Literature DB >> 8134421

Antileishmanial activity of a tetralone isolated from Ampelocera edentula, a Bolivian plant used as a treatment for cutaneous leishmaniasis.

A Fournet1, A A Barrios, V Muñoz, R Hocquemiller, F Roblot, A Cavé.   

Abstract

The stem bark of Ampelocera edentula Kuhlm. (Ulmaceae) is used by the Chimanes Indians from Bolivia for the treatment of cutaneous leishmaniasis caused by the protozoan Leishmania braziliensis. A chloroform extract of the stem barks was found to be active against extracellular forms of Leishmania ssp. and Trypanosoma cruzi at 50 micrograms/ml. Bioassay-guided fractionation of this extract allowed us to isolate one active compound. Its structure was elucidated by spectral and chemical studies as 4-hydroxy-1-tetralone. BALB/c mice infected with L. amazonensis (PH8) or L. venezuelensis were treated one day after the parasitic infection with 4-hydroxy-1-tetralone (25 mg/kg/day) or with reference drug, Glucantime (56 mg Sbv/kg/day) for 14 days. Lesion development was the criteria used to evaluate the disease severity. 4-Hydroxy-1-tetralone was slightly less effective than the reference drug against L. amazonensis or L. venezuelensis. Single treatment near the site of infection, 14 days after infection with L. amazonensis, with 4-hydroxy-1-tetralone (50 mg/kg) was more effective than Glucantime (112 mg/kg). This study is, to our knowledge, the first to show the activity of a tetralone for the experimental treatment of New World cutaneous leishmaniasis.

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Year:  1994        PMID: 8134421     DOI: 10.1055/s-2006-959397

Source DB:  PubMed          Journal:  Planta Med        ISSN: 0032-0943            Impact factor:   3.352


  3 in total

1.  Palladium-Catalyzed Dearomative syn-1,4-Oxyamination.

Authors:  Conghui Tang; Mikiko Okumura; Hejun Deng; David Sarlah
Journal:  Angew Chem Int Ed Engl       Date:  2019-09-20       Impact factor: 15.336

2.  Arenophile-Mediated Dearomative Reduction.

Authors:  Mikiko Okumura; Stephanie M Nakamata Huynh; Jola Pospech; David Sarlah
Journal:  Angew Chem Int Ed Engl       Date:  2016-11-23       Impact factor: 15.336

3.  Diastereoselective and enantioselective reduction of tetralin-1,4-dione.

Authors:  E Peter Kündig; Alvaro Enriquez-Garcia
Journal:  Beilstein J Org Chem       Date:  2008-10-22       Impact factor: 2.883

  3 in total

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