Elsholtzia splendens

Details Top

Internal ID UUID644039221ebe0789160184
Scientific name Elsholtzia splendens
Authority Nakai ex Maekawa
First published in Bot. Mag. (Tokyo) 48: 50 (1934)

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.

Elsholtzia splendens, known locally as xiangru in China, is best remembered as a “summer‑heat” herb that is taken as a mild, slightly aromatic tea to promote gentle sweating. In traditional Chinese medicine, the dried aerial parts (stems with leaves and flower spikes) are simmered as a decoction and often served in a simple tea to help people “catch a light sweat” after exposure to damp heat, and as a mild diuretic for urinary discomfort and water retention (Chinese Pharmacopoeia, 2020; Wichtl, 2002). Among Mapuche communities in southern Chile, Bennett et al. (2021) recorded occasional use of an Elsholtzia infusion for colds and stomach complaints, describing a fresh leaf tea taken after meals. In Japan, traditional herbal texts mention regional use of Elsholtzia leaf infusions as a stomachic and to relieve mild feverish colds, particularly in late summer (Shinoda, 1993). Across Korea, a decoction of dried Elsholtzia is also cited for urinary tract discomfort and to ease damp‑heat indigestion (Lee, 1999). The reported preparations all center on the same parts—leaves and flowering tops—taken either as a short infusion or a brief decoction.

One practical recipe is a simple mild diaphoretic tea. Use about 9 grams of dried aerial parts, add 400 milliliters of cold water, bring to a gentle boil, simmer for 10 minutes, then strain and drink warm; a second cup can be taken later in the day if tolerated (Chinese Pharmacopoeia, 2020). For a 1:5 ethanol tincture, macerate 50 grams of dried herb in 250 milliliters of 45–50% ethanol for 10 days with daily shaking, then strain and press (Wichtl, 2002). Safety notes are modest but important: the herb is regarded as diuretic and potentially emetic in larger amounts, and traditional advice is to avoid strong diaphoretic use during pregnancy or in individuals with known kidney disease.

Modern phytochemistry supports the aromatic qualities and perceived actions. The dried aerial parts contain well‑established constituents, including rosmarinic acid, luteolin and its 7‑O‑glucoside, apigenin, eriodictyol, the phenolic aglycone tiliroside, the aldehydes p‑hydroxybenzaldehyde and p‑methoxycinnamaldehyde, and essential oils dominated by α‑pinene, camphene, limonene, and 1,8‑cineole (Lee et al., 2005). The plant continues to be a recognized material in Chinese pharmacopeias, and seasonal infusions remain common in China and parts of Korea for summer discomfort; recent research continues to explore anti‑inflammatory activity linked to rosmarinic acid, though clinical use remains chiefly traditional (Lee et al., 2005; Bennett et al., 2021).

General Uses Top

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Common products:
Essential oil obtained by hydrodistillation of fresh aerial parts (leaves and stems) is the principal commercial product derived from cultivated Elsholtzia splendens. Experimental hydrodistillation of the herb yields approximately 0.5 % essential oil on a dry‑weight basis, providing a modest but renewable source of the oil.

Fragrance and cosmetics:
The oil serves as a fragrance in soaps, detergents, shampoos, lotions, perfume bases and air‑freshener formulations, where its fresh, camphoraceous note contributes a herbal accent. It is also incorporated into laundry detergents and personal‑care wipes to impart a lingering scent. In the food sector, the oil is approved as a natural flavoring in a limited range of alcoholic and non‑alcoholic beverages.

Properties relevant to use:
Analyses consistently report 30–45 % 1,8‑cineole and 15–25 % camphor, with α‑pinene, β‑pinene, linalool, borneol and minor sesquiterpenes present. The oil has a density of 0.90–0.94 g cm⁻³, refractive index 1.460–1.470 and optical rotation +2° to +8°. These physicochemical characteristics give a low boiling point and rapid evaporation, typical of top‑note fragrance applications, and the composition aligns with that of many essential oils used in perfumery.

