Botanical species · safety record

Corydalis solida

The EFSA Compendium of Botanicals holds 46 constituent measurements for Corydalis solida. 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: Corydalis solida (L.) Clairv.

46Constituent measurements
0Safety records
12Cited 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

  • Isoquinoline alkaloids11
  • Protopine4
  • Alkaloids3
  • Allocryptopine2
  • Bulbocapnine2
  • Corydaline2
  • Isoboldine2
  • Stylopine2
  • Tetrahydropalmatin2
  • Adlumidine1

Plant parts

  • Live plants27
  • Roots and other underground parts10
  • Aerial part of plants8
  • Unspecified1

Preparations

  • Solvent extraction43

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
AdlumidineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
AlkaloidsRoots and other underground partsSolvent extraction—GC-MSResolve DOI
AllocryptopineLive plants—0.005 Percent—Resolve DOI
AllocryptopineRoots and other underground partsSolvent extraction—Capillary (Zone) Electrophoresis (CE or CZE)Resolve DOI
Aporphine alkaloidsLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
BicucullineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
BulbocapnineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
CorydalineLive plantsSolvent extraction0.02 Percent—Resolve DOI
CorydalineRoots and other underground partsSolvent extraction—Capillary (Zone) Electrophoresis (CE or CZE)Resolve DOI
CorydineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
DehydronantenineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
DihydrosanguinarineLive plantsSolvent extraction—Nuclear Magnetic Resonance (NMR)Resolve DOI
DomesticineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
GlaucineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
IsoboldineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
Isoquinoline alkaloidsRoots and other underground partsSolvent extraction—Capillary (Zone) Electrophoresis (CE or CZE)Resolve DOI
Isoquinoline alkaloidsLive plantsSolvent extraction—Nuclear Magnetic Resonance (NMR)Resolve DOI
Isoquinoline alkaloidsLive plantsSolvent extraction—Nuclear Magnetic Resonance (NMR)Resolve DOI
Isoquinoline alkaloidsLive plantsSolvent extraction88 PercentStandard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
Isoquinoline alkaloidsUnspecified——UnspecifiedResolve DOI
NandazurineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
OxonantenineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
PalmatineRoots and other underground partsSolvent extraction—High Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
PredicentrineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
ProtopineLive plantsSolvent extraction0.014 Percent—Resolve DOI
ProtopineRoots and other underground partsSolvent extraction—Capillary (Zone) Electrophoresis (CE or CZE)Resolve DOI
ProtopineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
ScoulerineLive plantsSolvent extraction< 0.001 Percent—Resolve DOI
SinactineLive plantsSolvent extraction—Nuclear Magnetic Resonance (NMR)Resolve DOI
StylopineLive plantsSolvent extraction——Resolve DOI
StylopineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
TetrahydropalmatinLive plantsSolvent extraction0.01 Percent—Resolve DOI
TetrahydropalmatinRoots and other underground partsSolvent extraction—Capillary (Zone) Electrophoresis (CE or CZE)Resolve DOI
ThaliporphineLive plantsSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
AlkaloidsRoots and other underground partsSolvent extraction≥ 0.189 PercentGaschromatography (GC)No resolvable identifier
AlkaloidsRoots and other underground partsSolvent extraction≤ 0.888 PercentGaschromatography (GC)No resolvable identifier
BulbocapnineAerial part of plantsSolvent extraction—Nuclear Magnetic Resonance (NMR)No resolvable identifier
IsoboldineAerial part of plantsSolvent extraction—Nuclear Magnetic Resonance (NMR)No resolvable identifier
IsocorydineAerial part of plantsSolvent extraction—Nuclear Magnetic Resonance (NMR)No resolvable identifier
Isoquinoline alkaloidsAerial part of plants——Nuclear Magnetic Resonance (NMR)No resolvable identifier

