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Details

Stereochemistry ABSOLUTE
Molecular Formula C20H25ClN2O5
Molecular Weight 408.876
Optical Activity ( + )
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of AMLODIPINE, (R)-

SMILES

CCOC(=O)C1=C(COCCN)NC(C)=C([C@H]1C2=CC=CC=C2Cl)C(=O)OC

InChI

InChIKey=HTIQEAQVCYTUBX-QGZVFWFLSA-N
InChI=1S/C20H25ClN2O5/c1-4-28-20(25)18-15(11-27-10-9-22)23-12(2)16(19(24)26-3)17(18)13-7-5-6-8-14(13)21/h5-8,17,23H,4,9-11,22H2,1-3H3/t17-/m1/s1

HIDE SMILES / InChI

Molecular Formula C20H25ClN2O5
Molecular Weight 408.876
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 23:42:56 GMT 2025
Edited
by admin
on Mon Mar 31 23:42:56 GMT 2025
Record UNII
YUH55G7ZTY
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
AMLODIPINE, (R)-
Common Name English
(+)-AMLODIPINE
Preferred Name English
(R)-(+)-AMLODIPINE
Common Name English
(R)-AMLODIPINE
Common Name English
D-AMLODIPINE
Common Name English
3,5-PYRIDINEDICARBOXYLIC ACID, 2-((2-AMINOETHOXY)METHYL)-4-(2-CHLOROPHENYL)-1,4-DIHYDRO-6-METHYL-, 3-ETHYL 5-METHYL ESTER, (R)-
Systematic Name English
AMLODIPINE, (+)-
Common Name English
3,5-PYRIDINEDICARBOXYLIC ACID, 2-((2-AMINOETHOXY)METHYL)-4-(2-CHLOROPHENYL)-1,4-DIHYDRO-6-METHYL-, 3-ETHYL 5-METHYL ESTER, (4R)-
Systematic Name English
Code System Code Type Description
CAS
103129-81-3
Created by admin on Mon Mar 31 23:42:56 GMT 2025 , Edited by admin on Mon Mar 31 23:42:56 GMT 2025
PRIMARY
EPA CompTox
DTXSID90430938
Created by admin on Mon Mar 31 23:42:56 GMT 2025 , Edited by admin on Mon Mar 31 23:42:56 GMT 2025
PRIMARY
FDA UNII
YUH55G7ZTY
Created by admin on Mon Mar 31 23:42:56 GMT 2025 , Edited by admin on Mon Mar 31 23:42:56 GMT 2025
PRIMARY
PUBCHEM
9801597
Created by admin on Mon Mar 31 23:42:56 GMT 2025 , Edited by admin on Mon Mar 31 23:42:56 GMT 2025
PRIMARY
Related Record Type Details
RACEMATE -> ENANTIOMER
ENANTIOMER -> ENANTIOMER