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  2. 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.

  3. List of phytochemicals in food - Wikipedia

    en.wikipedia.org/wiki/List_of_phytochemicals_in_food

    Isoflavones (phytoestrogens) use the 3-phenylchromen-4-one skeleton (with no hydroxyl group substitution on carbon at position 2). Daidzein (formononetin) soy, alfalfa sprouts, red clover, chickpeas, peanuts, kudzu, other legumes. Genistein (biochanin A) soy, alfalfa sprouts, red clover, chickpeas, peanuts, other legumes. Glycitein soy. Isoflavanes

  4. List of Japanese ingredients - Wikipedia

    en.wikipedia.org/wiki/List_of_Japanese_ingredients

    pufferfish - flesh, skin, soft roe eaten as sashimi and hot pot (tecchiri); organs, etc. poisonous; roe also contain tetrodotoxin but a regional specialty food cures it in nuka until safe to eat. tilefish ( amadai ) - in a Kyoto-style preparation, it is roasted to be eaten scales and all; used in high-end surimi .

  5. Guanosine - Wikipedia

    en.wikipedia.org/wiki/Guanosine

    Guanosine (symbol G or Guo) is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a β-N 9-glycosidic bond.Guanosine can be phosphorylated to become guanosine monophosphate (GMP), cyclic guanosine monophosphate (cGMP), guanosine diphosphate (GDP), and guanosine triphosphate (GTP).

  6. Pickled Vegetable Salad with Soft-Boiled Eggs Recipe - AOL

    www.aol.com/food/recipes/pickled-vegetable-salad...

    Carefully lower the eggs into the saucepan and reduce the heat to moderate. Simmer the eggs for 6 minutes. Pour off the hot water and gently shake the eggs in the pan to crack the shells.

  7. Guanine - Wikipedia

    en.wikipedia.org/wiki/Guanine

    A Fischer–Tropsch synthesis can also be used to form guanine, along with adenine, uracil, and thymine. Heating an equimolar gas mixture of CO, H 2 , and NH 3 to 700 °C for 15 to 24 minutes, followed by quick cooling and then sustained reheating to 100 to 200 °C for 16 to 44 hours with an alumina catalyst, yielded guanine and uracil:

  8. Galega officinalis - Wikipedia

    en.wikipedia.org/wiki/Galega_officinalis

    The English name "goat's-rue" is a translation of the Latin Ruta capraria, used for the plant in 1554 when it was considered to be related to Ruta graveolens, or common rue. [9] The Latin specific epithet officinalis refers to plants with some medicinal, culinary or herbal attributes. [10] Galega bicolor is a synonym.

  9. Category:Guanidines - Wikipedia

    en.wikipedia.org/wiki/Category:Guanidines

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