CAS 149934-21-4
:9-Amino Minocycline Hydrochloride
Description:
9-Amino Minocycline Hydrochloride is a derivative of minocycline, a broad-spectrum antibiotic belonging to the tetracycline class. This compound is characterized by the presence of an amino group at the 9-position of the minocycline structure, which enhances its antibacterial activity and pharmacological properties. It is typically presented as a hydrochloride salt, which improves its solubility in aqueous solutions, making it suitable for various pharmaceutical formulations. The substance exhibits a wide range of antibacterial activity against both Gram-positive and Gram-negative bacteria, and it is often used in the treatment of infections, including those caused by resistant strains. Additionally, 9-Amino Minocycline Hydrochloride has anti-inflammatory properties, which can be beneficial in treating conditions like acne and other dermatological disorders. Its mechanism of action involves inhibiting bacterial protein synthesis by binding to the 30S ribosomal subunit. As with other tetracyclines, it is important to consider potential side effects and contraindications, including photosensitivity and interactions with certain metal ions.
Formula:C23H28N4O7·ClH
InChI:InChI=1S/C23H28N4O7.ClH/c1-26(2)12-7-11(24)17(28)14-9(12)5-8-6-10-16(27(3)4)19(30)15(22(25)33)21(32)23(10,34)20(31)13(8)18(14)29;/h7-8,10,16,28,30-31,34H,5-6,24H2,1-4H3,(H2,25,33);1H/t8-,10-,16-,23-;/m0./s1
InChI key:InChIKey=KYFXMIINWSZGCG-KBTHSJHISA-N
SMILES:O[C@]12[C@]([C@H](N(C)C)C(O)=C(C(N)=O)C1=O)(C[C@]3(C(=C2O)C(=O)C=4C(C3)=C(N(C)C)C=C(N)C4O)[H])[H].Cl
Synonyms:- (4S,4As,5Ar,12As)-9-Amino-4,7-Bis(Dimethylamino)-1,4,4A,5,5A,6,11,12A-Octahydro-3,10,12,12A-Tetrahydroxy-1,11-Dioxo-2-Naphthacenecarboxamide Hydrochloride
- (4S,4As,5Ar,12As)-9-Amino-4,7-Bis(Dimethylamino)-1,4,4A,5,5A,6,11,12A-Octahydro-3,10,12,12A-Tetrahydroxy-1,11-Dioxo-2-Naphthacenecarboxamide Hydrochloride (1:1)
- (4S,4aS,5aR,12aS)-9-amino-4,7-bis(dimethylamino)-3,10,12,12a-tetrahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide sulfate (1:1)
- 2-Naphthacenecarboxamide, 9-amino-4,7-bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-, hydrochloride (1:1), (4S,4aS,5aR,12aS)-
- 2-Naphthacenecarboxamide, 9-amino-4,7-bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-, monohydrochloride, [4S-(4α,4aα,5aα,12aα)]-
- 9-Aminominocycline hydrochloride
- 9-Amino-minocycline hydrochloride
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Found 9 products.
Tigecycline Related Compound B ((4S,4aS,5aR,12aS)-9-Amino-4,7-bis(dimethylamino)-3,10,12,12a-tetrahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2- carboxamide hydrochloride (1:x))
CAS:Aromatic cyclic amides (including cyclic carbamates) and their derivatives; salts thereofFormula:C23H28N4O7·HClColor and Shape:Off-White PowderMolecular weight:472.19589-Amino minocycline, HCl
CAS:Formula:C23H29ClN4O7Purity:95%Color and Shape:SolidMolecular weight:508.9520(4S,4aS,5aR,12aS)-9-Amino-4,7-bis(dimethylamino)-3,10,12,12a-tetrahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide hydrochloride
CAS:(4S,4aS,5aR,12aS)-9-Amino-4,7-bis(dimethylamino)-3,10,12,12a-tetrahydroxy-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide hydrochloridePurity:95%Molecular weight:508.95g/molTigecycline EP Impurity B HCl (Tigecycline Metabolite M6 HCl, 9-Amino Minocycline HCl)
CAS:Formula:C23H28N4O7·HClColor and Shape:Yellow SolidMolecular weight:472.50 36.469-Aminominocycline Hydrochloride (~90%)
CAS:Controlled Product<p>Applications 9-Aminominocycline Hydrochloride is a metabolite of Minocycline Hydrochloride (M344800); a second generation tetracycline antibiotic and antibacterial.<br>References Zbinovsky, V., et al.: Anal. Profiles Drug Subs., 6, 323 (1977); Oringer, R.J., et al.: J. Periodontol., 73, 835 (2002)<br></p>Formula:C23H28N4O7•HClPurity:~90%Color and Shape:NeatMolecular weight:508.959-Aminominocycline hydrochloride
CAS:<p>Aminominocycline hydrochloride is a synthetic, catalytic compound. It is used as a reaction solution in organic solvents and has been shown to be an effective inhibitor of sulfate-reducing bacteria, such as Desulfovibrio desulfuricans. Aminominocycline hydrochloride has been found to be effective against human serum at a flow rate of 1 mL/min, but not at higher flow rates, likely due to its ability to react with the chloride ion. This product can be used for analytical methods in the determination of triazine and high yield chloride. Aminominocycline hydrochloride is also known to react with monoclonal antibodies and can be used for the detection of pollutants.</p>Formula:C23H28N4O7·HClPurity:Min. 80 Area-%Color and Shape:Yellow PowderMolecular weight:508.95 g/mol









