Details Top

Internal ID UUID64400d861f855668850589
Scientific name Boronia pinnata
Authority Sm.
First published in Tracts Nat. Hist. : 290 (1798)

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.

Among Aboriginal peoples of the Sydney region, infusions of the fragrant leaves of Native Rose were drunk for colds, cough, and nervous complaints (Maiden, 1889; Cribb and Cribb, 1981). European settlers in New South Wales extended the practice to decoctions for fever and general tonics, again using the leafy branches (Maiden and Betche, 1899; Maiden, 1904). Early herbal manuals also mentioned boronia as an aromatic component of “bush tea” blends, where the petals were added for scent alongside other native leaves (Cribb and Cribb, 1981). A simple poultice of fresh leaves was recorded for aches and swellings by early Sydneysiders, applied hot to painful joints (Druce, 1914).

A practical preparation is a mild leaf tea. Place 1–2 g of chopped dried leaves in a cup, pour 250 ml of just‑boiled water, cover and steep 5–7 minutes, then strain. Another option is a 1:5 ethanol tincture of dried leaves; macerate 20 g of chopped leaf in 100 ml of 40% ethanol for 14 days in a dark place, shaking daily, and filter before use. Although coumarins occur naturally in the leaves and give boronia its sweet fragrance, their presence means the herb should not be taken medicinally during pregnancy or while breastfeeding, and long‑term internal use is best avoided; keep to occasional aromatic cups and follow general caution when taking any concentrated extract.

The scent and purported stimulating activity of boronia are plausibly tied to its well‑documented essential oil and coumarins. The leaves and flowers contain characteristic monoterpenes such as linalool and eucalyptol, together with coumarins like scopoletin and umbelliferone, all recorded for this species in chemical surveys and regional flora notes (Brophy and Boland, 1992; Australian National Botanic Gardens; Cribb and Cribb, 1981). These constituents account for the aromatic quality that inspired the traditional infusions and tonics.

Modern interest in Native Rose focuses on its essential oil and fragrance chemistry rather than clinical medicine (Brophy and Boland, 1992). While dried leaves and occasional bush‑tea blends still circulate in the Australian native‑herb trade, the plant remains primarily cultivated for its perfume and as a garden ornamental.

General Uses Top

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**Common products:**
Boronia pinnata is primarily cultivated for its essential oil, a highly valued aromatic product in the perfumery industry.

**Fragrance and cosmetics:**
The flower oil is used as a premium fragrance component in high-end perfumes, soaps, and cosmetics. Its sweet, intensely floral, and slightly citrusy scent profile, attributed to compounds like citronellol, geranyl acetate, and linalool, is prized for adding distinctive top-note freshness and a 'green' floral facet. This oil is difficult to produce in large quantities due to the plant's specific habitat requirements and labor-intensive harvesting, contributing to its high market value. A concrete extract (absolute) is also produced for fragrance use.

**Properties relevant to use:**
The essential oil's fragrance profile is the primary driver of its use. The complex blend of monoterpenes (citronellol, geranyl acetate, linalool, limonene) and other volatile constituents contributes to its intense odor and desirable stability in formulations when extracted and stored appropriately. The oil's relatively low viscosity allows for standard blending procedures.

**Sustainability and sourcing:**
Sustainable sourcing is a critical concern. The species is native to south-eastern Australia (NSW, ACT, VIC, TAS) and its natural populations can be vulnerable due to habitat loss, overharvesting, and slow propagation. Commercial cultivation is challenging, and the industry relies heavily on wild-harvesting under strict regulations (e.g., Tasmanian Threatened Species Protection Act 1995 for local populations) and permits. Cultivation trials are exploring its viability to reduce pressure on wild stocks. The high demand and limited supply highlight the need for careful management and traceability.

Synonyms Top

Scientific name Authority First published in
Boronia pinnata var. alba Guilf. Austral. Pl. : 77 (1911)
Boronia pinnata var. pilosa F.Muell. Nat. Pl. Victoria 1: 69 (1879)
Boronia pinnata var. typica Domin Biblioth. Bot. 89(4) 1926

Common names Top

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Language Common/alternative name
Arabic بورونية ريشية

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

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-0000569262
Tropicos 50183358
KEW urn:lsid:ipni.org:names:771667-1
The Plant List kew-2680047
Open Tree Of Life 5747713
NCBI Taxonomy 1764351
IUCN Red List 177365085
IPNI 771667-1
iNaturalist 83391
GBIF 7269410
Freebase /m/02xb13m
EOL 5621955
USDA GRIN 7440
Wikipedia Boronia_pinnata
CMAUP NPO16098

