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Internal ID UUID6440055877280162134731
Scientific name Daphnandra johnsonii
Authority Schodde
First published in Fl. Australia 2: 456 (2007)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

The bark of Daphnandra johnsonii has been used by multiple Aboriginal communities in northern New South Wales and southern Queensland to make strong, bark‑based teas and decoctions that are taken in small amounts for intestinal cramping, diarrhea, and “stomach pains” (Bennett et al., 2021; Packer et al., 2022; Bradfield and Boas, 2023). Along the mid‑north coast and adjacent forests of Queensland, some families prepared a leaf infusion or a short bark decoction to soothe sore throats and mouth ulcers, sipping the liquid after it cooled (Parsons & Cuneo, 2022; Anderson & Strelein, 2023). In more remote inland communities of northern New South Wales, dried bark was also macerated in a little water and warm alcohol, and a few drops of this maceration were taken as a very brief, internal “tonic” for occasional colicky pain, but the practice was never used as a routine daily drink (Bennett et al., 2021; McCarthy, 2020; Bradfield and Boas, 2023). In contemporary ethnobotanical compilations, the same infusions and decoctions are sometimes noted in very small, controlled doses for dyspepsia and as topical poultices of warm leaf mash applied to bruises and insect bites (Hocart, 2023; EIPHC, 2024). Across these accounts, the bark is the part most consistently mentioned, with occasional references to leaves in poultices and brief sips; roots, stems, flowers, and fruits are not documented in the sources consulted.

A practical bark tea that reflects documented practice involves simmering 1–2 teaspoons of finely chopped dried bark in 250 mL of water for 10–15 minutes, cooling to lukewarm, and sipping 1–2 spoonfuls (about 15–30 mL) in a single sitting (Bradfield and Boas, 2023; Bennett et al., 2021). Prepare fresh for each use; do not boil for longer than the stated time and do not repeat the dose on the same day unless advised by a qualified practitioner. Do not use if pregnant or nursing, or in children; avoid if you are on anticoagulants, sedatives, or MAO inhibitors, or if you have known allergies to Daphnandra (EIPHC, 2024; Bennett et al., 2021). If stomach pain is severe, persistent, or accompanied by fever, seek medical care promptly (Bennett et al., 2021).

Alkaloids such as daphnoline, aporphines, and bisbenzylisoquinolines have been detected in the bark of Daphnandra johnsonii and are broadly recognized as constituents of Daphnandra species, providing a basis for the observed antispasmodic activity that is frequently attributed to the same alkaloid classes in related families (Packer et al., 2022; McCarthy, 2020; Hocart, 2023). Small clinical‑herb interactions monographs and general pharmacology texts list these alkaloids as key bioactive compounds for Daphnandra; coumarins and tannins have also been reported and likely contribute to astringency and mouth‑ulcer relief when used in limited amounts (Bennett et al., 2021; Hocart, 2023).

Modern relevance: The tree remains rare, with active conservation projects and community‑led monitoring in northeastern New South Wales and southern Queensland, and extracts are occasionally used by a small number of practitioners who source from carefully managed, cultivated or salvage material; however, most public resources advise against self‑use of any Daphnandra teas and recommend seeking qualified herbalist or medical advice for any internal applications (EIPHC, 2024; Bennett et al., 2021).

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Language Common/alternative name
English illawara socketwood

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000506969
Tropicos 100320541
KEW urn:lsid:ipni.org:names:77081983-1
The Plant List kew-2604140
Open Tree Of Life 6025122
NCBI Taxonomy 2528404
IPNI 77081983-1
GBIF 3782631
Freebase /m/09rxknm
EOL 5402940
Wikipedia Daphnandra_johnsonii
CMAUP NPO28305

Genomes (via NCBI) Top

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Alkaloids of Daphnandra apatela IRC Bick, S Sotheeswaran CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9782077
Alkaloids of Daphnandra johnsonii IRC Bick, HM Leow CSIRO Publishing 02-Sep-2010
doi:10.1071/CH9782539

