In the paper entitled"Efficient adsorption of Mn(Ⅱ)by layered double hydroxides intercalated with di ethylenetriaminepentaacetic acid and the mechanistic study"in Journal of Environmental Sciences,volume 85...In the paper entitled"Efficient adsorption of Mn(Ⅱ)by layered double hydroxides intercalated with di ethylenetriaminepentaacetic acid and the mechanistic study"in Journal of Environmental Sciences,volume 85,page 56-65,there were problems with mathematical notation and dimensional errors in the calculation for Giibbs free energy.In Section 2.5:Adsorption isotherms and thermodynamics studies,authors calculated the Gibbs free energy change(△G°)展开更多
Objective: To investigate the effective compounds, potential targets and molecular mechanism of Kanglaite injection (KLTi) in the treatment of Non-Small Cell Lung Cancer (NSCLC) based on network pharmacology. Methods:...Objective: To investigate the effective compounds, potential targets and molecular mechanism of Kanglaite injection (KLTi) in the treatment of Non-Small Cell Lung Cancer (NSCLC) based on network pharmacology. Methods: The active compounds and targets of KLTi which extracted and isolated from Coix Seed were screened by Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP). The related genes of NSCLC were obtained by searching the Human Gene Database (GeneCards) and Online Mendelian Inheritance in Man (OMIM). The candidate targets of KLTi in the treatment of NSCLC were obtained after extracting the intersection network. The "drug-component-target-disease" network was constructed with the help of Cytoscape 3.7.2. The Protein- Protein Interaction networks were constructed on the STRING platform and core network modules were screened. The Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis of candidate genes were performed using Metascape platform, and a "pathway-target- compounds" network was constructed to further screen key genes and active compounds. Results: A total of 11 compounds, 22 candidate targets, 206 GO functions and 12 KEGG pathways were obtained. Conclusion: The active compounds of KLTi in the treatment of NSCLC are stigmasterol, stigmasterol α1 and ergosterol. The key targets are PGR, NCOA2, PTGS2, NR3C2, and PTGS1. The core GO functions included receptor activity and binding, neuronal signal transmission and hormone stimulation;KEGG mainly involves cancer pathways, neuroactive ligand-receptor interactions and calcium signaling pathways. This study reveals the molecular biological mechanism of KLTi in the treatment of NSCLC, which is speculated to be related to neuroendocrine, providing a new basis and therapeutic direction for subsequent clinical application and experimental research.展开更多
Carbon-supported single-atom catalysts were found to suffer reversible deactivation in catalytic hydrogenation,but the mechanism is still unclear.Herein,nitro compounds hydrogenation catalyzed by N-doped carbon-suppor...Carbon-supported single-atom catalysts were found to suffer reversible deactivation in catalytic hydrogenation,but the mechanism is still unclear.Herein,nitro compounds hydrogenation catalyzed by N-doped carbon-supported Co single atom(Co1/NC)was taken as a model to uncover the mechanism of the reversible deactivation phenomenon.Co1/NC exhibited moderate adsorption towards the substrate molecules(i.e.,nitro compounds or related intermediates),which could be strengthened by the confinement effect from the porous structure.Consequently,substrate molecules tend to accumulate within the pore channel,especially micropores that host Co1,making it difficult for the reactants to access the active sites and finally leading to their deactivation.The situation could be even worse when the substrate molecules possess a large size.Nevertheless,the catalytic activity of Co1/NC could be restored via a simple thermal treatment,which could remove the adsorbates within the pore channel,hence releasing active sites that were originally inaccessible to reactants.展开更多
This paper discloses the reaction mechanism of two consecutive but different visible light photo-induced chain processes for the rapid construction of spirobi[indene]skeletons.The first process is triggered by a photo...This paper discloses the reaction mechanism of two consecutive but different visible light photo-induced chain processes for the rapid construction of spirobi[indene]skeletons.The first process is triggered by a photo-induced single-electron-transfer(SET)of an electron donor-accepter(EDA)complex.The second process is initiated by a direct SET process between aryldiazonium salt and the excited allenic intermediate.In these two processes,another SET took place respectively on the in situ formed radical intermediate to realize a redox-neutral outcome.The mechanistic studies have been carried out by control experiments,kinetic and spectroscopic analyses,deuterium labeling experiments to support these two chain processes.展开更多
