Botanical species · safety record

Duboisia myoporoides

The EFSA Compendium of Botanicals holds 32 constituent measurements and 1 adverse-effect record for Duboisia myoporoides. 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: Duboisia myoporoides R.Br.

32Constituent measurements
1Safety records
10Cited sources
5Licensed products (Canada)

Regulatory presence

Health Canada's Licensed Natural Health Products Database holds 5 licensed products naming Duboisia myoporoides 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

  • Leaf
  • Leaves

What the records describe

Constituents measured

  • Tropane alkaloids6
  • Hyoscyamine5
  • Scopolamine4
  • Anabasine3
  • Nicotine3
  • Alkaloids2
  • Pelletierine2
  • Apoatropine1
  • Atropine1
  • Esculetin1

Plant parts

  • Leaves25
  • Shoot4
  • Aerial part of plants3
  • Unspecified1

Preparations

  • Solvent extraction31

Effect types

  • Systemic1

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
AlkaloidsLeavesSolvent extraction≥ 2220 Microgram/square decimetreGaschromatography (GC)Resolve DOI
AlkaloidsLeavesSolvent extraction≤ 8960 Microgram/square decimetreGaschromatography (GC)Resolve DOI
AnabasineLeavesSolvent extraction≥ 0.39 PercentChromatographic testsResolve DOI
AnabasineLeavesSolvent extraction≤ 1.4 PercentChromatographic testsResolve DOI
ApoatropineLeavesSolvent extractionMass Spectroscopy and hyphenated methods without chromatographyResolve DOI
EsculetinAerial part of plantsSolvent extractionHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
HyoscyamineLeavesSolvent extraction≤ 3 Milligram/gramUHPLC-MS-MSResolve DOI
HyoscyamineLeavesSolvent extraction≥ 2.5 Milligram/gramUHPLC-MS-MSResolve DOI
HyoscyamineLeavesSolvent extraction≥ 80 Microgram/square decimetreGaschromatography (GC)Resolve DOI
HyoscyamineLeavesSolvent extraction≤ 1590 Microgram/square decimetreGaschromatography (GC)Resolve DOI
HyoscyamineLeavesSolvent extraction1.5 Milligram/gramUHPLC-MS-MSResolve DOI
NicotineLeavesSolvent extraction≥ 0.06 PercentChromatographic testsResolve DOI
NicotineLeavesSolvent extraction≤ 0.3 PercentChromatographic testsResolve DOI
PelletierineLeavesSolvent extraction≥ 0.09 PercentChromatographic testsResolve DOI
PelletierineLeavesSolvent extraction≤ 0.25 PercentChromatographic testsResolve DOI
ScopolamineLeavesSolvent extraction≥ 2000 Microgram/square decimetreGaschromatography (GC)Resolve DOI
ScopolamineLeavesSolvent extraction≤ 7400 Microgram/square decimetreGaschromatography (GC)Resolve DOI
ScopolamineLeavesSolvent extraction12.71 Milligram/gramUHPLC-MS-MSResolve DOI
ScopoletinAerial part of plantsSolvent extractionHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
ScopolinAerial part of plantsSolvent extraction0.1 Milligram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
Tropane alkaloidsUnspecifiedUnspecifiedResolve DOI
Tropane alkaloidsLeavesSolvent extractionMass Spectroscopy and hyphenated methods without chromatographyResolve DOI
Tropane alkaloidsLeavesSolvent extraction≤ 0.09 PercentChromatographic testsResolve DOI
Tropane alkaloidsLeavesSolvent extraction≥ 0.08 PercentChromatographic testsResolve DOI
Tropane alkaloidsLeavesSolvent extraction0.06 Microgram/gramChromatographic testsResolve DOI
Tropane alkaloidsLeavesSolvent extractionHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
TropineLeavesSolvent extractionMass Spectroscopy and hyphenated methods without chromatographyResolve DOI
ValtropineLeavesSolvent extractionMass Spectroscopy and hyphenated methods without chromatographyResolve DOI
AnabasineShootSolvent extraction0.56 Percent AreaChromatographic testsNo resolvable identifier
AtropineShootSolvent extraction0.25 Percent AreaChromatographic testsNo resolvable identifier
NicotineShootSolvent extraction0.91 Percent AreaChromatographic testsNo resolvable identifier
ScopolamineShootSolvent extraction0.7 Percent AreaChromatographic testsNo resolvable identifier

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
SystemicLeavesCase 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. Fliniaux, MA., GilletManceau, F., Marty, D., Macek, T., Monti, JP., JacquinDubreuil, A. Evaluation of the relation between the endogenous scopoletin and scopolin level of some solanaceous and papaver cell suspensions and their ability to bioconvert scopoletin to scopolin . Plant science, 1997, vol. 123, no. 1-2, p. 205-210. DOI
  2. Foley, P. Duboisia myoporoides: The medical career of a native Australian plant. Historical records of australian science, 2006, vol. 17, no. 1, p. 31-69. DOI
  3. SHUKLA, YN., THAKUR, RS. TROPANE ALKALOIDS FROM DUBOISIA-MYOPOROIDES. Phytochemistry, 1992, vol. 31, no. 12, p. 4389-4390. DOI
  4. MORTIMER, PI., WILKINSON, S. THE OCCURRENCE OF NICOTINE, ANABASINE, AND ISOPELLETIERINE IN DUBOISIA-MYOPOROIDES . Journal of the chemical society, 1957, no. SEP, p. 3967-3970. DOI
  5. Ullrich, Sophie Friederike., Averesch, Nils J. H., Castellanos, Leonardo., Choi, Young Hae., Rothauer, Andreas., Kayser, Oliver. Discrimination of wild types and hybrids of Duboisia myoporoides and Duboisia leichhardtii at different growth stages using H-1 NMR-based metabolite profiling and tropane alkaloids-targeted HPLC-MS analysis . Phytochemistry, 2016, vol. 131, p. 44-56. DOI
  6. KITAMURA, Y., YAMASHITA, R., MIURA, H., WATANABE, M. PHLOEM TRANSPORT OF TROPANE AND PYRIDINE ALKALOIDS IN DUBOISIA-MYOPOROIDES . Journal of plant physiology, 1993, vol. 142, no. 5, p. 635-637.
  7. Mishra, S., Sangwan, R.S. Dynamics of tropane alkaloids in Duboisia myoporoides leaf during development. Journal of herbs, spices and medicinal plants, 1996, vol. 4, no. 3, p. 61-70. DOI
  8. Khanam, N., Khoo, C., Khan, AG. Effects of cytokinin-auxin combinations on cell arrangement in the basal stems and tropane alkaloid production in cultured non-rooted shoots of Duboisia myoporoides . Australian journal of botany, 2001, vol. 49, no. 4, p. 443-450. DOI
  9. Pellowe, Elizabeth., Poncia, Hugo D. M. Duboisia ingestion: An unusual cause of anticholinergic poisoning. Emergency medicine australasia, 2013, vol. 25, no. 3, p. 268-270. DOI
  10. Naumann, A., Kurtze, L., Kr�hmer, A., Hagels, H., Schulz, H. Discrimination of solanaceae taxa and quantification of scopolamine and hyoscyamine by ATR-FTIR spectroscopy. Planta medica, 2014, vol. 80, no. 15, p. 1315-1320. 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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