| pubmed-article:10450967 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:10450967 | lifeskim:mentions | umls-concept:C0001443 | lld:lifeskim |
| pubmed-article:10450967 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:10450967 | lifeskim:mentions | umls-concept:C0582118 | lld:lifeskim |
| pubmed-article:10450967 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:10450967 | lifeskim:mentions | umls-concept:C0243077 | lld:lifeskim |
| pubmed-article:10450967 | lifeskim:mentions | umls-concept:C1707689 | lld:lifeskim |
| pubmed-article:10450967 | pubmed:issue | 14 | lld:pubmed |
| pubmed-article:10450967 | pubmed:dateCreated | 1999-9-24 | lld:pubmed |
| pubmed-article:10450967 | pubmed:abstractText | Carbocylic coformycin (4) is a potent herbicide whose primary mode of action involves inhibition of adenosine 5'-monophosphate deaminase (AMPDA) following phosphorylation of the 5'-hydroxyl group in vivo. The search for more stable and accessible structures led to the synthesis of carbocyclic nebularine (8) and deaminoformycin (10). The latter compound is a good herbicide and its corresponding 5'-monophosphate 14 is a strong inhibitor of plant AMPDA (IC50 100 nM). | lld:pubmed |
| pubmed-article:10450967 | pubmed:language | eng | lld:pubmed |
| pubmed-article:10450967 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10450967 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:10450967 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:10450967 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:10450967 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:10450967 | pubmed:month | Jul | lld:pubmed |
| pubmed-article:10450967 | pubmed:issn | 0960-894X | lld:pubmed |
| pubmed-article:10450967 | pubmed:author | pubmed-author:EarnshawC GCG | lld:pubmed |
| pubmed-article:10450967 | pubmed:author | pubmed-author:DancerJ EJE | lld:pubmed |
| pubmed-article:10450967 | pubmed:author | pubmed-author:LindellS DSD | lld:pubmed |
| pubmed-article:10450967 | pubmed:author | pubmed-author:MoloneyB ABA | lld:pubmed |
| pubmed-article:10450967 | pubmed:author | pubmed-author:HewittB DBD | lld:pubmed |
| pubmed-article:10450967 | pubmed:author | pubmed-author:DudfieldP JPJ | lld:pubmed |
| pubmed-article:10450967 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:10450967 | pubmed:day | 19 | lld:pubmed |
| pubmed-article:10450967 | pubmed:volume | 9 | lld:pubmed |
| pubmed-article:10450967 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:10450967 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:10450967 | pubmed:pagination | 1985-90 | lld:pubmed |
| pubmed-article:10450967 | pubmed:dateRevised | 2000-12-18 | lld:pubmed |
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| pubmed-article:10450967 | pubmed:meshHeading | pubmed-meshheading:10450967... | lld:pubmed |
| pubmed-article:10450967 | pubmed:year | 1999 | lld:pubmed |
| pubmed-article:10450967 | pubmed:articleTitle | The design and synthesis of inhibitors of adenosine 5'-monophosphate deaminase. | lld:pubmed |
| pubmed-article:10450967 | pubmed:affiliation | AgrEvo UK Limited, Essex, England. stephen.lindell@agrevo.com | lld:pubmed |
| pubmed-article:10450967 | pubmed:publicationType | Journal Article | lld:pubmed |
| http://linkedlifedata.com/r... | http://linkedlifedata.com/r... | pubmed-article:10450967 | lld:chembl |
| http://linkedlifedata.com/r... | pubmed:referesTo | pubmed-article:10450967 | lld:pubmed |
