Amanote Research
Register
Sign In
Dynamic Formation of Imidazolidino Boronate Enables Design of Cysteine-Responsive Peptides
doi 10.1021/acs.orglett.7b03116.s001
Full Text
Open PDF
Abstract
Available in
full text
Date
Unknown
Authors
Unknown
Publisher
American Chemical Society (ACS)
Related search
A Janus Chelator Enables Biochemically Responsive MRI Contrast With Exceptional Dynamic Range
Journal of the American Chemical Society
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
Breathing Life Into Polycations: Functionalization With pH-Responsive Endosomolytic Peptides and Polyethylene Glycol Enables siRNA Delivery
Journal of the American Chemical Society
Biochemistry
Colloid
Catalysis
Chemistry
Surface Chemistry
Modulation of Ion Channels by Cysteine-Rich Peptides
Ion Channels DownUnder
Targeting RNA With Cysteine-Constrained Peptides
Bioorganic and Medicinal Chemistry Letters
Organic Chemistry
Molecular Medicine
Molecular Biology
Biochemistry
Clinical Biochemistry
Pharmaceutical Science
Drug Discovery
Computer-Aided Design of Mastoparan-Like Peptides Enables the Generation of Nontoxic Variants With Extended Antibacterial Properties
Formation of C(sp2)Boronate Esters by Borylative Cyclization of Alkynes Using BCl3
Angewandte Chemie
Incorporation of Anionic Monomer to Tune the Reversible Catechol-Boronate Complex for pH Responsive, Reversible Adhesion
Langmuir
Surfaces
Materials Science
Condensed Matter Physics
Interfaces
Electrochemistry
Spectroscopy
Medicine
Environmentally Responsive Peptides as Anticancer Drug Carriers☆
Advanced Drug Delivery Reviews
Pharmaceutical Science
Quaternization of Vinyl/Alkynyl Pyridine Enables Ultrafast Cysteine-Selective Protein Modification and Charge Modulation
Angewandte Chemie - International Edition
Catalysis
Chemistry