guanidine การใช้

• The factory makes guanidine nitrate, which is used in chemical explosives.
• The guanidine group of arginine residues condense with malondialdehyde to give 2-aminopyrimidines.
• Denaturants 6M-urea or 4M-guanidine hydrochloride did not destroy the protein.
• Fatal bone-marrow suppression, apparently dose related, can occur with guanidine.
• Note : this compound may also be recognized as "'guanidine "'thiocyanate.
• Durant was able to provide his expertise on guanidine chemistry to further the progress of the research.
• It is developed to explain the extraordinary stability of guanidinium cation and high basicity of the Guanidine.
• If you heat ammonium thiocyanate too hot you get an irreverable conversion to guanidine thiocyanate and ammonium trithiocarbonate.
• Lugduname is part of a family of extremely potent sweeteners which contain acetic acid functional groups attached to guanidine.
• Guanidine hydrochloride is indicated for the reduction of the symptoms of muscle weakness and easy fatigability associated with Eaton-Lambert syndrome.
• The toxicity was proposed to arise from the thiourea group, and similar guanidine analogues were investigated until the ultimate discovery of cimetidine.
• This is because guanidinium is the conjugate acid of guanidine and is called the guanidinium cation, [ CH 6 N 3 ] +.
• It was originally proposed that a hydrogen bond between the uracil and guanidine groups in the enol tautomer would make this the dominant form.
• This result was completely forgotten, as other guanidine analogs, such as the synthalins, took over and were themselves soon overshadowed by insulin.
• This reagent is part of the Lowry protein assay, and will also react with some nitrogen-containing compounds such as hydroxylamine and guanidine.
• Parsons tried to resolve GALCIT-27's stability issue with GALCIT-46, which replaced the former's ammonium nitrate with guanidine nitrate.
• This almost-correct molecule possesses a tricyclic guanidine group ( rings A, B & C ), along with a uracil ring ( D ).
• Strong and hindered non-nucleophilic guanidine bases are accessible from tetramethylurea in a simple manner, which are in contrast to the fused amidine bases DBU not alkylated.
• Jetex motors are powered by a solid pellet of guanidine nitrate, which burns to release a variety of gases in copious volume, leaving no solid residue or ash.
• With Tagamet imidazole is the the most obvious candidate for being a base with a pkB near 7, but I'm wondering why not the guanidine type residue?