Photo-amygdalin: light-dependent control over hydrogen cyanide release and cytotoxicity

Amygdalin is a natural glycosidic compound found in bitter almonds and apricot seeds. After enzymatic hydrolysis, amygdalin forms a cyanohydrin which spontaneously decays to release toxic hydrogen cyanide in a process called cyanogenesis. Due to this capacity to release cyanide, it has a long and controversial history of use as an anticancer therapeutic in alternative medicine. However, the inability to control amygdalin's cyanogenesis hinders its efficient medical use and renders it potentially dangerous. In this study we describe the design and development of 'photo-amygdalin', a compound whose cyanogenesis can be triggered by visible light. We synthesize photo-amygdalin inspired by the molecular structure of amygdalin, illustrate its capability to form hydrogen cyanide upon irradiation through a myoglobin test, and showcase its ability to significantly reduce the viability of a human cell line upon irradiation, proving it to be 100-fold more potent than potassium cyanide.

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Publication Details

Journal
Chemical Science
Published
2025-01-01
DOI
https://doi.org/10.1039/d5sc01248a
Citations
3
Primary Topic
Photochromic and Fluorescence Chemistry
Type
article
Field-Weighted Citation Impact
1.55

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article

Photo-amygdalin: light-dependent control over hydrogen cyanide release and cytotoxicity

Ainoa Guinart, Wiktor Szymański, Albert M. Schulte, Georgios Alachouzos et al.
3 citations
Chemical Science
Photochromic and Fluorescence Chemistry
1.55
article

Photo-amygdalin: light-dependent control over hydrogen cyanide release and cytotoxicity

Ainoa Guinart, Wiktor Szymański, Albert M. Schulte, Georgios Alachouzos, Ben L. Feringa
article en
3 citations

Abstract

Amygdalin is a natural glycosidic compound found in bitter almonds and apricot seeds. After enzymatic hydrolysis, amygdalin forms a cyanohydrin which spontaneously decays to release toxic hydrogen cyanide in a process called cyanogenesis. Due to this capacity to release cyanide, it has a long and controversial history of use as an anticancer therapeutic in alternative medicine. However, the inability to control amygdalin's cyanogenesis hinders its efficient medical use and renders it potentially dangerous. In this study we describe the design and development of 'photo-amygdalin', a compound whose cyanogenesis can be triggered by visible light. We synthesize photo-amygdalin inspired by the molecular structure of amygdalin, illustrate its capability to form hydrogen cyanide upon irradiation through a myoglobin test, and showcase its ability to significantly reduce the viability of a human cell line upon irradiation, proving it to be 100-fold more potent than potassium cyanide.

Chemical ScienceVol. 16(23)
University Medical Center Groningen (NL), University of Groningen (NL)
European Molecular Biology Organization, Ministerie van Onderwijs, Cultuur en Wetenschap, European Research Council, HORIZON EUROPE Marie Sklodowska-Curie Actions
Openalex Percentile: Top 18%
Photochromic and Fluorescence Chemistry
1.55
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Photo-amygdalin: light-dependent control over hydrogen cyanide release and cytotoxicity — Ainoa Guinart, Wiktor Szymański, et al. · Chemical Science (2025) | TGRS Research Map | TGRS