Botanical species · safety record

Annona reticulata

The EFSA Compendium of Botanicals holds 41 constituent measurements for Annona reticulata. 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: Annona reticulata L.

41Constituent measurements
0Safety records
17Cited sources
0Licensed products (Canada)

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

  • Acetogenins10
  • Liriodenine6
  • Reticuline4
  • Asimilobine3
  • Alkaloids2
  • Aporphine alkaloids2
  • Coclaurine2
  • Dopamine2
  • Isoquinoline alkaloids2
  • Michelalbine2

Plant parts

  • Leaves11
  • Roots and other underground parts11
  • Bark7
  • Fruit unspecified4
  • Seed4
  • Stem3
  • stalk3
  • Aerial part of plants1

Preparations

  • Solvent extraction39
  • Essential oil2

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
AcetogeninsBarkSolvent extraction—Nuclear Magnetic Resonance (NMR)Resolve DOI
AcetogeninsFruit unspecifiedSolvent extraction—Nuclear Magnetic Resonance (NMR)Resolve DOI
AcetogeninsLeavesSolvent extraction—Nuclear Magnetic Resonance (NMR)Resolve DOI
AcetogeninsSeedSolvent extraction—Nuclear Magnetic Resonance (NMR)Resolve DOI
LiriodenineAerial part of plantsSolvent extraction—HPLC-UVResolve DOI
LiriodenineRoots and other underground partsSolvent extraction≥ 0.24 Millimole/kilogramHPLC-UVResolve DOI
LiriodenineRoots and other underground partsSolvent extraction≤ 775.53 Millimole/kilogramHPLC-UVResolve DOI
LiriodenineBarkSolvent extraction—Standard Chromatographic tests (paper- thin layer- and column chromatography)Resolve DOI
MyrceneFruit unspecifiedEssential oil≥ 12.62 Milligram/kilogramDistillation-titrimetry (modified Monier-William method)Resolve DOI
MyrceneFruit unspecifiedEssential oil≤ 20.06 Milligram/kilogramDistillation-titrimetry (modified Monier-William method)Resolve DOI
AcetogeninsRoots and other underground partsSolvent extraction——No resolvable identifier
AcetogeninsSeedSolvent extraction——No resolvable identifier
AcetogeninsSeedSolvent extraction——No resolvable identifier
AcetogeninsFruit unspecifiedSolvent extraction—Nuclear Magnetic Resonance (NMR)No resolvable identifier
AcetogeninsLeavesSolvent extraction—Nuclear Magnetic Resonance (NMR)No resolvable identifier
AcetogeninsSeedSolvent extraction—Nuclear Magnetic Resonance (NMR)No resolvable identifier
AlkaloidsBarkSolvent extraction——No resolvable identifier
AlkaloidsRoots and other underground partsSolvent extraction——No resolvable identifier
AnonaineBarkSolvent extraction——No resolvable identifier
Aporphine alkaloidsLeavesSolvent extraction——No resolvable identifier
Aporphine alkaloidsRoots and other underground partsSolvent extraction——No resolvable identifier
AsimilobineBarkSolvent extraction——No resolvable identifier
AsimilobineLeavesSolvent extraction——No resolvable identifier
AsimilobineRoots and other underground partsSolvent extraction——No resolvable identifier
CoclaurineLeavesSolvent extraction—Nuclear Magnetic Resonance (NMR)No resolvable identifier
CoclaurineStem / stalkSolvent extraction—Nuclear Magnetic Resonance (NMR)No resolvable identifier
CorydineLeavesSolvent extraction——No resolvable identifier
DopamineLeavesSolvent extraction—Nuclear Magnetic Resonance (NMR)No resolvable identifier
DopamineStem / stalkSolvent extraction—Nuclear Magnetic Resonance (NMR)No resolvable identifier
GlaucineLeavesSolvent extraction——No resolvable identifier
Isoquinoline alkaloidsLeavesSolvent extraction—Nuclear Magnetic Resonance (NMR)No resolvable identifier
Isoquinoline alkaloidsStem / stalkSolvent extraction—Nuclear Magnetic Resonance (NMR)No resolvable identifier
LiriodenineLeavesSolvent extraction——No resolvable identifier
LiriodenineRoots and other underground partsSolvent extraction——No resolvable identifier
MichelalbineBarkSolvent extraction——No resolvable identifier
MichelalbineRoots and other underground partsSolvent extraction——No resolvable identifier
OxonantenineLeavesSolvent extraction——No resolvable identifier
ReticulineBarkSolvent extraction——No resolvable identifier
ReticulineRoots and other underground partsSolvent extraction——No resolvable identifier
ReticulineRoots and other underground partsSolvent extraction——No resolvable identifier

