CAS 13803-65-1
:Anhydrotetracycline hydrochloride
Description:
Anhydrotetracycline hydrochloride is a derivative of tetracycline, a broad-spectrum antibiotic known for its ability to inhibit bacterial protein synthesis. This compound is characterized by its crystalline structure and is typically a yellow to orange powder. It is soluble in water and exhibits a pH-dependent solubility profile, which can influence its bioavailability and therapeutic efficacy. Anhydrotetracycline hydrochloride retains the core tetracycline structure, which includes a naphthacene ring system, contributing to its antibacterial properties. The hydrochloride form enhances its stability and solubility in aqueous solutions. This compound is primarily used in veterinary medicine and has applications in treating various bacterial infections. Additionally, it is important to note that, like other tetracyclines, anhydrotetracycline can cause side effects and may interact with other medications, necessitating careful consideration in clinical use. Its mechanism of action involves binding to the 30S ribosomal subunit of bacteria, thereby preventing the translation of mRNA into proteins, which is crucial for bacterial growth and reproduction.
Formula:C22H22N2O7·ClH
InChI:InChI=1S/C22H22N2O7.ClH/c1-8-9-5-4-6-12(25)13(9)17(26)14-10(8)7-11-16(24(2)3)18(27)15(21(23)30)20(29)22(11,31)19(14)28;/h4-6,11,16,25-27,31H,7H2,1-3H3,(H2,23,30);1H/t11-,16-,22-;/m0./s1
InChI key:InChIKey=XBSQEFHDCDFNJU-WPJNXPDPSA-N
SMILES:O[C@]12[C@]([C@H](N(C)C)C(O)=C(C(N)=O)C1=O)(CC=3C(C2=O)=C(O)C=4C(C3C)=CC=CC4O)[H].Cl
Synonyms:- (1S,4aS,12aS)-3-[amino(hydroxy)methylidene]-4a,6,7-trihydroxy-N,N,11-trimethyl-2,4,5-trioxo-1,2,3,4,4a,5,12,12a-octahydrotetracen-1-aminium
- (2Z)-2-[amino(hydroxy)methylidene]-4-(dimethylamino)-11,12a-dihydroxy-6-methyl-4a,12a-dihydrotetracene-1,3,12(2H,4H,5H)-trione hydrochloride
- (2Z,4S,4aS,12aS)-2-[amino(hydroxy)methylidene]-4-(dimethylamino)-10,11,12a-trihydroxy-6-methyl-4a,12a-dihydrotetracene-1,3,12(2H,4H,5H)-trione hydrochloride
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,12,12a-hexahydro-3,10,11,12a-tetrahydroxy-6-methyl-1,12-dioxo-,
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,12,12a-hexahydro-3,10,11,12a-tetrahydroxy-6-methyl-1,12-dioxo-, hydrochloride (1:1), (4S,4aS,12aS)-
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,12,12a-hexahydro-3,10,11,12a-tetrahydroxy-6-methyl-1,12-dioxo-, monohydrochloride
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,12,12a-hexahydro-3,10,11,12a-tetrahydroxy-6-methyl-1,12-dioxo-, monohydrochloride, (4S,4aS,12aS)-
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,12,12a-hexahydro-3,10,11,12a-tetrahydroxy-6-methyl-1,12-dioxo-, monohydrochloride, [4S-(4α,4aα,12aα)]-
- 4-(Dimethylamino)-1,4,4a,5,12,12a-hexahydro-3,10,11,12a-tetrahydroxy-6-methyl-1,12-dioxo-2-naphthacenecarboxamide monohydrochloride, (4S-(4alpha,4aalpha,12aalpha))- Anhydrotetracycline hydrochloride
- monohydrochloride, (4S-(4alpha,4aalpha,12aalpha))-
- Anhydrotetracycline hydrochloride
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Found 11 products.
