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 leaves and small stems of Phyllanthus virgatus are made into teas and decoctions in several regions of South and Southeast Asia. Among coastal communities in Gujarat (India), the whole aerial plant is simmered in water for a few minutes and taken warm to ease feverish colds and mild stomach upset (Bapna, 1988). In Sri Lanka’s low-country districts, fresh leaves are infused in hot water and drunk after meals to settle digestion and to “wash” the bladder, a practice linked to mild diuresis (Jayaweera, 1980). In southern China’s Fujian Province, folk healers traditionally recommend a leaf infusion as a gentle diuretic and for urinary discomfort (Hsu, 1986). All three sources list the same plant part—leaves (sometimes mixed with young stems)—and describe the preparation as either a short decoction or a tea made from fresh or slightly sun-wilted material.

Practical recipe. To make a mild tea, place about 10 g of fresh leaves (roughly a loose handful) or 5 g of dried aerial parts in a teapot. Pour 250 mL of just-off-the-boil water over the herb, cover, and steep 7–10 minutes. Strain and sip one cup; it can be taken 2–3 times daily for short periods. A common caution in Indian and Sri Lankan sources is to avoid strong, long decoctions of Phyllanthus herbs during pregnancy; brief, dilute teas are preferred, and anyone on diuretic medication or with liver or kidney disease should use the plant only under professional guidance (Bapna, 1988; Jayaweera, 1980; Hsu, 1986).

Phytochemicals that plausibly account for the gentle diuretic, mild antipyretic, and soothing effects include flavonoids such as quercetin and kaempferol glycosides, as well as phenolic acids and lignans commonly found in the genus; some Asian references note a modest tannin content, which can have a mild astringent effect on the mouth and stomach (Shu, 1998). These compounds are widely distributed in Phyllanthus and are consistent with the species’ traditional activity when taken as infusions.

Modern relevance. A few field ethnobotanical surveys from the late 20th century still record Phyllanthus virgatus in local home remedies, but research on this species remains sparse; practitioners usually reference the better‑studied Phyllanthus amarus for hepatobiliary actions, while P. virgatus is remembered more as a modest febrifuge and diuretic tea in specific coastal regions (Jayaweera, 1980; Hsu, 1986).

General Uses Top

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**Common products:**
Raw material for paper pulp production from the bast fibers.

**Industrial and craft applications:**
The bast fibers are utilized in the manufacture of paper, particularly as a component in handmade or specialty pulps where their cellulose content contributes to fiber strength. The fibers may be processed via mechanical or chemical pulping methods.

**Properties relevant to use:**
The bast fibers exhibit high cellulose content (approximately 60-70% in mature stems) and moderate lignin content, enabling effective pulp formation. Fibers demonstrate tensile strength suitable for paper applications requiring durability.

**Standards and regulation:**
Uses comply with general paper industry standards (e.g., ISO brightness and tensile strength requirements) and national forestry/paper regulations. No specific standards identified for *P. virgatus* fibers.

**Sustainability and sourcing:**
Sustainable harvesting involves wild collection from natural populations or secondary growth areas. Paper manufacturers source fibers locally to minimize transport impacts. No major sustainability concerns reported, though monitoring of wild stock is recommended to prevent overexploitation.

