370677 Sigma-AldrichGuanosine 3ʹ,5ʹ-cyclic Monophosphorothioate, 8-(4-Chlorophenylthio)-, Rp-Isomer, Triethylammonium Salt - Calbiochem
A potent, cell-permeable, and metabolically-stable inhibitor of protein kinase G Iα, Iβ, and type II.
More>> A potent, cell-permeable, and metabolically-stable inhibitor of protein kinase G Iα, Iβ, and type II. Less<<MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.
同义词: Rp-8-pCPT-cGMPS, TEA, PKG Inhibitor III
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概述
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重要规格表
| Empirical Formula |
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| C₁₆H₁₅ClN₅O₆PS₂ · C₆H₁₅N |
Products
| 产品目录编号 | 包装 | 数量 / 包装 | |
|---|---|---|---|
| 370677-1UMOLCN | 塑胶安瓿;塑胶针药瓶 | 1 umol |
| Description | |
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| Overview | A potent, cell-permeable, and metabolically-stable inhibitor of protein kinase G Iα, Iβ, and type II. Significantly more lipophilic and membrane-permeable than Rp-cGMPS or Rp-8-Br-cGMPS (Cat. No. 370674). Note: 1 µmol = 0.61 mg. |
| Catalogue Number | 370677 |
| Brand Family | Calbiochem® |
| Synonyms | Rp-8-pCPT-cGMPS, TEA, PKG Inhibitor III |
| Product Information | |
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| ATP Competitive | N |
| Declaration | Sold under license of U.S. Patent 5,625,056, Patents DE 3,802,865.4, and DE 4,217,679 issued to BIOLOG LSI. |
| Form | Lyophilized |
| Hill Formula | C₁₆H₁₅ClN₅O₆PS₂ · C₆H₁₅N |
| Chemical formula | C₁₆H₁₅ClN₅O₆PS₂ · C₆H₁₅N |
| Hygroscopic | Hygroscopic |
| Reversible | N |
| Structure formula Image | |
| Quality Level | MQ100 |
| Applications |
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| Biological Information | |
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| Primary Target | PKG1α |
| Purity | ≥99% by HPLC |
| Physicochemical Information | |
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| Cell permeable | Y |
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| Safety Information according to GHS |
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| Specifications |
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| Global Trade Item Number | |
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| 产品目录编号 | GTIN |
| 370677-1UMOLCN | 04055977191707 |
Documentation
Guanosine 3ʹ,5ʹ-cyclic Monophosphorothioate, 8-(4-Chlorophenylthio)-, Rp-Isomer, Triethylammonium Salt - Calbiochem MSDS
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Guanosine 3ʹ,5ʹ-cyclic Monophosphorothioate, 8-(4-Chlorophenylthio)-, Rp-Isomer, Triethylammonium Salt - Calbiochem 分析证书
| 标题 | 批号 |
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| 370677 |
参考
| 参考信息概述 |
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| Abd Alla, S., et al. 1996. Eur. J. Biochem. 241, 498. Lee, S.J., et al. 1996. Dev. Biol. 180, 324. Van Uffelen, B.E., et al. 1996. J. Leukoc. Biol. 60, 94. Willmott, N., et al. 1996. J. Biol. Chem. 271, 3699. Butt, E., et al. 1994. Eur. J. Pharmacol. 269, 265. |