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CCT007093

CCT007093

Item no.	HY-15880-10mg
Manufacturer	MedChem Express
CASRN	176957-55-4
Amount	10 mg
Quantity options	100 mg 10 mM/1 mL 10 mg 1 mg 500 mg 50 mg 5 mg
Category	Oncology Inhibitors & Compound Libraries Small Molecules By Organ Colorectal Cancer Breast Cancer Brain Cancer
Type	Inhibitors
Specific against	other
Purity	98.34
Citations	[1]Lingling Zhang, et al. Inhibition of wild-type p53-induced phosphatase 1 promotes liver regeneration in mice by direct activation of mammalian target of rapamycin. Hepatology. 2015 Jun;61(6):2030-41.\|[2]S Rayter, et al. A chemical inhibitor of PPM1D that selectively kills cells overexpressing PPM1D. Oncogene. 2008 Feb 14;27(8):1036-44.
Smiles	O=C1/C(CC/C1=C\C2=CC=CS2)=C/C3=CC=CS3
ECLASS 10.1	32160490
ECLASS 11.0	32160490
UNSPSC	12000000
Alias	176957-55-4
Shipping Condition	Room temperature
Available
Manufacturer - Type	Reference compound
Manufacturer - Applications	Cancer-Kinase/protease
Manufacturer - Targets	Apoptosis; Autophagy; Phosphatase
Shipping Temperature	Room Temperature
Storage Conditions	-20°C, 3 years; 4°C, 2 years (Powder)
Molecular Weight	272.39
Product Description	CCT007093 is an effective protein phosphatase 1D (PPM1D Wip1) inhibitor. Wip1 inhibition can activate the mTORC1 pathway and enhance hepatocyte proliferation after hepatectomy[1][2].
Manufacturer - Research Area	Cancer
Solubility	DMF: 3.33 mg/mL (ultrasonic)\|DMSO: ≥ 2.8 mg/mL
Manufacturer - Pathway	Apoptosis; Autophagy; Metabolic Enzyme/Protease
Clinical information	No Development Reported

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HY-15880-10mg-safety-datasheet.pdf