Results 211 to 220 of about 132,389 (268)
A Noncovalent Click‐to‐Release Strategy to Control Bond Cleavage and Prodrug Activation
Extending the click‐to‐release concept beyond covalent ligation, we introduce a noncovalent click‐to‐release strategy based on cucurbituril‐adamantane (CB‐Ad) association. A supramolecular preassembly encapsulating a self‐immolative guest (SIG) is rationally designed to prevent premature release, while adding a high‐affinity Ad guest initiates the CB ...
Xuancheng Fu +9 more
wiley +1 more source
Independent validation of transgenerational inheritance of learned pathogen avoidance in <i>Caenorhabditis elegans</i>. [PDF]
Akinosho A +3 more
europepmc +1 more source
A membrane‐penetrating molecular device composed of triplex containing cholesterol‐modified acyclic L‐threoninol nucleic acid (L‐aTNA) was achieved. This device is applied to a photo‐triggered signal transduction system functioning on giant unilamellar vesicles. Abstract Membrane‐penetrating molecular devices are valuable biological tools.
Kaifu Liu +2 more
wiley +1 more source
Optimization of the genetic code expansion technology for intracellular labelling and single-molecule tracking of proteins in genomically re-coded <i>E. coli</i>. [PDF]
Ilievski F +5 more
europepmc +1 more source
An Expanded Toolbox for Versatile Chemical Editing of Adeno‐Associated Virus
We describe technology to introduce diverse non‐natural chemical functionalities site‐specifically into the capsid of adeno‐associated virus through genetic code expansion, and using them to engineer this leading vector for human gene therapy for enhanced tissue specificity and reduced immunogenicity Abstract Site‐specific incorporation of noncanonical
Quan Pham +6 more
wiley +1 more source
A powerful bioorthogonal toolbox boosting the development of immune theranostics. [PDF]
Liu S, Hua C, Li X, Yuan P, Xing B.
europepmc +1 more source
Reaction of Sodium Azide with 1,1'–Dicyclohexenyl–Diepoxides
Mohammad Raouf Darvich +3 more
openalex +1 more source
Stable BF2 Boracycles as Versatile Reagents for Selective Ortho C–H Functionalization
We report a robust, metal‐free and scalable synthesis of stable BF2 boracycles via directed ortho CH borylation, delivering isolable, shelf‐stable reagents without chromatographic purification. These BF2 boracycles exhibit unique and tunable reactivity, enabling highly selective ipso‐functionalization across a broad range of transformations.
Ganesh H. Shinde +11 more
wiley +1 more source

