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JK-P3

For Research Use Only. Not for use in diagnostic procedures. Catalog #: MBS3607674

JK-P3 is a pyrazole-based inhibitor of VEGFR-2 (IC50: 7.8 uM). JK-P3 inhibits FGFR 1/3 kinase activity in vitro, but has no effect on FGFR signaling in cell-based assays. More details

$215 / 1mL*10mM (in DMSO) +1 FREE 8GB USB
Product Documentation
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Sample Manual Insert View PDF
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Testing Data View PDF
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Certificate of Analysis (COA) View PDF
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QC Report View PDF
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Material Safety Data Sheet View PDF
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Technical Datasheet View PDF
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Protocol View PDF

Product Overview

Online Datasheet in PDF
Product Name
JK-P3, Biochemical
Full Product Name
JK-P3
Product Synonym Names
3, 4-Dimethoxy-N-(5-phenyl-1H-pyrazol-3-yl)-benzamide
Purity/Purification
>98% (HPLC)
Preparation and Storage
Store at -20 degree C
Stability: >=2 years
Shipping: Ice Pack
Molecular Weight
323.35
Target
GTPase
Receptor
VEGFR2
Chemical Name
3, 4-Dimethoxy-N-(5-phenyl-1H-pyrazol-3-yl)-benzamide
SMILES
COc1c(cc(cc1)C(=O)Nc1n[nH]c(c1)c1ccccc1)OC
Molecular Formula
C18H17N3O3
CAS Number
942655-44-9

Product Categories/Family for JK-P3 biochemical

Others

Structure of JK-P3 biochemical

Jk-P3 Biochemical – Cat# MBS3607674

Product References and Citations for JK-P3 biochemical

1. Antony M. Latham, et al. Identification of Receptor Tyrosine Kinase Inhibitors Using Cell Surface Biotinylation and Affinity Isolation. VEGF Signaling pp 121-131 Cite as

Other Notes

Small volumes of JK-P3 biochemical vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.

Searchable Terms for JK-P3 purchase

MBS3607674 is a biochemical targeting JK-P3.
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