TargetMol

Benzylideneacetone

Product Code:
 
TAR-TN6993
Supplier:
 
TargetMol
Regulatory Status:
 
RUO
Shipping:
 
cool pack
Storage:
 
-20°C
1 / 1

No additional charges, what you see is what you pay! *

CodeSizePrice
TAR-TN6993-1mL1 mL * 10 mM (in DMSO)£94.00
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here.
Quantity:
TAR-TN6993-1g1g£95.00
Special offer! Add £1 to your order to get a TargetMol CCK-8 Kit. Read more here.
Quantity:
Prices exclude any Taxes / VAT
Stay in control of your spending. These prices have no additional charges, not even shipping!
* Rare exceptions are clearly labelled (only 0.14% of items!).
Multibuy discounts available! Contact us to find what you can save.
This product comes from: United States.
Typical lead time: 10-14 working days.
Contact us for more accurate information.
  • Further Information
  • Documents
  • References
  • Show All

Further Information

Bioactivity:
Benzylideneacetone, a monoterpene produced by the insect pathogenic bacterium Xenorhabdus nematophila, is a phospholipase A2 (PLA2) inhibitor with inhibitory effects on arachidonoid biosynthesis and enhances baculovirus pathogenicity of Xylaria minor.
CAS:
122-57-6
Formula:
C10H10O
Molecular Weight:
146.19
Pathway:
Metabolism
Purity:
0.9952
SMILES:
O=C(C=CC=1C=CC=CC1)C
Target:
Endogenous Metabolite|Phospholipase

References

Yates RL, et al. Fluorometric determination of benzylideneacetone in fragrance products by liquid chromatography with post-column derivatization. J Assoc Off Anal Chem. 1988;71(5):965-967. Kim J, et al. Benzylideneacetone, an eicosanoid biosynthesis inhibitor enhances baculovirus pathogenicity in the diamondback moth, Plutella xylostella. J Invertebr Pathol. 2011;106(2):308-313. Kwon B, et al. Benzylideneacetone, an immunosuppressant, enhances virulence of Bacillus thuringiensis against beet armyworm (Lepidoptera: Noctuidae). J Econ Entomol. 2008;101(1):36-41. Pativada T, et al. Benzylideneacetone Derivatives Inhibit Osteoclastogenesis and Activate Osteoblastogenesis Independently Based on Specific Structure-Activity Relationship. J Med Chem. 2019;62(13):6063-6082.