GW806742X

  Cat. No.:  DC10503   Featured
Chemical Structure
579515-63-2
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More than 5000 active chemicals with high quality for research!
Field of application
GW806742X is a novel VEGFR inhibitor.
Cas No.: 579515-63-2
Chemical Name: 1-[4-[Methyl-[2-[(3-Sulfamoylphenyl)amino]pyrimidin-4-Yl]amino]phenyl]-3-[4-(Trifluoromethyloxy)phenyl]urea
Synonyms: GW806742X;3-(4-(Methyl(4-(3-(4-(trifluoromethoxy)phenyl)ureido)phenyl)amino)pyrimidin-2-ylamino)benzenesulfonamide;1-[4-[methyl-[2-[(3-Sulfamoylphenyl)amino]pyrimidin-4-Yl]amino]phenyl]-3-[4-(Trifluoromethyloxy)phenyl]urea;urea deriv. 23;MLKL compound 1;BDBM5832;GTPL9513;C25H22F3N7O4S;SYN1215;HMS3303M11;HMS3305G22;BCP29591;NSC756366;compound 23 [PMID: 15990302];1-[4-[methyl-[2-(3-sulfamoylanilino)pyrimidin-4-yl]amino]phenyl]-3-[4-(trifluoromethoxy)phenyl]urea;GW80674
SMILES: S(C1=C([H])C([H])=C([H])C(=C1[H])N([H])C1=NC([H])=C([H])C(=N1)N(C([H])([H])[H])C1C([H])=C([H])C(=C([H])C=1[H])N([H])C(N([H])C1C([H])=C([H])C(=C([H])C=1[H])OC(F)(F)F)=O)(N([H])[H])(=O)=O
Formula: C25H22F3N7O4S
M.Wt: 573.5469
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Description: GW806742X is a Mixed Lineage Kinase Domain-Like (MLKL) inhibitor which binds the MLKL pseudokinase domain with a Kd value of 9.3 μM and anti-necroptosis activity. GW806742X has activity against VEGFR2[1][2].
MSDS
COA
LOT NO. DOWNLOAD
2018-0101
2018-0101
Cat. No. Product name Field of application
DC7889 URMC-099 URMC-099 is an orally bioavailable, brain penetrant mixed lineage kinase (MLK) inhibitor with IC50 of 19 nM, 42 nM, 14 nM, and 150 nM, for MLK1, MLK2, MLK3, and DLK, respectively, and also inhibits LRRK2 activity with IC50 of 11 nM.
DC9817 Necrosulfonamide (NSA) Necrosulfonamide (NSA) is a very specific and potent necrosis inhibitor with an IC50 less than 0.2 uM.
DC10503 GW806742X GW806742X is a novel VEGFR inhibitor.
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