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isonicotinic acid/sarcoma
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10 risultati
Effect of isonicotinic acid hydrazide-copper complex on Rous sarcoma virus and its genome RNA.
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The copper complex of the antituberculous drug, insonicotinic acid hydrazide (INH), inhibits the RNA-dependent DNA polymerase of Rous sarcoma virus and inactivates its ability to malignantly transform chick embryo cells. The INH-copper complex binds to the 70S genome RNA of Rous sarcoma virus (RSV),
Inactivation and inhibition of Rous sarcoma virus by copper-binding ligands: thiosemicarbazones, 8-hydroxyquinolines, and isonicotinic acid hydrazide.
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We have shown that three types of copper-binding ligands, thiosemicarbazones, 8-hydroxyquinolines, and isonicotinic acid hydrazide and their copper complexes, inactivate the transforming ability of RSV and inhibit its RNA-dependent DNA polymerases. Three other compounds, 2-pyridine
[THE ULTRASTRUCTURE OF MOUSE ASCITES SARCOMA INDUCED BY ISONICOTINIC ACID HYDRAZIDE (INH)].
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[Antitumoral action of triethylene melamine-isonicotinic acid hydrazide association on Galliera sarcoma of the rat].
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[Inhibitory action of isonicotinic acid hydrazide on the development of Galliera sarcoma in the rat].
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[ON THE ELECTRON MICROSCOPIC STRUCTURE OF A NEW TRANSPLANTABLE MOUSE ASCITES SARCOMA INDUCED BY ISONICOTINIC ACID HYDRAZIDE (INH)].
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[Study of the influence of some antimetabolites of vitamin B 6 on the appearance and development of (solid) IRE reticulo-sarcoma in the rat. II. Isonicotinic acid hydrozide (INH)].
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Hyperthyroidism, niacin, and isonicotinic acid hydrazide (INAH): effects on sarcoma 180.
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Comparative study of tumorigenicity in mice administered transplacentally or neonatally with metabolites of tryptophan and its related compounds.
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Intermediate metabolites of tryptophan, 3-hydroxy-L-kynurenine (3-OHKY), 3-hydroxyanthranilic acid (3-OHAA) and anthranilic acid (AA), and an enzyme inhibitor from 3-OHKY to 3-OHAA, isonicotinic acid hydrazide (INH) with or without 3-OHKY at the maximum tolerated dose were injected s.c. to infant
Anti-tumor virus activity of copper-binding drugs.
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Several, structurally different, copper-binding ligands can inhibit the RNA-dependent DNA polymerase of Rous sarcoma virus (RSV) and can inactivate the ability of the virus to malignantly transform chick embryo cells. These ligands include the anti-microbial agents, thiosemicarbazones,
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