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18054229
Source:
http://linkedlifedata.com/resource/pubmed/id/18054229
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0007634
,
umls-concept:C0184511
,
umls-concept:C0243077
,
umls-concept:C0441655
,
umls-concept:C0812228
,
umls-concept:C0812230
,
umls-concept:C1527148
,
umls-concept:C1554184
,
umls-concept:C1998468
pubmed:issue
1
pubmed:dateCreated
2008-1-9
pubmed:abstractText
This letter describes the development of potent, allosteric dual Akt1 and Akt2 inhibitors with improved aqueous solubility (approximately 18 mg/mL) that translates into enhanced cell activity and caspase-3 induction.
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9107377
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Caspase 3
,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-akt
,
http://linkedlifedata.com/resource/pubmed/chemical/Quinoxalines
,
http://linkedlifedata.com/resource/pubmed/chemical/Serine Proteinase Inhibitors
,
http://linkedlifedata.com/resource/pubmed/chemical/Water
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
1464-3405
pubmed:author
pubmed-author:BarnettStanley FSF
,
pubmed-author:Defeo-JonesDeborahD
,
pubmed-author:DugganMark EME
,
pubmed-author:HartmanGeorge DGD
,
pubmed-author:HuberHans EHE
,
pubmed-author:JonesRaymond ERE
,
pubmed-author:LindsleyCraig WCW
,
pubmed-author:RobinsonRonald GRG
,
pubmed-author:ZhaoZhijianZ
pubmed:issnType
Electronic
pubmed:day
1
pubmed:volume
18
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
49-53
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:18054229-Caspase 3
,
pubmed-meshheading:18054229-Cell Line, Tumor
,
pubmed-meshheading:18054229-Enzyme Activation
,
pubmed-meshheading:18054229-HT29 Cells
,
pubmed-meshheading:18054229-Humans
,
pubmed-meshheading:18054229-Kinetics
,
pubmed-meshheading:18054229-Phosphorylation
,
pubmed-meshheading:18054229-Proto-Oncogene Proteins c-akt
,
pubmed-meshheading:18054229-Quinoxalines
,
pubmed-meshheading:18054229-Serine Proteinase Inhibitors
,
pubmed-meshheading:18054229-Solubility
,
pubmed-meshheading:18054229-Water
pubmed:year
2008
pubmed:articleTitle
Development of potent, allosteric dual Akt1 and Akt2 inhibitors with improved physical properties and cell activity.
pubmed:affiliation
Department of Medicinal Chemistry, Technology Enabled Synthesis Group, Merck & Co., PO Box 4, West Point, PA 19486, USA. zhijian_zhao@merck.com
pubmed:publicationType
Journal Article