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TargetLeukotriene B4 receptor 1
LigandBDBM50317628
Substrate/Competitorn/a
Meas. Tech.ChEMBL_632889 (CHEMBL1107471)
IC50 0.07±n/a nM
Citation Goodnow, RAHicks, ASidduri, AKowalczyk, ADominique, RQiao, QLou, JPGillespie, PFotouhi, NTilley, JCohen, NChoudhry, SCavallo, GTannu, SAVentre, JDLavelle, DTare, NSOh, HLamb, MKurylko, GHamid, RWright, MBPamidimukkala, AEgan, TGubler, UHoffman, AFWei, XLi, YLO'Neil, JMarcano, RPozzani, KMolinaro, TSantiago, JSinger, LHargaden, MMoore, DCatala, ARChao, LCHermann, GVenkat, RMancebo, HRenzetti, LM Discovery of novel and potent leukotriene B4 receptor antagonists. Part 1. J Med Chem53:3502-16 (2010) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Leukotriene B4 receptor 1
Name:Leukotriene B4 receptor 1
Synonyms:BLT | BLT1 | BLTR | CMKRL1 | Chemoattractant receptor-like 1 | G-protein coupled receptor 16 | GPR16 | LT4R1_HUMAN | LTB4-R 1 | LTB4R | Leukotriene B4 R1 | Leukotriene B4 receptor | Leukotriene B4 receptor 1 | P2RY7 | P2Y purinoceptor 7 | P2Y7
Type:Enzyme Catalytic Domain
Mol. Mass.:37582.68
Organism:Homo sapiens (Human)
Description:Q15722
Residue:352
Sequence:
MNTTSSAAPPSLGVEFISLLAIILLSVALAVGLPGNSFVVWSILKRMQKRSVTALMVLNL
ALADLAVLLTAPFFLHFLAQGTWSFGLAGCRLCHYVCGVSMYASVLLITAMSLDRSLAVA
RPFVSQKLRTKAMARRVLAGIWVLSFLLATPVLAYRTVVPWKTNMSLCFPRYPSEGHRAF
HLIFEAVTGFLLPFLAVVASYSDIGRRLQARRFRRSRRTGRLVVLIILTFAAFWLPYHVV
NLAEAGRALAGQAAGLGLVGKRLSLARNVLIALAFLSSSVNPVLYACAGGGLLRSAGVGF
VAKLLEGTGSEASSTRRGGSLGQTARSGPAALEPGPSESLTASSPLKLNELN
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50317628
n/a
NameBDBM50317628
Synonyms:4-{2-(2-Carboxy-ethyl)-3-[6-(3,5-di-pyridin-4-yl-phenoxy)-hexyl]-phenoxy}-butyric acid | CHEMBL1099326
TypeSmall organic molecule
Emp. Form.C35H38N2O6
Mol. Mass.582.686
SMILESOC(=O)CCCOc1cccc(CCCCCCOc2cc(cc(c2)-c2ccncc2)-c2ccncc2)c1CCC(O)=O
Structure
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