ChemicalBook > CAS DataBase List > J&J Ex-61
J&J Ex-61
J&J Ex-61
- CAS No.943540-75-8
- Chemical Name:J&J Ex-61
- CBNumber:CB01872310
- Molecular Formula:C19H13F2N7
- Formula Weight:377.35
- MOL File:943540-75-8.mol
J&J Ex-61 Property
- Density 1.50
- storage temp. Store at -20°C
- solubility insoluble in H2O; ≥18.85 mg/mL in DMSO; ≥3.25 mg/mL in EtOH with ultrasonic
- form Powder
- pka 3.92±0.10(Predicted)
- color Off-white to light yellow
- CAS DataBase Reference 943540-75-8
- FDA UNII 15UDG410PN
Safety
-
Symbol(GHS)
- Signal wordWarning
- Hazard statements H319-H317
- Precautionary statements P261-P264-P272-P280-P302+P352-P305+P351+P338-P333+P313-P321-P337+P313-P363-P501
J&J Ex-61 Chemical Properties,Usage,Production
- Uses JNJ-38877605 is a potent inhibitor of c-Met catalytic activity. Selective over other tyrosine and serine-threonine kinases (600-fold selectivity). Ability to block constitutive or HGF-stimulated phosphorylation of c-Met demonstrated in vitro. JNJ 38877605 reduces radiation-induced invasion, apoptosis and proliferation of cancer cells in vitro.
- Definition ChEBI: 6-[difluoro-[6-(1-methyl-4-pyrazolyl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl]quinoline is a member of quinolines.
- Biological Activity jnj-38877605 is a small-molecule atp-competitive inhibitor of the catalytic activity of c-met.extensive evidence that c-met signaling is involved in the progression and spread of several cancers and an enhanced understanding of its role in disease have generated considerable interest in c-met and hgf asmajor targets in anti-cancer drug development.
- in vitro jnj-38877605 showed ~600-fold selectivity for c-met compared with a panel of ~250 diverse tyrosine and serine-threonine kinases and was found to potently inhibit hgf-stimulated and constitutively activated c-met phosphorylation in vitro [1].
- in vivo jnj-38877605 showed excellent oral bioavailability approaching 100% in all examined species. in addition, jnj-38877605 in a single dose was observed toinhibit met phosphorylation in tumor xenografts for up to16 h. inhibition of met phosphorylation was associated withdose-dependent tumor growth inhibition using a range of oral dosing regimens [2].
- target c-Met
- References [1] pererat, l avrijssent, janssens b, et al. jnj-38877605: a selective met kinase inhibitor inducingregression of met-driven tumor models. presented at the 99th aacr annual meeting; 2008 apr 12 -16;
J&J Ex-61 Preparation Products And Raw materials
Raw materials
Preparation Products
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943540-75-8, J&J Ex-61Related Search:
- Inhibitors
- 信号转导通路激酶抑制剂
- 抑制剂
- 药靶配体
- 合成材料中间体-高分子材料
- 小分子抑制剂,天然产物
- 蛋白酪氨酸激酶
- 杂环
- 芳烃衍生物
- C19H13F2N7
- 943540-74-1
- 化合物JNJ38877605,10 MM DMSO 溶液
- JNJ-38877605,C-MET抑制剂
- 化合物JNJ38877605
- 6-[二氟[6-(1-甲基-1H-吡唑-4-基)-1,2,4-噻唑并[4,3-B]吡嗪-3-基]甲基]-喹啉
- 6-[二氟[6-(1-甲基-1H-吡唑-4-基)-1,2,4-三唑并[4,3-B]哒嗪-3-基]甲基]喹啉
- 6-[二氟[6-(1-甲基-1H-吡唑-4-基)-1,2,4-三唑并[4,3-B]哒嗪-3
- 943540-75-8
- JNJ-38877605, 10 mM in DMSO
- Venadaparib Impurity 19
- 6-[difluoro-[6-(1-methylpyrazol-4-yl)-[1,2,4]triazolo[3,4-f]...
- J&J Ex-61 USP/EP/BP
- 6-[difluoro-[6-(1-methylpyrazol-4-yl)-[1,2,4]triazolo[3,4-f]pyridazin-3-yl]methyl]quinoline
- JNJ38877605; JNJ-38877605
- CS-43
- 6-[difluoro-[6-(1-methylpyrazol-4-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl]quinoline
- JNJ 38877605 NEW
- JNJ 38877605 6-[Difluoro[6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]pyridazin-3-yl]methyl]quinoline
- 6-[Difluoro[6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]pyridazin-3-yl]methyl]quinoline JNJ 38877605
- JNJ-33877605
- JNJ-38877605
- 6-(Difluoro(6-(1-methyl-1H-pyrazol-4-yl)-[1,2,4]-triazolo[4,3-b]pyridazin-3-yl)methyl)quinolin
- 6-[Difluoro[6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]pyridazin-3-yl]methyl]quinoline
- Quinoline, 6-[difluoro[6-(1-methyl-1H-pyrazol-4-yl)-1,2,4-triazolo[4,3-b]pyridazin-3-yl]methyl]-
- J&J Ex-61