Call +41-61-926-60-40 Fax +41-61-926-60-49


AG-CN2-0171-C250 250 µg INQ
AG-CN2-0171-M001 1 mg INQ
Select size:

* Required Fields

Add to Cart
Call +41-61-926-60-40
Fax +41-61-926-60-49
Contact Us!

Additional Information

Product Data
Synonyms Anabellamide; Asjanin; Auranamide; NSC 306231; N-Benzoyl-phenylalanine-2-benzoylamino-3-phenylpropyl ester
Formula C32H30N2O4
MW 506.6
CAS 63631-36-7
Source/Host Isolated from Aspergillus sp.
Purity ≥95% (HPLC)
Appearance White solid.
Solubility Soluble in ethanol, methanol or DMSO.
Origin Manufactured by BioLinks K.K. with courtesy strain from The Kitasato Institute.
Product Type Chemical
Shipping and Handling
Shipping AMBIENT
Short Term Storage +4°C
Long Term Storage -20°C
Use/Stability Stable for at least 2 years after receipt when stored at -20°C.
MSDS Download Document Download

Product Description

  • Anticancer compound.
  • Cytotoxic against human breast cancer cells.
  • Induces autophagic cell death in MCF-7 cells.
  • Moderate radical scavenger.
  • Weak acetylcholinesterase (AChE) inhibitor.
  • Shows moderate trypanocidal activity.

Product References

  1. Two metabolites from Aspergillus flavipes: A.M. Clark, et al.; Lloyda 40, 146 (1977)
  2. Cytotoxic and anti-HIV principles from the rhizomes of Begonia nantoensis: P.W. Wu, et al.; Chem. Pharm. Bull. 52, 345 (2004)
  3. A new method for asperphenamate synthesis and its antimicrobial activity evaluation: A.M. Pomini, et al.; Nat. Prod. Res. 20, 537 (2006)
  4. Total synthesis and anticancer activity studies of the stereoisomers of asperphenamate and patriscabratine: L. Yuane, et al.; Chin. Chem. Lett. 21, 155 (2010)
  5. JNK-dependent Atg4 upregulation mediates asperphenamate derivative BBP-induced autophagy in MCF-7 cells: Y. Li, et al.; Toxicol. Appl. Pharmacol. 263, 21 (2012)
  6. Two new Penicillium species Penicillium buchwaldii and Penicillium spathulatum, producing the anticancer compound asperphenamate: J.C. Frisvad, et al.; FEMS Microbiol. Lett. 339, 77 (2013)
  7. In vitro acetylcholinesterase activity of peptide derivatives isolated from two species of Leguminosae: C.Q. Alves, et al.; Pharm. Biol. 51, 936 (2013)
  8. Antioxidant activity of compounds isolated from the root woods of Erythrina droogmansiana: A.J.G. Yaya, et al.; Int. J. Pharm. Sci. Drug Res. 6, 160 (2014)
  9. Two trypanocidal dipeptides from the roots of Zapoteca portoricensis (Fabaceae): N.J. Nwodo, et al.; Molecules 19, 5470 (2014)
No reviews for this product yet.