seesar optibrium software (Optibrium)
Structured Review

Seesar Optibrium Software, supplied by Optibrium, 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/seesar+software/optibrium+properties/pmc12155980-70-3-4
Average 90 stars, based on 1 article reviews
Images
1) Product Images from "Design, Synthesis, and Biological Evaluations of a Novel Resveratrol-Type Analogue Against VEGF"
Article Title: Design, Synthesis, and Biological Evaluations of a Novel Resveratrol-Type Analogue Against VEGF
Journal: Molecules
doi: 10.3390/molecules30112345
Figure Legend Snippet: ( A ) Design of resveratrol-type derivatives. ( B ) Synthetic route towards RE-1. (I) 1,3-dichloropropane, NaH, THF, 0 °C-rt, 8 h; (II) pterostilbene, NaH, THF, rt, 16 h, 26%. Docking studies of RES ( C ) and RE-1 ( D ) against VEGF protein. VEGF 1–165 (PDB code: 1FLT) domain was selected as a binding site and docking studies were performed using SEESAR software (13.0 version). RES: resveratrol.
Techniques Used: Binding Assay, Software
Related Articles
Molecular Weight:Article Title: Discovery of druggable potent inhibitors of serine proteases and farnesoid X receptor by ligand-based virtual screening to obstruct SARS-CoV-2. Article Snippet: The coronavirus, a subfamily of the coronavirinae family, is an RNA virus with over 40 variations that can infect humans, non-human mammals and birds.. There are seven types of human coronaviruses, including SARS-CoV-2, is responsible for the recent COVID-19 pandemic.. The current study is focused on the identification of drug molecules for the treatment of COVID-19 by targeting human proteases like transmembrane serine protease 2 (TMPRSS2), furin, cathepsin B, and a nuclear receptor named farnesoid X receptor (FXR). other:Article Title: A therapeutic small molecule enhances γ-oscillations and improves cognition/memory in Alzheimer’s disease model mice Article Snippet: Additionally, predictive analysis for brain permeability and other drug-like properties was done in silico using Article Title: Identification of potential inhibitors targeting yellow fever virus helicase through ligand and structure-based computational studies. Article Snippet: Yellow fever is a flavivirus having plus-sensed RNA which encodes a single polyprotein.. Host proteases cut this polyprotein into seven nonstructural proteins including a vital NS3 protein.. The present study aims to identify the most effective inhibitor against the helicase (NS3) using different advanced ligand and structure-based computational studies. Software:Article Title: Design, Synthesis, and Biological Evaluations of a Novel Resveratrol-Type Analogue Against VEGF Article Snippet: .. Furthermore, we employed Binding Assay:Article Title: Identification and characterization of domain-specific inhibitors of DENV NS3 and NS5 proteins by in silico screening methods. Article Snippet: .. The ligands were docked to the proteins onto the binding pockets identified and the properties such as estimated affinity, torsion quality, H-bond network, molecular clashes and |
