IP Library Granted Patent US 10,307,378
Granted Patent B2
US 10,307,378 · App. 15/827,162 · Granted Jun 4, 2019

Diester and triester based low molecular weight, biodegradeable cationic lipids for oligonucleotide delivery

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Quick Facts
Patent No.
US 10,307,378
App. No.
15/827,162
Granted
Jun 4, 2019
Kind
B2
Abstract

The instant invention provides for novel cationic lipids of Formula A that can be used in combination with other lipid components such as cholesterol and PEG-lipids to form lipid nanoparticles with oligonucleotides. It is an object of the instant invention to provide a cationic lipid scaffold that demonstrates enhanced efficacy along with lower liver toxicity as a result of lower lipid levels in the liver. The present invention employs low molecular weight cationic lipids with one short lipid chain coupled with inclusion of hydrolysable functionality in the lipid chains to enhance the efficiency and tolerability of in vivo delivery of siRNA.

Claims (34)

1. A cationic lipid of Formula A:

wherein:

R 1 and R 2 are each independently selected from the group consisting of H, (C 1 -C 6 )alkyl, heterocyclyl, and polyamine, wherein said alkyl, heterocyclyl and polyamine are optionally substituted with one to three R′;

or R 1 and R 2 can be taken together with the nitrogen to which they are attached to form a monocyclic heterocycle with 4-7 members optionally containing, in addition to the nitrogen, one or two additional heteroatoms selected from N, O and S, said monocyclic heterocycle is optionally substituted with one to three R′;

R 3 is selected from the group consisting of (C 4 -C 20 )alkyl and (C 4 -C 20 )alkenyl, said alkyl or alkenyl is optionally substituted with one to three R′;

R 4 is selected from the group consisting of (C 1 -C 16 )alkyl and (C 2 -C 16 )alkenyl, said alkyl or alkenyl is optionally substituted with one to three R′;

R 5 is selected from the group consisting of (C 4 -C 8 )alkyl and (C 4 -C 8 )alkenyl, said alkyl or alkenyl is optionally substituted with one to three R′;

R 6 is (C 1 -C 2 )alkyl optionally substituted with one to three R′;

Q 1 and Q 2 are each, independently, selected from the group consisting of a bond, —OC(O)—, —C(O)O—, —SC(O)—, —C(O)S—, —OC(S)—, —S—S—, —C(R″)═N—, —N═C(R″)—, —C(R″)═N—O—, —O—N═C(R″)—, —C(O)(NR″)—, —N(R″)C(O)—, C(S)(NR″)—, —N(R″)C(O)—, —N(R″)C(O)N(R″)—, —OC(O)O—, OSi(R″) 2 O—, —C(O)(CR″ 2 )C(O)O— and —OC(O)(CR″ 2 )C(O)—), with the proviso that when either Q 1 or Q 2 is a bond then the other is not a bond;

X is selected from the group consisting of —OC(O)—, —C(O)O—, —SC(O)—, —C(O)S—, —OC(S)—, —S—S—, —C(R″)═N—, —N═C(R″)—, —C(R″)═N—O—, —O—N═C(R″)—, —C(O)(NR″)—, —N(R″)C(O)—, C(S)(NR″)—, —N(R″)C(O)—, —N(R″)C(O)N(R″)—, —OC(O)O—, OSi(R″) 2 O—, —C(O)(CR″ 2 )C(O)O— and —OC(O)(CR″ 2 )C(O)—),

each occurrence of R′ is independently selected from the group consisting of halogen, R″, OR″, SR″, CN, CO 2 R″ or CON(R″) 2 ;

each occurrence of R″ is independently selected from the group consisting of H and (C 1 -C 6 )alkyl, wherein said alkyl is optionally substituted with halogen and OH; and

n is 1, 2, 3, 4 or 5;

or a pharmaceutically acceptable salt or stereoisomer thereof;

with the proviso that at least one of R 3 -Q 1 -R 4 or R 5 -Q 2 -R 6 is

2. A cationic lipid of Formula A according to claim 1 ,

wherein:

R 1 and R 2 are each methyl;

n is 3;

R 3 is selected from the group consisting of (C 4 -C 20 )alkyl and (C 4 -C 20 )alkenyl, said alkyl or alkenyl is optionally substituted with one to three R′;

R 4 is selected from the group consisting of (C 1 -C 16 )alkyl and (C 2 -C 16 )alkenyl, said alkyl or alkenyl is optionally substituted with one to three R′;

R 5 is selected from the group consisting of (C 4 -C 8 )alkyl and (C 4 -C 8 )alkenyl, said alkyl or alkenyl is optionally substituted with one to three R′;

R 6 is (C 1 -C 2 )alkyl optionally substituted with one to three R′;

Q 1 and Q 2 are each, independently, a bond or —C(O)O—, with the proviso that when either Q 1 or Q 2 is a bond then the other is not a bond; and

X is —C(O)O—;

or a pharmaceutically acceptable salt or stereoisomer thereof;

with the proviso that at least one of R 3 -Q 1 -R 4 or R 5 -Q 2 -R 6 is

3. A lipid nanoparticle comprising a cationic lipid of claim 1 .

4. The lipid nanoparticle of claim 3 , wherein the lipid nanoparticle further comprises an oligonucleotide.

5. The lipid nanoparticle of claim 4 , wherein the oligonucleotide is an siRNA or miRNA.

6. The lipid nanoparticle of claim 5 , wherein the oligonucleotide is an siRNA.

7. The lipid nanoparticle of claim 3 , wherein the lipid nanoparticle further comprises cholesterol and PEG-DMG.

8. The lipid nanoparticle of claim 3 , wherein the lipid nanoparticle further comprises cholesterol, PEG-DMG and DSPC.

9. The lipid nanoparticle of claim 3 , wherein the lipid nanoparticle further comprises cholesterol, PEG-C-DMA and DSPC.

Assignments (3)
SECURITY INTEREST Recorded Oct 1, 2025
From: ALNYLAM PHARMACEUTICALS, INC.; SIRNA THERAPEUTICS, INC.
To: BANK OF AMERICA, N.A.
Reel/Frame 072996/0337 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 20, 2019
From: COLLETTI, STEVEN L; STANTON, MATTHEW G
To: MERCK SHARP & DOHME CORP.
Reel/Frame 048378/0889 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 20, 2019
From: MERCK SHARP & DOHME CORP.
To: SIRNA THERAPEUTICS, INC.
Reel/Frame 048378/0895 →