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Results for "

Hypochlorous

" in MedChemExpress (MCE) Product Catalog:

7

Inhibitors & Agonists

4

Fluorescent Dye

1

Peptides

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-130025
    HKOCl-3
    1 Publications Verification

    		 Fluorescent Dye Others
    HKOCl-3 is a highly sensitive and selective fluorescent probe for detecting hypochlorous acid.Ex: 490 nm; Em 527 nm .
    HKOCl-3
  • HY-D1158
    HKOCl-4m

    		Fluorescent Dye Inflammation/Immunology
    HKOCl-4m is a selective and mitochondria-targeting rhodol-based fluorescent probe for monitoring mitochondrial hypochlorous acid (HOCl) .
    HKOCl-4m
  • HY-130027
    HKOCl-4
    1 Publications Verification

    BXY2142

    		 Fluorescent Dye Others
    HKOCl-4 (BXY2142) is a rhodol-based yellow fluorescent probe for the detection of hypochlorous acid with excellent sensitivity and selectivity . HKOCl-4 has longer absorption wavelength and better pH stability compared with fluorescein-based probes. Ex: 530 nm; Em 557 nm.
    HKOCl-4
  • HY-112669
    5-Chloro-2'-deoxyuridine
    1 Publications Verification

    5-Chlorodeoxyuridine; CldU

    		 Others Neurological Disease
    5-Chloro-2'-deoxyuridine, a thymine analog, is to study the potential of hypochlorous acid damage to DNA and DNA precursors.
    5-<em>Chloro</em>-2'-deoxyuridine
  • HY-D1265
    EtS-DMAB

    HClO-green

    		 Fluorescent Dye Others
    EtS-DMAB (HClO-green) is a fluorescent probe, which can selectively detect hypochlorous acid (HOCl) (λex=440 nm, λem=610 nm). EtS-DMAB is applied to image exogenous and endogenous HOCl in live cells .
    EtS-DMAB
  • HY-P1182
    C21

    		Histone Methyltransferase Cancer
    C21 is a potent, irreversible, and selective PRMT1 inhibitor with an IC50 of 1.8 μM. C21 inhibits PRMT6 with an IC50 of 8.8 μM .
    C21
  • HY-125039
    N-Acetyl lysyltyrosylcysteine amide
    2 Publications Verification

    		 Glutathione Peroxidase Cardiovascular Disease Neurological Disease
    N-Acetyl lysyltyrosylcysteine amide is a potent, reversible, specific, and non-toxic tripeptide inhibitor of myeloperoxidase (MPO). N-Acetyl lysyltyrosylcysteine amide effectively inhibits MPO generation of toxic oxidants in vivo. N-Acetyl lysyltyrosylcysteine amide reduces neuronal damage and preserves brain tissue and neurological function in the stroked brain. N-Acetyl lysyltyrosylcysteine amide inhibits MPO-dependent hypochlorous acid (HOCl) generation, protein nitration, and LDL oxidation .
    N-Acetyl lysyltyrosylcysteine amide

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