TIANFU CHEM Doxycycline

Details:

Doxycycline Basic information
Product Name: Doxycycline
Synonyms: (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;Doxycyclin hyclate;Doxycycline Base & Hyclate;6- Deoxy-5-hydroxytetracycline, 6-Deoxyoxytetracycline, Doxytetracycline, GS 3065, HydraMycin, MedeoMycin, VibraMycin;4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-4-(dimethylamino)-4;5-hydroxy-alpha-6-deoxytetracycline;5-hydroxy-alpha-6-deoxytetracyclinemonohydrate;6-alpha-deoxy-5-oxytetracycline
CAS: 564-25-0
MF: C22H24N2O8
MW: 444.44
EINECS: 209-271-1
Product Categories: FUNGICIDE;Intermediates & Fine Chemicals;Pharmaceuticals
Mol File: 564-25-0.mol
Doxycycline Structure
Doxycycline Chemical Properties
Melting point  206-209°C (dec.)
CAS DataBase Reference 564-25-0(CAS DataBase Reference)
EPA Substance Registry System 2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5, 5a,6,11,12a-octahydro-3,5, 10,12,12a-pentahydroxy-6- methyl-1,11-dioxo-, (4S,4aR,5S,5aR,6R,12aS)-(564-25-0)
Safety Information
Hazardous Substances Data 564-25-0(Hazardous Substances Data)

Doxycycline Usage And Synthesis
Chemical Properties Yellow Solid
Uses tetracycline antibiotics
Uses Doxycycline is a semi-synthetic tetracycline prepared by hydrogenolysis of oxytetracycline to remove the 6-hydroxy group. Although the synthesis was reported in 1958, it was not released for use until 1967. Doxycycline, together with minocycline, is regarded as a ‘third generation’ tetracycline largely replacing the analogues and pro-drugs produced in the early 1960s for mainstream antibiotic applications. Like all tetracyclines, doxycycline shows broad spectrum antibacterial and antiprotozoan activity and acts by binding to the 30S and 50S ribosomal subunits, blocking protein synthesis. Doxycycline has been extensively cited in the literature with over 10,000 references.
Definition ChEBI: Tetracycline in which the 5beta-hydrogen is replaced by a hydroxy group, while the 6alpha-hydroxy group is replaced by hydrogen. A semi-synthetic tetracycline antibiotic, it is used to inhibit bacterial protein synthesis a d treat non-gonococcal urethritis and cervicitis, exacerbations of bronchitis in patients with chronic obstructive pulmonary disease (COPD), and adult periodontitis.