K252b

Modify Date: 2024-01-02 12:30:18

K252b Structure
K252b structure
Common Name K252b
CAS Number 99570-78-2 Molecular Weight 453.446
Density 1.8±0.1 g/cm3 Boiling Point 769.8±60.0 °C at 760 mmHg
Molecular Formula C26H19N3O5 Melting Point N/A
MSDS USA Flash Point 419.4±32.9 °C

 Use of K252b


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].

 Names

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
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.8±0.1 g/cm3
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

 Safety Information

Hazard Codes Xi: Irritant;
RIDADR UN 1993 / PGIII

 Synthetic Route

 Articles1

More Articles
Cooperativity between extracellular adenosine 5'-triphosphate and activation of N-methyl-D-aspartate receptors in long-term potentiation induction in hippocampal CA1 neurons.

Neuroscience 113 , 617-628, (2002)

The mechanism of ATP-induced long-term potentiation (LTP) was studied pharmacologically using guinea-pig hippocampal slices. LTP, induced in CA1 neurons by 10 min application of 10 microM ATP, was blo...

 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