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Sedanolide (CAS 6415-59-4)

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Alternate Names:
3-butyl-3a,4,5,6-tetrahydro-3H-2-benzofuran-1-one
Application:
Sedanolide is an inducer of GST and inhibitor of Cox-1, Cox-2, Topo I, Topo II, and carcinogenesis
CAS Number:
6415-59-4
Purity:
≥98%
Molecular Weight:
194.27
Molecular Formula:
C12H18O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Sedanolide, a natural phthalide derived from celery seeds, is extensively studied in the field of agricultural and food science research due to its intriguing chemical properties. As a component contributing to the distinctive aroma and flavor of celery, sedanolide has been investigated for its role in plant chemistry and as a potential natural additive in food industries. Its mechanism of action is primarily associated with its capacity as a natural insecticidal and fungicidal agent, offering an alternative to synthetic chemicals in managing crop pests and diseases. In research settings, sedanolide is examined for its effectiveness in repelling insects and protecting plants against fungal pathogens, which can enhance crop yield and reduce spoilage. Studies have also explored sedanolide′s role in modulating plant growth and development, including its potential influence on germination and root growth. This makes it valuable for understanding plant-environment interactions and developing sustainable agricultural practices. Furthermore, sedanolide is researched for its antioxidant properties, contributing insights into its potential benefits in food preservation and extending the shelf life of perishable products.


Sedanolide (CAS 6415-59-4) References

  1. Mosquitocidal, nematicidal, and antifungal compounds from Apium graveolens L. seeds.  |  Momin, RA. and Nair, MG. 2001. J Agric Food Chem. 49: 142-5. PMID: 11305251
  2. Sedanolide, a natural phthalide from celery seed oil: effect on hydrogen peroxide and tert-butyl hydroperoxide-induced toxicity in HepG2 and CaCo-2 human cell lines.  |  Woods, JA., et al. 2001. In Vitr Mol Toxicol. 14: 233-40. PMID: 11846995
  3. Antioxidant, cyclooxygenase and topoisomerase inhibitory compounds from Apium graveolens Linn. seeds.  |  Momin, RA. and Nair, MG. 2002. Phytomedicine. 9: 312-8. PMID: 12120812
  4. Chemistry, technology, and nutraceutical functions of celery (Apium graveolens L.): an overview.  |  Sowbhagya, HB. 2014. Crit Rev Food Sci Nutr. 54: 389-98. PMID: 24188309
  5. Sedanolide induces autophagy through the PI3K, p53 and NF-κB signaling pathways in human liver cancer cells.  |  Hsieh, SL., et al. 2015. Int J Oncol. 47: 2240-6. PMID: 26500073
  6. Antibacterial activity of endosymbiotic bacterial compound from Pheretima sp. earthworms inhibit the growth of Salmonella Typhi and Staphylococcus aureus: in vitro and in silico approach.  |  Husain, DR. and Wardhani, R. 2021. Iran J Microbiol. 13: 537-543. PMID: 34557283
  7. Bifidobacterium longum R0175 protects mice against APAP-induced liver injury by modulating the Nrf2 pathway.  |  Li, S., et al. 2023. Free Radic Biol Med. 203: 11-23. PMID: 37003500
  8. Sedanolide Activates KEAP1-NRF2 Pathway and Ameliorates Hydrogen Peroxide-Induced Apoptotic Cell Death.  |  Tabei, Y., et al. 2023. Int J Mol Sci. 24: PMID: 38003720
  9. Sedanolide alleviates DSS-induced colitis by modulating the intestinal FXR-SMPD3 pathway in mice.  |  Li, S., et al. 2024. J Adv Res.. PMID: 38582300
  10. Chemoprevention of benzo[a]pyrene-induced forestomach cancer in mice by natural phthalides from celery seed oil.  |  Zheng, GQ., et al. 1993. Nutr Cancer. 19: 77-86. PMID: 8446516

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Sedanolide, 100 mg

sc-205972
100 mg
$154.00

Is SC-205972 trans or cis?

Asked by: Jz28sail
Thank you for your question. For the compound, sc-205972, we do not characterize whether it is cis or trans. If you have any further questions or concerns, please feel free to contact our Technical Service department by calling 800-457-3801 option 2, emailing scbt@scbt.com, or using the Live Chat function on our website.
Answered by: Tech Service 8
Date published: 2017-02-07
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Rated 5 out of 5 by from Momin et al (PubMed ID 11305251) found thatMomin et al (PubMed ID 11305251) found that sedanolide was a prostaglandin H endoperoxide synthase- (COX-1) and Cox-II inhibitor at pH 7 and also inhibited topoisomerase I/II activity. -SCBT Publication Review
Date published: 2015-05-12
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Sedanolide is rated 5.0 out of 5 by 1.
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