HBX 28258

HBX 28258 Suppliers list
Company Name: TargetMol Chemicals Inc.  
Tel: +1-781-999-5354; +1-00000000000
Email: marketing@targetmol.com
Company Name: HANGZHOU CLAP TECHNOLOGY CO.,LTD  
Tel: 86-571-88216897,88216896 13588875226
Email: sales@hzclap.com
Company Name: Nanjing Shizhou Biology Technology Co.,Ltd  
Tel: 025-85560043 15850508050
Email: cindy.huang@synzest.com
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.cn
Company Name: TargetMol Chemicals Inc.  
Tel: 13564774135
Email: marketing@targetmol.com

HBX 28258 manufacturers

  • HBX28258
  • HBX28258 pictures
  • $1980.00
  • 2026-07-27
  • CAS:1426544-54-8
  • Purity:
  • Supply Ability: 10g
HBX 28258 Basic information
Product Name:HBX 28258
Synonyms:HBX 28258;2-Acridinecarboxamide, 9-chloro-N-[3-[ethyl(phenylmethyl)amino]propyl]-5,6,7,8-tetrahydro-
CAS:1426544-54-8
MF:C26H30ClN3O
MW:435.99
EINECS:
Product Categories:
Mol File:1426544-54-8.mol
HBX 28258 Structure
HBX 28258 Chemical Properties
Safety Information
MSDS Information
HBX 28258 Usage And Synthesis
DescriptionHBX28258 is an inhibitor of recombinant human USP7 protein. It acts by binding the active site through covalent mechanism and selectively inactivating USP7 protein in human colon cancer and embryonic kidney cell.
UsesHBX 28258 is a selective USP7 inhibitor, with an IC50 of 22.6 μM. HBX 28258 can covalently binds to Cys223 located in the catalytic core of USP7, inhibits its deubiquitinating activity, promotes MDM2 protein degradation, and activates p53[1].
IC 50USP7: 22.6 μM (IC50)
References[1] Qi SM, et, al. Targeting USP7-Mediated Deubiquitination of MDM2/MDMX-p53 Pathway for Cancer Therapy: Are We There Yet Front Cell Dev Biol. 2020 Apr 2:8:233. DOI:10.3389/fcell.2020.00233
HBX 28258 Preparation Products And Raw materials
Tag:HBX 28258(1426544-54-8) Related Product Information
MTX115325 UCHL1 Protein, Rat (His) USP25 Protein, Human USP3 Protein, Human (Active, sf9, GST) P 22077 USP5-IN-1