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Plakinamine P, A Steroidal Alkaloid with Bactericidal Activity against Mycobacterium tuberculosis.
Rodrigues Felix, Carolina; Roberts, Jill C; Winder, Priscilla L; Gupta, Rashmi; Diaz, M Cristina; Pomponi, Shirley A; Wright, Amy E; Rohde, Kyle H.
Afiliação
  • Rodrigues Felix C; Biotechnology Department, Universidade Federal de Pelotas, Pelotas, RS 96010-610, Brazil.
  • Roberts JC; Harbor Branch Oceanographic Institute, Florida Atlantic University, Fort Pierce, FL 34946, USA.
  • Winder PL; Harbor Branch Oceanographic Institute, Florida Atlantic University, Fort Pierce, FL 34946, USA.
  • Gupta R; Division of Immunity and Pathogenesis, Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.
  • Diaz MC; Harbor Branch Oceanographic Institute, Florida Atlantic University, Fort Pierce, FL 34946, USA.
  • Pomponi SA; Harbor Branch Oceanographic Institute, Florida Atlantic University, Fort Pierce, FL 34946, USA.
  • Wright AE; Harbor Branch Oceanographic Institute, Florida Atlantic University, Fort Pierce, FL 34946, USA.
  • Rohde KH; Division of Immunity and Pathogenesis, Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL 32827, USA.
Mar Drugs ; 17(12)2019 Dec 16.
Article em En | MEDLINE | ID: mdl-31888140
ABSTRACT
Tuberculosis is the leading cause of death due to infectious disease worldwide. There is an urgent need for more effective compounds against this pathogen to control the disease. Investigation of the anti-mycobacterial activity of a deep-water sponge of the genus Plakina revealed the presence of a new steroidal alkaloid of the plakinamine class, which we have given the common name plakinamine P. Its structure is most similar to plakinamine L, which also has an acyclic side chain. Careful dissection of the nuclear magnetic resonance data, collected in multiple solvents, suggests that the dimethyl amino group at the 3 position is in an equatorial rather than axial position unlike previously reported plakinamines. Plakinamine P was bactericidal against M. tuberculosis, and exhibited moderate activity against other mycobacterial pathogens, such as M. abscessus and M. avium. Furthermore, it had low toxicity against J774 macrophages, yielding a selectivity index (SI, or IC50/MIC) of 8.4. In conclusion, this work provides a promising scaffold to the tuberculosis drug discovery pipeline. Future work to determine the molecular target of this compound may reveal a pathway essential for M. tuberculosis survival during infection.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esteroides / Alcaloides / Mycobacterium tuberculosis / Antituberculosos Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Esteroides / Alcaloides / Mycobacterium tuberculosis / Antituberculosos Idioma: En Ano de publicação: 2019 Tipo de documento: Article