Scientific name	Authority	First published in
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 patens	Miq. ex Müll.Arg.	Linnaea 32: 34 (1863)
Phyllanthus simplex var. brevipes	Müll.Arg.	Prodr. [A. P. de Candolle] 15(2): 392. 1866
Phyllanthus simplex var. myriocladus	Müll.Arg.	Linnaea 32: 33. 1863
Phyllanthus simplex var. pratensis	Müll.Arg.	Linnaea 32: 33. 1863
Diasperus virgatus	(G.Forst.) Kuntze	Revis. Gen. Pl. 2: 597 (1891)

Common names Top

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Filter by language:

Language	Common/alternative name
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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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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	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
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

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

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

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

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

An Immunohistochemical Analysis to Validate the Rationale behind the Enhanced Immunogenicity of D-Ribosylated Low Density Lipo-Protein

Akhter F, Khan MS, Singh S, Ahmad S

PLoS One

13-Nov-2014

PMCID:	PMC4231124
doi:	10.1371/journal.pone.0113144
PMID:	25393017

Alleviation of hyperglycemia and hyperlipidemia by Phyllanthus virgatus forst extract and its partially purified fraction in streptozotocin induced diabetic rats

Hashim A, Khan MS, Ahmad S

EXCLI J

12-Aug-2014

PMCID:	PMC4464522
PMID:	26417304

Antioxidant and α-Amylase Inhibitory Property of Phyllanthus virgatus L.: An In Vitro and Molecular Interaction Study

Hashim A, Khan MS, Khan MS, Baig MH, Ahmad S

Biomed Res Int

19-Jun-2013

PMCID:	PMC3703720
doi:	10.1155/2013/729393
PMID:	23957001

A nomenclator of Pacific oceanic island Phyllanthus (Phyllanthaceae), including Glochidion

Wagner WL, Lorence DH

PhytoKeys

12-Jul-2011

PMCID:	PMC3174446
doi:	10.3897/phytokeys.4.1581
PMID:	22171182

Hepatoprotective activity of the Phyllanthus species on tert-butyl hydroperoxide (t-BH)-induced cytotoxicity in HepG2 cells

Sharma SK, Arogya SM, Bhaskarmurthy DH, Agarwal A, Velusami CC

Pharmacogn Mag

01-Jul-2011

PMCID:	PMC3173898
doi:	10.4103/0973-1296.84237
PMID:	21969794

Biosynthesis and Function of Polyacetylenes and Allied Natural Products

Minto RE, Blacklock BJ

Prog Lipid Res

13-Mar-2008

PMCID:	PMC2515280
doi:	10.1016/j.plipres.2008.02.002
PMID:	18387369

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	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 COC(=O)C1=CC(=C(C(=C1)O)O)O	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 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
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 COCC1CC2=CC(=C3C(=C2C(C1COC)C4=CC(=C(C=C4)OC)OC)OCO3)OC	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 COCC1CC2=CC3=C(C=C2C(C1COC)C4=CC(=C(C=C4)OC)OC)OCO3	400.50	unknown	https://doi.org/10.1021/NP9603380
Phyltetralin	11223782	Click to see COCC1CC2=CC(=C(C=C2C(C1COC)C3=CC(=C(C=C3)OC)OC)OC)OC	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 CC1=C2CC(CCC2(CCC1=O)C)C(=C)C(=O)O	248.32	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Xanthoxylin	66654	Click to see CC(=O)C1=C(C=C(C=C1OC)OC)O	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 C1=CC=C2C(=C1)C(=CN2)C=O	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 C1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)S(=O)(=O)O)O	350.30	unknown	https://doi.org/10.1021/NP970336V
Kaempferide	5281666	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O	300.26	unknown	https://doi.org/10.1021/NP970336V
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1021/NP970336V
Kaempferol 8-C-sulfate	10500456	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)S(=O)(=O)O)O)O	366.30	unknown	https://doi.org/10.1021/NP970336V
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	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-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one	5353915	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/NP970336V
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 C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O	464.40	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-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 C1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)S(=O)(=O)O)OC4C(C(C(C(O4)CO)O)O)O	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 C1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)S(=O)(=O)O)OC4C(C(C(C(O4)CO)O)O)O	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 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
Myricetin 3-rhamnoside	5352000	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/NP970336V
Myricitrin	5281673	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)O)O	464.40	unknown	https://doi.org/10.1021/NP970336V
Quercetin 3-gentiobioside	5320834	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O	626.50	unknown	https://doi.org/10.1021/NP970336V
Quercetin-3-gentiobioside	13915961	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC5C(C(C(C(O5)CO)O)O)O)O)O)O)O)O	626.50	unknown	https://doi.org/10.1021/NP970336V
Quercitrin	5280459	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	https://doi.org/10.1021/NP970336V
Rutin	5280805	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	610.50	unknown	https://doi.org/10.1021/NP970336V
Vitamin P	5293655	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O	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 COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	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
4',5,7-Trihydroxy-3,6-dimethoxyflavone	5352032	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O	330.29	unknown	via CMAUP database
Jaceidin	5464461	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O	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'-Hydroxy-3,5,6,7-tetramethoxyflavone	13983731	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)OC)OC	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 COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)OC)O	344.30	unknown	via CMAUP database
Penduletin	5320462	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)OC	344.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3-Methoxytangeretin	11741814	Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC)OC	402.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
Brevifolincarboxylic acid	9838995	Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)O	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 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
[5-Hydroxy-3,4,6-tris[(3,4,5-trihydroxybenzoyl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	14188629	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)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	788.60	unknown	https://doi.org/10.1021/NP970336V
1,3,4,6-Tetragalloylglucose	471531	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)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O	788.60	unknown	https://doi.org/10.1021/NP970336V
1,4,6-tri-O-galloyl-beta-D-glucose	10077822	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)OC(=O)C4=CC(=C(C(=C4)O)O)O	636.50	unknown	https://doi.org/10.1021/NP970336V
1,4,6-Trigalloyl-beta-D-glucopyranose	14284610	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)OC(=O)C4=CC(=C(C(=C4)O)O)O	636.50	unknown	https://doi.org/10.1021/NP970336V
1,6-bis-O-galloyl-beta-D-glucose	440221	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
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 C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	952.60	unknown	https://doi.org/10.1021/NP970336V
[(1S,7S,9R,18R,19S,21R,22S)-7,8,8,12,13,22-hexahydroxy-21-(hydroxymethyl)-3,6,16-trioxo-2,17,20,23-tetraoxapentacyclo[16.3.1.17,11.04,9.010,15]tricosa-4,10,12,14-tetraen-19-yl] 3,4,5-trihydroxybenzoate	3086135	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)OC(=O)C4=CC(=O)C5(C(C4C6=C(O5)C(=C(C=C6C(=O)O3)O)O)(O)O)O)O	650.50	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 C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)OC(=O)C(C4C5=C(C(=C(C=C5C(=O)O3)O)O)OC4=O)CC(=O)O)O	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 C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)OC(=O)C(C4C5=C(C(=C(C=C5C(=O)O3)O)O)OC4=O)CC(=O)O)O	622.40	unknown	https://doi.org/10.1021/NP970336V
CID 338147	338147	Click to see C1C2C3C(C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C6=C5C7C(=CC(=O)C(C7(O)O)(O6)O)C(=O)O3)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	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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