Cas no 162616-70-8 (Isolupalbigenin)

Isolupalbigenin is a bioactive flavonoid compound derived from natural sources, known for its potential pharmacological properties. It exhibits notable antioxidant and anti-inflammatory effects, making it a subject of interest in medicinal chemistry and drug development. Structurally related to other flavones, isolupalbigenin demonstrates stability and selectivity in biological interactions, which may contribute to its therapeutic applications. Its mechanism of action involves modulation of cellular signaling pathways, particularly those related to oxidative stress and inflammation. Research suggests potential utility in neurodegenerative and metabolic disorders. The compound's purity and reproducibility are critical for experimental and clinical studies, ensuring reliable results in pharmacological investigations.
Isolupalbigenin structure
Isolupalbigenin structure
Product Name:Isolupalbigenin
CAS No:162616-70-8
MF:C25H26O5
MW:406.470947742462
CID:204499
PubChem ID:26238934
Update Time:2025-05-20

Isolupalbigenin Chemical and Physical Properties

Names and Identifiers

    • 4H-1-Benzopyran-4-one,5,7-dihydroxy-3-[4-hydroxy-3-(3-methyl-2-buten-1-yl)phenyl]-8-(3-methyl-2-buten-1-yl)-
    • Isolupalbigenin
    • 4H-1-Benzopyran-4-one,5,7-dihydroxy-3-[4-hydroxy-3-(3-methyl-2-butenyl)phenyl]-8-(3-methyl-2-butenyl)-(9CI)
    • 3',8-Di-(dimethylallyl)-genistein
    • 5,7-dihydroxy-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)chromen-4-one
    • 5,7-dihydroxy-3-(4-hydroxy-3-(3-methylbut-2-en-1-yl)phenyl)-8-(3-methylbut-2-en-1-yl)-4H-chromen-4-one
    • NCGC00384924-01!5,7-dihydroxy-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)chromen-4-one
    • HY-N8477
    • 162616-70-8
    • CS-0144675
    • AKOS040761899
    • CHEMBL461061
    • Isolupabigenin
    • CHEBI:143751
    • DA-64548
    • Inchi： 1S/C25H26O5/c1-14(2)5-7-17-11-16(8-10-20(17)26)19-13-30-25-18(9-6-15(3)4)21(27)12-22(28)23(25)24(19)29/h5-6,8,10-13,26-28H,7,9H2,1-4H3
    • InChI Key： FXJPTJQFJYNFKC-UHFFFAOYSA-N
    • SMILES： O1C=C(C(C2=C(C=C(C(C/C=C(\C)/C)=C12)O)O)=O)C1=CC=C(C(C/C=C(\C)/C)=C1)O

Computed Properties

  • Exact Mass: 406.17808
  • Monoisotopic Mass: 406.17802393g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 30
  • Rotatable Bond Count: 5
  • Complexity: 713
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 6.5
  • Topological Polar Surface Area: 87?2

Experimental Properties

  • Color/Form: Yellow powder
  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 621.5±55.0 °C at 760 mmHg
  • Flash Point: 212.3±25.0 °C
  • PSA: 86.99
  • Vapor Pressure: 0.0±1.9 mmHg at 25°C

Isolupalbigenin Security Information

Isolupalbigenin Pricemore >>

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Isolupalbigenin Related Literature

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Additional information on Isolupalbigenin

Comprehensive Overview of Isolupalbigenin (CAS No. 162616-70-8): Properties, Applications, and Research Insights

Isolupalbigenin (CAS No. 162616-70-8) is a bioactive flavonoid compound gaining significant attention in pharmaceutical and nutraceutical research. As a derivative of the lupalbigenin family, it exhibits unique structural and functional properties that make it a promising candidate for various therapeutic applications. This article delves into the chemical characteristics, potential health benefits, and current research trends surrounding this compound, addressing common queries such as "Isolupalbigenin benefits", "CAS 162616-70-8 uses", and "natural flavonoid sources".

The molecular structure of Isolupalbigenin features a distinctive flavone backbone with hydroxyl and methoxy substitutions, contributing to its antioxidant and anti-inflammatory properties. Recent studies highlight its potential in modulating cellular pathways related to oxidative stress, making it relevant to trending health topics like "natural anti-aging compounds" and "plant-based therapeutics". Researchers are particularly interested in its bioavailability and synergy with other phytochemicals, addressing frequent searches such as "how to enhance flavonoid absorption".

In the context of modern drug discovery, Isolupalbigenin demonstrates notable pharmacological activities. Preclinical studies suggest its potential in supporting metabolic health, aligning with current interests in "natural glucose metabolism regulators" and "plant-derived neuroprotective agents". The compound's mechanism of action involves interaction with various enzyme systems, particularly those related to cellular defense mechanisms, which responds to popular queries like "natural compounds for cellular health".

From a technical perspective, the isolation and characterization of Isolupalbigenin (CAS 162616-70-8) involve advanced chromatographic techniques, reflecting the growing demand for "high-purity natural compound isolation methods". Analytical data indicates stability under specific conditions, with optimal pH and temperature ranges that inform its potential formulation strategies - a topic frequently searched as "flavonoid stability in formulations".

The commercial availability of Isolupalbigenin has expanded with increasing interest in specialized phytochemicals. Current market trends show rising demand for "research-grade bioactive compounds" and "standardized plant extracts", positioning this compound as a valuable reference material. Quality control parameters typically include HPLC purity verification and spectroscopic confirmation, addressing professional concerns about "authenticity testing for rare flavonoids".

Future research directions for Isolupalbigenin may explore its potential in personalized nutrition and integrative medicine approaches, responding to emerging trends in "precision phytotherapy" and "tailored supplement formulations". Ongoing clinical investigations are expected to provide more definitive data on its bioavailability and therapeutic thresholds, answering frequent questions about "effective dosages of plant flavonoids" and "long-term safety of specialized phytochemicals".

For researchers and industry professionals, understanding the regulatory status of Isolupalbigenin (CAS 162616-70-8) remains crucial. Current classifications generally recognize it as a non-toxic natural product when used appropriately, aligning with searches for "GRAS status natural compounds" and "approved plant-derived actives". Documentation requirements typically include detailed characterization data and safety profiles, reflecting professional needs for "comprehensive phytochemical dossiers".

In conclusion, Isolupalbigenin represents an exciting area of phytochemical research with multiple potential applications. Its unique properties address current scientific and consumer interests in "bioactive plant compounds", "natural therapeutic alternatives", and "sustainable ingredient sourcing". As research progresses, this compound may offer novel solutions in health promotion and disease prevention strategies.

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