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Submit ReviewML T7 is a T cell immunoglobulin and mucin-containing molecule 3 (Tim-3) inhibitor; disrupts phosphatidylserine/CAECAM1 binding to Tim-3 (Kd = 7.0 μM and 7.4 μM for hTim-3 and mTim-3 respectively). ML T7 promotes cell proliferation, cytokine production and cytotoxicity of OT-I CD8+ cytotoxic T lymphocytes. ML T7 inhibits tumor growth in a syngeneic mouse model of hepatocellular carcinoma, increases NK cell tumor killing activity and DC maturation.
分子量 | 506.34 |
公式 | C27H17Cl2NO5 |
储存 | Store at -20°C |
纯度 | ≥98% (HPLC) |
CAS Number | 459789-75-4 |
PubChem ID | 3116616 |
InChI Key | OFJOQMMYCMPPEC-UHFFFAOYSA-N |
Smiles | ClC1=CC=C(C(Cl)=C1)N2C(C(C3C2=O)C(OC43C(C5=C(C4=O)C=CC=C5)=O)C6=CC=C(C=C6)C)=O |
上方提供的技术数据仅供参考。批次相关数据请参见分析证书。
Tocris products are intended for laboratory research use only, unless stated otherwise.
溶剂 | 最高浓度 mg/mL | 最高浓度 mM | |
---|---|---|---|
溶解性 | |||
DMSO | 50.63 | 100 |
以下数据基于产品分子量 506.34。 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.
浓度/溶剂体积/质量 | 1 mg | 5 mg | 10 mg |
---|---|---|---|
1 mM | 1.97 mL | 9.87 mL | 19.75 mL |
5 mM | 0.39 mL | 1.97 mL | 3.95 mL |
10 mM | 0.2 mL | 0.99 mL | 1.97 mL |
50 mM | 0.04 mL | 0.2 mL | 0.39 mL |
参考文献是支持产品生物活性的出版物。
Ma et al (2023) Identification of a small-molecule Tim-3 inhibitor to potentiate T cell-mediated antitumor immunotherapy in preclinical mouse models. Sci.Transl.Med. 15 PMID: 37967204
If you know of a relevant reference for ML T7, please let us know.
关键词: ML T7, ML T7 supplier, MLT7, ML, T7, T, cell, immunoglobulin, mucin, Tim3, Tim-3, inhibitor, phosphatidylserine, CEACAM1, cytokine, lymphocytes, HCC, hepatocellular, carcinoma, NK, natural, killer, Immune, Checkpoints, 8119, Tocris Bioscience
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Tocris offers the following scientific literature in this area to showcase our products. We invite you to request* your copy today!
*请注意,Tocris 仅会向正规科研企业/机构地址发送文献。
This poster summarizes the main metabolic pathways in cancer cells and highlights potential targets for cancer therapeutics. Genetic changes and epigenetic modifications in cancer cells alter the regulation of cellular metabolic pathways providing potential cancer therapeutic targets.