Botanical species · safety record

Nasturtium officinale

The EFSA Compendium of Botanicals holds 4 constituent measurements and 1 adverse-effect record for Nasturtium officinale. 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: Nasturtium officinale R.Br.

4Constituent measurements
1Safety records
4Cited sources
192Licensed products (Canada)

Regulatory presence

Health Canada's Licensed Natural Health Products Database holds 192 licensed products naming Nasturtium officinale 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.

Extract types on licence

  • Dry
  • Fresh

Source material stated

  • Aerial parts
  • Aerial parts extract
  • Fresh above ground parts
  • Fresh aerial part collected at flowering time
  • Herb
  • Herb top
  • Herb(s)
  • Leaf

What the records describe

Constituents measured

  • Glucosinolates2
  • Alkaloids1
  • Gluconasturtiin1

Plant parts

  • Leaves2
  • Live plants1
  • Seed1
  • Unspecified1

Preparations

  • Solvent extraction5

Effect types

  • Reproductive1

Target tissues

  • Uterus1

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
GluconasturtiinSeedSolvent extraction54 Millimole/kilogramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
AlkaloidsLive plantsSolvent extractionUnspecifiedNo resolvable identifier
GlucosinolatesLeavesSolvent extraction≤ 570.3 Microgram/gramColorimetry, Spectroscopy (Spectrometry) and PhotometryNo resolvable identifier
GlucosinolatesLeavesSolvent extraction≥ 293.2 Microgram/gramColorimetry, Spectroscopy (Spectrometry) and PhotometryNo 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
ReproductiveUterusUnspecifiedSolvent extractionRat (as animal)Reproduction toxicityNo resolvable identifier

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. Han, Hyejung., Kwon, Hoonjeong. Estimated dietary intake of thiocyanate from Brassicaceae family in Korean diet. Journal of toxicology and environmental health, part a: current issues, 2009, p. 1380-1387.
  2. Zalackas, C. Antidote to nicotine. comptes rendus hebdomadaires des seances de l'academie des sciences, 1905, p. 741-742.
  3. Williams, David J., Critchley, Christal., Pun, Sharon., Chaliha, Mridusmita., O'Hare, Timothy J. Differing mechanisms of simple nitrile formation on glucosinolate degradation in Lepidium sativum and Nasturtium officinale seeds . Phytochemistry, 2009, vol. 70, no. 11-12, p. 1401-1409. DOI
  4. Elbetieha, A., Al-Hamood, M.H., Alkofahi, A. Anti-implantation potential of some medicinal plants in female rats. Archives of std/hiv research, 1996, vol. 10, no. 3, p. 181-188.

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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