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Copper-free click chemistry is a bioorthogonal reaction first developed by Carolyn Bertozzi as an activated variant of an azide alkyne Huisgen cycloaddition, based on the work by Karl Barry Sharpless et al. Unlike CuAAC, Cu-free click chemistry has been modified to be bioorthogonal by eliminating a cytotoxic copper catalyst, allowing reaction ...
Orthogonal ligand-protein pairs (also known as re-engineered ligand-receptor interfaces or re-engineered enzyme-substrate interactions) are a protein-ligand binding pair made to be independent of the original binding pair. This is done by taking a mutant protein (naturally occurring or selectively engineered), which is activated by a different ...
Design of experiments with full factorial design (left), response surface with second-degree polynomial (right) The design of experiments ( DOE ), [ 1 ] also known as experiment design or experimental design , is the design of any task that aims to describe and explain the variation of information under conditions that are hypothesized to ...
Following hit confirmation, several compound clusters will be chosen according to their characteristics in the previously defined tests. An Ideal compound cluster will contain members that possess: high affinity towards the target (less than 1 μM) selectivity versus other targets; significant efficacy in a cellular assay
The line segments AB and CD are orthogonal to each other. In mathematics, orthogonality is the generalization of the geometric notion of perpendicularity.Whereas perpendicular is typically followed by to when relating two lines to one another (e.g., "line A is perpendicular to line B"), [1] orthogonal is commonly used without to (e.g., "orthogonal lines A and B").
Orthogonal tandem catalysis is a "one-pot reaction in which sequential catalytic processes occur through two or more functionally distinct, and preferably non-interfering, catalytic cycles". [7] This technique has been deployed in tandem alkane-dehydrogenation-olefin-metathesis catalysis [ 8 ] [ 9 ]
These combinations are chosen to satisfy two conditions. First, the total amount of s and p orbital contributions must be equivalent before and after hybridisation. Second, the hybrid orbitals must be orthogonal to each other. [27] [28] If two hybrid orbitals were not orthogonal, by definition they would have nonzero orbital overlap. Electrons ...
In organic chemistry, a ring flip (also known as a ring inversion or ring reversal) is the interconversion of cyclic conformers that have equivalent ring shapes (e.g., from a chair conformer to another chair conformer) that results in the exchange of nonequivalent substituent positions. [1]