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| 货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
|---|---|---|---|---|
| T288490-5mg |
5mg |
现货 ![]() |
| |
| T288490-10mg |
10mg |
现货 ![]() |
| |
| T288490-25mg |
25mg |
现货 ![]() |
| |
| T288490-50mg |
50mg |
期货 ![]() |
| |
| T288490-100mg |
100mg |
现货 ![]() |
|
| 别名 | 奥利索西 | 胆甾-4-烯-3-酮肟 |
|---|---|
| 英文别名 | Q27271076 | AKOS005145744 | XAA03387 | N-[(1R,3aS,3bS,9aR,9bS,11aR)-9a,11a-dimethyl-1-[(2R)-6-methylheptan-2-yl]-1H,2H,3H,3aH,3bH,4H,5H,7H,8H,9H,9aH,9bH,10H,11H,11aH-cyclopenta[a]phenanthren-7-ylidene]hydroxylamine | UNII-I2QN18P645 | (NZ)-N-[(8S,9S,10R,1 |
| 规格或纯度 | Moligand™, ≥98%(HPLC) |
| 英文名称 | TRO 19622 |
| 生化机理 | 神经保护和神经再生化合物。从轴突切开术诱导的细胞死亡中拯救运动神经元,并促进体内坐骨神经挤压后促进神经再生。直接结合到线粒体通透性孔的两个组件上,即电压依赖性阴离子通道(VDAC)和转运蛋白。被认为抑制了MPTP的开放。 |
| 储存温度 | -20°C储存,干燥 |
| 运输条件 | 超低温冰袋运输 |
| 产品介绍 |
application: TRO 19622 has been used as a mitochondrial permeability transition pore inhibitor in mouse neurons. TRO 19622 is also known to stimulate myelin repair in rat models of demyelination. |
| 纯度 | ≥98%(HPLC) |
| PubChem SID | 504769037 |
|---|---|
| 分子类型 | 小分子 |
| IIUPAC Name | (NZ)-N-[(8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-[(2R)-6-methylheptan-2-yl]-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-ylidene]hydroxylamine |
| INCHI | 1S/C27H45NO/c1-18(2)7-6-8-19(3)23-11-12-24-22-10-9-20-17-21(28-29)13-15-26(20,4)25(22)14-16-27(23,24)5/h17-19,22-25,29H,6-16H2,1-5H3/b28-21-/t19-,22+,23-,24+,25+,26+,27-/m1/s1 |
| InChi Key | QNTASHOAVRSLMD-FCARAQADSA-N |
| Smiles | CC(C)CCCC(C)C1CCC2C1(CCC3C2CCC4=CC(=NO)CCC34C)C |
| Isomeric SMILES | C[C@H](CCCC(C)C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CCC4=C/C(=N\O)/CC[C@]34C)C |
| PubChem CID | 21763506 |
| 分子量 | 399.65 |
| 溶解性 | 溶于DMSO, 最高浓度 (mg/mL): 19.98, 最高浓度(mM): 50;溶于ethanol, 最高浓度 (mg/mL): 7.99, 最高浓度(mM): 20 |
|---|---|
| 分子量 | 399.700 g/mol |
| XLogP3 | 8.800 |
| 氢键供体数Hydrogen Bond Donor Count | 1 |
| 氢键受体数Hydrogen Bond Acceptor Count | 2 |
| 可旋转键计数Rotatable Bond Count | 5 |
| 精确质量Exact Mass | 399.35 Da |
| 单同位素质量Monoisotopic Mass | 399.35 Da |
| 拓扑极表面积Topological Polar Surface Area | 32.600 Ų |
| 重原子数Heavy Atom Count | 29 |
| 形式电荷Formal Charge | 0 |
| 复杂度Complexity | 663.000 |
| 同位素原子数Isotope Atom Count | 0 |
| 定义的原子立体中心计数Defined Atom Stereocenter Count | 7 |
| 未定义的原子立体中心计数Undefined Atom Stereocenter Count | 0 |
| 定义的键立体中心计数Defined Bond Stereocenter Count | 1 |
| 未定义的键立体中心计数Undefined Bond Stereocenter Count | 0 |
| 所有立体化学键的总数The total count of all stereochemical bonds | 1 |
| 共价键合单元计数Covalently-Bonded Unit Count | 1 |
| 预防措施声明 |
P264: 处理后要彻底洗手。 |
|---|
| 1. Bordet T, Buisson B, Michaud M, Drouot C, Galéa P, Delaage P, Akentieva NP, Evers AS, Covey DF, Ostuni MA et al.. (2007) Identification and characterization of cholest-4-en-3-one, oxime (TRO19622), a novel drug candidate for amyotrophic lateral sclerosis.. J Pharmacol Exp Ther, 322 (2): (709-20). [PMID:17496168] |
| 2. Bernardi P, Bonaldo P. (2008) Dysfunction of mitochondria and sarcoplasmic reticulum in the pathogenesis of collagen VI muscular dystrophies.. Ann N Y Acad Sci, 1147 (303-11). [PMID:19076452] |
| 3. Lemasters JJ, Theruvath TP, Zhong Z, Nieminen AL. (2009) Mitochondrial calcium and the permeability transition in cell death.. Biochim Biophys Acta, 1787 (11): (1395-401). [PMID:19576166] |
| 4. Martin LJ. (2010) Olesoxime, a cholesterol-like neuroprotectant for the potential treatment of amyotrophic lateral sclerosis.. IDrugs, 13 (8): (568-80). [PMID:20721828] |