Results 331 to 340 of about 6,845,981 (383)

Molecular Recognition of Hydrophilic Molecules in Water by Combining the Hydrophobic Effect with Hydrogen Bonding.

Journal of the American Chemical Society, 2018
During the last half a century, great achievements have been made in molecular recognition in parallel with the invention of numerous synthetic receptors.
Huan Yao, Hua Ke, Xiaobin Zhang, San-Jiang Pan, Ming-Shuang Li, Liu-Pan Yang, G. Schreckenbach, Wei Jiang   +7 more
semanticscholar   +1 more source

Nucleoside Analogue-Based Supramolecular Nanodrugs Driven by Molecular Recognition for Synergistic Cancer Therapy.

Journal of the American Chemical Society, 2018
The utilization of nanotechnology for the delivery of a wide range of anticancer drugs has the potential to reduce adverse effects of free drugs and improve the anticancer efficacy. However, carrier materials and/or chemical modifications associated with
Dali Wang, Chunyang Yu, Li Xu, Leilei Shi, Gangsheng Tong, Jieli Wu, Hong Liu, D. Yan, Xinyuan Zhu   +8 more
semanticscholar   +1 more source

Molecular Recognition

ChemInform, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
openaire   +1 more source

Molecular Recognition via Base‐Pairing

ChemInform, 2007
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Jonathan L, Sessler, Candace M, Lawrence, Janarthanan, Jayawickramarajah   +2 more
openaire   +2 more sources

Polyvalent Carbocyanine Molecular Beacons for Molecular Recognitions

Journal of the American Chemical Society, 2004
Polyvalent carboxylate-terminating near-infrared (NIR) carbocyanine molecular beacons were prepared by homologation of reactive carboxyl groups of the beacon with imino diacetic acid. Their conjugation with unprotected d-(+)-glucosamine gave dendritic arrays of the carbohydrate on an inner NIR chromophore core.
Yunpeng, Ye, Sharon, Bloch, Samuel, Achilefu   +2 more
openaire   +2 more sources

Complexity in molecular recognition

Physical Chemistry Chemical Physics, 2011
The anomer selectivity of artificial carbohydrate receptors was studied using in silico methods in order to shed light on the thermodynamic driving forces at work during molecular recognition in general. The contributions of relevant intermolecular hydrogen bonds were investigated by means of generalized compliance constants in order to dissect ...
openaire   +2 more sources

Oligosaccharides in molecular recognition

Biochemical Society Transactions, 1988
Summary The development, organization and growth of complex organisms as well as their interactions with the environment involve an intricate array of molecular recognition events. There is an increased awareness of the involvement of oligosaccharides in many of these processes.
openaire   +2 more sources

DNA–psoralens molecular recognition using molecular dynamics

Il Farmaco, 1999
Furocoumarins are an important class of compounds for photochemotherapy used in the treatment of numerous diseases characterised by hyperproliferative conditions. Their photosensitising activity has been related to the ability to form covalent linkage with the pyrimidine bases of DNA upon UV-A irradiation.
BOGGIA, RAFFAELLA, FANCIULLO M., FINZI L., INCANI O., MOSTI, LUISA   +4 more
openaire   +2 more sources

Molecular recognition

Journal of Porphyrins and Phthalocyanines, 2000
The ‘marriage’ between porphyrin chemistry and the newly emerging molecular recognition science has opened up novel research opportunities leading to many biological and abiological applications. An overview of this fascinating research area is presented here.
openaire   +1 more source

Molecular Assembly and Molecular Recognition

1995
The use of molecular design for optimised molecular recognition and self-assembly for improved materials for chemical sensing is discussed. Peripheral substitution of phthalocyanines by alkyl, alkoxy, or crownether groups promotes self-assembly and provides control of local polarisability, optimising charge-transfer interaction energies for rapid ...
John D. Wright, Roeland J. M. Nolte
openaire   +1 more source