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Search results for sulfapyridine in Related Substance Name (approximate match)
Showing 1 - 5 of 5 results
Status:
US Approved Rx
(1977)
Source:
ANDA085828
(1977)
Source URL:
First approved in 1950
Source:
NDA007073
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
Sulfasalazine is an anti-inflammatory indicated for the treatment of ulcerative colitis and rheumatoid arthritis. The mode of action of Sulfasalazine or its metabolites, 5-aminosalicylic acid (5-ASA) and sulfapyridine (SP), is still under investigation, but may be related to the anti-inflammatory and/or immunomodulatory properties that have been observed in animal and in vitromodels, to its affinity for connective tissue, and/or to the relatively high concentration it reaches in serous fluids, the liver and intestinal walls, as demonstrated in autoradiographic studies in animals. In ulcerative colitis, clinical studies utilizing rectal administration of Sulfasalazine, SP and 5-ASA have indicated that the major therapeutic action may reside in the 5-ASA moiety. The relative contribution of the parent drug and the major metabolites in rheumatoid arthritis is unknown. Sulfasalazine is used for the treatment of Crohn's disease and rheumatoid arthritis as a second-line agent. Sulfasalazine is marketed under the trade name Azulfidine among others.
Status:
US Previously Marketed
Source:
M&B 693 by May & Baker
(1938)
Source URL:
First approved in 1938
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
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. It is also known, that sulfapyridine is one of the two primary metabolite of the anti-inflammatory drug salicylazosulfapyridine.
Status:
US Previously Marketed
Source:
M&B 693 by May & Baker
(1938)
Source URL:
First approved in 1938
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
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. It is also known, that sulfapyridine is one of the two primary metabolite of the anti-inflammatory drug salicylazosulfapyridine.
Status:
US Previously Marketed
Source:
M&B 693 by May & Baker
(1938)
Source URL:
First approved in 1938
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
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. It is also known, that sulfapyridine is one of the two primary metabolite of the anti-inflammatory drug salicylazosulfapyridine.
Status:
US Previously Marketed
Source:
M&B 693 by May & Baker
(1938)
Source URL:
First approved in 1938
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
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. It is also known, that sulfapyridine is one of the two primary metabolite of the anti-inflammatory drug salicylazosulfapyridine.