IP Library Granted Patent US 12,622,975
Granted Patent B2
US 12,622,975 · App. 17/761,496 · Granted May 12, 2026

Peptide-conjugated prodrugs

Inventors: Bing Xu (Newton, MA); Jiaqing Wang (Waltham, MA)
Assignee: BRANDEIS UNIVERSITY
A61K47/64A61P31/04
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Quick Facts
Patent No.
US 12,622,975
App. No.
17/761,496
Granted
May 12, 2026
Kind
B2
Abstract

The present disclosure relates to a conjugated prodrug comprising a peptide conjugated to an antibiotic molecules via a cleavable linker and pharmaceutical compositions thereof. Also disclosed are methods of enhancing the intracellular concentration of an antibiotic agent in a bacterium and methods of treating a patient for a bacterial infection.

Claims (30)

1 . A conjugated prodrug comprising:

a peptide comprising two to four amino acids, which peptide is conjugated to an antibiotic molecule via a cleavable linker, wherein:

(i) the peptide is selected from the group consisting of Gly-Gly, Gly-Gly-Gly, Gly-(D-Leu), Gly-(D-Ala), Gly-(D-Ser), Gly-Gly-Gly-Gly (SEQ ID NO: 1), Gly-Gly-(D-Phe), Gly-Gly-Phe, Gly-Phe-Gly, Gly-Gly-(D-Phe)-(D-Phe), Gly-Gly-Phe-Phe (SEQ ID NO: 3), Gly-Lys, and Gly-Asp;

(ii) the antibiotic molecule is not an aminoglycoside; and

(iii) wherein the cleavable linker forms an ester bond with the antibiotic molecule.

2 . The conjugated prodrug according to claim 1 , wherein the peptide is Gly-Gly-Gly-Gly (SEQ ID NO: 1), Gly-Gly-(D-Phe) (D-Phe), or Gly-Gly-Phe-Phe (SEQ ID NO: 3).

3 . The conjugated prodrug according to claim 1 , wherein the peptide is Gly-Gly, Gly-Gly-Gly, Gly-(D-Leu), Gly-(D-Ala), Gly-(D-Ser), Gly-Gly-(D-Phe), Gly-Gly-Phe, Gly-Phe-Gly, Gly-Lys, or Gly-Asp.

4 . The conjugated prodrug according to claim 1 , wherein the peptide is Gly-(D-Leu), Gly-(D-Ala), Gly-(L-Ser), Gly-Gly-(L-Phe), or Gly-Gly-(L-Phe)-(L-Phe).

5 . The conjugated prodrug according to claim 1 , wherein the peptide comprises a glycine residue covalently attached to the cleavable linker.

6 . The conjugated prodrug according to claim 1 , wherein the antibiotic molecule is selected from the group consisting of aminocoumarins, β-lactams, macrolides, ketolides, lincosamides, streptogramins, quinolones, rifamycins, tetracyclines, oxazolidinones, glycylcycline, amphenicals, and polymyxins.

7 . The conjugated prodrug according to claim 6 , wherein the antibiotic molecule is selected from the group consisting of chloramphenicol, N-(2-hydroxyacetyl)-ciprofloxacin, novobiocin, and benzylpenicillin (penicillin G).

8 . The conjugated prodrug according to claim 1 , wherein the antibiotic molecule is an efflux pump inhibitor.

9 . The conjugated prodrug according to claim 1 , wherein the cleavable linker is selected from the group consisting of:

—C(O)—(CH 2 ) n —C(O)— where n is an integer from 1 to 14,

—C(O)—(CH 2 ) m —CH═CH—C(O)— where m is an integer from 1 to 10,

—C(O)—CH—CH—C(O)—,

—C(O)-(1,2-cyclohexyl)-C(O)—,

—C(O)—Ar—C(O)— where Ar is a phenyl group, naphthyl group, or multi-ring aromatic group,

—C(O)—(CH 2 ) n —C(O)—(CH 2 ) q —C(O)—where n is an integer from 1 to 14 and q is from 1 to 10,

