Mycobacterium tuberculosis cell-wall and antimicrobial peptides: a mission impossible?

YM Jacobo-Delgado, A Rodríguez-Carlos… - Frontiers in …, 2023 - frontiersin.org
Mycobacterium tuberculosis (Mtb) is one of the most important infectious agents worldwide
and causes more than 1.5 million deaths annually. To make matters worse, the drug …

Therapeutic Potential of Marine-Derived Cyclic Peptides as Antiparasitic Agents

R Ribeiro, L Costa, E Pinto, E Sousa, C Fernandes - Marine Drugs, 2023 - mdpi.com
Parasitic diseases still compromise human health. Some of the currently available
therapeutic drugs have limitations considering their adverse effects, questionable efficacy …

BacPROTACs mediate targeted protein degradation in bacteria

FE Morreale, S Kleine, J Leodolter, S Junker, DM Hoi… - Cell, 2022 - cell.com
Hijacking the cellular protein degradation system offers unique opportunities for drug
discovery, as exemplified by proteolysis-targeting chimeras. Despite their great promise for …

Clp-targeting BacPROTACs impair mycobacterial proteostasis and survival

DM Hoi, S Junker, L Junk, K Schwechel, K Fischel… - Cell, 2023 - cell.com
Summary The ClpC1: ClpP1P2 protease is a core component of the proteostasis system in
mycobacteria. To improve the efficacy of antitubercular agents targeting the Clp protease …

Synthesis and Applications of Periodate for Fine Chemicals and Important Pharmaceuticals

S Arndt, PJ Kohlpaintner, K Donsbach… - … Process Research & …, 2022 - ACS Publications
An emerging interest for the application of periodate in the synthesis of active
pharmaceutical ingredients (APIs) and for the valorization of renewable feedstock is …

Total synthesis of apratoxin A and B using Matteson's homologation approach

O Andler, U Kazmaier - Organic & Biomolecular Chemistry, 2021 - pubs.rsc.org
Apratoxin A and B, two members of an interesting class of marine cyclodepsipeptides are
synthesized in a straightforward manner via Matteson homologation. Starting from a chiral …

Homo-BacPROTAC-induced degradation of ClpC1 as a strategy against drug-resistant mycobacteria

L Junk, VM Schmiedel, S Guha, K Fischel… - Nature …, 2024 - nature.com
Antimicrobial resistance is a global health threat that requires the development of new
treatment concepts. These should not only overcome existing resistance but be designed to …

Total Synthesis and Biological Evaluation of Modified Ilamycin Derivatives

J Greve, A Mogk, U Kazmaier - Marine Drugs, 2022 - mdpi.com
Ilamycins/rufomycins are marine cycloheptapeptides containing unusual amino acids.
Produced by Streptomyces sp., these compounds show potent activity against a range of …

Recent developments on the synthesis and bioactivity of ilamycins/rufomycins and cyclomarins, marine cyclopeptides that demonstrate anti-malaria and anti …

U Kazmaier, L Junk - Marine Drugs, 2021 - mdpi.com
Ilamycins/rufomycins and cyclomarins are marine cycloheptapeptides containing unusual
amino acids. Produced by Streptomyces sp., these compounds show potent activity against …

Steglich esterification: A versatile synthetic approach toward the synthesis of natural products, their analogues/derivatives

S Munawar, AF Zahoor, SM Hussain, S Ahmad… - Heliyon, 2024 - cell.com
The exploitation of natural products and their analogues in the field of pharmacology has
been regarded as of great importance. It can be attributed to the fact that these scaffolds …