Arimistane

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Description

Overview of Arimistane

Studies indicate that Arimistane, as an aromatase inhibitor, has been examined for its ability to influence aromatase-mediated biochemical processes.

Experimental findings suggest that suppression of aromatase activity may alter estrogen-associated biosynthetic pathways. These observations have led to continued investigation into androgen–estrogen regulatory dynamics in controlled research settings

Chemical Properties 

PubChem CID 150910
CAS Number 1420-49-1
Molecular Formula C19H24O2
2D Structure
Molar Mass 284.4 g/mol
3D Structure
Synonyms Androsta-3,5-diene-7,17-dione

1420-49-1

ARIMISTANE

77P0LYX19T

NSC-134910

Working Mechanism of Arimistane

Arimistane has been investigated in experimental research models for its interaction with the aromatase enzyme. 

The enzyme is responsible for the conversion of androgens into estrogen-related compounds. By influencing aromatase activity, this compound may alter estrogen-associated biosynthetic pathways in controlled laboratory systems. Arimistane is often utilized as a tool compound in studies examining androgen–estrogen regulatory dynamics and endocrine signaling processes.

Research Applications for Arimistane

Arimistane may be utilized in experimental settings to examine the regulation and inhibition of aromatase enzyme activity.

Researchers may explore how modulation of aromatase influences estrogen- and androgen–associated signaling dynamics within controlled laboratory models.

Choose Purerawz to Buy Arimistane

Purerawz provides Arimistane with verified purity and quality suitable for laboratory research. The compounds are handled and stored under conditions that maintain stability for experimental 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 usage. 

Reference Links

Martínez Brito, D., Leogrande, P., Colamonici, C., Curcio, D., Botre, F., & de la Torre, X. (2021). Arimistane: Degradation product or metabolite of 7-oxo-DHEA? Drug Testing and Analysis, 13(7), 1430–1439. https://doi.org/10.1002/dta.3036

Rohle, D., Wilborn, C., Taylor, L., Mulligan, C., Kreider, R., & Willoughby, D. (2007). Effects of eight weeks of an alleged aromatase inhibiting nutritional supplement 6-OXO (androst-4-ene-3,6,17-trione) on serum hormone profiles and clinical safety markers in resistance-trained, eugonadal males. Journal of the International Society of Sports Nutrition, 4(1). https://doi.org/10.1186/1550-2783-4-13

Dr. Helma Wennemers

Dr. Helma Wennemers is a globally recognized chemist shaping modern peptide science and molecular design through highly original research in applied biosciences.

Her work explores how precise molecular architecture can be engineered to create new functional systems in chemistry and life sciences. Her contributions continue to redefine contemporary chemical research through creativity, depth, and structural innovation.

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