JNJ-38877618

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Chemical Structure| 943540-74-7 同义名 : -
CAS号 : 943540-74-7
货号 : A967658
分子式 : C20H12F2N6
纯度 : 99%
分子量 : 374.35
MDL号 : MFCD31657377
存储条件:

Pure form Sealed in dry, 2-8°C

In solvent -20°C:3-6个月-80°C:12个月

溶解度 : -
动物实验配方:
生物活性
描述 JNJ-38877618 is a potent, highly selective, orally bioavailable Met kinase inhibitor with IC50s of 2 and 3 nM for wild type and mutant Met, respectively.
临床研究
NCT号 适应症或疾病 临床期 招募状态 预计完成时间 地点
NCT01964872 Healthy Volunteers Phase 1 Completed - United Kingdom ... 展开 >> Nottingham, United Kingdom 收起 <<
NCT03138083 Neoplasms Phase 1 Phase 2 Recruiting December 2020 France ... 展开 >> lNSTITUT GUSTAVE ROUSSY Recruiting Villejuif, France, 94805 Contact: Eric Angevin, MD          Netherlands Erasmus Mc Recruiting Rotterdam, Netherlands, 3000 CA Contact: Martijn Lolkema, MD/PhD          Universitair Medisch Centrum Utrecht Recruiting Utrecht, Netherlands, 3584 CX Contact: Filip De Vos, MD          United Kingdom University College London Hospitals Nhs Foundation Trust Recruiting London, United Kingdom, NW1 2BU Contact: Martin Forster, MD          The Christie Nhs Foundation Trust Recruiting Manchester, United Kingdom, M20 4BX Contact: Matthew G Krebs, MD PhD MRCP       Matthew.Krebs@christie.nhs.uk    The Newcastle Upon Tyne Hospitals Nhs Foundation Trust Recruiting Newcastle upon Tyne, United Kingdom, NE7 7DN Contact: Ruth Plummer, MD       Ruth.Plummer@newcastle.ac.uk    University of Oxford, Department of Oncology Recruiting Oxford, United Kingdom, OX3 7LE Contact: Sarah P Blagden, MD    +441865227212    sarah.blagden@oncology.ox.ac.uk 收起 <<
实验方案
1mg 5mg 10mg

1 mM

5 mM

10 mM

2.67mL

0.53mL

0.27mL

13.36mL

2.67mL

1.34mL

26.71mL

5.34mL

2.67mL