Chemical Structure : TMBIM6 antagonist BIA
CAS No.: 123134-61-2
货号: PC-28256Not For Human Use, Lab Use Only.
TMBIM6 antagonist BIA (Bax inhibitor-1 antagonist, TMBIM6 antagonist-1) is a specific small molecule TMBIM6 (Bax inhibitor-1, BI-1) antagonist, prevents TMBIM6 binding to mTORC2, decreases mTORC2 activity, also regulates TMBIM6-leaky Ca2+.
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 5 mg | ¥1280 | In stock | |
| 10 mg | ¥1980 | In stock | |
| 25 mg | ¥3280 | In stock | |
| 50 mg | Get quote | ||
| 100 mg | Get quote |
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TMBIM6 antagonist BIA (Bax inhibitor-1 antagonist, TMBIM6 antagonist-1) is a specific small molecule TMBIM6 (Bax inhibitor-1, BI-1) antagonist, prevents TMBIM6 binding to mTORC2, decreases mTORC2 activity, also regulates TMBIM6-leaky Ca2+.
BIA inhibits proliferation and cell viability of MCF7 and MDA-MB-231 cells highly expressed TMBIM6 with IC50 of 1.7-2.6 uM.
BIA reduces cell proliferation by inducing the dissociation of TMBIM6 from mTORC2 and ribosome, result in cell death.
BIA suppresses ER release of Ca2+ from TMBIM6. decreased cell migration in HT1080, MCF7, MDA-MB-231, and SKBR3 cells, but not TMBIM6 KO HT1080 cells.
BIA ( 1 mg/kg, vehicle 0.1% DMSO with saline) markedly impaired cell-driven tumor growth of injected HT1080 and MDA-MB-231 cells into immunocompromised mice.
BIA significantly attenuated inflammatory cell infiltration, goblet cell hyperplasia, airway remodelling and Th2-associated cytokine expression in the lungs of A. fumigatus-challenged mice.
Transmembrane B cell lymphoma 2-associated X protein (BAX) inhibitor motif-containing (TMBIM)6, an inhibitor of ER stress.
TMBIM6 is a Ca2+ channel-like protein that lowers the steady-state [Ca2+]ER, which is expressed in the endoplasmic reticulum (ER) membrane surface.
TMBIM6 is overexpressed in many cancer types.
| 分子量 | 268.27 | |
| 分子式 | C15H12N2O3 | |
| 外观性状 | Solid | |
| 储存条件 |
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| Solubility |
10 mM in DMSO |
|
| Chemical Name/SMILES |
1-(2-Aminophenyl)-3-(3-nitrophenyl)prop-2-en-1-one |
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1. Kim HK, et al. TMBIM6/BI-1 contributes to cancer progression through assembly with mTORC2 and AKT activation. Nat Commun. 2020 Aug 11;11(1):4012.
2. Yu YJ, et al. Br J Pharmacol. 2026 Oct;183(19):5975-5991.
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