| Reaction Details |
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 | Report a problem with these data |
| Target | Angiogenin |
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| Ligand | BDBM111447 |
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| Substrate/Competitor | n/a |
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| Meas. Tech. | Inhibition Kinetics with Angiogenin |
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| pH | 6±n/a |
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| Ki | 1.114e+6± 3e+3 nM |
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| Comments | extracted |
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| Citation |  Debnath, J; Dasgupta, S; Pathak, T Amino and carboxy functionalized modified nucleosides: a potential class of inhibitors for angiogenin. Bioorg Chem52:56-61 (2014) [PubMed] Article |
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| More Info.: | Get all data from this article, Assay Method |
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| Angiogenin |
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| Name: | Angiogenin |
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| Synonyms: | ANG | ANGI_HUMAN | RNASE5 |
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| Type: | Protein |
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| Mol. Mass.: | 16563.00 |
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| Organism: | Homo sapiens (Human) |
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| Description: | n/a |
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| Residue: | 147 |
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| Sequence: | MVMGLGVLLLVFVLGLGLTPPTLAQDNSRYTHFLTQHYDAKPQGRDDRYCESIMRRRGLT
SPCKDINTFIHGNKRSIKAICENKNGNPHRENLRISKSSFQVTTCKLHGGSPWPPCQYRA
TAGFRNVVVACENGLPVHLDQSIFRRP
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| BDBM111447 |
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| n/a |
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| Name | BDBM111447 |
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| Synonyms: | N-[2-Hydroxymethyl-5-(5-methyl-2,4-dioxo-3,4-dihydro- 2H-pyrimidin-1-yl)-tetrahydro-furan-3-yl]-malonamic acid (Compound 6) |
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| Type | Small organic molecule |
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| Emp. Form. | C13H17N3O7 |
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| Mol. Mass. | 327.29 |
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| SMILES | Cc1cn([C@H]2C[C@@H](NC(=O)CC(O)=O)[C@@H](CO)O2)c(=O)[nH]c1=O |r| |
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| Structure | 
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