h5-14H,3-4,15-16H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C19H24N2OS
Molecular Weight 328.472
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Phencarbamide is an anti-spasmodic and anticholinergic drug used during parturition. It has a specific antispasmodic action on the smooth muscle, both directly like papaverine and through the autonomic nervous system (atropine effect). It has also an analgesic effect of its own. Side-effects generally associated with the atropine group of drugs.

Approval Year

PubMed

PubMed

TitleDatePubMed
[On the pharmacology of the uterine action of phencarbamide].
1963
[PHENCARBAMIDE, A NEW SPASMOLYTIC COMBINED WITH DOLVIRAN].
1964 Jun
[EXPERIENCES WITH A NEW SPASMOLYTIC AGENT (ESCORPAL) IN OBSTETRICS].
1964 Jun 20
[SPASMOLYSIS IN OBSTETRICS: CLINICAL EXPERIENCE WITH PHENCARBAMIDE].
1964 Sep 26
[PRACTICAL EXPERIENCES WITH THE SPASMOLYTIC AGENT ESCORPAL IN OBSTETRICS].
1965 Jan 30
[Spasmolytic effect of phencarbamide on the uterine cervix during early puerperium].
1966 Aug 26
Propranolol-bunolol and phencarbamide in chloroform-induced ventricular fibrillation in mice.
1973 Jun
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:31:31 GMT 2023
Edited
by admin
on Fri Dec 15 16:31:31 GMT 2023
Record UNII
59H17J9F1B
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PHENCARBAMIDE
MI   USAN  
USAN  
Official Name English
ESCORPAL
Brand Name English
CARBAMOTHIOIC ACID, DIPHENYL-, S-(2-(DIETHYLAMINO)ETHYL) ESTER
Common Name English
FENCARBAMIDE [MART.]
Common Name English
PHENCARBAMIDE [USAN]
Common Name English
FENCARBAMIDE
INN   MART.   WHO-DD  
INN  
Official Name English
S-[2-(Diethylamino)ethyl] diphenylthiocarbamate
Systematic Name English
fencarbamide [INN]
Common Name English
Fencarbamide [WHO-DD]
Common Name English
PHENCARBAMIDE [MI]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C29704
Created by admin on Fri Dec 15 16:31:31 GMT 2023 , Edited by admin on Fri Dec 15 16:31:31 GMT 2023
NCI_THESAURUS C29696
Created by admin on Fri Dec 15 16:31:31 GMT 2023 , Edited by admin on Fri Dec 15 16:31:31 GMT 2023
Code System Code Type Description
NCI_THESAURUS
C66369
Created by admin on Fri Dec 15 16:31:31 GMT 2023 , Edited by admin on Fri Dec 15 16:31:31 GMT 2023
PRIMARY
EVMPD
SUB07546MIG
Created by admin on Fri Dec 15 16:31:31 GMT 2023 , Edited by admin on Fri Dec 15 16:31:31 GMT 2023
PRIMARY
SMS_ID
100000081246
Created by admin on Fri Dec 15 16:31:31 GMT 2023 , Edited by admin on Fri Dec 15 16:31:31 GMT 2023
PRIMARY
PUBCHEM
6008
Created by admin on Fri Dec 15 16:31:31 GMT 2023 , Edited by admin on Fri Dec 15 16:31:31 GMT 2023
PRIMARY
ECHA (EC/EINECS)
223-103-4
Created by admin on Fri Dec 15 16:31:31 GMT 2023 , Edited by admin on Fri Dec 15 16:31:31 GMT 2023
PRIMARY
MERCK INDEX
m395
Created by admin on Fri Dec 15 16:31:31 GMT 2023 , Edited by admin on Fri Dec 15 16:31:31 GMT 2023
PRIMARY Merck Index
FDA UNII
59H17J9F1B
Created by admin on Fri Dec 15 16:31:31 GMT 2023 , Edited by admin on Fri Dec 15 16:31:31 GMT 2023
PRIMARY
CAS
3735-90-8
Created by admin on Fri Dec 15 16:31:31 GMT 2023 , Edited by admin on Fri Dec 15 16:31:31 GMT 2023
PRIMARY
ChEMBL
CHEMBL2107472
Created by admin on Fri Dec 15 16:31:31 GMT 2023 , Edited by admin on Fri Dec 15 16:31:31 GMT 2023
PRIMARY
INN
1324
Created by admin on Fri Dec 15 16:31:31 GMT 2023 , Edited by admin on Fri Dec 15 16:31:31 GMT 2023
PRIMARY
EPA CompTox
DTXSID80190796
Created by admin on Fri Dec 15 16:31:31 GMT 2023 , Edited by admin on Fri Dec 15 16:31:31 GMT 2023
PRIMARY
Related Record Type Details
SALT/SOLVATE -> PARENT
SALT/SOLVATE -> PARENT
Related Record Type Details
ACTIVE MOIETY