R916562

  Cat. No.:  DC10995  
Chemical Structure
1037798-41-6
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More than 5000 active chemicals with high quality for research!
Field of application
R916562 (R562) is a potent, dual Axl/VEGF-R2 inhibitor with celluar IC50 of 136 nM for Axl.
Cas No.: 1037798-41-6
Chemical Name: 1H-1,2,4-Triazole-3,5-diamine, N3-[4-[4-(1R,2R,4S)-bicyclo[2.2.1]hept-2-yl-1-piperazinyl]phenyl]-1-(2-chloro-7-methylthieno[3,2-d]pyrimidin-4-yl)-
Synonyms: R 916562;R-916562;R562
SMILES: N(C1N=C(Cl)N=C2C(C)=CSC2=1)1C(N)=NC(NC2=CC=C(N3CCN([C@H]4CC5CC4CC5)CC3)C=C2)=N1
Formula: C26H30ClN9S
M.Wt: 536.099
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: R916562 (R562) is a potent, dual Axl/VEGF-R2 inhibitor with celluar IC50 of 136 nM for Axl; blocks growth of MDA-MB-231 breast carcinomas implanted subcutaneously in nu/nu mice, also shows efficacy in the Caki-1 human renal carcinoma xenograft model.
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
Cat. No. Product name Field of application
DC47331 AZ14145845 AZ14145845 is a highly selective type I1/2 dual Mer/Axl kinase inhibitor with in vivo efficacy.
DC11690 RU-302 RU-302 is a small molecule pan-TAM inhibitor that targets the TAM Ig1-Gas6 interface, blocks Gas6-dependent TAM activation.
DC10995 R916562 R916562 (R562) is a potent, dual Axl/VEGF-R2 inhibitor with celluar IC50 of 136 nM for Axl.
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