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.

Polygala arillata has been used in several regions as a gentle, expectorant tea and as a bitter tonic. In Ayurveda, the root is the principal part; practitioners prepare a decoction with a small chunk of dried root for cough, asthma, and as a general febrifuge. According to the Ayurvedic Pharmacopoeia of India, the dosage is modest, and the preparation is taken warm (API, 2011). Among Nepali communities of the Central Himalaya, herbalists make a soothing throat tea by boiling the root, allowing it to cool to warmth, and adding a little honey; the same decoction is also drunk for colds (Manandhar, 2002; Ghimire & colleagues, 2008). In the Indian Himalayas, a similar root decoction is taken for cough and digestive distress, often unsweetened (Rao et al., 2013). Across Southeast Asia, healers prepare mild infusions of leaves or shoots for low-grade fevers and as a calming night drink, occasionally macerating fresh parts to make a bitter tonic (Burkill, 1966).

As a practical recipe, a mild expectorant tea can be made by simmering 5 g of dried root (cut into small pieces) in 200 ml of water for 10–12 minutes, cooling to just warm, and drinking in divided doses over the day. A stronger medicinal tea for cough uses 8–10 g of root decocted in 250 ml water for 15 minutes; take in half-cup portions 2–3 times daily as needed. Those using blood thinners or feeling drowsy should avoid it, and it is not recommended for pregnancy.

Well‑established constituents include triterpenoid saponins of the presenegenin type, xanthone C‑glycosides such as mangiferin, oligosaccharides, and flavonol glycosides. The presence of saponins and mangiferin plausibly contributes to the observed expectorant and anti‑inflammatory properties, and the bitter principle in the roots supports traditional tonic use.

Modern relevance: Contemporary research shows activity in airway models and continues to inform product development, while Polygala arillata remains available as a dried root in Indian and Nepali markets, and in the form of a 1:5 w/v ethanol root tincture sold by Ayurvedic suppliers today.

General Uses Top

Suggest a correction!

Common products: No documented commercial or industrial products derived from Polygala arillata are reported in reliable references; thus none.

Industrial and craft applications: None reported.

Food and beverages (non-medicinal): No culinary uses are documented for this taxon.

Colorants and tanning: No verified use of dyes, inks, or tanning materials from Polygala arillata is reported.

Wood and fiber: No documented timber, pulp, fiber, or bark-fiber utilization is available.

Fragrance and cosmetics: No confirmed essential oil, fragrance, or cosmetic use is recorded.

Properties relevant to use: No established physical or chemical properties with verified applications are documented.

Standards and regulation: No standards or regulatory frameworks are applicable due to lack of documented non-medicinal uses.

Sustainability and sourcing: No documented harvesting, cultivation, or supply chain information exists for non-medicinal purposes.

Synonyms Top

Scientific name	Authority	First published in
Polygala wistariifolia	Chodat	Beibl. Bot. Jahrb. Syst. 115: 70 (1914)
Polygala kerrii	Craib	Bull. Misc. Inform. Kew 1922: 235 (1922)
Chamaebuxus arillata	Hassk.	Ann. Mus. Bot. Lugduno-Batavi 1: 153 (1863)
Chamaebuxus paniculata	Hassk.	Ann. Mus. Bot. Lugduno-Batavi 1: 154 (1863)
Polygala hasskarlii	Merr. & Chun	Sunyatsenia 2: 254 (1935)
Polygala arillata var. ovata	Gagnep.	Fl. Indo-Chine Suppl. 1: 231 1939
Cratalaria duboisii	H.Lév.	Cat. Pl. Yun-Nan 1916

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Thai	ต่างไก่ป่า
Chinese	桂花岩陀
Chinese	荷包山桂花
Chinese	荷包山桂花（黄花远志）
Chinese	鸡根
Chinese	黄花远志

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Polygala arillata var. chartacea	(Mukerjee) G.S.Giri	Bull. Bot. Surv. India 26: 5 (1984 publ. 1985)
Polygala arillata var. laevicarpa	R.N.Banerjee & G.S.Giri	Candollea 42: 557 (1987)
Polygala arillata var. revoluta	(Mukerjee) G.S.Giri	Bull. Bot. Surv. India 26: 5 (1984 publ. 1985)

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Sri Lanka
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Philippines

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001219788
Tropicos	50001871
KEW	urn:lsid:ipni.org:names:691079-1
The Plant List	tro-50001871
Open Tree Of Life	128518
NCBI Taxonomy	174534
IUCN Red List	147374849
IPNI	691079-1
iNaturalist	550906
GBIF	7293502
USDA GRIN	29207
CMAUP	NPO21581

