Reaction Details |
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Target | Methionine aminopeptidase 2 |
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Ligand | BDBM50353995 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_770260 (CHEMBL1831710) |
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IC50 | 11780±n/a nM |
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Citation | Hou, YP; Sun, J; Pang, ZH; Lv, PC; Li, DD; Yan, L; Zhang, HJ; Zheng, EX; Zhao, J; Zhu, HL Synthesis and antitumor activity of 1,2,4-triazoles having 1,4-benzodioxan fragment as a novel class of potent methionine aminopeptidase type II inhibitors. Bioorg Med Chem19:5948-54 (2011) [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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BDBM50353995 |
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n/a |
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Name | BDBM50353995 |
Synonyms: | CHEMBL1829278 |
Type | Small organic molecule |
Emp. Form. | C23H18N4O4S |
Mol. Mass. | 446.478 |
SMILES | [O-][N+](=O)c1ccccc1CSc1nnc(-c2ccc3OCCOc3c2)n1-c1ccccc1 |
Structure |
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