Cas no 469-06-7 (Isotachysterol)

Isotachysterol structure
Isotachysterol structure
Product Name:Isotachysterol
CAS No:469-06-7
MF:C28H44O
MW:396.648368835449
CID:331311
PubChem ID:9547231
Update Time:2025-07-17

Isotachysterol Chemical and Physical Properties

Names and Identifiers

    • 9,10-Secoergosta-5(10),6,8(14),22-tetraen-3-ol,(3b,6E,22E)- (9CI)
    • Isotachysterol
    • N,N-DIDESMETHYL ULIPRISTAL
    • (3R,6E,22E)-9,10-Secoergosta-5(10),6,8(14),22-tetraen-3-ol
    • Q27272259
    • (6E,22E)-(3S)-9,10-seco-5(10),6,8(14),22-ergostatetraen-3-ol
    • 469-06-7
    • 9,10-SECOERGOSTA-5(10),6,8(14),22-TETRAEN-3-OL, (3.BETA.,6E,22E)-
    • isotachysterol2
    • (1S)-3-[(E)-2-[(1R,7aR)-1-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-7a-methyl-1,2,3,5,6,7-hexahydroinden-4-yl]ethenyl]-4-methylcyclohex-3-en-1-ol
    • UNII-9A3Y6WT6UF
    • ISOTACHYSTEROL 2
    • 9A3Y6WT6UF
    • ERGOCALCIFEROL IMPURITY D [EP IMPURITY]
    • (6E,22E)-9,10-SECOERGOSTA-5(10),6,8(14),22-TETRAEN-3.BETA.-OL
    • 9,10-SECOERGOSTA-5(10),6,8(14),22-TETRAEN-3.BETA.-OL, (6E)-
    • LMST03010017
    • 3-CYCLOHEXEN-1-OL, 3-((1E)-2-((1R,7AR)-2,3,5,6,7,7A-HEXAHYDRO-7A-METHYL-1-((1R,2E,4R)-1,4,5-TRIMETHYL-2-HEXEN-1-YL)-1H-INDEN-4-YL)ETHENYL)-4-METHYL-, (1S)-
    • 6E-9,10-Secoergosta-5(10),6,8(14),22E-tetraen-3beta-ol
    • (1R)-3-[(E)-2-[(1R,7aR)-1-[(E,2R,5R)-5,6-dimethylhept-3-en-2-yl]-7a-methyl-1,2,3,5,6,7-hexahydroinden-4-yl]ethenyl]-4-methylcyclohex-3-en-1-ol
    • Inchi: 1S/C28H44O/c1-19(2)20(3)9-10-22(5)26-15-16-27-23(8-7-17-28(26,27)6)12-13-24-18-25(29)14-11-21(24)4/h9-10,12-13,19-20,22,25-26,29H,7-8,11,14-18H2,1-6H3/b10-9+,13-12+/t20-,22+,25-,26+,28+/m0/s1
    • InChI Key: WHIQZYTVWTZJNO-GMPZOFGBSA-N
    • SMILES: O[C@H]1CCC(C)=C(C1)/C=C/C1CCC[C@@]2(C)C=1CC[C@@H]2[C@@H](/C=C/[C@H](C)C(C)C)C

Computed Properties

  • Exact Mass: 396.33900
  • Monoisotopic Mass: 396.339216023g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 29
  • Rotatable Bond Count: 6
  • Complexity: 704
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 5
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 2
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 6.9
  • Topological Polar Surface Area: 20.2?2

Experimental Properties

  • Melting Point: 58-65°C
  • Solubility: Chloroform (Sparingly), Methanol (Slightly)
  • PSA: 20.23000
  • LogP: 7.78510

Isotachysterol Security Information

  • Storage Condition:Amber Vial, -86?°C Freezer, Under inert atmosphere

Isotachysterol Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
I902450-5mg
Isotachysterol
469-06-7
5mg
$ 200.00 2023-02-02
TRC
I902450-50mg
Isotachysterol
469-06-7
50mg
$ 1545.00 2023-02-02

Additional information on Isotachysterol

Isotachysterol (CAS No. 469-06-7): A Comprehensive Overview of Its Applications and Recent Research Findings

Isotachysterol, with the chemical identifier CAS No. 469-06-7, is a compound that has garnered significant attention in the field of pharmaceutical chemistry and biochemistry due to its unique structural properties and biological activities. This compound, belonging to the sterol family, has been extensively studied for its potential applications in medicine, particularly in the context of cholesterol metabolism and related therapeutic interventions.

