This work describes the inhibition effect of different concentration of an aqueous extracted of Peganum harmala seed on the corrosion of carbon steel in 1 M H2SO4 solution using potentiostatic polarization techniques ...This work describes the inhibition effect of different concentration of an aqueous extracted of Peganum harmala seed on the corrosion of carbon steel in 1 M H2SO4 solution using potentiostatic polarization techniques at the temperature range (298 - 328) K. The result showed that the inhibition efficiency increased with increasing of extract inhibitor concentration and temperature. The adsorption of inhibitor on carbon steel surface was fit into Langmuir adsorption isotherm. Kinetic and thermodynamic parameters governing the corrosion and the adsorption process were calculated and discussed.展开更多
Peganum harmala L.is a medicinal plant,and its seeds have been used to treat gastrointestinal cancer and malaria for a long time in North-Western China.In the present study,we aimed to probe the potential molecular ta...Peganum harmala L.is a medicinal plant,and its seeds have been used to treat gastrointestinal cancer and malaria for a long time in North-Western China.In the present study,we aimed to probe the potential molecular targets and pharmacological mechanisms of Peganum harmala L.seeds(PHS)on hepatocellular carcinoma(HCC)using network analysis and molecular docking.First,the chemical ingredients of PHS were obtained from TCMID and BATMAN-TCM databases,and the effective ingredients were screened by SwissADME.Furthermore,the target information of the effective ingredients was acquired from PharmMapper and SwissTargetPrediction databases.Secondly,HCC-related targets were obtained from Liverome,DisGeNET,and GeneCards databases.The intersection with the PHS was obtained.The“compounds-targets”was drawn using Cytoscape software,and PPI network diagrams were drawn using their intersection targets.GO analysis and KEGG enrichment analysis were carried out using the DAVID database.Finally,molecular docking was conducted between protein receptors and the active components using AutoDockTools.Our results showed 105 intersection targets of PHS with HCC.Moreover,10 core targets included ALB,AKT1,EGFR,CASP3,SRC,ESR1,MAPK3,MMP9,ANXA5,and MAPK1.Besides,404 GO functional annotations were obtained,including 287 biological processes,37 cell compositions,and 80 molecular functions.In addition,110 signaling molecules and pathways,including chemical oncogene receptors,PI3K-Akt pathway,HCC,and hepatitis B,were identified.The molecular docking results showed that the binding energies of the 10 core targets and the 12 active components were all less than–5 kcal/mol.In conclusion,this study expounded on the“component-target-pathway”interaction mechanism of PHS for the treatment of HCC,and it also provided a scientific basis for the clinical application of PHS.展开更多
文摘This work describes the inhibition effect of different concentration of an aqueous extracted of Peganum harmala seed on the corrosion of carbon steel in 1 M H2SO4 solution using potentiostatic polarization techniques at the temperature range (298 - 328) K. The result showed that the inhibition efficiency increased with increasing of extract inhibitor concentration and temperature. The adsorption of inhibitor on carbon steel surface was fit into Langmuir adsorption isotherm. Kinetic and thermodynamic parameters governing the corrosion and the adsorption process were calculated and discussed.
基金The National Natural Science Foundation of China(Grant No.81760637,81460539)the National Natural Science Foundation of Xinjiang(Grant No.2017D01C207)+1 种基金the Open Research Fund of Xinjiang Uygur Autonomous Region Key Laboratory(Grant No.XJDX1713)。
文摘Peganum harmala L.is a medicinal plant,and its seeds have been used to treat gastrointestinal cancer and malaria for a long time in North-Western China.In the present study,we aimed to probe the potential molecular targets and pharmacological mechanisms of Peganum harmala L.seeds(PHS)on hepatocellular carcinoma(HCC)using network analysis and molecular docking.First,the chemical ingredients of PHS were obtained from TCMID and BATMAN-TCM databases,and the effective ingredients were screened by SwissADME.Furthermore,the target information of the effective ingredients was acquired from PharmMapper and SwissTargetPrediction databases.Secondly,HCC-related targets were obtained from Liverome,DisGeNET,and GeneCards databases.The intersection with the PHS was obtained.The“compounds-targets”was drawn using Cytoscape software,and PPI network diagrams were drawn using their intersection targets.GO analysis and KEGG enrichment analysis were carried out using the DAVID database.Finally,molecular docking was conducted between protein receptors and the active components using AutoDockTools.Our results showed 105 intersection targets of PHS with HCC.Moreover,10 core targets included ALB,AKT1,EGFR,CASP3,SRC,ESR1,MAPK3,MMP9,ANXA5,and MAPK1.Besides,404 GO functional annotations were obtained,including 287 biological processes,37 cell compositions,and 80 molecular functions.In addition,110 signaling molecules and pathways,including chemical oncogene receptors,PI3K-Akt pathway,HCC,and hepatitis B,were identified.The molecular docking results showed that the binding energies of the 10 core targets and the 12 active components were all less than–5 kcal/mol.In conclusion,this study expounded on the“component-target-pathway”interaction mechanism of PHS for the treatment of HCC,and it also provided a scientific basis for the clinical application of PHS.