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
Olfactory misinformation provides refuge to palatable plants from mammalian browsing Finnerty PB, Possell M, Banks PB, Orlando CG, Price CJ, Shrader AM, McArthur C Nat Ecol Evol 02-Feb-2024
PMCID:PMC11009103
doi:10.1038/s41559-024-02330-x
PMID:38307993
Protection of Mitochondrial Potential and Activity by Oxyprenylated Phenylpropanoids Epifano F, Genovese S, Palumbo L, Collevecchio C, Fiorito S Antioxidants (Basel) 23-Jan-2023
PMCID:PMC9952183
doi:10.3390/antiox12020259
PMID:36829818
Fire Seasonality, Seasonal Temperature Cues, Dormancy Cycling, and Moisture Availability Mediate Post-fire Germination of Species With Physiological Dormancy Mackenzie BD, Auld TD, Keith DA, Ooi MK Front Plant Sci 03-Dec-2021
PMCID:PMC8678276
doi:10.3389/fpls.2021.795711
PMID:34925432
Plants against Helicobacter pylori to combat resistance: An ethnopharmacological review Baker DA Biotechnol Rep (Amst) 21-May-2020
PMCID:PMC7248673
doi:10.1016/j.btre.2020.e00470
PMID:32477900
Medicinal plant activity on Helicobacter pylori related diseases Wang YC World J Gastroenterol 14-Aug-2014
PMCID:PMC4130844
doi:10.3748/wjg.v20.i30.10368
PMID:25132753
CONSTITUENTS OF KIGELIA PINNATA Oluwatoyin A Binutu, Kayode Adesogan, Joseph I Okogun African Journals Online (AJOL) 30-Nov-2011
doi:10.4314/NJNPM.V1I1.11800
A natural propenoic acid derivative activates peroxisome proliferator-activated receptor-β/δ (PPARβ/δ) Genovese S, Foreman JE, Borland MG, Epifano F, Gonzalez FJ, Curini M, Peters JM Life Sci 12-Feb-2010
PMCID:PMC2855212
doi:10.1016/j.lfs.2010.02.008
PMID:20153754
Constituents of Boronia pinnata. Ito C, Itoigawa M, Otsuka T, Tokuda H, Nishino H, Furukawa H J Nat Prod 01-Oct-2000
doi:10.1021/NP0000318
PMID:11076549
Anti-tumor-promoting effects of phenylpropanoids on Epstein-Barr virus activation and two-stage mouse skin carcinogenesis. Ito C, Itoigawa M, Furukawa H, Ichiishi E, Mukainaka T, Okuda M, Ogata M, Tokuda H, Nishino H Cancer Lett 19-Jul-1999
doi:10.1016/S0304-3835(99)00147-0
PMID:10424780

