Synthesis of new piperazinyl-pyrrolo[1,2-a]quinoxaline derivatives as inhibitors of Candida albicans multidrug transporters by a Buchwald–Hartwig cross-coupling reaction

Author:

Guillon Jean12345,Nim Shweta6789,Moreau Stéphane12345,Ronga Luisa12345,Savrimoutou Solène12345,Thivet Elisabeth12345,Marchivie Mathieu101111213,Di Pietro Attilio1415161718,Prasad Rajendra1920219,Le Borgne Marc2223242526ORCID

Affiliation:

1. Univ. Bordeaux

2. INSERM U1212 – UMR CNRS 5320

3. ARNA Laboratory

4. UFR des Sciences Pharmaceutiques

5. F-33076 Bordeaux Cedex

6. School of Life Sciences

7. Jawaharlal Nehru University

8. 110067 New Delhi

9. India

10. CNRS

11. Bordeaux INP

12. ICMCB

13. UMR 5026

14. DRMP Group

15. IBCP

16. UMR 5086 (MMSB)

17. CNRS/Lyon I University

18. 69367 Lyon

19. Amity Institute of Integrative Sciences and Health

20. Amity University

21. Gurgaon 122413

22. Université de Lyon

23. Université Claude Bernard Lyon 1

24. Faculté de Pharmacie – ISPB

25. EA 4446 Bioactive Molecules and Medicinal Chemistry

26. SFR Santé Lyon-Est CNRS UMS3453 – INSERM US7

Abstract

Two series of piperazinyl-pyrrolo[1,2-a]quinoxaline derivatives were prepared via a Buchwald–Hartwig cross-coupling reaction and then evaluated for their ability to inhibit the drug efflux activity of two Candida albicans transporters.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

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