HBX41108 chemical structure
Chemical structureResearch use only
CAT. NO. DC8207Featured

HBX41108

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TotalUS$550
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Product overview

Description & Application

Inhibitor of ubiquitin-specific protease (USP) 7 activity (IC50 = 424 nM). Displays uncompetitive inhibition. Also inhibits USP7-mediated p53 deubiquitination (IC50 = 0.8 μM). Stabilizes p53 and inhibits cancer cell growth; induces p53-dependent apoptosis in p53 wild type and null isogenic cancer cell lines. For the detailed information of HBX41108 , the solubility of HBX41108 in water, the solubility of HBX41108 in DMSO, the solubility of HBX41108 in PBS buffer, the animal experiment (test) of HBX41108 , the cell expriment (test) of HBX41108 , the in vivo, in vitro and clinical trial test of HBX41108 , the EC50, IC50,and affinity,of HBX41108 , For the detailed information of HBX41108 , the solubility of HBX41108 in water, the solubility of HBX41108 in DMSO, the solubility of HBX41108 in PBS buffer, the animal experiment (test) of HBX41108 , the cell expriment (test) of HBX41108 , the in vivo, in vitro and clinical trial test of HBX41108 , the EC50, IC50,and affinity,of HBX41108 , Please contact DC Chemicals.

ParameterValue
Chemical Name7-Chloro-9-oxo-9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrile;7-Chloro-9-oxo-9H-indeno[1,2-b]-pyrazine-2,3-dicarbonitrile;7-Chloro-9-oxo-9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrile DISCONTINUED;HBX 41108
CAS No.924296-39-9
Synonyms7-Chloro-9-oxo-9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrile;7-Chloro-9-oxo-9H-indeno[1,2-b]-pyrazine-2,3-dicarbonitrile;7-Chloro-9-oxo-9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrile DISCONTINUED;HBX 41108
FormulaC13H3N4OCl
M.Wt266.64212
SMILESC1=CC2=C(C=C1Cl)C(=O)C3=C2N=C(C#N)C(=N3)C#N
Purity>98%
Storage2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

Biological Activity

Inhibitor of ubiquitin-specific protease (USP) 7 activity (IC50 = 424 nM). Displays uncompetitive inhibition. Also inhibits USP7-mediated p53 deubiquitination (IC50 = 0.8 μM). Stabilizes p53 and inhibits cancer cell growth; induces p53-dependent apoptosis in p53 wild type and null isogenic cancer cell lines. For the detailed information of HBX41108 , the solubility of HBX41108 in water, the solubility of HBX41108 in DMSO, the solubility of HBX41108 in PBS buffer, the animal experiment (test) of HBX41108 , the cell expriment (test) of HBX41108 , the in vivo, in vitro and clinical trial test of HBX41108 , the EC50, IC50,and affinity,of HBX41108 , For the detailed information of HBX41108 , the solubility of HBX41108 in water, the solubility of HBX41108 in DMSO, the solubility of HBX41108 in PBS buffer, the animal experiment (test) of HBX41108 , the cell expriment (test) of HBX41108 , the in vivo, in vitro and clinical trial test of HBX41108 , the EC50, IC50,and affinity,of HBX41108 , Please contact DC Chemicals.

In Vitro

No in vitro data are provided in the current product source. Contact us for further information.

In Vivo

No in vivo data are provided in the current product source. Contact us for further information.

References & source

DC Chemicals original product information

Published experimental findings depend on the model and assay conditions. They do not guarantee equivalent performance in every application. For laboratory research use only.

Product documentation

Refer to the certificate supplied with your lot for batch-specific release results.

Handling guide

2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO

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