KT5720
KT5720 Basic information
- Product Name:
- KT5720
- Synonyms:
-
- (9R,10S,12S)-2,3,9,10,11,12-HEXAHYDRO-10-HYDROXY-9-METHYL-1-OXO-9,12-EPOXY-1H-DIINDOLO[1,2,3-FG:3',2',1'-KL]PYRROLO[3,4-I][1,6]BENZODIAZOCINE-10-CARBOXYLIC ACID, HEXYL ESTER
- KT5720
- PROTEIN KINASE INHIBITOR KT 5720
- 9,12-Epoxy-1H-diindolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1,6]benzodiazocine-10-carboxylic acid, 2,3,9,10,11,12-hexahydro-10-hydroxy-9-methyl-1-oxo-, hexyl ester, (9R,10S,12S)-
- (9s,10s,12r)-2,3,9,10,11,12-hexahydro-10-hydroxy-9-methyl-1-oxo-9,12-epoxy-1h-diindolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1,6]benzodiazocine-10-carboxylic acid hexyl ester
- KT5720 - CAS 108068-98-0 - Calbiochem
- InSolution KT5720 - CAS 108068-98-0 - Calbiochem
- KT-5720 (KT5720)
- CAS:
- 108068-98-0
- MF:
- C32H31N3O5
- MW:
- 537.61
- EINECS:
- 810-587-2
- Product Categories:
-
- antibiotic
- Cyclic Nucleotide related
- Mol File:
- 108068-98-0.mol
KT5720 Chemical Properties
- Boiling point:
- 715.0±60.0 °C(Predicted)
- Density
- 1.49±0.1 g/cm3(Predicted)
- storage temp.
- −20°C
- solubility
- methanol: 5 mg/mL
- form
- powder
- pka
- 11.96±0.40(Predicted)
- color
- white
- Stability:
- Stable for 1 year from date of purchase as supplied. Solutions in DMSO may be stored at -20° for up to 3 months.
MSDS
- Language:English Provider:SigmaAldrich
KT5720 Usage And Synthesis
Description
Protein kinase A (PKA) regulates multiple signal transduction events via protein phosphorylation and is integral to all cellular responses involving the cyclic AMP second messenger system. KT 5720 is one of a family of compounds synthesized by the fungus Nocardiopsis sp. It blocks PKA signaling through competitive inhibition of ATP with a Ki value of 60 nM. Reported IC50 values vary widely depending upon ATP concentration tested and can range from 56 nM (low ATP) to 3 μM (physiologic ATP). Non-
Chemical Properties
White solid
Uses
KT 5720 is a potent, specific and cell-permeable inhibitor of PKA.
Definition
ChEBI: An organic heterooctacyclic compound that is 1H,1'H-2,2'-biindole in which the nitrogens have undergone formal oxidative coupling to positions 2 and 5 of hexyl (3S)-3-hydroxy-2-methyltetrahydrofuran-3- arboxylate (the 2R,3S,5S product), and in which the 3 and 3' positions of the biindole moiety have also undergone formal oxidative coupling to positions 3 and 4 of 1,5-dihydro-2H-pyrrol- -one.
Biological Activity
Potent, selective inhibitor of protein kinase A (K i = 60 nM). Has no effect on PKG or PKC (K i > 2 μ M). Reversibly arrests human skin fibroblasts in the G 1 phase. Also available as part of the Mixed Kinase Inhibitor Tocriset™ and PKA Tocriset™ .
Biochem/physiol Actions
Cell permeable: yes
storage
-20°C (desiccate)
References
1) Kase et al. (1987), K-252 compounds, novel and potent inhibitors of protein kinase C and cyclic nucleotide-dependent protein kinases; Biochem. Biophys. Res. Commun., 142 436 2) Cabell et al. (1993), Effects of selective inhibition of protein kinase C, cyclic AMP-dependent protein kinase, and Ca(2+)-calmodulin-dependent protein kinase on neurite development in cultured rat hippocampal neurons; Int. J. Dev. Neurosci., 11 357
KT5720Supplier
- Tel
- 010-82848833 400-666-7788
- jkinfo@jkchemical.com
- Tel
- 821-50328103-801 18930552037
- 3bsc@sina.com
- Tel
- 021-50135380
- shchemsky@sina.com
- Tel
- +86 21 61551611
- Tel
- 18149758185 18149758185
- sales-cpd@caerulumpharma.com
KT5720(108068-98-0)Related Product Information
- Adenosine 3',5'-cyclic monophosphate sodium salt
- 8-CHLORO-CAMP
- PROTEIN KINASE A INHIBITOR 14-22 AMIDE, CELL-PERMEABLE, MYRISTOYLATED
- 8-BROMOADENOSINE-3',5'-CYCLIC MONOPHOSPHOROTHIOATE, RP-ISOMER SODIUM SALT
- 9-ISOPROPYLCARBAZOLE
- 1-(1-METHYL-1H-INDOL-4-YL)METHYLAMINE 97
- KT5720
- N-Ethyl-3-carbazolecarboxaldehyde
- 9-CARBAZOLEPROPIONIC ACID
- K-252C
- K-252B
- 11,12-Dihydroindolo[2,3-a]carbazole
- 1-ethyl-1H-indole-4-carbaldehyde
- CARBAZOL-9-YL-METHANOL
- KT-5720
- KT5720 in Solution
- KT5720 (Selective PKA Inhibitor)
- KT5720 (semi-synthetic derivative of K525a), Selective PKA Inhibitor, 0.5376kD