Reaction Details |
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Target | Somatostatin receptor type 5 |
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Ligand | BDBM50064026 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_200528 (CHEMBL806598) |
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Ki | 3400±n/a nM |
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Citation | Hirschmann, R; Hynes, J; Cichy-Knight, MA; van Rijn, RD; Sprengeler, PA; Spoors, PG; Shakespeare, WC; Pietranico-Cole, S; Barbosa, J; Liu, J; Yao, W; Rohrer, S; Smith, AB Modulation of receptor and receptor subtype affinities using diastereomeric and enantiomeric monosaccharide scaffolds as a means to structural and biological diversity. A new route to ether synthesis. J Med Chem41:1382-91 (1998) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Somatostatin receptor type 5 |
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Name: | Somatostatin receptor type 5 |
Synonyms: | SOMATOSTATIN SST5 | SS-5-R | SS5-R | SS5R | SSR5_HUMAN | SSTR5 | Somatostatin receptor type 5 (SSTR5) |
Type: | Enzyme |
Mol. Mass.: | 39218.02 |
Organism: | Homo sapiens (Human) |
Description: | P35346 |
Residue: | 364 |
Sequence: | MEPLFPASTPSWNASSPGAASGGGDNRTLVGPAPSAGARAVLVPVLYLLVCAAGLGGNTL
VIYVVLRFAKMKTVTNIYILNLAVADVLYMLGLPFLATQNAASFWPFGPVLCRLVMTLDG
VNQFTSVFCLTVMSVDRYLAVVHPLSSARWRRPRVAKLASAAAWVLSLCMSLPLLVFADV
QEGGTCNASWPEPVGLWGAVFIIYTAVLGFFAPLLVICLCYLLIVVKVRAAGVRVGCVRR
RSERKVTRMVLVVVLVFAGCWLPFFTVNIVNLAVALPQEPASAGLYFFVVILSYANSCAN
PVLYGFLSDNFRQSFQKVLCLRKGSGAKDADATEPRPDRIRQQQEATPPAHRAAANGLMQ
TSKL
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BDBM50064026 |
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n/a |
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Name | BDBM50064026 |
Synonyms: | 5-{(2S,3S,4R,5S,6S)-3,4,5-Tris-benzyloxy-6-[2-(1H-indol-3-yl)-ethoxy]-tetrahydro-pyran-2-ylmethoxy}-pentylamine | CHEMBL282803 |
Type | Small organic molecule |
Emp. Form. | C42H50N2O6 |
Mol. Mass. | 678.8562 |
SMILES | NCCCCCOC[C@@H]1O[C@H](OCCc2c[nH]c3ccccc23)[C@@H](OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1OCc1ccccc1 |
Structure |
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