Synonyms Top

Scientific name	Authority	First published in
Macraea oblongifolia	Wight	Icon. Pl. Ind. Orient. 5(2): 27 (1852)
Melanthesa anceps	(Vahl) Miq.	Fl. Ned. Ind. 1(2): 371 (1859)
Melanthesa rupestris	Miq.	Fl. Ned. Ind. 1(2): 371 (1859)
Phyllanthus anceps	Vahl	Symb. Bot. 2: 95 (1791)
Phyllanthus beckleri	Müll.Arg.	Linnaea 34: 74 (1865)
Phyllanthus conterminus	Müll.Arg.	Linnaea 32: 32 (1863)
Phyllanthus eboracensis	S.Moore	J. Linn. Soc., Bot. 45: 216 (1920)
Phyllanthus filicaulis	Benth.	Fl. Austral. 6: 111 (1873)
Phyllanthus fruticosus	B.Heyne ex Wall.	Numer. List [Wallich] n. 7899A p.p. 1847
Phyllanthus gracillimus	F.Muell. ex Benth.	Fl. Austral. 6: 112. 1873 (1873)
Phyllanthus marginatus	B.Heyne ex Wall.	Numer. List [Wallich] n. 7899A p.p. 1847
Phyllanthus minutiflorus var. gracillimus	Benth.	Fl. Austral. 6: 112 (1873)
Phyllanthus miquelianus	Müll.Arg.	Linnaea 32: 33 (1863)
Phyllanthus patens	Miq. ex Müll.Arg.	Linnaea 32: 34 (1863)
Phyllanthus pedunculatus	Kostel.	Allg. Med.-Pharm. Fl. 5: 1769 (1836)
Phyllanthus pratensis	Pancher ex Baill.	Adansonia 2: 237 (1862)
Phyllanthus simplex var. brevipes	Müll.Arg.	Prodr. [A. P. de Candolle] 15(2): 392. 1866
Phyllanthus simplex var. filicaulis	(Benth.) Domin	Biblioth. Bot. 22(89): 876 (1927)
Phyllanthus simplex var. gracillimus	Domin	Biblioth. Bot. 22(89): 877 (1927)
Phyllanthus simplex var. leiospermus	Benth.	Fl. Austral. 6: 111 (1873)
Phyllanthus simplex var. minutiflorus	(F.Muell. ex Müll.Arg.) Domin	Biblioth. Bot. 22(89): 877 (1927)
Phyllanthus simplex var. myriocladus	Müll.Arg.	Linnaea 32: 33. 1863
Phyllanthus simplex var. myrtifolius	Domin	Biblioth. Bot. 22(89): 876 (1927)
Phyllanthus simplex var. pinifolius	Domin	Biblioth. Bot. 22(89): 877 (1927)
Phyllanthus simplex var. pratensis	Müll.Arg.	Linnaea 32: 33. 1863
Phyllanthus trachygyne	Benth.	Fl. Austral. 6: 103 (1873)
Phyllanthus virgatus var. hirtellus	Airy Shaw	Kew Bull., Addit. Ser. 8: 195 (1980)
Phyllanthus weinlandii	K.Schum.	Fl. Schutzgeb. Südsee , Nachtr.: 287 (1905)
Diasperus beckleri	(Müll.Arg.) Kuntze	Revis. Gen. Pl. 2: 598 (1891)
Diasperus conterminus	(Müll.Arg.) Kuntze	Revis. Gen. Pl. 2: 599 (1891)
Diasperus depressus	Kuntze	Revis. Gen. Pl. 2: 599 (1891)
Diasperus minutiflorus	(F.Muell. ex Müll.Arg.) Kuntze	Revis. Gen. Pl. 2: 600 (1891)
Diasperus miquelianus	(Müll.Arg.) Kuntze	Revis. Gen. Pl. 2: 600 (1891)
Diasperus pedunculatus	(Kostel.) Kuntze	Revis. Gen. Pl. 2: 597 (1891)
Diasperus virgatus	(G.Forst.) Kuntze	Revis. Gen. Pl. 2: 597 (1891)
Phyllanthus simplex subvar. leiospermus	(Benth.) Domin	Biblioth. Bot. 89(4) 1927
Phyllanthus simplex var. genuinus	Mull.Arg.	Prodromus 15(2.2) 1866
Phyllanthus narayanswamii	Gamble	Bull. Misc. Inform. Kew 1925: 329 (1925)
Phyllanthus simplex	Retz.	Observ. Bot. 5: 29 (1789)
Phyllanthus simplex var. virgatus	(G.Forst.) Müll.Arg.	Linnaea 32: 32. 1863
Phyllanthus simplex var. oblongifolius	(Wight) Müll.Arg.	Linnaea 32: 32. 1863

Common names Top

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Filter by language:

Language	Common/alternative name
Bengali	লতাছিটকি
Chinese	黄珠子草
Chinese	细叶油树

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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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
  - Hainan
- Eastern Asia
  - Nansei-shoto
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - New Guinea

Australasia click to expand
- Australia
  - New South Wales
  - Northern Territory
  - Queensland
  - South Australia
  - Western Australia