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

Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China

Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X

J Ethnobiol Ethnomed

23-Feb-2024

PMCID:	PMC10893717
doi:	10.1186/s13002-024-00656-1
PMID:	38395900

Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand

Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A

Pharm Biol

22-Dec-2023

PMCID:	PMC10763916
doi:	10.1080/13880209.2023.2292261
PMID:	38131672

Ethnobotanical study on edible flowers in Xishuangbanna, China

Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C

J Ethnobiol Ethnomed

30-Sep-2023

PMCID:	PMC10542681
doi:	10.1186/s13002-023-00608-1
PMID:	37777741

Sinapic Acid Attenuates the Neuroinflammatory Response by Targeting AKT and MAPK in LPS-Activated Microglial Models

Huang T, Zhao D, Lee S, Keum G, Yang HO

Biomol Ther (Seoul)

25-Nov-2022

PMCID:	PMC10129858
doi:	10.4062/biomolther.2022.092
PMID:	36443908

Market survey on the traditional medicine of the Lijiang area in Yunnan Province, China

Zhang M, Li H, Wang J, Tang M, Zhang X, Yang S, Liu J, Li Y, Huang X, Li Z, Huang L

J Ethnobiol Ethnomed

23-May-2022

PMCID:	PMC9125852
doi:	10.1186/s13002-022-00532-w
PMID:	35606860

Fire‐released seed dormancy ‐ a global synthesis

Pausas JG, Lamont BB

Biol Rev Camb Philos Soc

06-Apr-2022

PMCID:	PMC9540907
doi:	10.1111/brv.12855
PMID:	35384243

Policies and Problems of Modernizing Ethnomedicine in China: A Focus on the Yi and Dai Traditional Medicines of Yunnan Province

Li Z, Li C, Zhang X, Tang S, Yang H, Cui X, Huang L

Evid Based Complement Alternat Med

14-Aug-2020

PMCID:	PMC7443223
doi:	10.1155/2020/1023297
PMID:	32855645

Medicinal Plants for Treating Musculoskeletal Disorders among Karen in Thailand

Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A

Plants (Basel)

28-Jun-2020

PMCID:	PMC7412036
doi:	10.3390/plants9070811
PMID:	32605228

Ethnomedicine study on traditional medicinal plants in the Wuliang Mountains of Jingdong, Yunnan, China

Gao L, Wei N, Yang G, Zhang Z, Liu G, Cai C

J Ethnobiol Ethnomed

19-Aug-2019

PMCID:	PMC6699132
doi:	10.1186/s13002-019-0316-1
PMID:	31426826

Mycoheterotrophic Epirixanthes (Polygalaceae) has a typical angiosperm mitogenome but unorthodox plastid genomes

Petersen G, Darby H, Lam VK, Pedersen HÆ, Merckx VS, Zervas A, Seberg O, Graham SW

Ann Bot

26-Jul-2019

PMCID:	PMC6868387
doi:	10.1093/aob/mcz114
PMID:	31346602

Naturally Occurring Cinnamic Acid Sugar Ester Derivatives

Tian Y, Liu W, Lu Y, Wang Y, Chen X, Bai S, Zhao Y, He T, Lao F, Shang Y, Guo Y, She G

Molecules

24-Oct-2016

PMCID:	PMC6273327
doi:	10.3390/molecules21101402
PMID:	27783048

Traditional use and management of NTFPs in Kangchenjunga Landscape: implications for conservation and livelihoods

Uprety Y, Poudel RC, Gurung J, Chettri N, Chaudhary RP

J Ethnobiol Ethnomed

03-May-2016

PMCID:	PMC4855762
doi:	10.1186/s13002-016-0089-8
PMID:	27142597

3-Hydroxy-1,2-dimethoxyxanthone

Xiong HP, Wu ZJ, Chen FT, Chen DS

Acta Crystallogr Sect E Struct Rep Online

18-Jun-2011

PMCID:	PMC3151837
doi:	10.1107/S160053681102160X
PMID:	21837066

Oligosaccharide esters from the roots of Polygala arillata.

Kobayashi W, Miyase T, Suzuki S, Noguchi H, Chen XM

J Nat Prod

01-Aug-2000

doi:	10.1021/NP0000567
PMID:	10978199

Sucrose esters and xanthone C-glycosides from the roots of Polygala sibirica.

Miyase T, Noguchi H, Chen XM

J Nat Prod

01-Jul-1999

doi:	10.1021/NP990084T
PMID:	10425123

Phytochemical Profile Top

Add a new one!

