Reaction Details |
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Target | Glucagon-like peptide 2 receptor |
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Ligand | BDBM50183645 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_1586856 |
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EC50 | 0.130000±n/a nM |
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Citation | Wisniewski, K; Sueiras-Diaz, J; Jiang, G; Galyean, R; Lu, M; Thompson, D; Wang, YC; Croston, G; Posch, A; Hargrove, DM; Wisniewska, H; Laporte, R; Dwyer, JJ; Qi, S; Srinivasan, K; Hartwig, J; Ferdyan, N; Mares, M; Kraus, J; Alagarsamy, S; Rivière, PJ; Schteingart, CD Synthesis and Pharmacological Characterization of Novel Glucagon-like Peptide-2 (GLP-2) Analogues with Low Systemic Clearance. J Med Chem59:3129-39 (2016) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Glucagon-like peptide 2 receptor |
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Name: | Glucagon-like peptide 2 receptor |
Synonyms: | GLP-2 receptor | GLP-2-R | GLP-2R | GLP2R | GLP2R_HUMAN |
Type: | PROTEIN |
Mol. Mass.: | 63023.90 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_876141 |
Residue: | 553 |
Sequence: | MKLGSSRAGPGRGSAGLLPGVHELPMGIPAPWGTSPLSFHRKCSLWAPGRPFLTLVLLVS
IKQVTGSLLEETTRKWAQYKQACLRDLLKEPSGIFCNGTFDQYVCWPHSSPGNVSVPCPS
YLPWWSEESSGRAYRHCLAQGTWQTIENATDIWQDDSECSENHSFKQNVDRYALLSTLQL
MYTVGYSFSLISLFLALTLLLFLRKLHCTRNYIHMNLFASFILRTLAVLVKDVVFYNSYS
KRPDNENGWMSYLSEMSTSCRSVQVLLHYFVGANYLWLLVEGLYLHTLLEPTVLPERRLW
PRYLLLGWAFPVLFVVPWGFARAHLENTGCWTTNGNKKIWWIIRGPMMLCVTVNFFIFLK
ILKLLISKLKAHQMCFRDYKYRLAKSTLVLIPLLGVHEILFSFITDDQVEGFAKLIRLFI
QLTLSSFHGFLVALQYGFANGEVKAELRKYWVRFLLARHSGCRACVLGKDFRFLGKCPKK
LSEGDGAEKLRKLQPSLNSGRLLHLAMRGLGELGAQPQQDHARWPRGSSLSECSEGDVTM
ANTMEEILEESEI
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BDBM50183645 |
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n/a |
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Name | BDBM50183645 |
Synonyms: | CHEMBL3823818 |
Type | Small organic molecule |
Emp. Form. | C160H237N41O47 |
Mol. Mass. | 3486.8403 |
SMILES | CCCCC(NC(=O)C(CCC(O)=O)NC(=O)C(CC(O)=O)NC(=O)C(CO)NC(=O)C(Cc1ccccc1)NC(=O)C(CO)NC(=O)CNC(=O)C(CC(O)=O)NC(=O)CNC(=O)C(N)Cc1cnc[nH]1)C(=O)NC(CC(N)=O)C(=O)NC(C(C)O)C(=O)NC(C(C)CC)C(=O)NC(CC(C)C)C(=O)NC(CC(O)=O)C(=O)NC(Cc1ccc2ccccc2c1)C(=O)NC(CC(C)C)C(=O)NC(C)C(=O)NC(C)C(=O)NC(CCCNC(N)=N)C(=O)NC(CC(O)=O)C(=O)NC(Cc1ccccc1)C(=O)NC(C(C)CC)C(=O)NC(CC(N)=O)C(=O)NC(Cc1c[nH]c2ccccc12)C(=O)NC(CC(C)C)C(=O)NC(C(C)CC)C(=O)NC(CCC(N)=O)C(=O)NC(C(C)O)C(=O)NC(CCCCN)C(N)=O |
Structure |
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