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  2. Guanidinium chloride - Wikipedia

    en.wikipedia.org/wiki/Guanidinium_chloride

    At high concentrations of guanidinium chloride (e.g., 6 M), proteins lose their ordered structure, and they tend to become randomly coiled, i.e. they do not contain any residual structure. However, at concentrations in the millimolar range in vivo, guanidinium chloride has been shown to "cure" prion positive yeast cells (i.e. cells exhibiting a ...

  3. Guanidine - Wikipedia

    en.wikipedia.org/wiki/Guanidine

    Guanidine exists protonated, as guanidinium, in solution at physiological pH. Guanidinium chloride (also known as guanidine hydrochloride) has chaotropic properties and is used to denature proteins. Guanidinium chloride is known to denature proteins with a linear relationship between concentration and free energy of unfolding.

  4. Category:Guanidines - Wikipedia

    en.wikipedia.org/wiki/Category:Guanidines

    Printable version; In other projects ... Help. The general structure of a guanidine Subcategories. This category has the following 8 subcategories, out of 8 total ...

  5. File:Guanidin.svg - Wikipedia

    en.wikipedia.org/wiki/File:Guanidin.svg

    The following other wikis use this file: Usage on az.wikipedia.org Quanidin; Usage on bn.wikipedia.org গুয়ানিডিন; Usage on ca.wikipedia.org

  6. Wikipedia : WikiProject Pharmacology/Structural diagrams

    en.wikipedia.org/.../Structural_diagrams

    Molecular structure diagrams used in drug-related pharmacology articles should be created using a molecule editor program, such as ChemDraw, ChemSketch, or ISIS/Draw (ChemDraw and Isis/draw are commercial software packages, ChemSketch is freeware.

  7. Category:Guanidinium compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Guanidinium_compounds

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  8. Native chemical ligation - Wikipedia

    en.wikipedia.org/wiki/Native_chemical_ligation

    It involves the reaction of an unprotected peptide thioester with a second, unprotected peptide that has an N-terminal cysteine residue. It is carried out in aqueous solution at neutral pH, usually in 6 M guanidine.hydrochloride, in the presence of an arylthiol catalyst and typically gives near-quantitative yields of the desired ligation product.

  9. 7-Methyl-1,5,7-triazabicyclo (4.4.0)dec-5-ene - Wikipedia

    en.wikipedia.org/wiki/7-methyl-1,5,7...

    7-Methyl-1,5,7-triazabicyclo[4.4.0]dec-5-ene (mTBD) is a bicyclic strong guanidine base (pK a = 25.43 in CH 3 CN and pK a = 17.9 in THF). [3] mTBD, like 1,5,7-triazabicyclo[4.4.0]dec-5-ene and other guanidine super bases, can be used as a catalyst in a variety of chemical reactions. [4]