KT5720

KT5720__PKA kinase inhibitor Auristatin F

Product Name KT5720
Description

PKA kinase inhibitor

Purity >98% (TLC)
CAS No. 108068-98-0
Molecular Formula C32H31N3O5
Molecular Weight 537.6
Storage Temperature -20ºC
Shipping Temperature Shipped Ambient
Product Type Inhibitor
Solubility Soluble in methanol: clear colorless solution at 5 mg/ml
Source Synthetic
Appearance White powder
SMILES N47C1=C(C6=C(C2=C1N(C3=CC=CC=C23)email protected5OC@@4(C@(C5)(O)C(=O)OCCCCCC)C)C(NC6)=O)C8=C7C=CC=C8
InChI InChI=1S/C32H31N3O5/c1-3-4-5-10-15-39-30(37)32(38)16-23-34-21-13-8-6-11-18(21)25-26-20(17-33-29(26)36)24-19-12-7-9-14-22(19)35(28(24)27(25)34)31(32,2)40-23/h6-9,11-14,23,38H,3-5,10,15-17H2,1-2H3,(H,3
InChIKey ZHEHVZXPFVXKEY-UHFFFAOYSA-N
Safety Phrases Classification:
Specific target organ toxicity-single exposure (Category 1), H370

Safety Phrases:
S22 – Do not breathe dust.
S24/25 – Avoid contact with skin and eyes.
S36/37/39 – Wear suitable protective clothing, gloves and eye/face protection.

Hazard statements:
H370 Causes damage to organs.

Precautionary statements:
P260 Do not breathe dust/ fume/ gas/ mist/ vapours/ spray.
P264 Wash skin thoroughly after handling.
P270 Do not eat, drink or smoke when using this product.
P307 + P311 IF exposed: Call a POISON CENTER or doctor/ physician.
P321 Specific treatment (see supplemental first aid instructions on this label).
P405 Store locked up.
P501 Dispose of contents/ container to an approved waste disposal plant

Cite This Product KT5720 (StressMarq Biosciences Inc., Victoria BC CANADA, Catalog # SIH-457)
Alternative Names (9S,10S,12R)-2,3,9,10,11,12-Hexahydro-10-hydroxy-9-methyl-1-oxo-9,12-epoxy-1H-diindolo1,2,3-fg:3′,2′,1′-klpyrrolo3,4-i1,6benzodiazocine-10-carboxylic acid hexyl ester
Research Areas Cancer, Apoptosis, Cancer Growth Inhibitors, Cell Signaling, Tyrosine Kinase Inhibitors
PubChem ID 3844
Scientific Background KT5720 is a potent and selective inhibitor of protein kinase A (PKA). This compound blocks PKA signaling through competitive inhibition. It causes no significant effect on protein kinase C (PKC), protein kinase G (PKG) or myosin light chain kinase (mlCK). KT5720 has been shown to reversibly arrests human skin fibroblasts in the G1 phase. It is cell permeable.
References 1. Kase H., et al. (1987) Biochem. Biophys. Res. Comm. 142(2): 436–440.
2. Gadbois D.M., Crissman H.A., Tobey R.A., & Bradbury E.M. (1992) Pro. Na. Aca. Sci. USA. 89(18): 8626–8630.