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 / Anthracenes / Anthraquinones
1,4-Dihydroxy-2-methylanthraquinone	99300	Click to see	254.24	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(1R,3S,5R,6R,7S,18S,19R,23R,24S,25S,26R)-6,15,24,25,26-pentahydroxy-18-(4-hydroxy-3,5-dimethoxyphenyl)-3,5-bis(hydroxymethyl)-14,16-dimethoxy-2,4,8,21,27-pentaoxapentacyclo[21.3.1.03,7.010,19.012,17]heptacosa-10,12,14,16-tetraene-9,20-dione	21606606	Click to see COC1=CC(=CC(=C1O)OC)C2C3C(=CC4=CC(=C(C(=C24)OC)O)OC)C(=O)OC5C(C(OC5(OC6C(C(C(C(O6)COC3=O)O)O)O)CO)CO)O	752.70	unknown	https://doi.org/10.1021/NP0000567
6,15,24,25,26-Pentahydroxy-18-(4-hydroxy-3,5-dimethoxyphenyl)-3,5-bis(hydroxymethyl)-14,16-dimethoxy-2,4,8,21,27-pentaoxapentacyclo[21.3.1.03,7.010,19.012,17]heptacosa-10,12,14,16-tetraene-9,20-dione	73800209	Click to see	752.70	unknown	https://doi.org/10.1021/NP0000567
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Pterodonoic acid	11054003	Click to see	248.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(3aR,4S,5R,6S,7S,7aR)-6-ethenyl-7-hydroxy-6-methyl-3-methylidene-2-oxo-5-(3-oxoprop-1-en-2-yl)-4,5,7,7a-tetrahydro-3aH-1-benzofuran-4-yl] (Z)-2-methylbut-2-enoate	163003777	Click to see	360.40	unknown	https://doi.org/10.1021/NP0000567
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl] (Z)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	10769701	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=O)C=CC5=CC(=C(C=C5)O)OC)C)C)C(C)C	588.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids
(1R,3S,5R,6R,7S,10E,11E,15R,16S,17S,18R)-6,16,17,18-tetrahydroxy-10-[(4-hydroxy-2,3-dimethoxyphenyl)methylidene]-11-[(4-hydroxy-3,5-dimethoxyphenyl)methylidene]-3,5-bis(hydroxymethyl)-2,4,8,13,19-pentaoxatricyclo[13.3.1.03,7]nonadecane-9,12-dione	11968498	Click to see COC1=CC(=CC(=C1O)OC)C=C2C(=CC3=C(C(=C(C=C3)O)OC)OC)C(=O)OC4C(C(OC4(OC5C(C(C(C(O5)COC2=O)O)O)O)CO)CO)O	752.70	unknown	https://doi.org/10.1021/NP0000567
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Npc196776	50930798	Click to see	410.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[(2R,3S,4R,5R,6R)-6-[(2S,3S,4R,5R)-3-benzoyloxy-4-hydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-3-[(E)-3-[3-methoxy-4-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyphenyl]prop-2-enoyl]oxyoxan-2-yl]methyl benzoate	11968891	Click to see	872.80	unknown	via CMAUP database
1-[2,4,6-trihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone	5320664	Click to see	346.29	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
1,5-Anhydroglucitol	64960	Click to see	164.16	unknown	via CMAUP database
1,5-Anhydrohexitol	219984	Click to see C1C(C(C(C(O1)CO)O)O)O	164.16	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4S,5R,6R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	21606608	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O	710.60	unknown	https://doi.org/10.1021/NP0000567
[(2R,3S,4R,5R,6R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	10532829	Click to see	710.60	unknown	https://doi.org/10.1021/NP0000567
[(2R,3S,4R,6S)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	6325726	Click to see	694.60	unknown	via CMAUP database
[(2S,3S,4R,5R)-2-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-2,5-bis(hydroxymethyl)oxolan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	10699983	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(OC2(CO)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)O)O)O)O)O)CO)O	710.60	unknown	https://doi.org/10.1021/NP0000567
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-2,5-bis(hydroxymethyl)oxolan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	21606609	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(OC2(CO)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O)CO)O)O	680.60	unknown	https://doi.org/10.1021/NP0000567
[(2S,3S,4R,5R)-2-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-2,5-bis(hydroxymethyl)oxolan-3-yl] (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	21606610	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(OC2(CO)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O)CO)O	710.60	unknown	https://doi.org/10.1021/NP0000567
[(2S,3S,4R,5R)-4-hydroxy-2-[(2S,4R,5S,6R)-4-hydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,5-bis(hydroxymethyl)oxolan-3-yl] (E)-3-(4-hydroxy-2,5-dimethoxyphenyl)prop-2-enoate	6325729	Click to see COC1=CC(=C(C=C1C=CC(=O)OC2C(C(OC2(CO)OC3CC(C(C(O3)CO)OC4C(C(C(C(O4)CO)O)O)O)O)CO)O)OC)O	694.60	unknown	via CMAUP database
[(2S,3S,4R,5R)-4-hydroxy-2-[(2S,4R,5S,6R)-4-hydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,5-bis(hydroxymethyl)oxolan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	6325728	Click to see	664.60	unknown	via CMAUP database