40 of 46 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. MANSKE, RHF. THE ALKALOIDS OF FUMARIACEOUS PLANTS .51. CORYDALIS-SOLIDA (L) SWARTZ. Canadian journal of chemistry-revue canadienne de chimie, 1956, vol. 34, no. 1, p. 1-3. DOI
  2. Sturm, Sonja., Seger, Christoph., Stuppner, Hermann. Analysis of Central European Corydalis species by nonaqueous capillary electrophoresis-electrospray ion trap mass spectrometry . Journal of chromatography a, 2007, vol. 1159, no. 1-2, p. 42-50. DOI
  3. Berkov, Strahil., Bastida, Jaume., Nikolova, Milena., Viladomat, Francesc., Codina, Carles. Rapid TLC/GC-MS identification of acetylcholinesterase inhibitors in alkaloid extracts . Phytochemical analysis, 2008, vol. 19, no. 5, p. 411-419. DOI
  4. Iwasa, J., Naruto, S., Utsui, Y. Studies on the constituent of Corydalis sps. I. Application of thin-layer-and gas-chromatography to Corydalis alkaloids . . Yakugaku zasshi : journal of the pharmaceutical society of japan, 1966, vol. 86, no. 5, p. 396-9.
  5. Sturm, Sonia., Seger, Christoph., Godejohann, Markus., Spraul, Manfred., Stuppner, Hermann. Conventional sample enrichment strategies combined with high-performance liquid chromatography-solid phase extraction-nuclear magnetic resonance analysis allows analyte identification from a single minuscule Corydalis solida plant tuber . Journal of chromatography a, 2007, vol. 1163, no. 1-2, p. 138-144. DOI
  6. Ito, Chihiro., Itoigawa, Masataka., Tokuda, Harukuni., Kuchide, Masashi., Nishino, Hoyoku., Furukawa, Hiroshi. Chemopreventive activity of isoquinoline alkaloids from Corydalis plants. Planta medica, 2001, vol. 67, no. 5, p. 473-475.
  7. Doncheva, Tsvetelina., Yordanova, Gabriela., Vutov, Vassil., Kostova, Nadezhda., Philipov, Stefan. COMPARATIVE STUDY OF ALKALOID PROFILE OF CORYDALIS SLIVENENSIS VEL. AND CORYDALIS SOLIDA L. . Comptes rendus de l academie bulgare des sciences, 2015, vol. 68, no. 7, p. 843-846.
  8. KIRYAKOV, HG., ISKRENOVA, ES. MINOR ALKALOIDS OF CORYDALIS-BULBOSA, STRUCTURE OF BULBODIONE. Planta medica, 1984, vol. 50, no. 2, p. 136-138. DOI
  9. RAHIMIZADEH, M., MILLER, RR., ONUR, MA., GOZLER, T., SHAMMA, M. (+/-)-CORYSOLIDINE, A SPIROBENZYLISOQUINOLINE ALKALOID FROM CORYDALIS-SOLIDA . Phytochemistry, 1986, vol. 25, no. 9, p. 2245-2246. DOI
  10. SLAVIK, J., DOLEJS, L., SLAVIKOVA, L. ALKALOIDS OF THE PAPAVERACEAE .81. ALKALOIDS FROM CORYDALIS-SOLIDA (L) SW MASS-SPECTROMETRY OF QUATERNARY BENZYLISOQUINOLINE ALKALOIDS . Collection of czechoslovak chemical communications, 1985, vol. 50, no. 10, p. 2299-2309.
  11. KIRYAKOV, HG., ISKRENOVA, E., KUZMANOV, B., EVSTATIEVA, L. ALKALOIDS FROM CORYDALIS-BULBOSA - STRUCTURE OF CORYDIONE. Planta medica, 1981, vol. 43, no. 1, p. 51-55. DOI
  12. Sener, B., Temizer, H. Chemical Study on Protoberberine Alkaloids from Corydalis solida ssp. brachyloba. . Planta medica, 1988, vol. 54, no. 6, p. 584-584. 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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