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Details

Stereochemistry RACEMIC
Molecular Formula C36H41N3O6
Molecular Weight 611.7272
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of LERCANIDIPINE

SMILES

COC(=O)C1=C(C)NC(C)=C(C1C2=CC=CC(=C2)[N+]([O-])=O)C(=O)OC(C)(C)CN(C)CCC(C3=CC=CC=C3)C4=CC=CC=C4

InChI

InChIKey=ZDXUKAKRHYTAKV-UHFFFAOYSA-N
InChI=1S/C36H41N3O6/c1-24-31(34(40)44-6)33(28-18-13-19-29(22-28)39(42)43)32(25(2)37-24)35(41)45-36(3,4)23-38(5)21-20-30(26-14-9-7-10-15-26)27-16-11-8-12-17-27/h7-19,22,30,33,37H,20-21,23H2,1-6H3

HIDE SMILES / InChI

Molecular Formula C36H41N3O6
Molecular Weight 611.7272
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 17:54:59 UTC 2023
Edited
by admin
on Sat Dec 16 17:54:59 UTC 2023
Record UNII
V7XTJ4R0BH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
LERCANIDIPINE
INN   MI   WHO-DD  
INN  
Official Name English
Lercanidipine [WHO-DD]
Common Name English
3,5-PYRIDINEDICARBOXYLIC ACID, 1,4-DIHYDRO-2,6-DIMETHYL-4-(3-NITROPHENYL)-, 2-((3,3-DIPHENYLPROPYL)METHYLAMINO)-1,1-DIMETHYLETHYL METHYL ESTER
Common Name English
LERCANIDIPINE [MI]
Common Name English
lercanidipine [INN]
Common Name English
LERCANIL
Brand Name English
2-((3,3-DIPHENYLPROPYL)METHYLAMINO)-1,1-DIMETHYLETHYL METHYL (4RS)-2,6-DIMETHYL-4-(3-NITROPHENYL)-1,4-DIHYDROPYRIDINE-3,5-DICARBOXYLATE
Systematic Name English
Classification Tree Code System Code
WHO-ATC C09DB08
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
NCI_THESAURUS C333
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
WHO-ATC C08CA13
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
WHO-ATC C09BB02
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
WHO-VATC QC09BB02
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
WHO-VATC QC08CA13
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
Code System Code Type Description
MESH
C060343
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY
FDA UNII
V7XTJ4R0BH
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY
WIKIPEDIA
LERCANIDIPINE
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY
DRUG BANK
DB00528
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY
DRUG CENTRAL
4157
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY
INN
6971
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY
SMS_ID
100000092283
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY
PUBCHEM
65866
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY
NCI_THESAURUS
C81687
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY
ChEMBL
CHEMBL250270
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY
CAS
100427-26-7
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY
EPA CompTox
DTXSID2048327
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY
MERCK INDEX
m6770
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY Merck Index
EVMPD
SUB08437MIG
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY
RXCUI
135056
Created by admin on Sat Dec 16 17:55:00 UTC 2023 , Edited by admin on Sat Dec 16 17:55:00 UTC 2023
PRIMARY RxNorm
Related Record Type Details
SALT/SOLVATE -> PARENT
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
SALT/SOLVATE -> PARENT
TARGET -> INHIBITOR
Related Record Type Details
ACTIVE MOIETY