D003512Chemicals & DrugsD02.455.426.392.368.367.340D02.522.400110.999743Cyclohexanonesprns:fullNamefull nameprns:hasAuthorListauthor listprns:hasNetworkhas networkprns:hasPublicationVenuepublished inprns:informationResourceReferenceinformation resource referenceprns:isPrimaryPositionis primary positionprns:latitudelatitudeprns:longitudelongitudeprns:maxWeightmaximum weightprns:medlineTAjournal title abbreviationprns:meshDescriptorUIMeSH DescriptorUIprns:meshSemanticGroupNameMeSH semantic group nameprns:meshTreeNumberMeSH tree numberprns:minWeightminimum weightprns:numberOfAuthorsnumber of authorsprns:numberOfConnectionsnumber of connectionsprns:numberOfPublicationsnumber of publicationsprns:personIdPerson IDprns:personInPrimaryPositionperson in primary positionprns:positionInDepartmentposition in departmentprns:predicateNodepredicate nodeprns:publicationDatepublication dateprns:sortOrdersort orderprns:uniquenessWeightuniqueness weightprns:yearyearAcademic ArticleArticleDocumentbibo:pmidPubMed IdentifierDepartmentvivo:hrJobTitleHR job titleInformation ResourcePositionvivo:positionInOrganizationposition in organizationvivo:preferredTitlepreferred titlevivo:researchAreaOfresearch area ofvivo:subjectAreaForsubject area forrdf:predicatepredicaterdf:typetyperdfs:labellabelConceptAgentfoaf:firstNamefirst namefoaf:lastNamelast nameOrganizationPerson0.0513510.0513511research area of0.7079460.2054572subject area for30987350Al-Majid AM, Islam MS, Atef S, El-Senduny FF, Badria FA, Elshaier YAMM, Ali M, Barakat A, Motiur Rahman AFMMolecules (Basel, Switzerland)Synthesis of Pyridine-Dicarboxamide-Cyclohexanone Derivatives: Anticancer and a-Glucosidase Inhibitory Activities and In Silico Study. Molecules. 2019 Apr 04; 24(7).Molecules2019-04-04T00:00:002019Synthesis of Pyridine-Dicarboxamide-Cyclohexanone Derivatives: Anticancer and a-Glucosidase Inhibitory Activities and In Silico Study.11381131Zagnitko O, Jelenska J, Tevzadze G, Haselkorn R, Gornicki PProceedings of the National Academy of Sciences of the United States of AmericaAn isoleucine/leucine residue in the carboxyltransferase domain of acetyl-CoA carboxylase is critical for interaction with aryloxyphenoxypropionate and cyclohexanedione inhibitors. Proc Natl Acad Sci U S A. 2001 Jun 05; 98(12):6617-22.Proc Natl Acad Sci U S A2001-05-29T00:00:002001An isoleucine/leucine residue in the carboxyltransferase domain of acetyl-CoA carboxylase is critical for interaction with aryloxyphenoxypropionate and cyclohexanedione inhibitors.Mol Gen/Cell BioUniversity of ChicagoRobertHaselkornRobert Haselkorn41.78927490000000-87.601250000000001490Haselkorn, RobertProfessor Emeritustrue1Professor EmeritusProfessor Emeritus