Botanical species · safety record

Harungana madagascariensis

The EFSA Compendium of Botanicals holds 20 constituent measurements and 8 adverse-effect records for Harungana madagascariensis. 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: Harungana madagascariensis Lam. ex Poir.

20Constituent measurements
8Safety records
6Cited sources
0Licensed 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

No Health Canada licensed natural health product in the snapshot names this species as a medicinal ingredient under this exact binomial. Absence here means absence from this one register under this one name, not absence from trade, and not a safety verdict.

What the records describe

Constituents measured

  • Saponins5
  • Alkaloids4
  • Anthraquinone3
  • Anthraquinones2
  • Oxalates2
  • Anthracene derivatives1
  • Anthrones1
  • Cardiac glycosides1
  • Tannins1

Plant parts

  • Bark27
  • Live plants1

Preparations

  • Solvent extraction28

Effect types

  • Digestive5
  • Systemic2
  • Pulmonary and cardiac1

Target tissues

  • Digestive5
  • Blood coagulation1
  • Cardiovascular1
  • Urogenital1
  • haematological1

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
AlkaloidsBarkSolvent extraction≤ 1.14 Milligram/100 gramPhytochemical screeningResolve DOI
AlkaloidsBarkSolvent extraction≥ 0.36 Milligram/100 gramPhytochemical screeningResolve DOI
Anthracene derivativesBarkSolvent extractionStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
AnthraquinonesBarkSolvent extractionStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
AnthraquinonesBarkSolvent extractionPhytochemical screeningResolve DOI
AnthronesLive plantsSolvent extractionNuclear Magnetic Resonance (NMR)Resolve DOI
Cardiac glycosidesBarkSolvent extractionPhytochemical screeningResolve DOI
OxalatesBarkSolvent extraction≤ 4.63 Milligram/100 gramResolve DOI
OxalatesBarkSolvent extraction≥ 3.64 Milligram/100 gramResolve DOI
SaponinsBarkSolvent extraction≥ 0.37 Milligram/100 gramPhytochemical screeningResolve DOI
SaponinsBarkSolvent extraction≤ 0.48 Milligram/100 gramPhytochemical screeningResolve DOI
AlkaloidsBarkSolvent extraction≤ 2.45 PercentNo resolvable identifier
AlkaloidsBarkSolvent extraction≥ 0.6 PercentNo resolvable identifier
AnthraquinoneBarkSolvent extractionPhytochemical screeningNo resolvable identifier
AnthraquinoneBarkSolvent extraction≤ 0.54 PercentNo resolvable identifier
AnthraquinoneBarkSolvent extraction≥ 0.42 PercentNo resolvable identifier
SaponinsBarkSolvent extraction≥ 0.38 PercentNo resolvable identifier
SaponinsBarkSolvent extraction≤ 0.59 PercentNo resolvable identifier
SaponinsBarkSolvent extractionPhytochemical screeningNo resolvable identifier
TanninsBarkSolvent extractionPhytochemical screeningNo 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
DigestiveDigestiveBarkSolvent extractionSaccharomyces cerevisiae (as organism)In vitroResolve DOI
DigestiveDigestiveBarkSolvent extractionSaccharomyces cerevisiae (as organism)In vitroResolve DOI
DigestiveDigestiveBarkSolvent extractionSaccharomyces cerevisiae (as organism)In vitroResolve DOI
DigestiveDigestiveBarkSolvent extractionSaccharomyces cerevisiae (as organism)In vitroResolve DOI
DigestiveDigestiveBarkSolvent extractionSaccharomyces cerevisiae (as organism)In vitroResolve DOI
Pulmonary and cardiacBlood coagulationBarkSolvent extractionRat (as animal)Short-term toxicityResolve DOI
SystemicCardiovascular / haematologicalBarkSolvent extractionRat (as animal)Short-term toxicityResolve DOI
SystemicUrogenitalBarkSolvent extractionRat (as animal)Short-term toxicityResolve 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. Eze, Fredrick Nwude., Airouyuwa, Osamede Jennifer. Quantitative phytochemical evaluation of stem bark extracts of Harungana madagascariensis. British journal of pharmaceutical research, 2014, vol. 4, no. 17), 2068-207, p. 7 pp.
  2. Kouam, SF., Khan, SN., Krohn, K., Ngadjui, BT., Kapche, DGWF., Yapna, DB., Zareem, S., Moustafa, AMY., Choudhary, MI. alpha-glucosidase inhibitory anthranols, kenganthranols A-C, from the stem bark of Harungana madagascariensis . Journal of natural products, 2006, vol. 69, no. 2, p. 229-233. DOI
  3. Akah, P.A. Abortifacient activity of some Nigerian medicinal plants. Phytotherapy Research, 1994, vol. 8, no. 2, p. 106-108.
  4. Etame, R.M.E., Mouokeu, R.S., Ngane, R.A.N., Assam, J.P.A., Masoohe, A.M., Tientcheu, R., Hopogap, M.L., Etoa, F.X. Acute and sub-acute toxicity of Harungana madagascariensis LAM (Hypericaceae) stem bark methanol extract. Journal of applied pharmaceutical science, 2017, vol. 7, no. 3, p. 160-167. DOI
  5. Antia, Bassey Sunday., Ita, Basil Nse., Udo, Uwemedimo Emmanuel. Nutrient Composition and In Vitro Antioxidant Properties of Harungana madagascariensis Stembark Extracts . Journal of medicinal food, 2015, vol. 18, no. 5, p. 609-614. DOI
  6. IINUMA, M., TOSA, H., ITO, T., TANAKA, T., AQIL, M. 2 PRENYLATED ANTHRONES IN HARUNGANA-MADAGASCARIENSIS. Phytochemistry, 1995, vol. 40, no. 1, p. 267-270. 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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