Tinidazole
CAS: 19387-91-8
Ref. TM-T0893
1g | 92.00 € | ||
50mg | 45.00 € | ||
100mg | 57.00 € | ||
200mg | 68.00 € | ||
1ml*10 (DMSO) | 59.00 € |
Product Information
- CP12574
- 1-(2-Ethanesulfonyl-ethyl)-2-methyl-5-nitro-1H-imidazole
- 1-(2-Ethylsulfonylethyl)-2-methyl-5-nitroimidazole
- 1-(Ethylsulfonylethyl)-2-methyl-5-nitroimidazole
- 1-[2-(Ethylsulfonyl)ethyl]-2-methyl-5-nitro-1H-imidazode
- 1-[2-(ethylsulfonyl)ethyl]-2-methyl-5-nitro-1H-imidazole
- 1-[2′-(Ethylsulfonyl)-ethyl]-2-methyl-5-nitroimidazole
- 1H-Imidazole, 1-[2-(ethylsulfonyl)ethyl]-2-methyl-5-nitro-
- Amtiba
- Bioshik
- See more synonyms
- Cp 12574
- Diamicron
- Dramion
- Ethyl [2-(2-methyl-5-nitroimidazol-1-yl)ethyl] sulfone
- Fasigin
- Fasigyn
- Glongyn
- Imidazole, 1-[2-(ethylsulfonyl)ethyl]-2-methyl-5-nitro-
- Nordialex
- Pletil
- Protozol
- Simplotan
- Sorquetan
- Sporinex
- Tindamax
- Tini 300
- Tinidazol
- Tiprogyn
- Tricolam
- Trimonase
Tinidazole (CP12574)a is a 5-nitroimidazole derivative with the antiprotozoal property. Although the mechanism of action has not been fully elucidated, it has been suggested that tinidazole is metabolized and yields nitrite anions and metronidazole. Metronidazole's nitro group, in turn, is reduced via the parasite ferredoxin, thereby generating a series of free nitro radicals including nitro anions. Toxicity is achieved via depletion of sulfhydryl groups and DNA strand breaks with multiple hits having an additive effect and ultimately leading to cell death.
Chemical properties
Technical inquiry about: TM-T0893 Tinidazole
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