BAY-2416964 is a potent and orally active aryl hydrocarbon receptor (AHR) antagonist extracted from patent WO2018146010A1, example 192, has an IC50 of 341 nM. BAY2416964 specifically binds to AhR, inhibits AhR activation, and prevents AhR-mediated signaling. Abrogation of AhR activation prevents the activation of immune-tolerant dendritic cells (DCs) and regulatory T cells (Tregs) in the tumor microenvironment (TME). This may restore the immune response against tumor cells. .
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名称 | BAY-2416964 |
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Iupac 化学名称 | (S)-6-(4-chlorophenyl)-N-(1-hydroxypropan-2-yl)-2-(1-methyl-1H-pyrazol-4-yl)-3-oxo-2,3-dihydropyridazine-4-carboxamide |
同义词 | BAY-2416964; BAY 2416964; BAY2416964; |
英文同义词 | BAY-2416964; BAY 2416964; BAY2416964; |
分子式 | C18H18ClN5O3 |
分子量 | 387.824 |
Smile | O=C(C1=CC(C2=CC=C(Cl)C=C2)=NN(C3=CN(C)N=C3)C1=O)N[C@@H](C)CO |
InChiKey | YAGSZKAJPHGVOV-NSHDSACASA-N |
InChi | InChI=1S/C18H18ClN5O3/c1-11(10-25)21-17(26)15-7-16(12-3-5-13(19)6-4-12)22-24(18(15)27)14-8-20-23(2)9-14/h3-9,11,25H,10H2,1-2H3,(H,21,26)/t11-/m0/s1 |
Cas号 | 2242464-44-2 |
相关CAS号 | 2242464-44-2 |
包装 | 价格 | 库存 | 纯度 | 备货期 |
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大货 | 询价 | 询价 | 询价 |
外观性状 | Solid powder |
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纯度 | 98% Min. |
存储 | Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years). |
可溶性 | Soluble in DMSO |
处理方式 | Refer to MSDS |
运输条件 | Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs. |
海关编码 | 2934200090 |
Targets | |
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Mechanism | |
Cell study | |
Animal study | |
Clinical study |