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TargetAdenosylhomocysteinase
LigandBDBM50280298
Substrate/Competitorn/a
Meas. Tech.ChEBML_197371
Ki 112±n/a nM
Citation Liu, SWolfe, MSYuan, CAli, SMBorchardt, RT Synthesis and evaluation of 4′-5′-dehydro-5′-fluoroaristeromycins as S-adenosyl-L-homocysteine (AdoHcy) hydrolase inhibitors Bioorg Med Chem Lett2:1741-1744 (1992)    Article
More Info.:Get all data from this article,  Assay Method
 
Adenosylhomocysteinase
Name:Adenosylhomocysteinase
Synonyms:Adenosylhomocysteinase | Ahcy | SAHH_RAT
Type:PROTEIN
Mol. Mass.:47537.52
Organism:Rattus norvegicus
Description:ChEMBL_1507790
Residue:432
Sequence:
MADKLPYKVADIGLAAWGRKALDIAENEMPGLMRMREMYSASKPLKGARIAGCLHMTVET
AVLIETLVALGAEVRWSSCNIFSTQDHAAAAIAKAGIPVFAWKGETDEEYLWCIEQTLHF
KDGPLNMILDDGGDLTNLIHTKHPQLLSGIRGISEETTTGVHNLYKMMANGILKVPAINV
NDSVTKSKFDNLYGCRESLIDGIKRATDVMIAGKVAVVAGYGDVGKGCAQALRGFGARVI
ITEIDPINALQAAMEGYEVTTMDEACKEGNIFVTTTGCVDIILGRHFEQMKDDAIVCNIG
HFDVEIDVKWLNENAVEKVNIKPQVDRYLLKNGHRIILLAEGRLVNLGCAMGHPSFVMSN
SFTNQVMAQIELWTHPDKYPVGVHFLPKKLDEAVAEAHLGKLNVKLTKLTEKQAQYLGMP
INGPFKPDHYRY
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BDBM50280298
n/a
NameBDBM50280298
Synonyms:(1R,2S,3R)-3-(6-Amino-purin-9-yl)-5-[1-fluoro-meth-(Z)-ylidene]-cyclopentane-1,2-diol | CHEMBL49204
TypeSmall organic molecule
Emp. Form.C11H12FN5O2
Mol. Mass.265.2437
SMILESNc1ncnc2n(cnc12)[C@@H]1C\C(=C\F)[C@@H](O)[C@H]1O
Structure
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