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TargetCorticotropin-releasing factor receptor 1
LigandBDBM50413233
Substrate/Competitorn/a
Meas. Tech.ChEMBL_493722 (CHEMBL949477)
IC50>10000±n/a nM
Citation Di Fabio, RArban, RBernasconi, GBraggio, SBlaney, FECapelli, AMCastiglioni, EDonati, DFazzolari, ERatti, EFeriani, AContini, SGentile, GGhirlanda, DSabbatini, FMAndreotti, DSpada, SMarchioro, CWorby, ASt-Denis, Y Dihydropyrrole[2,3-d]pyridine derivatives as novel corticotropin-releasing factor-1 antagonists: mapping of the receptor binding pocket by in silico docking studies. J Med Chem51:7273-86 (2009) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Corticotropin-releasing factor receptor 1
Name:Corticotropin-releasing factor receptor 1
Synonyms:CRF-R | CRF-R2 Alpha | CRF1 | CRFR | CRFR1 | CRFR1_HUMAN | CRH-R 1 | CRHR | CRHR1 | Corticotropin releasing factor receptor 1 | Corticotropin-releasing factor receptor 1 (CRF-1) | Corticotropin-releasing factor receptor 1 (CRF1) | Corticotropin-releasing hormone receptor 1
Type:Enzyme
Mol. Mass.:50744.31
Organism:Homo sapiens (Human)
Description:P34998
Residue:444
Sequence:
MGGHPQLRLVKALLLLGLNPVSASLQDQHCESLSLASNISGLQCNASVDLIGTCWPRSPA
GQLVVRPCPAFFYGVRYNTTNNGYRECLANGSWAARVNYSECQEILNEEKKSKVHYHVAV
IINYLGHCISLVALLVAFVLFLRLRPGCTHWGDQADGALEVGAPWSGAPFQVRRSIRCLR
NIIHWNLISAFILRNATWFVVQLTMSPEVHQSNVGWCRLVTAAYNYFHVTNFFWMFGEGC
YLHTAIVLTYSTDRLRKWMFICIGWGVPFPIIVAWAIGKLYYDNEKCWFGKRPGVYTDYI
YQGPMILVLLINFIFLFNIVRILMTKLRASTTSETIQYRKAVKATLVLLPLLGITYMLFF
VNPGEDEVSRVVFIYFNSFLESFQGFFVSVFYCFLNSEVRSAIRKRWHRWQDKHSIRARV
ARAMSIPTSPTRVSFHSIKQSTAV
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50413233
n/a
NameBDBM50413233
Synonyms:CHEMBL458169
TypeSmall organic molecule
Emp. Form.C22H11F9N6S
Mol. Mass.562.414
SMILESCc1cc(-n2ccc(n2)-c2nccs2)c2nc(n(-c3ccc(cc3C(F)(F)F)C(F)(F)F)c2n1)C(F)(F)F |(10.43,-27.88,;11.76,-27.11,;11.77,-25.57,;13.09,-24.79,;13.09,-23.26,;11.84,-22.35,;12.31,-20.89,;13.85,-20.88,;14.33,-22.35,;14.76,-19.64,;16.3,-19.63,;16.77,-18.17,;15.53,-17.28,;14.28,-18.18,;14.43,-25.56,;15.9,-25.08,;16.82,-26.33,;15.9,-27.59,;15.44,-29.06,;13.93,-29.38,;13.46,-30.85,;14.5,-31.99,;16.01,-31.65,;16.47,-30.19,;17.98,-29.86,;19.5,-29.6,;17.68,-28.34,;18.26,-31.37,;14.03,-33.46,;15.49,-33.96,;12.58,-32.95,;13.57,-34.92,;14.43,-27.11,;13.1,-27.88,;18.36,-26.33,;19.9,-26.33,;18.36,-27.87,;18.36,-24.79,)|
Structure
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