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HDAC-IN-35
SKU
HY-146539-Get quote
Category Reference compound
Tags Cancer, Cell Cycle/DNA Damage;Epigenetics;Protein Tyrosine Kinase/RTK, HDAC;VEGFR
Products Details
Product Description
– HDAC-IN-35 (Compound 14) is a potent, selective HDAC and VEGFR-2 inhibitor, with IC50 values of 0.166 and 13.2 µM for HDAC6 and VEGFR-2, respectively[1].
Web ID
– HY-146539
Shipping
– Room temperature
Applications
– Cancer-Kinase/protease
Molecular Formula
– C17H13ClF3N3O3
References
– [1]Szu Lee, et al. Effect of phenylurea hydroxamic acids on histone deacetylase and VEGFR-2. Bioorg Med Chem. 2021 Nov 15;50:116454.
Molecular Weight
– 399.75
SMILES
– O=C(NO)/C=C/C1=CC=C(C=C1)NC(NC2=CC=C(C(C(F)(F)F)=C2)Cl)=O
Clinical Information
– No Development Reported
Research Area
– Cancer
Solubility
– 10 mM in DMSO
Target
– HDAC;VEGFR
Isoform
– HDAC1;HDAC6;HDAC8;VEGFR2/KDR/Flk-1
Pathway
– Cell Cycle/DNA Damage;Epigenetics;Protein Tyrosine Kinase/RTK
Product type
– Reference compound
Disclaimer: All products are for Research use only unless clearly stated otherwise on the product datasheet. Datasheets provided on the website are drafts for reference purpose only and you are requested to always refer to the hard copy included in the kit for your experimentation. Agdia Products are available for delivery only in Canada.