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Results for "

disproportionation

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5

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1

Biochemical Assay Reagents

1

Natural
Products

Cat. No. Product Name Target Research Areas Chemical Structure
  • HY-W001187
    Tempo
    10+ Cited Publications

    		 Mitochondrial Metabolism DNA/RNA Synthesis Reactive Oxygen Species (ROS) Cancer
    Tempo is a nitric oxide radical and a selective scavenger of ROS in mitochondria. Tempo is also an organocatalyst that disproportionates superoxide and oxidizes primary alcohols to aldehydes in a catalytic cycle. Tempo has mutagenic and antioxidant effects and can induceDNA strand breaks. Tempo also exerts cytotoxic and mutagenic properties in mouse lymphoma cells .
    Tempo
  • HY-15932
    TOOS

    TOOS sodium salt

    		 Biochemical Assay Reagents Others
    TOOS (TOOS sodium salt) is a highly water-soluble aniline derivative widely used in diagnostics and biological experiments. TOOS can be combined with 3-methyl-2-benzothiazolinone hydrazone hydrochloride (MBTH) to form a chromogenic system to measure oxidase activity. In the MBTH-TOOS chromogenic system, MBTH is catalytically oxidized to produce (-NH) free radicals, which react with TOOS to form colorless compounds. Furthermore, the colorless compound undergoes a disproportionation reaction to produce a blue-violet quinoid compound .
    TOOS
  • HY-N11424
    Bilirubin diglucuronide

    		Drug Metabolite Glycosyltransferase Metabolic Disease
    Bilirubin diglucuronide is a bilirubin glycoside conjugate with a 1-O-acyl β-D-glucuronide structure. Bilirubin diglucuronide is the major conjugated bilirubin (HY-N0323) and predominant pigment excreted in the bile of adult humans, rats, dogs and cats. Bilirubin diglucuronide is mainly synthesized via UDP-glucuronosyltransferase-mediated transfer of glucuronic acid from UDP-glucuronic acid to bilirubin monoglucuronide, or via enzymatic disproportionation of two moles of bilirubin monoglucuronide (predominantly producing the IXα configuration). In addition, Bilirubin diglucuronide can also be synthesized from bilirubin or its monoglucuronide in a UDP-glucuronic acid-dependent manner. Pretreatment with phenobarbital significantly enhances the formation process of Bilirubin diglucuronide .
    Bilirubin diglucuronide
  • HY-W012472
    1,3,5-Triisopropylbenzene

    		Environmental Pollutants Biochemical Assay Reagents Others
    1,3,5-Triisopropylbenzene is a symmetric aromatic hydrocarbon compound. 1,3,5-Triisopropylbenzene serves as a saturated crosslinker to participate in the "inverse vulcanization" reaction of elemental sulfur. 1,3,5-Triisopropylbenzene acts as a probe molecule to evaluate the external surface acidity and accessibility of zeolite materials. 1,3,5-Triisopropylbenzene is also used as fuel and fuel additive, lubricant and lubricant additive, as well as micelle swelling agent .
    1,3,5-Triisopropylbenzene
  • HY-W001187R
    Tempo (Standard)

    		Mitochondrial Metabolism DNA/RNA Synthesis Reactive Oxygen Species (ROS) Reference Standards Cancer
    Tempo (Standard) is the analytical standard of Tempo. This product is intended for research and analytical applications. Tempo is a nitric oxide radical and a selective scavenger of ROS in mitochondria. Tempo is also an organocatalyst that disproportionates superoxide and oxidizes primary alcohols to aldehydes in a catalytic cycle. Tempo has mutagenic and antioxidant effects and can induceDNA strand breaks. Tempo also exerts cytotoxic and mutagenic properties in mouse lymphoma cells [4].
    Tempo (Standard)

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