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Name | Lutropin-choriogonadotropic hormone receptor |
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Species | Homo sapiens (Human) |
Gene | LHCGR |
Synonym | lutropin-choriogonadotropic hormone receptor Luteinizing hormone receptor LSH-R LHR LH/CG-R [ Show all ] |
Disease | Heart disease Breast cancer Cancer Myelodysplastic syndrome Female infertility [ Show all ] |
Length | 699 |
Amino acid sequence | MKQRFSALQLLKLLLLLQPPLPRALREALCPEPCNCVPDGALRCPGPTAGLTRLSLAYLPVKVIPSQAFRGLNEVIKIEISQIDSLERIEANAFDNLLNLSEILIQNTKNLRYIEPGAFINLPRLKYLSICNTGIRKFPDVTKVFSSESNFILEICDNLHITTIPGNAFQGMNNESVTLKLYGNGFEEVQSHAFNGTTLTSLELKENVHLEKMHNGAFRGATGPKTLDISSTKLQALPSYGLESIQRLIATSSYSLKKLPSRETFVNLLEATLTYPSHCCAFRNLPTKEQNFSHSISENFSKQCESTVRKVNNKTLYSSMLAESELSGWDYEYGFCLPKTPRCAPEPDAFNPCEDIMGYDFLRVLIWLINILAIMGNMTVLFVLLTSRYKLTVPRFLMCNLSFADFCMGLYLLLIASVDSQTKGQYYNHAIDWQTGSGCSTAGFFTVFASELSVYTLTVITLERWHTITYAIHLDQKLRLRHAILIMLGGWLFSSLIAMLPLVGVSNYMKVSICFPMDVETTLSQVYILTILILNVVAFFIICACYIKIYFAVRNPELMATNKDTKIAKKMAILIFTDFTCMAPISFFAISAAFKVPLITVTNSKVLLVLFYPINSCANPFLYAIFTKTFQRDFFLLLSKFGCCKRRAELYRRKDFSAYTSNCKNGFTGSNKPSQSTLKLSTLHCQGTALLDKTRYTEC |
UniProt | P22888 |
Protein Data Bank | N/A |
GPCR-HGmod model | N/A |
3D structure model | No available structures or models |
BioLiP | N/A |
Therapeutic Target Database | T79473 |
ChEMBL | CHEMBL1854 |
IUPHAR | N/A |
DrugBank | BE0000134 |
Name | CHEMBL209634 |
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Molecular formula | C23H22N4O2S2 |
IUPAC name | 5-amino-4-(3-methoxyphenyl)-2-methylsulfanyl-N-(2-phenylethyl)thieno[2,3-d]pyrimidine-6-carboxamide |
Molecular weight | 450.575 |
Hydrogen bond acceptor | 7 |
Hydrogen bond donor | 2 |
XlogP | 5.5 |
Synonyms | SCHEMBL4328116 |
Inchi Key | ANFSNQLMLULUFN-UHFFFAOYSA-N |
Inchi ID | InChI=1S/C23H22N4O2S2/c1-29-16-10-6-9-15(13-16)19-17-18(24)20(31-22(17)27-23(26-19)30-2)21(28)25-12-11-14-7-4-3-5-8-14/h3-10,13H,11-12,24H2,1-2H3,(H,25,28) |
PubChem CID | 11604835 |
ChEMBL | CHEMBL209634 |
IUPHAR | N/A |
BindingDB | N/A |
DrugBank | N/A |
Structure | |
Lipinski's druglikeness | This ligand has a partition coefficient log P greater than 5. |
Parameter | Value | Reference | Database source |
---|---|---|---|
Efficacy | 25.6 % | PMID16789744 | ChEMBL |
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