U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C27H28N2O7
Molecular Weight 492.5204
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of CILNIDIPINE

SMILES

COCCOC(=O)C1=C(C)NC(C)=C(C1C2=CC(=CC=C2)[N+]([O-])=O)C(=O)OC\C=C\C3=CC=CC=C3

InChI

InChIKey=KJEBULYHNRNJTE-DHZHZOJOSA-N
InChI=1S/C27H28N2O7/c1-18-23(26(30)35-14-8-11-20-9-5-4-6-10-20)25(21-12-7-13-22(17-21)29(32)33)24(19(2)28-18)27(31)36-16-15-34-3/h4-13,17,25,28H,14-16H2,1-3H3/b11-8+

HIDE SMILES / InChI

Molecular Formula C27H28N2O7
Molecular Weight 492.5204
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 1
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 16:31:16 UTC 2023
Edited
by admin
on Fri Dec 15 16:31:16 UTC 2023
Record UNII
97T5AZ1JIP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
CILNIDIPINE
INN   JAN   MART.   MI   WHO-DD  
INN  
Official Name English
CILNIDIPINE [JAN]
Common Name English
cilnidipine [INN]
Common Name English
SISCARD
Brand Name English
FRC-8653
Code English
Cilnidipine [WHO-DD]
Common Name English
CILNIDIPINE [MART.]
Common Name English
ATELEC
Brand Name English
(±)-(E)-CINNAMYL 2-METHOXYETHYL 1,4-DIHYDRO-2,6-DIMETHYL-4-(M-NITROPHENYL)-3,5-PYRIDINEDICARBOXYLATE
Systematic Name English
CINALONG
Brand Name English
CILNIDIPINE [MI]
Common Name English
3,5-PYRIDINEDICARBOXYLIC ACID, 1,4-DIHYDRO-2,6-DIMETHYL-4-(3-NITROPHENYL)-, 3-(2-METHOXYETHYL) 5-((2E)-3-PHENYL-2-PROPEN-1-YL) ESTER
Systematic Name English
Classification Tree Code System Code
WHO-VATC QC08CA14
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
WHO-ATC C08CA14
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
Code System Code Type Description
MESH
C065927
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
CAS
132203-70-4
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
CAS
102106-21-8
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
NON-SPECIFIC STEREOCHEMISTRY
NCI_THESAURUS
C171754
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
MERCK INDEX
m3548
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY Merck Index
PUBCHEM
5282138
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
FDA UNII
97T5AZ1JIP
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
DRUG CENTRAL
642
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
IUPHAR
7767
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
EPA CompTox
DTXSID0046309
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
SMS_ID
100000091319
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
WIKIPEDIA
Cilnidipine
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
ChEMBL
CHEMBL452076
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
EVMPD
SUB06268MIG
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
INN
6880
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
DRUG BANK
DB09232
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
CHEBI
31399
Created by admin on Fri Dec 15 16:31:16 UTC 2023 , Edited by admin on Fri Dec 15 16:31:16 UTC 2023
PRIMARY
Related Record Type Details
TARGET -> INHIBITOR
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
ACTIVE MOIETY