Reaction Details |
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Target | Prolyl hydroxylase EGLN2 |
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Ligand | BDBM50324535 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_649378 (CHEMBL1219076) |
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IC50 | >100000±n/a nM |
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Citation | Hamada, S; Suzuki, T; Mino, K; Koseki, K; Oehme, F; Flamme, I; Ozasa, H; Itoh, Y; Ogasawara, D; Komaarashi, H; Kato, A; Tsumoto, H; Nakagawa, H; Hasegawa, M; Sasaki, R; Mizukami, T; Miyata, N Design, synthesis, enzyme-inhibitory activity, and effect on human cancer cells of a novel series of jumonji domain-containing protein 2 histone demethylase inhibitors. J Med Chem53:5629-38 (2010) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Prolyl hydroxylase EGLN2 |
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Name: | Prolyl hydroxylase EGLN2 |
Synonyms: | EGLN2 | EGLN2_HUMAN | EIT6 | Egl nine homolog 2 | Estrogen-induced tag 6 | HIF prolyl hydroxylase | HIF-PH1 | HIF-prolyl hydroxylase 1 | HPH-3 | Hypoxia-inducible factor prolyl hydroxylase | PHD1 | Prolyl hydroxylase domain-containing protein 1 | Prolyl hydroxylase domain-containing protein 1 (PHD1) |
Type: | Protein |
Mol. Mass.: | 43657.01 |
Organism: | Homo sapiens (Human) |
Description: | Q96KS0 |
Residue: | 407 |
Sequence: | MDSPCQPQPLSQALPQLPGSSSEPLEPEPGRARMGVESYLPCPLLPSYHCPGVPSEASAG
SGTPRATATSTTASPLRDGFGGQDGGELRPLQSEGAAALVTKGCQRLAAQGARPEAPKRK
WAEDGGDAPSPSKRPWARQENQEAEREGGMSCSCSSGSGEASAGLMEEALPSAPERLALD
YIVPCMRYYGICVKDSFLGAALGGRVLAEVEALKRGGRLRDGQLVSQRAIPPRSIRGDQI
AWVEGHEPGCRSIGALMAHVDAVIRHCAGRLGSYVINGRTKAMVACYPGNGLGYVRHVDN
PHGDGRCITCIYYLNQNWDVKVHGGLLQIFPEGRPVVANIEPLFDRLLIFWSDRRNPHEV
KPAYATRYAITVWYFDAKERAAAKDKYQLASGQKGVQVPVSQPPTPT
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BDBM50324535 |
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n/a |
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Name | BDBM50324535 |
Synonyms: | 3-{[9-(Dimethylamino)nonanoyl](hydroxy)amino}propanoicAcid Hydrochloride | CHEMBL1215519 | CHEMBL1229308 |
Type | Small organic molecule |
Emp. Form. | C14H28N2O4 |
Mol. Mass. | 288.3831 |
SMILES | CN(C)CCCCCCCCC(=O)N(O)CCC(O)=O |
Structure |
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