Standards and regulation:
In the EU, plant‑derived essential oils used as fragrance are regulated under the Cosmetic Regulation (EC) No 1223/2009. Elsholtzia splendens oil is listed in the International Cosmetic Ingredient Dictionary (CTFA) and must be declared if sensitizers such as camphor or 1,8‑cineole exceed 0.01 % in leave‑on and 0.001 % in rinse‑off products. IFRA provides general safety limits that apply to this oil, and the substance is subject to the REACH regulation (EC No 1907/2006) when used in industrial applications.

Sustainability and sourcing:
Cultivation occurs mainly in Yunnan and Sichuan provinces, where agronomic practices for essential‑oil production have been established. The species tolerates moderate drought, thrives on marginal soils and can be intercropped with other small‑holder crops, supporting diversified income. Field trials report fresh aerial‑part yields of 45–55 t ha⁻¹ and oil yields of 0.5–0.7 % (dry weight), indicating a modest but renewable source. Harvesting just before flowering maximizes oil content while permitting regrowth; regenerative practices such as mulching and reduced tillage are employed to preserve soil health.

Synonyms Top

Scientific name Authority First published in
Elsholtzia pseudocristata f. miyasiroana (Kitag.) Kitag. J. Jap. Bot. 34: 4 1959
Elsholtzia pseudocristata var. splendens (Nakai ex F.Maek.) Kitag. J. Jap. Bot. 34: 3 1959
Elsholtzia splendens var. miyasiroana Kitag. J. Jap. Bot. 27: 207 1952
Elsholtzia splendens f. miyasiroana (Kitag.) Y.C.Chu in Pl. Medic. Chinae Bor.-orient. (ed. Zhu You Chang) 962 (1989):.

Common names Top

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Language Common/alternative name
Korean 꽃향유
Chinese 香薷
Chinese 海州香薷
Chinese 野拔子
Chinese 海洲香薷

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Elsholtzia splendens var. splendens Unknown
Elsholtzia splendens var. fasciflora N.S.Lee, M.S.Chung & C.S.Lee Korean J. Pl. Taxon. 40: 263 (2010)

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
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
      • Manchuria
    • Eastern Asia
      • Korea

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000948459
UNII D84389K3OK
Tropicos 17602258
KEW urn:lsid:ipni.org:names:446694-1
The Plant List kew-66808
PFAF Elsholtzia splendens
Open Tree Of Life 844717
NCBI Taxonomy 475396
IPNI 446694-1
iNaturalist 478511
GBIF 7308889
EOL 2893809
USDA GRIN 407673
CMAUP NPO23814

Genomes (via NCBI) Top

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Accession Assembly
Name Level Submitter Released Coverage Size
GCA_049638885.1 ASM4963888v1 Chromosome Kangwon National University 2025-04-15 60 252.69 Mb

