IP Library Patent Application 17919202
Patent Application
App. No. 17/919,202

NOVEL THERAPEUTIC USE OF PLEUROMUTILINS

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Patent No.
US None
App. No.
17/919,202
Abstract

A compound of formula (I) wherein n is 0 to 4; m is 0 or 1 with the proviso that the sulphur atom and R 3 are in vicinal position (if m=0 then R 3 is in position 2′, and if m=1 then R 3 is on position 1′); R is ethyl or vinyl; R 1 is hydrogen or (C 1-6 )alkyl, R 2 is hydrogen or (C 3-6 )cycloalkyl, or unsubstituted (C 1-6 )alkyl, or (C 1-6 )alkyl substituted by one or more of hydroxy; preferably one or two, methoxy, halogen, (C 3-6 )cycloalkyl, or R 1 and R 2 together with the nitrogen atom to which they are attached form a 5 to 7 membered heterocyclic ring containing at least 1 nitrogen atom or 1 nitrogen and 1 additional heteroatom e. g. selected from N or O, or R 1 is hydroxy and R 2 is formyl; R 3 is OH, OR 4 , a halogen atom, or R 3 is bound to 2′ and represents —O—(CH 2 ) p —O— with p is 2 or 3; R 4 is unsubstituted (C 1-6 )alkyl or (C 3-6 )cycloalkyl, or a pharmaceutically acceptable salt, solvate, prodrug or metabolite thereof for the specific use in the treatment or prevention of a disease mediated by a virus.

Claims (83)

1 . A method for treating or preventing a disease mediated by a virus, comprising administering to a subject in need thereof a compound of formula (I)

wherein

n is 0 to 4;

m is 0 or 1 with the proviso that the sulphur atom and R 3 are in vicinal position, if m=0 then R 3 is in position 2′, and if m=1 then R 3 is on position 1′;

R is ethyl or vinyl;

R 1 is hydrogen or (C 1-6 )alkyl,

R 2 is hydrogen or

(C 3-6 )cycloalkyl, or

unsubstituted (C 1-6 )alkyl, or

(C 1-6 )alkyl substituted by one or more of

hydroxy,

methoxy,

halogen, or

(C 3-6 )cycloalkyl, or

R 1 and R 2 together with the nitrogen atom to which they are attached form a 5 to 7 membered heterocyclic ring containing at least 1 nitrogen atom or 1 nitrogen and 1 additional heteroatom selected from N or O, or

R 1 is hydroxy and R 2 is formyl;

R 3 is OH, OR 4 , or a halogen atom, or

R 3 is bound to 2′ and R 3 represents —O—(CH 2 ) p —O— with p being 2 or 3; and

R 4 is unsubstituted (C 1-6 )alkyl or (C 3-6 )cycloalkyl,

or a pharmaceutically acceptable salt, solvate, prodrug or metabolite thereof.

2 . The method according to claim 1 , wherein the compound or the pharmaceutically acceptable salt, solvate, prodrug or metabolite thereof is selected from formulae (II), (III), (IV), (V), and (VI)

wherein in each formula, n, R 1 and R 2 are defined as in claim 1 , and their pharmaceutically acceptable salts, solvates, prodrugs or metabolites.

3 . The method according to claim 1 , wherein the compound or the pharmaceutically acceptable salt, solvate, prodrug or metabolite thereof is selected from

14-O-{[(1R, 2R, 4R)-4-Amino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin;

14-O-{[(1S, 2S, 4S)-4-Amino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin;

14-O-{[(1R, 2R, 5S)-5-Amino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin;

14-O-{[(1S, 2S, 5R)-5-Amino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin;

14-O-{[(1R, 2R, 4S)-4-Amino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 4R) diastereomer thereof;

14-O-{[(1R, 2R, 5R)-5-Amino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin;

14-O-{[(1S, 2S, 5S)-5-Amino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin;

14-O-{[(1R, 2R, 3R)-3-Amino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 3S) diastereomer thereof;

14-O-{[(1R, 2R, 4R)-4-Diethylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 4S) diastereomer thereof;

14-O-{[(1R, 2R, 4R)-4-Ethylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 4S) diastereomer thereof;

14-O-{[(1R, 2R, 5S)-5-Ethylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 5R) diastereomer thereof;

14-O-{[(1R, 2R, 5S)-5-Diethylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 5R) diastereomer thereof;

14-O-{[(1R, 2R, 4S)-4-Diethylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 4R) diastereomer thereof;

14-O-{[(1R, 2R, 5R)-5-Diethylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 5S) diastereomer thereof;

14-O-{[(1R, 2R, 3R)-3-Ethylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 3S) diastereomer thereof;

14-O-{[(1R, 2R, 3R)-3-Diethylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 3S) diastereomer thereof;

14-O-{[(1R, 2R, 4S)-4-(Formyl-hydroxy-amino)-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 4R) diastereomer thereof;

14-O-{[(1R, 2R, 5S)-5-(Formyl-hydroxy-amino)-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 5R) diastereomer thereof;

14-O-{[(1R, 2R, 3R/S)-3-(Formyl-hydroxy-amino)-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 3R/S) diastereomer thereof;

14-O-{[(1R, 2R, 5S)-2-Hydroxy-5-methylamino-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 5R) diastereomer thereof;

14-O-{[(1R, 2R, 5S)-5-Allylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 5R) diastereomer thereof;

14-O-{[(1R, 2R, 5S)-2-Hydroxy-5-(2-methoxy-ethylamino)-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 5R) diastereomer thereof;

14-O-{[(1R, 2R, 4R*)-2-Hydroxy-4-(2-hydroxy-ethylamino)-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 4S*) diastereomer thereof;

