AdipoGen Life Sciences

Altenusin

CHF 170.00
In stock
AG-CN2-0143-M0011 mgCHF 170.00
AG-CN2-0143-M0055 mgCHF 620.00
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Product Details
Synonyms MS 341
Product Type Chemical
Properties
Formula

C15H14O6

MW 290.3
CAS 31186-12-6
Source/Host Chemicals Isolated from Penicillium sp.
Purity Chemicals ≥97% (HPLC)
Appearance Yellow solid.
Solubility Soluble in methanol, ethanol or DMSO.
InChi Key ADPBTBPPIIKLEH-UHFFFAOYSA-N
Smiles COC1=CC(O)=C(C(O)=O)C(=C1)C1=CC(O)=C(O)C=C1C
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light.
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
Documents
MSDS Download PDF
Product Specification Sheet
Datasheet Download PDF
Description
  • Antibiotic [7].
  • Antifungal penicillide [8].
  • Non-competitive, specific neutral sphingomyelinase (N-SMase) inhibitor [2].
  • Strong pp60c-Src inhibitor [3].
  • Inhibits cFMS receptor tyrosine kinase (CSF-1/m-CSF receptor tyrosine kinase) which is implicated in cancer and bone diseases [3].
  • Myosin light chain kinase inhibitor [1].
  • Exhibits anti-HIV-1 integrase activity [4].
  • Cytotoxic activity against mouse lymphoma cells [6].
  • Anti-protozoan, trypanothione reductase (TR) inhibitor [5].
  • Phytotoxin [9].
Product References
  1. Isolation of myosin light chain kinase inhibitors from microorganisms: dehydroaltenusin, altenusin, atrovenetinone, and cyclooctasulfur: S. Nakanishi, et al.; Biosci. Biotechnol. Biochem. 59, 1333 (1995)
  2. Alutenusin, a specific neutral sphingomyelinase inhibitor, produced by Penicillium sp. FO-7436: R. Uchida, et al.; J. Antibiot. 52, 572 (1999)
  3. Fungal Metabolites as Potent Protein Kinase Inhibitors: Identification of a Novel Metabolite and Novel Activities of Known Metabolites: M. Oyama, et al.; Lett. Drug Des. Disc. 1, 24 (2004)
  4. HIV-1 Integrase Inhibitors: 2003-2004 Update: R. Dayan, et al.; Med. Res. Rev. 26, 271 (2006)
  5. Altenusin, a biphenyl isolated from the endophytic fungus Alternaria sp., inhibits trypanothione reductase from Trypanosoma cruzi: B.B. Cota, et al.; FEMS Microbiol. Lett. 285, 177 (2008)
  6. Cytotoxic metabolites from the fungal endophyte Alternaria sp. and their subsequent detection in its host plant Polygonum senegalense: A.H. Aly, et al.; J. Nat. Prod. 71, 972 (2008)
  7. Polyketides with antimicrobial activity from the solid culture of an endolichenic fungus Ulocladium sp.: Q.X. Wang, et al.; Fitoterapia 83, 209 (2012)
  8. Antifungal activity of altenusin isolated from the endophytic fungus Alternaria sp. against the pathogenic fungus Paracoccidioides brasiliensis: S. Johann, et al.; Rev. Iberoam. Micol. 29, 205 (2012)
  9. Identification of Alternaria alternata mycotoxins by LC-SPE-NMR and their cytotoxic effects to soybean (Glycine max) cell suspension culture: G.D. de Souza, et al.; Molecules 18, 2528 (2013)
  10. Development of Acid Hydrolysis-Based UPLC–MS/MS Method for Determination of Alternaria Toxins and Its Application in the Occurrence Assessment in Solanaceous Vegetables and Their Products: H. Tang, et al.; Toxins 15, 201 (2023)
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