Product Details
5α-Hydroxy Laxogenin is a plant-derived steroidal sapogenin classified within the broader group of brassinosteroids. It is structurally related to naturally occurring compounds identified in certain plant species, including those within the Smilax genus.
In controlled research environments, this compound is examined for its structural characteristics and its interaction with intracellular signaling components. Its classification as a brassinosteroid-like molecule allows for investigation into pathways associated with plant-derived steroid analogs and their molecular behavior.
This compound is supplied strictly for laboratory research purposes and is not intended for consumption, medical, or diagnostic use.
Mechanism of Action
At the molecular level, 5α-Hydroxy Laxogenin is studied for its interaction with intracellular signaling pathways associated with protein turnover and cellular regulatory mechanisms. Research focuses on how this compound may influence signaling cascades involved in transcriptional activity and protein synthesis regulation.
Additionally, investigations explore its interaction with pathways related to proteolytic processes and regulatory signaling molecules. These studies are conducted in vitro to evaluate how structural features of brassinosteroid-like compounds contribute to pathway modulation and intracellular signaling dynamics.
The compound is also examined for its potential role in influencing receptor-independent signaling mechanisms, allowing researchers to better understand how plant-derived steroid analogs interact with cellular systems at the biochemical level.
Chemical Properties of 5α-Hydroxy Laxogenin
| Attribute | Details |
| Compound Name | 5α-Hydroxy Laxogenin |
| Classification | Steroidal sapogenin (brassinosteroid class) |
| Molecular Formula | C27H42O5 |
| Molecular Weight | 446.6 g/mol |
| CAS Number | 56786-63-1 |
| IUPAC Name | (1S,2S,4S,5’R,6R,7S,8R,9S,12S,13R,16S,18R)-16,18-dihydroxy-5′,7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2′-oxane]-19-one |
| Synonyms | 5alpha-Hydroxy laxogenin |
| Primary Function | Investigation of intracellular signaling and protein regulation pathways |
| Research Context | Brassinosteroid analog and molecular pathway analysis |
| Format | Research compound (non-consumable) |
| Stability | Stable under controlled laboratory storage conditions |
Research Applications
Intracellular Signaling Pathway Studies
5α-Hydroxy Laxogenin is utilized in experimental systems to examine signaling cascades associated with transcriptional regulation and intracellular communication. Researchers analyze how structural variations influence pathway activity at the molecular level.
Protein Turnover and Regulatory Mechanism Analysis
This compound is applied in studies investigating protein synthesis and degradation pathways. Its interaction with intracellular systems supports evaluation of how regulatory mechanisms maintain protein balance within controlled environments.
Brassinosteroid Analog Research
As a member of the brassinosteroid class, 5α-Hydroxy Laxogenin is used to explore structure-activity relationships among plant-derived steroidal compounds. These studies focus on molecular configuration, binding interactions, and pathway modulation.
Why Choose BehemothLabz to Buy 5α-Hydroxy Laxogenin for Research
BehemothLabz provides research-grade 5α-Hydroxy Laxogenin manufactured under controlled laboratory conditions with strict quality assurance protocols. Each batch undergoes analytical verification to ensure consistency in molecular composition and purity.
Comprehensive documentation, including laboratory testing reports and sourcing transparency, supports reproducibility in experimental settings. BehemothLabz maintains a compliance-focused approach, supplying compounds intended strictly for laboratory-based investigation and analytical research
Disclaimer
5α-Hydroxy Laxogenin is intended strictly for laboratory research and analytical purposes only. It is not intended for use in diagnostic procedures, therapeutic applications, or in vivo studies of any kind.
Any references to biochemical pathways, receptor interactions, or enzymatic processes are provided solely for informational and research-context purposes. This compound must be handled exclusively by qualified professionals in controlled laboratory environments in accordance with applicable regulations and safety guidelines.
Improper handling or use outside of controlled research settings is strictly prohibited.
References
- Beer, C., & Keiler, A. M. (2022). Androgenic properties of the dietary supplement 5α-hydroxy-laxogenin. Archives of toxicology, 96(7), 2139–2142. https://doi.org/10.1007/s00204-022-03283-5
- Avula, B., Chittiboyina, A. G., Bae, J. Y., Haider, S., Wang, Y. H., Wang, M., Zhao, J., Deuster, P. A., & Khan, I. A. (2019). The power of hyphenated chromatography-Time of flight mass spectrometry for unequivocal identification of spirostanes in bodybuilding dietary supplements. Journal of pharmaceutical and biomedical analysis, 167, 74–82. https://doi.org/10.1016/j.jpba.2018.12.045
