Chemical Structure : BTSA1
CAS No.: 314761-14-3
货号: PC-72944Not For Human Use, Lab Use Only.
BTSA1 (BAX Trigger Site Activator 1) is a potent, selective, orally bioavailable BAX trigger site activator, binds with high affinity (EC50=144 nM) and specificity to the N-terminal activation site.
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---|---|---|---|
10 mg | ¥1280 | In stock | |
25 mg | ¥2180 | In stock | |
50 mg | ¥3580 | In stock | |
100 mg | Get quote |
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BTSA1 (BAX Trigger Site Activator 1) is a potent, selective, orally bioavailable BAX trigger site activator, binds with high affinity (EC50=144 nM) and specificity to the N-terminal activation site.
BTSA1 competed FITC-BIM SAHBA2 with IC50 of 250 nM in competitive fluorescence polarization assays.
BTSA1 displays no affinity on anti-apoptotic BCL-2 proteins, BCL-XL, MCL-1 and BFL-1/A1.
BTSA1 induces conformational changes to BAX leading to BAX-mediated apoptosis, induces all steps of the BAX activation pathway.
BTSA1 induced BAX activation effectively and selectively promotes apoptosis of acute myeloid leukemia cells.
BTSA1 is effective against patient AML blasts and pre-leukemic stem cells without affecting normal hematopoietic progenitor cells and demonstrates significant synergy with Venetoclax.
分子量 | 430.504 | |
分子式 | C21H14N6OS2 | |
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 |
1H-Pyrazole-4,5-dione, 3-phenyl-1-(4-phenyl-2-thiazolyl)-, 4-[2-(2-thiazolyl)hydrazone] |
1. Denis E Reyna, et al. Cancer Cell. 2017 Oct 9;32(4):490-505.e10.
2. Liang T, et al. J Med Chem. 2020 Oct 22;63(20):12083-12099.
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