E2535
Eprosartan mesylate
≥98% (HPLC)
Synonym(s):
Eprosartan Monomethanesulfonate, SKF-108566J, Teveten
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About This Item
Empirical Formula (Hill Notation):
C23H24N2O4S · CH4O3S
CAS Number:
Molecular Weight:
520.62
NACRES:
NA.77
PubChem Substance ID:
UNSPSC Code:
12352200
MDL number:
Quality Level
assay
≥98% (HPLC)
form
powder
color
white to off-white
solubility
DMSO: >10 mg/mL
originator
Abbott
storage temp.
room temp
SMILES string
CS(O)(=O)=O.CCCCc1ncc(\C=C(/Cc2cccs2)C(O)=O)n1Cc3ccc(cc3)C(O)=O
InChI
1S/C23H24N2O4S.CH4O3S/c1-2-3-6-21-24-14-19(12-18(23(28)29)13-20-5-4-11-30-20)25(21)15-16-7-9-17(10-8-16)22(26)27;1-5(2,3)4/h4-5,7-12,14H,2-3,6,13,15H2,1H3,(H,26,27)(H,28,29);1H3,(H,2,3,4)/b18-12+;
InChI key
DJSLTDBPKHORNY-XMMWENQYSA-N
Gene Information
human ... AGTR1(185)
Biochem/physiol Actions
Angiotensin II type 1 (AT1) receptor antagonist; anti-hypertensive.
Features and Benefits
This compound is featured on the Angiotensin Receptors page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.
This compound was developed by Abbott. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.
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signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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Wilco de Jager et al.
BMC immunology, 10, 52-52 (2009-09-30)
Growing knowledge about cellular interactions in the immune system, including the central role of cytokine networks, has lead to new treatments using monoclonal antibodies that block specific components of the immune system. Systemic cytokine concentrations can serve as surrogate outcome
Global Trade Item Number
| SKU | GTIN |
|---|---|
| E2535-10MG | 04061833602744 |
| E2535-50MG | 04061833218495 |