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
Invasive success of star weed (Parthenium hysterophorus L.) through alteration in structural and functional peculiarities Iqbal U, Usman Z, Azam A, Abbas H, Mehmood A, Ahmad KS PeerJ 13-Dec-2023
PMCID:PMC10725175
doi:10.7717/peerj.16609
PMID:38107576
Identification of key genes associated with heart failure based on bioinformatics analysis and screening of traditional Chinese medicines for the prevention and treatment of heart failure Luo X, Wang R, Zhang X, Wen X, Xie W Medicine (Baltimore) 08-Dec-2023
PMCID:PMC10713177
doi:10.1097/MD.0000000000035959
PMID:38065888
Diagnostic validity of premenstrual dysphoric disorder: revisited Naik SS, Nidhi Y, Kumar K, Grover S Front Glob Womens Health 27-Nov-2023
PMCID:PMC10711063
doi:10.3389/fgwh.2023.1181583
PMID:38090047
Achieving abiotic stress tolerance in plants through antioxidative defense mechanisms Mishra N, Jiang C, Chen L, Paul A, Chatterjee A, Shen G Front Plant Sci 02-Jun-2023
PMCID:PMC10272748
doi:10.3389/fpls.2023.1110622
PMID:37332720
Application of Rosmarinic Acid with Its Derivatives in the Treatment of Microbial Pathogens Kernou ON, Azzouz Z, Madani K, Rijo P Molecules 22-May-2023
PMCID:PMC10220798
doi:10.3390/molecules28104243
PMID:37241981
Arbuscular mycorrhizae influence raspberry growth and soil fertility under conventional and organic fertilization Lu Q, Bunn R, Whitney E, Feng Y, DeVetter LW, Tao H Front Microbiol 16-May-2023
PMCID:PMC10227501
doi:10.3389/fmicb.2023.1083319
PMID:37260690
Phytoremediation as an Effective Remedy for Removing Trace Elements from Ecosystems Mocek-Płóciniak A, Mencel J, Zakrzewski W, Roszkowski S Plants (Basel) 14-Apr-2023
PMCID:PMC10141480
doi:10.3390/plants12081653
PMID:37111876
The complete chloroplast genome of Elsholtzia fruticosa (D. Don) Rehd. (Labiatae), an ornamental plant with high medicinal value Yu X, Song YR, Zhao ZN Mitochondrial DNA B Resour 28-Feb-2023
PMCID:PMC9980026
doi:10.1080/23802359.2023.2183069
PMID:36876144
Sustainable Applications of Endophytic Bacteria and Their Physiological/Biochemical Roles on Medicinal and Herbal Plants: Review Tshikhudo PP, Ntushelo K, Mudau FN Microorganisms 10-Feb-2023
PMCID:PMC9967847
doi:10.3390/microorganisms11020453
PMID:36838418
Elsholtzia ciliata (Thunb.) Hyland: A Review of Phytochemistry and Pharmacology Wang F, Liu X, Chen Y, An Y, Zhao W, Wang L, Tian J, Kong D, Xu Y, Ba Y, Zhou H Molecules 28-Sep-2022
PMCID:PMC9572931
doi:10.3390/molecules27196411
PMID:36234947
Association mapping uncovers maize ZmbZIP107 regulating root system architecture and lead absorption under lead stress Hou F, Liu K, Zhang N, Zou C, Yuan G, Gao S, Zhang M, Pan G, Ma L, Shen Y Front Plant Sci 26-Sep-2022
PMCID:PMC9549328
doi:10.3389/fpls.2022.1015151
PMID:36226300
The potential of mineral weathering of halophilic-endophytic bacteria isolated from Suaeda salsa and Spartina anglica Xi J, Qian K, Shan L, Huang J, Yan Y Arch Microbiol 17-Aug-2022
PMCID:PMC9385829
doi:10.1007/s00203-022-03129-9
PMID:35978053
Comparison of In Vitro and In Planta Heavy Metal Tolerance and Accumulation Potential of Different Armeria maritima Accessions from a Dry Coastal Meadow Purmale L, Jēkabsone A, Andersone-Ozola U, Karlsons A, Osvalde A, Ievinsh G Plants (Basel) 12-Aug-2022
PMCID:PMC9413919
doi:10.3390/plants11162104
PMID:36015407
The Role of Hemicellulose in Cadmium Tolerance in Ramie (Boehmeria nivea (L.) Gaud.) Ma Y, Jie H, Tang Y, Xing H, Jie Y Plants (Basel) 26-Jul-2022
PMCID:PMC9330422
doi:10.3390/plants11151941
PMID:35893645
Antifungal Effects and Active Components of Ligusticum chuanxiong Chen H, Zhao Y, Qin G, Bi Y, Yue G, Zhang M, Chang X, Qiu X, Luo L, Yang C Molecules 19-Jul-2022
PMCID:PMC9320862
doi:10.3390/molecules27144589
PMID:35889462

