Tag: M.W=300-350

Sanchez, Rafael S. published the artcileLight- and Redox-Controlled Fluorescent Switch Based on a Perylenediimide-Dithienylethene Dyad, Synthetic Route of 219537-97-0, the publication is Journal of Physical Chemistry C (2012), 116(12), 7164-7172, database is CAplus.

The development of luminescent materials that are sensitive to both optical and elec. stimuli is of high interest for the fabrication of future information-processing devices. In this study we report about a novel fluorescent mol. switch (1) that can be light- and redox-controlled. This compound has been synthesized by covalent tethering of a perylenediimide fluorophore (PDI) to a dithienylethene (DTE) unit. The photochromic properties of the DTE group are preserved in the dyad, which can be reversibly converted between open (1o) and closed (1c) states upon irradiation In addition, 1 displays electrochromicity, and its ring-opening process can be promoted quant. by electrochem. oxidation Whereas the open-ring state of the switch is highly fluorescent, the emission of the PDI group in 1c is quenched by energy transfer to the DTE group. This allows large fluorescence modulation between the two states of 1, which can be operated either as an all-optical switch or by a combination of photo- and electrochem. stimuli.

Journal of Physical Chemistry C published new progress about 219537-97-0. 219537-97-0 belongs to chlorides-buliding-blocks, auxiliary class Fused/Partially Saturated Cycles,Cyclopentenes, name is 5-Chloro-3-[2-(5-chloro-2-methylthien-3-yl)cyclopent-1-en-1-yl]-2-methylthiophene, and the molecular formula is C15H14Cl2S2, Synthetic Route of 219537-97-0.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Mahindra, Amit published the artcileAntiplasmodial activity of short peptide-based compounds, COA of Formula: C19H14Cl2, the publication is RSC Advances (2015), 5(29), 22674-22684, database is CAplus.

Three series of short peptide-based compounds were synthesized, which upon evaluation against chloroquine-sensitive (D6) and chloroquine-resistant (W2) strains of Plasmodium falciparum in vitro, produced IC₅₀ values ranging between 1.4-4.7 μg mL^-1. Importantly, higher antimalarial activity against the drug-resistant strain of P. falciparum (W2) was observed for the tested peptides, indicating their potential in the treatment of drug-resistant malaria parasites. The lack of cytotoxicity in all tested peptides provides evidence of their safety profile. The selected peptides were evaluated in an enzymic inhibitory assay against plasmepsin II, a potential target for antiplasmodial activity, also indicated from the results of the mol. docking studies.

RSC Advances published new progress about 42074-68-0. 42074-68-0 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Benzyl chloride,Benzene, name is 2-Chlorotrityl chloride, and the molecular formula is C19H14Cl2, COA of Formula: C19H14Cl2.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Rzuczek, Suzanne G. published the artcileFeatures of Modularly Assembled Compounds That Impart Bioactivity Against an RNA Target, Related Products of chlorides-buliding-blocks, the publication is ACS Chemical Biology (2013), 8(10), 2312-2321, database is CAplus and MEDLINE.

Transcriptomes provide a myriad of potential RNAs that could be the targets of therapeutics or chem. genetic probes of function. Cell-permeable small mols., however, generally do not exploit these targets, owing to the difficulty in the design of high affinity, specific small mols. targeting RNA. As part of a general program to study RNA function using small mols., we designed bioactive, modularly assembled small mols. that target the noncoding expanded RNA repeat that causes myotonic dystrophy type 1 (DM1), r-(CUG)^exp. Herein, we present a rigorous study to elucidate features in modularly assembled compounds that afford bioactivity. Different modular assembly scaffolds were investigated, including polyamines, α-peptides, β-peptides, and peptide tertiary amides (PTAs). On the basis of activity as assessed by improvement of DM1-associated defects, stability against proteases, cellular permeability, and toxicity, we discovered that constrained backbones, namely, PTAs, are optimal. Notably, we determined that r-(CUG)^exp is the target of the optimal PTA in cellular models and that the optimal PTA improves DM1-associated defects in a mouse model. Biophys. analyses were employed to investigate potential sources of bioactivity. These investigations show that modularly assembled compounds have increased residence times on their targets and faster on rates than the RNA-binding modules from which they were derived. Moreover, they have faster on rates than the protein that binds r-(CUG)^exp, the inactivation of which gives rise to DM1-associated defects. These studies provide information about features of small mols. that are programmable for targeting RNA, allowing for the facile optimization of therapeutics or chem. probes against other cellular RNA targets.

