Reaction Details |
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Target | Methionine aminopeptidase 2 |
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Ligand | BDBM50147349 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1848682 (CHEMBL4349223) |
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IC50 | 67±n/a nM |
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Citation | Zhao, Z; Song, H; Xie, J; Liu, T; Zhao, X; Chen, X; He, X; Wu, S; Zhang, Y; Zheng, X Research progress in the biological activities of 3,4,5-trimethoxycinnamic acid (TMCA) derivatives. Eur J Med Chem173:213-227 (2019) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Methionine aminopeptidase 2 |
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Name: | Methionine aminopeptidase 2 |
Synonyms: | Initiation factor 2-associated 67 kDa glycoprotein | MAP 2 | MAP2_HUMAN | METAP2 | MNPEP | MetAP 2 | Methionine aminopeptidase 2 (MetAP2) | Methionine aminopeptidases (HsMetAP2) | P67EIF2 | Peptidase M 2 | p67 |
Type: | Enzyme |
Mol. Mass.: | 52884.45 |
Organism: | Homo sapiens (Human) |
Description: | P50579 |
Residue: | 478 |
Sequence: | MAGVEEVAASGSHLNGDLDPDDREEGAASTAEEAAKKKRRKKKKSKGPSAAGEQEPDKES
GASVDEVARQLERSALEDKERDEDDEDGDGDGDGATGKKKKKKKKKRGPKVQTDPPSVPI
CDLYPNGVFPKGQECEYPPTQDGRTAAWRTTSEEKKALDQASEEIWNDFREAAEAHRQVR
KYVMSWIKPGMTMIEICEKLEDCSRKLIKENGLNAGLAFPTGCSLNNCAAHYTPNAGDTT
VLQYDDICKIDFGTHISGRIIDCAFTVTFNPKYDTLLKAVKDATNTGIKCAGIDVRLCDV
GEAIQEVMESYEVEIDGKTYQVKPIRNLNGHSIGQYRIHAGKTVPIVKGGEATRMEEGEV
YAIETFGSTGKGVVHDDMECSHYMKNFDVGHVPIRLPRTKHLLNVINENFGTLAFCRRWL
DRLGESKYLMALKNLCDLGIVDPYPPLCDIKGSYTAQFEHTILLRPTCKEVVSRGDDY
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BDBM50147349 |
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n/a |
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Name | BDBM50147349 |
Synonyms: | (R)-3-(S)-Amino-2-hydroxy-5-phenyl-pentanoic acid {4-[3-((E)-3,4,5-trimethoxy-phenyl)-acryloylamino]-phenyl}-amide | CHEMBL110292 |
Type | Small organic molecule |
Emp. Form. | C29H33N3O6 |
Mol. Mass. | 519.5888 |
SMILES | COc1cc(\C=C\C(=O)Nc2ccc(NC(=O)[C@@H](O)[C@H](N)CCc3ccccc3)cc2)cc(OC)c1OC |
Structure |
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