Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
23
pubmed:dateCreated
2006-11-10
pubmed:abstractText
A series of 5-arylamino-6-chloro-1H-indazole-4,7-diones were synthesized and evaluated for their inhibitory activity on protein kinase B/Akt. The compounds exhibited a potent Akt1 inhibitory activity. Further mechanistic study revealed that they might have dual inhibitory effects on both activity and phosphorylation of Akt1 in PC-3 tumor cell line.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0960-894X
pubmed:author
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
16
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6001-5
pubmed:dateRevised
2011-11-2
pubmed:meshHeading
pubmed-meshheading:16990001-Amination, pubmed-meshheading:16990001-Animals, pubmed-meshheading:16990001-Antineoplastic Agents, pubmed-meshheading:16990001-Catalysis, pubmed-meshheading:16990001-Cell Line, Tumor, pubmed-meshheading:16990001-Chlorine, pubmed-meshheading:16990001-Glycogen Synthase Kinase 3, pubmed-meshheading:16990001-Humans, pubmed-meshheading:16990001-Indazoles, pubmed-meshheading:16990001-Mice, pubmed-meshheading:16990001-Mice, Nude, pubmed-meshheading:16990001-Molecular Structure, pubmed-meshheading:16990001-Neoplasms, pubmed-meshheading:16990001-Phosphorylation, pubmed-meshheading:16990001-Protein Kinase Inhibitors, pubmed-meshheading:16990001-Proto-Oncogene Proteins c-akt, pubmed-meshheading:16990001-Structure-Activity Relationship, pubmed-meshheading:16990001-Xenograft Model Antitumor Assays
pubmed:year
2006
pubmed:articleTitle
Synthesis and biological evaluation of 5-arylamino-6-chloro-1H-indazole-4,7-diones as inhibitors of protein kinase B/Akt.
pubmed:affiliation
ILDONG Research Laboratories, ILDONG Pharmaceutical Co. Ltd., 260-5, Eonnam-Dong, Kuseong-Gu, Yongin, Kyongki-Do 449-910, Republic of Korea.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't