Linker Architectures as Steric Auxiliaries for Altering Enzyme-Mediated Payload Release from Bioconjugates-Reference-Cited by-同舟云学术

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Linker Architectures as Steric Auxiliaries for Altering Enzyme-Mediated Payload Release from Bioconjugates

Published:2021-09-29 Issue:10 Volume:32 Page:2257-2267
ISSN:1043-1802
Container-title:Bioconjugate Chemistry
language:en
Short-container-title:Bioconjugate Chem.

Author:

Giese Matthew¹^ORCID,Davis Paul D.¹,Woodman Robert H.¹,Hermanson Greg¹,Pokora Alex¹,Vermillion Melissa¹

Affiliation:

1. Quanta BioDesign, 7470 Montgomery Drive, Plain City, Ohio 43064, United States

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Pharmaceutical Science,Pharmacology,Biomedical Engineering,Bioengineering,Biotechnology

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.bioconjchem.1c00429

Reference48 articles.

1. The multifaceted roles of tumor-associated proteases and harnessing their activity for prodrug activation

2. Protease-Activated Drug Development

3. Harnessing albumin as a carrier for cancer therapies

4. Unlocking the potential of antibody–drug conjugates for cancer therapy

5. The Chemistry Behind ADCs

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. AJICAP-M: Traceless Affinity Peptide Mediated Conjugation Technology for Site-Selective Antibody–Drug Conjugate Synthesis;Organic Letters;2024-04-19

2. Biological Evaluation of Antibody-Drug Conjugates Produced by Tag-Free Lipoate Ligase A Modification;Biochemistry;2024-02-13

3. Novel formats of antibody conjugates: recent advances in payload diversity, conjugation, and linker chemistry;Expert Opinion on Biological Therapy;2023-11-02

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