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1.
Chem Commun (Camb) ; (24): 2494-6, 2007 Jun 28.
Article in English | MEDLINE | ID: mdl-17563807

ABSTRACT

3(2H)-Furanones can be prepared by a catalytic asymmetric protocol from enynones, which, if electron-rich, require only one reagent and involve two reactions in a single operation--a domino process.


Subject(s)
Furans/chemistry , Alkynes/chemistry , Catalysis , Furans/chemical synthesis , Models, Molecular , Molecular Structure , Stereoisomerism
2.
Bioorg Med Chem Lett ; 17(1): 136-41, 2007 Jan 01.
Article in English | MEDLINE | ID: mdl-17046252

ABSTRACT

Syntheses of aryloxyalkanoic acid hydroxyamides are described, all of which are potent inhibitors of histone deacetylase, some being more potent in vitro than trichostatin A (IC(50)=3 nM). Variation of the substituents on the benzene ring as well as fusion of a second ring have marked effects on potency, in vitro IC(50) values down to 1 nM being obtained.


Subject(s)
Amides/chemistry , Antineoplastic Agents/chemistry , Enzyme Inhibitors/chemistry , Histone Deacetylase Inhibitors , Amides/chemical synthesis , Amides/pharmacology , Antineoplastic Agents/chemical synthesis , Antineoplastic Agents/pharmacology , Enzyme Inhibitors/chemical synthesis , Enzyme Inhibitors/pharmacology , Histone Deacetylases/chemistry , Humans , Protein Conformation , Structure-Activity Relationship
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