chemdraw ultra version 8.0 (CambridgeSoft Corporation)
90
Structured Review
CambridgeSoft Corporation
chemdraw ultra version 8.0
Chemdraw Ultra Version 8.0, supplied by CambridgeSoft Corporation, 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/chemdraw+ultra+version+8%2E0/chemdraw/pm37154740-46-0-4
Average 90 stars, based on 1 article reviews
Chemdraw Ultra Version 8.0, supplied by CambridgeSoft Corporation, 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/chemdraw+ultra+version+8%2E0/chemdraw/pm37154740-46-0-4
Average 90 stars, based on 1 article reviews
chemdraw ultra version 8.0 - by Bioz Stars,
2026-09
90/100 stars
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other:Article Title: A quantum mechanical investigation of possible mechanisms for the nucleotidyl transfer reaction catalyzed by DNA polymerase beta. Article Snippet: Several quantum mechanical (QM) and hybrid quantum/molecular mechanical (QM/MM) studies have been employed recently to analyze the nucleotidyl transfer reaction in DNA polymerase â (pol â).. Our examination reveals strong dependence of the reported mechanism on the initial molecular model.. Thus, we explore here several model systems by QM methods to investigate pol â’s possible pathway variations. Article Title: Processes for preparing (E)-styrylbenzylsulfone compounds and uses thereof for treating proliferative disorders Article Snippet: The compounds, except for the α,b-unsaturated sulfonamides, were named using the “Structure to Name” program within Article Title: Molecular docking and antimalarial evaluation of hybrid para -aminobenzoic acid 1,3,5 triazine derivatives via inhibition of Pf -DHFR. Article Snippet: In this study, a structurally guided pharmacophore hybridization strategy is used to combine the two key structural scaffolds, para-aminobenzoic acid (PABA), and 1,3,5 triazine in search of new series of antimalarial agents.. A combinatorial library of 100 compounds was prepared in five different series as [4A (1–22), 4B (1–21), 4 C (1–20), 4D (1–19) and 4E (1–18)] using different primary and secondary amines, from where 10 compounds were finally screened out through molecular property filter analysis and molecular docking study as promising PABA substituted 1,3,5-triazine scaffold as an antimalarial agent.. The docking results showed that compounds 4A12 and 4A20 exhibited good binding interaction with Phe58, IIe164, Ser111, Arg122, Asp54 ( 424.19 to 360.34 kcal/mol) and Arg122, Phe116, Ser111, Phe58 ( 506.29 to 431.75 kcal/mol) against wild (1J3I) and quadruple mutant (1J3K) type of Pf-DHFR. Article Title: Substituted phenoxy-and phenylthio-derivatives for treating proliferative disorders Article Snippet: The compounds, except for the α,β-unsaturated sulfonamides, were named using the “Structure to Name” program within Article Title: Heteroaryl sulfones and sulfonamides and therapeutic uses thereof Article Snippet: The naming of compounds disclosed herein was done by employing the structure naming programs included |