Addition of thiols to o-quinone methide: New 2-hydroxy-3-phenylsulfanylmethyl[1,4]naphthoquinones and their activity against the human malaria parasite Plasmodium falciparum (3D7)

Título:

Autor:

David Rodrigues da Rocha

Ano:

2013

DOI:

10.1016/j.ejmech.2012.10.052

Revista:

European Journal of Medicinal Chemistry

ISSN:

02235234

Tags:

Malaria

Plasmodium falciparum

naphthoquinone

Phenylsulfanylmethyl[1

4]naphthoquinone

antimalarial

Idioma:

Inglês

Buscar essa publicação no Google Acadêmico

Publicações com a mesma autoria

4-(Dimethylamino)pyridine as Multivalent Catalyst in Organic Synthesis

Recent Advances in the Synthesis of New Antimycobacterial Agents Based on the 1H-1,2,3-Triazoles

Investigation of cobalt(III)-tpa complexes as potential bioreductively activated carriers for naphthoquinone-based drugs

Efficient Catalytic Oxidation of 3-Arylthio- and 3-Cyclohexylthio-lapachone Derivatives to New Sulfonyl Derivatives and Evaluation of Their Antibacterial Activities

Oxalyl Chloride: A Versatile Reagent in Organic Synthesis

(3,3?-Methylene)bis-2-hydroxy-1,4-naphthoquinones induce cytotoxicity against DU145 and PC3 cancer cells by inhibiting cell viability and promoting cell cycle arrest

Novel 1H-1,2,3-, 2H-1,2,3-, 1H-1,2,4- and 4H-1,2,4-triazole derivatives: a patent review (2008-2011)

Selective and sensitive pull down of amyloid fibrils produced in vitro and in vivo by the use of pentameric-thiophene-coupled resins.

Phosphomolybdic Acid (PMA)

Design and Synthesis of Carbohydrate Derivatives for Antagonistic Activity at Muscarinic Receptor