14-O-{[(1R, 2R, 4R*)-4-Cyclohexylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 4S*) diastereomer thereof;

14-O-{[(1R, 2R, 4R*)-4-Cyclopropylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 4S*) diastereomer thereof;

14-O-{[(1R, 2R, 5S*)-4-Cyclopropylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 5R*) diastereomer thereof;

14-O-{[(1R, 2R, 4S*)-4-Cyclopropylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 4R*) diastereomer thereof;

14-O-{[(1R, 2R, 5R*)-2-Hydroxy-5-morpholin-4-yl-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 5S*) diastereomer thereof;

14-O-{[(1R, 2R, 5S*)-2-Hydroxy-5-morpholin-4-yl-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S, 5R*) diastereomer thereof;

14-O-{[(1R, 2R, 5S)-5-Amino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-19,20-dihydro-mutilin and the (1S, 2S, 5R) diastereomer thereof;

14-O-{[(1R, 2R, 5S)-5-Ethylamino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-19,20-dihydro-mutilin and the (1S, 2S, 5R) diastereomer thereof;

14-O-{[(1R, 2R, 5R)-5-Amino-2-hydroxy-cyclohexylsulfanyl]-acetyl}-19,20-dihydro-mutilin and the (1S, 2S, 5S) diastereomer thereof;

14-O-{[(1R, 2R)-4-Aminomethyl-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S) diastereomers thereof;

14-O-{[5-Amino-2-chloro-cyclohexylsulfanyl]-acetyl}-mutilin;

14-O-{[4-Amino-2-chloro-cyclohexylsulfanyl]-acetyl}-mutilin;

14-O-[(4-Amino-1-hydroxy-cyclohexylmethylsulfanyl)-acetyl]-mutilin;

14-O-{[(1R, 2R)-2-Hydroxy-5-(3-methylamino-propyl)-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S) diastereomer thereof;

14-O-{[(1R, 2R)-2-Hydroxy-4-(3-methylamino-propyl)-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S) diastereomer thereof;

14-O-{[(1R, 2R)-5-(3-Amino-propyl)-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S) diastereomer thereof;

14-O-{[(1R, 2R)-4-(3-Amino-propyl)-2-hydroxy-cyclohexylsulfanyl]-acetyl}-mutilin and the (1S, 2S) diastereomer thereof;

14-O-{[(6R, 8R)-8-Amino-1,4-dioxa-spiro[4.5]dec-6-ylsulfanyl]-acetyl}-mutilin and the (6S, 8S) diastereomer thereof;

14-O-{[4-Amino-2-methoxy-cyclohexylsulfanyl]-acetyl}-mutilin;

14-O-{[5-Amino-2-methoxy-cyclohexylsulfanyl]-acetyl}-mutilin and their pharmaceutically acceptable salts, solvates, prodrugs or metabolites.

4 . The method according to claim 1 , wherein the compound or the pharmaceutically acceptable salt, solvate, prodrug or metabolite thereof is Lefamulin or its pharmaceutically acceptable salts, solvates, prodrugs or metabolites.

5 . The method according to claim 1 , wherein the compound or the pharmaceutically acceptable salt, solvate, prodrug or metabolite thereof is in form of a salt and/or a solvate.

6 . The method according to claim 1 , wherein the compound or the pharmaceutically acceptable salt, solvate, prodrug or metabolite thereof is Lefamulin in the form as Lefamulin acetate salt.

7 . The method according to claim 1 , wherein the disease is a respiratory disease.

8 . The method according to claim 1 , wherein the disease is an acute respiratory syndrome.

9 . The method according to claim 1 , wherein the virus is a positive- or negative-sense single-stranded RNA virus.

10 . The method according to claim 1 , wherein the disease is an airborne disease.

11 .- 15 . (canceled)

16 . The method according to claim 8 , wherein the acute respiratory syndrome includes Influenza, Severe Acute Respiratory Syndrome (SARS), Middle East Respiratory Syndrome (MERS) or COVID-19.

17 . The method according to claim 9 , wherein the virus is selected from Coronaviridae, Paramyxoviridae, Orthomyxoviridae, Flaviviridae, and Picornaviridae.

18 . The method according to claim 17 , wherein the Coranaviridae is human coronavirus.

19 . The method according to claim 17 , wherein the Paramyxoviridae is Paramyxovirinae or Pneumovirinae.

20 . The method according to claim 19 , wherein the Paramyxovirinae is Measles virus.

21 . The method according to claim 19 , wherein the Pneumovirinae is Respiratory Syncytial Virus.

22 . The method according to claim 17 , wherein the Orthomyxoviridae is Influenza virus.

23 . The method according to claim 17 , wherein the Flaviviridae is Dengue virus or Zika virus.

24 . The method according to claim 17 , wherein the Picornaviridae is Rhinovirus.

Assignments (3)
NUNC PRO TUNC ASSIGNMENT Recorded Apr 3, 2025
From: NABRIVA THERAPEUTICS GMBH
To: HONG KONG KING-FRIEND INDUSTRIAL COMPANY LTD.
Reel/Frame 070725/0291 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 9, 2025
From: NABRIVA THERAPEUTICS GMBH
To: HONG KONG KING-FRIEND INDUSTRIAL COMPANY LTD.
Reel/Frame 069806/0458 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 5, 2023
From: PAUKNER, SUSANNE; WICHA, WOLFGANG; GELONE, STEVEN PETER; ASCHER, GERD; RIEDL, ROSEMARIE
To: NABRIVA THERAPEUTICS GMBH
Reel/Frame 063854/0225 →