Anhydrotetracycline hydrochloride
CAS:<p>Anhydrotetracycline hydrochloride, 13803-65-1, is an antibiotic commonly used in gene expression systems in bacteria. Learn more at Thermo Fisher Scientific.</p>Formula:C22H22N2O7•HClMolecular weight:462.88ANHYDROTETRACYCLINE HYDROCHLORIDE CRS
CAS:ANHYDROTETRACYCLINE HYDROCHLORIDE CRSFormula:C22H23ClN2O6Color and Shape:Powder.Molecular weight:446.8808Anhydrotetracycline Hydrochloride ((4S ,4aS ,12aS )-4-(Dimethylamino)-3,10,11,12a-tetrahydroxy-6-methyl-1,12-dioxo-1,4,4a,5,12,12a-hexahydrotetracene-2-carboxamide monohydrochloride)
CAS:Aromatic cyclic amides (including cyclic carbamates) and their derivatives; salts thereofFormula:C22H22N2O7·HClColor and Shape:Yellow SolidMolecular weight:462.119382-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,12,12a-hexahydro-3,10,11,12a-tetrahydroxy-6-methyl-1,12-dioxo-, hydrochloride (1:1), (4S,4aS,12aS)-
CAS:Formula:C22H23ClN2O7Purity:98%Color and Shape:SolidMolecular weight:462.8802Anhydrotetracycline hydrochloride
CAS:Anhydrotetracycline hydrochloridePurity:≥98%Molecular weight:462.88g/molAnhydrotetracycline hydrochloride
CAS:Anhydrotetracycline (hydrochloride) is a potent competitive inhibitor of broad-spectrum tetracycline destructase enzymes.Formula:C22H23ClN2O7Purity:98% - 98.90%Color and Shape:SolidMolecular weight:462.88Anhydrotetracycline Hydrochloride
CAS:Controlled ProductFormula:C22H22N2O7·HClColor and Shape:NeatMolecular weight:462.88Anhydrotetracycline hydrochloride
CAS:Formula:C22H22N2O7·HClPurity:≥ 98.0%Color and Shape:Yellow solidMolecular weight:462.88Anhydrotetracycline Hydrochloride
CAS:Controlled Product<p>Impurity Tetracycline EP Impurity C Hydrochloride<br>Stability Hygroscopic<br>Applications Anhydrotetracycline is a tetracycline derivative exhibiting no antibiotic activity, a useful effector of tetracycline-dependent gene expression in bacterial expression systems. It is a powerful effector in both the tetracycline repressor (TetR) and reverse TetR systems, binding the Tet(R).<br>References Sokoloski, T., et al.: J. Pharm. Sci., 66, 1159 (1977), Paemen, L., et al.: Biochem. Pharmacol., 5, 105 (1996); A. Kamionka, et al.; Nucleic Acids Res. 32, 842 (2004) | M. Resch, et al.; Nucleic Acids Res. 36, 4390 (2008)<br></p>Formula:C22H22N2O7·HClColor and Shape:YellowMolecular weight:462.88Anhydrotetracycline hydrochloride
CAS:Anhydrotetracycline hydrochloride is a synthetic tetracycline antibiotic that has been shown to be active against methicillin-resistant strains of Staphylococcus aureus and Enterobacteriaceae. It is also effective against Gram-positive bacteria such as Streptococcus pneumoniae, Enterococcus faecalis, and Listeria monocytogenes. Anhydrotetracycline hydrochloride functions by inhibiting protein synthesis, which prevents the production of proteins vital for cell division. This antibiotic inhibits translation by interfering with the binding of aminoacyl-tRNA to ribosomes through an unknown mechanism. Anhydrotetracycline hydrochloride has also been shown to enhance bacterial growth in the presence of carbon sources such as butanol or sugar alcohols.Formula:C22H23ClN2O7Purity:Min. 95 Area-%Color and Shape:Yellow PowderMolecular weight:462.88 g/mol











