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Heterotandem bicyclic peptide complexes

a bicyclic peptide and complex technology, applied in the direction of peptides, drug compositions, peptides/protein ingredients, etc., can solve the problem of reducing the conformational flexibility of cyclic structures, and achieve the effect of preventing, suppressing or treating cancer

Pending Publication Date: 2022-09-29
BICYCLETX LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patent is about a type of peptide that can bind to both cancer cells and immune cells. This peptide can be used to prevent or treat cancer.

Problems solved by technology

Good binding properties result from a relatively large interaction surface formed between the peptide and the target as well as the reduced conformational flexibility of the cyclic structures.

Method used

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  • Heterotandem bicyclic peptide complexes
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  • Heterotandem bicyclic peptide complexes

Examples

Experimental program
Comparison scheme
Effect test

example 1

of BCY12375

[0162]

[0163]Procedure for Preparation of Palmitic Acid—PEG10-N3

[0164]A mixture of Palmitic acid (100.0 mg, 282.89 μmol, 1.0 eq.), compound 2 (150.0 mg, 284.84 μmol, 1.0 eq.), and DIEA (74.5 mg, 574.11 μmol, 100.0 μL, 2.0 eq.) was dissolved in DMF (2 mL). The reaction mixture was stirred at 30° C. for 2 hr. LC-MS showed compound 1 was consumed completely and one main peak with desired m / z (MW: 765.03, observed m / z: 765.22) was detected. The reaction mixture was concentrated under reduced pressure to remove solvent and produced a residue. The residue was then purified by prep-HPLC (neutral condition). Palmitic acid—PEG10-N3 (79.0 mg, 99.41 μmol, 35.14% yield, 96.27% purity) was obtained as a white solid.

[0165]Procedure for Preparation of Palmitic Acid—PEG10-BCY12023

[0166]A mixture of compound 3 (50.0 mg, 22.07 μmol, 1.0 eq.), compound 2 (17.0 mg, 22.22 μmol, 1.0 eq.), and THPTA (10.0 mg, 23.02 μmol, 1.0 eq.) was dissolved in t-BuOH / H2O (1:1, 1 mL, pre-degassed and purged wi...

example 2

of BCY12021

[0171]

[0172]Procedure for Preparation of Palmitic Acid—PEG10-BCY11144

[0173]A mixture of compound 3 (160.0 mg, 69.45 μmol, 1.0 eq.), compound 4 (56.0 mg, 72.20 μmol, 1.0 eq.), and THPTA (35.0 mg, 80.55 μmol, 1.1 eq.) was dissolved in t-BuOH / H2O (1:1, 2 mL, pre-degassed and purged with N2 for 3 times), and then CuSO4 (0.4 M, 56.0 μL, 1.0 eq.) and VcNa (30.0 mg, 151.43 μmol, 2.2 eq.) were added under N2. The pH of this solution was adjusted to 8 by dropwise addition of 0.2 M NH4HCO3 (in 1:1 t-BuOH / H2O), and the solution turned to light yellow. The reaction mixture was stirred at 40° C. for 16 hr under N2 atmosphere. LC-MS showed one main peak with desired m / z (calculated MW: 3068.70, observed m / z: 1533.81 ([M / 2+H]+), 1023.43 ([M / 3+H]+)) was detected. The reaction mixture was filtered and concentrated under reduced pressure to give a residue. The crude product was purified by prep-HPLC (TFA condition), and Palmitic acid—PEG10-BCY11144 (150.0 mg, 46.83 μmol, 67.42% yield, 95.8...

example 3

of BCY11468

[0178]

[0179]Procedure for Preparation of COM113

[0180]A mixture of compound 1 (50.0 mg, 124.4 μmol, 1.0 eq), EDCl (95.4 mg, 497.7 μmol, 4.0 eq), HOBt (55.5 mg, 410.6 μmol, 3.3 eq), and DMAP (15.2 mg, 124.4 μmol, 1.0 eq) was dissolved in 2 mL DMF, and then DIEA (134.9 mg, 1.04 mmol, 181.8 μL, 8.4 eq) was added to generate a homogenous solution. Next, compound 2 (200.0 mg, 379.8 μmol, 3.05 eq) dissolved in DMF (2 mL) was added to this solution dropwise. The reaction mixture was stirred at 30° C. for 16 hr. LC-MS showed compound 1 was consumed completely and one main peak with desired m / z (MW: 1891.19, observed m / z: 945.8600 ([M / 2+H+]) and 612.4400 ([(M−3H2O) / 3+H+])) was detected. The reaction mixture was directly purified by prep-HPLC (TFA condition), resulting in COM113 (161 mg, 85.67 μmol, 68% yield) as a yellow oil after lyophilization.

[0181]Procedure for Preparation of COM113-BCY8928

[0182]COM113 (50.0 mg, 26.44 μmol, 1.0 eq) and BCY8928 (53.0 mg, 23.9 μmol, 0.9 eq) were ...

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PUM

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Abstract

The present invention relates to heterotandem bicyclic peptide complexes which comprise a first peptide ligand, which binds to a component present on a cancer cell, conjugated via a linker to a second peptide ligand, which binds to a component present on an immune cell. The invention also relates to the use of said heterotandem bicyclic peptide complexes in preventing, suppressing or treating cancer.

Description

FIELD OF THE INVENTION[0001]The present invention relates to heterotandem bicyclic peptide complexes which comprise a first peptide ligand, which binds to a component present on a cancer cell, conjugated via a linker to a second peptide ligand, which binds to a component present on an immune cell. The invention also relates to the use of said heterotandem bicyclic peptide complexes in preventing, suppressing or treating cancer.CROSS REFERENCE TO RELATED APPLICATIONS[0002]This application is a divisional of U.S. patent application Ser. No. 17 / 062,662, filed on Oct. 5, 2020, which claims the benefit of U.S. Provisional Application No. 62 / 910,129, filed on Oct. 3, 2019, the entire disclosures of which are hereby incorporated herein by reference.REFERENCE TO SEQUENCE LISTING[0003]A Sequence Listing is being submitted electronically via EFS in the form of a text file, created Mar. 21, 2022, and named 189822_SL.txt (35,391 bytes), the contents of which are incorporated herein by reference...

Claims

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Application Information

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Patent Type & Authority Applications(United States)
IPC IPC(8): C07K11/02
CPCC07K11/02C07K7/08C07K14/00A61P35/00C07K2319/00A61K38/00A61K47/64A61K47/60C07K14/70578C07K14/70532C07K14/70503C07K14/715A61K47/543A61K47/545
Inventor MUDD, GEMMAUPADHYAYA, PUNITMCDONNELL, KEVIN
Owner BICYCLETX LTD
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