LW6

Item no.	HY-13671-50mg
Manufacturer	MedChem Express
CASRN	934593-90-5
Amount	50 mg
Quantity options	100 mg 10mM/1mL 10 mg 25 mg 50 mg 5 mg
Category	Oncology Inhibitors & Compound Libraries Small Molecules By Organ Colorectal Cancer
Type	Inhibitors
Specific against	other
Purity	98.93
Formula	C26H29NO5
Citations	[1]Naik R, et al. Synthesis and structure-activity relationship study of chemical probes as hypoxia induced factor-1α/malate dehydrogenase 2 inhibitors. J Med Chem. 2014 Nov 26;57(22):9522-38.<br/>[2]Lee K, et al. LW6, a novel HIF-1 inhibitor, promotes proteasomal degradation of HIF-1alpha via upregulation of VHL in a colon cancer cell line. Biochem Pharmacol. 2010 Oct 1;80(7):982-9.<br/>[3]Song JG, et al. Discovery of LW6 as a new potent inhibitor of breast cancer resistance protein.<br/>[4]Sato M, et al. LW6, a hypoxia-inducible factor 1 inhibitor, selectively induces apoptosis in hypoxic cells through depolarization of mitochondria in A549 human lung cancer cells. Mol Med Rep. 2015 Sep;12(3):3462-8.
Smiles	O=C(OC)C1=CC=C(O)C(NC(COC2=CC=C(C3(C4)CC5CC4CC(C5)C3)C=C2)=O)=C1
ECLASS 10.1	32160490
ECLASS 11.0	32160490
UNSPSC	12000000
Alias	HIF-1α inhibitor; LW8
Available
Product Description	LW6 (HIF-1α inhibitor) is a novel HIF-1 inhibitor with an IC50 of 4.4 μM. LW6 decreases HIF-1α protein expression without affecting HIF-1β expression.
StorageTemperature	-20°C, 3 years; 4°C, 2 years (Powder)
Shipping	Room Temperature
Manufacturers Applications	Cancer-programmed cell death
MolecularWeight	435.51
Clinical Information	No Development Reported
Manufacturers Research Area	Cancer
Solubility	DMF : 17.24 mg/mL (ultrasonic)\|DMSO : 25 mg/mL (ultrasonic)
Target	Apoptosis; HIF/HIF Prolyl-Hydroxylase
Manufacturers Target	Apoptosis; HIF/HIF Prolyl-Hydroxylase
Manufacturers Pathway	Apoptosis; Metabolic Enzyme/Protease
Manufacturers Product type	Reference compound

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HY-13671-50mg-safety-datasheet.pdf