IP Library Granted Patent US 9,512,073
Granted Patent B2
US 9,512,073 · App. 13/662,002 · Granted Dec 6, 2016

Amino acid-, peptide-and polypeptide-lipids, isomers, compositions, and uses thereof

Inventors: Yizhou Dong (Dublin, OH); Kevin Thomas Love (Boston, MA); Robert S. Langer (Newton, MA); Daniel Griffith Anderson (Framingham, MA); Delai Chen (Cambridge, MA); Yi Chen (Cambridge, MA); Arturo Jose Vegas (Belmont, MA); Akinleye C. Alabi (Ithaca, NY); Yunlong Zhang (Cambridge, MA)
Assignee: Massachusetts Institute of Technology
C07C323/58C07C229/12C07C229/22C07C229/24C07C229/26C07C229/36C07C237/08C07C237/12C07C271/22C07C279/14C07D207/16C07D209/20C07D209/24C07D233/64C07D241/08C07D265/32C07D403/06C07D413/06C07D487/04C07D487/06C12N15/87C12N15/88C12Q1/025G01N33/15
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,512,073
App. No.
13/662,002
Granted
Dec 6, 2016
Kind
B2
Abstract

Described herein are compounds and compositions characterized, in certain embodiments, by conjugation of various groups, such as lipophilic groups, to an amino or amide group of an amino acid, a linear or cyclic peptide, a linear or cyclic polypeptide, or structural isomer thereof, to provide compounds of the present invention, collectively referred to herein as “APPLs”. Such APPLs are deemed useful for a variety of applications, such as, for example, improved nucleotide delivery. Exemplary APPLs include, but are not limited to, compounds of Formula (I), (II), (III), (IV), (V), and (VI), and salts thereof, as described herein: wherein m, n, p, R′, R 1 , R 2 , R 3 , R 4 , R 5 , R 8 , Z, W, Y, and Z are as defined herein.

Claims (83)

1. A compound of Formula (III):

or salt thereof;

wherein:

p is an integer of between 1 and 9, inclusive;

each instance of Q is independently O, S, or NR Q , wherein R Q is hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, optionally substituted heteroaryl, a nitrogen protecting group, or a group of the formula (i), (ii), or (iii);

each instance of R 1 is independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, optionally substituted heteroaryl, halogen, —OR A1 , —N(R A1 ) 2 , —SR A1 , or a group of formula (iv); wherein each occurrence of R A1 is independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, optionally substituted heteroaryl, an oxygen protecting group when attached to an oxygen atom, a sulfur protecting group when attached to an sulfur atom, a nitrogen protecting group when attached to a nitrogen atom, or two R A1 groups are joined to form an optionally substituted heterocyclic or optionally substituted heteroaryl ring;

provided least one instance of R 1 is a group of formula:

L is an optionally substituted alkylene, optionally substituted alkenylene, optionally substituted alkynylene, optionally substituted heteroalkylene, optionally substituted heteroalkenylene, optionally substituted heteroalkynylene, optionally substituted carbocyclylene, optionally substituted heterocyclylene, optionally substituted arylene, or optionally substituted heteroarylene;

R 6 and R 7 are each independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, optionally substituted heteroaryl, a nitrogen protecting group, or a group of the formula (i), (ii), or (iii);

each instance of R 2 is independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, optionally substituted heteroaryl, a nitrogen protecting group, or a group of the formula (i), (ii), or (iii); and

Formulae (i), (ii), and (iii) are:

wherein:

each instance of formula (i) is independently formula (i-a) or formula (i-b):

each instance of R′ is independently hydrogen or optionally substituted alkyl;

X is O, S, or NR X , wherein R X is hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, optionally substituted heteroaryl, or a nitrogen protecting group;

Y is O, S, or NR Y , wherein R Y is hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, optionally substituted heteroaryl, or a nitrogen protecting group;

R P is hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, optionally substituted heteroaryl, an oxygen protecting group when attached to an oxygen atom, a sulfur protecting group when attached to a sulfur atom, or a nitrogen protecting group when attached to a nitrogen atom; and

R L is optionally substituted C 6-50 alkyl, optionally substituted C 6-50 alkenyl, optionally substituted C 6-50 alkynyl, optionally substituted heteroC 6-50 alkyl optionally substituted heteroC 6-50 alkenyl, optionally substituted heteroC 6-50 alkynyl, or a polymer;

provided that at least one instance of R Q , R 2 , R 6 , or R 7 is a group of the formula (i), (ii), or (iii).

