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New developments in RiPP discovery, enzymology and engineering
Covering: up to June 2020 Ribosomally-synthesized and post-translationally modified
peptides (RiPPs) are a large group of natural products. A community-driven review in 2013 …
peptides (RiPPs) are a large group of natural products. A community-driven review in 2013 …
Diversification of phage-displayed peptide libraries with noncanonical amino acid mutagenesis and chemical modification
Sitting on the interface between biologics and small molecules, peptides represent an
emerging class of therapeutics. Numerous techniques have been developed in the past 30 …
emerging class of therapeutics. Numerous techniques have been developed in the past 30 …
Methods for generating and screening libraries of genetically encoded cyclic peptides in drug discovery
Drug discovery has traditionally focused on using libraries of small molecules to identify
therapeutic drugs, but new modalities, especially libraries of genetically encoded cyclic …
therapeutic drugs, but new modalities, especially libraries of genetically encoded cyclic …
Peptide therapeutics: targeting the undruggable space
N Tsomaia - European journal of medicinal chemistry, 2015 - Elsevier
Rapid advancements in genomics have brought a better understanding of molecular
mechanisms for various pathologies and identified a number of highly attractive target …
mechanisms for various pathologies and identified a number of highly attractive target …
Therapeutics targeting the fibrinolytic system
The function of the fibrinolytic system was first identified to dissolve fibrin to maintain
vascular patency. Connections between the fibrinolytic system and many other physiological …
vascular patency. Connections between the fibrinolytic system and many other physiological …
Phage selection of cyclic peptides for application in research and drug development
Conspectus Cyclic peptides can bind to protein targets with high affinities and selectivities,
which makes them an attractive modality for the development of research reagents and …
which makes them an attractive modality for the development of research reagents and …
A Cysteine‐Directed Proximity‐Driven Crosslinking Method for Native Peptide Bicyclization
Efficient and site‐specific modification of native peptides and proteins is desirable for
synthesizing antibody‐drug conjugates as well as for constructing chemically modified …
synthesizing antibody‐drug conjugates as well as for constructing chemically modified …
Identification of highly selective covalent inhibitors by phage display
Molecules that covalently bind macromolecular targets have found widespread applications
as activity-based probes and as irreversibly binding drugs. However, the general reactivity of …
as activity-based probes and as irreversibly binding drugs. However, the general reactivity of …
Selection-based discovery of druglike macrocyclic peptides
Macrocyclic peptides are an emerging class of therapeutics that can modulate protein–
protein interactions. In contrast to the heavily automated high-throughput screening systems …
protein interactions. In contrast to the heavily automated high-throughput screening systems …
Disulfide-directed multicyclic peptide libraries for the discovery of peptide ligands and drugs
S Lu, S Fan, S **ao, J Li, S Zhang, Y Wu… - Journal of the …, 2023 - ACS Publications
Multicyclic peptides with stable 3D structures are a kind of novel and promising peptide
formats for drug design and discovery as they have the potential to combine the best …
formats for drug design and discovery as they have the potential to combine the best …