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<<Synonyme: Rp-8-pCPT-cGMPS, TEA, PKG Inhibitor III
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Übersicht
Replacement Information |
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Key Spec Table
Empirical Formula |
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C₁₆H₁₅ClN₅O₆PS₂ · C₆H₁₅N |
Preis & Verfügbarkeit
Bestellnummer | Verfügbarkeit | Verpackung | St./Pkg. | Preis | Menge | |
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370677-1UMOL |
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Kst.-Ampulle | 1 umol |
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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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Materials Information |
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Safety Information according to GHS |
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Product Usage Statements |
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Supplemental Information |
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Specifications |
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Global Trade Item Number | |
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Bestellnummer | GTIN |
370677-1UMOL | 04055977191707 |
Documentation
Guanosine 3ʹ,5ʹ-cyclic Monophosphorothioate, 8-(4-Chlorophenylthio)-, Rp-Isomer, Triethylammonium Salt - Calbiochem SDB
Titel |
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Guanosine 3ʹ,5ʹ-cyclic Monophosphorothioate, 8-(4-Chlorophenylthio)-, Rp-Isomer, Triethylammonium Salt - Calbiochem Analysenzertifikate
Titel | Chargennummer |
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370677 |
Literatur
Übersicht |
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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. |