目錄:MedChemExpress LLC>>生化試劑>> PHT-7.3 | MCE
CAS | 1614225-93-2 | 純度 | 98.50% |
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分子量 | 433.52 | 分子式 | C??H??N?O?S |
供貨周期 | 現(xiàn)貨 | 規(guī)格 | 5 mg |
貨號 | HY-128590 | 應(yīng)用領(lǐng)域 | 醫(yī)療衛(wèi)生,化工,生物產(chǎn)業(yè),制藥 |
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CAS No. : 1614225-93-2
產(chǎn)品活性:PHT-7.3 is a selective inhibitor of connector enhancer of kinase suppressor of Ras 1 (Cnk1) pleckstrin homology (PH) domain (Kd=4.7 μM). PHT-7.3 inhibits mut-KRas, but not wild-type KRas cancer cell and tumor growth and signaling. PHT-7.3 has antitumor activity.
研究領(lǐng)域:GPCR/G Protein
作用靶點(diǎn):Ras
In Vivo: PHT-7.3 (200 mg/kg; i.p.; daily; for 20 days) exhibits cytostatic antitumor activity in the mut-KRas(G12S) A549 xenograft and mut-KRasG12V H441 xenograft.
相關(guān)產(chǎn)品:Bioactive Compound Library Plus | GPCR/G Protein Compound Library | Kinase Inhibitor Library | Anti-Cancer Compound Library | Ferroptosis Compound Library | Glutamine Metabolism Compound Library | Anti-Pancreatic Cancer Compound Library | Anti-Blood Cancer Compound Library | Angiogenesis-Related Compound Library | Anti-Liver Cancer Compound Library | Anti-Colorectal Cancer Compound Library | Heterocyclic Compound Library | Membrane Protein-targeted Compound Library | Membrane Receptor-targeted Compound Library | LC-2 | KRAS G12C inhibitor 54 | MRTX1133 | AZA1 | RBC10 | CFL-137 | Deltarasin hydrochloride | BDP9066 | CCG-100602 | KRAS inhibitor-4 | KRas G12R inhibitor 1 | MRTX0902 | KRAS G12C inhibitor 25 | Antitumor agent-60 | KRAS G12C inhibitor 30 | KRas G12C inhibitor 1 | Spiclomazine hydrochloride | GGTI-286 hydrochloride | 6H05 | AZD4625 | SOS1-IN-6 | Antineoplaston A10 | Opnurasib | K-Ras-IN-1 | BI-0474 | Diazepinomicin | K20 | BQU57 | KRAS G12D inhibitor 12 | KRas G12C inhibitor 3
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