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Submit ReviewSID 26681509 is a potent and reversible human cathepsin L inhibitor (IC50 = 56 nM). Displays no inhibitory activity at cathepsin G. Antimalarial; inhibits leishmaniasis.
SID 26681509 is also offered as part of the Tocriscreen 2.0 Max. 了解 Tocris 化合物库的更多信息。
分子量 | 539.65 |
公式 | C27H33N5O5S |
储存 | Store at -20°C |
纯度 | ≥97% (HPLC) |
CAS Number | 958772-66-2 |
PubChem ID | 16725315 |
InChI Key | OTIWAYTTYNFEKL-QFIPXVFZSA-N |
Smiles | O=C(NNC(SCC(NC1=C(CC)C=CC=C1)=O)=O)[C@H](CC2=CNC3=C2C=CC=C3)NC(OC(C)(C)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 | 26.98 | 50 | |
ethanol | 5.4 | 10 |
以下数据基于产品分子量 539.65。 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 |
---|---|---|---|
0.5 mM | 3.71 mL | 18.53 mL | 37.06 mL |
2.5 mM | 0.74 mL | 3.71 mL | 7.41 mL |
5 mM | 0.37 mL | 1.85 mL | 3.71 mL |
25 mM | 0.07 mL | 0.37 mL | 0.74 mL |
参考文献是支持产品生物活性的出版物。
Shah et al (2008) Kinetic characterization and molecular docking of a novel, potent and selective slow-binding inhibitor of human cathepsin L. Mol.Pharmacol. 74 34 PMID: 18403718
Myers et al (2008) Identification and synthesis of a unique thiocarbazate cathepsin L inhibitor. Bioorg.Med.Chem.Lett. 18 210 PMID: 18060772
If you know of a relevant reference for SID 26681509, please let us know.
关键词: SID 26681509, SID 26681509 supplier, SID26681509, cathepsin, L, inhibitors, inhibits, cysteine, protease, antimalarial, Cathepsin, Calcium-Sensitive, Proteases, 3625, Tocris Bioscience
引用文献是使用了 Tocris 产品的出版物。 SID 26681509 的部分引用包括:
Rui et al (2021) Integrated transcriptomic analysis of human tuberculosis granulomas and a biomimetic model identifies therapeutic targets. J Clin Invest 131 PMID: 34128839
您是否知道使用了 Tocris SID 26681509 的优秀论文? 请告知我们.
平均评分: 5 (Based on 1 Review.)
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