ACS Chemical Biology published new progress about 42074-68-0. 42074-68-0 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Benzyl chloride,Benzene, name is 2-Chlorotrityl chloride, and the molecular formula is C19H14Cl2, Related Products of chlorides-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Sun, Cai-Li published the artcileSupramolecular Polymer-Based Fluorescent Microfibers for Switchable Optical Waveguides, COA of Formula: C15H14Cl2S2, the publication is ACS Applied Materials & Interfaces (2018), 10(31), 26526-26532, database is CAplus and MEDLINE.

We report the switchable optical waveguide microfibers based on fluorescent supramol. polymer for the first time. The pillar[5]arene-based supramol. polymeric microfibers were prepared easily from the viscous solution of bispillar[5]arene host (bisP5A) and diphenylanthracene-derived guest (GD). The resulting microfibers act as an active optical waveguide material with long propagation distance (400 μm) and low optical propagation loss (0.01 dB/μm). When photoresponsive dithienylethene-derived guest (GDTE) was added, the resulting ternary microfibers show switchable optical waveguide by the noninvasive control of UV/vis light with negligible fatigue over four cycles. This convenient preparation method is also applied for the quadruple-hydrogen-bonded fluorescent supramol. polymeric microfibers which imply good light propagation property with an optical loss coefficient of 0.02 dB/μm.

ACS Applied Materials & Interfaces published new progress about 219537-97-0. 219537-97-0 belongs to chlorides-buliding-blocks, auxiliary class Fused/Partially Saturated Cycles,Cyclopentenes, name is 5-Chloro-3-[2-(5-chloro-2-methylthien-3-yl)cyclopent-1-en-1-yl]-2-methylthiophene, and the molecular formula is C12H14BNO2, COA of Formula: C15H14Cl2S2.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Yao, Shengxin published the artcileLow-symmetry porphyrin analogues with flexible open-form dithienylethene moieties: Intense near IR Q bands, SDS of cas: 219537-97-0, the publication is Dyes and Pigments (2021), 109440, database is CAplus.

Two low-symmetry porphyrinoids with a dithienylethene (DTE) moiety incorporated into the core macrocycle, that contain either a CHO or a bridging Me ether group, have been serendipitously synthesized through a Rothemund condensation reaction. X-ray crystal structures demonstrate that CHO and bridging Me ether groups on the DTE moiety changes the conformation of the macrocycle and significantly influences the relative energies of the frontier orbitals of the porphyrinoid π-system and results in a remarkable enhancement and broadening of the Q bands in the 450-800 nm region compared to those of conventional tetrapyrrolic porphyrins. The introduction of a DTE moiety provides an effective strategy for achieving the intense near-IR region absorption that is required for many of the practical applications of porphyrinoids, through a disruption of the macrocyclic π-system that is similar to that of naturally occurring corrins.

Dyes and Pigments published new progress about 219537-97-0. 219537-97-0 belongs to chlorides-buliding-blocks, auxiliary class Fused/Partially Saturated Cycles,Cyclopentenes, name is 5-Chloro-3-[2-(5-chloro-2-methylthien-3-yl)cyclopent-1-en-1-yl]-2-methylthiophene, and the molecular formula is C19H14O2, SDS of cas: 219537-97-0.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Coudret, Christophe published the artcileElectrochemical oxidation mechanism of photochromic switches: electrodimerisation, ring closure or ring opening?, Recommanded Product: 5-Chloro-3-[2-(5-chloro-2-methylthien-3-yl)cyclopent-1-en-1-yl]-2-methylthiophene, the publication is Portugaliae Electrochimica Acta (2007), 25(1), 89-101, database is CAplus.

