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≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C,Desiccated Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
FNDR-20123 is a safe, first-in-class, and orally active anti-malarial HDAC inhibitor with IC 50 s of 31 nM and 3 nM for Plasmodium and human HDAC , respectively. FNDR-20123 exerts anti-malarial activity against Plasmodium falciparum asexual stage (IC 50 =
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IC50& Target:human HDAC 3 nM (IC 50 ) Plasmodium HDAC 31 nM (IC 50 ) HDAC1 25 nM (IC 50 ) HDAC2 29 nM (IC 50 ) HDAC3 2 nM (IC 50 ) HDAC6 11 nM (IC 50 ) HDAC8 282 nM (IC 50 ) Plasmodium
In Vitro:FNDR-20123 is active against all resistant strains tested so far, which will be highly valuable in eliminating the rapidly evolving drug-resistant parasite. MCE has not independently confirmed the accuracy of these methods. They are for reference onl
In Vivo:FNDR-20123 (10-50mg/kg; p.o.; bw for 4 days) is also able to reduce parasitaemia significantly in a mouse model for P. falciparum infection. MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model
Biological Activity:FNDR-20123 is a safe, first-in-class, and orally active anti-malarial HDAC inhibitor with IC 50 s of 31 nM and 3 nM for Plasmodium and human HDAC , respectively. FNDR-20123 exerts anti-malarial activity against Plasmodium falciparum asexual stage (IC 50 =
| Peso molecular | 413.9 |
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Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →| Solubilidad | DMSO : 31.25 mg/mL (75.50 mM; Need ultrasonic) |
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