O1385

Ozagrel hydrochloride hydrate

≥98% (HPLC), solid

• Synonym(e): (E)-3-[4-(Imidazol-1-ylmethyl)phenyl]propenoic acid hydrochloride hydrate, OKY-046
• Empirische Formel (Hill-System): C₁₃H₁₂N₂O₂ · HCl · xH₂O
• CAS-Nummer: 78712-43-3
• Molekulargewicht: 264.71 (anhydrous basis)
• MDL-Nummer: MFCD00911569
• UNSPSC-Code: 12352200
• PubChem Substanz-ID: 24897942
• NACRES: NA.77

Eigenschaften

• Assay: ≥98% (HPLC)
• Form: solid
• Lagerbedingungen: desiccated
• Farbe: white to off-white
• Löslichkeit: H₂O: soluble
• Lagertemp.: room temp
• SMILES String: O.Cl.OC(=O)\C=C\c1ccc(Cn2ccnc2)cc1
• InChI: 1S/C13H12N2O2.ClH.H2O/c16-13(17)6-5-11-1-3-12(4-2-11)9-15-8-7-14-10-15;;/h1-8,10H,9H2,(H,16,17);1H;1H2/b6-5+;;
• InChIKey: OWIZTYOMGVTSDP-TXOOBNKBSA-N

Beschreibung

Anwendung

Ozagrel hydrochloride hydrate has been used as a thromboxane synthase inhibitor:

• in high cholesterol-diet rats (HC) to test its effect on arteriolar constriction
• to pre-treat mice to test its effect on lipopolysaccharide (LPS)-induced behavioral changes
• to test its effect on arteriolar vasoconstriction in hyperglycemic mice

Biochem./physiol. Wirkung

Ozagrel is useful in treating lacunar and thrombotic stroke. It blocks vasoconstriction and platelet aggregation. Ozagrel aids in improving the prostacyclin (PGI2)/ thromboxane A2 (TXA2) in the acute phase of cerebral ischemia. It improves endothelial dysfunction in L-methionine-induced hyperhomocysteinemia (HHcy)-induced vascular cognitive impairment and dementia (VCID).

Ozagrel is a selective thromboxane A₂ synthase (TXA₂) inhibitor.

Sicherheitshinweise

• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 2
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: Eyeshields, Gloves, type N95 (US)