2. The compound of claim 1 , wherein each instance of Q is O.

3. The compound of claim 1 , wherein at least one instance of R 2 is hydrogen.

4. The compound of claim 1 , wherein each instance of R 1 is a group of formula (iv).

5. The compound of claim 1 , wherein L is an optionally substituted alkylene.

6. The compound of claim 1 , wherein the group of formula (iv) is of formula:

wherein q is an integer between 1 and 50, inclusive.

7. The compound of claim 1 , wherein the compound is selected from the group consisting of:

and salts thereof.

8. The compound of claim 1 , wherein the compound is selected from the group consisting of:

and salts thereof.

9. A composition comprising a compound of claim 1 or salt thereof, and an excipient.

10. The composition of claim 9 , wherein the composition is a pharmaceutical composition, a cosmetic composition, a nutraceutical composition, or a composition with non-medical application.

11. The compound of claim 1 , wherein at least one instance of R Q , R 2 , R 6 , or R 7 is a group of the formula (i), and further provided neither R Q , R 2 , R 6 , nor R 7 is a group of the formula (ii) or (iii).

12. The compound of claim 1 , wherein at least one instance of R Q , R 2 , R 6 , or R 7 is a group of the formula (ii), and further provided neither R Q , R 2 , R 6 , nor R 7 is a group of the formula (i) or (iii).

13. The compound of claim 1 , wherein at least one instance of R Q , R 2 , R 6 , or R 7 is a group of the formula (iii), and further provided neither R Q , R 2 , R 6 , nor R 7 is a group of the formula (i) or (ii).

14. The compound of claim 1 , wherein the compound is selected from the group consisting of:

and salts thereof,

wherein:

R 1 is selected from the group consisting of —H, —CH 3 , —CH(CH 3 ) 2 , —CH(CH 3 )(CH 2 CH 3 ), —CH 2 CH(CH 3 ) 2 ,

provided at least one R 1 is a group of formula:

and

R 6 and R 7 are each independently selected from the group consisting of hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, optionally substituted carbocyclyl, optionally substituted heterocyclyl, optionally substituted aryl, optionally substituted heteroaryl, a nitrogen protecting group when attached to a nitrogen atom, an oxygen protecting group when attached to an oxygen atom, a sulfur protecting group when attached to a sulfur atom, and a group of formula (i), (ii), or (iii).

15. The compound of claim 1 , wherein p is 1.

16. The compound of claim 14 , wherein p is 1.

17. The compound of claim 1 , wherein at least one instance of R 6 or R 7 is a group of the formula (i), (ii), or (iii).

18. The compound of claim 14 , wherein at least one instance of R 6 or R 7 is a group of the formula (i), (ii), or (iii).

19. The compound of claim 1 , wherein R L is optionally substituted C 6-20 alkyl, optionally substituted C 6-20 alkenyl, optionally substituted C 6-20 alkynyl, optionally substituted heteroC 6-20 alkyl, optionally substituted heteroC 6-20 alkenyl, or optionally substituted heteroC 6-20 alkynyl.

20. The compound of claim 19 , wherein R L is optionally substituted C 6-20 alkyl.

21. The compound of claim 20 , wherein R L is unsubstituted C 6-20 alkyl.

22. The compound of claim 1 , wherein each instance of R 1 is independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, or a group of formula (iv), provided at least one instance of R 1 is a group of formula:

23. The compound of claim 22 , wherein the group of formula (iv) is of formula:

wherein q is an integer between 1 and 10, inclusive.

24. The compound of claim 23 , wherein q is 4.

25. The compound of claim 1 , wherein each instance of R 2 is independently hydrogen or a group of the formula (i), (ii), or (iii).

26. The compound of claim 1 , wherein X is NR X , wherein R X is hydrogen, optionally substituted alkyl, or a nitrogen protecting group.

27. The compound of claim 1 , wherein X is O.

28. The compound of claim 1 , wherein X is S.

29. The compound of claim 1 , wherein Y is O.

30. The compound of claim 29 , wherein R P is hydrogen or an oxygen protecting group.

31. The compound of claim 1 , wherein:

optionally substituted refers to a carbon atom of a group which may be unsubstituted or independently substituted with halogen, —CN, —NO 2 , —N 3 , —SO 2 H, —SO 3 H, —OH, —OR aa , —N(R bb ) 2 , —SH, —SR aa , —SSR cc , —C(═O)R aa , —CO 2 H, —CHO, —CO 2 R aa , —OC(═O)R aa , —OCO 2 R aa , —C(═O)N(R bb ) 2 , —OC(═O)N(R bb ) 2 , —NR bb C(═O)R aa , —R bb CO 2 R aa , —NR bb C(═O)N(R bb ) 2 , —C(═O)NR bb SO 2 R aa , —NR bb SO 2 R aa , —SO 2 N(R bb ) 2 , —SO 2 R aa , —SO 2 OR aa , —OSO 2 R aa , —S(═O)R aa , —OS(═O)R aa , —Si(R aa ) 3 , C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 3-10 carbocyclyl, 3-14 membered heterocyclyl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, C 6-14 aryl, or 5-14 membered heteroaryl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, wherein each alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl, and heteroaryl is independently substituted with 0, 1, 2, 3, 4, or 5 R dd groups; or two geminal hydrogens of the carbon atom are replaced with the group ═O, ═S, or ═NR bb ;

