| Weight | 457.432 g/mol |
|---|---|
| Formula | C20H27NO11 |
| Hydrogen Acceptors | 12 |
| Hydrogen Donors | 7 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 7 |
amygdalin (29883-15-6)
Laetrile · Neoamygdalin · Amygdaloside
Score:
#1259 in Biochemistry
,
#3114 in Biology
,
#3894 in Chemistry
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- Enzyme Catalysis: Tool to Make and Break Amygdalin Hydrogelators From Renewable Resources: A Delivery Model for Hydrophobic Drugs (Journal of the American Chemical Society, 2006)
- A clinical trial of amygdalin (Laetrile) in the treatment of human cancer. (The New England Journal of Medicine, 1982)
- Amygdalin in almond nectar and pollen facts and possible roles (Plant Systematics and Evolution, 2016)
- Amygdalin Induces Apoptosis through Regulation of Bax and Bcl-2 Expressions in Human DU145 and LNCaP Prostate Cancer Cells (Biological & Pharmaceutical Bulletin, 2006)
- Tissue and Subcellular Localization of Enzymes Catabolizing (R)-Amygdalin in Mature Prunus serotina Seeds. (Plant Physiology, 1992)
- A Pharmacologic and Toxicological Study of Amygdalin (JAMA, 1981)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Laetrile
- Neoamygdalin
- Amygdaloside
- Mandelonitrile-beta-Gentiobioside
- Mandelonitrile beta Gentiobioside
-
SMILESC1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O
-
InChIKeyXUCIJNAGGSZNQT-UHFFFAOYSA-N
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