Product Details – 4-Andro
4-Andro, also known as 4-androstenediol, is a synthetic prohormone compound studied as a metabolic precursor within steroidogenic pathways. It is utilized in biochemical research to investigate enzymatic conversion processes, steroidal pathway interactions, and ligand formation in controlled experimental systems.
In laboratory settings, 4-Andro serves as a model compound for examining precursor-to-ligand transformation and the role of enzymatic activity in modulating steroidal signaling pathways.
Mechanism of Action
4-Andro is studied for its role as a substrate in enzymatic biotransformation pathways. Specifically, it undergoes conversion via enzymes such as 3β-hydroxysteroid dehydrogenase (3β-HSD) and 17β-hydroxysteroid dehydrogenase (17β-HSD), resulting in the formation of downstream androgenic ligands.
These ligands are then analyzed for their interaction with androgen receptors (AR), leading to receptor activation and subsequent transcriptional modulation.
Furthermore, research involving 4-Andro focuses on enzymatic conversion efficiency, ligand-receptor binding dynamics, and downstream signaling pathway activation in vitro. Its non-methylated structure is also examined in studies evaluating enzyme interaction profiles and metabolic processing within controlled biochemical environments.
Chemical Properties of 4-Andro
| Property | Value |
| Chemical Formula | C19H30O2 |
| Molar Mass | 290.447 g/mol |
| CAS Number | 1156-92-9 |
| Synonyms | Androst-4-ene-3β,17β-diol, 4-Andro |
| IUPAC Name | (3S,8R,9S,10R,13S,14S,17S)-10,13-dimethyl-2,3,6,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,17-diol |
Research Applications
Enzymatic Conversion Studies
4-Andro is widely used in laboratory research to examine steroidogenic enzyme activity, particularly involving 3β-HSD and 17β-HSD. Studies focus on substrate conversion rates and intermediate formation within biochemical pathways.
Androgen Receptor Interaction Analysis
The compound is applied in studies investigating ligand binding to androgen receptors. Research includes receptor activation, binding affinity, and conformational changes associated with ligand-receptor complexes.
Steroidogenic Pathway Research
4-Andro is utilized to explore multi-step steroidogenic pathways, including precursor transformation and downstream signaling processes in controlled in vitro systems.
Structure–Activity Relationship (SAR) Studies
This compound is relevant in SAR investigations analyzing how structural features influence enzymatic conversion, receptor interaction, and signaling pathway engagement.
Why Choose BehemothLabz to Buy 4-Andro for Research
Behemoth Labz provides research-grade 4-andro capsules for sale. They are manufactured under controlled laboratory conditions with strict quality assurance protocols. Each batch undergoes analytical verification to ensure consistency in molecular composition and purity. You will always find pure 4 andro for sale here.
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
Retatrutide 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
- Broeder C. E. (2003). Oral andro-related prohormone supplementation: do the potential risks outweigh the benefits?. Canadian journal of applied physiology = Revue canadienne de physiologie appliquee, 28(1), 102–116. https://doi.org/10.1139/h03-009
- Broeder, C. E., Quindry, J., Brittingham, K., Panton, L., Thomson, J., Appakondu, S., Breuel, K., Byrd, R., Douglas, J., Earnest, C., Mitchell, C., Olson, M., Roy, T., & Yarlagadda, C. (2000). The Andro Project: physiological and hormonal influences of androstenedione supplementation in men 35 to 65 years old participating in a high-intensity resistance training program. Archives of internal medicine, 160(20), 3093–3104. https://doi.org/10.1001/archinte.160.20.3093
