BFH772

Item number	Size	Delivery time	Price
TGM-T3599-2mg	2 mg	7 - 10 business days*	40.00€
TGM-T3599-5mg	5 mg	7 - 10 business days*	60.00€
TGM-T3599-1mL	1 ml	7 - 10 business days*	67.00€
TGM-T3599-10mg	10 mg	7 - 10 business days*	103.00€
TGM-T3599-25mg	25 mg	7 - 10 business days*	198.00€
TGM-T3599-50mg	50 mg	7 - 10 business days*	295.00€
TGM-T3599-100mg	100 mg	7 - 10 business days*	560.00€

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Description: BFH772, a structure analogue of BAW2881, is a potent and selective VEGF inhibitor.... more

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Product information "BFH772"

Description: BFH772, a structure analogue of BAW2881, is a potent and selective VEGF inhibitor. BFH772 is highly effective at targeting VEGFR2 kinase with an IC50 value of 3 nM. BFH772 inhibits the ligand induced autophosphorylation of RET, PDGFR, and KIT kinases, with IC50 values ranging between 30 and 160 nM. Target: VEGFR. Smiles: OCc1cc(Oc2ccc3c(cccc3c2)C(=O)Nc2cccc(c2)C(F)(F)F)ncn1. References: Bold G, et al. J Med Chem. 2016, 59(1):132-46.

Keywords:	BFH-722
Supplier:	TargetMol
Supplier-Nr:	T3599

Properties

Application:	VEGFR2 inhibitor
MW:	439.39 D
Formula:	C23H16F3N3O3

Database Information

CAS :	890128-81-1\| Matching products
KEGG ID :	K05098 \| Matching products

Handling & Safety

Storage:	+4°C
Shipping:	+4°C (International: +4°C)

Caution
Our products are for laboratory research use only: Not for administration to humans!

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