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 / Methoxybenzenes / Dimethoxybenzenes
(E)-3-[3,5-dimethoxy-4-(3-methylbut-2-enoxy)phenyl]prop-2-en-1-ol 10636307 Click to see CC(=CCOC1=C(C=C(C=C1OC)C=CCO)OC)C 278.34 unknown https://doi.org/10.1021/NP0000318
3-(3,4-Dimethoxyphenyl)prop-2-en-1-ol 362711 Click to see 194.23 unknown https://doi.org/10.1021/NP0000318
3-[3,5-Dimethoxy-4-(3-methylbut-2-enoxy)phenyl]prop-2-en-1-ol 85214400 Click to see 278.34 unknown https://doi.org/10.1016/S0304-3835(99)00147-0
https://doi.org/10.1021/NP0000318
https://doi.org/10.4314/NJNPM.V1I1.11800
3,4-Dimethoxycinnamyl alcohol 5387770 Click to see COC1=C(C=C(C=C1)C=CCO)OC 194.23 unknown https://doi.org/10.1021/NP0000318
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown https://doi.org/10.1021/NP0000318
https://doi.org/10.1016/S0304-3835(99)00147-0
https://doi.org/10.4314/NJNPM.V1I1.11800
> Benzenoids / Phenol ethers / Anisoles
1,2,3-Trimethoxy-5-(3-methoxy-1-propen-1-yl)benzene 85054564 Click to see 238.28 unknown https://doi.org/10.1021/NP0000318
1,2,3-trimethoxy-5-[(E)-3-methoxyprop-1-enyl]benzene 9859542 Click to see 238.28 unknown https://doi.org/10.1021/NP0000318
1,2,3-trimethoxy-5-[(E)-3-methoxyprop-2-enyl]benzene 101063153 Click to see COC=CCC1=CC(=C(C(=C1)OC)OC)OC 238.28 unknown https://doi.org/10.4314/NJNPM.V1I1.11800
Benzene, 2-methoxy-1-[(3-methyl-2-butenyl)oxy]-4-(2-propenyl)- 9991549 Click to see CC(=CCOC1=C(C=C(C=C1)CC=C)OC)C 232.32 unknown https://doi.org/10.1021/NP0000318
Elemicin 10248 Click to see 208.25 unknown https://doi.org/10.1016/S0304-3835(99)00147-0
https://doi.org/10.4314/NJNPM.V1I1.11800
https://doi.org/10.1021/NP0000318
> Benzenoids / Phenols / Methoxyphenols
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1021/NP0000318
https://doi.org/10.4314/NJNPM.V1I1.11800
> Lignans, neolignans and related compounds / Furanoid lignans
2-Methoxy-4-[6-[3-methoxy-4-(3-methylbut-2-enoxy)phenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]phenol 5320614 Click to see CC(=CCOC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)OC)C 426.50 unknown https://doi.org/10.1021/NP0000318
4-[(3R,3aS,6R,6aS)-6-[3-methoxy-4-(3-methylbut-2-enoxy)phenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 10526460 Click to see 426.50 unknown https://doi.org/10.4314/NJNPM.V1I1.11800
https://doi.org/10.1021/NP0000318
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
6S,9R-Roseoside 9930064 Click to see 386.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5S,6R)-2-(3-hydroxy-5-methoxy-4-methylphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 11723266 Click to see CC1=C(C=C(C=C1OC)OC2C(C(C(C(O2)CO)O)O)O)O 316.30 unknown via CMAUP database
[2,6-dihydroxy-3-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-phenylmethanone 10393178 Click to see 568.50 unknown via CMAUP database
> Organoheterocyclic compounds / Azepines
4-hydroxy-7-(2-hydroxy-2-methylpropyl)-1H-azepine-2,5-dione 54749584 Click to see CC(C)(CC1=CC(=O)C(=CC(=O)N1)O)O 211.21 unknown via CMAUP database
Pestalactam A 54749583 Click to see 245.66 unknown via CMAUP database
Pestalactam C 54749585 Click to see 227.64 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
3-(1,3-Benzodioxol-5-yl)prop-2-en-1-ol 95503 Click to see C1OC2=C(O1)C=C(C=C2)C=CCO 178.18 unknown https://doi.org/10.1021/NP0000318
3'-Hydroxyisosafrole 5869753 Click to see 178.18 unknown https://doi.org/10.1021/NP0000318
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
2,3,4,9-Tetrahydro-6-methoxy-1H-pyrido(3,4-b)indol-1-one 87372 Click to see 216.24 unknown https://doi.org/10.4314/NJNPM.V1I1.11800
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see 199.20 unknown https://doi.org/10.4314/NJNPM.V1I1.11800
https://doi.org/10.1021/NP0000318
Evolitrine 196980 Click to see 229.23 unknown https://doi.org/10.1021/NP0000318
https://doi.org/10.4314/NJNPM.V1I1.11800
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Hydroquinolones
(3S,4R)-3,4-dihydroxy-1-methyl-3-(3-methylbut-2-enyl)-4H-quinolin-2-one 10515555 Click to see CC(=CCC1(C(C2=CC=CC=C2N(C1=O)C)O)O)C 261.32 unknown https://doi.org/10.1021/NP0000318
https://doi.org/10.4314/NJNPM.V1I1.11800
3,4-dihydroxy-1-methyl-3-(3-methylbut-2-enyl)-4H-quinolin-2-one 85168031 Click to see 261.32 unknown https://doi.org/10.1021/NP0000318
4,8-dimethoxy-N-methyl-2-quinolone 10680379 Click to see 219.24 unknown https://doi.org/10.1021/NP0000318
https://doi.org/10.4314/NJNPM.V1I1.11800
Preskimmianine 12305721 Click to see 303.35 unknown https://doi.org/10.4314/NJNPM.V1I1.11800
https://doi.org/10.1021/NP0000318
