U0126

U0126
Identifiers
	IUPAC name 1,4-Diamino-2,3-dicyano-1,4-bis(2-aminophenylthio)butadiene;
CAS Number	218601-62-8 ;
PubChem CID	3006531;
ChemSpider	2276356 ;
UNII	8027P94HLL;
ChEBI	CHEBI:90693 ;
ChEMBL	ChEMBL34704 ;
CompTox Dashboard (EPA)	DTXSID4040470 ;
Chemical and physical data
Formula	C18H16N6S2
Molar mass	380.49 g·mol−1
3D model (JSmol)	Interactive image;
	SMILES c1cc(c(cc1)S/C(=C(/C(=C(/Sc2c(cccc2)N)\N)/C#N)\C#N)/N)N;
	InChI InChI=1S/C18H16N6S2/c19-9-11(17(23)25-15-7-3-1-5-13(15)21)12(10-20)18(24)26-16-8-4-2-6-14(16)22/h1-8H,21-24H2/b17-11+,18-12+ ; Key:DVEXZJFMOKTQEZ-JYFOCSDGSA-N ;
	(what is this?) (verify)

U0126 is a highly selective inhibitor of both MEK1 and MEK2, a type of MAPK/ERK kinase.[1][2] U0126 was found to functionally antagonize AP-1 transcriptional activity via noncompetitive inhibition of the dual specificity kinase MEK with IC₅₀ of 72 nM for MEK1 and 58 nM for MEK2. U0126 inhibited anchorage-independent growth of Ki-ras-transformed rat fibroblasts by simultaneously blocking both extracellular signal-regulated kinase (ERK) and mammalian target of rapamycin (mTOR)-p70(S6K) pathways.[3] The effects of U0126 on the growth of eight human breast cancer cell lines shown that U0126 selectively repressed anchorage-independent growth of MDA-MB231 and HBC4 cells, two lines with constitutively activated ERK.[4] Loss of contact with substratum triggers apoptosis in many normal cell types, a phenomenon termed anoikis. U0126 sensitized MDA-MB231 and HBC4 to anoikis, i.e., upon treatment with U0126, cells deprived of anchorage entered apoptosis.

U0126 is also a weak inhibitor of PKC, Raf, ERK, JNK, MEKK, MKK-3, MKK-4/SEK, MKK-6, Cdk2 and Cdk4.

Its potential for wiping long-term memories in rats has been studied at the Center for Neural Science at New York University.[5]

References

Favata, M., et al., Identification of a novel inhibitor of mitogen-activated protein kinase. J. Biol. Chem. 273, 18623, (1998)
DeSilva, D., et al., Inhibition of mitogen-activated protein kinase blocks T cell proliferation but does not induce or prevent anergy. J. Immunol. 160, 4175, (1998)
Duncia, J.V., et al., MEK inhibitors: The chemistry and biological activity of U0126, its analogs, and cyclization products. Bioorg. Med. Chem. Lett. 8, 2839-2844, (1998)
Fukazawa, H., et al., Mitogen-activated protein/extracellular signal-regulated kinase kinase (MEK) inhibitors restore anoikis sensitivity in human breast cancer cell lines with a constitutively activated extracellular-regulated kinase (ERK) pathway. Mol. Cancer Ther., 303-309, (2002)
Smith, Kerri (2007-03-11). "Wipe out a single memory". Nature Magazine. Retrieved 2017-12-31.

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.

[1] Favata, M., et al., Identification of a novel inhibitor of mitogen-activated protein kinase. J. Biol. Chem. 273, 18623, (1998)

[2] DeSilva, D., et al., Inhibition of mitogen-activated protein kinase blocks T cell proliferation but does not induce or prevent anergy. J. Immunol. 160, 4175, (1998)

[3] Duncia, J.V., et al., MEK inhibitors: The chemistry and biological activity of U0126, its analogs, and cyclization products. Bioorg. Med. Chem. Lett. 8, 2839-2844, (1998)

[4] Fukazawa, H., et al., Mitogen-activated protein/extracellular signal-regulated kinase kinase (MEK) inhibitors restore anoikis sensitivity in human breast cancer cell lines with a constitutively activated extracellular-regulated kinase (ERK) pathway. Mol. Cancer Ther., 303-309, (2002)

[5] Smith, Kerri (2007-03-11). "Wipe out a single memory". Nature Magazine. Retrieved 2017-12-31.

U0126

See also

References