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Chemical Structure
Chemical Structure
Chemical Structure

Narciclasine [29477-83-6]

Research Use Only
AG-CN2-0524
AdipoGen Life Sciences
CAS Number29477-83-6
Product group Chemicals
Estimated Purity>98%
Molecular Weight307.3
Price on request
Packing Size
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Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    Narciclasine [29477-83-6]
  • Delivery Days Customer
    10
  • CAS Number
    29477-83-6
  • Certification
    Research Use Only
  • Estimated Purity
    >98%
  • Hazard Information
    Danger,Non-hazardous
  • Molecular Formula
    C14H13NO7
  • Molecular Weight
    307.3
  • Scientific Description
    Chemical. CAS: 29477-83-6. Formula: C14H13NO7. MW: 307.3. Plant growth modulator/inhibitor. Anticancer agent. Exhibits antiproliferative and pro-apoptotic effects in carcinoma cells and displays cytotoxic activity against a panel of 60 cancer cell lines. Shown to promote autophagy-induced apoptosis and to slow cell cycle progression. Inhibits protein synthesis by interacting with the 60S ribosome subunit. Regulates the Rho/ROCK/LIM kinase/cofilin pathway. Stimulates RhoA activation and induces actin polymerization. Anti-obesity agent. Attenuates diet-induced obesity (DIO) in mice by promoting oxidative metabolism in skeletal muscle and energy expenditure. Anti-inflammatory agent suppressing NF-kappaB-dependent gene transcription. Antiviral agent in vitro. Antifungal agent. Shown to inhibit amyloid plaque formation in an Alzheimers disease model. - Plant growth modulator/inhibitor. Anticancer agent. Exhibits antiproliferative and pro-apoptotic effects in carcinoma cells and displays cytotoxic activity against a panel of 60 cancer cell lines. Shown to promote autophagy-induced apoptosis and to slow cell cycle progression. Inhibits protein synthesis by interacting with the 60S ribosome subunit. Regulates the Rho/ROCK/LIM kinase/cofilin pathway. Stimulates RhoA activation and induces actin polymerization. Anti-obesity agent. Attenuates diet-induced obesity (DIO) in mice by promoting oxidative metabolism in skeletal muscle and energy expenditure. Anti-inflammatory agent suppressing NF-kappaB-dependent gene transcription. Antiviral agent in vitro. Antifungal agent. Shown to inhibit amyloid plaque formation in an Alzheimers disease model.
  • SMILES
    OC1=C(C(N[C@]2([H])C3=C[C@H](O)[C@@H](O)[C@H]2O)=O)C3=CC4=C1OCO4
  • Storage Instruction
    2°C to 8°C,-20°C
  • UNSPSC
    12352200