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DSM502CAS No. : 2426616-55-7
MCE 國(guó)際站:DSM502
產(chǎn)品活性:DSM502 是一種基于吡咯的二氫乳清酸脫氫酶 (DHODH) 抑制劑。DSM502 對(duì) Plasmodium DHODH 和 Plasmodium 寄生蟲(chóng)表現(xiàn)出納摩爾級(jí)效力,對(duì)哺乳動(dòng)物 DHODH 沒(méi)有抑制作用。
研究領(lǐng)域:Metabolic Enzyme/Protease | Anti-infection
作用靶點(diǎn):Dihydroorotate Dehydrogenase | Parasite
In Vitro: DSM502 shows inhibitory activity against P. falciparum DHODH (PfDHODH, IC50=20 nM), P. vivax DHODH (PvDHODH, IC50=14 nM) and Pf3D7 cells (EC50=14 nM), with no inhibition of the human enzyme.
In Vivo: DSM502 (10 and 50 mg/kg; p.o. once daily for 4 days) results in 97% parasite clearance in confirmatory SCID study compared to 85% clearance in the GSK study.
DSM502 (18.3 and 50 mg/kg; a single p.o.) exhibits high oral bioavailability (>100%, >100%), apparent t1/2 (2.6, 3.6 h) and Cmax (8.4, 42.3 μM) in mice.
DSM502 (2.8 mg/kg; a single i.v.) exhibits apparent t1/2 (2.8 h), plasma clearance (26.1 mL/min/kg), and Vss (1.2 L/kg) in mice.
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