Description Features In vitro
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GSK 343

Description Features In vitro
Product Name
GSK 343
CAS No.
1346704-33-3
Chemical Name
GSK 343
Synonyms
GSK343;CS-728;GSK 343;GSK-343;GSK343, >=98%;GSK-343/GSK343;GSK 343 USP/EP/BP;GSK343;GSK 343;GSK-343;1-Isopropyl-N-((6-methyl-2-oxo-4-propyl-1,2-dihydropyridin-3-yl)methyl)-6-(2-(4-methylpiperazi;1-(1-Methylethyl)-N-[(6-methyl-2-oxo-4-propyl-1,2-dihydro-3-pyridinyl)methyl]-6-[2-(4-methyl-1-piper
CBNumber
CB52666625
Molecular Formula
C31H39N7O2
Formula Weight
541.69
MOL File
1346704-33-3.mol
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GSK 343 Property

Boiling point:
797.4±60.0 °C(Predicted)
Density 
1.26±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
DMSO: soluble15mg/mL, clear
form 
powder
pka
11.84±0.10(Predicted)
color 
, white to beige to brown
InChIKey
ULNXAWLQFZMIHX-UHFFFAOYSA-N
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Safety

Hazard Codes 
Xn
Risk Statements 
22
WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML0766
Product name
GSK343
Purity
≥98% (HPLC)
Packaging
5mg
Price
$148
Updated
2024/03/01
Sigma-Aldrich
Product number
SML0766
Product name
GSK343
Purity
≥98% (HPLC)
Packaging
25mg
Price
$234.8
Updated
2024/03/01
Cayman Chemical
Product number
14094
Product name
GSK343
Purity
≥95%
Packaging
1mg
Price
$37
Updated
2024/03/01
Cayman Chemical
Product number
14094
Product name
GSK343
Purity
≥95%
Packaging
5mg
Price
$116
Updated
2024/03/01
Cayman Chemical
Product number
14094
Product name
GSK343
Purity
≥95%
Packaging
10mg
Price
$161
Updated
2024/03/01
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GSK 343 Chemical Properties,Usage,Production

Description

GSK343 is a potent and selective EZH2 inhibitor with IC50 of 4 nM in a cell-free assay, showing 60 fold selectivity against EZH1, and >1000 fold selectivity against other histone methyltransferases.

Features

A chemical probe for the SGC epigenetics initiative. Potential use in a variety of solid tumors.

In vitro

GSK343 inhibits trimethylation of H3K27 (H3K27me3) with IC50 of 174 nM in HCC1806 breast cancer cells. GSK343 potently inhibits cell proliferation in breast cancer cells and prostate cancer cells, and the prostate cancer cell line LNCaP is the most sensitive to GSK343, with IC50 of 2.9 μM. GSK343 significantly suppresses the growth of EOC cells cultured in 3D matrigel extracellular matrix (ECM), which mimics the tumor microenvironment in vivo. In addition, GSK343 also induces apoptosis of EOC cells in 3D and significantly inhibits the invasion of EOC cells.

Uses

GSK343 has been used:

  • as an inhibitor of?enhancer of zeste homolog 2 (EZH2) to assess the impact of chromatin condensation on?cell migration
  • as histone methyl transferase inhibitor, to suppress the Polyandrocarpa misakiensis, mitochondrial non-coding-region (NCR) PmNCR?reporter gene expression, facilitated?by TC14-3
  • as a supplement in the growth medium to inhibit the generation of H3K27me3 or to inhibit RNA polymerase II
  • as EZH2 inhibitor to treat castration-resistant neuroendocrine prostate cancer (CRPC-NE)

Definition

ChEBI: GSK343 is a member of the class of indazoles that is 1-isopropyl-1H-indazole-4-carboxamide in which the nitrogen of the carboxamide group is substituted by a (6-methyl-2-oxo-4-propyl-1,2-dihydropyridin-3-yl)methyl group and in which the indazole ring is substituted at position 6 by a 2-(4-methylpiperazin-1-yl)pyridin-4-yl group. A highly potent and selective EZH2 inhibitor (IC50 = 4 nM). It has a role as an EC 2.1.1.43 (enhancer of zeste homolog 2) inhibitor, an apoptosis inducer and an antineoplastic agent. It is a N-alkylpiperazine, a secondary carboxamide, an aminopyridine, a pyridone, a N-arylpiperazine and a member of indazoles.

