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Results for "

T7405

" in TargetMol Product Catalog.
  • Inhibitors & Agonists
    6
    TargetMol | All_Pathways
  • Natural Products
    2
    TargetMol | Natural_Products
  • Piperidolate
    T740582-98-4
    Piperidolate inhibits intestinal cramp induced by acetylcholine
    • $34
    In Stock
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    TargetMol | Inhibitor Sale
  • Pyridinium bisretinoid A2E
    A2E
    T74051173449-96-2
    Pyridinium bisretinoid A2E (A2E) is a fluorescent chromophore isolated from lipofuscin in retinal pigment epithelium, a lipophilic cation and weak photosensitizer with cytotoxicity. A2E promotes apoptosis under blue light exposure and induces autophagy under photoactivation, damaging membrane integrity in a concentration-dependent manner.
    • $829
    In Stock
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    QTY
    TargetMol | Inhibitor Hot
  • Allyl methyl trisulfide
    T7405034135-85-8
    Allyl methyl trisulfide, a volatile organic compound found in garlic (Allium sativum L.) essential oil, exhibits antibacterial, antioxidant, and antitumor activities [1].
    • Inquiry Price
    Inquiry
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  • Polyinosinic-polycytidylic acid potassium
    T7405231852-29-6
    Polyinosinic-polycytidylic acid potassium (Poly(I:C) potassium), a synthetic double-stranded RNA analog, serves as an agonist for toll-like receptor 3 (TLR3) and retinoic acid-inducible gene I (RIG-I)-like receptors (RIG-I and MDA5), offering applications in immunotherapy. Its sodium variant enhances both innate and adaptive immune responses when used as a vaccine adjuvant and is instrumental in modifying the tumor microenvironment. Additionally, Poly(I:C) potassium can directly induce apoptosis in cancer cells [1] [2] [3].
    • $50
    7-10 days
    Size
    QTY
  • epi-Aszonalenin A
    T74056908853-14-5
    Epi-Aszonalenin A, a benzodiazepine fungal metabolite initially derived from Aspergillus novofumigatus, functions as a psychoactive agent [1].
    • $436
    35 days
    Size
    QTY
  • Targaprimir-96 TFA
    T74059
    Targaprimir-96 TFA, a potent inhibitor of microRNA-96 (miR-96) processing, selectively reduces miR-96 production in cancer cells, thereby inducing apoptosis. This compound exhibits low nanomolar affinity binding to primary miR-96 (pri-miR-96), targeting it specifically in breast cancer cells while remaining inactive in normal breast cells [1].
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