Reaction Details |
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Target | Ribonuclease pancreatic |
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Ligand | BDBM50298711 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_588021 (CHEMBL1048356) |
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Ki | 7000±n/a nM |
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Citation | Debnath, J; Dasgupta, S; Pathak, T Nucleoside-amino acid conjugates: An alternative route to the design of ribonuclease A inhibitors. Bioorg Med Chem17:4921-7 (2009) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Ribonuclease pancreatic |
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Name: | Ribonuclease pancreatic |
Synonyms: | CAM-RNase A | RNAS1_BOVIN | RNASE1 | RNAse A | RNS1 |
Type: | Enzyme |
Mol. Mass.: | 16468.79 |
Organism: | Bison bison (American bison) |
Description: | carboxamidomethylated RNase A |
Residue: | 150 |
Sequence: | MALKSLVLLSLLVLVLLLVRVQPSLGKETAAAKFERQHMDSSTSAASSSNYCNQMMKSRN
LTKDRCKPVNTFVHESLADVQAVCSQKNVACKNGQTNCYQSYSTMSITDCRETGSSKYPN
CAYKTTQANKHIIVACEGNPYVPVHFDASV
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BDBM50298711 |
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n/a |
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Name | BDBM50298711 |
Synonyms: | (2R,3R,4R,5R)-2-(4-amino-2-oxopyrimidin-1(2H)-yl)-4-hydroxy-5-(hydroxymethyl)tetrahydrofuran-3-yl dihydrogen phosphate | CHEMBL582887 | CYTIDINE-2'-MONOPHOSPHATE |
Type | Small organic molecule |
Emp. Form. | C9H14N3O8P |
Mol. Mass. | 323.1965 |
SMILES | Nc1ccn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2OP(O)(O)=O)c(=O)n1 |r| |
Structure |
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