Target
Adenosylhomocysteinase
Ligand
BDBM50370520
Substrate
n/a
Meas. Tech.
ChEMBL_302948 (CHEMBL841783)
Ki
550±n/a nM
Citation
 Wnuk, SFLewandowska, ESacasa, PRCrain, LNZhang, JBorchardt, RTDe Clercq, E Stereoselective synthesis of sugar-modified enyne analogues of adenosine and uridine. Interaction with S-adenosyl-L-homocysteine hydrolase and antiviral and cytotoxic effects. J Med Chem 47:5251-7 (2004) [PubMed]  Article 
Target
Name:
Adenosylhomocysteinase
Synonyms:
AHCY | Adenosylhomocysteinase | SAHH | SAHH_HUMAN
Type:
PROTEIN
Mol. Mass.:
47714.06
Organism:
Homo sapiens (Human)
Description:
ChEMBL_1507791
Residue:
432
Sequence:
MSDKLPYKVADIGLAAWGRKALDIAENEMPGLMRMRERYSASKPLKGARIAGCLHMTVETAVLIETLVTLGAEVQWSSCNIFSTQDHAAAAIAKAGIPVYAWKGETDEEYLWCIEQTLYFKDGPLNMILDDGGDLTNLIHTKYPQLLPGIRGISEETTTGVHNLYKMMANGILKVPAINVNDSVTKSKFDNLYGCRESLIDGIKRATDVMIAGKVAVVAGYGDVGKGCAQALRGFGARVIITEIDPINALQAAMEGYEVTTMDEACQEGNIFVTTTGCIDIILGRHFEQMKDDAIVCNIGHFDVEIDVKWLNENAVEKVNIKPQVDRYRLKNGRRIILLAEGRLVNLGCAMGHPSFVMSNSFTNQVMAQIELWTHPDKYPVGVHFLPKKLDEAVAEAHLGKLNVKLTKLTEKQAQYLGMSCDGPFKPDHYRY
  
Inhibitor
Name:
BDBM50370520
Synonyms:
CHEMBL611098
Type:
Small organic molecule
Emp. Form.:
C13H13N5O3
Mol. Mass.:
287.274
SMILES:
Nc1ncnc2n(cnc12)C1O[C@H](\C=C\C#C)[C@@H](O)[C@H]1O |r|
Structure:
Search PDB for entries with ligand similarity: