Reaction Details |
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Target | 72 kDa type IV collagenase |
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Ligand | BDBM240828 |
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Substrate/Competitor | n/a |
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Meas. Tech. | MMP-2 Inhibition Assay |
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IC50 | 212970±1350 nM |
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Citation | Zhang, X; Zhang, L; Zhang, J; Feng, J; Yuan, Y; Fang, H; Xu, W Design, synthesis and preliminary activity evaluation of novel 3-amino-2-hydroxyl-3-phenylpropanoic acid derivatives as aminopeptidase N/CD13 inhibitors. J Enzyme Inhib Med Chem28:545-51 (2013) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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72 kDa type IV collagenase |
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Name: | 72 kDa type IV collagenase |
Synonyms: | Gelatinase 2 (MMP-2) |
Type: | Protein |
Mol. Mass.: | 73661.44 |
Organism: | Sus scrofa (Pig) |
Description: | Q95JA4 |
Residue: | 661 |
Sequence: | MTEARGARGALAGPLRALCVLGCLLGRAAAAPSPIIKFPGDVAPKTDKELAVQYLNTFYG
CPKESCNLFVLKDTLKKMQKFFGLPQTGELDQSTIETMRKPRCGNPDVANYNFFPRKPKW
DKTQITYRIIGYTPDLDPETVDDAFARAFRVWSDVTPLRFSRIHDGEADIMINFGRWEHG
DGYPFDGKDGLLAHAFAPGPGVGGDSHFDDDELWTLGEGQVVRVKYGNADGEYCKFPFSF
NGKEYNSCTDTGRSDGFLWCSTTYNFDKDGKYGFCPHEALFTMGGNADGQPCKFPFRFQG
TSYNSCTTEGRTDGYRWCGTTEDYDRDKKYGFCPETAMSTVGGNSEGAPCVFPFTFLGNK
HESCTSAGRSDGKLWCATTANYDDDRKWGFCPDQGYSLFLVAAHEFGHAMGLEHSEDPGA
LMAPIYTYTKNFRLSHDDVKGIQELYGASPDIDTGTGPTPTLGPVTPEICKQDIVFDGIS
QIRGEIFFFKDRFIWRTVTPRDKPMVAPAGATFWPELPEKIDAVYEAPQEEKAVFFAGNE
YWVYSASTLERGYPKPLTSLGLPPDVQKVDAAFNWSKNKKTYIFAGDKFWRYNEVKKKMD
PGFPKLIADAWNAIPDNLDAVVDLQGGGHSYFFKGAYYLKLENQSLKSVKFGSIKSDWLG
C
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BDBM240828 |
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n/a |
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Name | BDBM240828 |
Synonyms: | (2R,3S)-3-amino-2-hydroxy-N-((S)-2-(hydroxyamino)-2-oxo-1-phenylethyl)-3-phenylpropanamide hydrochloride (7e) |
Type | Small organic molecule |
Emp. Form. | C17H19N3O4 |
Mol. Mass. | 329.3505 |
SMILES | N[C@H]([C@@H](O)C(=O)N[C@H](C(=O)NO)c1ccccc1)c1ccccc1 |r| |
Structure |
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