Reaction Details Report a problem with these data
Target
Heat shock protein beta-1
Ligand
BDBM50263167
Substrate
n/a
Meas. Tech.
ChEMBL_489080 (CHEMBL987300)
IC50
6±n/a nM
Citation
Angell, RM; Angell, TD; Bamborough, P; Bamford, MJ; Chung, CW; Cockerill, SG; Flack, SS; Jones, KL; Laine, DI; Longstaff, T; Ludbrook, S; Pearson, R; Smith, KJ; Smee, PA; Somers, DO; Walker, AL Biphenyl amide p38 kinase inhibitors 4: DFG-in and DFG-out binding modes. Bioorg Med Chem Lett 18:4433-7 (2008) [PubMed] Article
More Info.:
Target
Name:
Heat shock protein beta-1
Synonyms:
HSP27 | HSP28 | HSPB1 | HSPB1_HUMAN
Type:
PROTEIN
Mol. Mass.:
22781.73
Organism:
Homo sapiens (Human)
Description:
ChEMBL_1500622
Residue:
205
Sequence:
MTERRVPFSLLRGPSWDPFRDWYPHSRLFDQAFGLPRLPEEWSQWLGGSSWPGYVRPLPPAAIESPAVAAPAYSRALSRQLSSGVSEIRHTADRWRVSLDVNHFAPDELTVKTKDGVVEITGKHEERQDEHGYISRCFTRKYTLPPGVDPTQVSSSLSPEGTLTVEAPMPKLATQSNEITIPVTFESRAQLGGPEAAKSDETAAK
Inhibitor
Name:
BDBM50263167
Synonyms:
3,4,5,6-Tetrahydro-2H-[1,2']bipyridinyl-4'-carboxylic acid [4'-(cyclopropylmethyl-carbamoyl)-6-methyl-biphenyl-3-yl]-amide | CHEMBL476141 | D3RKN_34
Type:
Small organic molecule
Emp. Form.:
C29H32N4O2
Mol. Mass.:
468.59
SMILES:
Cc1ccc(NC(=O)c2ccnc(c2)N2CCCCC2)cc1-c1ccc(cc1)C(=O)NCC1CC1