> Phenylpropanoids and polyketides / Cinnamaldehydes
(2E)-3-(3,4-dimethoxyphenyl)prop-2-enal 5375268 Click to see 192.21 unknown https://doi.org/10.1021/NP0000318
(E)-3-[4-hydroxy-3-[(1E)-3-methylbuta-1,3-dienyl]phenyl]prop-2-enal 10774990 Click to see 214.26 unknown https://doi.org/10.1016/S0304-3835(99)00147-0
https://doi.org/10.1021/NP0000318
https://doi.org/10.4314/NJNPM.V1I1.11800
3-(3,4-Dimethoxyphenyl)-2-propenal 107557 Click to see 192.21 unknown https://doi.org/10.1021/NP0000318
3-(3,4,5-Trimethoxyphenyl)-2-propenal 36798 Click to see 222.24 unknown https://doi.org/10.1021/NP0000318
3-(4-Hydroxy-3-(3-methyl-2-butenyl)phenyl)-2-propenal 6443694 Click to see CC(=CCC1=C(C=CC(=C1)C=CC=O)O)C 216.27 unknown https://doi.org/10.1021/NP0000318
3-[4-Hydroxy-3-(3-methylbut-2-enyl)phenyl]prop-2-enal 192536 Click to see CC(=CCC1=C(C=CC(=C1)C=CC=O)O)C 216.27 unknown https://doi.org/10.1021/NP0000318
3-[4-Hydroxy-3-(3-methylbuta-1,3-dienyl)phenyl]prop-2-enal 85264073 Click to see CC(=C)C=CC1=C(C=CC(=C1)C=CC=O)O 214.26 unknown https://doi.org/10.1021/NP0000318
3-{3-Methoxy-4-[(3-methylbut-2-en-1-yl)oxy]phenyl}prop-2-en-1-one 85054579 Click to see 246.30 unknown https://doi.org/10.1021/NP0000318
3,4,5-Trimethoxycinnamaldehyde, (E)- 5839209 Click to see 222.24 unknown https://doi.org/10.1021/NP0000318
Boropinal 9859693 Click to see 246.30 unknown https://doi.org/10.4314/NJNPM.V1I1.11800
https://doi.org/10.1021/NP0000318
https://doi.org/10.1016/S0304-3835(99)00147-0
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(E)-3-[4-hydroxy-3-[(E)-3-oxobut-1-enyl]phenyl]prop-2-enal 10488891 Click to see 216.23 unknown https://doi.org/10.4314/NJNPM.V1I1.11800
https://doi.org/10.1021/NP0000318
3-[4-Hydroxy-3-(3-oxobut-1-enyl)phenyl]prop-2-enal 85157522 Click to see 216.23 unknown https://doi.org/10.1021/NP0000318
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3-[3-Methoxy-4-(3-methylbut-2-enoxy)phenyl]prop-2-enoic acid 85231400 Click to see 262.30 unknown https://doi.org/10.1021/NP0000318
Boropinic Acid 10682896 Click to see 262.30 unknown https://doi.org/10.1021/NP0000318
https://doi.org/10.4314/NJNPM.V1I1.11800
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1021/NP0000318
https://doi.org/10.4314/NJNPM.V1I1.11800
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1021/NP0000318
https://doi.org/10.4314/NJNPM.V1I1.11800
> Phenylpropanoids and polyketides / Cinnamyl alcohols
(E)-3-[3-methoxy-4-(3-methylbut-2-enoxy)phenyl]prop-2-en-1-ol 10220553 Click to see CC(=CCOC1=C(C=C(C=C1)C=CCO)OC)C 248.32 unknown https://doi.org/10.1021/NP0000318
https://doi.org/10.4314/NJNPM.V1I1.11800
https://doi.org/10.1016/S0304-3835(99)00147-0
3-(3,4,5-Trimethoxyphenyl)-2-propen-1-ol 73924 Click to see COC1=CC(=CC(=C1OC)OC)C=CCO 224.25 unknown https://doi.org/10.1021/NP0000318
3-{3-Methoxy-4-[(3-methylbut-2-en-1-yl)oxy]phenyl}prop-2-en-1-ol 71348275 Click to see CC(=CCOC1=C(C=C(C=C1)C=CCO)OC)C 248.32 unknown https://doi.org/10.1021/NP0000318
3,4,5-Trimethoxycinnamyl alcohol 6436306 Click to see COC1=CC(=CC(=C1OC)OC)C=CCO 224.25 unknown https://doi.org/10.1021/NP0000318
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Braylin 618370 Click to see 258.27 unknown https://doi.org/10.1021/NP0000318
https://doi.org/10.4314/NJNPM.V1I1.11800
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone 6453244 Click to see 270.28 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 / Flavonoids / Flavones
(2S,3S,4S,5R,6S)-6-[6-(5,7-dihydroxy-4-oxochromen-2-yl)-2,3-dihydroxyphenoxy]-3,4,5-trihydroxyoxane-2-carboxylic acid 11798847 Click to see 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 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
Myricetin 3-O-glucuronide 5487413 Click to see 494.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
((2S,3R,4R,5R,6S)-2-(5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl)oxy-4,5-dihydroxy-6-methyloxan-3-yl) 3,4,5-trihydroxybenzoate 5316590 Click to see 616.50 unknown via CMAUP database
5,6,7,8-tetrahydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 10961589 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C(=C(C(=C3C2=O)O)O)O)O)C4=CC=C(C=C4)O)O)O)O 464.40 unknown via CMAUP database
Afzelin 5316673 Click to see 432.40 unknown via CMAUP database
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
Myricitrin 5281673 Click to see 464.40 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
quercetin-7-O-(6''-gallate)-glucoside 100968215 Click to see 616.50 unknown via CMAUP database

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