| Identification | Back Directory | [Name]
7-Chloro-9-oxo-9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrile | [CAS]
924296-39-9 | [Synonyms]
CS-1900
HBX 41108
HBX 41108;HBX-41108
7-chloro-5-oxo-5H-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 HBX 41108 | [Molecular Formula]
C13H3ClN4O | [MDL Number]
MFCD16251537 | [MOL File]
924296-39-9.mol | [Molecular Weight]
266.64 |
| Chemical Properties | Back Directory | [Melting point ]
220(dec.)℃ | [Boiling point ]
604.9±55.0 °C(Predicted) | [density ]
1.66 | [storage temp. ]
Store at -20°C | [solubility ]
insoluble in H2O; ≥1.83 mg/mL in EtOH with gentle warming and ultrasonic; ≥13.35 mg/mL in DMSO | [form ]
solid | [pka]
-9.42±0.20(Predicted) | [color ]
Light yellow to yellow | [InChI]
1S/C13H3ClN4O/c14-6-1-2-7-8(3-6)13(19)12-11(7)17-9(4-15)10(5-16)18-12/h1-3H | [InChIKey]
BIGPXXAUSQLTQR-UHFFFAOYSA-N | [SMILES]
O=C(C1=C2C=CC(Cl)=C1)C3=C2N=C(C(C#N)=N3)C#N |
| Hazard Information | Back Directory | [Uses]
7-Chloro-9-oxo-9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrile is used in the synthesis and biological evaluation of 9-Oxo-9H-indeno[1,2-b]pyrazine-2,3-dicarbonitrile analogues as potential Inhibitors of deubiquitinating enzymes.
| [Biological Activity]
hbx 41108 is a potent inhibitor of usp7 with ic50 value of 424 nm [1].ubiquitin-specific-processing protease 7 (usp7) is a ubiquitin specific protease and removes ubiquitin from specific protein substrates. usp7 can deubiquitinate p53, protecting p53 from mdm2-mediated degradation and involving the oncogenic stabilization of p53.hbx 41108 is an uncompetitive and reversible usp7 inhibitor. hbx 41108 inhibited usp7-mediated p53 deubiquitination with ic50 value of 0.8 μm in a dose-dependent way and was only weakly active against the aspartic, serine and metalloproteases tested with ic50 > 10 μm. in hct116 cells, hbx 41108 increased the levels of p53 and p21cip1/waf, which was the product of p53 target genes. in hek293 cells, hbx 41108 increased the level of polyubiquitinated forms of p53 and reduced mdm2 levels. in hct116 colon cancer cells, hbx 41108 inhibited cell proliferation with ic50 value of 1 μm in a dose-dependent way and induced apoptosis in a dose-dependent manner [1]. in cos7 cells, hbx 41108 inhibited pparγ stability induced by usp7 and decreased the basal transcriptional activity of pparγ by 70% [2]. | [in vivo]
HBX 41108 (100 mg/kg/day for 14 days, i.p.) can promote wound healing and reduce blood sugar levels in diabetic rats [3].
| [IC 50]
USP7: 424 nM (IC50); hTPH2 | [storage]
Store at -20°C | [References]
[1]. colland f, formstecher e, jacq x, et al. small-molecule inhibitor of usp7/hausp ubiquitin protease stabilizes and activates p53 in cells. mol cancer ther, 2009, 8(8): 2286-2295.
[2]. lee kw, cho jg, kim cm, et al. herpesvirus-associated ubiquitin-specific protease (hausp) modulates peroxisome proliferator-activated receptor γ (pparγ) stability through its deubiquitinating activity. j biol chem, 2013, 288(46): 32886-32896. |
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| Company Name: |
Henan Alpha Chemical Co., Ltd.
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| Telephone: |
0371-55055611 18137792234 |
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https://www.chemicalbook.com/ShowSupplierProductsList31206/0.htm |
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