Zobrazeno 1 - 10
of 1 935
pro vyhledávání: '"peptoid"'
Autor:
Roeya Refaei, Kyueui Lee, Goun Amy Lee, Paul Demian, Fouad El Mansouri, Phillip B. Messersmith, Mouad Lamrani, Mohamed Khaddor, Nabil Allali
Publikováno v:
Journal of Functional Biomaterials, Vol 15, Iss 6, p 154 (2024)
This research evolves into a comparative study of three different phenolic composites as coatings for rigid contact lenses, with a particular emphasis on enhancing their antifouling properties and hydrophobicity. The primary layer, comprised of diver
Externí odkaz:
https://doaj.org/article/466a3885c9bb4b02ba0281bbd7902402
Autor:
Vivek Kumar, Jennifer S. Lin, Natalia Molchanova, John A. Fortkort, Carolin Reckmann, Stefan Bräse, Håvard Jenssen, Annelise E. Barron, Archana Chugh
Publikováno v:
FEBS Open Bio, Vol 13, Iss 3, Pp 519-531 (2023)
Visceral leishmaniasis (VL) is among the most neglected tropical diseases in the world. Drug cell permeability is essential for killing the intracellular residing parasites responsible for VL, making cell‐permeating peptides a logical choice to add
Externí odkaz:
https://doaj.org/article/6b75aec485214b3d80572638e6c7579d
Autor:
Kang Yang, Di Liu, Lei Feng, Liugen Xu, Yangang Jiang, Xiran Shen, Amjad Ali, Jianwei Lu, Li Guo
Publikováno v:
Polymers, Vol 16, Iss 7, p 990 (2024)
The development of nontoxic and efficient antifreeze agents for organ cryopreservation is crucial. However, the research remains highly challenging. In this study, we designed and synthesized a series of peptoid oligomers using the solid-phase submon
Externí odkaz:
https://doaj.org/article/ecb77809908d4d249085c2cdd0eb556b
Autor:
Maxim Lebedev, Aaron B. Benjamin, Sathish Kumar, Natalia Molchanova, Jennifer S. Lin, Kent J. Koster, Julian L. Leibowitz, Annelise E. Barron, Jeffrey D. Cirillo
Publikováno v:
Pharmaceutics, Vol 16, Iss 4, p 464 (2024)
New antiviral agents are essential to improving treatment and control of SARS-CoV-2 infections that can lead to the disease COVID-19. Antimicrobial peptoids are sequence-specific oligo-N-substituted glycine peptidomimetics that emulate the structure
Externí odkaz:
https://doaj.org/article/7b24857c92f74ec191ebd9ad305568d0
Autor:
Singhamahapatra Anadi, Pattnaik Chinmayee, Kar Prasad Bishnu, Nayak Chandra Ganesh, Sahoo Narayan Laxmi, Sahoo Satyanarayan
Publikováno v:
Journal of the Serbian Chemical Society, Vol 88, Iss 7-8, Pp 715-727 (2023)
The present work describes the synthesis of a new class of glycolipids with systematic variations in the linkage region, as well as in the aglycon part using Cu(I) catalyzed click reaction. The linkage region between sugar and the aglycon part was di
Externí odkaz:
https://doaj.org/article/2cd1e49c2d404071af8f116520528547
Autor:
Minsang Kim, Yeongmi Cheon, Dongmin Shin, Jieun Choi, Josefine Eilsø Nielsen, Myeong Seon Jeong, Ho Yeon Nam, Sung‐Hak Kim, Reidar Lund, Håvard Jenssen, Annelise E. Barron, Seongsoo Lee, Jiwon Seo
Publikováno v:
Advanced Science, Vol 10, Iss 24, Pp n/a-n/a (2023)
Abstract Antimicrobial peptides (AMPs) are promising therapeutics in the fight against multidrug‐resistant bacteria. As a mimic of AMPs, peptoids with N‐substituted glycine backbone have been utilized for antimicrobials with resistance against pr
Externí odkaz:
https://doaj.org/article/b83c343184e24617b1e454cf97703cb1
Akademický článek
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Akademický článek
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Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 18, Iss 1, Pp 845-854 (2022)
The synthesis and conformational analysis of the first series of peptoid oligomers composed of consecutive N-(alkylamino)glycine units is investigated. We demonstrate that N-(methylamino)glycine homooligomers can be readily synthesized in solution us
Externí odkaz:
https://doaj.org/article/4ec3b50909ef476e917615fc1881876e
Autor:
Valeria Cafaro, Andrea Bosso, Ilaria Di Nardo, Assunta D’Amato, Irene Izzo, Francesco De Riccardis, Marialuisa Siepi, Rosanna Culurciello, Nunzia D’Urzo, Emiliano Chiarot, Antonina Torre, Elio Pizzo, Marcello Merola, Eugenio Notomista
Publikováno v:
Pharmaceuticals, Vol 16, Iss 10, p 1386 (2023)
Cationic antimicrobial peptides (CAMPs) are powerful molecules with antimicrobial, antibiofilm and endotoxin-scavenging activities. These properties make CAMPs very attractive drugs in the face of the rapid increase in multidrug-resistant (MDR) patho
Externí odkaz:
https://doaj.org/article/b64d9ebe3a774c0c965d4b7b351d0214