Biological Activity

gsk343 is a selective and sam-competitive inhibitor of the histone lysine methyltransferase ezh2 with ic50 value of 4 nm [1].ezh2 (enhancer of zestehomolog 2) is a catalytic subunit of the protein complex (polycomb repressive complex 2, prc2). it catalyzes the methylation of h3k27 through transferring the methyl group of sam to h3k27. the trimethylation of h3k27 subsequently results in the transcription suppression of target genes such as runx3, foxc1 and brca1. the overexpression and mutation of ezh2 have been found in many sorts of tumors demonstrating that ezh2 is an attractive target for the treatment of cancers. as a potent ezh2 inhibitor, gsk343 inhibits the activity of the enzyme via competing with the cofactor sam [1, 2].gsk343 is a selective ezh2 inhibitor. it showed no significant inhibitory effects on other enzymes requiring sam as cofactor, including dnmt, mll, prmt and setmar. gsk343 exerted a certain degree of effective on ezh1 with ic50 value of 240 nm since ezh1 was quite homologous to ezh2. in cultured hcc1806 breast cancer cells, treatment of gsk343 dose-dependently reduced h3k27me3 with ic50 value of 174 nm. besides that, gsk343 was found to inhibit cell proliferation in some breast and prostate cancer cells. in lncap cells, gsk343 suppressed cell growth with ic50 value of 2.9 μm. in human eoc cells, gsk343 notably inhibited cell invasion and induced cell apoptosis. gsk343 was also found to induce lc3-ii accumulation and autophagy in a549, mda-mb-231 and hepg2 cell. it enhanced the antitumor activity of sorafenib which was a multikinase inhibitor and could decrease the expression of ezh2 in hepg2 cells [1, 3 and 4].gsk343 is only used as a tool to investigate ezh2 in vitro because of its high clearance in the animal model [1].

Biochem/physiol Actions

GSK343 is a potent, specific inhibitor of the histone H3-lysine 27 (H3K27) methyltransferase EZH2. GSK343 inhibits EZH2 enzymatic activity with an IC50 of 4 nM. The compound displays 60 fold selectivity for EZH2 vs. EZH1, and 1000 fold or greater selectivity against other histone methyltransferases. The IC50 for inhibition of H3K27 methylation is < 200 nM in HCC1806 cells. For full characterization details, please visit the GSK343 probe summary on the Structural Genomics Consortium (SGC) website.To learn about other SGC chemical probes for epigenetic targets, visit sigma.com/sgc

target

EZH2

storage

Store at -20°C

References

[1] verma s k, tian x, lafrance l v, et al. identification of potent, selective, cell-active inhibitors of the histone lysine methyltransferase ezh2. acs medicinal chemistry letters, 2012, 3(12): 1091-1096.
[2] ferraro a, boni t, pintzas a. ezh2 regulates cofilin activity and colon cancer cell migration by targeting itga2 gene. plos one, 2014, 9(12): e115276.
[3] amatangelo m, garipov a, li h, et al. three-dimensional culture sensitizes epithelial ovarian cancer cells to ezh2 methyltransferase inhibition. cell cycle, 2013, 12(13): 2113-2119.
[4] liu t p, lo h l, wei l s, et al. s-adenosyl-l-methionine-competitive inhibitors of the histone methyltransferase ezh2 induce autophagy and enhance drug sensitivity in cancer cells. anti-cancer drugs, 2015, 26(2): 139.

GSK 343 Preparation Products And Raw materials

Raw materials

Preparation Products

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GSK 343 Suppliers

Shanghai Boyle Chemical Co., Ltd.
Tel
Fax
86-21-57758967
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sales@boylechem.com
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China
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J & K SCIENTIFIC LTD.
Tel
010-82848833 400-666-7788
Fax
86-10-82849933
Email
jkinfo@jkchemical.com
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China
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94657
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Jinan Trio PharmaTech Co., Ltd.
Tel
+86 (531) 88811783
Fax
+86 (531) 55696010 QQ 1762738062
Email
sales@trio-pharmatech.com (International market)
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China
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ChemCell Biomedicine Co.,Ltd.
Tel
020-13556033878 2965585218 13556033878
Fax
0086-0757-85406358
Email
chemcell@hotmail.com
Country
China
ProdList
369
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Wuhan Fortuna Chemical Co., Ltd
Tel
027-59207852 13308628970
Fax
QQ3130921841
Email
buy@fortunachem.com
Country
China
ProdList
2866
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Dalian Meilun Biotech Co., Ltd.
Tel
0411-62910999 13889544652
Email
meilunui@163.com
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China
ProdList
4727
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NCE Biomedical Co.,Ltd.
Tel
4000-027-021 |24 +86-13986109188 | +86-15623472865 | +81-08033611988
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+86-27-87599188
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China
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Haoyuan Chemexpress Co., Ltd.
Tel
021-58950125
Fax
(86) 21-58955996
Email
info@chemexpress.com
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China
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7552
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UHN Shanghai Research & Development Co., Ltd.
Tel
021-58958002 18930822973
Fax
+86 (21) 5895-8628
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sales@uhnshanghai.com
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China
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Shanghai Aladdin Bio-Chem Technology Co.,LTD
Tel
400-400-6206333 18521732826
Fax
021-50323701
Email
market@aladdin-e.com
Country
China
ProdList
25003
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View Lastest Price from GSK 343 manufacturers

