Reaction Details |
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Target | Galanin receptor type 2 |
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Ligand | BDBM50273367 |
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Substrate/Competitor | n/a |
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Ki | 2.75±n/a nM |
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Comments | PDSP_3165 |
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Citation | Smith, KE; Walker, MW; Artymyshyn, R; Bard, J; Borowsky, B; Tamm, JA; Yao, WJ; Vaysse, PJ; Branchek, TA; Gerald, C; Jones, KA Cloned human and rat galanin GALR3 receptors. Pharmacology and activation of G-protein inwardly rectifying K+ channels. J Biol Chem273:23321-6 (1998) [PubMed] Article |
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More Info.: | Get all data from this article |
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Galanin receptor type 2 |
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Name: | Galanin receptor type 2 |
Synonyms: | GALR2_RAT | Galanin R2 | Galanin receptor 2 | Galanin receptor type 2 | Galnr2 | Galr2 |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 40697.04 |
Organism: | RAT |
Description: | Galanin R2 GALR2 RAT::O08726 |
Residue: | 372 |
Sequence: | MNGSGSQGAENTSQEGGSGGWQPEAVLVPLFFALIFLVGTVGNALVLAVLLRGGQAVSTT
NLFILNLGVADLCFILCCVPFQATIYTLDDWVFGSLLCKAVHFLIFLTMHASSFTLAAVS
LDRYLAIRYPLHSRELRTPRNALAAIGLIWGLALLFSGPYLSYYRQSQLANLTVCHPAWS
APRRRAMDLCTFVFSYLLPVLVLSLTYARTLRYLWRTVDPVTAGSGSQRAKRKVTRMIII
VAVLFCLCWMPHHALILCVWFGRFPLTRATYALRILSHLVSYANSCVNPIVYALVSKHFR
KGFRKICAGLLRPAPRRASGRVSILAPGNHSGSMLEQESTDLTQVSEAAGPLVPPPALPN
CTASSRTLDPAC
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BDBM50273367 |
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n/a |
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Name | BDBM50273367 |
Synonyms: | (2S,3S)-2-((S)-2-((S)-2-((S)-1-(2-((S)-2-((S)-2-((S)-2-(2-((S)-2-((S)-2-((S)-4-amino-2-((S)-2-((2S,3R)-2-((S)-2-(2-aminoacetamido)-3-(1H-indol-3-yl)propanamido)-3-hydroxybutanamido)-4-methylpentanamido)-4-oxobutanamido)-3-hydroxypropanamido)propanamido)acetamido)-3-(4-hydroxyphenyl)propanamido)-4-methylpentanamido)-4-methylpentanamido)acetyl)pyrrolidine-2-carboxamido)-3-(1H-imidazol-5-yl)propanamido)propanamido)-3-methylpentanoic acid | CHEMBL499980 | Galanin (1-16) | Galanin (1-16), porcine | Galanin (1-16), rat |
Type | Small organic molecule |
Emp. Form. | C78H116N20O21 |
Mol. Mass. | 1669.877 |
SMILES | CC[C@H](C)[C@H](NC(=O)[C@H](C)NC(=O)[C@H](Cc1cnc[nH]1)NC(=O)[C@@H]1CCCN1C(=O)CNC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](Cc1ccc(O)cc1)NC(=O)CNC(=O)[C@H](C)NC(=O)[C@H](CO)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@@H](NC(=O)[C@H](Cc1c[nH]c2ccccc12)NC(=O)CN)[C@@H](C)O)C(O)=O |r| |
Structure |
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