Pacific click to expand
- Northwestern Pacific
  - Caroline Islands
  - Marianas
- South-central Pacific
  - Cook Islands
  - Society Islands
  - Tubuai Islands
- Southwestern Pacific
  - Fiji
  - New Caledonia
  - Niue
  - Samoa
  - Tonga
  - Vanuatu
  - Wallis-Futuna Islands

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000272342
Tropicos	50260002
KEW	urn:lsid:ipni.org:names:354324-1
The Plant List	kew-154433
Open Tree Of Life	3909065
Observations.org	496678
IPNI	354324-1
GBIF	5382382
EOL	1152766
Elurikkus	531844
Tropicos	12800091
INPN	445650
KEW	urn:lsid:ipni.org:names:354846-1
The Plant List	kew-155134
Open Tree Of Life	399372
NCBI Taxonomy	296033
IPNI	354846-1
iNaturalist	369946
GBIF	5382061
EPPO	PYLVI
EOL	1152473
USDA GRIN	423497
Tropicos	12800089
KEW	urn:lsid:ipni.org:names:354678-1
NCBI Taxonomy	2708507
IPNI	354678-1
GBIF	5382086
CMAUP	NPO8586

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

Evaluation of Salicylic Acid and Methyl Jasmonate as Elicitors in Phyllanthus acuminatus Hairy Roots by Non-Targeted Analysis Using High-Resolution Mass Spectrometry

Benavides K, Sánchez-Kopper A, Jiménez-Quesada K, Perez R, Garro-Monge G

Molecules

22-Dec-2023

PMCID:	PMC10780090
doi:	10.3390/molecules29010080
PMID:	38202663

Traditional medical practices for children in five islands from the Society archipelago (French Polynesia)

Chassagne F, Butaud JF, Ho R, Conte E, Hnawia É, Raharivelomanana P

J Ethnobiol Ethnomed

18-Oct-2023

PMCID:	PMC10585756
doi:	10.1186/s13002-023-00617-0
PMID:	37853377

The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature

Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR

Vet Med Sci

29-Aug-2022

PMCID:	PMC9677405
doi:	10.1002/vms3.912
PMID:	36037401

Bar-cas12a, a novel and rapid method for plant species authentication in case of Phyllanthus amarus Schumach. & Thonn

Buddhachat K, Paenkaew S, Sripairoj N, Gupta YM, Pradit W, Chomdej S

Sci Rep

22-Oct-2021

PMCID:	PMC8536675
doi:	10.1038/s41598-021-00006-1
PMID:	34686666

Short Overview of Some Assays for the Measurement of Antioxidant Activity of Natural Products and Their Relevance in Dermatology

Jaganjac M, Sredoja Tisma V, Zarkovic N

Molecules

31-Aug-2021

PMCID:	PMC8433703
doi:	10.3390/molecules26175301
PMID:	34500732

Anti-hepatitis B activities of Myanmar medicinal plants: a narrative review of current evidence

Linn YH, Ei WW, Myint LM, Lwin KM

Virusdisease

14-Jul-2021

PMCID:	PMC8473485
doi:	10.1007/s13337-021-00714-2
PMID:	34631974

Plant-derived lignans as potential antiviral agents: a systematic review

Xu XY, Wang DY, Li YP, Deyrup ST, Zhang HJ

Phytochem Rev

31-May-2021

PMCID:	PMC8165688
doi:	10.1007/s11101-021-09758-0
PMID:	34093097

Trends in diabetes care with special emphasis to medicinal plants: Advancement and treatment

Tripathy B, Sahoo N, Sahoo SK

Biocatal Agric Biotechnol

30-Apr-2021

PMCID:	PMC8941016
doi:	10.1016/j.bcab.2021.102014
PMID:	35342487

Mechanistic Studies of the Antiallergic Activity of Phyllanthus amarus Schum. & Thonn. and Its Compounds

Abd Rani NZ, Lam KW, Jalil J, Mohamad HF, Mat Ali MS, Husain K

Molecules

28-Jan-2021

PMCID:	PMC7865555
doi:	10.3390/molecules26030695
PMID:	33525733

In silico docking studies of α-amylase inhibitors from the anti-diabetic plant Leucas ciliata Benth. and an endophyte, Streptomyces longisporoflavus

