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Chemical Structure
Chemical Structure
Chemical Structure

Curvularin [10140-70-2]

Research Use Only
AG-CN2-0147
AdipoGen Life Sciences
CAS Number10140-70-2
Product group Chemicals
Estimated Purity>95%
Molecular Weight292.3
Price on request
Packing Size
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Overview

  • Supplier
    AdipoGen Life Sciences
  • Product Name
    Curvularin [10140-70-2]
  • Delivery Days Customer
    10
  • CAS Number
    10140-70-2
  • Certification
    Research Use Only
  • Estimated Purity
    >95%
  • Molecular Formula
    C16H20O5
  • Molecular Weight
    292.3
  • Scientific Description
    Antibiotic [1]. Antiprotozoal [1]. Antifungal and phytotoxic compound [1, 6]. Anti-inflammatory [7]. TGF-beta signaling inhibitor [8] Anticancer compound [2, 9]. Inhibits expression of inducible nitric oxide synthase (iNOS; NOSII) [4, 5]. Cell division inhibitor [3]. Acetylcholinesterase (AChE) inhibitor [9]. - Chemical. CAS: 10140-70-2. Formula: C16H20O5. MW: 292.3. Isolated from Penicillium sp. FKI-1938 Antibiotic. Antiprotozoal. Antifungal and phytotoxic compound. Anti-inflammatory. TGF-beta signaling inhibitor Anticancer compound. Inhibits expression of inducible nitric oxide synthase (iNOS; NOSII). Cell division inhibitor. Acetylcholinesterase (AChE) inhibitor.
  • SMILES
    C[C@H]1CCCCCC(=O)C2=C(O)C=C(O)C=C2CC(=O)O1
  • Storage Instruction
    -20°C,2°C to 8°C
  • UNSPSC
    12352200

References

  • Antimicrobial properties of fungal macrolide antibiotics: V. Betina & D. Micekova; Z. Allg. Mikrobiol. 12, 355 (1972)
  • Curvularin from Penicillium baradicum Baghdadi NRRL 3754, and biological effects: R.F. Vesonder, et al.; J. Environ. Sci. Health 11, 289 (1976)
  • Structural study of curvularin, a cell division inhibitor: E.L. Ghisalberti, et al.; Austral. J. Chem. 46, 571 (1993)
  • Sporogen, S14-95, and S-curvularin, three inhibitors of human inducible nitric-oxide synthase expression isolated from fungi: Y. Yao, et al.; Mol. Pharmacol. 63, 383 (2003)
  • Inhibitors of inducible NO synthase expression: total synthesis of (S)-curvularin and its ring homologues: S. Elzner, et al.; ChemMedChem 3, 924 (2008)
  • Isolation and Difference in Anti-Staphylococcus aureus Bioactivity of Curvularin Derivates from Fungus Eupenicillium sp.: L.W. Xie, et al.; Appl. Biochem. Biotechnol. 159, 284 (2009)
  • The anti-inflammatory fungal compound (S)-curvularin reduces proinflammatory gene expression in an in vivo model of rheumatoid arthritis: N. Schmidt, et al.; J. Pharmacol. Exp. Ther. 343, 106 (2012)
  • Inhibition of TGF-beta signaling by the fungal lactones (S)-curvularin, dehydrocurvularin, oxacyclododecindione and galiellalactone: K. Rudolph, et al.; Cytokine 61, 285 (2013)
  • Metabolite profiling and biological activities of bioactive compounds produced by Chrysosporium lobatum strain BK-3 isolated from Kaziranga National Park, Assam, India: C.G. Kumar, et al.; SpringerPlus 2, 122 (2013)