probit analysis using litchfield and wilcoxon (GraphPad Software Inc)
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probit analysis using litchfield and wilcoxon
Probit Analysis Using Litchfield And Wilcoxon, supplied by GraphPad Software 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/probit+analysis+using+litchfield+and+wilcoxon+or+graphpad+prism%C2%AE+software/probit+analysis+using+litchfield+and+wilcoxon/pmc09721285-158-18-20
Average 90 stars, based on 1 article reviews
Probit Analysis Using Litchfield And Wilcoxon, supplied by GraphPad Software 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/probit+analysis+using+litchfield+and+wilcoxon+or+graphpad+prism%C2%AE+software/probit+analysis+using+litchfield+and+wilcoxon/pmc09721285-158-18-20
Average 90 stars, based on 1 article reviews
probit analysis using litchfield and wilcoxon - by Bioz Stars,
2026-10
90/100 stars
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Concentration Assay:Article Title: Absolute configuration and biological profile of two thiazinooxadiazol-3-ones with L-type calcium channel activity: a study of the structural effects. Article Snippet: In the framework of our interest in racemic thiazinooxadiazol-3-ones we determined the absolute configuration and the biological activity as L-type calcium channel blockers of two compounds that differ in the length of the acetal chain, which could affect the pharmacological profile.. We observed an interesting inversion of the stereoselectivity, with the activity residing on the R-form for a short chain compound (n = 1) and on the S-form for a long chain one (n = 12).. The length of the linear acetal chain appears to be able to invert the stereoselectivity of such a class of compounds, and in silico simulations suggested that this different behaviour might be explained by different hydrophilic and hydrophobic interactions with the binding site. Software:Article Title: Absolute configuration and biological profile of two thiazinooxadiazol-3-ones with L-type calcium channel activity: a study of the structural effects. Article Snippet: In the framework of our interest in racemic thiazinooxadiazol-3-ones we determined the absolute configuration and the biological activity as L-type calcium channel blockers of two compounds that differ in the length of the acetal chain, which could affect the pharmacological profile.. We observed an interesting inversion of the stereoselectivity, with the activity residing on the R-form for a short chain compound (n = 1) and on the S-form for a long chain one (n = 12).. The length of the linear acetal chain appears to be able to invert the stereoselectivity of such a class of compounds, and in silico simulations suggested that this different behaviour might be explained by different hydrophilic and hydrophobic interactions with the binding site. |