Drug intelligence / Profile preview

amygdalin

Development stage
Preclinical
Modality
Classical Binding Small Molecules → Small Molecules, Covalent Small Molecules → Small Molecules, Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Oral, Intravenous, Intramuscular
01

Overview

Amygdalin is a naturally occurring cyanogenic glycoside found in the seeds of many fruits, especially apricots, bitter almonds, apples, peaches, cherries, and plums. It has been promoted as an alternative cancer treatment since the 1950s under various names including laetrile and "vitamin B17," though it is not a vitamin. When metabolized in the body—especially when taken orally—amygdalin is broken down by beta-glucosidase enzymes to produce prunasin and mandelonitrile; these are further hydrolyzed to benzaldehyde and hydrocyanic acid (cyanide), which is highly toxic. The proposed mechanism for anticancer activity involves selective toxicity of cyanide toward cancer cells; however, this theory has not been substantiated in humans or clinical trials. Amygdalin also exhibits anti-inflammatory effects via immunomodulation of Treg cells and inhibition of COX-2/iNOS pathways in animal studies. Despite anecdotal claims for use against cancer or pain relief, there is no reliable evidence supporting its efficacy for any medical condition. Its use carries significant risk due to potential cyanide poisoning[1][2][3][4][5].

Other names
laetrilevitamin B17mandelonitrile-beta-glucuronidemandelonitrile beta-D-gentiobiosidenitrilosidepurasin
02

Targets

AKT1 (Proto-oncogene serine/threonine-protein kinase Akt1)BCL-2 (BCL-2 family)BGL (beta-Glucosidase)CDK2 (Cyclin-dependent kinase 2)PTGS2 (Prostaglandin-Endoperoxide Synthase 2)FAK (Focal adhesion kinase)ILK (Integrin-linked kinase)NOS2 (Nitric Oxide Synthase 2)COX7C (Cytochrome c oxidase subunit 7C, mitochondrial)IL1B (Interleukin-1 beta)TNFA (Tumor necrosis factor alpha (soluble))

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