Chemical Name: (3,4-Dihydroxy-5-nitrophenyl)(4-methylphenyl)methanone. Alternate Names: Ro 40-7592
COMT inhibitor, TTR aggregation inhibitor
Molekulargewicht:
273.24
Reinheit:
98% by TLC, NMR (Conforms)
Formulierung:
Yellow solid
CAS Nummer:
[134308-13-7]
Formel:
C14H11NO5
Anwendungsbeschreibung:
Catechol O-methyltransferase inhibitor (COMT), inhibiting both brain and peripheral enzymes.1 Potent inhibitor of alpha-synuclein and beta-amyloid oligomerization and fibrillogenesis protecting against extracellular toxicity.2 Binds to transthyretin (TTR) with high affinity (21 to 58 nM) and inhibits TTR aggregation in human plasma and prevents TTR-induced cytotoxicity in vitro. Stabilizes TTR in mice and humans in vivo.3 Inhibits O-methylation of exogenous polyphenols such as EGCG.4 Cell permeable. Orally bioavailable
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