Product: | Balsalazide | ||||||||
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Catalog Number: | 4799 | ||||||||
CAS Number: | 80573-04-2 | ||||||||
Synonyms: |
5-[Bis(2-chloroethyl)-amino]-1-methyl-1H-benzimidazole-2-butanoic Acid Hydrochloride; Cytostasan; Ribomustin |
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Pricing: |
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Formula: | C17H13N3Na2O6 • H2O | ||||||||
Chemical Purity: | >99% | ||||||||
Molecular Weight: | 401.28 | ||||||||
Structure: | |||||||||
Appearance: | Solid | ||||||||
Category: | Unlabeled Reference Standards | ||||||||
Stability: | Stable under recommended storage conditions | ||||||||
Storage: |
Keep container tightly closed in a dry and well-ventilated place. Recommended storage temperature: 2-8°C. Light sensitive |
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Transportation: |
Non-hazardous for transport |
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Literature References: |
Kimura, I., et al., Effects of BX661A, a new therapeutic agent for ulcerative colitis, on reactive oxygen species in comparison with salazosulfapyridine and its metabolite sulfapyridine. Arzneimittelforschung 48, 1007-11, (1998); Kumamoto, T., et al., Inhibition by aminosalicylates of lipid peroxidation in large intestinal mucosa after mesenteric ischemia/reperfusion in the rat. Jpn. J. Pharmacol. 75, 187-9, (1997); MacGregor, D.J., et al., Chemoprevention of colon cancer carcinogenesis by balsalazide: inhibition of azoxymethane-induced aberrant crypt formation in the rat colon and intestinal tumor formation in the B6-Min/+ mouse. Int. J. Oncol. 17, 173-9, (2000); Simmonds, N.J., et al., Antioxidant effects of aminosalicylates and potential new drugs for inflammatory bowel disease: assessment in cell-free systems and inflamed human colorectal biopsies. Aliment. Pharmacol. Ther. 13, 363-72, (1999); Merck 14,945 |
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MSDS: | |||||||||
Description: |
Balsalazide has antioxidative and anti-inflammatory properties. It inhibits superoxide production and was found to scavenge hypochlorite radicals.1 Balsalazide was shown to inhibit lipid peroxidation in rat intestinal mucosa.2 It was also shown to inhibit azoxymethane-induced colon carcinogenesis.3 In vivo, basalazide is cleaved through azoreduction to produce 4-aminobenzoyl-β-alanine, an inert carrier moiety, and 5-aminosalicylic acid (5-ASA). |