Anti-fungals compounds targeting the synthesis of fungal sphingolipids

Patent metadata

Field	Value
Publication number	US-11858880-B2
Application number	US-202217837548-A
Country	US
Kind code	B2
Filing date	Jun 10, 2022
Priority date	Jun 16, 2017
Publication date	Jan 2, 2024
Grant date	Jan 2, 2024

Abstract

The present invention provides a compound having the structure:

and use of the compound for inhibiting the growth of or killing

First claim

What is claimed is:

1. A method of inhibiting the growth of a fungus comprising contacting the fungus with an effective amount of the compound having the structure:

wherein
R 1 is —H, alkyl, alkenyl, or alkynyl;
R 2 is —H, alkyl, alkenyl, or alkynyl;
R 3 , R 4 , R 5 , and R 6 are each independently —H, halogen, C 1 -C 6 alkyl, —OH, —O—(C 1 -C 6 alkyl), —CHF 2 , —CF 3 , —OCHF 2 or —OCF 3 , or
R 3 and R 4 are each independently —H, halogen, C 1 -C 6 alkyl, —OH, —O—(C 1 -C 6 alkyl), —CHF 2 , —CF 3 , —OCHF 2 or —OCF 3 , and R 5 and R 6 combine to form a fused aryl or fused heteroaryl, which are each unsubstituted or substituted, or
R 3 and R 6 are each independently —H, halogen, C 1 -C 6 alkyl, —OH, —O—(C 1 -C 6 alkyl), —CHF 2 , —CF 3 , —OCHF 2 or —OCF 3 , and R 4 and R 5 combine to form a fused aryl or fused heteroaryl, which are each unsubstituted or substitute, or
R 5 and R 6 are each independently —H, halogen, C 1 -C 6 alkyl, —OH, —O—(C 1 -C 6 alkyl), —CHF 2 , —CF 3 , —OCHF 2 or —OCF 3 , and R 3 and R 4 combine to form a fused aryl or fused heteroaryl, which are each unsubstituted or substituted; and
A is an aryl or heteroaryl, which are each unsubstituted or substituted,
wherein when R 3 , R 4 , and R 6 are each —H and R 5 is —OH or —OCH 3 , or R 3 , R 5 , and R 6 are each —H and R 4 is —Br, then A is other than ortho-tolyl or meta-bromophenyl,
or a pharmaceutically acceptable salt or ester thereof, so as to thereby inhibit the growth of the fungus.

2. A method of inhibiting fungal sphingolipid synthesis in a fungus comprising contacting the fungus with an effective amount of the compound having the structure:

wherein
R 1 is —H, alkyl, alkenyl, or alkynyl;
R 2 is —H, alkyl, alkenyl, or alkynyl;
R 3 , R 4 , R 5 , and R 6 are each independently —H, halogen, C 1 -C 6 alkyl, —OH, —O—(C 1 -C 6 alkyl), —CHF 2 , —CF 3 , —OCHF 2 or —OCF 3 , or
R 3 and R 4 are each independently —H, halogen, C 1 -C 6 alkyl, —OH, —O—(C 1 -C 6 alkyl), —CHF 2 , —CF 3 , —OCHF 2 or —OCF 3 , and R 5 and R 6 combine to form a fused aryl or fused heteroaryl, which are each unsubstituted or substituted, or
R 3 and R 6 are each independently —H, halogen, C 1 -C 6 alkyl, —OH, —O—(C 1 -C 6 alkyl), —CHF 2 , —CF 3 , —OCHF 2 or —OCF 3 , and R 4 and R 5 combine to form a fused aryl or fused heteroaryl, which are each unsubstituted or substitute, or
R 5 and R 6 are each independently —H, halogen, C 1 -C 6 alkyl, —OH, —O—(C 4 -C 6 alkyl), —CHF 2 , —CF 3 , —OCHF 2 or —OCF 3 , and R 3 and R 4 combine to form a fused aryl or fused heteroaryl, which are each unsubstituted or substituted; and
A is an aryl or heteroaryl, which are each unsubstituted or substituted,
wherein when R 3 , R 4 , and R 6 are each —H and R 5 is —OH or —OCH 3 , or R 3 , R 5 , and R 6 are each —H and R 4 is —Br, then A is other than ortho-tolyl or meta-bromophenyl, or a pharmaceutically acceptable salt or ester thereof, so as to thereby inhibit sphingolipid synthesis in the fungus.