The molecular structure of Isotachysterol distinguishes it from other sterols through its specific isomeric configuration. This configuration imparts distinct biochemical properties that make it a valuable candidate for research in lipid metabolism. Recent studies have highlighted its role in modulating cholesterol levels, making it a promising candidate for the development of novel therapeutic agents targeting hypercholesterolemia and related cardiovascular disorders.

In the realm of academic research, Isotachysterol has been investigated for its potential to interact with cellular receptors and enzymes involved in cholesterol homeostasis. Studies have demonstrated that this compound can influence the activity of HMG-CoA reductase, a key enzyme in the mevalonate pathway responsible for cholesterol synthesis. The ability to modulate this enzyme suggests that Isotachysterol could be a viable therapeutic option for managing elevated cholesterol levels.

Moreover, recent advancements in biochemical research have uncovered the potential of Isotachysterol in combating age-related macular degeneration (AMD). AMD is a leading cause of irreversible vision loss, primarily due to oxidative stress and inflammation in the retinal pigment epithelium (RPE). Preclinical studies have indicated that Isotachysterol possesses antioxidant properties that can protect against oxidative damage and reduce inflammation, thereby potentially slowing the progression of AMD.

The structural uniqueness of Isotachysterol, as evidenced by its chemical formula and isomeric configuration, has also led to investigations into its potential role in anti-inflammatory therapies. Chronic inflammation is a hallmark of various diseases, including rheumatoid arthritis and inflammatory bowel disease. Research has shown that sterols, including Isotachysterol, can modulate inflammatory pathways by interacting with nuclear factor kappa B (NF-κB) and other transcription factors involved in inflammation.

In addition to its therapeutic applications, Isotachysterol has been explored for its potential role in enhancing cellular health and longevity. Studies have suggested that this compound can improve mitochondrial function by protecting against oxidative stress and promoting ATP production. This property makes it an attractive candidate for research aimed at extending healthy lifespan and mitigating age-related decline.

The synthesis and characterization of Isotachysterol have also been subjects of interest in synthetic chemistry. Researchers have developed novel synthetic routes to produce this compound with high purity and yield, enabling more extensive research into its biological activities. These advancements have not only facilitated preclinical studies but also opened avenues for industrial-scale production if future clinical trials validate its efficacy.

The pharmacokinetic properties of Isotachysterol, including its absorption, distribution, metabolism, and excretion (ADME), have been carefully evaluated to understand its potential as a drug candidate. Initial studies have revealed that this compound exhibits good oral bioavailability and moderate tissue distribution, suggesting that it could be administered orally for therapeutic purposes. Further research is ongoing to optimize these pharmacokinetic profiles for improved therapeutic efficacy.

The safety profile of Isotachysterol has also been a focus of recent studies. Toxicological assessments have been conducted to evaluate potential side effects and determine safe dosage ranges. Preliminary results indicate that Isotachysterol is well-tolerated at moderate doses but may cause mild gastrointestinal discomfort at higher concentrations. These findings are crucial for guiding future clinical trials and ensuring patient safety if this compound progresses to human testing.

The interdisciplinary nature of research on Isotachysterol underscores its significance in both academic and industrial settings. Collaboration between chemists, biochemists, pharmacologists, and clinicians has been instrumental in uncovering its diverse applications. This collaborative approach not only accelerates the pace of discovery but also ensures that research findings are translated into tangible benefits for patients.

In conclusion, Isotachysterol (CAS No. 469-06-7) represents a promising compound with multifaceted applications in pharmaceuticals and biotechnology. Its unique structural properties, coupled with recent research findings on its biological activities, position it as a valuable candidate for further exploration in therapeutic interventions targeting hypercholesterolemia, AMD, inflammation, and age-related decline. As research continues to uncover new insights into its mechanisms of action and pharmacological properties, the potential for harnessing the benefits of this compound remains highly promising.

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