Literature DB >> 4328024

Inactivation of Rous sarcoma virus on contact with N-ethyl isatin -thiosemicarbazone.

W Levinson, B Woodson, J Jackson.   

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Year:  1971        PMID: 4328024     DOI: 10.1038/newbio232116a0

Source DB:  PubMed          Journal:  Nat New Biol        ISSN: 0090-0028


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  6 in total

1.  Preferential inhibition of ribonucleic acid synthesis by a new thiosemicarbazone possessing antibacterial and antiparasitic properties.

Authors:  R E Brown; F A Stancato; A D Wolfe
Journal:  Antimicrob Agents Chemother       Date:  1981-02       Impact factor: 5.191

2.  Inactivation of herpes simplex virus by thiosemicarbazones and certain cations.

Authors:  W Levinson; V Coleman; B Woodson; A Rabson; J Lanier; J Whitcher; C Dawson
Journal:  Antimicrob Agents Chemother       Date:  1974-04       Impact factor: 5.191

3.  Inactivation of lambda phage infectivity and lambda deoxyribonucleic acid transfection by N-methyl-isatin beta-thiosemicarbazone-copper complexes.

Authors:  W Levinson; R Helling
Journal:  Antimicrob Agents Chemother       Date:  1976-01       Impact factor: 5.191

4.  Inhibition of RNA-dependent DNA polymerase of Rous sarcoma virus by thiosemicarbazones and several cations.

Authors:  W Levinson; A Faras; B Woodson; J Jackson; J M Bishop
Journal:  Proc Natl Acad Sci U S A       Date:  1973-01       Impact factor: 11.205

5.  Inhibition of granulocyte-macrophage colony formation in vitro by substituted isatin thiosemicarbazones.

Authors:  T A McNeill
Journal:  Antimicrob Agents Chemother       Date:  1973-08       Impact factor: 5.191

6.  N-methylisatin-beta-thiosemicarbazone derivative (SCH 16) is an inhibitor of Japanese encephalitis virus infection in vitro and in vivo.

Authors:  Liba Sebastian; Anita Desai; Madhusudana N Shampur; Yogeeswari Perumal; D Sriram; Ravi Vasanthapuram
Journal:  Virol J       Date:  2008-05-22       Impact factor: 4.099

  6 in total

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