(6E)-N-[(4Z)-2,5-Dimethyl-4-(p-tolyl­imino)cyclo­hexa-2,5-dienyl­idene]-4-methyl­aniline

The title compound, C22H22N2, was prepared by the reaction of 4-amino­toluene with sodium carbonate, sodium hydroxide and potassium permanganate. The mol­ecule is disposed about a crystallographic inversion centre with one half-mol­ecule comprising the asymmetric unit. The dihedral angle between the terminal and central benzene rings is 88.05 (1)°. The crystal packing is stabilized by van der Waals forces

An optimal scaling scheme for DCO-OFDM based visible light communications

DC-biased optical orthogonal frequency-division multiplexing (DCO-OFDM) is widely used in visible light communication (VLC) systems to provide high data rate transmission. As intensity modulation with direct detection (IM/DD) is employed to modulate the OFDM signal, scale up the amplitude of the signal can increase the effective transmitted electrical power whereas more signals are likely to be clipped due to the limited dynamic range of LEDs, resulting in severe clipping distortion. Thus, it is crucial to scale the signal to find a tradeoff between the effective electrical power and the clipping distortion. In this paper, an optimal scaling scheme is proposed to maximize the received signal-to-noise-plus-distortion ratio (SNDR) with the constraint of the radiated optical power in a practical scenario where DC bias is fixed for a desired dimming level. Simulation results show that the system with the optimal scaling factor outperforms that with fixed scaling factor under different equivalent noise power in terms of the bit error ratio (BER) performance

GOPlan: Goal-conditioned Offline Reinforcement Learning by Planning with Learned Models

Offline goal-conditioned RL (GCRL) offers a feasible paradigm to learn general-purpose policies from diverse and multi-task offline datasets. Despite notable recent progress, the predominant offline GCRL methods have been restricted to model-free approaches, constraining their capacity to tackle limited data budgets and unseen goal generalization. In this work, we propose a novel two-stage model-based framework, Goal-conditioned Offline Planning (GOPlan), including (1) pretraining a prior policy capable of capturing multi-modal action distribution within the multi-goal dataset; (2) employing the reanalysis method with planning to generate imagined trajectories for funetuning policies. Specifically, the prior policy is based on an advantage-weighted Conditioned Generative Adversarial Networks that exhibits distinct mode separation to overcome the pitfalls of out-of-distribution (OOD) actions. For further policy optimization, the reanalysis method generates high-quality imaginary data by planning with learned models for both intra-trajectory and inter-trajectory goals. Through experimental evaluations, we demonstrate that GOPlan achieves state-of-the-art performance on various offline multi-goal manipulation tasks. Moreover, our results highlight the superior ability of GOPlan to handle small data budgets and generalize to OOD goals.Comment: Spotlight Presentation at Goal-conditioned Reinforcement Learning Workshop at NeurIPS, 202

Scoulerine promotes cytotoxicity and attenuates stemness in ovarian cancer by targeting PI3K/AKT/mTOR axis

In women, ovarian cancer is a common gynecological cancer associated with poor prognosis, reoccurrence and chemoresistance. Scoulerine, a benzylisoquinoline alkaloid, has been reported effective against several carcinomas. Thus, we investigated the impact of scoulerine on ovarian cancer cells (OVCAR3). Cell viability was assessed by MTT assay, migration was determined by Boyden Chamber assay, while the invasion was monitored by Boyden Chamber assay using the matrigel. The stemness properties of OVCAR3 cells were observed by tumorsphere assay. Epithelial to mesenchymal transition (EMT) and stemness-related protein markers were monitored by real-time PCR analysis and immunoblotting. Scoulerine inhibits the viability of OVCAR3 cells with the IC50 observed at 10 µmol L–1 after 48 h treatment. Scoulerine inhibited the colony-forming ability, migration and invasiveness of OVCAR3 cells in a dose-dependent fashion. Scoulerine treatment also drastically reduced the spheroid-forming ability of OVCAR3 cells. The mesenchymal and stemness-related markers like N-cadherin, vimentin, CD-44, Oct-4, Sox-2 and Aldh1A1 were downregulated, whereas the epithelial markers like E-cadherin and CD-24 were upregulated in scoulerine-treated cells. The upstream PI3K/Akt/mTOR-axis was downregulated in scoulerine-treated cells. We concluded that scoulerine successfully perturbs the cancerous properties of OVCAR3 cells by targeting the PI3K/Akt/mTOR axis. In vivo studies revealed a substantial decrease in tumor mass and volume after scoulerine treatment. Furthermore, scoulerine treatment was found to decrease oxidative stress factors in ovarian cancer mice model. Scoulerine is a potential anticancer agent against ovarian cancer and can be considered as a lead molecule for this malignancy, provided further investigations are performed

