INCB040093

  Cat. No.:  DC11631  
Chemical Structure
1262440-25-4
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More than 5000 active chemicals with high quality for research!
Field of application
A novel potent, selective, orally available PI3Kδ inhibitor with IC50 of 31 nM.
Cas No.: 1262440-25-4
Chemical Name: 6-(3-fluorophenyl)-3-methyl-7-((1S)-1-(9H-purin-6-ylamino)ethyl)-5H-(1,3)thiazolo(3,2-a)pyrimidin-5-one
Synonyms: INCB 040093;INCB-040093;Dezapelisib
SMILES: C12SC=C(C)N1C(=O)C(C1=CC=CC(F)=C1)=C([C@H](NC1=C3C(=NC=N1)NC=N3)C)N=2
Formula: C20H16FN7Os
M.Wt: 421.454
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: A novel potent, selective, orally available PI3Kδ inhibitor with IC50 of 31 nM; displays 74 to >900-fold selectivity for the other PI3K family members, and does not inhibit a panel of 57 additional kinases; potently inhibits cellular proliferation CD19+ human or CD21+ canine primary B cells with IC50 of 1-3 nM, reduces anti-FcR-induced basophil activation in the presence of human whole blood (IC50=33 nM); demonstrates promising efficacy in patients with Hodgkin's lymphoma in clinical studies.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
Cat. No. Product name Field of application
DC8652 TGR-1202 hydrochloride(Umbralisib) TGR-1202 hydrochloride is an orally available, next generation PI3Kdelta inhibitor, inhibits PI3Kδ activity in enzyme and cell based assays with IC50 and EC50 values of 22.2 and 24.3 nM respectively.
DC10150 Tenalisib Tenalisib (RP6530) is a novel, potent, and selective PI3Kδ and PI3Kγ inhibitor with IC50 values of 25 and 33 nM, respectively.
DC11631 INCB040093 A novel potent, selective, orally available PI3Kδ inhibitor with IC50 of 31 nM.
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