—C(O)—(CH 2 ) m —CH═CH—C(O)—(CH 2 ) q —C(O)—where m is an integer from 1 to 14 and q is from 1 to 10,

—C(O)—CH═CH—C(O)—(CH 2 ) q —C(O)—where q is an integer from 1 to 10,

—C(O)-(1,2-cyclohexyl)-C(O)—(CH 2 ) q —C(O)—where q is an integer from 1 to 10, and

—C(O)—Ar—C(O)—(CH 2 ) q —C(O)—where Ar is a phenyl group, naphthyl group, or multi-ring aromatic group and q is an integer from 1 to 10.

10 . The conjugated prodrug according to claim 1 , which is selected from the group consisting of:

wherein n is an integer from 1 to 14, q is an integer from 1 to 10, and Z is the peptide.

11 . The conjugated prodrug according to claim 10 , wherein the peptide comprises a glycine residue covalently attached to the cleavable linker.

12 . The conjugated prodrug according to claim 1 , wherein the cleavable linker is —C(O)—(CH 2 ) n —C(O)—, where n is an integer from 1 to 14.

13 . A pharmaceutical composition comprising a pharmaceutically acceptable carrier and a conjugated prodrug according to claim 1 .

14 . A method of enhancing intracellular concentration of an antibiotic agent in a bacterium, the method comprising:

contacting a bacterium with an effective amount of the conjugated prodrug according to claim 1 , whereby said conjugated prodrug is taken up by the bacterium and said linker is cleaved intracellularly to release the antibiotic agent from said prodrug, causing an increase in the intracellular concentration of the antibiotic agent.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 9, 2022
From: XU, BING; WANG, JIAQING
To: BRANDEIS UNIVERSITY
Reel/Frame 062037/0347 →
Continuity (2)
Provisional Application 62902371 · Sep 18, 2019
Related Publication 20220387610A1 · Dec 8, 2022
References Cited (11)
US 20170348337A1 · Schmidt et al. · 2017 [cited by applicant]
WO WO2016025627A1 · 2016 [cited by examiner]
International Search Report and Written Opinion for corresponding Application No. PCT/US2020/051410 (mailed Feb. 4, 2021). [cited by applicant]
Weitz et al., “Functional and Structural Characterization of a Prokaryotic Peptide Transporter with Features Similar to Mammalian PEPT1,” J. Biol. Chem. 282(5):2832-2839 (2007). [cited by applicant]
Garai et al., “Bacterial Peptide Transporters: Messengers of Nutrition to Virulence,” Virulence 8(3):297-309 (2017). [cited by applicant]
Prabhala et al., “The Prototypical Proton-Coupled Oligopeptide Transporter YdgR from [cited by applicant]
Li et al., “The Challenge of Efflux-mediated Antibiotic Resistance in Gram-negative Bacteria,” Clin. Microbiol. Rev. 28:337-418 (2015). [cited by applicant]
Zhou et al., “Taurine Boosts Cellular Uptake of Small D-Peptides for Enzyme-Instructed Intracellular Molecular Self-Assembly,” J. Am. Chem. Soc. 137(32):10040-10043 (2015). [cited by applicant]
Li et al., “Enzyme-Instructed Intracellular Molecular Self-Assembly to Boost Activity of Cisplatin Against Drug-Resistant Ovarian Cancer Cells,” Angew. Chem. Int. Ed. 54(45):13307-13311 (2015). [cited by applicant]
Li et al., “Selectively Inducing Cancer Cell Death by Intracellular Enzyme-Instructed Self-Assembly (EISA) of Dipeptide Derivatives,” Adv. Healthc. Mater. 6(15):1601400 (2017). [cited by applicant]
Chen et al., “Bacteria-Targeting Conjugates Based on Antimicrobial Peptide for Bacteria Diagnosis and Therapy,” Mol. Pharm. 12(7):2505-2516 (2015). [cited by applicant]