Name | (5R,6S,8S)-6-hydroxy-5-methyl-13-oxo-5,6,7,8,14,15-hexahydro-13H-5,8-epoxy-4b,8a,14-triazadibenzo[b,h]cycloocta[1,2,3,4-jkl]cyclopenta[e]-as-indacene-6-carboxylic acid |
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Synonyms |
9,12-Epoxy-1H-diindolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1,6]benzodiazocine-10-carboxylicacid,2,3,9,10,11,12-hexahydro-10-hydroxy-9-methyl-1-oxo-,(9S,10R,12R)
K-252b solution MFCD00132117 (15R,16S,18S)-16-Hydroxy-15-methyl-3-oxo-28-oxa-4,14,19-triazaoctacyclo[12.11.2.1.0.0.0.0.0]octacosa-1,6,8,10,12,20,22,24,26-nonaene-16-carboxylic acid 6,9-Epoxy-15H-diindolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1,6]benzodiazocine-7-carboxylic acid, 6,7,8,9,16,17-hexahydro-7-hydroxy-6-methyl-15-oxo-, (6R,7S,9S)- (5R,6S,8S)-6-hydroxy-5-methyl-13-oxo-5,6,7,8,14,15-hexahydro-13H-5,8-epoxy-4b,8a,14-triazadibenzo[b,h]cycloocta[1,2,3,4-jkl]cyclopenta[e]-as-indacene-6-carboxylic acid |
Description | K-252b, an indolocarbazole isolated from the actinomycete Nocardiopsis, is a PKC inhibitor. K-252b can be used to inhibit extracellular kinases of cells in culture because it can’t pass through cell membrane freely [1][2][3]. |
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Related Catalog | |
Target |
PKC[1]. |
References |
Density | 1.8±0.1 g/cm3 |
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Boiling Point | 769.8±60.0 °C at 760 mmHg |
Molecular Formula | C26H19N3O5 |
Molecular Weight | 453.446 |
Flash Point | 419.4±32.9 °C |
Exact Mass | 453.132477 |
PSA | 105.72000 |
LogP | 3.57 |
Vapour Pressure | 0.0±2.8 mmHg at 25°C |
Index of Refraction | 1.903 |
Hazard Codes | Xi: Irritant; |
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RIDADR | UN 1993 / PGIII |
Precursor 9 | |
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DownStream 1 | |