Nanoscale tools to selectively destroy cancer cells
Literature Information
Pierre-Luc Boudreault, Mathieu Arseneault, François Otis, Normand Voyer
We present experimental data that demonstrate the potential of synthetic crown ether modified peptide nanostructures to act as selective and efficient chemotherapeutic agents that operate by attacking and destroying cell membranes.
Recommended Journals

Journal of Enzyme inhibition and Medicinal Chemistry

Advanced Engineering Materials

Journal of Medical Biochemistry

Current Pharmaceutical Biotechnology

Coloration Technology

European Journal of Organic Chemistry

Molecules

CrystEngComm

Photochemical & Photobiological Sciences

Mini-Reviews in Medicinal Chemistry
Related Literature
Olefin/paraffin solubility in a solid polymer electrolyte membrane
T. C. Merkel, Z. He, A. Morisato, I. Pinnau
DOI: 10.1039/B301420G
Synthesis and reactions of a novel 3,4-didehydropyroglutamate derivative
Makoto Oba, Naohiro Nishiyama, Kozaburo Nishiyama
DOI: 10.1039/B300554B
A new axially-chiral photochemical switch
Silvia Pieraccini, Stefano Masiero, Gian Piero Spada, Giovanni Gottarelli
DOI: 10.1039/B211421F
Aziridinyl anions from a chiral, nonracemic 2-isopropylidineaziridine: surprisingly diastereoselective alkylation reactions
J. F. Hayes, N. Prévost, I. Prokeš, M. Shipman, A. M. Z. Slawin, H. Twin
DOI: 10.1039/B303252C
Template synthesis of porous gold microspheres
Dmitry G. Shchukin
DOI: 10.1039/B304259F
A novel concept to activate enediynes for DNA cleavage
Michael Schmittel, Giampietro Viola, Francesco Dall’Acqua, Guido Morbach
DOI: 10.1039/B211783E
Addition of the ortho-C–H bonds of phenol across an olefin catalysed by a chiral iridium(i) diphosphine complex
Romano Dorta, Antonio Togni
DOI: 10.1039/B211672C
Hydrogen bonded molecular assembly by reversible cyclization reaction of anthracene
Masashi Ikegami, Ikuma Ohshiro, Tatsuo Arai
DOI: 10.1039/B304034H
Room-temperature heterogeneous hydroxylation of phenol with hydrogen peroxide over Fe2+, Co2+ ion-exchanged Naβ zeolite
Jung-Nam Park, Chul Wee Lee
DOI: 10.1039/B212296K
Formation of surface-grafted copolymer brushes with continuous composition gradients
Michael R. Tomlinson, Jan Genzer
DOI: 10.1039/B303823H
You might also like
What are the main uses of (3.beta.)-3-Hydroxy-N,N-dimethyl-chol-5-en-24-amide (CAS: 79066-03-8)?
(3.beta.)-3-Hydroxy-N,N-dimethyl-chol-5-en-24-amide (CAS: 79066-03-8) is primari...
What regulatory guidelines apply to 5-(aminomethyl)-2-methoxyphenol (CAS: 89702-89-6)?
5-(Aminomethyl)-2-methoxyphenol (CAS: 89702-89-6) is classified under GHS as a s...
What is Thieno[2,3-c]pyridin-7(6H)-one (CAS: 28981-13-7)?
Thieno[2,3-c]pyridin-7(6H)-one (CAS: 28981-13-7) is a heterocyclic organic compo...
Is 1-[(6-Methoxy-3-pyridinyl)methyl]-4-piperidinamine dihydrochloride (CAS: 1185311-28-7) safe?
1-[(6-Methoxy-3-pyridinyl)methyl]-4-piperidinamine dihydrochloride is generally ...
What regulatory guidelines apply to [(2E)-3-Phenyl-2-propen-1-yl]phosphonic acid (CAS: 146404-58-2)?
[(2E)-3-Phenyl-2-propen-1-yl]phosphonic acid (CAS: 146404-58-2) is regulated und...
What regulatory guidelines apply to 6-Bromo-7-methoxyquinoline (CAS: 1620515-86-7)?
6-Bromo-7-methoxyquinoline (CAS: 1620515-86-7) falls under the scope of the Glob...
What industries use (2R)-1-(1-Benzofuran-2-yl)-N-propyl-2-pentanamine (CAS: 260550-89-8)?
This compound is primarily used in the pharmaceutical industry for the developme...
What are the main uses of 1-Ethyl-7-[2-methyl-6-(4H-1,2,4-triazol-3-yl)-3-pyridinyl]-3,5-dihydropyrazino[2,3-b]pyrazin-2(1H)-one (CAS: 1228013-15-7)?
1-Ethyl-7-[2-methyl-6-(4H-1,2,4-triazol-3-yl)-3-pyridinyl]-3,5-dihydropyrazino[2...
Are there alternatives to {5-(Acryloylamino)-2-[(dimethylamino)methyl]phenyl}boronic acid (CAS: 1217500-78-1) in synthesis?
Alternative reagents such as 2-[(dimethylamino)methyl]phenylboronic acid or rela...
What is 3-(Piperidin-4-yloxy)pyridine (CAS: 310881-48-2)?
3-(Piperidin-4-yloxy)pyridine (CAS: 310881-48-2) is an organic compound with the...
Source Journal
Chemical Communications

ChemComm publishes urgent research which is of outstanding significance and interest to experts in the field, while also appealing to the journal’s broad chemistry readership. Our communication format is ideally suited to short, urgent studies that are of such importance that they require accelerated publication. Our scope covers all topics in chemistry, and research at the interface of chemistry and other disciplines (such as materials science, nanoscience, physics, engineering and biology) where there is a significant novelty in the chemistry aspects. Major topic areas covered include: Analytical Chemistry Catalysis Chemical Biology and medicinal chemistry Computational Chemistry and Machine Learning Energy and sustainable chemistry Environmental Chemistry Green Chemistry Inorganic Chemistry Materials Chemistry Nanoscience Organic Chemistry Physical Chemistry Polymer Chemistry Supramolecular Chemistry
![(3E)-3-[4-Hydroxy-3,5-bis(2-methyl-2-propanyl)benzylidene]dihydro-2(3H)-furanone structure (3E)-3-[4-Hydroxy-3,5-bis(2-methyl-2-propanyl)benzylidene]dihydro-2(3H)-furanone structure](https://static.chemtradehub.com/structs/102/102271-49-8-cba7.webp)



![N-[(6-Bromo-3-pyridinyl)methyl]ethanamine structure N-[(6-Bromo-3-pyridinyl)methyl]ethanamine structure](https://static.chemtradehub.com/structs/120/120740-05-8-ca55.webp)