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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 保质期:
Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year
- 英文名:
Atractyloside potassium salt
- 库存:
现询
- 供应商:
北京索莱宝科技有限公司
- CAS号:
102130-43-8
- 规格:
1mg/50mg/100mg/20mg/10mg/5mg
| 规格: | 1mg | 产品价格: | ¥476.0 |
|---|---|---|---|
| 规格: | 50mg | 产品价格: | ¥4853.0 |
| 规格: | 100mg | 产品价格: | ¥9050.0 |
| 规格: | 20mg | 产品价格: | ¥2400.0 |
| 规格: | 10mg | 产品价格: | ¥1800.0 |
| 规格: | 5mg | 产品价格: | ¥1131.0 |
| 基本信息 | |
| CAS | No.102130-43-8 |
| 中文名称 | 苍术苷钾盐 |
| 英文名称 | Atractyloside potassium salt |
| 别名 | 苍术苷钾盐;苍术苷; |
| 分子式 | C30H44K2O16S2 |
| 分子量 | 802.99 |
| 溶解性 | Soluble in Water/DMSO |
| 纯度 | HPLC≥98% |
| 外观(性状) | White to off-white Solid |
| 储存条件 | Powder:2-8℃,2 years;Insolvent(母液):-20℃,6 months;-80℃,1 year |
| MDL | MFCD00078810 |
| SMILES | [H][C@@]12C(C(O)=O)C[C@@H](O[C@H]3[C@@H]([C@H]([C@@H]([C@@H](CO)O3)OS(=O)(O[K])=O)OS(=O)(O[K])=O)OC(CC(C)C)=O)C[C@@]1(C)[C@@]4([H])[C@@]5([C@@H](O)C([C@H](CC4)C5)=C)CC2 |
| InChIKey | IUCNQFHEWLYECJ-VCQILIGCSA-L |
| InChI | InChI=1S/C30H46O16S2.2K/c1-14(2)9-22(32)44-25-24(46-48(39,40)41)23(45-47(36,37)38)20(13-31)43-28(25)42-17-10-18(27(34)35)19-7-8-30-11-16(15(3)26(30)33)5-6-21(30)29(19,4)12-17;;/h14,16-21,23-26,28,31,33H,3,5-13H2,1-2,4H3,(H,34,35)(H,36,37,38)(H,39,40,41);;/q;2*+1/p-2/t16-,17-,18-,19-,20-,21+,23-,24+,25-,26+,28+,29-,30-;;/m1../s1 |
| PubChem CID | 12299879 |
| 靶点 | Others |
| 通路 | Others |
| 背景说明 | Atractyloside potassium salt是高效、特异性的线粒体 ADP/ATP 转运抑制剂。 |
| 生物活性 | Atractyloside Dipotassium Salt is an inhibitor of ADP/ATP Translocase. ATP-ADP translocase (AAT) is a mitochondrial ADP/ATP carrier. It transports ATP from the mitochondrial matrix to the cytoplasm and transports ADP from the cytoplasm to the mitochondrial matrix. In Ehrlich ascites tumor cells, atractyloside (3 mM) inhibited cells growth by 70%. The mitochondria became spherical shaped with translucent matrix rid of cristae. When transfered to normal medium, proliferation and macromolecular synthesis recovered to normal levels within 3 to 6 h.In the sarcoplasmic reticulum vesicles from the rabbit skeletal muscle with 10 μM of cytoplasmic Ca2+, atractyloside reduced the rate of choline+ influx through the Ca2+ channels to 60%. Also, it inhibited about half of Ca2+ channels incorporated into planar bilayers. In mitochondrial membranes isolated from a rat heart muscle, atractyloside (5-100 μM) inhibited the chloride channels in dose-dependent way [1-3]. |
| 数据来源文献 | [1]. Yamaguchi N, Kagari T, Kasai M. Inhibition of the ryanodine receptor calcium channel in the sarcoplasmic reticulum of skeletal muscle by an ADP/ATP translocase inhibitor, atractyloside. Biochem Biophys Res Commun, 1999, 258(2): 247-251. [2]. Pick-Kober KH, Schneider F. Proliferation, macromolecular synthesis and energy metabolism of in vitro grown Ehrlich ascites tumor cells after inhibition of ATP-ADP translocation by atractyloside. Eur J Cell Biol, 1984, 34(2): 323-329. [3]. Malekova L, Kominkova V, Ferko M, et al. Bongkrekic acid and atractyloside inhibits chloride channels from mitochondrial membranes of rat heart. Biochim Biophys Acta, 2007, 1767(1): 31-44. |
| 单位 | 瓶 |
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