Reaction Details |
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Target | Adenosylhomocysteinase |
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Ligand | BDBM50408149 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_196553 (CHEMBL801948) |
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Ki | 224±n/a nM |
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Citation | Wnuk, SF; Yuan, CS; Borchardt, RT; Balzarini, J; De Clercq, E; Robins, MJ Anticancer and antiviral effects and inactivation of S-adenosyl-L-homocysteine hydrolase with 5'-carboxaldehydes and oximes synthesized from adenosine and sugar-modified analogues. J Med Chem40:1608-18 (1997) [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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BDBM50408149 |
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n/a |
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Name | BDBM50408149 |
Synonyms: | CHEMBL2093112 |
Type | Small organic molecule |
Emp. Form. | C10H12N6O4 |
Mol. Mass. | 280.2401 |
SMILES | Nc1ncnc2n(cnc12)[C@@H]1O[C@H](CN=O)[C@@H](O)[C@@H]1O |r| |
Structure |
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