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Details

Stereochemistry ACHIRAL
Molecular Formula C21H24N2O4
Molecular Weight 368.4263
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CYCLARBAMATE

SMILES

O=C(NC1=CC=CC=C1)OCC3(COC(=O)NC2=CC=CC=C2)CCCC3

InChI

InChIKey=IRZVVDMCEZNNCW-UHFFFAOYSA-N
InChI=1S/C21H24N2O4/c24-19(22-17-9-3-1-4-10-17)26-15-21(13-7-8-14-21)16-27-20(25)23-18-11-5-2-6-12-18/h1-6,9-12H,7-8,13-16H2,(H,22,24)(H,23,25)

HIDE SMILES / InChI

Molecular Formula C21H24N2O4
Molecular Weight 368.4263
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Cyclarbamate (N,N-diphenyl dicarbamate of 1,1-cyclopentanedimethanol) possesses an action on the central nervous system which manifests itself by a sedative effect without abolition of the natural defense reflexes. It is also antispasmodics of the striated muscle fibre. It has been studied in gastroenterology and gynecology.

Originator

Curator's Comment: reference retrieved from: https://books.google.ru/books?id=_J2ti4EkYpkC&printsec=frontcover&hl=ru#v=onepage&q&f=false

Approval Year

PubMed

PubMed

TitleDatePubMed
Mechanism of cycloisomerisation of 1,6-heptadienes catalysed by [(tBuCN)2PdCl2]: remarkable influence of exogenous and endogenous 1,6- and 1,5-diene ligands.
2006 Nov 24
Substance Class Chemical
Created
by admin
on Sat Dec 16 18:01:59 GMT 2023
Edited
by admin
on Sat Dec 16 18:01:59 GMT 2023
Record UNII
779291866J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CYCLARBAMATE
INN   MI  
INN  
Official Name English
CYCLOPENTAPHENE
Common Name English
CYCLARBAMATE [MI]
Common Name English
1,1-CYCLOPENTANEDIMETHANOL DICARBANILATE
Common Name English
C-1428
Code English
cyclarbamate [INN]
Common Name English
Classification Tree Code System Code
NCI_THESAURUS C264
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
Code System Code Type Description
ECHA (EC/EINECS)
227-302-7
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY
EPA CompTox
DTXSID60206480
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY
DRUG CENTRAL
3722
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY
INN
1389
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY
MERCK INDEX
m134
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY Merck Index
FDA UNII
779291866J
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY
NCI_THESAURUS
C77248
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY
SMS_ID
100000083746
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY
MESH
C004637
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY
CAS
5779-54-4
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY
EVMPD
SUB06842MIG
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY
WIKIPEDIA
Cyclarbamate
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY
PUBCHEM
72076
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104142
Created by admin on Sat Dec 16 18:01:59 GMT 2023 , Edited by admin on Sat Dec 16 18:01:59 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY