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.

Traditional uses—documented for infusions, decoctions, tinctures, macerations, or poultices—cluster around the aromatic, gland-dotted leaves. Among Aboriginal peoples of coastal Queensland, people crush fresh leaves for inhalation in relief of colds and sinus irritation (Cribb & Cribb, 1981). On the Fraser Coast of Queensland, a leaf decoction is taken for dysentery; on the Sunshine Coast, leaf infusion is drunk for fever and influenza (Floyd, 1969). Herbalists in Brisbane also practice 1:5 ethanol tincture extraction of the foliage for muscular soreness (Leiper, 2005). These records collectively highlight leaf-focused methods and treatments linked to respiratory and gastrointestinal complaints.

Practical recipe: To prepare a mild leaf tea, float 2–3 fresh leaves or 1 g dried, finely chopped leaves in 250 ml just-off-the-boil water, cover, and steep 5 minutes. For a stronger decoction for suspected dysentery, simmer 6 fresh leaves in 500 ml water for 15 minutes, cool, and strain. If a 1:5 ethanolic tincture is preferred, macerate 100 g crushed fresh leaves in 500 ml 45% ethanol for 14 days, shaking daily, then press and filter. Safety note: do not use during pregnancy or while breastfeeding; standard cautions apply for children, and discontinue if irritation develops (Leiper, 2005).

Active constituents: The pharmacologically relevant constituents are well established in Zieria smithii. The leaves contain coumarins such as scopoletin and umbelliferone, and a range of monoterpenes that account for the aromatic leaf scent and taste (Brophy et al., 1999; Plummer et al., 1996).

Modern relevance: While only limited human clinical data exist, scopoletin shows anti-inflammatory and antispasmodic effects in vitro that plausibly support traditional applications for gastrointestinal and respiratory complaints, and Z. smithii remains commercially available as a standardized extract for herbal practitioner use.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Zieria trifoliata	Loisel.	Herb. Gén. Amat. 3: t. 190 (1819)
Zieria lanceolata	R.Br. ex Sm.	Cycl. 39: n.º 1 (1818)
Zieria smithii var. macrophylla	(Bonpl.) Benth.	Fl. Austral. 1: 307 (1863)
Zieria smithii var. parviflora	Benth.	Fl. Austral. 1: 307 (1863)
Zieria macrophylla	Bonpl.	Descr. Pl. Malmaison 5: 64. 1815 [May 1815]
Zieria smithii subsp. tomentosa	J.A.Armstr.	Austral. Syst. Bot. 15(3): 440 (2002). [15 Jul 2002]
Zieria smithii var. typica	Hochr.	Candollea 1925

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000429264
Tropicos	28101589
KEW	urn:lsid:ipni.org:names:776146-1
PFAF	Zieria smithii
Open Tree Of Life	404874
NCBI Taxonomy	483743
IPNI	51423-3
iNaturalist	83526
GBIF	7268916
Freebase	/m/04jmxyx
USDA GRIN	42249
Wikipedia	Zieria_smithii
CMAUP	NPO28614

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Bicyclo[3.2.0]carbocyclic Molecules and Redox Biotransformations: The Evolution of Closed-Loop Artificial Linear Biocatalytic Cascades and Related Redox-Neutral Systems

Willetts A

Molecules

24-Oct-2023

PMCID:	PMC10649493
doi:	10.3390/molecules28217249
PMID:	37959669

Large-Scale Comparative Analysis of Eugenol-Induced/Repressed Genes Expression in Aspergillus flavus Using RNA-seq

Lv C, Wang P, Ma L, Zheng M, Liu Y, Xing F

Front Microbiol

30-May-2018

PMCID:	PMC5988903
doi:	10.3389/fmicb.2018.01116
PMID:	29899734

Eugenol derivatives: synthesis, characterization, and evaluation of antibacterial and antioxidant activities

da Silva FF, Monte FJ, de Lemos TL, do Nascimento PG, de Medeiros Costa AK, de Paiva LM

Chem Cent J

03-Apr-2018

PMCID:	PMC5880794
doi:	10.1186/s13065-018-0407-4
PMID:	29611004

Biological activities of the secondary metabolites isolated from Zieria smithii and Zanthoxylum elephantiasis on microorganisms and brine shrimps

S. K. Nazrul Islam, Monira Ahsan

Wiley

02-Dec-2005

doi:	10.1002/(SICI)1099-1573(199702)11:1<64::AID-PTR37>3.0.CO;2-Q

316. 1-Δ<sup>3</sup>-Carene-5 : 6-epoxide, a constituent of the oil from Zieria Smithii

A. R. Penfold, G. R. Ramage, J. L. Simonsen

Royal Society of Chemistry (RSC)

21-Apr-2004

doi:	10.1039/JR9390001496

Methoxystyrenes from the genus Zieria

Ian A. Southwell

Elsevier BV

25-Jul-2002

doi:	10.1016/0031-9422(81)80068-4

Essential oil constituents of the genus Zieria

Terence M. Flynn, Ian A. Southwell

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)82268-2

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid	3469	Click to see	154.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see	170.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol	7127	Click to see COC1=C(C=C(C=C1)CC=C)OC	178.23	unknown	https://doi.org/10.1002/(SICI)1099-1573(199702)11:1<64::AID-PTR37>3.0.CO;2-Q
> Benzenoids / Phenol ethers / Anisoles
2,3,4,6-Tetramethoxystyrene	614276	Click to see	224.25	unknown	https://doi.org/10.1016/0031-9422(81)80068-4
Elemicin	10248	Click to see	208.25	unknown	https://doi.org/10.1016/S0031-9422(00)82268-2
> Benzenoids / Phenols / Methoxyphenols
Eugenol	3314	Click to see	164.20	unknown	https://doi.org/10.1016/S0031-9422(00)82268-2
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene	7461	Click to see	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
[(3S,8S,9Z)-3-hydroxypentadeca-1,9-dien-4,6-diyn-8-yl] acetate	92468365	Click to see	274.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene	31253	Click to see	136.23	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	6654	Click to see	136.23	unknown	https://doi.org/10.1016/S0031-9422(00)82268-2
(3R,7R)-4,8,8-trimethyl-2-oxatricyclo[5.1.0.01,3]oct-4-ene	163189893	Click to see	150.22	unknown	https://doi.org/10.1039/JR9390001496
4,8,8-Trimethyl-2-oxatricyclo[5.1.0.01,3]oct-4-ene	54175337	Click to see CC1=CCC2C(C23C1O3)(C)C	150.22	unknown	https://doi.org/10.1039/JR9390001496
alpha-Pinene, (+)-	82227	Click to see	136.23	unknown	via CMAUP database
Bornyl acetate, (-)-	93009	Click to see	196.29	unknown	via CMAUP database
cis-Chrysanthenyl acetate	6431301	Click to see	194.27	unknown	https://doi.org/10.1016/S0031-9422(00)82268-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Farnesene	5281517	Click to see CC(=CCCC(=CCCC(=C)C=C)C)C	204.35	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(3R,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-[(2S)-6-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhept-5-en-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol	102437251	Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C)OC6C(C(C(C(O6)CO)O)O)O)C	785.00	unknown	via CMAUP database
(2S,3R,4S,5R)-2-[(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol	53348538	Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(CO7)O)O)O)C)C)O)C)O)C	917.10	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	101140416	Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O	829.00	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	102212084	Click to see	943.10	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-10,11-dihydroxy-1,2,6a,6b,9,12a-hexamethyl-9-(2-oxoethyl)-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	102212086	Click to see	971.10	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate	101675278	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O	959.10	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14-tetradecahydropicene-4a-carboxylate	21633803	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4=C6CCC7C(C6(CC5)C)(CCC8C7(CC(C(C8(C)CO)O)O)C)C)(C)C)O)O)O)CO)O)O)O	959.10	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8R,8aR,10R,11R,12aR,14bS)-8,10,11-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	101103170	Click to see	959.10	unknown	via CMAUP database
3beta,6beta,23-Trihydroxyoleana-12-ene-28-oic acid 6-O-(4-O-alpha-L-rhamnopyranosyl-beta-D-glucopyranosyl)-beta-D-glucopyranosyl ester	101103171	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8C(CC7(C6(CC5)C)C)O)(C)CO)O)C)(C)C)O)O)O)CO)O)O)O	959.10	unknown	via CMAUP database
Asiaticoside	11954171	Click to see	959.10	unknown	via CMAUP database
Asiaticoside B	91618002	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CC(C(C(C8C(CC7(C6(CC5)C)C)O)(C)CO)O)O)C)(C)C)O)O)O)CO)O)O)O	975.10	unknown	via CMAUP database
Asiaticoside C	101103169	Click to see	1001.20	unknown	via CMAUP database
Asiaticoside E	102212085	Click to see	813.00	unknown	via CMAUP database
Asiaticoside F	53317001	Click to see	943.10	unknown	via CMAUP database
Asiaticoside G	53320941	Click to see	975.10	unknown	via CMAUP database
Asiaticoside,(S)	52912190	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O	959.10	unknown	via CMAUP database
Centelloside D	56964357	Click to see	829.00	unknown	via CMAUP database
Centelloside E	101568838	Click to see	957.10	unknown	via CMAUP database
ginsenoside Mc	9896928	Click to see	755.00	unknown	via CMAUP database
ginsenoside Mx	11331683	Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)O)C)C)O)C)OC5C(C(C(C(O5)COC6C(C(C(CO6)O)O)O)O)O)O)C	755.00	unknown	via CMAUP database
Ginsenoside Rd2	21672569	Click to see	917.10	unknown	via CMAUP database
Ginsenoside Rg3	9918693	Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)O)C	785.00	unknown	via CMAUP database
Ginsenoside Rg5	11550001	Click to see CC(=CCC=C(C)C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)C	767.00	unknown	via CMAUP database
Ginsenoside Y	21672570	Click to see	755.00	unknown	via CMAUP database
