J4649

JNJ-10198409

≥98% (HPLC), solid

• 동의어(들): 3-Fluoro-N-(6,7-dimethoxy-2,4-dihydroindeno[1,2-c]pyrazol-3-yl)phenylamine, N-(3-fluorophenyl)-2,4-dihydro-6,7-dimethoxy-Indeno[1,2-c]pyrazol-3-amine, RWJ 540973
• 실험식(Hill 표기법): C₁₈H₁₆FN₃O₂
• CAS Number: 627518-40-5
• Molecular Weight: 325.34
• UNSPSC 코드: 51111800
• PubChem Substance ID: 329815736
• NACRES: NA.77

속성

• 분석: ≥98% (HPLC)
• 형태: solid
• 색상: off-white
• solubility: DMSO: >10 mg/mL; H₂O: <2 mg/mL
• 주관자: Johnson & Johnson
• 저장 온도: −20°C
• SMILES string: COc1cc2Cc3c(Nc4cccc(F)c4)n[nH]c3-c2cc1OC
• InChI: 1S/C18H16FN3O2/c1-23-15-7-10-6-14-17(13(10)9-16(15)24-2)21-22-18(14)20-12-5-3-4-11(19)8-12/h3-5,7-9H,6H2,1-2H3,(H2,20,21,22)
• InChI key: ZDNURMVOKAERHZ-UHFFFAOYSA-N

설명

생화학적/생리학적 작용

JNJ-10198409 is a potent ATP-competitive inhibitor of Platelet-Derived Growth Factor receptor tyrosine kinase (PDGF-RTK) with both antiangiogenic and a direct tumor cell antiproliferative activity. It is selective for PDGF-β kinase with IC₅₀ values of 4.2 nM for PDGF-β and 45 nM for PDGF-α kinase.

특징 및 장점

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 PAF Receptor and PDGFR pages of the Handbook of Receptor Classification and Signal Transduction. To browse other handbook pages, click here.

This compound was developed by Johnson & Johnson. To browse the list of other pharma-developed compounds and Approved Drugs/Drug Candidates, click here.

안전성 정보

• Storage Class Code: 11 - Combustible Solids
• WGK: WGK 3
• Flash Point (°F): Not applicable
• Flash Point (°C): Not applicable