RET-IN-3

  Cat. No.:  DC40626  
Chemical Structure
2414374-53-9
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More than 5000 active chemicals with high quality for research!
Field of application
RET-IN-3 (compound 34) is a selective RETV804M kinase inhibitor, with an IC50 of 19 nM.
Cas No.: 2414374-53-9
Chemical Name: RET-IN-3
SMILES: CN(C)CCCNC1=NC2=C(C3=CC(OCO4)=C4C=C3)C=NN2C=C1
Formula: C18H21N5O2
M.Wt: 339.39
Sotrage: Powder-20°C3 years4°C2 yearsIn solvent-80°C6 months-20°C1 month
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
Cat. No. Product name Field of application
DC47314 TPX-0046 TPX-0046 is a novel RET/SRC inhibitor with a mean IC50 of 17 nM for RETG810R in Ba/F3 cell proliferation assay.,RET [1]() SRC [1]()
DC47129 Zeteletinib Zeteletinib (BOS-172738) shows selective inhibitory activity against RET, PDGFR, KIT, NTRK and FLT3 kinases. Zeteletinib has antitumor activity.
DC47018 Vepafestinib Vepafestinib (compound 6) is a RET inhibitor (extracted from patent WO2019039439).
DC40626 RET-IN-3 RET-IN-3 (compound 34) is a selective RETV804M kinase inhibitor, with an IC50 of 19 nM.
DC40625 WF-47-JS03 WF-47-JS03 is a potent and selective RET kinase inhibitor with IC50s of 1.7 nM and 5.3 nM for KIF5B-RET transfected Ba/F3 cells and CCDC6-RET transfected LC-2/ad lung cancer cells, respectively. WF-47-JS03 demonstrates >500-fold selectivity against kinase insert domain receptor (KDR). Effective brain penetration.
DC10058 BBT594 BBT594 (NVP-BBT594), is potent and selective inhibitor of RET and JAK2.
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