First-principles design of ferromagnetic monolayer MnO2_2 at the complex interface

Rapidly increasing interest in low-dimensional materials is driven by the emerging requirement to develop nanoscale solid-state devices with novel functional properties that are not available in three-dimensional bulk phases. Among the well-known low-dimensional systems, complex transition metal oxide interface holds promise for broad applications in electronic and spintronics devices. Herein, intriguing metal-insulator and ferromagnetic-antiferromagnetic transitions are achieved in monolayer MnO$_2$ that is sandwiched into SrTiO$_3$-based heterointerface systems through interface engineering. By using first-principles calculations, we modeled three types of SrTiO$_3$-based heterointerface systems with different interface terminations and performed a comparative study on the spin-dependent magnetic and electronic properties that are established in the confined MnO$_2$ monolayer. First-principles study predicts that metal-insulator transition and magnetic transition in the monolayer MnO$_2$ are independent on the thickness of capping layers. Moreover, 100$\%$ spin-polarized two-dimensional electron gases accompanied by robust room temperature magnetism are uncovered in the monolayer MnO$_2$. Not only is the buried MnO$_2$ monolayer a new interface phase of fundamental physical interest, but it is also a promising candidate material for nanoscale spintronics applications. Our study suggests interface engineering at complex oxide interfaces is an alternative approach to designing high-performance two-dimensional materials.Comment: 24 pages, 7 figure

Elucidation of mechanisms of action of Wei-Sheng-Fang-Yi-Bao-Dan in the treatment of COVID-19 and depression using network pharmacology and molecular docking

Purpose: To investigate the mechanisms of action of Wei-Sheng-Fang-Yi-Bao-Dan (WSFYBD) in the treatment of COVID-19 and depression using network pharmacology and molecular docking. Methods: First, the bioactive components and target genes of WSFYBD were retrieved from TCMSP database. The relevant gene targets of depression and COVID-19 were obtained from databases. The core WSFYBD genes for treatment were separately obtained by determining gene intersection. Cytoscape 3.8.0 software was used to draw the visual interactive networks. STRING database was employed to construct protein-protein interaction networks, while Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) functional enrichment analyses were used to determine the function and pathway of target genes via a Bioconductor/R. Finally, AutoDockTools software was employed for molecular docking. Results: A total of 105 potential bio-active components and 35 target genes of WSFYBD for COVID-19 therapy were identified. Also, 1905 GO entries (p < 0.05) and 158 related signal pathways (p < 0.05) for COVID-19 were obtained. Similarly, 114 potential bio-active components of WSFYBD and 127 potential therapeutic targets of depression were identified. Moreover, 1948 GO entries (p < 0.05) and 177 related signal pathways for depression were retrieved (p < 0.05). Docking results showed the main bio-active components were closely bound to the core targets. Conclusion: The mechanisms for treating COVID-19 show that WSFYBD directly acts on SARS-CoV-2 virus to prevent it from entering the host cell, or inhibits virus replication. Secondly, WSFYBD ameliorates depression by acting on key targets that control over-activated cytokines. Therefore, WSFYBD has potentials for the management of COVID-19 and depression