Objective:The objective of this study was to investigate the potential mechanisms of ephedra-gypsum in the treatment ofrespiratory diseases(RDs)using network pharmacology and molecular docking techniques.Materials and...Objective:The objective of this study was to investigate the potential mechanisms of ephedra-gypsum in the treatment ofrespiratory diseases(RDs)using network pharmacology and molecular docking techniques.Materials and Methods:The TCMSP and UniProt databases were used to mine the active components and targets of ephedra-gypsum,and the targets of RD were screened using the Online Mendelian Inheritance in Man(OMIM)and GeneCards databases.The protein-protein interaction network graph was created using the drug-disease intersection targets in the STRING database.The network diagram was analyzed using Cytoscape 3.9.1's topology function.The gene ontology(GO)and KEGG enrichment analyses were performed using the DAVID platform.Molecular docking bioactivity validation of the main active components and core targets was performed using AutoDock and PyMOL software.Results:Twenty-four compounds were screened,and 113 drug-disease targets overlapped.In total,358 biological processes,67 molecular functions,38 cellular components of GO,and 139 pathways were identified.Molecular docking analysis demonstrated the strong binding ability of tumor protein 53(TP53)-luteolin.Conclusion:The core components of ephedra-gypsum,such as quercetin,luteolin,kaempferol,and CaSO_(4)·2H_(2)O,act on key targets,such as tumor necrosis factor(TNF),interleukin-6(IL-6),TP53,and IL-1β through cytokine-mediated signaling pathways,infiammatory responses,cell proliferation,and apoptosis.This could be useful for the treatment of RD.展开更多
MCRs for preparation of chromenopyridines under reflux conditions and chromenes at room temperature conditions from different salicylaldehydes,malononitrile and different thiols(mol ratio- 1:2:1) were established....MCRs for preparation of chromenopyridines under reflux conditions and chromenes at room temperature conditions from different salicylaldehydes,malononitrile and different thiols(mol ratio- 1:2:1) were established.Mechanistic investigation suggests that the MCRs undergo different pathways at different temperatures and catalyzed by different organic bases.The structure of chromenopyridine and chromene are confirmed by crystal X-ray crystallography.展开更多
Photooxidation provides a promising strategy for removing the dominant indoor pollutant of HCHO,while the underlying photooxidation mechanism is still unclear,especially the exact role of H2O molecules.Herein,we utili...Photooxidation provides a promising strategy for removing the dominant indoor pollutant of HCHO,while the underlying photooxidation mechanism is still unclear,especially the exact role of H2O molecules.Herein,we utilize in-situ spectral techniques to unveil the H2O-mediated HCHO photooxidation mechanism.As an example,the synthetic defective Bi2WO6 ultrathin sheets realize high-rate HCHO photooxidation with the assistance of H2O at room temperature.In-situ electron paramagnetic resonance spectroscopy demonstrates the existence of•OH radicals,possibly stemmed from H2O oxidation by the photoexcited holes.Synchrotron-radiation vacuum ultraviolet photoionization mass spectroscopy and H218O isotope-labeling experiment directly evidence the formed•OH radicals as the source of oxygen atoms,trigger HCHO photooxidation to produce CO2,while in-situ Fourier transform infrared spectroscopy discloses the HCOO*radical is the main photooxidation intermediate.Density-functional-theory calculations further reveal the•OH formation process is the rate-limiting step,strongly verifying the critical role of H2O in promoting HCHO photooxidation.This work first clearly uncovers the H2O-mediated HCHO photooxidation mechanism,holding promise for high-efficiency indoor HCHO removal at ambient conditions.展开更多
