CAS 126643-37-6|KT5823

Introduction:Basic information about CAS 126643-37-6|KT5823, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common NameKT5823
CAS Number126643-37-6Molecular Weight495.52600
Density1.52g/cm3Boiling Point629.2ºC at 760mmHg
Molecular FormulaC29H25N3O5Melting Point/
MSDSChineseUSAFlash Point334.3ºC

Names

Namekt 5823
SynonymMore Synonyms

KT5823 BiologicalActivity

DescriptionKT5823, a selective the cGMP-dependent protein kinase (PKG) inhibitor with an Ki value of 0.23 μM, it also inhibits PKA and PKC with Ki values of 10 μM and 4 μM, respectively[1]. KT5823 is a staurosporine-related protein kinase inhibitor, increases thyroid-stimulating hormone-induced (Na+/I- symporter) NIS expression, and iodide uptake in thyroid cells[2]. KT5823 arrests cells after the G0/G1 boundary and causes increases in the levels of apoptotic DNA fragmentation[3].
Related CatalogSignaling Pathways >>Apoptosis >>ApoptosisSignaling Pathways >>Epigenetics >>PKCSignaling Pathways >>Protein Tyrosine Kinase/RTK >>PKAResearch Areas >>OthersSignaling Pathways >>Stem Cell/Wnt >>PKASignaling Pathways >>TGF-beta/Smad >>PKC
Target

PKA:10 μM (Ki)

PKC:4 μM (Ki)

References

[1]. 1.Gadbois DM, et al. Multiple kinase arrest points in the G1 phase of nontransformed mammalian cells are absent in transformed cells. Proc Natl Acad Sci U S A. 1992 Sep 15;89(18):8626-30.

[2]. Wyatt TA, et al. KT5823 activates human neutrophils and fails to inhibit cGMP-dependent protein kinase phosphorylation of vimentin. Res Commun Chem Pathol Pharmacol. 1991 Oct;74(1):3-14.

[3]. Chan SL, et al. Guanylyl cyclase inhibitors NS2028 and ODQ and protein kinase G (PKG) inhibitor KT5823 trigger apoptotic DNA fragmentation in immortalized uterine epithelial cells: anti-apoptotic effects of basal cGMP/PKG. Mol Hum Reprod. 2003 Dec;9(12):775-83.

Chemical & Physical Properties

Density1.52g/cm3
Boiling Point629.2ºC at 760mmHg
Molecular FormulaC29H25N3O5
Molecular Weight495.52600
Flash Point334.3ºC
Exact Mass495.17900
PSA74.93000
LogP4.58930
Vapour Pressure9.67E-16mmHg at 25°C
Index of Refraction1.763
InChIKeyQTYMDECKVKSGSM-YMUMJAELSA-N
SMILESCOC(=O)C1(OC)CC2OC1(C)n1c3ccccc3c3c4c(c5c6ccccc6n2c5c31)C(=O)N(C)C4

Safety Information

Personal Protective EquipmentEyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter
Hazard CodesXi
RIDADRNONH for all modes of transport

Articles32

More Articles
Brain natriuretic peptide constitutively downregulates P2X3 receptors by controlling their phosphorylation state and membrane localization.

Mol. Pain 11 , 71, (2015)

ATP-gated P2X3 receptors are important transducers of nociceptive stimuli and are almost exclusively expressed by sensory ganglion neurons. In mouse trigeminal ganglion (TG), P2X3 receptor function is...

Interaction between bradykinin and natriuretic peptides via RGS protein activation in HEK-293 cells.

Am. J. Physiol. Cell Physiol. 303(12) , C1260-8, (2012)

In this study, the interaction of natriuretic peptides (NP) and bradykinin (BK) signaling pathways was identified by measuring membrane potential (V(m)) and intracellular Ca(2+) using the patch-clamp ...

Cytoprotective effect of 1-nitro-2-phenylethane in mice pancreatic acinar cells subjected to taurocholate: putative role of guanylyl cyclase-derived 8-nitro-cyclic-GMP.

Biochem. Pharmacol. 91(2) , 191-201, (2014)

The nitroderivative 1-nitro-2-phenylethane (NPE) was recently described as a compound possessing heme-dependent soluble guanylyl cyclase (sGC) stimulating properties in vascular smooth muscle cells. I...

Synonyms

MFCD00132119
(9S,10R,12R)-2,3,9,10,11,12-hexahydro-10-methoxy-2,9-dimethyl-1-oxo-9,12-epoxy-1H-diindolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-l][1,6]benzodiazocine-10-carboxylic acid methyl ester
CAS 55989-13-4|3-(4-Chlorophenyl)piperidine
CAS 21102-95-4|BMY 7378 dihydrochloride
Recommended......
TOP