CAS 24390-14-5
:Doxiciclina hiclato
Descripción:
Doxiciclina hiclato es un antibiótico de amplio espectro que pertenece a la clase de las tetraciclinas, utilizado principalmente para tratar diversas infecciones bacterianas, incluidas las infecciones del tracto respiratorio, infecciones del tracto urinario y ciertas condiciones de la piel. Se caracteriza por su capacidad para inhibir la síntesis de proteínas en las bacterias al unirse a la subunidad ribosomal 30S, impidiendo así el crecimiento y la reproducción de los microorganismos. Doxiciclina hiclato es un derivado semisintético de la tetraciclina, que mejora su estabilidad y absorción en el tracto gastrointestinal. La sustancia se administra típicamente por vía oral y es conocida por su vida media relativamente larga, lo que permite una dosificación una o dos veces al día. También es efectiva contra ciertas infecciones protozoarias y se utiliza en el tratamiento del acné y como profilaxis para la malaria. Los efectos secundarios comunes pueden incluir trastornos gastrointestinales, fotosensibilidad y efectos potenciales en el desarrollo de huesos y dientes en niños. Debido a su amplia actividad, Doxiciclina hiclato es una herramienta valiosa tanto en medicina humana como veterinaria.
Fórmula: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
Clave InChI: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
Sinónimos:- (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
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Encontrado 23 productos.
Doxycycline Hyclate
CAS:Fórmula:C22H24N2O8C2H6O·HClH2OPureza:>97.0%(HPLC)Forma y color:Light yellow to Amber to Dark green powder to crystalPeso molecular: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>Fórmula:C46H58Cl2N4O18Forma y color:Powder or crystals or crystalline powder, YellowPeso molecular:1025.88DOXYCYCLINE HYCLATE CRS
CAS:DOXYCYCLINE HYCLATE CRSFórmula:C46H58Cl2N4O18Forma y color:Crystalline Powder. Yellow. Powder.Peso molecular:1025.875DOXYCYCLINE FOR SYSTEM SUITABILITY CRS
CAS:DOXYCYCLINE FOR SYSTEM SUITABILITY CRSFórmula:C46H58Cl2N4O18Forma y color:Crystalline Powder. Yellow. Powder.Peso molecular:1025.875Doxycycline hyclate
CAS:Doxycycline hyclateFórmula:C22H24N2O8 / C22H25ClN2O8Pureza:83.1% / 89.9%Forma y color:YellowPeso molecular:444.15327 / 480.12994Doxycycline Hyclate
CAS:Tetracyclines and their derivatives; salts thereofFórmula:C12H24N2O8C2H6O·ClHH2OForma y color:Light Yellow PowderPeso molecular: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:Fórmula:C46H58Cl2N4O18Pureza:95%Forma y color:SolidPeso molecular:1025.8747Doxycycline hyclate
CAS:Fórmula:C22H24N2O8·HCl·5H2O·5C2H6OPureza:95.0 - 102.0 % (C22H25ClN2O8, anhydrous and ethanol free basis)Forma y color:Yellow, crystalline powder, hygroscopicPeso molecular:512.94Doxycycline hyclate 100 µg/mL in Acetonitrile
CAS:Fórmula:C22H24N2O8·C2H6OClH·H2OForma y color:Single SolutionPeso molecular:1025.87Doxycycline hyclate
CAS:Producto controladoFórmula:C22H24N2O8·C2H6OClH·H2OForma y color:NeatPeso molecular:1025.87PharmaVetResiMix 5 Tetracyclines-v10 10 µg/mL in Methanol
CAS:Producto controladoForma y color:MixtureDoxycycline Hyclate
CAS:Producto controladoFórmula:C22H24N2O8·C2H6OClH·H2OForma y color:NeatPeso molecular:1025.87Doxycycline (hyclate)
CAS:Doxycycline hyclate (WC2031) is a synthetic tetracycline derivative with similar antimicrobial activity. Doxycycline hyclate is also an inhibitor of MMP.Fórmula:C22H24N2O8·HClC2H6OH2OPureza:97.48% - >99.99%Forma y color:Yellow Crystallien PowderPeso molecular:512.90Doxycycline Hyclate
CAS:Fórmula:C22H24N2O8(C2H6O)HCl(H2O)Peso molecular:444.44 : 1/2(46.07) : 36.5 : 1/2(18.0)Doxycycline Hyclate
CAS:Producto controlado<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>Fórmula:C22H24N2O8·C2H6O·2ClH·H2OForma y color:YellowPeso molecular:1025.87Doxycycline-d3 Hyclate (Major)
CAS:Producto controlado<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>Fórmula:(C22H21D3N2O8)•2HCl•xH2O•C2H6OForma y color:NeatPeso molecular: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>Fórmula:C22H24N2O8•HCl•(C2H6O)0•(H2O)0Pureza:Min. 95 Area-%Forma y color:PowderPeso molecular:512.94 g/molDoxycycline hyclate
CAS:<p>Antibiotic; anti-protozoal; anti-helmintic; protein synthesis inhibitor</p>Fórmula:C22H24N2O8•HCl•(C2H6O)0•(H2O)0Pureza:Min. 95 Area-%Forma y color:Yellow PowderPeso molecular:512.94 g/molDoxycycline Hyclate (DXH), 800U/mg
CAS:Fórmula:C22H24N2O8·HClH2OC2H6OForma y color:Yellow, Hygroscopic crystalline powderPeso molecular:512.94Doxycycline hydrochloride hemiethanolate hemihydrate, Antibiotic for Culture Media Use Only
CAS:<p>Doxycycline is an antibiotic that inhibits bacterial growth by inhibiting protein synthesis, respiratory chain, DNA gyrase, DNA topoisomerase IV. Doxycycline inhibits papaverine by blocking the expression of both cytochrome P450 and epoxide hydrolase. Doxycycline is commonly found in studies for bacterial infections, drug therapy, histopathological studies, cell culture and chemometric analysis.</p>Fórmula:C22H24N2O8·HClH2OC2H6OPureza:Min. 97.0 Area-%Peso molecular:512.90 g/mol
















