IP Library Granted Patent US 9,872,849
Granted Patent B2
US 9,872,849 · App. 14/811,341 · Granted Jan 23, 2018

Diterpenoid membranolide compounds having anti-leishmania activity and uses thereof

Inventors: Bill J. Baker (Tampa, FL); Christopher G. Witowski (Clearwater, FL); John Alan Maschek (Salt Lake City, UT); Brian Vesely (Tampa, FL); Dennis E. Kyle (Lithia, FL)
Assignee: UNIVERSITY OF SOUTH FLORIDA
A61K31/365A61K31/343A61K31/366A61K45/06
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Quick Facts
Patent No.
US 9,872,849
App. No.
14/811,341
Granted
Jan 23, 2018
Kind
B2
Abstract

In a screening program, the Antarctic sponge Dendrilla membranosa was found to produce diterpenoid secondary metabolites with activity against the leishmaniasis-causing parasite Leishmania donovani . The present invention concerns compositions useful for control of Leishmania spp. parasites in vitro and in vivo and treatment of leishmaniasis; methods for treatment of leishmaniasis; and methods for controlling Leishmania spp. parasites in vitro and in vivo.

Claims (14)

1. A composition comprising at least one anti- Leishmania agent; and at least one other compound having the following chemical structure:

or a pharmaceutically acceptable salt thereof; or,

or a pharmaceutically acceptable salt thereof.

2. The composition of claim 1 , wherein the at least one anti- Leishmania agent is an antimonial, amphotericin B, miltefosine, pentamidine, aminoglycoside-amino-cyclitol antibiotic, azole, 4-methyl-6-methoxy-8-aminoquinoline, or nucleoside analogue, or a combination thereof.

3. The composition of claim 1 , wherein the at least one other compound has the following chemical structure:

or a pharmaceutically acceptable salt thereof.

4. The composition of claim 3 , wherein the at least one anti- Leishmania agent is an antimonial, amphotericin B, miltefosine, pentamidine, aminoglycoside-amino-cyclitol antibiotic, azole, 4-methyl-6-methoxy-8-aminoquinoline, or nucleoside analogue, or a combination thereof.

5. The composition of claim 1 , wherein the at least one other compound has the following chemical structure:

or a pharmaceutically acceptable salt thereof.

6. The composition of claim 5 , wherein the at least one anti- Leishmania agent is an antimonial, amphotericin B, miltefosine, pentamidine, aminoglycoside-amino-cyclitol antibiotic, azole, 4-methyl-6-methoxy-8-aminoquinoline, or nucleoside analogue, or a combination thereof.

7. The composition of claim 1 , wherein the at least one other compound comprises a compound having the chemical structure:

or a pharmaceutically acceptable salt thereof; and a compound having the chemical structure:

or a pharmaceutically acceptable salt thereof.

8. The composition of claim 7 , wherein the at least one anti- Leishmania agent is an antimonial, amphotericin B, miltefosine, pentamidine, aminoglycoside-amino-cyclitol antibiotic, azole, 4-methyl-6-methoxy-8-aminoquinoline, or nucleoside analogue, or a combination thereof.

Assignments (2)
CONFIRMATORY LICENSE Recorded Feb 15, 2018
From: UNIVERSITY OF SOUTH FLORIDA
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 045346/0703 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 6, 2017
From: BAKER, BILL J.; WITOWSKI, CHRISTOPHER G.; MASCHEK, JOHN ALAN; VESELY, BRIAN; KYLE, DENNIS E.
To: UNIVERSITY OF SOUTH FLORIDA
Reel/Frame 042919/0950 →
Continuity (2)
Provisional Application 62032243 · Aug 1, 2014
Related Publication 20160030388A1 · Feb 4, 2016