Cas no 99119-69-4 (Kushenol I)

Kushenol I is a naturally occurring flavonoid compound derived from the roots of Sophora flavescens, a plant traditionally used in herbal medicine. This bioactive molecule exhibits notable pharmacological properties, including anti-inflammatory, antioxidant, and potential anticancer activities. Its chemical structure, characterized by a flavone backbone with hydroxyl and prenyl substituents, contributes to its interaction with cellular targets such as enzymes and signaling pathways. Kushenol I is of interest in research for its ability to modulate oxidative stress and inflammatory responses, making it a candidate for therapeutic development. Its purity and stability are critical for reproducibility in experimental studies, ensuring reliable data in biochemical and pharmacological investigations.
Kushenol I structure
Kushenol I structure
Product Name:Kushenol I
CAS No:99119-69-4
MF:C26H30O7
MW:454.512208461761
CID:1991662
PubChem ID:20832634
Update Time:2025-11-01

Kushenol I Chemical and Physical Properties

Names and Identifiers

    • (2R,3R)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-8-[5-hydroxy-5-methyl-2-(prop-1-en-2-yl)hexyl]-5-methoxy-2,3-dihydro-4H-chromen-4-one
    • 4H-1-benzopyran-4-one, 2-(2,4-dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-8-[5-hydroxy-5-methyl-2-(1-methylethenyl)hexyl]-5-methoxy-, (2R,3R)-
    • 2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]chromen-4-one
    • Kushenol I
    • 4H-1-Benzopyran-4-one,2-(2,4-dihydroxyphenyl)-2,3-dihydro-3,7-dihydroxy-5-methoxy-8-((2R)-5-methyl-2-(1-methylethenyl)-4-hexenyl)-,(2R,3R)
    • Kushenol C
    • NSC 668937
    • (2R,3R)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-[(2R)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one
    • (2R,3R)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-[(2R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl]-3,4-dihydro-2H-1-benzopyran-4-one
    • KushenolI
    • HY-N2286
    • AKOS032946014
    • MS-28270
    • DTXSID80243958
    • (2R,3R)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-((R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl)chroman-4-one
    • CS-0019614
    • 99119-69-4
    • DA-64799
    • 1ST165710
    • Inchi： 1S/C26H30O7/c1-13(2)6-7-15(14(3)4)10-18-20(29)12-21(32-5)22-23(30)24(31)26(33-25(18)22)17-9-8-16(27)11-19(17)28/h6,8-9,11-12,15,24,26-29,31H,3,7,10H2,1-2,4-5H3/t15-,24+,26-/m1/s1
    • InChI Key： QKEDJCCCNZWOBS-SGOPFIAHSA-N
    • SMILES： O1C2C(=C(C=C(C=2C[C@H](C(=C)C)C/C=C(\C)/C)O)OC)C([C@@H]([C@H]1C1C=CC(=CC=1O)O)O)=O

Computed Properties

  • Exact Mass: 438.16800
  • Monoisotopic Mass: 454.19915329g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 4
  • Hydrogen Bond Acceptor Count: 7
  • Heavy Atom Count: 33
  • Rotatable Bond Count: 7
  • Complexity: 730
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 3
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 5
  • Topological Polar Surface Area: 116?2

Experimental Properties

  • Color/Form: Powder
  • Density: 1.270±0.06 g/cm3 (20 oC 760 Torr),
  • Boiling Point: 722.434°C at 760 mmHg
  • Flash Point: 242.43°C
  • Refractive Index: 1.614
  • Solubility: Insuluble (2.6E-3 g/L) (25 oC),
  • PSA: 131.36000
  • LogP: 5.07910

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Kushenol I Suppliers

Amadis Chemical Company Limited
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(CAS:99119-69-4)Kushenol I
Order Number:A1205982
Stock Status:in Stock
Quantity:10mg/25mg/20mg
Purity:99%
Pricing Information Last Updated:Friday, 30 August 2024 03:43
Price ($):276.0/552.0/251.0

Kushenol I Related Literature

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Additional information on Kushenol I

Exploring Kushenol I (CAS No. 99119-69-4): A Comprehensive Guide to Its Properties and Applications

In the realm of natural compounds, Kushenol I (CAS No. 99119-69-4) stands out as a bioactive flavonoid with significant potential in various fields, including pharmacology and nutraceuticals. This compound, derived from the roots of Sophora flavescens, has garnered attention for its unique structural properties and therapeutic benefits. Researchers and industry professionals alike are increasingly interested in its applications, particularly in the context of anti-inflammatory and antioxidant activities, which align with current health trends focused on natural remedies and preventive care.

The chemical structure of Kushenol I features a prenylated flavonoid backbone, which contributes to its distinct biological activities. Studies have highlighted its ability to modulate cellular pathways, making it a candidate for further exploration in neuroprotection and metabolic health. These properties resonate with modern consumer interests, such as brain health supplements and natural anti-aging solutions, which are frequently searched topics in health forums and scientific databases.

From a technical perspective, Kushenol I (CAS No. 99119-69-4) exhibits notable solubility characteristics, favoring organic solvents like methanol and dimethyl sulfoxide (DMSO). This makes it suitable for formulation in lab settings and industrial applications. Its stability under varying pH conditions further enhances its versatility, addressing common challenges faced in drug delivery systems and functional food development—areas where user queries often focus on bioavailability enhancement and shelf-life optimization.

Recent advancements in extraction and purification techniques have improved the yield of Kushenol I, making it more accessible for research and commercial use. Innovations such as supercritical fluid extraction and high-performance liquid chromatography (HPLC) are frequently discussed in scientific circles, reflecting the growing demand for sustainable extraction methods—a hot topic in both academic and eco-conscious consumer communities.

Beyond its biochemical attributes, Kushenol I is also being explored for its potential in cosmeceuticals, where its anti-tyrosinase activity could contribute to skin brightening products. This aligns with the surge in searches for natural alternatives to synthetic skincare ingredients, a trend driven by increasing awareness of clean beauty standards. The compound’s compatibility with liposomal encapsulation further positions it as a promising ingredient for advanced dermatological formulations.

In summary, Kushenol I (CAS No. 99119-69-4) represents a multifaceted compound with applications spanning health, wellness, and biotechnology. Its alignment with contemporary interests—such as plant-based therapeutics, green chemistry, and personalized medicine—ensures its relevance in both scientific literature and consumer-driven markets. As research continues to uncover its full potential, this compound is poised to play a pivotal role in the future of natural product innovation.

99119-69-4 (Kushenol I) Related Products

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Amadis Chemical Company Limited
(CAS:99119-69-4)Kushenol I
A1205982
Purity:99%/99%/99%
Quantity:10mg/25mg/20mg
Price ($):276.0/552.0/251.0
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