Reaction Details |
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Target | Adenosylhomocysteinase |
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Ligand | BDBM50366808 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEBML_196550 |
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Ki | 4000±n/a nM |
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Citation | Guillerm, G; Guillerm, D; Vandenplas-Vitkowski, C; Glapski, C; De Clercq, E Inactivation of S-adenosyl-L-homocysteine hydrolase with novel 5'-thioadenosine derivatives. Antiviral effects. Bioorg Med Chem Lett13:1649-52 (2003) [PubMed] |
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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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BDBM50366808 |
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n/a |
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Name | BDBM50366808 |
Synonyms: | CHEMBL603565 |
Type | Small organic molecule |
Emp. Form. | C12H15N5O3S |
Mol. Mass. | 309.344 |
SMILES | Nc1ncnc2n(cnc12)C1O[C@H](CSC=C)[C@@H](O)[C@H]1O |r| |
Structure |
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