Results 121 to 130 of about 7,864 (178)

Naphthyl Ester Synthesis Using 1,3-Dicyclohexylcarbodiimide

Synthesis, 2004
AbstractFor Abstract see ChemInform Abstract in Full Text.
Gulay Zengin
exaly   +2 more sources

Reaction of dicyclohexylcarbodiimide with mitochondrial proteins

Biochimica Et Biophysica Acta - Bioenergetics, 1993
Ilmo E Hassinen, I E Hassinen
exaly   +3 more sources

Dicyclohexylcarbodiimide — An inhibitor of oxidative phosphorylation

Biochemical and Biophysical Research Communications, 1966
Abstract This communication reports some of the properties of a new inhibitor of oxidative phosphorylation, DCCD ∗ , whose mode of action is similar to oligomycin and aurovertin (Lardy et al., 1958). Low titres of DCCD inhibit the ccupled respiration of mitochondria and the ATP-driven partial reactions of oxidative phosphorylation catalysed by ETPH.
R B, Beechey, C T, Holloway, I G, Knight, A M, Roberton   +3 more
openaire   +2 more sources

Sensitivity of methanogenic bacteria to dicyclohexylcarbodiimide

Canadian Journal of Microbiology, 1982
Methanospirillum hungatei strains GP1 and JF1 when exposed to the adenosinetriphosphatase inhibitor N,N′-dicyclohexylcarbodiimide experienced a marked decline in growth rates, methane synthesis activities, and intracellular ATP concentrations. Although growth was inhibited, the intracellular ATP concentrations of all other methanogens tested were ...
Sprott, G., Jarrell, K.
openaire   +3 more sources

1,3-Dicyclohexylcarbodiimide

2010
[538-75-0] C13H22N2 (MW 206.33) InChI = 1/C13H22N2/c1-3-7-12(8-4-1)14-11-15-13-9-5-2-6-10-13/h12-13H,1-10H2 InChIKey = QOSSAOTZNIDXMA-UHFFFAOYAO (powerful dehydrating agent commonly used for the preparation of amides,2 esters,3 and anhydrides;4 used with DMSO for the mild oxidation of alcohols to ketones;5 used in the ...
Jeffrey S. Albert, Andrew D. Hamilton, Amy C. Hart   +2 more
openaire   +1 more source

Dicyclohexylcarbodiimide-binding sites in the myelin proteolipid

Neurochemical Research, 1984
Dicyclohexylcarbodiimide (DCCD), an inhibitor of proton translocation, has been shown to bind preferentially to the myelin proteolipid and to inhibit proton movement in liposomes containing the proteolipid (Lin, L. and Lees, M. 1982. Proc. Natl. Acad. Sci. USA 79:941-945). In the present study the location of the DCCD-binding site(s) in the sequence of
L F, Lin, M B, Lees
openaire   +2 more sources

Dicyclohexylcarbodiimide as inducer of mitochondrial Ca2+ release

Journal of Bioenergetics and Biomembranes, 1990
The effect of the alkylating reagent dicyclohexylcarbodiimide (DCCD) on mitochondrial Ca2+ content was studied. The results obtained indicate that DCCD at a concentration of 100 microM induces mitochondrial Ca2+ efflux. This reaction is accompanied by an increasing energy drain on the system, stimulation of oxygen consumption, and mitochondrial ...
E, Chávez, C, Zazueta, E, Díaz
openaire   +2 more sources

Dicyclohexylcarbodiimide-sensitive ATPase in Halobacterium saccharovorum

Archives of Biochemistry and Biophysics, 1985
Membranes from Halobacterium saccharovorum contained a cryptic ATPase which required Mg2+ or Mn2+ and was activated by Triton X-100. The optimal pH for ATP hydrolysis was 9-10. ATP or GTP were hydrolyzed at the same rate while ITP, CTP, and UTP were hydrolyzed at about half that rate. The products of ATP hydrolysis were ADP and phosphate.
H, Kristjansson, L I, Hochstein
openaire   +2 more sources

MHC restriction in contact hypersensitivity to dicyclohexylcarbodiimide

Food and Chemical Toxicology, 2002
Mouse ear swelling tests were performed using different strains of mice with dicyclohexylcarbodiimide (DCC), diisopropylcarbodiimide (DIC), di-p-tolylcarbodiimide (DTC), and positive control chemicals, such as dinitrochlorobenzene (DNCB) and oxazolone (OXA).
H, Kato, M, Hayashi, Y, Fukumori, H, Kaneko   +3 more
openaire   +2 more sources

Light-induced reaction of dicyclohexylcarbodiimide with bacteriorhodopsin

Biochemical and Biophysical Research Communications, 1981
Abstract Bacteriorhodopsin solubilized in Triton X-100 micelles undergoes a light-induced reaction with [14C]-dicyclohexylcarbodiimide at pH 7.5. The reaction has three consequences: 1) incorporation of radioactivity into bacteriorhodopsin, 2) irreversible bleaching of the retinal chromophore, and 3) alteration of the CNBr cleavage pattern.
R, Renthal, N, Dawson, L, Villarreal
openaire   +2 more sources