Informations sur le produit
- (2Z,4S,4aS,5aS,6S,12aS)-2-[amino(hydroxy)methylidene]-7-chloro-4-(dimethylamino)-6,10,11,12a-tetrahydroxy-6-methyl-4a,5a,6,12a-tetrahydrotetracene-1,3,12(2H,4H,5H)-trione hydrochloride
- (2Z,4S,4aS,6S,12aS)-2-[amino(hydroxy)methylidene]-7-chloro-4-(dimethylamino)-6,10,11,12a-tetrahydroxy-6-methyl-4a,5a,6,12a-tetrahydrotetracene-1,3,12(2H,4H,5H)-trione hydrochloride
- 2-Naphthacenecarboxamide, 7-chloro-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, hydrochloride (1:1), (4S,4aS,5aS,6S,12aS)-
- 2-Naphthacenecarboxamide, 7-chloro-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride
- 2-Naphthacenecarboxamide, 7-chloro-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride, (4S,4aS,5aS,6S,12aS)-
- 2-Naphthacenecarboxamide, 7-chloro-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride, [4S-(4α,4aα,5aα,6β,12aα)]-
- 7-Chlorotetracycline hydrochloride
- 7-Chlorotetracycline monohydrochloride
- Aureociclina
- Aureocycline
- Voir d'autres synonymes
- Aureomycin monohydrochloride
- Aureovit 12C80
- Aurofac 100
- Biomycin hydrochloride
- Chlortetracycline hydrochloride
- Chlortetracyclinium chloride
- Fermycin Soluble
- Isphamycin
- NSC 13252
This is the deuterated form of chlortetracycline hydrochloride (CTC), an antibiotic that is used mainly to treat bacterial infections. Chlortetracycline hydrochloride is a tetracycline antibiotic composed of chlortetracycline, a β-lactam ring, and hydrochloride, a hydrogen chloride salt. It has two active forms: the ionized form and the free base form. The ionized form is responsible for its action on bacteria because it can easily cross the lipid bilayer membrane of Gram-positive bacteria. Chlortetracycline hydrochloride has additive effects with other antibiotics such as erythromycin and tetracyclines, which may lead to treatment efficiency in time-sensitive infections. Furthermore, it enhances microglial activation against pathogens, providing protection against intracellular pathogens implicated in neurodegenerative diseases.