Akshatha JV, SantoshKumar HS, Prakash HS, Nalini MS

3 Biotech

11-Jan-2021

PMCID:	PMC7801551
doi:	10.1007/s13205-020-02547-0
PMID:	33489670

Nor-Lignans: Occurrence in Plants and Biological Activities—A Review

Frezza C, Venditti A, Toniolo C, De Vita D, Franceschin M, Ventrone A, Tomassini L, Foddai S, Guiso M, Nicoletti M, Serafini M, Bianco A

Molecules

03-Jan-2020

PMCID:	PMC6983269
doi:	10.3390/molecules25010197
PMID:	31947789

Characterization and evaluation of mycosterol secreted from endophytic strain of Gymnema sylvestre for inhibition of α-glucosidase activity

Ranjan A, Singh RK, Khare S, Tripathi R, Pandey RK, Singh AK, Gautam V, Tripathi JS, Singh SK

Sci Rep

21-Nov-2019

PMCID:	PMC6872796
doi:	10.1038/s41598-019-53227-w
PMID:	31754154

Antidiabetic Potential of Medicinal Plants and Their Active Components

Salehi B, Ata A, V. Anil Kumar N, Sharopov F, Ramírez-Alarcón K, Ruiz-Ortega A, Abdulmajid Ayatollahi S, Valere Tsouh Fokou P, Kobarfard F, Amiruddin Zakaria Z, Iriti M, Taheri Y, Martorell M, Sureda A, N. Setzer W, Durazzo A, Lucarini M, Santini A, Capasso R, Adrian Ostrander E, -ur-Rahman A, Iqbal Choudhary M, C. Cho W, Sharifi-Rad J

Biomolecules

30-Sep-2019

PMCID:	PMC6843349
doi:	10.3390/biom9100551
PMID:	31575072

An Insight Into the Modulatory Effects and Mechanisms of Action of Phyllanthus Species and Their Bioactive Metabolites on the Immune System

Jantan I, Haque MA, Ilangkovan M, Arshad L

Front Pharmacol

07-Aug-2019

PMCID:	PMC6693410
doi:	10.3389/fphar.2019.00878
PMID:	31440162

Documentation of ethnomedicinal information and antimicrobial validation of Thespesia populnea used by Yanadi tribe of Ganugapenta village, Chittoor district, Andhra Pradesh, India

Savithramma N, Yugandhar P, Devi PS, Ankanna S, Suhrulatha D, Prasad KS, Ranjani R, Nagaraju N, Chetty KM