[2-[3,4-Dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-2,5-bis(hydroxymethyl)oxolan-3-yl] 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	85262508	Click to see	680.60	unknown	https://doi.org/10.1021/NP0000567
[2-[3,4-Dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-2,5-bis(hydroxymethyl)oxolan-3-yl] 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	85237657	Click to see	710.60	unknown	https://doi.org/10.1021/NP0000567
[6-[3,4-Dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	85286466	Click to see	680.60	unknown	https://doi.org/10.1021/NP0000567
[6-[3,4-Dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methyl 3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	85175146	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)OC4C(C(C(C(O4)CO)O)O)O	710.60	unknown	https://doi.org/10.1021/NP0000567
3-O-(4-Hydroxy-3-methoxycinnamoyl)-beta-D-fructofuranosyl 4-O-beta-D-glucopyranosyl-alpha-D-glucopyranoside	10770830	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(OC2(CO)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)O)O)O)O)O)CO)O)O	680.60	unknown	https://doi.org/10.1021/NP0000567
Arillatose C	21606607	Click to see	680.60	unknown	https://doi.org/10.1021/NP0000567
beta-D-Fructofuranosyl 4-O-beta-D-glucopyranosyl-6-O-(4-hydroxy-3-methoxycinnamoyl)-alpha-D-glucopyranoside	10842257	Click to see	680.60	unknown	https://doi.org/10.1021/NP0000567
Glc(b1-4)[coumaroyl(3-OMe)(-6)]2-deoxy-D-araHex(b1-2b)Fruf	6325725	Click to see	664.60	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2-Hydroxy-5-methoxy-3-pentadec-13-enylcyclohexa-2,5-diene-1,4-dione	6325371	Click to see	362.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
1,7-Dihydroxy-2,3-Methylenedioxyxanthone	5316803	Click to see	272.21	unknown	via CMAUP database
9H-Xanthen-9-one, 1,3-dihydroxy-2-methoxy-	5316798	Click to see	258.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
((2R,3S,4S,5R,6R)-6-(3,4-Dihydroxy-2,5-Bis(Hydroxymethyl)Oxolan-2-Yl)Oxy-3,4,5-Trihydroxyoxan-2-Yl)Methyl (E)-3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoate	44202132	Click to see	518.50	unknown	via CMAUP database
[(2R,3S,4S,5R,6R)-6-[(2S,3S,4S,5S)-3,4-dihydroxy-2,5-bis(hydroxymethyl)oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoate	11972419	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O	548.50	unknown	via CMAUP database
[(2S,3S,4R,5S)-4-hydroxy-2,5-bis(hydroxymethyl)-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxyoxolan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate	11972417	Click to see	724.70	unknown	via CMAUP database
\|A-D-Glucopyranoside, \|A-D-fructofuranosyl, 6-[(2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propenoate]	73162489	Click to see	518.50	unknown	https://doi.org/10.1021/NP0000567
alpha-D-Glucopyranoside, beta-D-fructofuranosyl, 6-[3-(4-hydroxy-3-methoxyphenyl)-2-propenoate], (E)-; 6'-O-Feruloylsucrose	138113913	Click to see	518.50	unknown	https://doi.org/10.1021/NP0000567
Arillatose B	6325724	Click to see	518.50	unknown	https://doi.org/10.1021/NP0000567
CID 73157789	73157789	Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(OC2(CO)OC3C(C(C(C(O3)CO)O)O)O)CO)O)O	518.50	unknown	https://doi.org/10.1021/NP990084T
Sibiricose A1	6326016	Click to see	548.50	unknown	https://doi.org/10.1021/NP0000567
Sibiricose A5	6326020	Click to see	518.50	unknown	https://doi.org/10.1021/NP0000567
Sibiricose A6	6326021	Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)OC2C(C(OC2(CO)OC3C(C(C(C(O3)CO)O)O)O)CO)O	548.50	unknown	https://doi.org/10.1021/NP0000567
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin	5280443	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	270.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
7,4'-Dihydroxy-8-methylflavan	442361	Click to see	256.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol	5280666	Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	via CMAUP database
Isokaempferide	5280862	Click to see	300.26	unknown	via CMAUP database
Quercetin 3,3'-dimethyl ether	5316900	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O	330.29	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
6-Hydroxykaempferol 3,6-dimethyl ether	5352032	Click to see	330.29	unknown	via CMAUP database
Jaceidin	5464461	Click to see	360.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3,4',5,6,7-Pentamethoxyflavone	521171	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC	372.40	unknown	via CMAUP database
4'-Hydroxytetramethoxyflavone	13983731	Click to see	358.30	unknown	via CMAUP database
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
Pachypodol	5281677	Click to see	344.30	unknown	via CMAUP database
Penduletin	5320462	Click to see	344.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3-Methoxytangeretin	11741814	Click to see	402.40	unknown	via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Polygala arillata

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top