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Name | Cysteinyl leukotriene receptor 1 |
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Species | Homo sapiens (Human) |
Gene | CYSLTR1 |
Synonym | LTD4 receptor LTD4 leukotriene D4 receptor HMTMF81 HG55 [ Show all ] |
Disease | N/A |
Length | 337 |
Amino acid sequence | MDETGNLTVSSATCHDTIDDFRNQVYSTLYSMISVVGFFGNGFVLYVLIKTYHKKSAFQVYMINLAVADLLCVCTLPLRVVYYVHKGIWLFGDFLCRLSTYALYVNLYCSIFFMTAMSFFRCIAIVFPVQNINLVTQKKARFVCVGIWIFVILTSSPFLMAKPQKDEKNNTKCFEPPQDNQTKNHVLVLHYVSLFVGFIIPFVIIIVCYTMIILTLLKKSMKKNLSSHKKAIGMIMVVTAAFLVSFMPYHIQRTIHLHFLHNETKPCDSVLRMQKSVVITLSLAASNCCFDPLLYFFSGGNFRKRLSTFRKHSLSSVTYVPRKKASLPEKGEEICKV |
UniProt | Q9Y271 |
Protein Data Bank | N/A |
GPCR-HGmod model | Q9Y271 |
3D structure model | This predicted structure model is from GPCR-EXP Q9Y271. |
BioLiP | N/A |
Therapeutic Target Database | N/A |
ChEMBL | CHEMBL1798 |
IUPHAR | 269 |
DrugBank | BE0000705 |
Name | CHEMBL1213921 |
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Molecular formula | C36H23BrN2O6 |
IUPAC name | 6-bromo-4-oxo-3-(quinolin-2-ylmethoxy)-2-[3-(quinolin-2-ylmethoxy)phenyl]chromene-8-carboxylic acid |
Molecular weight | 659.492 |
Hydrogen bond acceptor | 8 |
Hydrogen bond donor | 1 |
XlogP | 7.1 |
Synonyms | BDBM50323892 6-bromo-4-oxo-3-(quinolin-2-ylmethoxy)-2-(3-(quinolin-2-ylmethoxy)phenyl)-4H-chromene-8-carboxylic acid 2-[3-[(2-Quinolyl)methoxy]phenyl]-3-[(2-quinolyl)methoxy]-4-oxo-6-bromo-4H-1-benzopyran-8-carboxylic acid |
Inchi Key | AJCUVQGKLQCMGU-UHFFFAOYSA-N |
Inchi ID | InChI=1S/C36H23BrN2O6/c37-24-17-28-32(40)35(44-20-26-15-13-22-7-2-4-11-31(22)39-26)33(45-34(28)29(18-24)36(41)42)23-8-5-9-27(16-23)43-19-25-14-12-21-6-1-3-10-30(21)38-25/h1-18H,19-20H2,(H,41,42) |
PubChem CID | 10532372 |
ChEMBL | CHEMBL1213921 |
IUPHAR | N/A |
BindingDB | 50323892 |
DrugBank | N/A |
Structure | |
Lipinski's druglikeness | This ligand is heavier than 500 daltons. This ligand has a partition coefficient log P greater than 5. |
Parameter | Value | Reference | Database source |
---|---|---|---|
IC50 | 63.0 nM | PMID20621485 | BindingDB,ChEMBL |
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