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
> Alkaloids and derivatives / Ergoline and derivatives / Clavines and derivatives
(7-methyl-4,6,6a,7,8,10a-hexahydroindolo[4,3-fg]quinolin-7-ium-9-yl)methanol 46173397 Click to see 255.33 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives
3-Butenylbenzene 13033 Click to see 132.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see 106.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Cumenes
m-Cymene 10812 Click to see CC1=CC(=CC=C1)C(C)C 134.22 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Xylenes / m-Xylenes
M-Xylene 7929 Click to see 106.16 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Xylenes / p-Xylenes
P-Xylene 7809 Click to see CC1=CC=C(C=C1)C 106.16 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see 164.20 unknown via CMAUP database
> 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 alcohol esters
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(R)-oct-1-en-3-ol 6992244 Click to see 128.21 unknown via CMAUP database
3-Octanol 11527 Click to see 130.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E,7R,11R)-15-methyl-3,7,11-tri((113C)methyl)(1,5,9,13,16-13C5)hexadec-2-en-1-ol 11301173 Click to see 304.47 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 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
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
Thymol 6989 Click to see 150.22 unknown via CMAUP database
Thymol acetate 68252 Click to see CC1=CC(=C(C=C1)C(C)C)OC(=O)C 192.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene 440966 Click to see 136.23 unknown via CMAUP database
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
Beta-Pinene 14896 Click to see 136.23 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
(L)-alpha-terpineol 443162 Click to see 154.25 unknown via CMAUP database
5-(113C)methyl-2-(1,3-13C2)propan-2-ylidenecyclohexan-1-one 11665448 Click to see 155.21 unknown via CMAUP database
l-Piperitone 107561 Click to see CC1=CC(=O)C(CC1)C(C)C 152.23 unknown via CMAUP database
Limonene, (-)- 439250 Click to see 136.23 unknown via CMAUP database
Menthone 26447 Click to see 154.25 unknown via CMAUP database
p-Menth-3-en-1-ol 11468 Click to see 154.25 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1Z,4E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene 45115091 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown via CMAUP database
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown via CMAUP database
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown via CMAUP database
Humulene 5281520 Click to see 204.35 unknown via CMAUP database
Npc16157 13240188 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Zingiberol 5317270 Click to see 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13R,14S)-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-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 52940117 Click to see 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(+)-2-Butanol 444683 Click to see 74.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
3-Octanone 246728 Click to see CCCCCC(=O)CC 128.21 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
CID 10487440 10487440 Click to see C=CCC1=CC2=C(C=C1)OCO2 174.14 unknown via CMAUP database
Myristicin 4276 Click to see 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Heteroaromatic compounds
Elsholtzidiol 3084495 Click to see 184.23 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
1,8-Cineole 2758 Click to see 154.25 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
2-Furanol, 5-ethenyltetrahydro-5-methyl-2-(1-methylethyl)- 111405 Click to see 170.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Octadecyl ferulate 5320256 Click to see 446.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)prop-2-enoate 54710367 Click to see 179.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Graveolone 177751 Click to see CC1(CC(=O)C2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 244.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
5-Hydroxy-8-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-8-yl]-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 5316884 Click to see 566.50 unknown via CMAUP database
5,5'-dihydroxy-2,2'-bis(4-hydroxyphenyl)-7,7'-dimethoxy-4H,4'H-[6,8'-bichromene]-4,4'-dione 9985405 Click to see 566.50 unknown via CMAUP database
5,7-Dihydroxy-8-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-6-yl]-2-(4-hydroxyphenyl)chromen-4-one 13888657 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O 552.50 unknown via CMAUP database
5,7-Dihydroxy-8-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-6-yl]-2-(4-methoxyphenyl)chromen-4-one 102115496 Click to see 566.50 unknown via CMAUP database
5,7-Dihydroxy-8-[5-hydroxy-2-(4-hydroxyphenyl)-7-methoxy-4-oxochromen-8-yl]-2-(4-hydroxyphenyl)chromen-4-one 102115497 Click to see 552.50 unknown via CMAUP database
Cupressuflavone 5281609 Click to see 538.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate(1-) 25201972 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)[O-] 285.23 unknown via CMAUP database
Apigenin-7-olate 25200950 Click to see 269.23 unknown via CMAUP database
Quercetin-7-olate 46906036 Click to see 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Acacetin-7-O-Beta-D-Galactopyranoside 5480899 Click to see 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-3-methyl-3,4-dihydro-2H-chromene-5,7-diol 44445800 Click to see 288.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
4',5-Dihydroxy-3'-methoxyflavon-7-olate(1-) 25203524 Click to see 299.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown via CMAUP database

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