population-based adme simulator version 15 Search Results


90
Bayer AG filapixant
Filapixant, supplied by Bayer AG, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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filapixant - by Bioz Stars, 2026-08
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Molegro ApS virtual docker mvd
RM5 and NLRP3 Docking by <t>MVD</t> 5.5. This figure illustrates the docking of RM5 to the NLRP3 protein <t>using</t> <t>Molegro</t> Virtual Docker (MVD) 5.5. The blue color represents the crystal structure of NLRP3, while the light brown indicates the docking structure of RM5. The superimposition of these structures demonstrates the alignment and binding conformation of RM5 within the NLRP3 active site, validating the accuracy of the docking protocol.
Virtual Docker Mvd, supplied by Molegro ApS, 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/population-based+adme+simulator+version+15/pmc11311378-234-6-6?v=Molegro+ApS
Average 90 stars, based on 1 article reviews
virtual docker mvd - by Bioz Stars, 2026-08
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HeartFlow Inc ffrct physiological models
RM5 and NLRP3 Docking by <t>MVD</t> 5.5. This figure illustrates the docking of RM5 to the NLRP3 protein <t>using</t> <t>Molegro</t> Virtual Docker (MVD) 5.5. The blue color represents the crystal structure of NLRP3, while the light brown indicates the docking structure of RM5. The superimposition of these structures demonstrates the alignment and binding conformation of RM5 within the NLRP3 active site, validating the accuracy of the docking protocol.
Ffrct Physiological Models, supplied by HeartFlow Inc, 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/population-based+adme+simulator+version+15/10__1161_slash_circinterventions__118__007577-51-26-74?v=HeartFlow+Inc
Average 90 stars, based on 1 article reviews
ffrct physiological models - by Bioz Stars, 2026-08
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SAS institute charmm19/sas
RM5 and NLRP3 Docking by <t>MVD</t> 5.5. This figure illustrates the docking of RM5 to the NLRP3 protein <t>using</t> <t>Molegro</t> Virtual Docker (MVD) 5.5. The blue color represents the crystal structure of NLRP3, while the light brown indicates the docking structure of RM5. The superimposition of these structures demonstrates the alignment and binding conformation of RM5 within the NLRP3 active site, validating the accuracy of the docking protocol.
Charmm19/Sas, supplied by SAS institute, 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/population-based+adme+simulator+version+15/10__1021_slash_ja057216r-264-0-28?v=SAS+institute
Average 90 stars, based on 1 article reviews
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DNASTAR lasergene molecular biology suite18
RM5 and NLRP3 Docking by <t>MVD</t> 5.5. This figure illustrates the docking of RM5 to the NLRP3 protein <t>using</t> <t>Molegro</t> Virtual Docker (MVD) 5.5. The blue color represents the crystal structure of NLRP3, while the light brown indicates the docking structure of RM5. The superimposition of these structures demonstrates the alignment and binding conformation of RM5 within the NLRP3 active site, validating the accuracy of the docking protocol.
Lasergene Molecular Biology Suite18, supplied by DNASTAR, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/population-based+adme+simulator+version+15/10__1007_slash_s10462___020___09951___1-928-105-105?v=DNASTAR
Average 93 stars, based on 1 article reviews
lasergene molecular biology suite18 - by Bioz Stars, 2026-08
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RenderX Inc xsl•fo renderx session details
RM5 and NLRP3 Docking by <t>MVD</t> 5.5. This figure illustrates the docking of RM5 to the NLRP3 protein <t>using</t> <t>Molegro</t> Virtual Docker (MVD) 5.5. The blue color represents the crystal structure of NLRP3, while the light brown indicates the docking structure of RM5. The superimposition of these structures demonstrates the alignment and binding conformation of RM5 within the NLRP3 active site, validating the accuracy of the docking protocol.
Xsl•Fo Renderx Session Details, supplied by RenderX Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
xsl•fo renderx session details - by Bioz Stars, 2026-08
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Image Search Results


RM5 and NLRP3 Docking by MVD 5.5. This figure illustrates the docking of RM5 to the NLRP3 protein using Molegro Virtual Docker (MVD) 5.5. The blue color represents the crystal structure of NLRP3, while the light brown indicates the docking structure of RM5. The superimposition of these structures demonstrates the alignment and binding conformation of RM5 within the NLRP3 active site, validating the accuracy of the docking protocol.

Journal: International Journal of Molecular Sciences

Article Title: High-Throughput Molecular Modeling and Evaluation of the Anti-Inflammatory Potential of Açaí Constituents against NLRP3 Inflammasome

doi: 10.3390/ijms25158112

Figure Lengend Snippet: RM5 and NLRP3 Docking by MVD 5.5. This figure illustrates the docking of RM5 to the NLRP3 protein using Molegro Virtual Docker (MVD) 5.5. The blue color represents the crystal structure of NLRP3, while the light brown indicates the docking structure of RM5. The superimposition of these structures demonstrates the alignment and binding conformation of RM5 within the NLRP3 active site, validating the accuracy of the docking protocol.

Article Snippet: The docking simulations were performed using Molegro Virtual Docker (MVD) with the following parameters based on the literature: X = 17.03; Y = 35.46; Z = 125.55; the grid resolution: 0.30 Å; the number of runs: 10; the population size: 50; the maximum iterations: 1500; the energy threshold: 100.0; and the binding site radius (around the active site): 15 Å.

Techniques: Binding Assay