The F1F0-ATPase binding site of dibutyltin-3-hydroxyflavone: Interactions with venturicidin, oligomycin and DCCD-Reference-Cited by-同舟云学术

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The F1F0-ATPase binding site of dibutyltin-3-hydroxyflavone: Interactions with venturicidin, oligomycin and DCCD

Published:1993-10 Issue:6 Volume:7 Page:401-406
ISSN:0268-2605
Container-title:Applied Organometallic Chemistry
language:en
Short-container-title:Appl. Organomet. Chem.

Author:

Griffiths David E,Usta Julnar,Tian Ya Min

Publisher

Wiley

Subject

Inorganic Chemistry,General Chemistry

Reference15 articles.

1. Organotin-flavone complexes: A new class of fluorescent probes for F1F0ATPase

2. Dibutyltin-3-hydroxyflavone bromide: A fluorescent inhibitor of F1F0-ATPase

3. and unpublished studies

4. and Biochem. Soc. Trans., 1993, 21: (in press)

5. Interaction of [14C]dicyclohexylcarbodiimide with complex V (Mitochondrial Adenosine Triphosphate Synthetase Complex)

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1. ChemInform Abstract: The F1F0-ATPase Binding Site of Dibutyltin-3-hydroxyflavone: Interactions with Venturicidin, Oligomycin, and DCCD.;ChemInform;2010-08-19

2. Safety and Environmental Effects;PATAI'S Chemistry of Functional Groups;2009-12-15

3. Studies in aryltin chemistry: part 7. Spectroscopic and fungicidal studies of somep-substituted tri-aryltin acetates, oxides and hydroxides;Applied Organometallic Chemistry;1997-12

4. The vacuolar H+-ATPase: a universal proton pump of eukaryotes;Biochemical Journal;1997-06-15

5. Interaction of Organotins with a Vacuolar-Type H+-ATPase;Biochemical and Biophysical Research Communications;1996-10

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