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FNDR-20123 (free base)
SKU
HY-131708-Get quote
Category Reference compound
Tags Anti-infection;Cell Cycle/DNA Damage;Epigenetics, HDAC;Parasite, Infection
Products Details
Product Description
– FNDR-20123 free base is a safe, first-in-class, and orally active anti-malarial HDAC inhibitor with IC50s of 31 nM and 3 nM for Plasmodium and human HDAC, respectively. FNDR-20123 free base exerts anti-malarial activity against Plasmodium falciparum asexual stage (IC50=41 nM) and sexual blood stage (IC50=190 nM for male gametocytes). FNDR-20123 free base inhibits HDAC1, HDAC2, HDAC3, HDAC6, and HDAC8 (IC50=25, 29, 2, 11, and 282 nM, respectively) and inhibits Class III HDAC isoforms at nanomolar concentrations[1].
Web ID
– HY-131708
Shipping
– Room temperature
Applications
– COVID-19-anti-virus
Molecular Formula
– C21H23N5O2
References
– [1]Potluri V, et al. Discovery of FNDR-20123, a histone deacetylase inhibitor for the treatment of Plasmodium falciparum malaria. Malar J. 2020;19(1):365. Published 2020 Oct 12.
CAS Number
– 1267502-34-0
Molecular Weight
– 377.44
SMILES
– O=C(NO)C1=CC=C(CN2N=NC(C3=CC=C(CN4CCCC4)C=C3)=C2)C=C1
Clinical Information
– No Development Reported
Research Area
– Infection
Solubility
– DMSO : 35.71 mg/mL (ultrasonic)
Target
– HDAC;Parasite
Isoform
– HDAC;HDAC1;HDAC2;HDAC3;HDAC6;HDAC8;Plasmodium
Pathway
– Anti-infection;Cell Cycle/DNA Damage;Epigenetics
Product type
– Reference compound
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