Computer-Aided Design of Orally Bioavailable Pyrrolidine Carboxamide Inhibitors of Enoyl-Acyl Carrier Protein Reductase of Mycobacterium tuberculosis with Favorable Pharmacokinetic Profiles

Eitemau Tebyg

• Structure-Based Design and in Silico Screening of Virtual Combinatorial Library of Benzamides Inhibiting 2-trans Enoyl-Acyl Carrier Protein Reductase of Mycobacterium tuberculosis with Favorable Predicted Pharmacokinetic Profiles
  gan: Kouman, Koffi Charles, et al.
  Cyhoeddwyd: (2019)
• Virtual design of novel Plasmodium falciparum cysteine protease falcipain-2 hybrid lactone–chalcone and isatin–chalcone inhibitors probing the S2 active site pocket
  gan: Koffi N’Guessan Placide Gabin Allangba, et al.
  Cyhoeddwyd: (2019-01-01)
• Virtual design of novel Plasmodium falciparum cysteine protease falcipain-2 hybrid lactone–chalcone and isatin–chalcone inhibitors probing the S2 active site pocket
  gan: Allangba, Koffi N’Guessan Placide Gabin, et al.
  Cyhoeddwyd: (2019)
• Design of Thymidine Analogues Targeting Thymidilate Kinase of Mycobacterium tuberculosis
  gan: Owono Owono, Luc Calvin, et al.
  Cyhoeddwyd: (2013)
• Pyrrolidine Carboxamides as a Novel Class of Inhibitors of Enoyl Acyl Carrier Protein Reductase (InhA) from Mycobacterium tuberculosis
  gan: He, Xin, et al.
  Cyhoeddwyd: (2006)