The Configuration of Tadalafil and Tadalafil Analogues Found in Dietary Supplements].

Tomohide Fukiwake, Midori Yamazaki, Kazunaga Takahashi, Takahiro Doi, Masami Kawaguchi, Keigo Enomoto, Hiroki Yoshino, Katsuya Uchimoto, Maki Nishimura

Shokuhin eiseigaku zasshi. Journal of the Food Hygienic Society of Japan 2021

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This study determined the configuration of the isomers of tadalafil, nortadalafil, and homotadalafil in dietary supplements. The products purchased over the Internet studied included a honey product and a tablet, which contained tadalafil, and a candy, which contained nortadalafil and homotadalafil. Each of the pharmaceutical ingredients isolated from the products was measured with circular dichroism (CD).As a result, the CD spectrum of each isolated pharmaceutical ingredient was found to align with the standard CD spectrum of the 6R,12aR isomer, confirmed that each isolated tadalafil or tadalafil analogue included in a 6R,12aR isomer. According to a report, among the stereoisomers of tadalafil, the 6R,12aR isomers have the most potent inhibitory activities of phosphodiesterase-type-5. From the report, the potential strength of the inhibitory activity of the 6R,12aR isomers of nortadalafil and homotadalafil was suggested. Therefore, it seemed that the 6R,12aR isomer often used in the product.

Citation

Tomohide Fukiwake, Midori Yamazaki, Kazunaga Takahashi, Takahiro Doi, Masami Kawaguchi, Keigo Enomoto, Hiroki Yoshino, Katsuya Uchimoto, Maki Nishimura. The Configuration of Tadalafil and Tadalafil Analogues Found in Dietary Supplements]. Shokuhin eiseigaku zasshi. Journal of the Food Hygienic Society of Japan. 2021;62(2):65-72