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    Offer Omeprazole 73590-58-6/ ycgsales2011@ gmail.com

    Offer Omeprazole 73590-58-6/ ycgsales2011@ gmail.com

    Price:
    negotiate
    Quantity Order:
    Payment Method:
    Telegraphic Transfer (T/T)
    Pack. & Delivery:
    pack: 1kg foil bag/ tin

    Specification :

    CAS: 73590-58-6
    MF: C17H19N3O3S
    MW: 345.42
    EINECS:
    Product Categories: Drug bulk; Active Pharmaceutical Ingredients; Omeprazole; Intermediates & Fine Chemicals; Pharmaceuticals; API' s; ATPase
    Mol File: 73590-58-6.mol
    mp 156° C
    storage temp. 2-8° C
    solubility H2O: 0.5 mg/ mL
    form solid
    color white
    Merck 6845
    Stability: Stable, but hygroscopic and photosensitive. Incompatible with strong oxidizing agents. Store in the dark.
    Chemical Properties White Crystalline Solid
    Usage Binds covalently to proton pump. It inhibits gastric secretion. Used as an anttiulcerative
    Biological Activity H + , K + -ATPase inhibitor ( IC 50 = 5.8 ¼ M) that displays antisecretory and antiulcer activity. Inhibits gastric acid secretion ( IC 50 = 0.16 ¼ M for histamine-induced acid formation) and reduces gastric lesion formation induced by a variety of ulcerative stimuli. Antibacteral against Helicobacter pylori in vitro . Also inhibits CYP2C19, CYP2C9 and CYP3A ( K i values are 3.1, 40.1 and 84.4 ¼ M respectively) and blocks swelling-dependent chloride channels ( ICIswell) .
    Raw materials Chloroform--> 3-Chloroperoxybenzoic acid--> o-Phenylenediamine--> 3, 5-Dimethyl-4-methoxy-2-pyridinemethanol--> Pota ssium ethylxanthate--> Benzimidazole--> 5-Methoxy-2-mercaptobenzimidazole
    Packing: 1kg net/ foil bag or tin.
    Delivery: Express courier.
    The min. order is 10 grams.
    a proton pump inhibitor used in the treatment of dyspepsia, peptic ulcer disease ( PUD) , gastroesophageal reflux disease ( GORD/ GERD) , laryngopharyngeal reflux ( LPR) and Zollinger– Ellison syndrome. Omeprazole is a competitive inhibitor of the enzymes CYP2C19 and CYP2C9, and may therefore interact with drugs that depend on them for metabolism, such as diazepam, escitalopram, and warfarin; the concentrations of these drugs may increase if they are used concomitantly with omeprazole.[ 13] Clopidogrel ( Plavix) is an inactive prodrug that partially depends on CYP2C19 for conversion to its active form; inhibition of CYP2C19 blocks the activation of clopidogrel, thus reducing its effects and potentially increasing the risk of stroke or heart attack in people taking clopidogrel to prevent these events.[ 14] [ 15] Omeprazole is also a competitive inhibitor of p-glycoprotein, as are other PPIs.
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