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Journal ArticleDOI

The synthesis of pyrimido[4,5-c] pyridazines and pyrido[2,3-d]pyrimidines related to toxoflavin and fervenulin

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TLDR
In this paper, 4-deazatoxoflavin and 4deazafervenulin analogs have been prepared with the required intermediates, including 3,5,7-trimethyl-1,2,3,4,4-tetrahydropyrido[2, 3,d]-2, 4-pyrimidinedione.
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This article is published in Journal of Heterocyclic Chemistry.The article was published on 1975-12-01. It has received 21 citations till now. The article focuses on the topics: Toxoflavin.

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Book ChapterDOI

Uracils: Versatile Starting Materials in Heterocyclic Synthesis

TL;DR: This chapter provides a brief review on uracil and its chemistry and has pointed out by some selective but typical examples that show uracils and their derivatives possess considerable synthetic potential.
Journal ArticleDOI

Regiospecific one-pot synthesis of pyrimido[4,5-d]pyrimidine derivatives in the solid state under microwave irradiations.

TL;DR: This procedure provides a convenient method for the direct synthesis of pyrimido[4,5-d]pyrimidines in excellent yields when carried out in the solid state and under microwave irradiations.
Journal ArticleDOI

PLK1 as a potential drug target in cancer therapy

TL;DR: The data suggest that PLK1 may serve as a target for discovering small molecule anticancer agents, and low micromolar antiproliferative activity towards SW620, a human colon cancer cell line, most likely through cell cycle arrest at the G2/M phase.
Journal ArticleDOI

A novel synthesis of 3-(substituted)pyrimido[4,5-c]pyridazine-5,7(1H,6H)-diones

TL;DR: An improved synthesis of 3-(substituted)pyrimido[4,5-c]pyridazine-5,7(1H,6H)-diones, a known subclass of 4-deazatoxoflavins, is reported.
Journal ArticleDOI

A Novel Synthesis of Fused Uracils: Indenopyrimidopyridazines, Pyrimidopyridazines, and Pyrazolopyrimidines for Antimicrobial and Antitumor Evalution

TL;DR: A variety of different compounds of fused uracils were prepared simply by the heating of 6-hydrazinyl-1-methyl-, 6-Hydrazinyl -1-propyl-, or 6- Hydrazinyl, 1,3-dipropyluracil under reflux with ninhydrin, isatin, benzylidene malononitrile, benzylylidene ethyl cyanoacetate, benzil, and phenacyl brom
References
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Journal ArticleDOI

On the origin of the toxicity of toxoflavin.

TL;DR: The mechanism of action of toxoflavin appears to act as an electron-carrier which makes possible a by-passing of the cytochrome-system and the final result of this electron-transfer is the production of hydrogen-peroxide.
Journal ArticleDOI

On toxoflavin, the yellow poison of pseudomonas cocovenenans

TL;DR: In this article, a new investigation of the structure of Pseudomonas cocovenenans was carried out, leading to an entirely different structure and simplified the isolation of toxoflavin.
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