1,4-Bis-(2,3-epoxypropylamino)-9,10-anthracenedione and related compounds as potent antifungal and antimicrobial agents

doi:10.1016/S0960-894X(97)10176-7

Paper

1,4-Bis-(2,3-epoxypropylamino)-9,10-anthracenedione and related compounds as potent antifungal and antimicrobial agents

Published Dec 16, 1997 · Zev Lidert, D. Young, M. M. Bowers-Daines

Bioorganic & Medicinal Chemistry Letters

UNKNOWN SJR score

4

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0

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Abstract

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Study Snapshot

1,4-Bis-(2,3-epoxypropylamino)-9,10-anthracenedione and related compounds show potent antifungal and antimicrobial activity, effectively controlling downy mildew at 12 ppm.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Paper

1,4-Bis-(2,3-epoxypropylamino)-9,10-anthracenedione and related compounds as potent antifungal and antimicrobial agents

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References

A 2.|E|-Bit Distributed Algorithm for the Directed Euler Trail Problem

The new distributed Euler trail algorithm requires only 2 middot;E| one-bit messages to effectively solve the directed Euler trail problem in an Euler diagraph.

Effects of zarilamide on microtubules and nuclear division in Phytophthora capsici and tobacco suspension-cultured cells

Zarilamide inhibits nuclear division in Phytophthora capsici and tobacco plants by destroying the microtubule cytoskeleton and causing mitosis inhibition.

Citations

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This study demonstrates that enantiomerically pure 2-(aryloxymethyl)aziridines can efficiently transform into chiral N-(2-bromo-3-aryloxypropyl)amines through regio- and stereospecific ring opening of intermediate aziridinium salts by bromid

A new approach towards 2-amino-1-aryloxy-3-methoxypropanes from 1-arylmethyl-2-(bromomethyl)aziridines

This study presents a new method for preparing 2-amino-1-aryloxy-3-methoxypropanes from 1-arylmethyl-2-(bromomethyl)aziridines, achieving high yields and regioselective ring opening.