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Details

Stereochemistry ABSOLUTE
Molecular Formula C26H33N5O3
Molecular Weight 463.5719
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Valsartan Ethyl Ester, L-

SMILES

CCCCC(=O)N(CC1=CC=C(C=C1)C2=C(C=CC=C2)C3=NN=NN3)[C@@H](C(C)C)C(=O)OCC

InChI

InChIKey=BTSNVLAJCYDJEU-DEOSSOPVSA-N
InChI=1S/C26H33N5O3/c1-5-7-12-23(32)31(24(18(3)4)26(33)34-6-2)17-19-13-15-20(16-14-19)21-10-8-9-11-22(21)25-27-29-30-28-25/h8-11,13-16,18,24H,5-7,12,17H2,1-4H3,(H,27,28,29,30)/t24-/m0/s1

HIDE SMILES / InChI

Molecular Formula C26H33N5O3
Molecular Weight 463.5719
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 Sat Dec 16 19:52:08 GMT 2023
Edited
by admin
on Sat Dec 16 19:52:08 GMT 2023
Record UNII
9K9ZK2M3DP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Valsartan Ethyl Ester, L-
Common Name English
N-(1-Oxopentyl)-N-[[2′-(2H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-L-valine ethyl ester
Systematic Name English
(S)-Ethyl 2-(N-((2'-(2H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)pentanamido)-3-methylbutanoate
Systematic Name English
Ethyl N-((2'-(1H-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl)methyl)-N-pentanoyl-L-valinate
Systematic Name English
Ethyl (2S)-3-methyl-2-(N-{[2'-(1H-1,2,3,4-tetrazol-5-yl)-[1,1'-biphenyl]-4-yl]methyl}pentanamido)butanoate
Systematic Name English
Valsartan Ethyl Ester
Common Name English
L-Valine, N-(1-oxopentyl)-N-[[2′-(2H-tetrazol-5-yl)[1,1′-biphenyl]-4-yl]methyl]-, ethyl ester
Systematic Name English
Code System Code Type Description
PUBCHEM
58153804
Created by admin on Sat Dec 16 19:52:09 GMT 2023 , Edited by admin on Sat Dec 16 19:52:09 GMT 2023
PRIMARY
CAS
1111177-30-0
Created by admin on Sat Dec 16 19:52:09 GMT 2023 , Edited by admin on Sat Dec 16 19:52:09 GMT 2023
PRIMARY
FDA UNII
9K9ZK2M3DP
Created by admin on Sat Dec 16 19:52:09 GMT 2023 , Edited by admin on Sat Dec 16 19:52:09 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> ENANTIOMER