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Chemical Structure
Chemical Structure
Chemical Structure

Quinolactacin A [386211-68-3,386211-69-4]

Research Use Only
AG-CN2-0164
AdipoGen Life Sciences
CAS Number386211-69-4
DownloadMSDS
Product group Chemicals
Estimated Purity>95%
Molecular Weight270.3
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Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    Quinolactacin A [386211-68-3, 386211-69-4]
  • Delivery Days Customer
    10
  • CAS Number
    386211-69-4
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Hazard Information
    Warning
  • Molecular Formula
    C16H18N2O2
  • Molecular Weight
    270.3
  • Scientific Description
    Antibiotic [1-3]. Acetylcholinesterase (AChE) inhibitor [3]. Anti-inflammatory compound [1, 4]. Tumor necrosis factor (TNF) inhibitor [1, 4]. - Chemical. CAS: Quinolactacin A1: 386211-68-3/Quinolactacin A2: 386211-69-4. Formula: C16H18N2O2. MW: 270.3. Isolated from Penicillium citrinum. Antibiotic. Acetylcholinesterase (AChE) inhibitor. Anti-inflammatory compound. Tumor necrosis factor (TNF) inhibitor.
  • SMILES
    [H][C@](C)(CC)C1([H])NC(=O)C2=C1N(C)C1=CC=CC=C1C2=O
  • Storage Instruction
    2°C to 8°C,-20°C
  • UNSPSC
    12352200

References

  • Quinolactacins A, B and C: Novel Quinolone Compounds from Penicillium sp. EPF-6 I. Taxonomy, Production, Isolation and Biological Properties: N. Kakinuma, et al.; J. Antibiot. 53, 1247 (2000)
  • Quinolactacins A, B and C: Novel Quinolone Compounds from Penicillium sp. EPF-6 II. Physico-chemical Properties and Structure Elucidation: S. Takahashi, et al.; J. Antibiot. 53, 1252 (2000)
  • Quinolactacins Al and A2, new acetylcholinesterase inhibitors from Penicillium citrinum: W.G. Kim, et al.; J. Antibiot. 54, 831 (2001)
  • Biosynthesis of quinolactacin A, a TNF production inhibitor: T. Sasaki, et al.; J. Antibiot. 59, 418 (2006)