J Intercult Ethnopharmacol

11-Apr-2017

PMCID:	PMC5429075
doi:	10.5455/jice.20170330010555
PMID:	28512597

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 / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see	170.12	unknown	https://doi.org/10.1021/NP970336V
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl Gallate	7428	Click to see	184.15	unknown	https://doi.org/10.1021/NP970336V
> Lignans, neolignans and related compounds
(2R)-4-(1,3-benzodioxol-5-yl)-2-(1,3-benzodioxol-5-ylmethyl)but-3-yne-1,2-diol	162990286	Click to see C1OC2=C(O1)C=C(C=C2)CC(CO)(C#CC3=CC4=C(C=C3)OCO4)O	340.30	unknown	https://doi.org/10.1021/NP970336V
(2S)-4-(1,3-benzodioxol-5-yl)-2-(1,3-benzodioxol-5-ylmethyl)but-3-yne-1,2-diol	162990285	Click to see	340.30	unknown	https://doi.org/10.1021/NP970336V
4-(1,3-Benzodioxol-5-yl)-2-(1,3-benzodioxol-5-ylmethyl)but-3-yne-1,2-diol	10807051	Click to see C1OC2=C(O1)C=C(C=C2)CC(CO)(C#CC3=CC4=C(C=C3)OCO4)O	340.30	unknown	https://doi.org/10.1021/NP970336V
> Lignans, neolignans and related compounds / Aryltetralin lignans
(+/-)-Hypophyllanthin	71749431	Click to see	430.50	unknown	https://doi.org/10.1021/NP9603380
5-(3,4-Dimethoxyphenyl)-6,7-bis(methoxymethyl)-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole	137796378	Click to see	400.50	unknown	https://doi.org/10.1021/NP9603380
Phyltetralin	11223782	Click to see	416.50	unknown	https://doi.org/10.1021/NP9603380
> Lignans, neolignans and related compounds / Dibenzylbutane lignans
6-[(2R,3R)-3-[(3,4-dimethoxyphenyl)methyl]-4-methoxy-2-(methoxymethyl)butyl]-4-methoxy-1,3-benzodioxole	13989915	Click to see COCC(CC1=CC(=C(C=C1)OC)OC)C(CC2=CC3=C(C(=C2)OC)OCO3)COC	432.50	unknown	https://doi.org/10.1021/NP9603380
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
Hinokinin	442879	Click to see C1C(C(C(=O)O1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5	354.40	unknown	https://doi.org/10.1021/NP9603380
> 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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Xanthoxylin	66654	Click to see	196.20	unknown	https://doi.org/10.1021/NP970336V
> Organoheterocyclic compounds / Indoles and derivatives / Indolecarboxylic acids and derivatives
Indole-3-carboxylic acid	69867	Click to see C1=CC=C2C(=C1)C(=CN2)C(=O)O	161.16	unknown	https://doi.org/10.1021/NP9603380 https://doi.org/10.1021/NP970336V
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole-3-Carboxaldehyde	10256	Click to see	145.16	unknown	https://doi.org/10.1021/NP970336V
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
3-chloro-10a-[(3-chloro-6-hydroxy-2,2,6-trimethylcyclohexyl)methyl]-6,8-dihydroxy-2,2-dimethyl-4,4a-dihydro-3H-benzo[g]chromene-5,10-dione	78167274	Click to see CC1(C(CCC(C1CC23C(CC(C(O2)(C)C)Cl)C(=O)C4=C(C3=O)C=C(C=C4O)O)(C)O)Cl)C	499.40	unknown	https://doi.org/10.1021/NP9603380
> 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 / Flavones / Flavonols
3,5,7-Trihydroxy-4-oxo-2-phenylchromene-8-sulfonic acid	10738015	Click to see	350.30	unknown	https://doi.org/10.1021/NP970336V
Kaempferide	5281666	Click to see	300.26	unknown	https://doi.org/10.1021/NP970336V
Kaempferol	5280863	Click to see	286.24	unknown	https://doi.org/10.1021/NP970336V
Kaempferol 8-C-sulfate	10500456	Click to see	366.30	unknown	https://doi.org/10.1021/NP970336V
Quercetin	5280343	Click to see	302.23	unknown	https://doi.org/10.1021/NP970336V
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one	51402807	Click to see	464.40	unknown	https://doi.org/10.1021/NP970336V
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-4H-1-benzopyran-3-yl 6-deoxyhexopyranoside	5353915	Click to see	448.40	unknown	https://doi.org/10.1021/NP970336V
3-[5-(1,2-Dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	13179952	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/NP970336V
5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxy-2-(3,4,5-Trihydroxyphenyl)Chromen-4-One	5352000	Click to see	464.40	unknown	https://doi.org/10.1021/NP970336V
5,7-dihydroxy-4-oxo-2-phenyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromene-8-sulfonic acid	10530351	Click to see	512.40	unknown	https://doi.org/10.1021/NP970336V
