1982
DOI: 10.1016/0166-3542(82)90052-3
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Inhibition of avian myeloblastosis virus reverse transcriptase and virus inactivation by metal complexes of isonicotinic acid hydrazide

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Cited by 10 publications
(3 citation statements)
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“…The result is inactivation of the pathogen. Also copper complexes can form radicals that inactivate viruses (Vasudevachari and Antony, 1982). Copper may also disrupt enzyme structures and functions by binding to sulfur or carboxylate containing groups and amino groups holes in the cell membranes, thereby compromising the integrity of cells of proteins and can interact with lipids, causing their peroxidation and opening holes in the cell membranes, thereby compromising the integrity of cells.…”
Section: Discussionmentioning
confidence: 99%
“…The result is inactivation of the pathogen. Also copper complexes can form radicals that inactivate viruses (Vasudevachari and Antony, 1982). Copper may also disrupt enzyme structures and functions by binding to sulfur or carboxylate containing groups and amino groups holes in the cell membranes, thereby compromising the integrity of cells of proteins and can interact with lipids, causing their peroxidation and opening holes in the cell membranes, thereby compromising the integrity of cells.…”
Section: Discussionmentioning
confidence: 99%
“…Despite its long history of use, the antimicrobial capabilities of chitosan against a spectrum of Gram-positive and Gram-negative bacteria were formally recognised in 1979 [1] and a whole range of studies began [2][3][4][5][6][7][8][9][10]. The antimicrobial ability of this natural animal-based polysaccharide relies on a number of factors including pH, microorganism species, metal ion content, molecular weight, degree of deacetylation and so forth [11][12][13].…”
Section: Introductionmentioning
confidence: 99%
“…It has been reported that CunINH inhibits the multiplication of avian myeloblastosis virus by blocking the process of reverse transcription (Vasudevachari & Antony, 1985a). This inhibition was shown to be due to preferential binding of CuHINH to the enzyme reverse transcriptase (Vasudevachari & Antony, 1982). Recently, it has been shown that Cu'^NH cleaves pBR322 form I DNA into smaller fragments (Vasudevachari & Antony, 1985b).…”
mentioning
confidence: 99%