The asymmetric hydroxylation of inactive carbon atoms in organic compounds remains an important reaction in the industrial synthesis of valuable chiral compounds.Fe(II)and 2-ketoglutarate-dependent dioxygenases(Fe/2-k...The asymmetric hydroxylation of inactive carbon atoms in organic compounds remains an important reaction in the industrial synthesis of valuable chiral compounds.Fe(II)and 2-ketoglutarate-dependent dioxygenases(Fe/2-kg DOs)are the largest known subgroups of mononuclear nonheme-Fe(II)-dependent oxygenases,catalyzing various oxidation reactions of C-H bonds.Recent developments in Fe/2-kg DO-related researches have coupled concepts from bioinformatics,synthetic biology,and computational biology to establish effective biotransformation systems.The most well-studied and characterized activ-ity of the Fe/2-kg DOs is substrate hydroxylation,with regard to which mechanistic studies involving the Fe center assist in engineering the protein frameworks of these enzymes to obtain the desired catalytic enhancements.Amino acids are typical substrates of Fe/2-kg DOs and are usually converted into hydroxyl amino acids,which are widely used as intermediates in pharmaceutical and fine chemical industries.Herein,we have reviewed prior structural and mechanistic studies on Fe/2-kg DOs,as well as studies on the Fe/2-kg DO-mediated selective C-H oxidation process for selective hydroxyl amino acid synthesis,which will further our journey along the promising path of building complexity via C-H bond oxidation.Further,new bioinformatics techniques should be adopted with structure-based protein rational design to mine sequence databases and shrink mutant libraries to produce a diverse panel of functional Fe/2-kg DOs capable of catalyzing targeted reactions.展开更多
基金funded by the National Natural Science Foundation of China(Nos.31971551,31470573 and 31070478)the Tianjin Key Projects of Scientific and Technological Support(Nos.17YFZCNC00220 and 18YFZCNC01270)
文摘In the paper entitled"Efficient adsorption of Mn(Ⅱ)by layered double hydroxides intercalated with di ethylenetriaminepentaacetic acid and the mechanistic study"in Journal of Environmental Sciences,volume 85,page 56-65,there were problems with mathematical notation and dimensional errors in the calculation for Giibbs free energy.In Section 2.5:Adsorption isotherms and thermodynamics studies,authors calculated the Gibbs free energy change(△G°)
基金2018 National Key RESEARCH and Development Plan"Research on Modernization of Traditional Chinese Medicine"(No.2018YFC1707405)NSFC(No.81273946,81473463,81774289)+2 种基金Beijing Science and Technology Plan Major Fund supported projects(No.D161100005116004)Beijing Science and Technology Nova Crossover Project(NO.Z171100001117128)Independent topic selection of Chinese Academy of TCM(No.ZZ11-028)
文摘Objective: To investigate the effective compounds, potential targets and molecular mechanism of Kanglaite injection (KLTi) in the treatment of Non-Small Cell Lung Cancer (NSCLC) based on network pharmacology. Methods: The active compounds and targets of KLTi which extracted and isolated from Coix Seed were screened by Traditional Chinese Medicine Systems Pharmacology Database and Analysis Platform (TCMSP). The related genes of NSCLC were obtained by searching the Human Gene Database (GeneCards) and Online Mendelian Inheritance in Man (OMIM). The candidate targets of KLTi in the treatment of NSCLC were obtained after extracting the intersection network. The "drug-component-target-disease" network was constructed with the help of Cytoscape 3.7.2. The Protein- Protein Interaction networks were constructed on the STRING platform and core network modules were screened. The Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis of candidate genes were performed using Metascape platform, and a "pathway-target- compounds" network was constructed to further screen key genes and active compounds. Results: A total of 11 compounds, 22 candidate targets, 206 GO functions and 12 KEGG pathways were obtained. Conclusion: The active compounds of KLTi in the treatment of NSCLC are stigmasterol, stigmasterol α1 and ergosterol. The key targets are PGR, NCOA2, PTGS2, NR3C2, and PTGS1. The core GO functions included receptor activity and binding, neuronal signal transmission and hormone stimulation;KEGG mainly involves cancer pathways, neuroactive ligand-receptor interactions and calcium signaling pathways. This study reveals the molecular biological mechanism of KLTi in the treatment of NSCLC, which is speculated to be related to neuroendocrine, providing a new basis and therapeutic direction for subsequent clinical application and experimental research.
基金the National Natural Science Foundation of China(Nos.22008221 and 22238013)the Foundation of State Key Laboratory of Biobased Material and Green Papermaking,Qilu University of Technology,Shandong Academy of Sciences(No.GZKF202010).
