Skip to main content
University of California San Francisco
UCSF School of Medicine | Department of Pediatrics UCSF Medical Center

Bis-alkylamine quindolone derivatives as new antimalarial leads.

  • Read more about Bis-alkylamine quindolone derivatives as new antimalarial leads.

Comparison of the antiplasmodial and falcipain-2 inhibitory activity of beta-amino alcohol thiolactone-chalcone and isatin-chalcone hybrids.

  • Read more about Comparison of the antiplasmodial and falcipain-2 inhibitory activity of beta-amino alcohol thiolactone-chalcone and isatin-chalcone hybrids.

Synthesis, antimalarial and antitubercular activity of acetylenic chalcones.

  • Read more about Synthesis, antimalarial and antitubercular activity of acetylenic chalcones.

Antimalarial activity of azadipeptide nitriles.

  • Read more about Antimalarial activity of azadipeptide nitriles.

Antiparasitic activities of novel, orally available fumagillin analogs.

  • Read more about Antiparasitic activities of novel, orally available fumagillin analogs.

Design, synthesis and structure-activity relationships of (1H-pyridin-4-ylidene)amines as potential antimalarials.

  • Read more about Design, synthesis and structure-activity relationships of (1H-pyridin-4-ylidene)amines as potential antimalarials.

Artemisinin-dipeptidyl vinyl sulfone hybrid molecules: design, synthesis and preliminary SAR for antiplasmodial activity and falcipain-2 inhibition.

  • Read more about Artemisinin-dipeptidyl vinyl sulfone hybrid molecules: design, synthesis and preliminary SAR for antiplasmodial activity and falcipain-2 inhibition.

Imidazolidin-4-one peptidomimetic derivatives of primaquine: synthesis and antimalarial activity.

  • Read more about Imidazolidin-4-one peptidomimetic derivatives of primaquine: synthesis and antimalarial activity.

Design and synthesis of novel 2-pyridone peptidomimetic falcipain 2/3 inhibitors.

  • Read more about Design and synthesis of novel 2-pyridone peptidomimetic falcipain 2/3 inhibitors.

Cryptolepine analogues containing basic aminoalkyl side-chains at C-11: synthesis, antiplasmodial activity, and cytotoxicity.

  • Read more about Cryptolepine analogues containing basic aminoalkyl side-chains at C-11: synthesis, antiplasmodial activity, and cytotoxicity.

Pagination

  • Previous page ‹‹
  • Page 2
  • Next page ››
Subscribe to Bioorganic & medicinal chemistry letters

Pediatrics Home

MAKE A GIFT

© 2026 The Regents of the University of California. The University of California San Francisco  |  UCSF Department of Pediatrics                                                                                   Accessibility  Privacy Policy  Terms of Use  A-Z Website List