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Antiparasitic activities of new lawsone Mannich bases.
Al Nasr, Ibrahim; Jentzsch, Jana; Winter, Isabel; Schobert, Rainer; Ersfeld, Klaus; Koko, Waleed S; Mujawah, Adil A H; Khan, Tariq A; Biersack, Bernhard.
Afiliação
  • Al Nasr I; College of Science and Arts in Unaizah, Qassim University, Unaizah, Saudi Arabia.
  • Jentzsch J; College of Science and Arts in Ar Rass, Qassim University, Ar Rass, Saudi Arabia.
  • Winter I; Laboratory of Molecular Parasitology, University of Bayreuth, Bayreuth, Germany.
  • Schobert R; Laboratory of Molecular Parasitology, University of Bayreuth, Bayreuth, Germany.
  • Ersfeld K; Organic Chemistry Laboratory, University of Bayreuth, Bayreuth, Germany.
  • Koko WS; Laboratory of Molecular Parasitology, University of Bayreuth, Bayreuth, Germany.
  • Mujawah AAH; College of Science and Arts in Ar Rass, Qassim University, Ar Rass, Saudi Arabia.
  • Khan TA; College of Science and Arts in Ar Rass, Qassim University, Ar Rass, Saudi Arabia.
  • Biersack B; College of Applied Health Sciences in Ar Rass, Qassim University, Ar Rass, Saudi Arabia.
Arch Pharm (Weinheim) ; 352(11): e1900128, 2019 Nov.
Article em En | MEDLINE | ID: mdl-31536649
A series of new lawsone Mannich bases derived from salicylaldehydes or nitrofurfural were prepared and tested for their activities against Leishmania major, Toxoplasma gondii, and Trypanosoma brucei brucei parasites. The hydrochloride salts 5a and 6a of the Mannich bases 2a and 3a, derived from unsubstituted salicylaldehyde and long-chained alkyl amines, were selectively and strongly active against T. gondii cells and appear to be new promising drug candidates against this parasite. Compound 6a showed an even higher activity against T. gondii than the known lawsone Mannich base 1b. Compound 4a, derived from salicylaldehyde and 2-methylaminopyridine, was also distinctly active against T. gondii cells. The derivatives 3a (salicyl derivative), 3b (3,5-dichloro-2-hydroxyphenyl derivative), and 3d (5-nitrofuranyl derivative) as well as the hydrochlorides 6a and 6b were also efficacious against T. b. brucei cells with compounds 3a and 3b being more selective for T. b. brucei over Vero cells when compared with the known control compound 1b. The derivatives 5a, 5c, 6a, and 6c proved to be up to five times more active than 1b against L. major promastigotes and up to four times more efficacious against L. major amastigotes.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Toxoplasma / Trypanosoma brucei brucei / Naftoquinonas / Leishmania major / Antiparasitários Idioma: En Revista: Arch Pharm (Weinheim) Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Arábia Saudita

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Toxoplasma / Trypanosoma brucei brucei / Naftoquinonas / Leishmania major / Antiparasitários Idioma: En Revista: Arch Pharm (Weinheim) Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Arábia Saudita