Career Henan Chemical Co
Product
GSK 343 1346704-33-3
Price
US $1.00/g
Min. Order
1g
Purity
99%
Supply Ability
200kg
Release date
2020-01-13

1346704-33-3, GSK 343Related Search:


  • 1H-Indazole-4-carboxamide, N-[(1,2-dihydro-6-methyl-2-oxo-4-propyl-3-pyridinyl)methyl]-1-(1-methylethyl)-6-[2-(4-methyl-1-piperazinyl)-4-pyridinyl]-
  • 1-(1-Methylethyl)-N-[(6-methyl-2-oxo-4-propyl-1,2-dihydro-3-pyridinyl)methyl]-6-[2-(4-methyl-1-piperazinyl)-4-pyridinyl]-1H-indazole-4-carboxamide GSK343
  • GSK 343
  • GSK343
  • GSK-343
  • GSK-343/GSK343
  • 1-(1-Methylethyl)-N-[(6-Methyl-2-oxo-4-propyl-1,2-dihydro-3-pyridinyl)Methyl]-6-[2-(4-Methyl-1-piperazinyl)-4-pyridinyl]-1H-indazole-4-carboxaMide
  • N-[(1,2-Dihydro-6-methyl-2-oxo-4-propyl-3-pyridinyl)methyl]-1-(1-methylethyl)-6-[2-(4-methyl-1-piperazinyl)-4-py
  • N-[(1,2-Dihydro-6-methyl-2-oxo-4-propyl-3-pyridinyl)methyl]-1-(1-methylethyl)-6-[2-(4-methyl-1-piperazinyl)-4-pyridinyl]-1H-indazole-4-carboxamide
  • N-[(6-Methyl-2-oxo-4-propyl-1,2-dihydropyridin-3-yl)methyl]-6-[2-(4-methylpiperazin-1-yl)pyridin-4-yl]-1-(propan-2-yl)-1H-<WBR
  • GSK343, >=98%
  • 1-Isopropyl-N-((6-methyl-2-oxo-4-propyl-1,2-dihydropyridin-3-yl)methyl)-6-(2-(4-methylpiperazi
  • N-[(6-METHYL-2-OXO-4-PROPYL-1H-PYRIDIN-3-YL)METHYL]-6-[2-(4-METHYLPIPERAZIN-1-YL)PYRIDIN-4-YL]-1-PROPAN-2-YLINDAZOLE-4-CARBOXAMIDE
  • N-((2-hydroxy-6-methyl-4-propylpyridin-3-yl)methyl)-1-isopropyl-6-(2-(4-methylpiperazin-1-yl)pyridin-4-yl)-1H-indazole-4-carboxamide
  • GSK343;GSK 343;GSK-343
  • 1-isopropyl-n-[(6-methyl-2-oxo-4-propyl-1,2-dihydro-3-pyridinyl)m Ethyl]-6-[2-(4-methyl-1-piperazinyl)-4-pyridinyl]-1h-indazole-4-c Arboxamide
  • CS-728
  • GSK 343 USP/EP/BP
  • 1-Isopropyl-N-((6-methyl-2-oxo-4-propyl-1,2-dihydropyridin-3-yl)methyl)-6-(2-(4-methylpiperazin-1-yl)pyridin-4-yl)-1H-indazole-4-carboxamide
  • 1-(1-Methylethyl)-N-[(6-methyl-2-oxo-4-propyl-1,2-dihydro-3-pyridinyl)methyl]-6-[2-(4-methyl-1-piper
  • 1346704-33-3
  • C31H39N7O2
  • API
  • Inhibitors