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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

    The general structure of a guanidine. Guanidines are a group of organic compounds sharing a common functional group with the general structure (R 1 R 2 N)(R 3 R 4 N)C=N−R 5. The central bond within this group is that of an imine, and the group is related structurally to amidines and ureas.

  4. Category:Guanidines - Wikipedia

    en.wikipedia.org/wiki/Category:Guanidines

    Download QR code; Print/export Download as PDF; Printable version; ... Help. The general structure of a guanidine Subcategories. This category has the following 9 ...

  5. 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.

  6. 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

  7. Chaotropic agent - Wikipedia

    en.wikipedia.org/wiki/Chaotropic_agent

    A chaotropic agent is a substance which disrupts the structure of, and denatures, macromolecules such as proteins and nucleic acids (e.g. DNA and RNA).Chaotropic solutes increase the entropy of the system by interfering with intermolecular interactions mediated by non-covalent forces such as hydrogen bonds, van der Waals forces, and hydrophobic effects.

  8. Category:Guanidinium compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Guanidinium_compounds

    Download QR code; Print/export Download as PDF; Printable version; In other projects Wikimedia Commons; Wikidata item; ... Guanidine nitrate; Guanidinium chloride;

  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]