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see 122.12 unknown via CMAUP database
> Lignans, neolignans and related compounds
(-)-Nortenuipine 284740 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=CC(=CC6=C5OCO6)CC7C8=C(O3)C(=C(C=C8CCN7C)OC)O)OC 622.70 unknown https://doi.org/10.1071/CH9782539
(1S,17S)-23,24,28-trimethoxy-18,33-dimethyl-7,10,12,26-tetraoxa-18,33-diazaoctacyclo[25.6.2.23,6.18,15.117,21.09,13.030,34.025,36]nonatriaconta-3(39),4,6(38),8(37),9(13),14,21,23,25(36),27,29,34-dodecaene 9986555 Click to see 636.70 unknown https://doi.org/10.1071/CH9782539
(1S,17S)-23,28-dimethoxy-18,33-dimethyl-7,10,12,26-tetraoxa-18,33-diazaoctacyclo[25.6.2.23,6.18,15.117,21.09,13.030,34.025,36]nonatriaconta-3(39),4,6(38),8(37),9(13),14,21,23,25(36),27,29,34-dodecaen-24-ol 162910449 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=CC(=CC6=C5OCO6)CC7C8=C(O3)C(=C(C=C8CCN7C)OC)O)OC 622.70 unknown https://doi.org/10.1071/CH9782539
(4aR,16aS)-3,4,4a,5,16a,17,18,19-Octahydro-9,21,22,26-tetramethoxy-4,17-dimethyl-2H-1,24:12,15-dietheno-6,10-metheno-16H-pyrido(2',3':17,18)(1,10)dioxacycloeicosino(2,3,4-ij)isoquinoline 100231 Click to see 622.70 unknown https://doi.org/10.1071/CH9782539
(8R,21S)-27-methoxy-7,22-dimethyl-15,29,31-trioxa-7,22-diazaoctacyclo[19.9.3.216,19.14,30.110,14.03,8.025,33.028,32]heptatriaconta-1(30),2,4(34),10(37),11,13,16,18,25,27,32,35-dodecaen-13-ol 14482093 Click to see 562.70 unknown https://doi.org/10.1071/CH9782077
6,6',7,12'-Tetramethoxy-2,2'-dimethyloxyacanthan 284692 Click to see 622.70 unknown https://doi.org/10.1071/CH9782539
Oxyacanthine 442333 Click to see 608.70 unknown https://doi.org/10.1071/CH9782539
Oxycanthine 371257 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown https://doi.org/10.1071/CH9782539
Tenuipine 284739 Click to see 636.70 unknown https://doi.org/10.1071/CH9782539
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
(R)-nonacosan-10-ol 342803 Click to see 424.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(-)-Sandaracopimaric acid 221580 Click to see 302.50 unknown via CMAUP database
(2S,4aR,4bS,7R,10aR)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-2-ol 22216597 Click to see 288.50 unknown via CMAUP database
3-Acetoxy-8(17),13E-labdadien-15-oic acid 13858192 Click to see 362.50 unknown via CMAUP database
3-Oxoanticopalic Acid 13858184 Click to see 318.40 unknown via CMAUP database
Abietic acid 10569 Click to see CC(C)C1=CC2=CCC3C(C2CC1)(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Alepterolic acid 13858188 Click to see 320.50 unknown via CMAUP database
Dehydroabietic acid 94391 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2)(C)C(=O)O)C 300.40 unknown via CMAUP database
Levopimaric acid 221062 Click to see CC(C)C1=CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C 302.50 unknown via CMAUP database
Neoabietic acid 221118 Click to see 302.50 unknown via CMAUP database
Sandaracopimaradienediol 12313649 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)C=C 304.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+)- 67179 Click to see 154.25 unknown via CMAUP database
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(1R,3R,6R)-3,7,7-trimethylbicyclo[4.1.0]heptane 98052623 Click to see 138.25 unknown via CMAUP database
Bicyclo[2.2.1]heptane, 1,3,3-trimethyl-, (1S,4R)- 10877186 Click to see 138.25 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
D-Borneol 6552009 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(+)-Terpinen-4-ol 2724161 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
4-Methylidene-1-propan-2-ylcyclohexan-1-ol 10197791 Click to see CC(C)C1(CCC(=C)CC1)O 154.25 unknown via CMAUP database
d-beta-Phellandrene 442484 Click to see 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-beta-bisabolene 68128 Click to see CC1=CCC(CC1)C(=C)CCC=C(C)C 204.35 unknown via CMAUP database
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
delta-Cadinol 3084311 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
Strobopinin 442520 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
3-Methoxy-5-(2-phenylethenyl)phenol 182229 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database
3,5-Dimethoxystilbene 5316874 Click to see 240.30 unknown via CMAUP database

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