eprosartan (Q784717)

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angiotensin II receptor antagonist used for the treatment of high blood pressure.
  • Eprozar®
  • SK-108566
  • Teveten®
  • (E)-3-[2-n-butyl-1-{(4-carboxyphenyl)methyl}-1H-imidazol-5-yl]-2-(2-thienyl)methyl-2-propenoic acid
  • (E)-2-butyl-1-(p-carboxybenzyl)-alpha-2-thenylimidazole-5-acrylic acid
  • (E)-alpha{[2-butyl-1-[(4-carboxyphenyl)methyl]-1H-imidazole-5-yl]methylene}-2-thiopheneproprionic acid
  • (e)-3-[2-N-Butyl-1-{(4-carboxyphenyl)methyl}-1H-imidazol-5-yl]-2-(2-thienyl)methyl-2-propenoic acid
  • (e)-Alpha{[2-butyl-1-[(4-carboxyphenyl)methyl]-1H-imidazole-5-yl]methylene}-2-thiopheneproprionic acid
  • (e)-2-Butyl-1-(P-carboxybenzyl)-alpha-2-thenylimidazole-5-acrylic acid
  • Éprosartan
  • Eprosartanum
  • Eprosartan
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Language Label Description Also known as
English
eprosartan
angiotensin II receptor antagonist used for the treatment of high blood pressure.
  • Eprozar®
  • SK-108566
  • Teveten®
  • (E)-3-[2-n-butyl-1-{(4-carboxyphenyl)methyl}-1H-imidazol-5-yl]-2-(2-thienyl)methyl-2-propenoic acid
  • (E)-2-butyl-1-(p-carboxybenzyl)-alpha-2-thenylimidazole-5-acrylic acid
  • (E)-alpha{[2-butyl-1-[(4-carboxyphenyl)methyl]-1H-imidazole-5-yl]methylene}-2-thiopheneproprionic acid
  • (e)-3-[2-N-Butyl-1-{(4-carboxyphenyl)methyl}-1H-imidazol-5-yl]-2-(2-thienyl)methyl-2-propenoic acid
  • (e)-Alpha{[2-butyl-1-[(4-carboxyphenyl)methyl]-1H-imidazole-5-yl]methylene}-2-thiopheneproprionic acid
  • (e)-2-Butyl-1-(P-carboxybenzyl)-alpha-2-thenylimidazole-5-acrylic acid
  • Éprosartan
  • Eprosartanum
  • Eprosartan

Statements

has use
medication
0 references
chemical structure
Eprosartan.svg
512 × 393; 8 KB
0 references
mass
424.146 dalton
1 reference
stated in
PubChem
PubChem CID
5281037
language of work or name
English
title
133040-01-4 (English)
retrieved
18 November 2016
chemical formula
C₂₃H₂₄N₂O₄S
1 reference
stated in
PubChem
PubChem CID
5281037
language of work or name
English
title
133040-01-4 (English)
retrieved
18 November 2016
canonical SMILES
CCCCC1=NC=C(N1CC2=CC=C(C=C2)C(=O)O)C=C(CC3=CC=CS3)C(=O)O
1 reference
stated in
PubChem
PubChem CID
5281037
language of work or name
English
title
133040-01-4 (English)
retrieved
18 November 2016
isomeric SMILES
CCCCC1=NC=C(N1CC2=CC=C(C=C2)C(=O)O)/C=C(\CC3=CC=CS3)/C(=O)O
1 reference
stated in
PubChem
PubChem CID
5281037
language of work or name
English
title
133040-01-4 (English)
retrieved
18 November 2016
significant drug interaction
Commons category
Eprosartan
0 references

Identifiers

Reaxys registry number
4338002
1 reference
stated in
ChEBI
ChEBI ID
4814
language of work or name
English
title
eprosartan (English)
retrieved
3 October 2016
MassBank accession ID
MSBNK-Eawag-EA277601
0 references
MSBNK-Eawag-EA277602
0 references
MSBNK-Eawag-EA277603
0 references
MSBNK-Eawag-EA277604
0 references
MSBNK-Eawag-EA277605
0 references
MSBNK-Eawag-EA277606
0 references
MSBNK-Eawag-EA277607
0 references
MSBNK-Eawag-EA277608
0 references
MSBNK-Eawag-EA277609
0 references
MSBNK-Eawag-EA277610
0 references
MSBNK-Eawag-EA277611
0 references
MSBNK-Eawag-EA277612
0 references
MSBNK-Eawag-EA277613
0 references
MSBNK-Eawag-EA277614
0 references
MSBNK-Eawag-EA277651
0 references
MSBNK-Eawag-EA277652
0 references
MSBNK-Eawag-EA277653
0 references
MSBNK-Eawag-EA277654
0 references
MSBNK-Eawag-EA277655
0 references
MSBNK-Eawag-EA277656
0 references
MSBNK-Eawag-EA277657
0 references
MSBNK-Eawag-EA277658
0 references
MSBNK-Eawag-EA277659
0 references
MSBNK-Eawag-EA277660
0 references
MSBNK-Eawag-EA277661
0 references
MSBNK-Eawag-EA277662
0 references
MSBNK-Eawag-EA277663
0 references
MSBNK-Eawag-EA277664
0 references
SPLASH
HSDB ID
7521
1 reference
stated in
Hazardous Substances Data Bank
HSDB ID
7521
publication date
28 October 2019
title
EPROSARTAN (English)
retrieved
10 May 2021
LiverTox ID
Eprosartan
0 references
KEGG ID
D04040
1 reference
stated in
ChEBI
ChEBI ID
4814
language of work or name
English
title
eprosartan (English)
retrieved
3 October 2016
C07467
1 reference
stated in
ChEBI
ChEBI ID
4814
language of work or name
English
title
eprosartan (English)
retrieved
3 October 2016
 
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