40 of 41 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. Yang, Tsang Hsiung., Cheng, Mu Ying. The alkaloids of Annona reticulata L. II. Taiwan yaoxue zazhi, 1987, vol. 39, no. 3, p. 195-201.
  2. Santos, Alfredo C. Alkaloid from Anona Reticulata Linnaeus. Philippine journal of science, 1930, vol. 43, p. 561-4.
  3. Chang, Fang-Rong., Chen, Keh-Shaw., Ko, Feng-Nien., Teng, Che-Ming., Wu, Yang-Chang. Bioactive alkaloids from Annona reticulata. Chinese pharmaceutical journal, 1995, vol. 47, no. 5, p. 483-491.
  4. Jamkhande, P.G., Wattamwar, A.S., Chandak, P.G. In vitro anthelmintic efficacy of ethno-medicinal plant Annona reticulata L. roots against Indian earthworms (Pheretima posthuma). Indian journal of natural products and resources, 2014, vol. 5, no. 2, p. 152-157.
  5. Gopinath, K. W., Govindachari, T. R., Pai, B. R., Viswanathan, N. The structure of reticuline, a new alkaloid from Anona reticulata. Chemische berichte, 1959, vol. 92, p. 776-9.
  6. Liu, Dong., Yu, Jingguang., Sun, Lan., Luo, Xiuzhen., Guo, Shaorong., Lin, Jitian. Chemical constituents of the seeds from Annona reticulata (Annonaceae). Tianran chanwu yanjiu yu kaifa, 1998, vol. 10, no. 2, p. 1-7.
  7. TAM, VT., HIEU, PQC., CHAPPE, B., ROBLOT, F., FIGADERE, B., CAVE, A. ACETOGENINS OF ANNONACEAE .37. RETICULATAIN-1 AND RETICULATAIN-2 WITH RETICULATAMONE - 3 NEW POLYKETIDES FROM THE SEEDS OF ANNONA-RETICULATA . Bulletin de la societe chimique de france, 1995, vol. 132, no. 3, p. 324-329.
  8. Pino, JA., Marbot, R., Fuentes, V. Characterization of volatiles in bullock's heart (Annona reticulata L.) fruit cultivars from Cuba . Journal of agricultural and food chemistry, 2003, vol. 51, no. 13, p. 3836-3839. DOI
  9. Castro-Moreno, Marisol., Leonor Tinoco-Ojanguren, Clara., del Rocio Cruz-Ortega, Ma., Rosa Gonzalez-Esquinca, Alma. Influence of seasonal variation on the phenology and liriodenine content of Annona lutescens (Annonaceae) . Journal of plant research, 2013, vol. 126, no. 4, p. 529-537. DOI
  10. SAAD, JM., HUI, YH., RUPPRECHT, JK., ANDERSON, JE., KOZLOWSKI, JF., ZHAO, GX., WOOD, KV., MCLAUGHLIN, JL. RETICULATACIN - A NEW BIOACTIVE ACETOGENIN FROM ANNONA-RETICULATA (ANNONACEAE) . Tetrahedron, 1991, vol. 47, no. 16-17, p. 2751-2756. DOI
  11. Araya, H., Maeda, U., Hara, N., Prasad, S., Begum, A. S., Sahai, M., Fujimoto, Y. Potent biologically active tetrahydrofuranic acetogenins from custard apple (Annona reticulate Linn) seeds. Meiji daigaku nogakubu kenkyu hokoku, 2012, vol. 62, no. 1, p. 1-9.
  12. Chen, YY., Chang, FR., Yen, HF., Wu, YC. Epomusenins A and B, two acetogenins from fruits of Rollinia mucosa. PHYTOCHEMISTRY, 1996, vol. 42, no. 4, p. 1081-1083. DOI
  13. Forgacs, P., Desconclois, J.F., Mansard, D. Dopamine and tetrahydroisoquinoline alkaloids of Annona reticulata DOPAMINE ET ALCALOIDES TETRAHYDROISOQUINOLEIQUES D'ANNONA RETICULATA L. ANNONACEES . Plantes medicinales et phytotherapie, 1981, vol. 15, no. 1, p. 10-15.
  14. WU, YC., CHANG, FR., DUH, CY., WANG, SK. ANNORETICUIN AND ISOANNORETICUIN - 2 NEW CYTOTOXIC ACETOGENINS FROM ANNONA-RETICULATA . Heterocycles, 1992, vol. 34, no. 4, p. 667-674.
  15. CHANG, FR., WU, YC., DUH, CY. STUDIES ON THE ACETOGENINS OF FORMOSAN ANNONACEOUS PLANTS .2. CYTOTOXIC ACETOGENINS FROM ANNONA-RETICULATA . Journal of natural products, 1993, vol. 56, no. 10, p. 1688-1694. DOI
  16. Yu, J. G., Liu, D., Xu, L. Z., Yang, S. L. Studies on chemical structures of two iso-acetogenins from Annona reticulata . Yaoxue xuebao, 1997, vol. 32, no. 12, p. 914-919.
  17. Chang, FR., Chen, JL., Chiu, HF., Wu, MJ., Wu, YC. Acetogenins from seeds of Annona reticulata. Phytochemistry, 1998, vol. 47, no. 6, p. 1057-1061. 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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