IP Library Granted Patent US 9,919,057
Granted Patent B2
US 9,919,057 · App. 14/865,778 · Granted Mar 20, 2018

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); Jeon Yang (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)
Assignee: LegoChem Biosciences, Inc.
A61K47/48715A61K47/48A61K47/48384A61K47/48584C07D249/04C07K19/00
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Quick Facts
Patent No.
US 9,919,057
App. No.
14/865,778
Granted
Mar 20, 2018
Kind
B2
Abstract

Provided 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 (66)

1. A compound represented by the following Chemical Formula 1:

G is a glucuronic acid moiety or

 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)—, —C(O)NR′—, —C(O)O—, —SO 2 NR′—, —P(O)R″NR′—, —SONR′—, or —PO 2 NR′—, in each case where the C(O), S, or P is directly bound to the phenyl ring, and R′ and R″ are each independently hydrogen, (C 1 -C 8 )alkyl, (C 3 -C 8 )cycloalkyl, (C 1 -C 8 )alkoxy, (C 1 -C 8 )alkylthio, mono- or di-(C 1 -C 8 )alkylamino, (C 3 -C 20 )heteroaryl or (C 6 -C 20 )aryl;

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

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;

wherein either:

A) L is an alkylene chain having 1 to 50 carbon atoms and satisfies at least one of the following (i) to (iv):

(i) the alkylene includes at least one unsaturated bond,

(ii) the alkylene includes at least one heteroarylene,

(iii) at least one carbon atom of the alkylene is replaced with one or more hetero atoms selected from nitrogen (N), oxygen (O), and sulfur (S), and P

(iv) the alkylene is substituted with one or more alkyls having 1 to 20 carbon atoms; or

B) L includes at least one isoprenyl derivative unit represented by the following Chemical Formula A, which is recognized by an isoprenoid transferase

and

R 1 and R 2 are each independently hydrogen, (C 1 -C 8 )alkyl, or (C 3 -C 8 )cycloalkyl.

2. The compound of claim 1 , wherein G is

R 3 is hydrogen or a carboxyl protecting group, and R 4 (s) are each independently hydrogen or a hydroxyl protecting group.

3. The compound of claim 1 , wherein W is —C(O)—, —C(O)NR′—, or —C(O)O—.

4. The compound of claim 1 , wherein the linker L is an alkylene having 1 to 50 carbon atoms and satisfies at least one of the following (i) to (iv):

(i) the alkylene includes at least one unsaturated bond,

(ii) the alkylene includes at least one heteroarylene,

(iii) at least one carbon atom of the alkylene is replaced with one or more hetero atoms selected from nitrogen (N), oxygen (O), and sulfur (S), and

(iv) the alkylene is substituted with one or more alkyls having 1 to 20 carbon atoms.

5. The compound of claim 1 , wherein the linker L includes at least one isoprenyl derivative unit represented by the following Chemical Formula A, which is recognized by an isoprenoid transferase:

6. The compound of claim 5 , wherein the linker L further includes 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.

7. The compound of claim 6 , wherein the linker L further includes a connection unit represented by the following 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.

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

9. The compound of claim 8 , 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.

10. The compound of claim 8 , wherein the antibody is covalently bonded to the linker L through the amino acid motif.

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

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

13. The compound of claim 8 , wherein the isoprenoid transferase is farnesyl protein transferase (FTase) or geranylgeranyl transferase (GGTase).

14. 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.

15. The compound of claim 14 , 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.

16. The compound of claim 14 , wherein the antibody is a monoclonal antibody.

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

18. 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.

19. The compound of claim 8 , 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.

20. The compound of claim 19 , selected from compounds having the following structures:

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;

B is a drug having a structure selected from the following structures

and

y is an integer of 1 to 10.

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 Dec 11, 2015
From: KIM, YONG ZU; PARK, TAE KYO; WOO, SUNG HO; KIM, SUN YOUNG; CHO, JONG UN; JUNG, DOO HWAN; YANG, JEON; 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
To: LEGOCHEM BIOSCIENCES, INC.
Reel/Frame 037267/0232 →
Priority Claims (2)
KR 10-2014-0064360 · May 28, 2014 · national
KR 10-2015-0073161 · May 26, 2015 · national
Continuity (2)
Continuation PCTKR2015005299 · May 27, 2015
Related Publication 20160184451A1 · Jun 30, 2016