Product Details: 4-Andro (Transdermal Liquid Form)
4-Andro, also known as 4-DHEA, is a laboratory compound derived from dehydroepiandrosterone (DHEA). This compound is classified as a positional isomer of DHEA. Because its structure is slightly different, it may behave differently in controlled studies. Research has reported variations in receptor interaction and signaling activity when compared with standard DHEA compounds.
Mechanism of Action
4-Andro is studied as a precursor compound in biochemical systems. In experimental conditions, it may undergo enzymatic conversion through pathways involving enzymes such as 17β-hydroxysteroid dehydrogenase.
Following this conversion, resulting metabolites may interact with androgen receptors located in certain cell types. These interactions are associated with signaling pathways that are linked to protein regulation and cellular function in preclinical studies.
Properties of 4-Andro (Transdermal Liquid Form)
- Molecular Formula: C₁₉H₃₀O₂
- Molecular Weight: 290.44 g/mol
- CAS Number: 1156-92-9
- PubChem CID: 220401
- 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
- Synonyms: Androst-4-ene-3β,17β-diol, 4-DHEA [5]
Research Applications of 4-Andro
Androgen Pathway Studies
4-Andro is used in controlled studies that examine androgen-related signaling. It may help researchers observe how precursor compounds interact with receptors. [3]Protein Synthesis Observation
Some studies focus on how androgen-related pathways connect with protein regulation signals. Changes in cellular activity are measured under laboratory conditions. [4]
Metabolic and Cellular Activity Research
This compound is also explored in studies involving metabolic signaling and cellular response. Current findings remain limited and require further investigation. [2]
Why Buy 4-Andro from BehemothLabz
Behemoth Labz has established itself as a reliable and reputable source for research compounds since 2014. We take pride in offering the highest-quality products that are backed by independent, third-party-issued Certificates of Analysis for identification, purity, and concentration.
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Disclaimer: This information is for educational purposes. We do not allow the human consumption of our products. All our products are sold for laboratory and research experiments.
Please make sure you go through the Terms and Conditions. Please research the scientific uses of this product before making any purchases. Make note that the packaging and labels of the product may differ from those shown on the website.
References
- Labrie, F. (1991). Intracrinology. Molecular and Cellular Endocrinology, 78(3), C113–C118. https://pubmed.ncbi.nlm.nih.gov/1936571/
- Traish, A. M., et al. (2011). Dehydroepiandrosterone (DHEA)—a precursor steroid or an active hormone in human physiology. The Journal of Sexual Medicine, 8(11), 2960–2982. https://pubmed.ncbi.nlm.nih.gov/21995863/
- Penning, T. M. (2015). Human hydroxysteroid dehydrogenases and pre-receptor regulation. Steroids, 103, 139–147. https://pubmed.ncbi.nlm.nih.gov/26278090/
- Basaria, S. (2010). Androgen abuse in athletes: detection and consequences. The Journal of Clinical Endocrinology & Metabolism, 95(4), 1533–1543. https://pubmed.ncbi.nlm.nih.gov/20139227/
- PubChem. (n.d.). 4-Androstenediol (CID: 220401). National Center for Biotechnology Information. https://pubchem.ncbi.nlm.nih.gov/compound/220401
