AdipoGen Life Sciences

Meleagrin

CHF 190.00
In stock
AG-CN2-0451-M0011 mgCHF 190.00
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Product Details
Synonyms 6-O-Methyloxaline
Product Type Chemical
Properties
Formula

C23H23N5O4

MW 433.5
CAS 71751-77-4
Source/Host Chemicals Isolated from Penicillium sp.
Purity Chemicals ≥90% (HPLC)
Appearance Yellow adhered film.
Solubility Soluble in DMSO or ethanol.
InChi Key JTJJJLSLKZFEPJ-ZAYCRUKZSA-N
Smiles CON1C2=C(C=CC=C2)[C@@]2(C=C(O)C(=O)N3C(=CC4=CN=CN4)C(=O)N[C@@]123)C(C)(C)C=C
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Handling Advice Protect from light.
Protect from moisture.
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
  • Mycotoxin.
  • Alkaloid antibiotic.
  • Bacterial enoyl-acyl carrier protein reductase (FabI) inhibitor.
  • Antineoplastic activity.
  • Moderate cytotoxicity against A-549 and HL-60 cell lines. Induces cell cycle arrest through G2/M phase, presumably by inhibiting tubulin polymerization.
  • Antifouling agent against the barnacle Balanus amphitrite.
Product References
  1. Studies on fungal products. VII. The structures of meleagrin and 9-O-p-bromobenzoylmeleagrin: K. Kawai, et al.; Chem. Pharm. Bull. 32, 94 (1984)
  2. Study of the alkaloid composition of the food-infecting penicilles: T.A. Reshetilova, et al.; Food Addit. Contam. 12, 461 (1995)
  3. Production of mycotoxins on artificially and naturally infested building materials: K.F. Nielsen, et al.; Mycopathologia 145, 43 (1999)
  4. Alkaloids from a deep ocean sediment-derived fungus Penicillium sp. and their antitumor activities: L. Du, et al.; J. Antibiot. 63, 165 (2010)
  5. iTRAQ-based proteomic profiling of the barnacle Balanus amphitrite in response to the antifouling compound meleagrin: Z. Han, et al.; J. Proteome Res. 12, 2090 (2013)
  6. Meleagrin, a new FabI inhibitor from Penicillium chryosogenum with at least one additional mode of action: C.J. Zheng, et al.; PLoS One 8, e78922 (2013)
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