Chemical Structure : JB170
CAS No.: 2705844-82-0
货号: PC-24082Not For Human Use, Lab Use Only.
JB170 is a potent, highly selective PROTAC degrader of Aurora A with DC50 of 28 nM and Dmax of 300 nM in MV4-11 cells, linking alisertib to the cereblon-binding molecule Thalidomide.
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---|---|---|---|
5 mg | ¥1880 | In stock | |
10 mg | ¥2980 | In stock | |
25 mg | ¥4980 | In stock | |
50 mg | Get quote | ||
100 mg | Get quote |
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JB170 is a potent, highly selective PROTAC degrader of Aurora A with DC50 of 28 nM and Dmax of 300 nM in MV4-11 cells, linking alisertib to the cereblon-binding molecule Thalidomide.
JB170 selectively binds AURORA-A (EC50=193 nM) over AURORA-B (EC50=1.4 µM).
JB170 reduces AURORA-A levels by inducing proteolysis, induces AURORA-A ubiquitylation by CEREBLON followed by proteolysis via the proteasome.
JB170 induces S-phase arrest in in MV4-11 cells, induces apoptosis in cancer cells.
分子量 | 963.37 | |
分子式 | C48H44ClFN8O11 | |
外观性状 | Solid | |
储存条件 |
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Solubility |
10 mM in DMSO |
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Chemical Name/SMILES |
4-((9-Chloro-7-(2-fluoro-6-methoxyphenyl)-5H-benzo[c]pyrimido[4,5-e]azepin-2-yl)amino)-N-(2-(2-(2-(2-((2-(2,6-dioxopiperidin-3-yl)-1,3-dioxoisoindolin-4-yl)oxy)acetamido)ethoxy)ethoxy)ethyl)-2-methoxybenzamide |
1. Adhikari B, et al. Nat Chem Biol. 2020;16(11):1179-1188.
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