Reaction Details |
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Target | Adenosylhomocysteinase |
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Ligand | BDBM50373102 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_466720 (CHEMBL937441) |
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IC50 | 90700±n/a nM |
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Citation | Ando, T; Iwata, M; Zulfiqar, F; Miyamoto, T; Nakanishi, M; Kitade, Y Synthesis of 2-modified aristeromycins and their analogs as potent inhibitors against Plasmodium falciparum S-adenosyl-L-homocysteine hydrolase. Bioorg Med Chem16:3809-15 (2008) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Adenosylhomocysteinase |
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Name: | Adenosylhomocysteinase |
Synonyms: | AHCY | Adenosylhomocysteinase | SAHH | SAHH_HUMAN |
Type: | PROTEIN |
Mol. Mass.: | 47714.06 |
Organism: | Homo sapiens (Human) |
Description: | ChEMBL_1507791 |
Residue: | 432 |
Sequence: | MSDKLPYKVADIGLAAWGRKALDIAENEMPGLMRMRERYSASKPLKGARIAGCLHMTVET
AVLIETLVTLGAEVQWSSCNIFSTQDHAAAAIAKAGIPVYAWKGETDEEYLWCIEQTLYF
KDGPLNMILDDGGDLTNLIHTKYPQLLPGIRGISEETTTGVHNLYKMMANGILKVPAINV
NDSVTKSKFDNLYGCRESLIDGIKRATDVMIAGKVAVVAGYGDVGKGCAQALRGFGARVI
ITEIDPINALQAAMEGYEVTTMDEACQEGNIFVTTTGCIDIILGRHFEQMKDDAIVCNIG
HFDVEIDVKWLNENAVEKVNIKPQVDRYRLKNGRRIILLAEGRLVNLGCAMGHPSFVMSN
SFTNQVMAQIELWTHPDKYPVGVHFLPKKLDEAVAEAHLGKLNVKLTKLTEKQAQYLGMS
CDGPFKPDHYRY
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BDBM50373102 |
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n/a |
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Name | BDBM50373102 |
Synonyms: | CHEMBL261619 |
Type | Small organic molecule |
Emp. Form. | C11H16N6O3 |
Mol. Mass. | 280.2831 |
SMILES | Nc1nc(N)c2ncn([C@@H]3C[C@H](CO)[C@@H](O)[C@H]3O)c2n1 |
Structure |
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