Sulfapyridine (2-sulfaniyl aminopyridine)
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Sulfapyridine (2-sulfaniyl aminopyridine) annotated bibliography by Merck & Co.

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Published by Merck & Co. Inc. in Rahway, N.J .
Written in English

Subjects:

  • Sulphapyridine -- Bibliography

Book details:

Edition Notes

GenreBibliography.
Classifications
LC ClassificationsZ6665.S9 M52 1941b
The Physical Object
Pagination122 p. ;
Number of Pages122
ID Numbers
Open LibraryOL6419040M
LC Control Number41012270
OCLC/WorldCa7702981

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Sulfapyridine may cause blood problems, especially if it is taken for a long time. If your symptoms do not improve within a few days, or if they become worse, check with your doctor. Sulfapyridine may cause blood problems. These problems may result in a greater chance of certain infections, slow healing, and bleeding of the gums. Therefore, you. Sulfapyridine. Sulfapyridine is a sulfonamide metabolite of sulfasalazine which seems to be mainly responsible for the adverse effects noted by the parent drug (Jafri and Pasricha, ). From: Reference Module in Biomedical Sciences, Related terms: Methotrexate; Sulfamethoxazole; Tumor Necrosis Factor Alpha; Mesalazine; Prodrug; Enzymes; Sulfasalazine; Dapsone. Aqueous solution is neutral. (NTP, ) Sulfapyridine is a sulfonamide consisting of pyridine with a 4-aminobenzenesulfonamido group at the 2-position. It has a role as an antiinfective agent, a dermatologic drug, a xenobiotic, an environmental contaminant and a drug allergen.   Descriptions. Sulfapyridine is a sulfa medicine. It is used to help control dermatitis herpetiformis (Duhring's disease), a skin problem. It may also be used for other problems as determined by your doctor. However, this medicine will not work for any kind of infection as other sulfa medicines do. This medicine may cause some serious side effects.

Sulfapyridine is a competitive inhibitor of the bacterial enzyme dihydropteroate synthetase. It was used to treat of infections in humans in particular, dermatitis herpetiformis (Duhring's disease), a skin problem, but that usage was discontinued by manufacturer. Stanley L. Marks, in Canine and Feline Gastroenterology, Sulfasalazine. The drug consists of sulfapyridine linked to mesalamine (previously called 5-aminosalicylic acid) by an azo bond that is cleaved by colonic bacteria with subsequent release of the active moiety of the drug, mesalamine. Sulfapyridine is almost completely absorbed in the colon, metabolized in the liver, and excreted in. All mass spectra in this site (plus many more) are available from the NIST/EPA/NIH Mass Spectral Library. Please see the following for information about the library and its accompanying search program. Symbol which looks like a small house Solid circle with an upward pointer in it. Jump to content.

Book: All Authors / Contributors: Merck & Co. OCLC Number: Notes: "Composed of abstracts from the literature of and " Includes author index. Description: 2 preliminary leaves, pages ; 28 cm: Other Titles: Annotated bibliography, March , sulfapyridine. It was discovered by Lionel Whitby at the British firm May & Baker Ltd and logged in their Test Book on 2 November, under Code No M&B It was successfully used to treat Winston Churchill 's bacterial pneumonia in ‘Sulfapyridine is a competitive inhibitor of bacterial para-aminobenzoic acid (PABA), a substrate of the enzyme dihydropteroate synthetase.’ Word of the day gi. Sulfapyridine melting point standard, also called Sulfapyridine, is a metabolite of sulfasalazine. It is an antibiotic and is mostly used in treating rheumatoid arthritis. Sulfapyridine is a short acting sulfonamide, which can be substituted for dapsone and it does not cause neuropathy.