Reaction Details |
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Target | Cannabinoid receptor 2 |
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Ligand | BDBM50399122 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_876706 (CHEMBL2183177) |
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Ki | 25±n/a nM |
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Citation | Yang, P; Myint, KZ; Tong, Q; Feng, R; Cao, H; Almehizia, AA; Alqarni, MH; Wang, L; Bartlow, P; Gao, Y; Gertsch, J; Teramachi, J; Kurihara, N; Roodman, GD; Cheng, T; Xie, XQ Lead discovery, chemistry optimization, and biological evaluation studies of novel biamide derivatives as CB2 receptor inverse agonists and osteoclast inhibitors. J Med Chem55:9973-87 (2012) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Cannabinoid receptor 2 |
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Name: | Cannabinoid receptor 2 |
Synonyms: | CANNABINOID CB2 | CB-2 | CB2 | CB2A | CB2B | CNR2 | CNR2_HUMAN | CX5 | Cannabinoid CB2 receptor | Cannabinoid receptor 2 (CB2) | Cannabinoid receptor 2 (CB2R) | hCB2 |
Type: | G Protein-Coupled Receptor (GPCR) |
Mol. Mass.: | 39690.94 |
Organism: | Homo sapiens (Human) |
Description: | P34972 |
Residue: | 360 |
Sequence: | MEECWVTEIANGSKDGLDSNPMKDYMILSGPQKTAVAVLCTLLGLLSALENVAVLYLILS
SHQLRRKPSYLFIGSLAGADFLASVVFACSFVNFHVFHGVDSKAVFLLKIGSVTMTFTAS
VGSLLLTAIDRYLCLRYPPSYKALLTRGRALVTLGIMWVLSALVSYLPLMGWTCCPRPCS
ELFPLIPNDYLLSWLLFIAFLFSGIIYTYGHVLWKAHQHVASLSGHQDRQVPGMARMRLD
VRLAKTLGLVLAVLLICWFPVLALMAHSLATTLSDQVKKAFAFCSMLCLINSMVNPVIYA
LRSGEIRSSAHHCLAHWKKCVRGLGSEAKEEAPRSSVTETEADGKITPWPDSRDLDLSDC
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BDBM50399122 |
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n/a |
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Name | BDBM50399122 |
Synonyms: | CHEMBL2179734 |
Type | Small organic molecule |
Emp. Form. | C23H39N3O2 |
Mol. Mass. | 389.5747 |
SMILES | CCCCCC(=O)NC(NC(=O)CCCCC)c1ccc(cc1)N(CC)CC |
Structure |
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