Results 11 to 20 of about 43,444 (345)

The Taming of the Maleimide: Fabrication of Maleimide‐Containing ‘Clickable’ Polymeric Materials

open access: yesThe Chemical Record, 2017
AbstractFunctional polymers are widely employed in various areas of biomedical sciences. In order to tailor them for desired applications, facile and efficient functionalization of these polymeric materials under mild and benign conditions is important.
Oz, Yavuz, Sanyal, Amitav
openaire   +4 more sources

N-(3-Chlorophenyl)maleimide [PDF]

open access: yesActa Crystallographica Section E Structure Reports Online, 2008
Le composé du titre, C(10)H(6) ClNO(2), a un angle dièdre de 46,46 (5) ° entre les cycles benzène et maléimide. Un court contact intermoléculairehalogène-oxygène est observé, avec une distance Cl O de 3,0966 (13) Å. Interactions O, ce qui donne lieu à des feuilles parallèles à (100).
Rodolfo Moreno‐Fuquen   +2 more
openaire   +4 more sources

A novel application of maleimide for advanced drug delivery: in vitro and in vivo evaluation of maleimide-modified pH-sensitive liposomes

open access: yesInternational Journal of Nanomedicine, 2013
Tianshu Li, Shinji TakeokaDepartment of Life Science and Medical Bioscience, Graduate School of Advanced Science and Engineering, Waseda University (TWIns), Shinjuku-ku, Tokyo, JapanAbstract: Maleimide is a stable and easy-to-handle moiety that rapidly ...
Li T, Takeoka S
doaj   +1 more source

S‐Nitrosothiols as Thiol‐Protecting Groups for Controlled Thiol‐Maleimide Crosslinking of Homogeneous Soft Hydrogels

open access: hybridAdvanced Materials, EarlyView.
Rapid thiol‐maleimide addition frequently outpaces mixing, resulting in heterogeneous hydrogels. S‐nitrosothiols act as thiol‐protecting groups, allowing uniform mixing with maleimide‐functionalized polymers before gelation. Sodium thiosulfate or sodium ascorbate then regenerates thiols on demand, triggering controlled thiol‐maleimide crosslinking ...
Julian A. Serna   +7 more
openalex   +2 more sources

Clusteroluminescence in Maleimide: from Well-Known Phenomenon to Unknown Mechanism [PDF]

open access: yes, 2022
Maleimide compounds have a long history related to colour reactions. It has been reported that maleimide yields bright colour when it reacts with basic reagents.
Ben Zhong, Tang   +5 more
core   +2 more sources

Unexpected Fluorescent Behavior of Maleimide Based Zwitterionic Molecule: Aggregation Induced Emission [PDF]

open access: yes, 2022
A novel traditional fluorophore free bright blue light emitting small organic molecule with aqueous solubility consisting N-substituted maleimide with zwitterionic side chain was explored.
Dr. Ishita, Mukherjee
core   +2 more sources

Breaking The Monotony: Cobalt and Maleimide as a New Entrant to the Catellani Reaction [PDF]

open access: yes, 2022
A catalytic system was discovered for the intramolecular C-H amidation of N-phenoxy acetamide derivatives. For the first time, a cobalt catalyst was employed for the Catellani reaction.
Tanmayee, Nanda   +8 more
core   +2 more sources

Studies About A biocompatible Maleimide-modified Dextran And Hyaluronic Acid Hydrogel System [PDF]

open access: yes, 2023
This article discussed a novel hydrogel, which was created through Michael addition. Two precursors dextran functionalized maleimide groups and hyaluronic acid functionalized thiol groups were designed, prepared, and characterized by NMR.
Song, Jiang, Tianjin, Zhang
core   +1 more source

Dynamics of AF488 C5-maleimide-stained competence pili. A+B) Images of time-laps microscopy were acquired every 20 s.

open access: yes, 2023
Yellow arrow indicates pilus formation, orange pilus retraction. Movies were acquired in the GFP-channel. C) Colocalization of fluorescently labelled DNA with C5 Maleimide-stained competence pili in BF-, GFP, and TxRed-channel. Scale bars 2 μm.
Sven Holtrup (6871598)   +3 more
core   +1 more source

Bisindolyl Maleimides and Indolylmaleimide Derivatives—A Review of Their Synthesis and Bioactivity

open access: yesPharmaceuticals, 2023
The evolution of bisindolyl maleimides and indolyl maleimide derivatives and their unique biological activities have stimulated great interest in medicinal chemistry programs.
Louise N. Cooney   +5 more
doaj   +1 more source

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