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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. Category:Guanidines - Wikipedia

    en.wikipedia.org/wiki/Category:Guanidines

    العربية; Azərbaycanca; تۆرکجه; Български; Bosanski; Català; Deutsch; Ελληνικά; Español; Esperanto; Euskara; فارسی; Français; Galego

  4. Guanine - Wikipedia

    en.wikipedia.org/wiki/Guanine

    The first isolation of guanine was reported in 1844 by the German chemist Julius Bodo Unger (1819–1885), who obtained it as a mineral formed from the excreta of sea birds, which is known as guano and which was used as a source of fertilizer; guanine was named in 1846. [3]

  5. Guano - Wikipedia

    en.wikipedia.org/wiki/Guano

    Guano is a highly effective fertilizer due to the high content of nitrogen, phosphate, and potassium, all key nutrients essential for plant growth. Guano was also, to a lesser extent, sought for the production of gunpowder and other explosive materials.

  6. Biguanide - Wikipedia

    en.wikipedia.org/wiki/Biguanide

    In the 1920s, guanidine compounds were discovered in Galega extracts. Animal studies showed that these compounds lowered blood glucose levels. Some less toxic derivatives, synthalin A and synthalin B, were used for diabetes treatment, but after the discovery of insulin, their use declined.

  7. Guanidinium chloride - Wikipedia

    en.wikipedia.org/wiki/Guanidinium_chloride

    This dosage may be gradually increased to a total daily dosage of 35 mg/kg (16 mg/pound) of body weight per day or up to the development of side effects. Side effects may include increased peristalsis, diarrhea, paresthesia (tingling and numbness), and nausea. Fatal bone-marrow suppression, apparently dose related, can occur with guanidine. [7]

  8. Guanidinopropionic acid - Wikipedia

    en.wikipedia.org/wiki/Guanidinopropionic_acid

    Studies on animals (rats, monkeys, hamsters) show that acidic guanidine derivatives such as β-GPA can ameliorate hyperglycemia in animal models of noninsulin-dependent diabetes. [ 4 ] Though the oral availability of β-GPA is well established, the basic uptake mechanism has not been studied yet.

  9. Sulfaguanidine - Wikipedia

    en.wikipedia.org/wiki/Sulfaguanidine

    Sulfaguanidine is a sulfonamide.. Sulfaguanidine is a guanidine derivative of sulfanilamide used in veterinary medicine. Sulfaguanidine is poorly absorbed from the gut which makes it suitable for the treatment of bacillary dysentery and other enteric infections.