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TargetCorticotropin-releasing factor receptor 1
LigandBDBM50413236
Substrate/Competitorn/a
Meas. Tech.ChEMBL_493722 (CHEMBL949477)
IC50 8317.64±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:
BDBM50413236
n/a
NameBDBM50413236
Synonyms:CHEMBL458780
TypeSmall organic molecule
Emp. Form.C21H12F6N6OS
Mol. Mass.510.415
SMILESCc1cc(-n2ccc(n2)-c2nccs2)c2[nH]c(=O)n(-c3ccc(cc3C(F)(F)F)C(F)(F)F)c2n1 |(21.34,-6.37,;22.68,-5.6,;22.68,-4.05,;24.01,-3.28,;24,-1.74,;22.75,-.84,;23.23,.63,;24.77,.63,;25.25,-.83,;25.68,1.87,;27.22,1.88,;27.69,3.34,;26.44,4.23,;25.19,3.34,;25.34,-4.05,;26.82,-3.57,;27.73,-4.82,;29.27,-4.82,;26.82,-6.08,;27.29,-7.53,;26.26,-8.68,;26.73,-10.14,;28.24,-10.46,;29.27,-9.31,;28.79,-7.85,;29.82,-6.7,;30.91,-5.6,;28.7,-5.65,;30.94,-7.76,;28.72,-11.93,;29.11,-13.41,;30.2,-11.49,;27.25,-12.37,;25.34,-5.6,;24.01,-6.37,)|
Structure
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