KO-947

KO-947 Suppliers list
Company Name: Shanghai Boyle Chemical Co., Ltd.  
Tel:
Email: sales@boylechem.com
Company Name: BOC Sciences  
Tel: 1-631-485-4226; 16314854226
Email: info@bocsci.com
Company Name: Nanjing Norris-Pharm Technology Co., Ltd  
Tel: 13901585132
Email: sales@norris-pharm.com
Company Name: HangZhou YuHao Chemical Technology Co., Ltd.  
Tel: 0571-82693216
Email: info@yuhaochemical.com
Company Name: Shanghai Lollane Biological Technology Co.,Ltd.  
Tel: 021-52996696,15000506266 15000506266
Email:

KO-947 manufacturers

  • KO-947
  • KO-947 pictures
  • $44.00
  • 2026-07-27
  • CAS:1695533-89-1
  • Purity: 97.84%
  • Supply Ability: 10g
KO-947 Basic information
Product Name:KO-947
Synonyms:KO-947;6-benzyl-3-(pyridin-4-yl)-5,6-dihydro-1H-pyrazolo[4,3-g]quinazolin-7(8H)-one;KO947;KO-947;KO 947;7H-Pyrazolo[4,3-g]quinazolin-7-one, 1,5,6,8-tetrahydro-6-(phenylmethyl)-3-(4-pyridinyl)-;Inhibitor,ERK,KO-947,inhibit,KO 947,Extracellular signal regulated kinases,KO947;6-benzyl-3-(pyridin-4-yl)-1H,5H,6H,7H,8H-pyrazolo[4,3-g]quinazolin-7-one;KO-947 ,S8569
CAS:1695533-89-1
MF:C21H17N5O
MW:355.39
EINECS:
Product Categories:
Mol File:1695533-89-1.mol
KO-947 Structure
KO-947 Chemical Properties
Boiling point 704.1±60.0 °C(Predicted)
density 1.354±0.06 g/cm3(Predicted)
storage temp. 4°C, protect from light
solubility DMSO:66.75(Max Conc. mg/mL);187.82(Max Conc. mM)
form A crystalline solid
pka13.32±0.20(Predicted)
color White to off-white
Safety Information
MSDS Information
KO-947 Usage And Synthesis
DescriptionKO947 is an ERK inhibitor (IC50 = <50 nM for ERK2). It is greater than 50-fold selective for ERK over a panel of 450 kinases. KO947 reduces phosphorylation of the ERK target p90 ribosomal S6 kinase (RSK) in A375 cancer cells containing constitutively active B-RAFV600E with an IC50 value of less than 250 nM. It inhibits proliferation of A375 cells, as well as mutant K-Ras-expressing HCT116 and H358 cancer cell lines (IC50s = 50-250 nM for all).
UsesKO-947 is a potent and selective inhibitor of ERK1/2 kinases with potential utility in MAPK pathway dysregulated tumors.
in vivo

In cell-line derived xenograft studies, KO-947 profoundly suppresses ERK signaling for up to five days after a single dose and induces regressions in RAS- and RAF-mutant melanoma, NSCLC and pancreatic cancer models on administration schedules ranging from daily to weekly. Intermittent dosing enables comparable antitumor activity at reduced dose-intensity[1].

IC 50ERK1; ERK2
References[1] Burrows F, et al. KO-947, a potent ERK inhibitor with robust preclinical single agent activity in MAPK pathway dysregulated tumors [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 5168. doi:10.1158/1538-7445.AM2017-5168.
KO-947 Preparation Products And Raw materials
Tag:KO-947(1695533-89-1) Related Product Information
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