SML0509

JK-P3

≥98% (HPLC)

• 同義詞: 3,4-Dimethoxy-N-(5-phenyl-1H-pyrazol-3-yl)-benzamide
• 經驗公式（希爾表示法）: C₁₈H₁₇N₃O₃
• CAS號碼: 942655-44-9
• 分子量：: 323.35
• MDL號碼: MFCD22666405
• 分類程式碼代碼: 12352200
• PubChem物質ID: 329825518
• NACRES: NA.77

屬性

• 化驗: ≥98% (HPLC)
• 形狀: powder
• 顏色: white to beige
• 溶解度: DMSO: 5 mg/mL (clear solution)
• 儲存溫度: 2-8°C
• SMILES 字串: COc1ccc(cc1OC)C(=O)Nc2cc([nH]n2)-c3ccccc3
• InChI: 1S/C18H17N3O3/c1-23-15-9-8-13(10-16(15)24-2)18(22)19-17-11-14(20-21-17)12-6-4-3-5-7-12/h3-11H,1-2H3,(H2,19,20,21,22)
• InChI 密鑰: QAZJUVDICQNITG-UHFFFAOYSA-N

描述

生化／生理作用

JK-P3 is a VEGFR-2 inhibitor.

JK-P3 is a pyrazole-based inhibitor of VEGFR-2 (IC₅₀ = 7.8 μM). JK-P3 inhibits FGFR 1/3 kinase activity in vitro, but has no effect on FGFR signaling in cell-based assays. The compound blocks wound healing and tube formation in HUVEC without effecting endothelial cell proliferation.

特點和優勢

This compound is a featured product for Kinase Phosphatase Biology research. Click here to discover more featured Kinase Phosphatase Biology products. Learn more about bioactive small molecules for other areas of research at sigma.com/discover-bsm.

This compound is featured on the FGFR page of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

安全資訊

• 象形圖: GHS07
• 訊號詞: Warning
• 危險聲明: H302
• 危險分類: Acute Tox. 4 Oral
• 儲存類別代碼: 13 - Non Combustible Solids
• 水污染物質分類（WGK）: WGK 3
• 閃點（°F）: Not applicable
• 閃點（°C）: Not applicable