2017
DOI: 10.21767/2254-6081.100160
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Review on Pharmacological Activity of Amygdalin

Abstract: Amygdalin is obtained from the pebbles of rosaceous fruits, like apricots, almond, cherries, peaches and plums. It is a plant glucoside which is traditionally used as antitumor drug. It produces synergistic effect if it combines with conditional chemotherapy drugs. Amygdalin also used to cure many other diseases like to control asthma, improve immune system, causes apoptosis of human renal fibroblast, inhibit hyperglycemia. Amygdalin is banning to use as antitumor drug by FDA due to lack evidences of cure in c… Show more

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Cited by 32 publications
(18 citation statements)
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“…After oral administration, amygdalin produces more toxic hydrocyanic acid in the organism. In rats, the fatal dose (LD 50 ) of oral administration of amygdalin is 880 mg kg −1 body weight [ 43 ]. The human lethal dose for intravenous injection is 5 g. Humans can present systemic toxicity after oral administration of amygdalin, 4 g per day for half a month or intravenous injection for a month.…”
Section: Resultsmentioning
confidence: 99%
“…After oral administration, amygdalin produces more toxic hydrocyanic acid in the organism. In rats, the fatal dose (LD 50 ) of oral administration of amygdalin is 880 mg kg −1 body weight [ 43 ]. The human lethal dose for intravenous injection is 5 g. Humans can present systemic toxicity after oral administration of amygdalin, 4 g per day for half a month or intravenous injection for a month.…”
Section: Resultsmentioning
confidence: 99%
“…Excessive consumption of seeds may have a negative effect on the body, causing a number of adverse reactions of the following types: diarrhea, vomiting, abdominal pain and in extreme cases may lead to death ( Table 3 ). Human lethal dose of intravenous injection of amygdalin is 5 g [ 28 ]. No data are available for other fruits of Poland’s climate zone.…”
Section: Amygdalin As a Member Of Cyanogenic Glycosides—their Sources Toxicity And Anticancer Activitymentioning
confidence: 99%
“…Laetrile is degraded to gentiobiose and Lmandelonitrile. Gentiobiose is further hydrolysed to glucose while L-mandelonitrile into hydrogen cyanide and benzaldehyde (13). The chemical structure of laetrile is D-mandelonitrile-β-D-glucoside-6-β-glucoside (Figure 1).…”
Section: Chemistry Of Laetrilementioning
confidence: 99%