Antifungal drugs

Diethyl pyrocarbonate reacts selectively with the single-stranded loops of cruciform structures. The irreversible inactivation of ribonuclease with diethylpyrocarbonate has been studied.

Diethyl pyrocarbonate reacts selectively with the single-stranded loops of cruciform structures. The irreversible inactivation of ribonuclease with diethylpyrocarbonate has been studied.

Diethyl pyrocarbonate reacts selectively with the single-stranded loops of cruciform structures. The irreversible inactivation of ribonuclease with diethylpyrocarbonate has been studied.

Diethyl pyrocarbonate (DEP) is a bactericidal agent and decomposes in water to CO 2 and ethanol. DEP inhibits enzymes such as DNase and RNase without affecting nucleic acids.

Diethyl pyrocarbonate (DEP) is a bactericidal agent and decomposes in water to CO 2 and ethanol. DEP inhibits enzymes such as DNase and RNase without affecting nucleic acids.

Diethyl pyrocarbonate (DEP) is a bactericidal agent and decomposes in water to CO 2 and ethanol. DEP inhibits enzymes such as DNase and RNase without affecting nucleic acids.

Diethyl pyrocarbonate (DEP) is a bactericidal agent and decomposes in water to CO 2 and ethanol. DEP inhibits enzymes such as DNase and RNase without affecting nucleic acids.

Diethyl Pyrocarbonate (DEPC) is a chemical use to inactivate RNase enzymes and is sensitive to moisture and pH. It decomposes at 155°C, to ethanol and carbon dioxide in aqueous solution.

Diethyl Pyrocarbonate (DEPC) is a chemical use to inactivate RNase enzymes and is sensitive to moisture and pH. It decomposes at 155°C, to ethanol and carbon dioxide in aqueous solution.

Diethyl Pyrocarbonate (DEPC) is a chemical use to inactivate RNase enzymes and is sensitive to moisture and pH. It decomposes at 155°C, to ethanol and carbon dioxide in aqueous solution.

Diethyl Pyrocarbonate (DEPC) is a chemical use to inactivate RNase enzymes and is sensitive to moisture and pH. It decomposes at 155°C, to ethanol and carbon dioxide in aqueous solution.

Application Diethyl tert -butylmalonate has been used in the preparation of enantiomers of 4- tert -butyl-3-isopropyl-2,6,7-trioxa-1-phosphabicyclo[2.2.