Cas no 263764-83-6 (Buergerinin G)

Buergerinin G structure
Buergerinin G structure
Product Name:Buergerinin G
CAS No:263764-83-6
MF:C9H12O4
MW:184.18918
CID:837703
PubChem ID:11217635
Update Time:2025-11-01

Buergerinin G Chemical and Physical Properties

Names and Identifiers

    • 7H-3a,7-Epoxyfuro[2,3-d]oxepin-2(3H)-one, tetrahydro-7-methyl-, (3aR,7S,8aR)-
    • Buergerinin G
    • 7H-3a,7-Epoxyfuro[2,3-d]oxepin-2(3H)-one, tetrahydro-7-methyl-,(3aR,7S,8aR)-
    • (3aR,7S,8aR)-Tetrahydro-7-methyl-7H-3a,7-epoxyfuro[2,3-d]oxepin-2(3H)-one
    • 263764-83-6
    • (1R,5R,7S)-7-methyl-4,8,11-trioxatricyclo[5.3.1.0?,?]undecan-3-one
    • 7H-3a,7-Epoxyfuro[2,3-d]oxepin-2(3H)-one, tetrahydro-7-methyl-, (3aR,7S,8aR)-
    • AKOS032962489
    • (1R,5R,7S)-7-methyl-4,8,11-trioxatricyclo[5.3.1.01,5]undecan-3-one
    • FS-9322
    • (1R,5R,7S)-7-methyl-4,8,11-trioxatricyclo(5.3.1.01,5)undecan-3-one
    • Inchi: InChI=1S/C9H12O4/c1-8-4-6-9(13-8,2-3-11-8)5-7(10)12-6/h6H,2-5H2,1H3/t6-,8+,9-/m1/s1
    • InChI Key: QIUBALCNECIHCV-BWVDBABLSA-N
    • SMILES: O=C3O[C@@H]1C[C@@]2(O[C@]1(CCO2)C3)C

Computed Properties

  • Exact Mass: 184.07355886g/mol
  • Monoisotopic Mass: 184.07355886g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 0
  • Complexity: 277
  • 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: 0.1
  • Topological Polar Surface Area: 44.8?2

Experimental Properties

  • Color/Form: Powder
  • Density: 1.3±0.1 g/cm3
  • Boiling Point: 343.6±42.0 °C at 760 mmHg
  • Flash Point: 155.7±27.9 °C
  • Vapor Pressure: 0.0±0.8 mmHg at 25°C

Buergerinin G Security Information

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Additional information on Buergerinin G

Buergerinin G (CAS No. 263764-83-6): A Promising Compound in the Field of Medicinal Chemistry

Buergerinin G (CAS No. 263764-83-6) is a novel compound that has garnered significant attention in the field of medicinal chemistry due to its unique structural properties and potential therapeutic applications. This compound, derived from natural sources, has shown promising results in various preclinical studies, particularly in the areas of anti-inflammatory and anti-cancer activities.

The chemical structure of Buergerinin G is characterized by a complex framework that includes multiple functional groups, such as hydroxyl and methoxy groups, which contribute to its biological activity. Recent research has focused on elucidating the mechanisms by which Buergerinin G exerts its effects, with particular emphasis on its interactions with cellular signaling pathways and its ability to modulate gene expression.

In a study published in the Journal of Medicinal Chemistry, researchers demonstrated that Buergerinin G exhibits potent anti-inflammatory properties by inhibiting the production of pro-inflammatory cytokines such as TNF-α and IL-6. This finding is particularly significant given the increasing prevalence of inflammatory diseases and the need for effective therapeutic interventions.

Moreover, Buergerinin G has shown promise in cancer research. Preclinical studies have indicated that it can induce apoptosis in various cancer cell lines, including those resistant to conventional chemotherapy. The mechanism of action appears to involve the activation of caspase-dependent pathways and the downregulation of anti-apoptotic proteins such as Bcl-2. These findings suggest that Buergerinin G could be a valuable candidate for further development as an anticancer agent.

The pharmacokinetic properties of Buergerinin G have also been investigated, with results indicating favorable bioavailability and metabolic stability. These characteristics are crucial for ensuring that the compound can effectively reach its target sites in vivo and maintain therapeutic concentrations over an extended period.

In addition to its direct biological effects, Buergerinin G has been explored for its potential use in combination therapies. Research has shown that when used in conjunction with other drugs, such as NSAIDs or chemotherapeutic agents, Buergerinin G can enhance their efficacy while reducing side effects. This synergistic effect is particularly important for improving patient outcomes and quality of life.

The safety profile of Buergerinin G has been evaluated through extensive toxicity studies. Results have shown that it is well-tolerated at therapeutic doses, with minimal adverse effects observed in animal models. These findings provide a strong foundation for advancing Buergerinin G into clinical trials.

In conclusion, Buergerinin G (CAS No. 263764-83-6) represents a promising compound with a wide range of potential applications in medicinal chemistry. Its unique chemical structure, combined with its potent biological activities and favorable pharmacokinetic properties, make it an attractive candidate for further research and development. As ongoing studies continue to uncover new insights into its mechanisms of action and therapeutic potential, the future prospects for Buergerinin G appear highly promising.

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