GSK9311

GSK9311 Suppliers list
Company Name: TargetMol Chemicals Inc.
Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Products Intro: Product Name:GSK9311
CAS:1923851-49-3
Purity:98.00% Package:10 mg;100 mg;2 mg;25 mg;5 mg;50 mg Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Zhejiang J&C Biological Technology Co.,Limited
Tel: +1-2135480471 +1-2135480471
Email: sales@sarms4muscle.com
Products Intro: Product Name:GSK9311
CAS:1923851-49-3
Purity:99% Package:5KG;1KG Remarks:GSK9311
Company Name: InvivoChem
Tel: +1-708-310-1919 +1-13798911105
Email: sales@invivochem.cn
Products Intro: Product Name:GSK9311
CAS:1923851-49-3
Purity:98% Package:5mg Remarks:V2727
Company Name: TargetMol Chemicals Inc.
Tel:
Email: support@targetmol.com
Products Intro: Product Name:GSK9311
CAS:1923851-49-3
Package:2mg;108USD
Company Name: ShenZhen Trendseen Biological Technology Co.,Ltd.
Tel: 13417589054
Email: trendseenbio@gmail.com
Products Intro: Product Name:GSK9311
CAS:1923851-49-3
Purity:99% Package:1kg;25kg

GSK9311 manufacturers

  • GSK9311
  • GSK9311 pictures
  • $108.00 / 2mg
  • 2024-10-24
  • CAS:1923851-49-3
  • Min. Order:
  • Purity:
  • Supply Ability: 10g
GSK9311 Basic information
Product Name:GSK9311
Synonyms:GSK9311;GSK9311 >=98% (HPLC);Benzamide, N-[2,3-dihydro-1,3-dimethyl-6-[(2R)-2-methyl-1-piperazinyl]-2-oxo-1H-benzimidazol-5-yl]-N-ethyl-2-methoxy-;GSK 9311 hydrochloride;BRPF1 bromodomain inhibitor GS9311;GSK 9311;GSK-9311
CAS:1923851-49-3
MF:C24H31N5O3
MW:437.53
EINECS:
Product Categories:
Mol File:1923851-49-3.mol
GSK9311 Structure
GSK9311 Chemical Properties
Boiling point 625.5±55.0 °C(Predicted)
density 1.204±0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : ≥ 30 mg/mL (68.57 mM)
pka8.82±0.40(Predicted)
form Solid
color White to off-white
optical activity[α]/D 90 to 100°, c =0.3 in methanol
Safety Information
MSDS Information
GSK9311 Usage And Synthesis
Biological ActivityGSK9311 is a negative control for the SGC epigenetic probe GSK6853. GSK9311 exhibits 125- and 185-fold reduced potency than its structural analog GSK6853 toward BRPF1 in cell-free and cell-based assays (pIC50 = 6.0/GSK9311 vs. 8.1/GSK6853 in ligand competition binding assay by TR-FRET; IC50 = 3.7 μM/GSK9311 vs. 20 nM/GSK6853 against NanoLuc-BRPF1 bromodomain interaction with Histone H3.3-HaloTag in HEK293 cells), and therefore serves as a good inactive control compound in BRPF1 inhibition studies employing GSK6853. For characterization details of the active probe, GSK6853, please visit the GSK6853 probe summary on the Structural Genomics Consortium (SGC) website.

GSK6853, the active probe, is available from Sigma. To learn more about and purchase GSK6853, click here.

To learn about other SGC chemical probes for epigenetic targets, visit sigma.com/sgc
GSK9311 Preparation Products And Raw materials
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