or refers to a nitrogen atom of a group which may be unsubstituted or independently substituted with —OH, —OR aa , —C(═O)R aa , —C(═O)N(R cc ) 2 , —CO 2 R aa , —SO 2 R aa , C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 3-10 carbocyclyl, 3-14 membered heterocyclyl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, C 6-14 aryl, and 5-14 membered heteroaryl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, or two R cc groups attached to an N atom are joined to form a 3-14 membered heterocyclyl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen or 5-14 membered heteroaryl ring having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, wherein each alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl, and heteroaryl is independently substituted with 0, 1, 2, 3, 4, or 5 R dd groups;

each of R aa is independently C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 3-10 carbocyclyl, 3-14 membered heterocyclyl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, C 6-14 aryl, and 5-14 membered heteroaryl, or two R aa groups are joined to form a 3-14 membered heterocyclyl or 5-14 membered heteroaryl ring having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, wherein each alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl, and heteroaryl is independently substituted with 0, 1, 2, 3, 4, or 5 R dd groups;

each of R bb is independently hydrogen, —OH, —OR aa , —N(R cc ) 2 , —CN, —C(═O)R aa , —C(═O)N(R cc ) 2 , —CO 2 R aa , —SO 2 R aa , —SO 2 N(R cc ) 2 , —SO 2 R cc , —SO 2 OR cc , —SOR aa , C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 3-10 carbocyclyl, 3-14 membered heterocyclyl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, C 6-14 aryl, or 5-14 membered heteroaryl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, or two R bb groups are joined to form a 3-14 membered heterocyclyl or 5-14 membered heteroaryl ring, wherein each alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl, and heteroaryl is independently substituted with 0, 1, 2, 3, 4, or 5 R dd groups;

each of R cc is independently hydrogen, C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 3-10 carbocyclyl, 3-14 membered heterocyclyl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, C 6-14 aryl, or 5-14 membered heteroaryl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, or two R cc groups are joined to form a 3-14 membered heterocyclyl or 5-14 membered heteroaryl ring, wherein each alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl, and heteroaryl is independently substituted with 0, 1, 2, 3, 4, or 5 R dd groups;

each of R dd is independently halogen, —CN, —NO 2 , —N 3 , —SO 2 H, —SO 3 H, —OH, —OR ee , —N(R ff ) 2 , —SH, —SR ee , —SSR ee , —C(═O)R ee , —CO 2 H, —CO 2 R ee , —OC(═O)R ee , —OCO 2 R ee , —C(═O)N(R ff ) 2 , —OC(═O)N(R ff ) 2 , —NR ff C(═O)R ee , —NR ff CO 2 R ee , —NR ff C(═O)N(R ff ) 2 , —NR ff SO 2 R ee , —SO 2 N(R ff ) 2 , —SO 2 R ee , —SO 2 OR ee , —OSO 2 R ee , —S(═O)R ee , —Si(R ee ) 3 , C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 3-10 carbocyclyl, 3-10 membered heterocyclyl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, C 6-10 aryl, 5-10 membered heteroaryl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, wherein each alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl, and heteroaryl is independently substituted with 0, 1, 2, 3, 4, or 5 R gg groups, or two geminal R dd substituents can be joined to form ═O;

each of R ee is independently C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 3-10 carbocyclyl, C 6-10 aryl, 3-10 membered heterocyclyl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, and 5-10 membered heteroaryl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, wherein each alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl, and heteroaryl is independently substituted with 0, 1, 2, 3, 4, or 5 R gg groups;

each of R ff is independently hydrogen, C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 3-10 carbocyclyl, 3-10 membered heterocyclyl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, C 6-10 aryl and 5-10 membered heteroaryl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, or two R ff groups are joined to form a 3-14 membered heterocyclyl or 5-14 membered heteroaryl ring, wherein each alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aryl, and heteroaryl is independently substituted with 0, 1, 2, 3, 4, or 5 R gg groups;

each of R gg is independently halogen, —CN, —NO 2 , —N 3 , —SO 2 H, —SO 3 H, —OH, —OC 1-10 alkyl, —N(C 1-10 alkyl), —SH, —SC 1-10 alkyl, —SS(C 1-10 alkyl), —C(═O)(C 1-10 alkyl), —CO 2 H, —CO 2 (C 1-10 alkyl), —OC(═O)(C 1-10 alkyl), —OCO 2 (C 1-10 alkyl), —C(═O)NH 2 , —C(═O)N(C 1-10 alkyl) 2 , —OC(═O)NH(C 1-10 alkyl), —NHC(═O)(C 1-10 alkyl), —N(C 1-10 alkyl)C(═O)(C 1-10 alkyl), —NHCO 2 (C 1-10 alkyl), —NHC(═O)N(C 1-10 alkyl), —NHC(═O)NH(C 1-10 alkyl), —NHC(═O)NH 2 , —NHSO 2 (C 1-10 alkyl), —SO 2 N(C 1-10 alkyl), —SO 2 NH(C 1-10 alkyl), —SO 2 NH 2 , —SO 2 C 1-10 alkyl, —SO 2 OC 1-10 alkyl, —OSO 2 C 1-6 alkyl, —SOC 1-6 alkyl, —Si(C 1-10 alkyl) 3 , C 1-10 alkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 3-10 carbocyclyl, C 6-10 aryl, 3-10 membered heterocyclyl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen, 5-10 membered heteroaryl having ring carbon atoms and 1-4 ring heteroatoms selected from oxygen, sulfur, and nitrogen; or two geminal R gg substituents can be joined to form ═O;

a nitrogen protecting group is selected from the group consisting of —OH, —OR aa , —N(R cc ) 2 , —C(═O)R aa , —C(═O)N(R cc ) 2 , —CO 2 R aa , —SO 2 R aa , —C(═NR cc )R aa , —C(═NR cc )OR aa , —C(═NR cc )N(R cc ) 2 , —SO 2 N(R cc ) 2 , —SO 2 R cc , —SO 2 OR cc , —SOR aa , —C(═S)N(R cc ) 2 , —C(═O)SR cc , —C(═S)SR cc , C 1-10 alkyl, aralkyl, heteroaralkyl, C 2-10 alkenyl, C 2-10 alkynyl, C 3-10 carbocyclyl, 3-14 membered heterocyclyl, C 6-14 aryl, and 5-14 membered heteroaryl groups, wherein each alkyl, alkenyl, alkynyl, carbocyclyl, heterocyclyl, aralkyl, aryl, and heteroaryl is independently substituted with 0, 1, 2, 3, 4, or 5 R dd groups; and

an oxygen protecting group and a sulfur protecting group are independently selected from the group consisting of —R aa , —N(R bb ) 2 , —C(═O)SR aa , —C(═O)R aa , —CO 2 R aa , —C(═O)N(R bb ) 2 , —C(═NR bb )R aa , —C(═NR bb )OR aa , —C(═NR bb )N(R bb ) 2 , —S(═O)R aa , —SO 2 R aa , and —Si(R aa ) 3 .

32. The compound of claim 31 , wherein:

p is 1;

Q is O;

each instance of R 1 is independently hydrogen, optionally substituted alkyl, optionally substituted alkenyl, optionally substituted alkynyl, or a group of formula (iv), provided at least one instance of R 1 is a group of formula:

L is an optionally substituted alkylene, optionally substituted alkenylene, optionally substituted alkynylene, optionally substituted heteroalkylene, optionally substituted heteroalkenylene, or optionally substituted heteroalkynylene;

R 6 and R 7 are each independently hydrogen or a group of formula (i) or (ii), provided at least one instance of R 6 and R 7 is a group of formula (i) or (ii);

each instance of R 2 is independently hydrogen or a group of the formula (i) or (ii);

X is O, S, or NR X , wherein R X is hydrogen, optionally substituted alkyl, or a nitrogen protecting group;

Y is O;

R P is hydrogen or an oxygen protecting group; and

R L is optionally substituted C 6-20 alkyl, optionally substituted C 6-20 alkenyl, optionally substituted C 6-20 alkynyl, optionally substituted heteroC 6-20 alkyl, optionally substituted heteroC 6-20 alkenyl, or optionally substituted heteroC 6-20 alkynyl.

33. The compound of claim 8 , wherein the compound is:

or salt thereof.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 20, 2013
From: DONG, YIZHOU; LOVE, KEVIN THOMAS; LANGER, ROBERT S., SC.D; ANDERSON, DANIEL GRIFFITH; CHEN, DELAI; CHEN, YI; VEGAS, ARTURO JOSE; ALABI, AKINLEYE; ZHANG, YUNLONG
To: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
Reel/Frame 029836/0495 →
CONFIRMATORY LICENSE Recorded Nov 15, 2012
From: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 029302/0789 →
Continuity (2)
Provisional Application 61552423 · Oct 27, 2011
Related Publication 20130158021A1 · Jun 20, 2013