5,7-dihydroxy-4-oxo-2-phenyl-3-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromene-8-sulfonic acid	163104403	Click to see	512.40	unknown	https://doi.org/10.1021/NP970336V
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	https://doi.org/10.1021/NP970336V
Isoquercitrin	5484006	Click to see	464.40	unknown	https://doi.org/10.1021/NP970336V
Myricitrin	5281673	Click to see	464.40	unknown	https://doi.org/10.1021/NP970336V
Quercetin 3-O-gentiobioside	5320834	Click to see	626.50	unknown	https://doi.org/10.1021/NP970336V
Quercetin-3-gentiobioside	13915961	Click to see	626.50	unknown	https://doi.org/10.1021/NP970336V
Quercitrin	5280459	Click to see	448.40	unknown	https://doi.org/10.1021/NP970336V
Rutin	5280805	Click to see	610.50	unknown	https://doi.org/10.1021/NP970336V
Vitamin P	5293655	Click to see	610.50	unknown	https://doi.org/10.1021/NP970336V
> 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
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
Brevifolincarboxylic acid	9838995	Click to see	292.20	unknown	https://doi.org/10.1021/NP970336V
> Phenylpropanoids and polyketides / Tannins
(3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl) 3,4,5-trihydroxybenzoate	4628122	Click to see	332.26	unknown	https://doi.org/10.1021/NP970336V
[4,5-Dihydroxy-3,6-bis[(3,4,5-trihydroxybenzoyl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	14284610	Click to see	636.50	unknown	https://doi.org/10.1021/NP970336V
[5-Hydroxy-3,4,6-tris[(3,4,5-trihydroxybenzoyl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	14188629	Click to see	788.60	unknown	https://doi.org/10.1021/NP970336V
1,3,4,6-Tetra-O-Galloyl-Beta-D-Glucopyranoside	471531	Click to see	788.60	unknown	https://doi.org/10.1021/NP970336V
1,4,6-Tri-O-Galloyl-Beta-D-Glucose	10077822	Click to see	636.50	unknown	https://doi.org/10.1021/NP970336V
1,6-bis-O-galloyl-beta-D-glucose	440221	Click to see	484.40	unknown	https://doi.org/10.1021/NP970336V
1,6-Digalloyl-beta-D-glucopyranose	3332212	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O	484.40	unknown	https://doi.org/10.1021/NP970336V
beta-Glucogallin	124021	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O	332.26	unknown	https://doi.org/10.1021/NP970336V
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(57R,58S,510R,511R,519S)-14,15,16,24,25,26,52,53,516,517,517-Undecahydroxy-55,513,515,3,8-pentaoxo-55,57,58,510,511,513,515,516,517,517a-decahydro-4,7-dioxa-5(19,10)-1,16-epoxy-7,11-methanodibenzo[i,k][1,4,7]trioxacyclotridecina-1,2(1,2)-dibenzenacyclooctaphane-58-yl 3,4,5-trihydroxybenzoate	138991573	Click to see	952.60	unknown	https://doi.org/10.1021/NP970336V
[(1S,8R,9R,18R,19S,21R,22S)-7,7,8,12,13,22-hexahydroxy-21-(hydroxymethyl)-3,6,16-trioxo-2,17,20,23-tetraoxapentacyclo[16.3.1.18,11.04,9.010,15]tricosa-4,10,12,14-tetraen-19-yl] 3,4,5-trihydroxybenzoate	101921699	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)OC(=O)C4=CC(=O)C(C5(C4C6=C(O5)C(=C(C=C6C(=O)O3)O)O)O)(O)O)O	650.50	unknown	https://doi.org/10.1021/NP970336V
2-[(4R,5S,7R,8S,11S,12S,20S)-16,17,20-trihydroxy-7-(hydroxymethyl)-2,10,13-trioxo-5-(3,4,5-trihydroxybenzoyl)oxy-3,6,9,14-tetraoxatetracyclo[10.6.1.14,8.015,19]icosa-1(18),15(19),16-trien-11-yl]acetic acid	162861175	Click to see	622.40	unknown	https://doi.org/10.1021/NP970336V
2-[16,17,20-Trihydroxy-7-(hydroxymethyl)-2,10,13-trioxo-5-(3,4,5-trihydroxybenzoyl)oxy-3,6,9,14-tetraoxatetracyclo[10.6.1.14,8.015,19]icosa-1(18),15(19),16-trien-11-yl]acetic acid	85124357	Click to see	622.40	unknown	https://doi.org/10.1021/NP970336V
beta-D-Glucopyranose, cyclic 2-7:4-5-(3,6-dihydro-2,9,10,11,11-pentahydroxy-3-oxo-2,6-methano-2H-1-benzoxocin-5,7-dicarboxylate) 1-(3,4,5-trihydroxybenzoate), (2(2S))-	3086135	Click to see	650.50	unknown	https://doi.org/10.1021/NP970336V
CID 338147	338147	Click to see	952.60	unknown	https://doi.org/10.1021/NP970336V
Corilagin	73568	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O	634.50	unknown	https://doi.org/10.1021/NP970336V

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Phyllanthus virgatus

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