Botanical species · safety record

Mandragora officinarum

The EFSA Compendium of Botanicals holds 19 constituent measurements and 3 adverse-effect records for Mandragora officinarum. This page reports what those source records contain and how to reach them. It carries no effect estimate, no dose and no recommendation.

Accepted name in source: Mandragora officinarum L.

19Constituent measurements
3Safety records
8Cited sources
22Licensed products (Canada)

Regulatory presence

Health Canada's Licensed Natural Health Products Database holds 22 licensed products naming Mandragora officinarum as a medicinal ingredient, matched on the exact Latin binomial. A licence records that a product met the regulator's requirements for sale in Canada. It is not evidence that the product works.

Source material stated

  • Dried root(s)
  • New material
  • Root

What the records describe

Constituents measured

  • Eugenol2
  • Isoeugenol2
  • Tropane alkaloids2
  • Alkaloids1
  • Angelicin1
  • Apoatropine1
  • Atropine1
  • Calystegine a1
  • Calystegine b1
  • Cinnamyl alcohol1

Plant parts

  • Fruit unspecified9
  • Roots and other underground parts7
  • Unspecified2
  • Live plants1

Preparations

  • Solvent extraction15

Effect types

  • Neurotoxicity2

Target tissues

  • Neurologic: central nervous system2
  • Heart1

Recorded constituents

What analytical work has found in this species, at which plant part and preparation. A measured constituent is a fact about material, not about effect.

SubstancePlant partPreparationConcentrationAnalytical methodSource
AlkaloidsRoots and other underground partsSolvent extractionStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
AngelicinUnspecifiedSolvent extractionStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
ApoatropineRoots and other underground partsSolvent extractionStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
AtropineRoots and other underground partsSolvent extractionStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
Calystegine aSolvent extractionStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
Calystegine bSolvent extractionStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
Cinnamyl alcoholFruit unspecifiedSolvent extraction1.93 PercentGC-MSResolve DOI
CoumarinsUnspecifiedSolvent extractionStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
CuscohygrineRoots and other underground partsSolvent extractionStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
EugenolFruit unspecifiedSolvent extraction2.37 PercentGC-MSResolve DOI
EugenolFruit unspecifiedSolvent extraction2.37 PercentGC-MSResolve DOI
HyoscyamineFruit unspecified25.6 Microgram/gramGC-MS (Q)Resolve DOI
IsoeugenolFruit unspecifiedSolvent extraction1.63 PercentGC-MSResolve DOI
IsoeugenolFruit unspecifiedSolvent extraction1.63 PercentGC-MSResolve DOI
ScopineRoots and other underground partsSolvent extractionStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
ScopolamineFruit unspecified0.7 Microgram/gramGC-MS (Q)Resolve DOI
Tropane alkaloidsRoots and other underground parts≥ 0.2 PercentResolve DOI
Tropane alkaloidsRoots and other underground parts≤ 0.6 PercentResolve DOI
WithanolidesLive plantsSolvent extractionStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI

Recorded adverse effects

Adverse effects reported in the source literature, most often in animal or laboratory models at a stated preparation and dose.

EffectTarget tissuePlant partPreparationTest organismTest typeSource
NeurotoxicityNeurologic: central nervous systemFruit unspecifiedHuman (as organism)Case reportResolve DOI
NeurotoxicityNeurologic: central nervous systemFruit unspecifiedHuman (as organism)Case reportResolve DOI
Not statedHeartHuman (as organism)Case reportResolve DOI

Cited sources

The literature the compendium cites for this species. Metatron Health has no relationship with these authors or journals and earns nothing from citing them.

  1. Nikolaou, Panagiota., Papoutsis, Ioannis., Stefanidou, Maria., Dona, Artemis., Maravelias, Constantinos., Spiliopoulou, Chara., Athanaselis, Sotirios. ACCIDENTAL POISONING AFTER INGESTION OF APHRODISIAC BERRIES: DIAGNOSIS BY ANALYTICAL TOXICOLOGY . Journal of emergency medicine, 2012, vol. 42, no. 6, p. 662-665. DOI
  2. Hanus, LO., Rezanka, T., Spizek, J., Dembitsky, VM. Substances isolated from Mandragora species. Phytochemistry, 2005, vol. 66, no. 20, p. 2408-2417. DOI
  3. Fleisher, Z., Fleisher, A. The odoriferous principles of mandrake, Mandragora officinarum L.: Aromatic plants of the holy land and the Sinai. Part IX. Journal of essential oil research, 1992, vol. 4, no. 2, p. 187-188. DOI
  4. Drager, B., vanAlmsick, A., Mrachatz, G. Distribution of calystegines in several Solanaceae. Planta medica, 1995, vol. 61, no. 6, p. 577-579. DOI
  5. Tsiligianni, Ioanna G., Vasilopoulos, Theodoros K., Papadokostakis, Polyvios K., Arseni, Georgia K., Eleni, Astrinaki., Lionis, Christos D. A two cases clinical report of mandragora poisoning in primary care in Crete, Greece: two case report. . Cases journal, 2009, vol. 2, p. 9331-9331. DOI
  6. FLEISHER, A., FLEISHER, Z. THE FRAGRANCE OF BIBLICAL MANDRAKE. Economic botany, 1994, vol. 48, no. 3, p. 243-251. DOI
  7. Liersch, R. Mandragora - Portrait of a medicinal plant Mandragora - Portr�t einer arzneipflanze . Zeitschrift fur phytotherapie, 2006, vol. 27, no. 2, p. 98-102. DOI
  8. Suleiman, Rami K., Abu Zarga, Musa., Sabri, Salim S. New withanolides from Mandragora officinarum: First report of withanolides from the Genus Mandragora . Fitoterapia, 2010, vol. 81, no. 7, p. 864-868. DOI

Boundary

A constituent measurement is a fact about material at a stated preparation, not a statement about what that material does in a person. An adverse-effect or genotoxicity record is an observation reported in a source, most often in an animal or laboratory model. Neither is a Metatron Health conclusion about causality, human risk or benefit, and the absence of a record is not proof that a preparation is safe. Nothing here is diagnosis, prescribing or individual medical care.

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