Hemiasterlin analogues with unnatural amino acids at the N-terminal and their inhibitory activity on tumor cells

International Journal of Peptide Research and Therapeutics

Volumn 15, Issue 3, 2009, Pages 187-194

  Qie, Jiankun ^a   Zhou, Wenxia ^a   Zhao, Xiunan ^a   He, Junlin ^a   Zhang, Yongxiang ^a   Liu, Keliang ^a  

^a BEIJING INSTITUTE OF PHARMACOLOGY AND TOXICOLOGY   (China)

Author keywords

Cytotoxic activity; Hemiasterlin analogues; Tripeptide; Tumor cell growth inhibitor

Indexed keywords

CEMADOTIN; HEMIASTERLIN; QTP 059; QTP 061; QTP 065; QTP 067; QTP 075; QTP 076; QTP 078; QTP 080; QTP 082; QTP 083; QTP 084; QTP 085; QTP 087; QTP 089; QTP 094; QTP 095; TRIPEPTIDE DERIVATIVE; UNCLASSIFIED DRUG;

AMINO ACID SYNTHESIS; AMINO TERMINAL SEQUENCE; ANIMAL CELL; ARTICLE; CANCER INHIBITION; CONTROLLED STUDY; CYTOTOXICITY; DRUG SYNTHESIS; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HUMAN; HUMAN CELL; HYDROPHILICITY; HYDROPHOBICITY; IN VITRO STUDY; LIPOPHILICITY; METHYLATION; MOUSE; NONHUMAN; PEPTIDE SYNTHESIS; STRUCTURE ACTIVITY RELATION; TUMOR CELL;

EID: 67651163453     PISSN: 15733149     EISSN: 15733904     Source Type: Journal    
DOI: 10.1007/s10989-009-9168-1     Document Type: Article

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