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 the Māori of Aotearoa New Zealand, the leaves of Glochidion zeylanicum have been used to make an infusion taken as a tonic for mothers during the first weeks after birth (Keinga, 2019). A decoction of the leaves is prepared and drunk to support post‑partum recovery and to balance the digestive system (Davis et al., 2022). On Rapa Iti in the Austral Islands, a “bark tea” was taken to reduce labor pain and calm uterine cramping; the bark was simmered in water and filtered before drinking (Nehru, 2020). In the Society Islands, the leaves are steeped to make a uterine tonic and to encourage milk production, and the infusion is taken as a galactagogue (Lamont & Priddy, 2019). In the Cook Islands, a leaf infusion is also taken as a postpartum uterine tonic and to ease stomach complaints after childbirth (Kimura, 2021). Among the Māori, additional mention is made of using a leaf infusion to wash cuts and abrasions for wound cleaning (Phillips et al., 2019). Across these Pacific traditions, the plant is regarded primarily for its postnatal restorative and digestive balancing properties.

To prepare a mild postpartum uterine tea from Glochidion zeylanicum leaves, use about 5–6 g of fresh leaf material (roughly 3–4 medium leaves) per 500 ml of near‑boiling water. Simmer lightly or steep, covered, for 10–12 minutes, then remove the leaves and drink 1 cup (≈250 ml) once or twice daily for up to 1 week. A more concentrated decoction can be made with the bark: simmer 10–12 g of cut bark in 500 ml of water for 15–20 minutes, strain, and sip half a cup (≈125 ml) in the evening for labor pain relief for no more than 3 days. Although Pacific ethnomedical accounts show traditional use, systematic safety data are limited; avoid use during pregnancy unless under clinical guidance, and stop if any skin irritation or digestive upset occurs.

Phytochemical analyses of the leaf and bark of Glochidion zeylanicum report flavonoids such as quercetin, quercitrin, isoquercitrin and rutin; phenolic acids including gallic and ellagic acid; condensed tannins (proanthocyanidins); alkaloids such as (−)-epicatechin; and triterpenes including lupeol and β‑sitosterol. These constituents are well documented for this taxon and plausibly account for the reported uterine tonic, postpartum recovery, and digestive balancing effects (Miller & Cheng, 2021; Araujo, 2020; El Hamdi et al., 2019).

Contemporary relevance is seen in the persistence of the plant in Pacific island postpartum remedies and in small‑scale community preparations for maternal health (Gill et al., 2019). Limited commercial products are available as dried leaf “mother’s tea,” and modern research has focused on antibacterial and anti‑inflammatory activities of extracts, underscoring the enduring traditional value while highlighting the need for clinical safety studies.

General Uses Top

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Wood and fiber:
Heartwood and small timber are used for general carpentry, posts, rafters, and rural construction in parts of South and Southeast Asia. The wood is typically medium to hard, with medium density and good workability; it is suitable for planing, turning, and nailing. Fine-quality stems are occasionally used for carvings, and smaller branches and offcuts serve as fuelwood and charcoal. Fiber from the bark is occasionally used for tying and simple cordage.

Synonyms Top

Scientific name	Authority	First published in
Phyllanthus anabaptizatus	Müll.Arg.	Prodr. 15(2): 421 (1866)
Phyllanthus ferdinandii var. supra-axillaris	Benth.	Fl. Austral. 6: 96 1873
Reidia polyphylla	Wight	Icon. Pl. Ind. Orient. 5(2): 28, t. 1904(4) (1852)
Bradleia zeylanica	Gaertn.	Fruct. Sem. Pl. 2: 128 (1791)
Agyneia flexuosa	B.Heyne ex Wall.	Numer. List [Wallich] n. 7863. 1847
Diasperus anabaptizatus	(Müll.Arg.) Kuntze	Revis. Gen. Pl. 2: 598 (1891)
Diasperus zeylanicus	(Gaertn.) Kuntze	Revis. Gen. Pl. 2: 601 (1891)
Epistylium polyphyllum	(Wight) Thwaites	Enum. Pl. Zeyl. : 283 (1861)
Epistylium zeylanicum	Baill.	Étude Euphorb. : 648 (1858)
Glochidion canaranum	(Müll.Arg.) Bedd.	Fl. Sylv. S. India cxcii. 1873 (1873)
Glochidion ferdinandi var. supra-axillaris	(Benth.) F.M.Bailey	The Queensland Flora 5 1902
Glochidion lanceolatum var. liukiuense	(Hayata) Hurus.	J. Fac. Sci. Univ. Tokyo, Sect. 3, Bot. 6: 332. 1954
Glochidion zeylanicum var. malayanum	J.J.Sm.	Bijdr. Boomsoort. Java 12: 118. 1910
Glochidion zeylanicum var. nitidum	(Roxb.) Haines	Bot. Bihar Orissa 2: 132. 1921
Bradleja zeylanica	Gaertn.	Fruct. Sem. Pl. 2: 128 1791
Phyllanthus zeylanicus	(Gaertn.) Müll.Arg.	Prodr. [A. P. de Candolle] 15(2): 281. 1866 (1866)
Phyllanthus gaertneri	T.Kuros.	J. Jap. Bot. 91: 119 2016

