CAS 24390-14-5
:Doxycycline hyclate
Description:
Doxycycline hyclate is a broad-spectrum antibiotic belonging to the tetracycline class, primarily used to treat various bacterial infections, including respiratory tract infections, urinary tract infections, and certain skin conditions. It is characterized by its ability to inhibit protein synthesis in bacteria by binding to the 30S ribosomal subunit, thereby preventing the growth and reproduction of the microorganisms. Doxycycline hyclate is a semi-synthetic derivative of tetracycline, which enhances its stability and absorption in the gastrointestinal tract. The substance is typically administered orally and is known for its relatively long half-life, allowing for once or twice daily dosing. It is also effective against certain protozoal infections and is used in the treatment of acne and as prophylaxis for malaria. Common side effects may include gastrointestinal disturbances, photosensitivity, and potential effects on bone and teeth development in children. Due to its broad activity, doxycycline hyclate is a valuable tool in both human and veterinary medicine.
Formula:C22H24N2O8C2H6O·ClHH2O
InChI:InChI=1S/C22H24N2O8.C2H6O.ClH.H2O/c1-7-8-5-4-6-9(25)11(8)16(26)12-10(7)17(27)14-15(24(2)3)18(28)13(21(23)31)20(30)22(14,32)19(12)29;1-2-3;;/h4-7,10,14-15,17,25,27-29,32H,1-3H3,(H2,23,31);3H,2H2,1H3;1H;1H2/t7-,10+,14+,15-,17-,22-;;;/m0.../s1
InChI key:InChIKey=JRNIHERUNQWMMW-WBYAVNBMSA-N
SMILES:O[C@]12[C@]([C@H](N(C)C)C(O)=C(C(N)=O)C1=O)([C@@H](O)[C@]3(C(=C2O)C(=O)C=4C([C@@H]3C)=CC=CC4O)[H])[H].Cl.C(C)O.O
Synonyms:- (1S,3Z,4aS,11R,11aR,12S,12aR)-3-[amino(hydroxy)methylidene]-4a,6,7,12-tetrahydroxy-N,N,11-trimethyl-2,4,5-trioxo-1,2,3,4,4a,5,11,11a,12,12a-decahydrotetracen-1-aminium chloride
- (2E,4S,4aR,5S,5aR,6R,12aS)-2-[amino(hydroxy)methylidene]-4-(dimethylamino)-5,10,11,12a-tetrahydroxy-6-methyl-4a,5a,6,12a-tetrahydrotetracene-1,3,12(2H,4H,5H)-trione - ethanol (2:1) dihydrochloride hydrate
- (2Z,4S,4aR,5S,5aR,6R)-2-[amino(hydroxy)methylidene]-4-(dimethylamino)-5,10,11,12a-tetrahydroxy-6-methyl-4a,5a,6,12a-tetrahydrotetracene-1,3,12(2H,4H,5H)-trione hydrochloride
- (2Z,4S,4aR,5S,5aR,6R,12aS)-2-[amino(hydroxy)methylidene]-4-(dimethylamino)-5,10,11,12a-tetrahydroxy-6-methyl-4a,5a,6,12a-tetrahydrotetracene-1,3,12(2H,4H,5H)-trione - ethanol (2:1) dihydrochloride hydrate
- (4S,4Ar,5S,5Ar,6R,12As)-4-(Dimethylamino)-1,4,4A,5,5A,6,11,12A-Octahydro-3,5,10,12,12A-Pentahydroxy-6-Methyl-1,11-Dioxo-2-Naphthacenecarboxamide Hydrochloride
- (4S,4aR,5S,5aR,6R,12aS)-4-(dimethylamino)-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-1,4,4a,5,5a,6,11,12a-octahydrotetracene-2-carboxamide-ethanol hydrochloride hydrate (2:1:2:1)
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, hydrochloride, (4S,4aR,5S,5aR,6R,12aS)-, compd. with ethanol, hydrate (2:2:1:1)
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride, (4S,4aR,5S,5aR,6R,12aS)-, compd. with ethanol (2:1), monohydrate
- 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, monohydrochloride, [4S-(4α,4aα,5α,5aα,6α,12aα)]-, compd. with ethanol (2:1), monohydrate
- 2-Naphthacenecarboxamide, 4β-(dimethylamino)-1,4,4aβ,5,5aβ,6,11,12a-octahydro-3,5β,10,12,12aβ-pentahydroxy-6β-methyl-1,11-dioxo-, monohydrochloride, compd. with ethyl alc. (2:1), monohydrate
- 4-(Dimethylamino)-1,4,4A,5,5A,6,11,12A-Octahydro-3,5,10,12,12A-Pentahydroxy-6-Methyl-1,11-Dioxo-2-Na
- 4-(Dimethylamino)-3,5,10,12,12A-Pentahydroxy-6-Methyl-1,11-Dioxo-1,4,4A,5,5A,6,11,12A-Octahydrotetracene-2-Carboxamide
- 4-(Dimethylamino)-3,5,10,12,12A-Pentahydroxy-6-Methyl-1,11-Dioxo-1,4,4A,5,5A,6,11,12A-Octahydrotetracene-2-Carboxamide-Ethanol (2:1) Dihydrochloride Hydrate
- 6-Desoxy-5-hydroxytetracycline hydrochloride hemihydrate hemiethanolate
- Atridox
- BioPure MTAD
- Doryx
- Dox-T 100
- Doxitrat
- Doxy 100
- Doxycycline Hyclate
- Doxycycline Hyclate Monohydrate
- Doxycycline Hydrate
- Doxycycline Hydrochlocide
- Doxycycline Hydrochloride
- Doxycycline Hydrochloride Anhydrous
- Doxycycline Hydrochloride Hemiethanolate Hemihydrate
- Doxycycline hyclate COS
- Doxyprex