文摘Carbon-supported single-atom catalysts were found to suffer reversible deactivation in catalytic hydrogenation,but the mechanism is still unclear.Herein,nitro compounds hydrogenation catalyzed by N-doped carbon-supported Co single atom(Co1/NC)was taken as a model to uncover the mechanism of the reversible deactivation phenomenon.Co1/NC exhibited moderate adsorption towards the substrate molecules(i.e.,nitro compounds or related intermediates),which could be strengthened by the confinement effect from the porous structure.Consequently,substrate molecules tend to accumulate within the pore channel,especially micropores that host Co1,making it difficult for the reactants to access the active sites and finally leading to their deactivation.The situation could be even worse when the substrate molecules possess a large size.Nevertheless,the catalytic activity of Co1/NC could be restored via a simple thermal treatment,which could remove the adsorbates within the pore channel,hence releasing active sites that were originally inaccessible to reactants.
基金support from the Strategic Priority Research Program of the Chinese Academy of Sciences(Grant No.XD2000000)the National Natural Science Foundation of China(21421091,21372250,21121062,21302203,20732008,21772037,21772226,21861132014 and 91956115).
文摘This paper discloses the reaction mechanism of two consecutive but different visible light photo-induced chain processes for the rapid construction of spirobi[indene]skeletons.The first process is triggered by a photo-induced single-electron-transfer(SET)of an electron donor-accepter(EDA)complex.The second process is initiated by a direct SET process between aryldiazonium salt and the excited allenic intermediate.In these two processes,another SET took place respectively on the in situ formed radical intermediate to realize a redox-neutral outcome.The mechanistic studies have been carried out by control experiments,kinetic and spectroscopic analyses,deuterium labeling experiments to support these two chain processes.
基金supported by Grants from the National Natural Science Foundation of China(grant no.U20A20404)National College Students'Innovation and Entrepreneurship Training Program(202210752014).
文摘Objective:The objective of this study was to investigate the potential mechanisms of ephedra-gypsum in the treatment ofrespiratory diseases(RDs)using network pharmacology and molecular docking techniques.Materials and Methods:The TCMSP and UniProt databases were used to mine the active components and targets of ephedra-gypsum,and the targets of RD were screened using the Online Mendelian Inheritance in Man(OMIM)and GeneCards databases.The protein-protein interaction network graph was created using the drug-disease intersection targets in the STRING database.The network diagram was analyzed using Cytoscape 3.9.1's topology function.The gene ontology(GO)and KEGG enrichment analyses were performed using the DAVID platform.Molecular docking bioactivity validation of the main active components and core targets was performed using AutoDock and PyMOL software.Results:Twenty-four compounds were screened,and 113 drug-disease targets overlapped.In total,358 biological processes,67 molecular functions,38 cellular components of GO,and 139 pathways were identified.Molecular docking analysis demonstrated the strong binding ability of tumor protein 53(TP53)-luteolin.Conclusion:The core components of ephedra-gypsum,such as quercetin,luteolin,kaempferol,and CaSO_(4)·2H_(2)O,act on key targets,such as tumor necrosis factor(TNF),interleukin-6(IL-6),TP53,and IL-1β through cytokine-mediated signaling pathways,infiammatory responses,cell proliferation,and apoptosis.This could be useful for the treatment of RD.
基金supported by the National High Technology Research and Development Program of China(863 Program,No.2012AA02A701)the National High Technology Research and Development Program of China(863 Program,No. 2013AA031901)Program for Changjiang Scholars and Innovative Research Team in University(No.IRT1066)
文摘MCRs for preparation of chromenopyridines under reflux conditions and chromenes at room temperature conditions from different salicylaldehydes,malononitrile and different thiols(mol ratio- 1:2:1) were established.Mechanistic investigation suggests that the MCRs undergo different pathways at different temperatures and catalyzed by different organic bases.The structure of chromenopyridine and chromene are confirmed by crystal X-ray crystallography.
