1-Andro

Description

1-Andro Overview

1-Andro, also referred to as 1-Androsterone or 1-DHEA (3β-hydroxy-androst-1-ene-17-one), is classified as a prohormone-type compound. Prohormones are chemical precursors that may undergo enzymatic transformation into hormonally active metabolites during metabolic processes.

In biochemical research contexts, 1-Andro has been examined for its potential conversion into 1-testosterone (dihydroboldenone). This androgenic compound has been investigated for its anabolic properties and its interaction with androgen receptors in experimental studies. Experimental findings have explored how such metabolites interact with androgen-sensitive biological pathways and tissues in controlled study environments.

Chemical and Molecular Properties

Property	Information
CAS Number	23633-63-8
Molecular Formula	C19H28O2
Molecular Mass	288.4 g/mol
Synonyms	1-Androsterone, U5M72D8OWZ, DTXSID20737265, 1-Dehydroepiandrosterone
IUPAC Name	(3R,5S,8R,9S,10R,13S,14S)-3-hydroxy-10,13-dimethyl-3,4,5,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-17-one
Storage	15-30°C (59-86°F)

Mechanism of Action

From a biochemical perspective, prohormone compounds such as 1-Andro may undergo enzymatic transformations during metabolic processing.

Research literature suggests that 1-Andro may be metabolically converted into 1-testosterone, an androgen investigated for its interaction with androgen receptor pathways. These receptor interactions are of interest in studies examining:

• Androgen-responsive signaling mechanisms
• Hormone precursor metabolism
• Steroidogenic enzymatic pathways

Potential Research Applications

In controlled laboratory environments, 1-Andro may be investigated as a steroidal precursor compound for studies involving androgen-related metabolic pathways and biochemical signaling mechanisms. Researchers may utilize this compound as a reference material when examining hormone precursor transformations and receptor-associated processes.

Steroidogenesis and Metabolic Conversion Studies

1-Andro may be examined in experimental models exploring steroidogenic pathways, particularly those involving the enzymatic conversion of precursor compounds into biologically active metabolites.

Androgen Receptor Signaling Research

1-Andro has been investigated for its interaction with androgen receptor pathways due to the metabolites associated with it. Studies often focus on how 1‑Andro metabolites bind to androgen receptors in experimental settings.

Hormone Precursor Biochemistry

Researchers may study 1-Andro to better understand the biochemical characteristics of prohormone-type compounds, including their structural properties, metabolic stability, and enzymatic transformation patterns.

Note: 1‑Androsterone is not approved by the FDA for any medical or human use. It is intended for laboratory and research purposes only.

Where to Buy 1-Androsterone?

PureRawz supplies high-quality 1-Andro designed for laboratory and research purposes. The compound is produced under controlled conditions to support consistency in studies examining biochemical pathways and compound interactions in experimental settings.

All the products are subjected to strict quality assurance procedures and are verified by an independent third-party Certificate of Analysis (COA). This documentation confirms important parameters such as compound identity, purity, and overall product quality to support reliable research use.

Disclaimer

This information is for educational purposes only and not medical advice. Products are for research use only. Research must follow IRB or IACUC guidelines. Verify information independently before purchasing. By ordering, you agree to our Terms and Conditions. If you are not 100% satisfied with the product you received, please contact us at support@staging.purerawz.co

ATTENTION: All our products are for LABORATORY AND RESEARCH PURPOSES ONLY, not for veterinary or human use.

Reference Links

PubChem. (2024). 1-Androsterone. Nih.gov; PubChem. https://pubchem.ncbi.nlm.nih.gov/compound/1-Androsterone

Therina du Toit, Groessl, M., Emanuele Pignatti, Swart, A. C., & Fluck, C. E. (2025). Characterization of Steroid Metabolic Pathways in Established Human and Mouse Cell Models. International Journal of Molecular Sciences, 26(19), 9721-9721. https://doi.org/10.3390/ijms26199721

Friedel, A., Geyer, H., Kamber, M., Laudenbach-Leschowsky, U., Schanzer, W., Thevis, M., Vollmer, G., Zierau, O., & Diel, P. (2006). 17β-Hydroxy-5alpha-androst-1-en-3-one (1-testosterone) is a potent androgen with anabolic properties. Toxicology Letters, 165(2), 149-155. https://doi.org/10.1016/j.toxlet.2006.03.001