Simple photochromic dithienylethylenes with either perfluoro or perhydro cyclopentene ring, and a variety of substituents were prepared and their electrochem. behavior explored by cyclic voltammetry. All present 2 electron irreversible oxidation waves in their open form, but the radical cation of the open isomers can follow 3 different reaction pathways: dimerization, ring closure, or ring reopening. Whereas the chloro derivative follows a dimerization mechanism (EC₂E mechanism), the phenylthio substituted compound displays an efficient oxidative ring closure (ECE or DISP1 mechanism). Interesting electrochromic behavior is associated with this compound, a redox process occurring in the range 0.5-1.5 V is observed by monitoring the absorption species changes (colored species) in function of the applied potential. Also, electrochromic properties are also found in the corresponding ring closed isomers. Depending on the substituents on the thiophene ring and the perfluoro or perhydro cyclopentene ring, open isomers can be obtained from oxidation (chem. or electrochem.) of the corresponding ring closed isomers via EC mechanism. These observations should be taken into account for the potential design of 3-state conjugated systems and photoelec. mol. switching.

Portugaliae Electrochimica Acta published new progress about 219537-97-0. 219537-97-0 belongs to chlorides-buliding-blocks, auxiliary class Fused/Partially Saturated Cycles,Cyclopentenes, name is 5-Chloro-3-[2-(5-chloro-2-methylthien-3-yl)cyclopent-1-en-1-yl]-2-methylthiophene, and the molecular formula is C15H14Cl2S2, Recommanded Product: 5-Chloro-3-[2-(5-chloro-2-methylthien-3-yl)cyclopent-1-en-1-yl]-2-methylthiophene.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Kapp, Tobias G. published the artcileModification and functionalization of the guanidine group by tailor-made precursors, Application In Synthesis of 42074-68-0, the publication is Journal of Visualized Experiments (2017), e54873/1-e54873/7, database is CAplus and MEDLINE.

The guanidine group is one of the most important pharmacophoric groups in medicinal chem. The only amino acid carrying a guanidine group is arginine. In this article, an easy method for the modification of the guanidine group in peptidic ligands is provided, with an example of RGD-binding integrin ligands. It was recently demonstrated that the distinct modification of the guanidine group in these ligands allows for the selective modulation of the subtype (e.g., between the subtypes αv and α5). Moreover, a formerly unknown strategy for the functionalization via the guanidine group was demonstrated, and the synthetic approach is reviewed in this document. The modifications described here involve terminally (Nω) alkylated and acetylated guanidine groups. For the synthesis, tailor-made precursor mols. are synthesized, which are then subjected to a reaction with an orthogonally deprotected amine to transfer the pre-modified guanidine group. For the synthesis of alkylated guanidines, precursors based on N,N′-Di-Boc-1H-pyrazole-1-carboxamidine are used to synthesize acylated compounds, the precursor of choice being a correspondingly acylated derivative of N-Boc-S-methylisothiourea, which can be obtained in one- and two-step reactions.

Journal of Visualized Experiments published new progress about 42074-68-0. 42074-68-0 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Benzyl chloride,Benzene, name is 2-Chlorotrityl chloride, and the molecular formula is C19H14Cl2, Application In Synthesis of 42074-68-0.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Larsson, Malin published the artcileIdentification of potential aryl hydrocarbon receptor ligands by virtual screening of industrial chemicals, Application In Synthesis of 42074-68-0, the publication is Environmental Science and Pollution Research (2018), 25(3), 2436-2449, database is CAplus and MEDLINE.

