Chemistry:KT5720
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Revision as of 08:48, 28 June 2021 by imported>QCDvac (update)
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Names | |
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IUPAC name
(5R,6S,8S)-Hexyl 6-hydroxy-5-methyl-13-oxo-6,7,8,13,14,15-hexahydro-5H-16-oxa-4b,8a,14-triaza-5,8-methanodibenzo[b,h]cycloocta[jkl]cyclopenta[e]-as-indacene-6-carboxylate
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Other names
KT 5720
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Identifiers | |
3D model (JSmol)
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ChEBI | |
ChemSpider | |
PubChem CID
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UNII | |
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Properties | |
C32H31N3O5 | |
Molar mass | 537.616 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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Infobox references | |
Tracking categories (test):
KT5720 is a kinase inhibitor with specificity towards protein kinase A.[1] It is a semi-synthetic derivative of K252a[2] and analog of staurosporine.
References
- ↑ Makarevich, A. V.; Sirotkin, A. V.; Rafay, J. (2010). "Comparison of Effects of Protein Kinase A, Mitogen-activated Protein Kinase, and Cyclin-dependent Kinase Blockers on Rabbit Ovarian Granulosa Cell Functions". Hormone and Metabolic Research 42 (13): 936–43. doi:10.1055/s-0030-1267226. PMID 20972940.
- ↑ CID 3844 from PubChem
![]() | Original source: https://en.wikipedia.org/wiki/KT5720.
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