Weight | 280.309 g/mol |
---|---|
Formula | C11H12N4O3S |
Hydrogen Acceptors | 6 |
Hydrogen Donors | 2 |
Aromatic Rings | 2 |
Rotatable Bonds | 4 |
SULFALENE (152-47-6)
Longum · Sulfapyrazinmethoxine · Kelfizine
Score:
#403 in Microbiology
,
#1294 in Biochemistry
,
#3174 in Biology
,
#3971 in Chemistry
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- The genome sequence of Bifidobacterium longum reflects its adaptation to the human gastrointestinal tract (Proceedings of the National Academy of Sciences of the United States of America, 2002)
- Synbiotic therapy (Bifidobacterium longum/Synergy 1) initiates resolution of inflammation in patients with active ulcerative colitis: a randomised controlled pilot trial (Gut, 2005)
- The genome sequence of Bifidobacterium longum subsp. infantis reveals adaptations for milk utilization within the infant microbiome (Proceedings of the National Academy of Sciences of the United States of America, 2008)
- Assessment of psychotropic-like properties of a probiotic formulation ( Lactobacillus helveticus R0052 and Bifidobacterium longum R0175) in rats and human subjects (British Journal of Nutrition, 2011)
- Effect of Bifidobacterium longum and inulin on gut bacterial metabolism and carcinogen-induced aberrant crypt foci in rats. (Carcinogenesis, 1998)
- Adhesion, autoaggregation and hydrophobicity of 13 strains of Bifidobacterium longum (Letters in Applied Microbiology, 2000)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Longum
- Sulfapyrazinmethoxine
- Kelfizine
- Sulfamethoxypyrazine
- Sulfametopyrazine
- Sulphametopyrazine
- Sulfamethopyrazine
- Sulphalene
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SMILESCOC1=NC=CN=C1NS(=O)(=O)C2=CC=C(C=C2)N
-
InChIKeyKXRZBTAEDBELFD-UHFFFAOYSA-N
- Pubchem - SULFALENE
- Wikipedia - sulfalene
Sulfalene (INN, USAN) or sulfametopyrazine (BAN) is a long-acting sulfonamide antibacterial used for the treatment of chronic bronchitis, urinary tract infections and malaria. As of 2014 there were only two countries in which it is currently still marketed: Thailand and Ireland. It was discovered by researchers at Farmitalia and first published in 1960 and was marketed as Kelfizina.
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