3. A method of inhibiting fungal sphingolipid synthesis in a fungus in a mammal without substantially inhibiting mammalian sphingolipid synthesis comprising administering to the mammal an effective amount of the compound of having the structure:

wherein
R 4 is —H, alkyl, alkenyl, or alkynyl;
R 2 is —H, alkyl, alkenyl, or alkynyl;
R 3 , R 4 , R 5 , and R 6 are each independently —H, halogen, C 1 -C 6 alkyl, —OH, —O—(C 1 -C 6 alkyl), —CHF 2 , —CF 3 , —OCHF 2 or —OCF 3 , or
R 3 and R 4 are each independently —H, halogen, C 1 -C 6 alkyl, —OH, —O—(C 1 -C 6 alkyl), —CHF 2 , —CF 3 , —OCHF 2 or —OCF 3 , and R 5 and R 6 combine to form a fused aryl or fused heteroaryl, which are each unsubstituted or substituted, or
R 3 and R 6 are each independently —H, halogen, C 1 -C 6 alkyl, —OH, —O—(C 1 -C 6 alkyl), —CHF 2 , —CF 3 , —OCHF 2 or —OCF 3 , and R 4 and R 5 combine to form a fused aryl or fused heteroaryl, which are each unsubstituted or substitute, or
R 5 and R 6 are each independently —H, halogen, C 1 -C 6 alkyl, —OH, —O—(C 1 -C 6 alkyl), —CHF 2 , —CF 3 , —OCHF 2 or —OCF 3 , and R 3 and R 4 combine to form a fused aryl or fused heteroaryl, which are each unsubstituted or substituted; and
A is an aryl or heteroaryl, which are each unsubstituted or substituted,
wherein when R 3 , R 4 , and R 6 are each —H and R 5 is —OH or —OCH 3 , or R 3 , R 5 , and R 6 are each —H and R 4 is —Br, then A is other than ortho-tolyl or meta-bromophenyl, or a pharmaceutically acceptable salt or ester thereof, so as to thereby inhibit fungal sphingolipid synthesis in the fungus in the mammal without substantially inhibiting mammalian sphingolipid synthesis.

4. The method of claim 1 , wherein the compound has the structure:

or a pharmaceutically acceptable salt thereof.

5. The method of claim 1 , further comprising contacting the fungus with an effective amount of an anti-fungal agent.

6. The method of claim 3 , further comprising administering to the mammal an effective amount of an anti-fungal agent.

7. The method of claim 6 , wherein the amount of the compound and the amount of the anti-fungal agent when taken together is more effective to inhibit the growth of the fungus than the anti-fungal agent alone, or more effective to inhibit fungal sphingolipid synthesis than the anti-fungal agent alone.

8. The method of claim 6 , wherein the amount of the compound and the amount of the anti-fungal agent when taken together is more effective to inhibit fungal sphingolipid synthesis without substantially inhibiting mammalian sphingolipid synthesis in the mammal than the anti-fungal agent alone.

9. The method of claim 5 , wherein the anti-fungal agent is fluconazole, amphotericin B, caspofungin, tunicamycin or aureobasidin A.

10. The method of claim 1 , wherein the fungus is Cryptococcus Neoformans, Cryptococcus gattii, Candida albicans, Candida krusei, Candida glabrata, Candida parapsilosis, Candida guilliermondii, Aspergillus fumigatus, Rhizopus oryzae, Rhizopus spp., Blastomyces dermatitis, Histoplasma capsulatum, Coccidioides spp., Paecilomyces variotii, Pneumocystis murina, Pneumocystis jiroveci, Histoplasma capsulatum, Aspergillus spp., dimorphic fungi or mucorales fungi.

11. The method of claim 1 , wherein the fungus is other than Cryptococcus Neoformans.

12. The method of claim 1 , wherein the fungus is Cryptococcus gattii, Candida albicans, Candida krusei, Candida glabrata, Candida parapsilosis, Candida guilliermondii, Aspergillus fumigatus, Rhizopus oryzae, Rhizopus spp., Blastomyces dermatitis, Histoplasma capsulatum, Coccidioides spp., Paecilomyces variotii, Pneumocystis murina, Pneumocystis jiroveci, Histoplasma capsulatum, Aspergillus spp., dimorphic fungi or mucorales fungi.

13. The method of claim 2 , wherein the fungal sphingolipid is glucosylceramide (GlcCer).

14. The method of any claim 2 , wherein the compound has the structure:

Assignees

• Univ New York State Res Found

Inventors

• Ojima Iwao
• Del Poeta Maurizio
• Lazzarini Cristina
• Hanarahalli Krupanandan
• Sun Yi

Classifications

• C07C251/86 Primary

  having doubly-bound carbon atoms of hydrazone groups bound to carbon atoms of six-membered aromatic rings · CPC title

• A01N37/28

  containing the group [IMAGE cpc-sch-A01N-0937.gif]; Thio analogues thereof · CPC title

• A61K31/195

  having an amino group · CPC title

• A61P31/10

  Antimycotics · CPC title

• C07D213/86

  Hydrazides; Thio or imino analogues thereof · CPC title