Target
Dual specificity mitogen-activated protein kinase kinase 1
Ligand
BDBM50141438
Substrate
n/a
Meas. Tech.
ChEBML_124012
IC50
8±n/a nM
Citation
 Wityak, JHobbs, FWGardner, DSSantella, JBPetraitis, JJSun, JHFavata, MFDaulerio, AJHoriuchi, KYCopeland, RAScherle, PAJaffe, BDTrzaskos, JMMagolda, RLTrainor, GLDuncia, JV Beyond U0126. Dianion chemistry leading to the rapid synthesis of a series of potent MEK inhibitors. Bioorg Med Chem Lett 14:1483-6 (2004) [PubMed]  Article
Target
Name:
Dual specificity mitogen-activated protein kinase kinase 1
Synonyms:
Dual specificity mitogen-activated protein kinase (MEK) | Dual specificity mitogen-activated protein kinase kinase 1 (MEK) | Dual specificity mitogen-activated protein kinase kinase 1 (MEK1) | Dual specificity mitogen-activated protein kinase kinase 1/Mitogen-activated protein kinase 1/RAF proto-oncogene serine/threonine-protein kinase | Dual specificity mitogen-activated protein kinase kinase MEK1/2 | ERK activator kinase 1 | MAP kinase kinase 1 | MAP2K1 | MAPK/ERK kinase 1 | MAPK/ERK kinase 1 (MEK1) | MEK-1 | MEK1 | MP2K1_HUMAN | Mitogen-activated protein kinase 1 (MEK1) | PRKMK1 | VHL-MAP2K1/MAP2K2
Type:
Other Protein Type
Mol. Mass.:
43439.03
Organism:
Homo sapiens (Human)
Description:
Full-length human MEK-1 was generated by PCR and purified as a fusion protein from Escherichia coli lysates.
Residue:
393
Sequence:
MPKKKPTPIQLNPAPDGSAVNGTSSAETNLEALQKKLEELELDEQQRKRLEAFLTQKQKVGELKDDDFEKISELGAGNGGVVFKVSHKPSGLVMARKLIHLEIKPAIRNQIIRELQVLHECNSPYIVGFYGAFYSDGEISICMEHMDGGSLDQVLKKAGRIPEQILGKVSIAVIKGLTYLREKHKIMHRDVKPSNILVNSRGEIKLCDFGVSGQLIDSMANSFVGTRSYMSPERLQGTHYSVQSDIWSMGLSLVEMAVGRYPIPPPDAKELELMFGCQVEGDAAETPPRPRTPGRPLSSYGMDSRPPMAIFELLDYIVNEPPPKLPSGVFSLEFQDFVNKCLIKNPAERADLKQLMVHAFIKRSDAEEVDFAGWLCSTIGLNQPSTPTHAAGV
  
Inhibitor
Name:
BDBM50141438
Synonyms:
4-({3-[(Z)-2-Amino-1-cyano-2-(2-hydroxy-phenylsulfanyl)-vinyl]-phenyl}-hydroxy-methyl)-benzonitrile | CHEMBL35598
Type:
Small organic molecule
Emp. Form.:
C23H17N3O2S
Mol. Mass.:
399.465
SMILES:
OC(c1ccc(cc1)C#N)c1cccc(c1)C(C#N)C(=N)Sc1ccccc1O
Structure:
Search PDB for entries with ligand similarity: