CUDC-101，HDAC/EGFR/HER2 Inhibitor

Overview
Catalog #	bs-60092c-5-mg-solid
Product Name	CUDC-101，HDAC/EGFR/HER2 Inhibitor
Specifications
Storage Buffer	Powder
Storage Condition	Store in dry, dark place at -20C for 1 year.
Target
Product Information	Molecular Weight: 434.49 Formula: C24 H26 N4 O4 CAS Number: 1012054-59-9 InChi Key: PLIVFNIUGLLCEK-UHFFFAOYSA-N InChi: InChI=1S/C24H26N4O4/c1-3-17-9-8-10-18(13-17)27-24-19-14-22(21(31-2)15-20(19)25-16-26-24)32-12-7-5-4-6-11-23(29)28-30/h1,8-10,13-16,30H,4-7,11-12H2,2H3,(H,28,29)(H,25,26,27) Smiles: COC1C=C2N=CN=C(NC3C=CC=C(C=3)C#C)C2=CC=1OCCCCCCC(=O)NO Purity: 98.0 Solubility: DMSO up to 100 mM Appearance: Solid Power. Shelf Life: 1.0 years
Description	CUDC-101 is a potent multi-target inhibitor targeting HDAC, EGFR and HER2 with IC50 of 4.4 nM, 2.4 nM, and 15.7 nM, respectively.It is specific for class I and class II HDACs, not for class III Sir-type HDACs, and has > 50-fold selectivity against other protein kinases. CUDC-101 displays broad antiproliferative activity in many human cancer cell types with IC50 of 0.04-0.80 μM, exhibiting a higher potency than erlotinib, lapatinib, and combinations of vorinostat with either erlotinib or lapatinib in most cases. It can inhibit EGFR and Her2 phosphorylation, reduce cell proliferation and induce apoptosis in HCC827 non-small cell lung cancer (NSCLC) xenografts. It inhibits EGFR and induces upregulation of acetylated histone H3 in a dosedependent fashion. In vivo CUDC-101 promotes tumor regression in various cancer xenograft models such as non-small cell lung cancer (NSCLC), liver, breast, head and neck, colon, and pancreatic cancers. Currently it is in Phase I clinical trials for advanced head and neck, gastric, breast, liver and non-small cell lung cancer tumors.