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ZM 323881 HCl
Cat. No.:
OB0225WX-2536
Appearance:
Solid
Purity:
≥99%
Identity:
Confirmed by NMR, and HPLC.
Size:
Add to basket
Product Overview
Description:
ZM 323881 is a potent VEGFR2 antagonist with an IC50 of less than 2 nM, showing nearly no inhibitory effect on VEGFR1, PDGFR-beta, or EGFR.
Synonym:
193000-39-4; ZM 323881 hydrochloride; ZM323881 hydrochloride; ZM323881 (hydrochloride); ZM-323881 hydrochloride; 4-fluoro-2-methyl-5-[(7-phenylmethoxyquinazolin-4-yl)amino]phenol;hydrochloride; 5-{[7-(benzyloxy)quinazolin-4-yl]amino}-4-fluoro-2-methylphenol hydrochloride; 5-((7-(benzyloxy)quinazolin-4-yl)amino)-4-fluoro-2-methylphenol hydrochloride; ZM323881 HCl; 5-[(7-Benzyloxyquinazolin-4-yl)amino]-4-fluoro-2-methylphenol hydrochloride; MFCD08703130; ZM 323881 monohydrochloride; ZM-323881 monohydrochloride; 7-benzyloxy-4-(2-fluoro-5-hydroxy-4-methylanilino)quinazoline hydrochloride; 4-Fluoro-2-methyl-5-[[7-(phenylmethoxy)-4-quinazolinyl]amino]phenol Hydrochloride; 5-((7-Benzyloxyquinazolin-4-yl )amino)-4-fluoro-2-methylphenol hydrochloride; 5-{[7-(Benzyloxy)-4-quinazolinyl]amino}-4-fluoro-2-methylphenol hydrochloride (1:1); 7-(benzyloxy)-N-(2-fluoro-5-hydroxy-4-methylphenyl)quinazolin-4-aminium chloride
CAS No.:
193000-39-4
Compound CID:
22624897
Formula:
C22H18FN3O2·HCl
Formula Weight:
411.86
Specification
Stability:
3 years in powder form.
Storage:
Storage at -20°C.
Applications:
ZM 323881 HCl is applied in vascular biology as a potent and selective VEGFR2 inhibitor to investigate the molecular mechanisms of endothelial cell signaling and the inhibition of angiogenesis.
Library Information
Target:
VEGFR
Receptor:
VEGFR2
Pathways:
Protein tyrosine kinase
Plate Number:
L6700-05
Empty Location:
a1-h1; a12-h12
Container:
96-well plate
Formulation:
10mM DMSO
DMSO Max Solubility:
10 mg/mL; 24.28 mM
ALogP:
5.876
HBA_Count:
3
HBD_Count:
2
Rotatable Bond:
5





