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Results for "

dopal

" in TargetMol Product Catalog.
  • Inhibitors & Agonists
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    TargetMol | All_Pathways
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    TargetMol | Natural_Products
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    TargetMol | Cell_Research_Reagents
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  • DOPAL
    T375335707-55-1
    DOPAL is an aldehyde product of the oxidative deamination of dopamine by monoamine oxidase.[1] It can be further oxidized to 3,4-dihydroxyphenylacetic acid (DOPAC) by aldehyde dehydrogenase (ALDH) and, to a lesser extent reduced to 3,4-dihydroxyphenyl ethanol (DOPET). DOPAL is toxic to neurons.[2],[3] It can also oligomerize and precipitate α-synuclein, an event associated with Parkinson's disease.[2] Mice lacking cytosolic and mitochondrial forms of ALDH display increased levels of DOPAL as well as neurodegeneration and motor dysfunction characteristic of Parkinson's disease.[4]
    • $415
    35 days
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  • 8-Oxopseudopalmatine
    T131397
    8-Oxopseudopalmatine is a useful organic compound for research related to life sciences and the catalog number is T131397.
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  • Pseudopalmatine
    TN600919716-66-6
    Pseudopalmatine exhibits antiplasmodial activity. It also shows anti-acetylcholinesterase (AChE) activity, with IC50 values of 1.8uM.
    • $1,598
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  • 2-Azidopalmitoyl-CoA
    2-Azidopalmitoyl coenzyme A
    TYD-02422
    2-Azidopalmitoyl-CoA (2-Azidopalmitoyl coenzyme A) is a derivative of coenzyme A.
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  • RU-SKI 43
    RUSKI 43
    T127971043797-53-0In house
    RU-SKI 43 is a potent and selective hedgehog acyltransferase (Hhat) inhibitor with an IC50 of 850 nM. It exhibits anticancer activity and is a potential treatment for lung adenocarcinomas. RU-SKI 43 reduces Gli-1 activation through smoothening-independent non-canonical signaling and inhibits Akt and mTOR pathway activity.
    • $45
    In Stock
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  • 15-Azido-pentadecanoic acid
    Azido Palmitic Acid
    T84775118162-46-2
    15-Azido-pentadecanoic acid, also known as Azido Palmitic Acid, serves as a click chemistry reagent due to its azide group. This compound is instrumental in the identification and characterization of post-translationally palmitylated proteins through a straightforward two-step labeling and detection methodology [1]. It can partake in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with alkyne-bearing molecules and also engage in strain-promoted alkyne-azide cycloaddition (SPAAC) with molecules featuring DBCO or BCN groups, showcasing its versatility in biochemical applications.
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    8-10 weeks
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