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TargetCorticotropin-releasing factor receptor 1
LigandBDBM50413237
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:
BDBM50413237
n/a
NameBDBM50413237
Synonyms:CHEMBL488592
TypeSmall organic molecule
Emp. Form.C22H14F6N6S
Mol. Mass.508.442
SMILESCc1nc2c(cc(C)nc2n1-c1ccc(cc1C(F)(F)F)C(F)(F)F)-n1ccc(n1)-c1nccs1 |(.44,-25.52,;-1.1,-25.52,;-2.01,-24.26,;-3.48,-24.74,;-4.82,-23.98,;-6.15,-24.75,;-6.15,-26.29,;-7.48,-27.06,;-4.81,-27.06,;-3.48,-26.29,;-2.01,-26.77,;-1.53,-28.23,;-2.56,-29.38,;-2.09,-30.84,;-.58,-31.16,;.45,-30.01,;-.03,-28.55,;1,-27.4,;2.08,-26.3,;-.13,-26.35,;2.11,-28.46,;-.1,-32.62,;.29,-34.11,;1.37,-32.19,;-1.58,-33.07,;-4.82,-22.44,;-6.07,-21.54,;-5.6,-20.07,;-4.06,-20.07,;-3.58,-21.53,;-3.15,-18.82,;-1.61,-18.82,;-1.14,-17.35,;-2.39,-16.47,;-3.63,-17.36,)|
Structure
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