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Details

Stereochemistry RACEMIC
Molecular Formula C15H21NO2
Molecular Weight 247.3327
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of CICLONICATE

SMILES

C[C@@H]1C[C@H](CC(C)(C)C1)OC(=O)C2=CC=CN=C2

InChI

InChIKey=GQSGZTBDVNUIQS-DGCLKSJQSA-N
InChI=1S/C15H21NO2/c1-11-7-13(9-15(2,3)8-11)18-14(17)12-5-4-6-16-10-12/h4-6,10-11,13H,7-9H2,1-3H3/t11-,13-/m1/s1

HIDE SMILES / InChI

Molecular Formula C15H21NO2
Molecular Weight 247.3327
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Ciclonicate is a vasodilator and is used in cerebral and peripheral vascular disorders. Ciclonicate, given orally, markedly reduced basal and stimulated lipolysis. In 24-h-fasted rats its antilipolytic activity was long-lasting. Cyclonicate would influence not only triglyceride hydrolysis, but also free fatty acid utilization by adipose tissue.

Approval Year

Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:34:15 GMT 2023
Edited
by admin
on Fri Dec 15 16:34:15 GMT 2023
Record UNII
7H634NXI03
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CICLONICATE
INN   MART.   MI   WHO-DD  
INN  
Official Name English
CICLONICATE [MART.]
Common Name English
TRANS-3,3,5-TRIMETHYLCYCLOHEXYL NICOTINATE
Systematic Name English
CICLONICATE [MI]
Common Name English
Ciclonicate [WHO-DD]
Common Name English
ciclonicate [INN]
Common Name English
Classification Tree Code System Code
WHO-VATC QC04AC07
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
WHO-ATC C04AC07
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
Code System Code Type Description
SMS_ID
100000081888
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
FDA UNII
7H634NXI03
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
MERCK INDEX
m3538
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY Merck Index
PUBCHEM
10444661
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
NCI_THESAURUS
C167024
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
DRUG BANK
DB13709
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
ECHA (EC/EINECS)
258-561-4
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
EVMPD
SUB06243MIG
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
EPA CompTox
DTXSID001023827
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
MESH
C032821
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
WIKIPEDIA
CICLONICATE
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
CAS
53449-58-4
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
INN
3808
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
ChEMBL
CHEMBL2104521
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
DRUG CENTRAL
3908
Created by admin on Fri Dec 15 16:34:15 GMT 2023 , Edited by admin on Fri Dec 15 16:34:15 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY