IP Library Granted Patent US 10,980,890
Granted Patent B2
US 10,980,890 · App. 16/545,869 · Granted Apr 20, 2021

Compounds comprising self-immolative group

Inventors: Yong Zu Kim (Daejeon, KR); Tae Kyo Park (Daejeon, KR); Sung Ho Woo (Daejeon, KR); Sun Young Kim (Daejeon, KR); Jong Un Cho (Daejeon, KR); Doo Hwan Jung (Daejeon, KR); Ji Young Min (Daejeon, KR); Hyang Sook Lee (Daejeon, KR); Yun Hee Park (Daejeon, KR); Jeong Hee Ryu (Daejeon, KR); Kyu Man Oh (Daejeon, KR); Yeong Soo Oh (Daejeon, KR); Jeiwook Chae (Daejeon, KR); Ho Young Song (Daejeon, KR); Chul-Woong Chung (Daejeon, KR); Jeon Yang (Daejeon, KR)
Assignee: LegoChem Biosciences, Inc.
A61K47/549A61K47/50A61K47/6801A61K47/6803A61K47/6811A61K47/6813A61K47/6855A61K47/6871A61K47/6889A61K47/69C07D249/04C07D487/04C07D519/00C07K16/32C07K19/00A61K2039/505C07K2317/24C07K2317/94
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Quick Facts
Patent No.
US 10,980,890
App. No.
16/545,869
Granted
Apr 20, 2021
Kind
B2
Abstract

Provided herein are compounds comprising a self-immolative group, and the compounds comprising a self-immolative group according to the present invention may include a protein (for example, an oligopeptide, a polypeptide, an antibody, or the like) having substrate-specificity for a target and an active agent (for example, a drug, a toxin, a ligand, a detection probe, or the like) having a specific function or activity.

Claims (81)

1. A compound represented by Chemical Formula 1:

G is

wherein R 3 is hydrogen or a carboxyl protecting group, and each R 4 is independently hydrogen or a hydroxyl protecting group;

A is an antibody,

B is an active agent;

W is —C(O)NR′— wherein the C(O) is directly bound to the phenyl ring, and R′ is hydrogen or (C 1 -C 8 )alkyl;

each Z is independently hydrogen, halogen, cyano, or nitro;

n is an integer of 1 to 3;

R 1 and R 2 are each hydrogen; and

L comprises an alkylene chain having 1 to 50 carbon atoms and a binding unit represented by Chemical Formula B, C, D, or E:

L 1 is a single bond or alkylene having 1 to 30 carbon atoms;

R 11 is hydrogen or alkyl having 1 to 10 carbon atoms; and

L 2 is alkylene having 1 to 30 carbon atoms.

2. The compound of claim 1 , wherein G is

R 3 and R 4 are each hydrogen.

3. The compound of claim 1 , wherein L further comprises a connection unit represented by Chemical Formula F or G:

—(CH 2 ) r (V(CH 2 ) p ) q —  [Chemical Formula F]

—(CH 2 CH 2 X) w —  [Chemical Formula G]

V is a single bond, —O—, —S—, —NR 21 —, —C(O)NR 22 —, —NR 23 C(O)—, —NR 24 SO 2 —, or —SO 2 NR 25 —;

X is —O—, (C 1 -C 8 )alkylene, or —NR 21 —;

R 21 to R 25 are each independently hydrogen, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkyl(C 6 -C 20 )aryl, or (C 1 -C 6 )alkyl(C 3 -C 20 )heteroaryl;

r is an integer of 1 to 10;

p is an integer of 0 to 10;

q is an integer of 1 to 10; and

w is an integer of 1 to 10.

4. The compound of claim 1 , wherein:

i) G is

wherein R 3 and R 4 are each hydrogen; and

ii) L further comprises a connection unit represented by Chemical Formula F or G:

—(CH 2 ) r (V(CH 2 ) p ) q —  [Chemical Formula F]

—(CH 2 CH 2 X) w —  [Chemical Formula G]

wherein,

V is a single bond, —O—, —S—, —NR 21 —, —C(O)NR 22 —, —NR 23 C(O)—, —NR 24 SO 2 —, or —SO 2 NR 25 —;

X is —O—, (C 1 -C 8 )alkylene, or —NR 21 —;

R 21 to R 25 are each independently hydrogen, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkyl(C 6 -C 20 )aryl, or (C 1 -C 6 )alkyl(C 3 -C 20 )heteroaryl;

r is an integer of 1 to 10;

p is an integer of 0 to 10;

q is an integer of 1 to 10; and

w is an integer of 1 to 10.

5. The compound of claim 1 , wherein:

i) G is

wherein R 3 and R 4 are each hydrogen;

ii) L further comprises a connection unit represented by Chemical Formula F or G:

—(CH 2 ) r (V(CH 2 ) p ) q —  [Chemical Formula F]

—(CH 2 CH 2 X) w —  [Chemical Formula G]

wherein,

V is a single bond, —O—, —S—, —NR 21 —, —C(O)NR 22 —, —NR 23 C(O)—, —NR 24 SO 2 —, or —SO 2 NR 25 —;

X is —O—, (C 1 -C 8 )alkylene, or —NR 21 —;

R 21 to R 25 are each independently hydrogen, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkyl(C 6 -C 20 )aryl, or (C 1 -C 6 )alkyl(C 3 -C 20 )heteroaryl;

r is an integer of 1 to 10;

p is an integer of 0 to 10;

q is an integer of 1 to 10; and

w is an integer of 1 to 10; and

iii) L further comprises at least one isoprenyl derivative unit represented by Chemical Formula A

6. The compound of claim 1 , wherein the antibody comprises an amino acid motif recognizable by an isoprenoid transferase.

