Botanical species · safety record

Fumaria officinalis

The EFSA Compendium of Botanicals holds 67 constituent measurements for Fumaria officinalis. 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: Fumaria officinalis L.

67Constituent measurements
0Safety records
6Cited sources
60Licensed products (Canada)

Also recorded as

Synonyms are carried from the source compendium. A species may be traded and studied under more than one name, which is exactly how a safety record gets lost.

Regulatory presence

Health Canada's Licensed Natural Health Products Database holds 60 licensed products naming Fumaria officinalis 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

Source material stated

  • Aerial parts
  • Flower
  • Flowering aerial part(s)
  • Flowering aerial plant
  • Flowering top(s)
  • Fresh aerial part
  • Fresh aerial part collected at flowering time
  • Fresh aerial parts collected at flowering time

What the records describe

Constituents measured

  • Isoquinoline alkaloids7
  • Protopine7
  • Fumarophycine6
  • Stylopine6
  • Fumarilin5
  • Cryptopine4
  • Fumaritine4
  • Parfumine4
  • Sinactine4
  • Sanguinarine3

Plant parts

  • Aerial part of plants61
  • Unspecified4
  • Leaves2

Preparations

  • Solvent extraction55

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
3,4-dihydroxybenzoic acidAerial part of plantsSolvent extractionGC-MSResolve DOI
AdlumineAerial part of plantsSolvent extraction2 PercentGC-MSResolve DOI
AlkaloidsAerial part of plantsSolvent extraction540 Milligram/100 gramGC-MSResolve DOI
ChelidonineUnspecifiedSolvent extraction650 Microgram/gramMass Spectroscopy and hyphenated methods without chromatographyResolve DOI
CoptisineAerial part of plantsSolvent extraction≤ 0.9 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
CoptisineAerial part of plantsSolvent extraction≥ 0.3 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
CorytuberineAerial part of plantsSolvent extraction≤ 2.6 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
CorytuberineAerial part of plantsSolvent extraction≥ 0.6 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
CryptopineAerial part of plantsSolvent extraction≤ 7.3 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
CryptopineAerial part of plantsSolvent extraction≥ 2.8 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
CryptopineAerial part of plantsSolvent extraction11 PercentGC-MSResolve DOI
CryptopineAerial part of plantsSolvent extraction9.9 PercentGC-MSResolve DOI
DihydrosanguinarineAerial part of plantsSolvent extraction< 2 PercentGC-MSResolve DOI
FumarilinAerial part of plantsSolvent extraction2.5 PercentGC-MSResolve DOI
FumarilinAerial part of plantsSolvent extraction≤ 3.9 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FumarilinAerial part of plantsSolvent extraction≥ 2 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FumarilinAerial part of plantsSolvent extraction3 PercentGC-MSResolve DOI
FumarilinAerial part of plantsSolvent extraction7.3 PercentGC-MSResolve DOI
FumaritineAerial part of plantsSolvent extraction≤ 3.4 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FumaritineAerial part of plantsSolvent extraction≥ 2.7 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FumaritineAerial part of plantsSolvent extraction6 PercentGC-MSResolve DOI
FumaritineAerial part of plantsSolvent extraction6.8 PercentGC-MSResolve DOI
FumarophycineAerial part of plantsSolvent extraction≤ 29.8 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FumarophycineAerial part of plantsSolvent extraction≥ 17.1 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FumarophycineAerial part of plantsSolvent extraction≤ 37.4 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FumarophycineAerial part of plantsSolvent extraction≥ 19.3 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
FumarophycineAerial part of plantsSolvent extraction24 PercentGC-MSResolve DOI
FumarophycineAerial part of plantsSolvent extraction10.3 PercentGC-MSResolve DOI
Isoquinoline alkaloidsAerial part of plantsSolvent extraction≥ 624.4 Milligram/100 gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
Isoquinoline alkaloidsAerial part of plantsSolvent extraction≤ 1386.1 Milligram/100 gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
Isoquinoline alkaloidsAerial part of plantsSolvent extraction1.9 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
Isoquinoline alkaloidsUnspecifiedSolvent extractionMass Spectroscopy and hyphenated methods without chromatographyResolve DOI
Isoquinoline alkaloidsAerial part of plantsSolvent extraction≤ 3 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
Isoquinoline alkaloidsAerial part of plantsSolvent extraction0.8 PercentGC-MSResolve DOI
P-coumaric acidAerial part of plantsSolvent extractionGC-MSResolve DOI
ParfumineAerial part of plantsSolvent extraction10.1 PercentGC-MSResolve DOI
ParfumineAerial part of plantsSolvent extraction≤ 5.4 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
ParfumineAerial part of plantsSolvent extraction≥ 4 PercentHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
ParfumineAerial part of plantsSolvent extraction3 PercentGC-MSResolve DOI
ProtopineUnspecifiedSolvent extraction3726.6 Microgram/gramMass Spectroscopy and hyphenated methods without chromatographyResolve DOI

40 of 67 records are shown, ordered so that records carrying a resolvable reference come first.

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. Sousek, J., Guedon, D., Adam, T., Bochorakova, H., Taborska, E., Valka, I., Simanek, V. Alkaloids and organic acids content of eight Fumaria species. PHYTOCHEMICAL ANALYSIS, 1999, vol. 10, no. 1, p. 6-11. DOI
  2. Paltinean, Ramona., Toiu, Anca., Wauters, Jean Noel., Frederich, Michel., Tits, Monique., Angenot, Luc., Tamas, Mircea., Crisan, Gianina. PHYTOCHEMICAL ANALYSIS OF FUMARIA OFFICINALIS L. (FUMARIACEAE). Farmacia, 2016, vol. 64, no. 3, p. 409-413.
  3. Suau, R., Cabezudo, B., Rico, R., Najera, F., Lopez-Romero, JM. Direct determination of alkaloid contents in Fumaria species by GC-MS. Phytochemical analysis, 2002, vol. 13, no. 6, p. 363-367. DOI
  4. Vrancheva, Radka Z., Ivanov, Ivan G., Aneva, Ina Y., Dincheva, Ivayla N., Badjakov, Ilian K., Pavlov, Atanas I. Alkaloid profiles and acetylcholinesterase inhibitory activities of Fumaria species from Bulgaria . Zeitschrift fur naturforschung section c-a journal of biosciences, 2016, vol. 71, no. 1-2, p. 9-14. DOI
  5. Och, Anna., Szewczyk, Katarzyna., Pecio, Lukasz., Stochmal, Anna., Zaluski, Daniel., Bogucka-Kocka, Anna. UPLC-MS/MS Profile of Alkaloids with Cytotoxic Properties of Selected Medicinal Plants of the Berberidaceae and Papaveraceae Families. . Oxidative medicine and cellular longevity, 2017, vol. 2017, p. 9369872-9369872. DOI
  6. Sharma, Uday Raj., Surendra, V., Goli, Divakar. Evaluation of Analgesic activity of Ethanolic extracts of Fumaria officinalis Linn. in experimental animals. Journal of fundamental pharmaceutical research, 2014, vol. 2, no. 1, p. 49-56.

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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