Date published: 2025-11-1

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(E)-2′-Hydroxychalcone (CAS 888-12-0)

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Alternate Names:
(E)-o-Hydroxyphenyl Styryl Ketone; NSC 170284
Application:
(E)-2′-Hydroxychalcone is a chalcone derivative
CAS Number:
888-12-0
Molecular Weight:
224.25
Molecular Formula:
C15H12O2
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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(E)-2′-Hydroxychalcone, a natural phenolic compound, has garnered significant attention in scientific research due to its diverse pharmacological properties and potential applications. Its mechanism of action primarily involves modulation of various cellular signaling pathways and enzyme activities. Researchers have identified (E)-2′-hydroxychalcone as a potent antioxidant, capable of scavenging reactive oxygen species and mitigating oxidative stress-induced cellular damage. Additionally, this compound exhibits anti-inflammatory properties by inhibiting the production of pro-inflammatory mediators and cytokines, thereby attenuating inflammatory responses implicated in various pathological conditions. Moreover, (E)-2′-hydroxychalcone has shown promising anticancer activity through multiple mechanisms, including induction of apoptosis, inhibition of cell proliferation, and suppression of angiogenesis and metastasis. Its ability to target multiple signaling pathways involved in cancer progression makes it a promising candidate for the development of novel anticancer agents. Furthermore, (E)-2′-hydroxychalcone has been investigated for its antimicrobial activity against various bacterial and fungal pathogens, highlighting its potential in combating infectious diseases. Ongoing research endeavors continue to explore the potential of (E)-2′-hydroxychalcone and explain its underlying mechanisms of action, paving the way for the development of novel pharmacological interventions targeting oxidative stress, inflammation, cancer, and infectious diseases.


(E)-2′-Hydroxychalcone (CAS 888-12-0) References

  1. Cloning, Functional Characterization, and Catalytic Mechanism of a Bergaptol O-Methyltransferase from Peucedanum praeruptorum Dunn.  |  Zhao, Y., et al. 2016. Front Plant Sci. 7: 722. PMID: 27252733
  2. Enantioselective photochemistry through Lewis acid-catalyzed triplet energy transfer.  |  Blum, TR., et al. 2016. Science. 354: 1391-1395. PMID: 27980203
  3. Antifungal activity of 2'-hydroxychalcone loaded in nanoemulsion against Paracoccidioides spp.  |  Medina-Alarcón, KP., et al. 2020. Future Microbiol. 15: 21-33. PMID: 32043361
  4. 2'-Hydroxychalcone Induces Autophagy and Apoptosis in Breast Cancer Cells via the Inhibition of the NF-κB Signaling Pathway: In Vitro and In Vivo Studies.  |  Wang, X., et al. 2024. Nutrients. 16: PMID: 38398837
  5. Chemoprevention of 4-nitroquinoline 1-oxide-induced rat oral carcinogenesis by the dietary flavonoids chalcone, 2-hydroxychalcone, and quercetin.  |  Makita, H., et al. 1996. Cancer Res. 56: 4904-9. PMID: 8895742

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

(E)-2'-Hydroxychalcone, 2.5 g

sc-206560
2.5 g
$330.00