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Reaction Details
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TargetPlatelet-activating factor receptor
LigandBDBM50286022
Substrate/Competitorn/a
Meas. Tech.ChEBML_155151
Ki 120±n/a nM
Citation Sheppard, GSDavidsen, SKCarrera, GMPireh, DHolms, JHHeyman, HRSteinman, DHCurtin, MLConway, RGRhein, DAAlbert, DHTapang, PMagoc, TJSummers, JB Synthesis and evaluation of water soluble indole pyrrolothiazole paf antagonists Bioorg Med Chem Lett5:2913-2918 (1995)    Article
More Info.:Get all data from this article,  Assay Method
 
Platelet-activating factor receptor
Name:Platelet-activating factor receptor
Synonyms:PAF-R | PTAFR | PTAFR_CAVPO | Platelet activating factor receptor | Platelet-activating factor receptor
Type:Protein
Mol. Mass.:39005.63
Organism:Cavia porcellus
Description:n/a
Residue:342
Sequence:
MELNSSSRVDSEFRYTLFPIVYSIIFVLGIIANGYVLWVFARLYPSKKLNEIKIFMVNLT
VADLLFLITLPLWIVYYSNQGNWFLPKFLCNLAGCLFFINTYCSVAFLGVITYNRFQAVK
YPIKTAQATTRKRGIALSLVIWVAIVAAASYFLVMDSTNVVSNKAGSGNITRCFEHYEKG
SKPVLIIHICIVLGFFIVFLLILFCNLVIIHTLLRQPVKQQRNAEVRRRALWMVCTVLAV
FVICFVPHHMVQLPWTLAELGMWPSSNHQAINDAHQVTLCLLSTNCVLDPVIYCFLTKKF
RKHLSEKLNIMRSSQKCSRVTTDTGTEMAIPINHTPVNPIKN
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50286022
n/a
NameBDBM50286022
Synonyms:5-{(R)-7-[1-Dimethylcarbamoyl-6-(4-fluoro-phenyl)-1H-indole-3-carbonyl]-1H-pyrrolo[1,2-c]thiazol-3-yl}-1-[(E)-pyridine-3-carbonylimino]-1,2-dihydro-pyridinium | CHEMBL98090
TypeSmall organic molecule
Emp. Form.C35H28FN6O3S
Mol. Mass.631.698
SMILESCN(C)C(=O)n1cc(C(=O)c2ccn3[C@H](SCc23)c2ccc[n+](NC(=O)c3cccnc3)c2)c2ccc(cc12)-c1ccc(F)cc1
Structure
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