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Vitamin B12 test kit

Pazopanib

Cat. No.: 0225LY-0517
Appearance: Solid
Purity: ≥99%
Identity: Confirmed by NMR, HPLC, and LC-MS.
Size:
Pazopanib
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Product Overview

Description: Pazopanib acts as an inhibitor of several protein tyrosine kinases, including FGFR1, c-Kit, PDGFRβ, and VEGFR1–3, with IC50 values ranging from 10 nM to 146 nM, contributing to its antitumor efficacy.
Synonym: GW786034; 444731-52-6; 5-((4-((2,3-Dimethyl-2H-indazol-6-yl)(methyl)amino)pyrimidin-2-yl)amino)-2-methylbenzenesulfonamide; 5-[[4-[(2,3-Dimethylindazol-6-yl)-methylamino]pyrimidin-2-yl]amino]-2-methylbenzenesulfonamide
CAS No.: 444731-52-6
Compound CID: 10113978
Formula: C21H23N7O2S
Formula Weight: 437.52

Specification

Targets&IC50: VEGFR2: 30 nM; VEGFR3: 47 nM; VEGFR1: 10 nM; PDGFR: 84 nM; c-Kit: 74 nM
Relative Density: 1.40 g/cm3
Stability: 3 years in powder form.
Storage: Storage at -20°C.
Applications: Pazopanib can be used in angiogenesis research to evaluate the simultaneous inhibition of VEGFR, PDGFR, and c-Kit receptors.

Library Information

Target: FGFR; VEGFR; c-Kit; PDGFR
Receptor: c-Kit; FGFR; PDGFR; VEGFR1; VEGFR2; VEGFR3
Pathways: Tyrosine kinase/adaptors; Angiogenesis; Autophagy
Plate Number: AOCL-7
Plate Location: f10
Empty Location: a1-h1; a12-h12
Container: 96-well plate
Formulation: 10mM DMSO
DMSO Max Solubility: 25 mg/mL; 57.14 mM
Water Max Solubility: <1 mg/mL (insoluble or slightly soluble)
Ethanol Max Solubility: <1 mg/mL
ALogP: 3.741
HBA_Count: 5
HBD_Count: 2
Rotatable Bond: 5
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