We have developed a virtual screening procedure to identify potential ligands to the aryl hydrocarbon receptor (AhR) among a set of industrial chems. AhR is a key target for dioxin-like compounds, which is related to these compounds’ potential to induce cancer and a wide range of endocrine and immune system-related effects. The virtual screening procedure included an initial filtration aiming at identifying chems. with structural similarities to 66 known AhR binders, followed by 3 enrichment methods run in parallel. These include two ligand-based methods (structural fingerprints and nearest neighbor anal.) and one structure-based method using an AhR homol. model. A set of 6445 commonly used industrial chems. was processed, and each step identified unique potential ligands. Seven compounds were identified by all three enrichment methods, and these compounds included known activators and suppressors of AhR. Only approx. 0.7% (41 compounds) of the studied industrial compounds was identified as potential AhR ligands and among these, 28 compounds have to our knowledge not been tested for AhR-mediated effects or have been screened with low purity. We suggest assessment of AhR-related activities of these compounds and in particular 2-chlorotrityl chloride, 3-p-hydroxyanilino-carbazole, and 3-(2-chloro-4-nitrophenyl)-5-(1,1-dimethylethyl)-1,3,4-oxadiazol-2(3H)-one.

Environmental Science and Pollution Research published new progress about 42074-68-0. 42074-68-0 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Benzyl chloride,Benzene, name is 2-Chlorotrityl chloride, and the molecular formula is C19H14Cl2, Application In Synthesis of 42074-68-0.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Park, Jihye published the artcilePhotochromic metal-organic frameworks: Reversible control of singlet oxygen generation, Recommanded Product: 5-Chloro-3-[2-(5-chloro-2-methylthien-3-yl)cyclopent-1-en-1-yl]-2-methylthiophene, the publication is Angewandte Chemie, International Edition (2015), 54(2), 430-435, database is CAplus and MEDLINE.

The controlled generation of singlet oxygen is of great interest owing to its potential applications including industrial wastewater treatment, photochem., and photodynamic therapy. Two photochromic metal-organic frameworks, PC-PCN and SO-PCN, have been developed. A photochromic reaction has been successfully realized in PC-PCN while maintaining its single crystallinity. In particular, as a solid-state material which inherently integrates the photochromic switch and photosensitizer, SO-PCN has demonstrated reversible control of ¹O₂ generation. Addnl., SO-PCN shows catalytic activity towards photooxidation of 1,5-dihydroxynaphthalene.

Angewandte Chemie, International Edition published new progress about 219537-97-0. 219537-97-0 belongs to chlorides-buliding-blocks, auxiliary class Fused/Partially Saturated Cycles,Cyclopentenes, name is 5-Chloro-3-[2-(5-chloro-2-methylthien-3-yl)cyclopent-1-en-1-yl]-2-methylthiophene, and the molecular formula is C15H14Cl2S2, Recommanded Product: 5-Chloro-3-[2-(5-chloro-2-methylthien-3-yl)cyclopent-1-en-1-yl]-2-methylthiophene.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics

Spengler, Jan published the artcileUse of an Internal Reference for the Quantitative HPLC-UV Analysis of Solid-Phase Reactions: A Case Study of 2-Chlorotrityl Chloride Resin, HPLC of Formula: 42074-68-0, the publication is ACS Combinatorial Science (2013), 15(5), 229-234, database is CAplus and MEDLINE.

Here we evaluated the use of internal reference compounds for the rapid assessment of reactions performed in solid-phase. An internal reference compound (com. available) was bound to the resin, together with the substrate, and cleaved with the products after completion of the reaction. The peak area of the reference compound in the HPLC-UV chromatograms can be correlated directly with those of other compounds present in the reaction mixture, thereby allowing a quant. interpretation of the chromatograms with respect to conversion and yield. The usefulness of this method was demonstrated by optimization of a protocol for the synthesis of proline-based tripeptides.

ACS Combinatorial Science published new progress about 42074-68-0. 42074-68-0 belongs to chlorides-buliding-blocks, auxiliary class Chloride,Benzyl chloride,Benzene, name is 2-Chlorotrityl chloride, and the molecular formula is C14H14, HPLC of Formula: 42074-68-0.

Referemce:
https://en.wikipedia.org/wiki/Chloride,
Chlorides – an overview | ScienceDirect Topics