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Details

Stereochemistry ABSOLUTE
Molecular Formula C34H38N3O7P.ClH
Molecular Weight 668.116
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of EFONIDIPINE HYDROCHLORIDE, (R)-

SMILES

Cl.CC1=C([C@@H](C2=CC=CC(=C2)[N+]([O-])=O)C(=C(C)N1)P3(=O)OCC(C)(C)CO3)C(=O)OCCN(CC4=CC=CC=C4)C5=CC=CC=C5

InChI

InChIKey=OXVTXPCIJDYQIS-JSSVAETHSA-N
InChI=1S/C34H38N3O7P.ClH/c1-24-30(33(38)42-19-18-36(28-15-9-6-10-16-28)21-26-12-7-5-8-13-26)31(27-14-11-17-29(20-27)37(39)40)32(25(2)35-24)45(41)43-22-34(3,4)23-44-45;/h5-17,20,31,35H,18-19,21-23H2,1-4H3;1H/t31-;/m1./s1

HIDE SMILES / InChI

Molecular Formula ClH
Molecular Weight 36.461
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Molecular Formula C34H38N3O7P
Molecular Weight 631.6552
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Targets

Targets

Primary TargetPharmacologyConditionPotency
Target ID: O54898
Gene ID: NA
Gene Symbol: Cacna1g
Target Organism: Rattus norvegicus (Rat)
Substance Class Chemical
Created
by admin
on Sat Dec 16 10:38:29 UTC 2023
Edited
by admin
on Sat Dec 16 10:38:29 UTC 2023
Record UNII
084B99HW0I
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
EFONIDIPINE HYDROCHLORIDE, (R)-
Common Name English
(-)-EFONIDIPINE HYDROCHLORIDE
Common Name English
3-PYRIDINECARBOXYLIC ACID, 5-(5,5-DIMETHYL-2-OXIDO-1,3,2-DIOXAPHOSPHORINAN-2-YL)-1,4-DIHYDRO-2,6-DIMETHYL-4-(3-NITROPHENYL)-, 2-(PHENYL(PHENYLMETHYL)AMINO)ETHYL ESTER, MONOHYDROCHLORIDE, (4R)-
Systematic Name English
Code System Code Type Description
FDA UNII
084B99HW0I
Created by admin on Sat Dec 16 10:38:29 UTC 2023 , Edited by admin on Sat Dec 16 10:38:29 UTC 2023
PRIMARY
CAS
330548-22-6
Created by admin on Sat Dec 16 10:38:29 UTC 2023 , Edited by admin on Sat Dec 16 10:38:29 UTC 2023
PRIMARY
PUBCHEM
76963365
Created by admin on Sat Dec 16 10:38:29 UTC 2023 , Edited by admin on Sat Dec 16 10:38:29 UTC 2023
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER