E2535

Eprosartanmesylat

≥98% (HPLC)

• Synonym(e): Eprosartan Monomethanesulfonate, SKF-108566J, Teveten
• Empirische Formel (Hill-System): C₂₃H₂₄N₂O₄S · CH₄O₃S
• CAS-Nummer: 144143-96-4
• Molekulargewicht: 520.62
• NACRES: NA.77
• PubChem Substance ID: 329799032
• UNSPSC Code: 12352200
• MDL number: MFCD08141807
• Assay: ≥98% (HPLC)
• Form: powder
• Quality level: 100

Eigenschaften

• Quality Level: 100
• 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)

Beschreibung

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.

Sicherheitshinweise

• pictograms: GHS07
• signalword: Warning
• hcodes: H315,H319
• pcodes: P264 - P280 - P302 + P352 - P305 + P351 + P338 - P332 + P313 - P337 + P313
• Hazard Classifications: Eye Irrit. 2 - Skin Irrit. 2
• Lagerklasse: 11 - Combustible Solids
• wgk: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable