Juxtaposition of chemical and mutation-induced developmental defects in zebrafish reveal a copper-chelating activity for kalihinol F

Chemistry and Biology

Volumn 20, Issue 6, 2013, Pages 753-763

  Sandoval, Imelda T ^a,c   Manos, Elizabeth J ^a,c   Van Wagoner, Ryan M ^b   Delacruz, Richard Glenn C ^d   Edes, Kornelia ^a,c   Winge, Dennis R ^d   Ireland, Chris M ^b   Jones, David A ^a,b,c  

^a UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF UTAH   (United States)

^c UNIVERSITY OF UTAH   (United States)

^d UNIVERSITY OF UTAH HEALTH SCIENCES CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CHELATING AGENT; COPPER; HEME; HEMOGLOBIN; KALIHINOL F; TRIACYLGLYCEROL; UNCLASSIFIED DRUG;

ANGIOGENESIS; ARTICLE; CHELATION; COPPER DEFICIENCY; CYTOTOXICITY; DRUG MECHANISM; DRUG SCREENING; EMBRYO DEVELOPMENT; FATTY ACID METABOLISM; GENE EXPRESSION; GENE MUTATION; HEMATOPOIESIS; NONHUMAN; NOTOCHORD; OSSIFICATION; PHENOTYPE; PIGMENTATION; PRIORITY JOURNAL; STRUCTURE ACTIVITY RELATION; ZEBRA FISH;

ANIMALS; CELL SURVIVAL; CHELATING AGENTS; COPPER; DITERPENES; EMBRYO, NONMAMMALIAN; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HEP G2 CELLS; HUMANS; MUTATION; NITRILES; NOTOCHORD; PHENOTYPE; ZEBRAFISH;

DANIO RERIO;

EID: 84879401445     PISSN: 10745521     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.chembiol.2013.05.008     Document Type: Article

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