The invention relates to pseudomycin natural products including pseudomycins Aâ and Bâ, methods for making such pseudomycins, and methods employing antifungal activity of these pseudomycins. NMR and mass spectrometry indicate formula (I) for pseudomycin Aâ. NMR and mass spectrometry indicate formula (II) for pseudomycin Bâ.
Matthew David Belvo - Greenfield IN, US Adam Joseph Kreuzman - Greenwood IN, US Palaniappan Kulanthaivel - Carmel IN, US Tim Allen Smitka - Indianapolis IN, US
Assignee:
Eli Lilly and Company - Indianapolis IN
International Classification:
A61K038/14 A16K038/16
US Classification:
514 8, 530317, 530322
Abstract:
Provided are novel lipoglycopeptides exhibiting bacterial signal peptidase inhibitory activity. Also provided are actinomycete strains that produce these lipoglycopeptides, methods of producing such lipoglycopeptides by culturing these strains, pharmaceutical compositions comprising these lipoglycopeptides, and methods of treating bacterial infections comprising contacting bacteria susceptible to treatment with the present bacterial signal peptidase inhibitor lipoglycopeptides. These lipoglycopeptides are useful in human and veterinary medicine.
Palaniappan Kulanthaivel - Carmel IN Matthew David Belvo - Greenfield IN James William Martin - Coatesville IN Thomas John Perun - Indianapolis IN Douglas Joseph Zeckner - Greenwood IN
The invention relates to pseudomycin natural products including pseudomycins Aâ and Bâ, methods for making such pseudomycins, and methods employing antifungal activity of these pseudomycins. NMR and mass spectrometry indicate a formula for pseudomycin Aâ of: NMR and mass spectrometry indicate a formula for pseudomycin Bâ of:.