Eprosartan Mesylate

HCID 5282474

Basic information

CAS
144143-96-4
Standard SMILES
CCCCc1ncc(/C=C(\Cc2cccs2)C(=O)O)n1Cc1ccc(C(=O)O)cc1.CS(=O)(=O)O
InChIKey
DJSLTDBPKHORNY-XMMWENQYSA-N
Molecular formula
C24H28N2O7S2
Average molar mass
520.6 g/mol
Monoisotopic mass
520.13379358

Names & identifiers

Preferred name
Eprosartan Mesylate
IUPAC
4-[[2-butyl-5-[(E)-2-carboxy-3-thiophen-2-ylprop-1-enyl]imidazol-1-yl]methyl]benzoic acid;methanesulfonic acid
English name
Eprosartan mesylate
Molecular formula
C24H28N2O7S2
Molecular weight
520.62

Names & synonyms

EPROSARTAN MESYLATETevetenEprosartan mesilateeprosartan methanesulfonateEprosartan MonomethanesulfonateSK&F 108566-JDTXSID7044217UNII-8N2L1NX8S3SK&F-108566-J8N2L1NX8S3DTXCID5024217CHEBI:48409
Show more names
Eprosartan MyslateEposartan mesylateMonomethanesulfonateEprosartanMesylate>Eprosartan mesylate, >=99%Eprosartan mesylate USP/EP/BPSunitinib and its interMediate
(E)-2-Butyl-1-(p-carboxybenzyl)-alpha-2-thenylimidazole-5-acrylic acid, monomethanesulfonateTEVETEN HCT COMPONENT EPROSARTAN MESYLATE2-Thiophenepropanoic acid, alpha-((2-butyl-1-((4-carboxyphenyl)methyl)-1H-imidazol-5-yl)methylene)-, (E)-, monomethanesulfonateEPROSARTAN MESILATE (MART.)EPROSARTAN MESILATE [MART.]EPROSARTAN MESYLATE (USP-RS)EPROSARTAN MESYLATE [USP-RS](E)-alpha-((2-butyl-1-((4-carboxyphenyl)methyl)-1H-imidazol-5-yl)methylene)-2-thiophenepropanoic acid monomethanesulfonate

Database identifiers

CAS
144143-96-4
PubChem CID
5282474
DTXSID
DTXSID7044217
ChEMBL
CHEMBL1200987
ChEBI
CHEBI:48409
UNII
8N2L1NX8S3

Properties

Computed structural properties

Topological polar surface area
183 Ų
Hydrogen bond donors
3
Hydrogen bond acceptors
9
Rotatable bonds
10
Heavy atoms
35

Physicochemical properties

Melting point
248 · 248-250°
storage temp.
Sealed in dry,Room Temperature
solubility
10 mg/mL · DMSO: >10mg/mL
form
powder
color
white to off-white
Merck
14 · 14,3635

Safety & regulation

Toxicology

Drug Induced Liver Injury · 6 items

Drug Induced Liver Injury Rank (DILIrank 2.0)

Eprosartan mesylate

Ambiguous-DILI-concern

3

Adverse reactions

DOI:10.1016/j.drudis.2016.02.015

Effects During Pregnancy and Lactation · 1 item

◉ Summary of Use during Lactation;Eprosartan is no longer marketed in the US. Because no information is available on the use of eprosartan during breastfeeding, an alternate drug may be preferred, especially while nursing a newborn or preterm infant.;◉ Effects in Breastfed Infants;Relevant published information was not found as of the revision date.;◉ Effects on Lactation and Breastmilk;Relevant published information was not found as of the revision date.

Safety data

wgk
3
rtecs
XN0282400
hs_code
29349990
risk_code
36/37/38
Signal word
Warning
Symbol(GHS)
GHS07

Chemistry & industry

Applications

UsesEprosartan Mesylate is an angiotensin II receptor antagonists. Eprosartan Mesylate is used as an antihypertensive agent.

Suppliers100 total

国药集团化学试剂有限公司86-21-63210123 · [email protected]
北京华美互利生物化工010-56205725 · [email protected]
梯希爱(上海)化成工业发展有限公司021-67121386 · [email protected]
上海阿拉丁生化科技股份有限公司400-6206333 13167063860 · [email protected]
Shandong chuangyingchemical Co., Ltd.18853181302 · [email protected]

Additional notes

DefinitionChEBI: Eprosartan methanesulfonate is a methanesulfonate salt. It has a role as an antihypertensive agent. It contains an eprosartan.

Related reactions

6 records

Compound notes

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