基金This work was financially supported by National Key R&D Program of China(Nos.2019YFA0210004 and 2017YFA0207301)the National Natural Science Foundation of China(Nos.21975242 and 21890754)+5 种基金the Strategic Priority Research Program of Chinese Academy of Sciences(No.XDB36000000)Youth Innovation Promotion Association of CAS(No.CX2340007003)Major Program of Development Foundation of Hefei Center for Physical Science and Technology(No.2020HSC-CIP003)Key Research Program of Frontier Sciences of CAS(No.QYZDYSSW-SLH011)the Fok Ying-Tong Education Foundation(No.161012)Supercomputing USTC and National Supercomputing Center in Shenzhen are acknowledged for computational support.
文摘Photooxidation provides a promising strategy for removing the dominant indoor pollutant of HCHO,while the underlying photooxidation mechanism is still unclear,especially the exact role of H2O molecules.Herein,we utilize in-situ spectral techniques to unveil the H2O-mediated HCHO photooxidation mechanism.As an example,the synthetic defective Bi2WO6 ultrathin sheets realize high-rate HCHO photooxidation with the assistance of H2O at room temperature.In-situ electron paramagnetic resonance spectroscopy demonstrates the existence of•OH radicals,possibly stemmed from H2O oxidation by the photoexcited holes.Synchrotron-radiation vacuum ultraviolet photoionization mass spectroscopy and H218O isotope-labeling experiment directly evidence the formed•OH radicals as the source of oxygen atoms,trigger HCHO photooxidation to produce CO2,while in-situ Fourier transform infrared spectroscopy discloses the HCOO*radical is the main photooxidation intermediate.Density-functional-theory calculations further reveal the•OH formation process is the rate-limiting step,strongly verifying the critical role of H2O in promoting HCHO photooxidation.This work first clearly uncovers the H2O-mediated HCHO photooxidation mechanism,holding promise for high-efficiency indoor HCHO removal at ambient conditions.
基金Financial supports from the National Natural Science Foundation of China(NSFC)(No.21676120)the 111 Project(No.111-2-06)+5 种基金the High-End Foreign Experts Recruitment Program(No.G20190010083)the Program for Advanced Talents within Six Industries of Jiangsu Province(No.2015-NY-007)the National Program for Support of Top-Notch Young Professionals,the Fundamental Research Funds for the Central Universities(No.JUSRP51504)the Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions,Top-Notch Academic Programs Project of Jiangsu Higher Education Institutions,the Jiangsu Province“Collaborative Innovation Center for Advanced Industrial Fermentation”Industry Development Program,the Postgraduate Research&Practice Innovation Program of Jiangsu Province(No.KYCX19_1833)the Program for the Key Laboratory of Enzymes of Suqian(No.M201803)the National First-Class Discipline Program of Light Industry Technology and Engineering(No.LITE2018-09)are greatly appreciated。
文摘The asymmetric hydroxylation of inactive carbon atoms in organic compounds remains an important reaction in the industrial synthesis of valuable chiral compounds.Fe(II)and 2-ketoglutarate-dependent dioxygenases(Fe/2-kg DOs)are the largest known subgroups of mononuclear nonheme-Fe(II)-dependent oxygenases,catalyzing various oxidation reactions of C-H bonds.Recent developments in Fe/2-kg DO-related researches have coupled concepts from bioinformatics,synthetic biology,and computational biology to establish effective biotransformation systems.The most well-studied and characterized activ-ity of the Fe/2-kg DOs is substrate hydroxylation,with regard to which mechanistic studies involving the Fe center assist in engineering the protein frameworks of these enzymes to obtain the desired catalytic enhancements.Amino acids are typical substrates of Fe/2-kg DOs and are usually converted into hydroxyl amino acids,which are widely used as intermediates in pharmaceutical and fine chemical industries.Herein,we have reviewed prior structural and mechanistic studies on Fe/2-kg DOs,as well as studies on the Fe/2-kg DO-mediated selective C-H oxidation process for selective hydroxyl amino acid synthesis,which will further our journey along the promising path of building complexity via C-H bond oxidation.Further,new bioinformatics techniques should be adopted with structure-based protein rational design to mine sequence databases and shrink mutant libraries to produce a diverse panel of functional Fe/2-kg DOs capable of catalyzing targeted reactions.