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TG 100572

Chemical Structure : TG 100572

CAS No.: 867334-05-2

TG 100572 (TG100572;TG-100572)

Catalog No.: PC-42431Not For Human Use, Lab Use Only.

TG100572 is a potent, dual receptor tyrosine kinase/Src kinase inhibitor with IC50 of 2-16 nM for VEGFR, FGFR and PDGFR, 0.1-5 nM for Src family.

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Purity & Documentation Purity: >98% (HPLC) Select Batch:

Biological Activity

TG100572 is a potent, dual receptor tyrosine kinase/Src kinase inhibitor with IC50 of 2-16 nM for VEGFR, FGFR and PDGFR, 0.1-5 nM for Src family.
TG100572 inhibits vascular endothelial cell proliferation in vitro (ED50=610 nM) and blocks VEGF-induced phosphorylation of ERK, induces apoptosis.
TG100572 significant suppresses laser-induced choroidal neovascularization (CNV) in a murine model.

Physicochemical Properties

M.Wt 475.9699
Formula C26H26ClN5O2
Appearance Solid
CAS No.
Storage
Solide Powder
-20 °C 12 Months; 4°C 6 Months
In Solvent
-80 °C 6 Months; -20°C 6 Months
Shipping
Solubility

10 mM in DMSO

Chemical Name/SMILES

Phenol, 4-chloro-3-[5-methyl-3-[[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]amino]-1,2,4-benzotriazin-7-yl]-

References

1. Doukas J, et al. J Cell Physiol. 2008 Jul;216(1):29-37.

2. Sharma S, et al. J Virol. 2011 Jun;85(12):5995-6007.

3. Palanki MS, et al. J Med Chem. 2008 Mar 27;51(6):1546-59.

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