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  • DC Chemicals Limited
  • China
  • Product Name: HBX41108
  • Price: $550.0/100mg $900.0/250mg $1800.0/1g
  • Purity: 98.0%
  • Stocking Period: 3 Day
  • Contact: Tony Cao

924296-39-9

924296-39-9 structure
924296-39-9 structure
  • Name: HBX 41108
  • Chemical Name: 7-Chloro-9-oxo-9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrile
  • CAS Number: 924296-39-9
  • Molecular Formula: C13H3ClN4O
  • Molecular Weight: 266.64200
  • Catalog: Signaling Pathways Apoptosis Apoptosis
  • Create Date: 2018-12-21 18:12:38
  • Modify Date: 2024-01-02 17:13:44
  • HBX 41108 is an uncompetitive inhibitor of ubiquitin-specific protease 7 (USP7) with an IC50 of 424 nM. HBX 41108 inhibits USP7-mediated p53 deubiquitination to stabilize p53 and inhibits cancer cell growth. HBX 41108 induces p53-dependent apoptosis in p53 wild type and null isogenic cancer cell lines[1][2].

Name 7-Chloro-9-oxo-9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrile
Synonyms 7-chloro-9-oxoindeno[1,2-b]pyrazine-2,3-dicarbonitrile
HBX41108
Description HBX 41108 is an uncompetitive inhibitor of ubiquitin-specific protease 7 (USP7) with an IC50 of 424 nM. HBX 41108 inhibits USP7-mediated p53 deubiquitination to stabilize p53 and inhibits cancer cell growth. HBX 41108 induces p53-dependent apoptosis in p53 wild type and null isogenic cancer cell lines[1][2].
Related Catalog
References

[1]. Colland F, et al. Small-molecule inhibitor of USP7/HAUSP ubiquitin protease stabilizes and activates p53 in cells. Mol Cancer Ther. 2009 Aug;8(8):2286-95.

[2]. Colombo M, et al. Synthesis and biological evaluation of 9-oxo-9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrile analogues as potential inhibitors of deubiquitinating enzymes. ChemMedChem. 2010 Apr 6;5(4):552-8.

Density 1.66g/cm3
Boiling Point 604.9ºC at 760 mmHg
Molecular Formula C13H3ClN4O
Molecular Weight 266.64200
Flash Point 319.6ºC
Exact Mass 266.00000
PSA 90.43000
LogP 2.08476
Index of Refraction 1.725

~40%

924296-39-9 structure

924296-39-9

Literature: Hybrigenics S.A. Patent: EP1749822 A1, 2007 ; Location in patent: Page/Page column 28 ; EP 1749822 A1

~%

924296-39-9 structure

924296-39-9

Literature: ChemMedChem, , vol. 5, # 4 p. 552 - 558
Precursor  2

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