Reaction Details |
| Report a problem with these data |
Target | D-aspartate oxidase |
---|
Ligand | BDBM50004955 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_556667 (CHEMBL958954) |
---|
IC50 | >5000±n/a nM |
---|
Citation | Sparey, T; Abeywickrema, P; Almond, S; Brandon, N; Byrne, N; Campbell, A; Hutson, PH; Jacobson, M; Jones, B; Munshi, S; Pascarella, D; Pike, A; Prasad, GS; Sachs, N; Sakatis, M; Sardana, V; Venkatraman, S; Young, MB The discovery of fused pyrrole carboxylic acids as novel, potent D-amino acid oxidase (DAO) inhibitors. Bioorg Med Chem Lett18:3386-91 (2008) [PubMed] Article |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
D-aspartate oxidase |
---|
Name: | D-aspartate oxidase |
Synonyms: | D-Aspartate Oxidase (DDO) | DASOX | DDO | OXDD_HUMAN |
Type: | Oxidoreductase |
Mol. Mass.: | 37543.06 |
Organism: | Homo sapiens (Human) |
Description: | Recombinant human DDO expressed and purified from sf9 insect cells, was used in enzyme assays. |
Residue: | 341 |
Sequence: | MDTARIAVVGAGVVGLSTAVCISKLVPRCSVTIISDKFTPDTTSDVAAGMLIPHTYPDTP
IHTQKQWFRETFNHLFAIANSAEAGDAGVHLVSGWQIFQSTPTEEVPFWADVVLGFRKMT
EAELKKFPQYVFGQAFTTLKCECPAYLPWLEKRIKGSGGWTLTRRIEDLWELHPSFDIVV
NCSGLGSRQLAGDSKIFPVRGQVLQVQAPWVEHFIRDGSGLTYIYPGTSHVTLGGTRQKG
DWNLSPDAENSREILSRCCALEPSLHGACNIREKVGLRPYRPGVRLQTELLARDGQRLPV
VHHYGHGSGGISVHWGTALEAARLVSECVHALRTPIPKSNL
|
|
|
BDBM50004955 |
---|
n/a |
---|
Name | BDBM50004955 |
Synonyms: | 1H-Indole-2-carboxylic acid | CHEMBL278390 | Indol-2-carboxylic acid | Indole-2-carboxylate |
Type | Small organic molecule |
Emp. Form. | C9H7NO2 |
Mol. Mass. | 161.1574 |
SMILES | OC(=O)c1cc2ccccc2[nH]1 |
Structure |
|