2-(hydroxymethyl)anthraquinone

Known as: HMAQ-one 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1980-2015
01219802015

Papers overview

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2015
2015
Natural product drugs play a dominant role in pharmaceutical care. Nature is an attractive source of new therapeutic candidate… (More)
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2013
2013
Photoremovable protecting groups (PRPGs) were demonstrated as a delivery device for controlled release of pheromone under both UV… (More)
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2011
2011
Non-structural carbohydrates and phenolic compounds are implicated in the natural durability of wood. In order to find the… (More)
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2009
2009
The formal intramolecular photoredox reaction initially discovered for the parent 2-(hydroxymethyl)anthraquinone (1) has been… (More)
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2008
2008
The formal intramolecular photoredox reaction initially discovered for the parent 2-(hydroxymethyl)anthraquinone (1) in aqueous… (More)
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2006
2006
The growth-inhibiting activity of Tabebuia impetiginosa Martius ex DC dried inner bark-derived constituents against Helicobacter… (More)
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2006
2006
Inclusion of 2-(hydroxymethyl)anthraquinone in zeolite NaY leads to a solid, photoactivated, reusable oxygen sensor capable of… (More)
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2002
2002
The title compound undergoes a novel excited state intramolecular redox reaction in which the 'distal' side chain benzylic… (More)
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1992
1992
In an attempt to produce better cytotoxic analogues, chemotherapeutic antineoplastic radicals including an alkylating nitrogen… (More)
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1980
1980
Hypoxic cells of solid tumors are an obstacle to effective cancer therapy. Since hypoxic cells remote from the tumor blood supply… (More)
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