- Ethanol, compd. with (4S,4aR,5S,5aR,6R,12aS)-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide monohydrochloride (1:2), monohydrate
- Ethanol, compd. with [4S-(4α,4aα,5α,5aα,6α,12aα)]-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide monohydrochloride (1:2), monohydrate
- Monodoks
- Periostat
- Tetraclean
- See more synonyms
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Doxycycline Hyclate
CAS:Formula:C22H24N2O8C2H6O·HClH2OPurity:>97.0%(HPLC)Color and Shape:Light yellow to Amber to Dark green powder to crystalMolecular weight:512.94Doxycycline hyclate
CAS:<p>Doxycycline hyclate, 24390-14-5, is an antibiotic which inhibits bacterial growth by preventing polypeptide formation. Learn more at Thermo Fisher Scientific.</p>Formula:C46H58Cl2N4O18Color and Shape:Powder or crystals or crystalline powder, YellowMolecular weight:1025.88DOXYCYCLINE HYCLATE CRS
CAS:<p>DOXYCYCLINE HYCLATE CRS</p>Formula:C46H58Cl2N4O18Color and Shape:Crystalline Powder. Yellow. Powder.Molecular weight:1025.875DOXYCYCLINE FOR SYSTEM SUITABILITY CRS
CAS:<p>DOXYCYCLINE FOR SYSTEM SUITABILITY CRS</p>Formula:C46H58Cl2N4O18Color and Shape:Crystalline Powder. Yellow. Powder.Molecular weight:1025.875Doxycycline hyclate
CAS:Doxycycline hyclateFormula:C22H24N2O8 / C22H25ClN2O8Purity:83.1% / 89.9%Color and Shape:YellowMolecular weight:444.15327 / 480.12994Doxycycline Hyclate
CAS:<p>Tetracyclines and their derivatives; salts thereof</p>Formula:C12H24N2O8C2H6O·ClHH2OColor and Shape:Light Yellow PowderMolecular weight:1025.892-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-, hydrochloride, (4S,4aR,5S,5aR,6R,12aS)-, compd. with ethanol, hydrate (2:2:1:1)
CAS:Formula:C46H58Cl2N4O18Purity:95%Color and Shape:SolidMolecular weight:1025.8747Doxycycline hyclate
CAS:Formula:C22H24N2O8·HCl·5H2O·5C2H6OPurity:95.0 - 102.0 % (C22H25ClN2O8, anhydrous and ethanol free basis)Color and Shape:Yellow, crystalline powder, hygroscopicMolecular weight:512.94Doxycycline hyclate 100 µg/mL in Acetonitrile
CAS:Formula:C22H24N2O8·C2H6OClH·H2OColor and Shape:Single SolutionMolecular weight:1025.87Doxycycline hyclate
CAS:Controlled ProductFormula:C22H24N2O8·C2H6OClH·H2OColor and Shape:NeatMolecular weight:1025.87PharmaVetResiMix 5 Tetracyclines-v10 10 µg/mL in Methanol
CAS:Controlled ProductColor and Shape:MixtureDoxycycline Hyclate
CAS:Controlled ProductFormula:C22H24N2O8·C2H6OClH·H2OColor and Shape:NeatMolecular weight:1025.87Doxycycline (hyclate)
CAS:<p>Doxycycline hyclate (WC2031) is a synthetic tetracycline derivative with similar antimicrobial activity. Doxycycline hyclate is also an inhibitor of MMP.</p>Formula:C22H24N2O8·HClC2H6OH2OPurity:97.48% - >99.99%Color and Shape:Yellow Crystallien PowderMolecular weight:512.90Doxycycline Hyclate
CAS:Formula:C22H24N2O8(C2H6O)HCl(H2O)Molecular weight:444.44 : 1/2(46.07) : 36.5 : 1/2(18.0)Doxycycline Hyclate
CAS:Controlled Product<p>Applications Antibacterial.<br>References Fabre, et al.: Chemotherapia, 11, 73 (1966), Goldenthal, et al.: Toxicol. Appl. Pharmacol., 18, 185 (1971), Polson, A.M., et al.: J. Periodontol., 68, 110 (1997),<br></p>Formula:C22H24N2O8·C2H6O·2ClH·H2OColor and Shape:YellowMolecular weight:1025.87Doxycycline-d3 Hyclate (Major)
CAS:Controlled Product<p>Applications Doxycycline-d3 Hyclate, is the labeled analogue of Doxycycline Hyclate (D561500), acting as an Antibacterial.<br>References Fabre, et al.: Chemotherapia, 11, 73 (1966), Goldenthal, et al.: Toxicol. Appl. Pharmacol., 18, 185 (1971), Polson, A.M., et al.: J. Periodontol., 68, 110 (1997),<br></p>Formula:(C22H21D3N2O8)•2HCl•xH2O•C2H6OColor and Shape:NeatMolecular weight:2447.452364618Doxycycline hyclate - Bio-X ™
CAS:<p>Doxycycline is a tetracycline antibiotic that is used to treat a range of bacterial infections. It is a broad-spectrum antibiotic. This drug inhibits bacterial protein synthesis by binding to its 30S prokaryotic ribosomal subunit. It also inhibits the production of essential proteins required for the bacterial to survive.</p>Formula:C22H24N2O8•HCl•(C2H6O)0•(H2O)0Purity:Min. 95 Area-%Color and Shape:PowderMolecular weight:512.94 g/mol















