CAS 23313-80-6
:Epitetracycline hydrochloride
Description:
Epitetracycline hydrochloride is a semi-synthetic derivative of tetracycline, classified as an antibiotic. It exhibits broad-spectrum antibacterial activity, primarily targeting Gram-positive and Gram-negative bacteria by inhibiting protein synthesis through binding to the 30S ribosomal subunit. This compound is characterized by its stability in acidic conditions, which enhances its bioavailability. Epitetracycline hydrochloride is typically administered orally and is known for its therapeutic applications in treating various infections, including respiratory and urinary tract infections. The hydrochloride form improves solubility in water, facilitating its use in pharmaceutical formulations. Additionally, it possesses anti-inflammatory properties, making it useful in treating conditions like acne. However, like other tetracyclines, it may cause side effects such as gastrointestinal disturbances and photosensitivity. It is important to note that the use of epitetracycline hydrochloride should be guided by susceptibility testing to avoid resistance development. Overall, this compound plays a significant role in modern medicine, particularly in the treatment of bacterial infections.
Formula:C22H24N2O8·ClH
InChI:InChI=1S/C22H24N2O8.ClH/c1-21(31)8-5-4-6-11(25)12(8)16(26)13-9(21)7-10-15(24(2)3)17(27)14(20(23)30)19(29)22(10,32)18(13)28;/h4-6,9-10,15,25,27-28,31-32H,7H2,1-3H3,(H2,23,30);1H/t9-,10-,15+,21+,22-;/m0./s1
InChI key:InChIKey=XMEVHPAGJVLHIG-DXDJYCPMSA-N
SMILES:O[C@@]12[C@@](C[C@]3(C(=C1O)C(=O)C=4C([C@@]3(C)O)=CC=CC4O)[H])([C@@H](N(C)C)C(O)=C(C(N)=O)C2=O)[H].Cl
Synonyms:- Epitetracycline hydrochloride
- 2-Naphthacenecarboxamide, 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), (4R,4aS,5aS,6S,12aS)-
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride, (4R,4aS,5aS,6S,12aS)-
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride, [4R-(4α,4aβ,5aβ,6α,12aβ)]-
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride, 4-epimer
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Found 10 products.
Epitetracycline Hydrochloride
CAS:Tetracyclines and their derivatives; salts thereofFormula:C22H24N2O8·HClColor and Shape:Yellow PowderMolecular weight:480.129944-Epitetracycline hydrochloride
CAS:Formula:C22H25ClN2O8Purity:98%Color and Shape:SolidMolecular weight:480.8955PharmaVetResiMix 5 Tetracyclines-v10 10 µg/mL in Methanol
CAS:Controlled ProductColor and Shape:Colourless4-Epitetracycline hydrochloride
CAS:Controlled ProductFormula:C22H24N2O8·ClHColor and Shape:NeatMolecular weight:480.904-Epitetracycline Hydrochloride
CAS:Controlled ProductFormula:C22H24N2O8·ClHColor and Shape:NeatMolecular weight:480.904-epi-Tetracycline Hydrochloride
CAS:Controlled Product<p>Applications Metabolite of Tetracycline (T291400). This compound is a contaminant of emerging concern (CECs).<br>References Diana, J., et al.: J. Pharm. Biomed. Anal., 39, 523 (2005), Fritz, J., et al.: Food Chem., 105, 1297 (2007), Gratacos-Cubarsi, M., et al.: J. Agric. Food Chem., 55, 4610 (2007),<br></p>Formula:C22H24N2O8·ClHColor and Shape:YellowMolecular weight:480.904-Epitetracycline hydrochloride
CAS:<p>Epitetracycline is an epimer of the antibiotic tetracycline . Epimers of tetracycline form without catalysis and are considered degradation products. Epitetracycline has decreased activity as an antibiotic or a Tet repressor effector but may have stronger toxic effects in animals.</p>Formula:C22H25ClN2O8Color and Shape:SolidMolecular weight:480.904-Epitetracycline hydrochloride
CAS:<p>4-Epitetracycline hydrochloride is a tetracycline antibiotic derivative, which is a secondary metabolite derived from bacterial sources, particularly Streptomyces species. It functions primarily by inhibiting protein synthesis in bacteria through binding to the 30S ribosomal subunit, preventing the attachment of aminoacyl-tRNA to the RNA-ribosome complex. This action hinders bacterial growth by interfering with vital processes necessary for bacterial survival and replication.</p>Formula:C22H25ClN2O8Purity:Min. 95%Color and Shape:PowderMolecular weight:480.9 g/mol