7. The compound of claim 6 , wherein L further comprises at least one isoprenyl moiety represented by Chemical Formula A

8. The compound of claim 7 , wherein the antibody further comprises a spacer unit comprising an amino acid, an oligopeptide, or a polypeptide between the antibody and the amino acid motif.

9. The compound of claim 7 , wherein the antibody is covalently bonded to L through the amino acid motif.

10. The compound of claim 7 , wherein the amino acid motif is at a C-terminus of the antibody.

11. The compound of claim 10 , wherein the C-terminus of the antibody is a C-terminus of a light chain or a heavy chain of the antibody.

12. The compound of claim 7 , wherein the amino acid motif is CYYX, XXCC, XCXC, or CXX, C representing cysteine, Y representing an aliphatic amino acid, and X representing an amino acid that determines a substrate specificity of the isoprenoid transferase.

13. The compound of claim 12 , wherein the amino acid motif is (G) z CVIM (SEQ ID NO: 1) or (G) z CVLL (SEQ ID NO: 2), G representing a glycine unit, and z being an integer of 0 to 20.

14. The compound of claim 12 , wherein the isoprenoid transferase is farnesyl protein transferase (FTase) or geranylgeranyl transferase (GGTase).

15. The compound of claim 1 , wherein the antibody is selected from intact polyclonal antibodies, intact monoclonal antibodies, antibody fragments, single chain Fv (scFv) mutants, multispecific antibodies, bispecific antibodies, chimeric antibodies, humanized antibodies, human antibodies, fusion proteins including an antigen determination portion of an antibody, and other modified immunoglobulin molecules including an antigen recognition site.

16. The compound of claim 1 , wherein the antibody is a monoclonal antibody.

17. The compound of claim 1 , wherein the antibody is selected from muromonab-CD3, abciximab, rituximab, daclizumab, palivizumab, infliximab, trastuzumab, etanercept, basiliximab, gemtuzumab ozogamicin, alemtuzumab, ibritumomab tiuxetan, adalimumab, alefacept, omalizumab, efalizumab, tositumomab-I 131 , cetuximab, bevacizumab, natalizumab, ranibizumab, panitumumab, eculizumab, rilonacept, certolizumab pegol, romiplostim, belimumab, anti-CD20, tocilizumab, atlizumab, mepolizumab, pertuzumab, tremelimumab, ticilimumab, inotuzumab ozogamicin, aflibercept, catumaxomab, pregovomab, motavizumab, efumgumab, raxibacumab, and veltuzumab.

18. The compound of claim 1 , wherein the active agent is a drug, a toxin, an affinity ligand, a detection probe, or a combination thereof.

19. The compound of claim 1 , wherein the active agent is an immunomodulatory compound, an anticancer agent, an antiviral agent, an antibacterial agent, an antifungal agent, an antiparasitic agent, or a combination thereof.

20. The compound of claim 1 , wherein the compound is selected from:

wherein:

Z is hydrogen, (C 1 -C 8 )alkyl, halogen, cyano, or nitro;

X is —O—, (C 1 -C 8 )alkylene, or —NR 21 —;

R 21 is hydrogen, (C 1 -C 6 )alkyl, (C 1 -C 6 )alkyl(C 6 -C 20 )aryl, or (C 1 -C 6 )alkyl(C 3 -C 20 )heteroaryl;

n is an integer of 1 to 3, and when n is an integer of 2 or more, each of the Z(s) are the same as or different from each other;

r is an integer of 1 to 10;

q is an integer of 1 to 10;

w is an integer of 1 to 10;

x is an integer of 0 to 10;

g is an integer of 1 to 10.

21. A method of treating a disease selected from an autoimmune disorder, a cancer, a viral infection, a bacterial infection, a fungal infection, and a parasitic infection, comprising administering the compound of claim 1 .

22. The method of claim 21 , wherein the disease is cancer.

Assignments (2)
CHANGE OF NAME Recorded May 28, 2024
From: LEGOCHEM BIOSCIENCES, INC.
To: LIGACHEM BIOSCIENCES INC.
Reel/Frame 067540/0341 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 28, 2019
From: KIM, YONG ZU; PARK, TAE KYO; WOO, SUNG HO; KIM, SUN YOUNG; CHO, JONG UN; JUNG, DOO HWAN; MIN, JI YOUNG; LEE, HYANG SOOK; PARK, YUN HEE; RYU, JEONG HEE; OH, KYU MAN; OH, YEONG SOO; CHAE, JEIWOOK; SONG, HO YOUNG; CHUNG, CHUL-WOONG; YANG, JEON
To: LEGOCHEM BIOSCIENCES, INC.
Reel/Frame 050203/0082 →
Priority Claims (2)
KR 10-2014-0064360 · May 28, 2014 · national
KR 10-2015-0073161 · May 26, 2015 · national
Continuity (3)
Continuation 16005245 · Jun 11, 2018
Continuation 14898932
Related Publication 20200069816A1 · Mar 5, 2020
Cited By (8)
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