ArtNr |
HY-101666-50mg |
Hersteller |
MedChem Express
|
CAS-Nr. |
924296-39-9 |
Menge |
50 mg |
Quantity options |
100 mg
10 mM/1 mL
10 mg
1 ea
1 mg
25 mg
50 mg
5 mg
|
Kategorie |
|
Typ |
Inhibitors |
Specific against |
other |
Purity |
99.61 |
Formula |
C13H3ClN4O |
Citations |
[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. [3]Li X, Wang T, et al. Inhibition of USP7 suppresses advanced glycation end-induced cell cycle arrest and senescence of human umbilical vein endothelial cells through ubiquitination of p53. Acta Biochim Biophys Sin (Shanghai). 2022 Mar 25;54(3):311-320. [4]Li X, Wang T, et al. Inhibition of USP7 suppresses advanced glycation end-induced cell cycle arrest and senescence of human umbilical vein endothelial cells through ubiquitination of p53. Acta Biochim Biophys Sin (Shanghai). 2022 Mar 25;54(3):311-320. [5]Nawa Y, et al. Functional characterization of the neuron-restrictive silencer element in the human tryptophan hydroxylase 2 gene expression. J Neurochem. 2017 Sep;142(6):827-840. |
Smiles |
N#CC1=C(C#N)N=C2C(C(C3=C2C=CC(Cl)=C3)=O)=N1 |
ECLASS 10.1 |
32160490 |
ECLASS 11.0 |
32160490 |
UNSPSC |
12000000 |
Versandbedingung |
Raumtemperatur |
Lieferbar |
|
Manufacturer - Type |
Reference compound |
Manufacturer - Applications |
Cancer-programmed cell death |
Manufacturer - Targets |
Apoptosis; Deubiquitinase; MDM-2/p53 |
Shipping Temperature |
Room Temperature |
Storage Conditions |
4°C (Powder, sealed storage, away from moisture) |
Molecular Weight |
266.64 |
Product Description |
HBX 41108 is an 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. BX 41108 can be used in cancer and diabetes research[1][2][3][4]. |
Manufacturer - Research Area |
Cancer; Metabolic Disease |
Solubility |
DMSO : 250 mg/mL (ultrasonic; warming; heat to 60°C) |
Manufacturer - Pathway |
Apoptosis; Cell Cycle/DNA Damage |
Isoform |
USP7 |
Clinical information |
No Development Reported |
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