3,4-Dimethoxy-N-(5-phenyl-1H-pyrazol-3-yl)-benzamide
- Product Name
- 3,4-Dimethoxy-N-(5-phenyl-1H-pyrazol-3-yl)-benzamide
- CAS No.
- 942655-44-9
- Chemical Name
- 3,4-Dimethoxy-N-(5-phenyl-1H-pyrazol-3-yl)-benzamide
- Synonyms
- JK-P3;JK-P3, 10 mM in DMSO;3,4-Dimethoxy-N-(5-phenyl-1H-pyrazol-3-yl)-benzamide;Benzamide, 3,4-dimethoxy-N-(5-phenyl-1H-pyrazol-3-yl)-;JK-P3,Inhibitor,HUVEC,Anti-angiogenesis,FGFR,VEGFR,JK P3,Fibroblast growth factor receptor,JKP3,Anti-cancer,inhibit,Endothelial cells,JK-P-3,Vascular endothelial growth factor receptor
- CBNumber
- CB32750670
- Molecular Formula
- C18H17N3O3
- Formula Weight
- 323.35
- MOL File
- 942655-44-9.mol
3,4-Dimethoxy-N-(5-phenyl-1H-pyrazol-3-yl)-benzamide Property
- storage temp.
- 2-8°C
- solubility
- DMSO: soluble5mg/mL (clear solution)
- form
- powder
- color
- white to beige
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H302Harmful if swallowed
- Precautionary statements
-
P264Wash hands thoroughly after handling.
P264Wash skin thouroughly after handling.
P270Do not eat, drink or smoke when using this product.
P301+P312IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell.
P330Rinse mouth.
P501Dispose of contents/container to..…
N-Bromosuccinimide Price
- Product number
- SML0509
- Product name
- JK-P3
- Purity
- ≥98% (HPLC)
- Packaging
- 5mg
- Price
- $127
- Updated
- 2022/05/15
- Product number
- J0012
- Product name
- JK-P3
- Packaging
- 5MG
- Price
- $82
- Updated
- 2026/03/19
- Product number
- J0012
- Product name
- JK-P3
- Packaging
- 25MG
- Price
- $268
- Updated
- 2026/03/19
- Product number
- 42183
- Product name
- JK-P3,98%(HPLC)
- Purity
- 98%(HPLC)
- Packaging
- 5MG
- Price
- $131.04
- Updated
- 2021/12/16
- Product number
- 6471DD
- Product name
- 3,4-Dimethoxy-N-(5-phenyl-1H-pyrazol-3-yl)benzamide
- Packaging
- 5mg
- Price
- $220
- Updated
- 2021/12/16
3,4-Dimethoxy-N-(5-phenyl-1H-pyrazol-3-yl)-benzamide Chemical Properties,Usage,Production
Uses
JK-P3 is a potent and pan VEGFR2 inhibitor, with IC50s of 7.83 μM, 27 μM and 5.18 μM for VEGFR2, FGFR1 and FGFR3, respectively. JK-P3 can inhibit VEGF-A-stimulated VEGFR2 activation and intracellular signalling, also inhibits endothelial monolayer wound closure and angiogenesis, as well as fibroblast growth factor receptor kinase activity in vitro. JK-P3 has anti-angiogenic activity[1].
IC 50
VEGFR2: 7.83 μM (IC50); FGFR1: 27 μM (IC50); FGFR3: 5.18 μM (IC50)
References
[1] Kankanala J, et al. A combinatorial in silico and cellular approach to identify a new class of compounds that target VEGFR2 receptor tyrosine kinase activity and angiogenesis. Br J Pharmacol. 2012;166(2):737-748. DOI:10.1111/j.1476-5381.2011.01801.x
3,4-Dimethoxy-N-(5-phenyl-1H-pyrazol-3-yl)-benzamide Preparation Products And Raw materials
Raw materials
Preparation Products
3,4-Dimethoxy-N-(5-phenyl-1H-pyrazol-3-yl)-benzamide Suppliers
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