Reaction Details |
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Target | Oxytocin receptor |
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Ligand | BDBM50103475 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_145034 (CHEMBL753728) |
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Ki | 0.3±n/a nM |
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Citation | Carnazzi, E; Aumelas, A; Mouillac, B; Breton, C; Guillou, L; Barberis, C; Seyer, R Design, synthesis and pharmacological characterization of a potent radioiodinated and photoactivatable peptidic oxytocin antagonist. J Med Chem44:3022-30 (2001) [PubMed] |
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More Info.: | Get all data from this article, Assay Method |
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Oxytocin receptor |
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Name: | Oxytocin receptor |
Synonyms: | OT-R | OXTR | OXYR_HUMAN | Oxytocin |
Type: | Enzyme Catalytic Domain |
Mol. Mass.: | 42793.26 |
Organism: | Homo sapiens (Human) |
Description: | Oxytocin OXTR HEK293::B2R9L7 |
Residue: | 389 |
Sequence: | MEGALAANWSAEAANASAAPPGAEGNRTAGPPRRNEALARVEVAVLCLILLLALSGNACV
LLALRTTRQKHSRLFFFMKHLSIADLVVAVFQVLPQLLWDITFRFYGPDLLCRLVKYLQV
VGMFASTYLLLLMSLDRCLAICQPLRSLRRRTDRLAVLATWLGCLVASAPQVHIFSLREV
ADGVFDCWAVFIQPWGPKAYITWITLAVYIVPVIVLAACYGLISFKIWQNLRLKTAAAAA
AEAPEGAAAGDGGRVALARVSSVKLISKAKIRTVKMTFIIVLAFIVCWTPFFFVQMWSVW
DANAPKEASAFIIVMLLASLNSCCNPWIYMLFTGHLFHELVQRFLCCSASYLKGRRLGET
SASKKSNSSSFVLSHRSSSQRSCSQPSTA
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BDBM50103475 |
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n/a |
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Name | BDBM50103475 |
Synonyms: | Pmp-Tyr-Ile-Thr-Asn-Cys-Pro-Orn-phe(I,N3)-NH2 | Pmp-Tyr-Ile-Thr-Asn-Cys-Pro-Orn-phe(I125,N3)-NH2 |
Type | Small organic molecule |
Emp. Form. | C57H84IN15O13S2 |
Mol. Mass. | 1378.404 |
SMILES | CC[C@H](C)[C@H](NC(=O)[C@H](Cc1ccc(OC)cc1)NC(=O)CC1(CCCCC1)SCCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CS)C(=O)N1CCCC1C(=O)NC(CCCN)C(=O)NC(Cc1ccc(N=[N+]=[N-])c(I)c1)C(N)=O |
Structure |
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