Reaction Details |
| Report a problem with these data |
Target | Metabotropic glutamate receptor 2 |
---|
Ligand | BDBM50078230 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_106214 (CHEMBL713202) |
---|
Ki | 3000±n/a nM |
---|
Citation | Wichmann, J; Adam, G; Kolczewski, S; Mutel, V; Woltering, T Structure-activity relationships of substituted 5H-thiazolo[3,2-a]pyrimidines as group 2 metabotropic glutamate receptor antagonists. Bioorg Med Chem Lett9:1573-6 (1999) [PubMed] |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Metabotropic glutamate receptor 2 |
---|
Name: | Metabotropic glutamate receptor 2 |
Synonyms: | GRM2_RAT | Gprc1b | Grm2 | Mglur2 |
Type: | PROTEIN |
Mol. Mass.: | 95786.41 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_105034 |
Residue: | 872 |
Sequence: | MESLLGFLALLLLWGAVAEGPAKKVLTLEGDLVLGGLFPVHQKGGPAEECGPVNEHRGIQ
RLEAMLFALDRINRDPHLLPGVRLGAHILDSCSKDTHALEQALDFVRASLSRGADGSRHI
CPDGSYATHSDAPTAVTGVIGGSYSDVSIQVANLLRLFQIPQISYASTSAKLSDKSRYDY
FARTVPPDFFQAKAMAEILRFFNWTYVSTVASEGDYGETGIEAFELEARARNICVATSEK
VGRAMSRAAFEGVVRALLQKPSARVAVLFTRSEDARELLAATQRLNASFTWVASDGWGAL
ESVVAGSERAAEGAITIELASYPISDFASYFQSLDPWNNSRNPWFREFWEERFHCSFRQR
DCAAHSLRAVPFEQESKIMFVVNAVYAMAHALHNMHRALCPNTTHLCDAMRPVNGRRLYK
DFVLNVKFDAPFRPADTDDEVRFDRFGDGIGRYNIFTYLRAGSGRYRYQKVGYWAEGLTL
DTSFIPWASPSAGPLPASRCSEPCLQNEVKSVQPGEVCCWLCIPCQPYEYRLDEFTCADC
GLGYWPNASLTGCFELPQEYIRWGDAWAVGPVTIACLGALATLFVLGVFVRHNATPVVKA
SGRELCYILLGGVFLCYCMTFVFIAKPSTAVCTLRRLGLGTAFSVCYSALLTKTNRIARI
FGGAREGAQRPRFISPASQVAICLALISGQLLIVAAWLVVEAPGTGKETAPERREVVTLR
CNHRDASMLGSLAYNVLLIALCTLYAFKTRKCPENFNEAKFIGFTMYTTCIIWLAFLPIF
YVTSSDYRVQTTTMCVSVSLSGSVVLGCLFAPKLHIILFQPQKNVVSHRAPTSRFGSAAP
RASANLGQGSGSQFVPTVCNGREVVDSTTSSL
|
|
|
BDBM50078230 |
---|
n/a |
---|
Name | BDBM50078230 |
Synonyms: | 2-(2,6-Dichloro-phenyl)-5-(2-ethoxy-phenyl)-7-methyl-5H-thiazolo[3,2-a]pyrimidine-6-carboxylic acid 2-dimethylamino-ethyl ester | CHEMBL435174 |
Type | Small organic molecule |
Emp. Form. | C26H27Cl2N3O3S |
Mol. Mass. | 532.482 |
SMILES | CCOc1ccccc1C1N2C=C(SC2=NC(C)=C1C(=O)OCCN(C)C)c1c(Cl)cccc1Cl |c:12,16,19| |
Structure |
|