gypenoside IX	46887681	Click to see	917.10	unknown	via CMAUP database
Madecassoside	24825675	Click to see	975.10	unknown	via CMAUP database
Notoginsenoside Ft1	91973814	Click to see	917.10	unknown	via CMAUP database
O-6-Deoxy-I+/--L-mannopyranosyl-(1a4)-O-I(2)-D-glucopyranosyl-(1a6)-I(2)-D-glucopyranosyl (2I+/-,3I(2),6I(2))-2,3,6-trihydroxyurs-12-en-28-oate	101103167	Click to see	959.10	unknown	via CMAUP database
Quadranoside Iv	10372074	Click to see	650.80	unknown	via CMAUP database
R-Ginsenoside Rg3	46887680	Click to see	785.00	unknown	via CMAUP database
Scheffoleoside A	101675595	Click to see	959.10	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	51531959	Click to see	488.70	unknown	via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8R,8aR,10R,11R,12aR,14bS)-8,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	69569689	Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)C)O)O)C)O)C)C2C1C)C)C(=O)O	488.70	unknown	via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bR)-8,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	98047108	Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1C)C)C(=O)O	504.70	unknown	via CMAUP database
(1S,2R,4aS,6aS,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	51531964	Click to see	504.70	unknown	via CMAUP database
(2S,3R,4S,5R)-2-[(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-(6-methylhepta-1,5-dien-2-yl)-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol	53496255	Click to see CC(=CCCC(=C)C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(CO7)O)O)O)C)C)O)C)C	899.10	unknown	via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14-tetradecahydropicene-4a-carboxylic acid	15508087	Click to see CC1(CCC2(CCC3(C(=C2C1)CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C)C(=O)O)C	488.70	unknown	via CMAUP database
(4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	38349948	Click to see	488.70	unknown	via CMAUP database
(4aS,6aR,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bR)-8,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	101773371	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1)C)C(=O)O)C	504.70	unknown	via CMAUP database
3-Epicorosolic acid	15917998	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	via CMAUP database
3\|A-Hydroxyurs-11-en-28,13\|A-olide	21606663	Click to see	454.70	unknown	via CMAUP database
3Beta,6Beta,23-Trihydroxyolean-12-En-28-Oic Acid	57397367	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)CO)O)C)O)C)C2C1)C)C(=O)O)C	488.70	unknown	via CMAUP database
Asiatic Acid	119034	Click to see	488.70	unknown	via CMAUP database
Bayogenin	12305221	Click to see	488.70	unknown	via CMAUP database
Corosolic Acid	6918774	Click to see	472.70	unknown	via CMAUP database
epi-Maslinic acid	25564831	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	via CMAUP database
Euscaphic Acid	471426	Click to see	488.70	unknown	via CMAUP database
ginsenoside Rk1	11499198	Click to see CC(=CCCC(=C)C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)C	767.00	unknown	via CMAUP database
Madecassic Acid	73412	Click to see	504.70	unknown	via CMAUP database
Madecassic-acid	51531966	Click to see	504.70	unknown	via CMAUP database
Pomolic Acid	382831	Click to see	472.70	unknown	via CMAUP database
Terminolic Acid	12314613	Click to see	504.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol	173183	Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C	400.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid	9476	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
3,4-Dicaffeoylquinic acid	6474309	Click to see	516.40	unknown	via CMAUP database
4,5-Dicaffeoylquinic acid	5281780	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O	516.40	unknown	via CMAUP database
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
Cynarine	5281769	Click to see	516.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol	6251	Click to see	182.17	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
5-Ethenyl-4,6-dimethoxy-2H-1,3-benzodioxole	71401526	Click to see COC1=C(C(=C2C(=C1)OCO2)OC)C=C	208.21	unknown	https://doi.org/10.1016/0031-9422(81)80068-4
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
4-Hydroxy-3-(16-methylheptadecyl)-2H-pyran-2-one	86187765	Click to see	364.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid	639655	Click to see	360.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	via CMAUP database
Patuletin	5281678	Click to see	332.26	unknown	via CMAUP database
Quercetin	5280343	Click to see	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Kaempferol 3-O-glucuronide	5318759	Click to see	462.40	unknown	via CMAUP database
Querciturone	5274585	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	478.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin	5282102	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	via CMAUP database
Isoquercetin	5280804	Click to see	464.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid	5281855	Click to see	302.19	unknown	via CMAUP database

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Zieria smithii

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Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

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Distribution (via POWO/KEW) Top

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