discovery studio visualizer v. 17.2 (Dassault Systemes)
90
Structured Review
Dassault Systemes
discovery studio visualizer v. 17.2
Discovery Studio Visualizer V. 17.2, supplied by Dassault Systemes, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/discovery+studio+visualizer+v%2E17%2E2/discovery+studio+modeling+environment+release+2017/pm40159997-293-6-10
Average 90 stars, based on 1 article reviews
Discovery Studio Visualizer V. 17.2, supplied by Dassault Systemes, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/discovery+studio+visualizer+v%2E17%2E2/discovery+studio+modeling+environment+release+2017/pm40159997-293-6-10
Average 90 stars, based on 1 article reviews
discovery studio visualizer v. 17.2 - by Bioz Stars,
2026-10
90/100 stars
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Related Articles
Software:Article Title: Identification of a novel binding mechanism of Quinoline based molecules with lactate dehydrogenase of Plasmodium falciparum . Article Snippet: Dassault Systèmes BIOVIA, Discovery Studio Visualizer, v.17.2, San Diego: Article Title: Novel recombinant keratin degrading subtilisin like serine alkaline protease from Bacillus cereus isolated from marine hydrothermal vent crabs Article Snippet: Figure 3 Structural predictions. ( a ) I-TASSER structure prediction ( https://zhanglab.ccmb.med.umich.edu/I-TASSER/ ) and image retrieved from Article Title: Design, Synthesis and Assay of Novel Methylxanthine-Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors. Article Snippet: ; Richmond, Article Title: Synthesis of cytotoxic urs-12-ene- and 28-norurs-12-ene- type conjugates with amino- and mercapto-1,3,4-oxadiazoles and mercapto-1,2,4-triazoles. Article Snippet: A small library of 2-mercapto-1,3,4-oxadiazoles, 2-amino-1,3,4-oxadiazoles and 3-mercapto-1,2,4triazoles attached to the urs-12-eneand 28-nor-urs-12-ene skeleton has been obtained.. Ursolic acid derived hydrazides have been identified as useful starting materials for the developed synthesis.. Ursolic acid hydrazide provided access to oxadiazoles attached directly to C-17 of the ursane core, but synthesis of structurally related 3-mercapto-1,2,4-triazoles was not possible in this way due to steric hindrance of the triterpenoid. Article Title: Role of Circular RNA MMP9 in Glioblastoma Progression: From Interaction With hnRNPC and hnRNPA1 to Affecting the Expression of BIRC5 by Sequestering miR-149. Article Snippet: Glioblastoma multiforme (GBM) presents a significant challenge in neurooncology due to its aggressive behavior and selfrenewal capacity.. Circular RNAs (circRNAs), a subset of noncoding RNAs (ncRNAs) generated through mRNA backsplicing, are gaining attention as potential targets for GBM research.. In our study, we sought to explore the functional role of circMMP9 (circular form of matrix metalloproteinase9) as a promising therapeutic target for GBM through bioinformatic predictions and human data analysis. Article Title: Synthesis and evaluation of 99m Tc-labeled 1-(2-Pyridyl)piperazine derivatives as radioligands for 5HT 7 receptors. Article Snippet: Glioblastoma multiform (GBM) is one of the most aggressive tumors of the central nervous system in humans.. GBM overexpresses serotonin-7 receptors (5-HT7Rs); hence, this study aims to develop 5-HT7R targeted radiotracers.. Aryl piperazine derivatives can act as ligands for 5-HT7R. Ligand Binding Assay:Article Title: Identification of a novel binding mechanism of Quinoline based molecules with lactate dehydrogenase of Plasmodium falciparum . Article Snippet: Dassault Systèmes BIOVIA, Discovery Studio Visualizer, v.17.2, San Diego: Article Title: Novel recombinant keratin degrading subtilisin like serine alkaline protease from Bacillus cereus isolated from marine hydrothermal vent crabs Article Snippet: Figure 3 Structural predictions. ( a ) I-TASSER structure prediction ( https://zhanglab.ccmb.med.umich.edu/I-TASSER/ ) and image retrieved from Article Title: Design, Synthesis and Assay of Novel Methylxanthine-Alkynylmethylamine Derivatives as Acetylcholinesterase Inhibitors. Article Snippet: ; Richmond, Article Title: Synthesis of cytotoxic urs-12-ene- and 28-norurs-12-ene- type conjugates with amino- and mercapto-1,3,4-oxadiazoles and mercapto-1,2,4-triazoles. Article Snippet: A small library of 2-mercapto-1,3,4-oxadiazoles, 2-amino-1,3,4-oxadiazoles and 3-mercapto-1,2,4triazoles attached to the urs-12-eneand 28-nor-urs-12-ene skeleton has been obtained.. Ursolic acid derived hydrazides have been identified as useful starting materials for the developed synthesis.. Ursolic acid hydrazide provided access to oxadiazoles attached directly to C-17 of the ursane core, but synthesis of structurally related 3-mercapto-1,2,4-triazoles was not possible in this way due to steric hindrance of the triterpenoid. Article Title: Role of Circular RNA MMP9 in Glioblastoma Progression: From Interaction With hnRNPC and hnRNPA1 to Affecting the Expression of BIRC5 by Sequestering miR-149. Article Snippet: Glioblastoma multiforme (GBM) presents a significant challenge in neurooncology due to its aggressive behavior and selfrenewal capacity.. Circular RNAs (circRNAs), a subset of noncoding RNAs (ncRNAs) generated through mRNA backsplicing, are gaining attention as potential targets for GBM research.. In our study, we sought to explore the functional role of circMMP9 (circular form of matrix metalloproteinase9) as a promising therapeutic target for GBM through bioinformatic predictions and human data analysis. Article Title: Synthesis and evaluation of 99m Tc-labeled 1-(2-Pyridyl)piperazine derivatives as radioligands for 5HT 7 receptors. Article Snippet: Glioblastoma multiform (GBM) is one of the most aggressive tumors of the central nervous system in humans.. GBM overexpresses serotonin-7 receptors (5-HT7Rs); hence, this study aims to develop 5-HT7R targeted radiotracers.. Aryl piperazine derivatives can act as ligands for 5-HT7R. |