In the present paper, we report the synthesis via catalytic Michael reaction and biological results of a series of 3-heteryl substituted pyrrolidine-2,5-dione derivatives as moderate inhibitors against M. tuberculosis H37Rv growth. Some of them present also inhibition activities against InhA.

Synthesis of 3-heteryl substituted pyrrolidine-2,5-diones via catalytic Michael reaction and evaluation of their inhibitory activity against InhA and Mycobacterium tuberculosis

MORI, GIORGIA;PASCA, MARIA ROSALIA;
2014-01-01

Abstract

In the present paper, we report the synthesis via catalytic Michael reaction and biological results of a series of 3-heteryl substituted pyrrolidine-2,5-dione derivatives as moderate inhibitors against M. tuberculosis H37Rv growth. Some of them present also inhibition activities against InhA.
2014
Medical Research, Diagnosis & Treatment contains studies of existing and developing diagnostic and therapeutic techniques, as well as specific classes of clinical intervention. Resources in this category emphasize the difference between normal and disease states, with the ultimate goal of more effective diagnosis and intervention. Specific areas of interest include pathology and histochemical analysis of tissue, clinical chemistry and biochemical analysis of medical samples, diagnostic imaging, radiology and radiation, surgical research, anesthesiology and anesthesia, transplantation, artificial tissues, and medical implants. Resources focused on the disease, diagnosis, and treatment of specific organs or physiological systems are excluded and are covered in the Medical Research: Organs & Systems category.
Esperti anonimi
Inglese
Internazionale
STAMPA
71C
46
52
7
antitubercular agents; InhA
9
info:eu-repo/semantics/article
262
Matviiuk, T; Mori, Giorgia; Lherbet, C; Rodriguez, F; Pasca, MARIA ROSALIA; Gorichko, M; Guidetti, B; Voitenko, Z; Baltas, M.
1 Contributo su Rivista::1.1 Articolo in rivista
none
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/760284
Citazioni
  • ???jsp.display-item.citation.pmc??? 9
  • Scopus 45
  • ???jsp.display-item.citation.isi??? 44
social impact