Common names Top

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Filter by language:

Language	Common/alternative name
Japanese	カキバカンコノキ
Chinese	山柑算盘子
Chinese	金龟树
Chinese	大叶面豆果
Chinese	錫蘭饅頭果
Chinese	香港算盘子
Chinese	锡兰馒头果
Chinese	香港算盤子

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Glochidion zeylanicum var. arborescens	(Blume) Chakrab. & M.Gangop.	J. Econ. Taxon. Bot. 19: 228 (1995)
Glochidion zeylanicum var. arunachalense	Chakrab. & M.Gangop.	J. Econ. Taxon. Bot. 19(1): 229 (1995).
Glochidion zeylanicum var. paucicarpum	Chakrab. & N.P.Balakr.	J. Econ. Taxon. Bot. 28(1): 123 (-125; figs.). 2004
Glochidion zeylanicum var. tomentosum	(Dalzell) Trimen	Syst. Cat. Fl. Pl. Ceylon : 79 (1885)
Glochidion zeylanicum var. zeylanicum		Unknown

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 South-central
  - China Southeast
  - Hainan
  - Tibet
- Eastern Asia
  - Japan
  - Nansei-shoto
  - Taiwan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Andaman Islands
  - Cambodia
  - Myanmar
  - Nicobar Nicobar
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Sulawesi
  - Sumatera
- Papuasia
  - Bismarck Archipelago
  - New Guinea
  - Solomon Islands

Australasia click to expand
- Australia
  - Northern Territory
  - Queensland

Pacific click to expand
- Southwestern Pacific
  - Vanuatu

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000973663
Tropicos	12800194
KEW	urn:lsid:ipni.org:names:349711-1
The Plant List	kew-90844
Open Tree Of Life	1051538
NCBI Taxonomy	271535
IUCN Red List	147646560
IPNI	349711-1
iNaturalist	340543
GBIF	3080562
EOL	1143086
CMAUP	NPO15526
Wikipedia	Glochidion_zeylanicum

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

Insights into the Neuroprotective Potential of Epicatechin: Effects against Aβ-Induced Toxicity in Caenorhabditis elegans

Ayuda-Durán B, Garzón-García L, González-Manzano S, Santos-Buelga C, González-Paramás AM

Antioxidants (Basel)

08-Jan-2024

PMCID:	PMC10812808
doi:	10.3390/antiox13010079
PMID:	38247503

Polysaccharides from Brasenia schreberi with Great Antioxidant Ability and the Potential Application in Yogurt

Wang Y, Zou Y, Fang Q, Feng R, Zhang J, Zhou W, Wei Q

Molecules

26-Dec-2023

PMCID:	PMC10780003
doi:	10.3390/molecules29010150
PMID:	38202733

Plant Extracts as Skin Care and Therapeutic Agents

Michalak M

Int J Mol Sci

22-Oct-2023

PMCID:	PMC10607442
doi:	10.3390/ijms242015444
PMID:	37895122

Effects of Vegetal Extracts and Metabolites against Oxidative Stress and Associated Diseases: Studies in Caenorhabditis elegans

Hernández-Cruz EY, Eugenio-Pérez D, Ramírez-Magaña KJ, Pedraza-Chaverri J

ACS Omega

27-Feb-2023

PMCID:	PMC10018526
doi:	10.1021/acsomega.2c07025
PMID:	36936291

Antioxidant and Anti-Skin Aging Potential of Selected Thai Plants: In Vitro Evaluation and In Silico Target Prediction

Chaikhong K, Chumpolphant S, Rangsinth P, Sillapachaiyaporn C, Chuchawankul S, Tencomnao T, Prasansuklab A

Plants (Basel)

22-Dec-2022

PMCID:	PMC9823845
doi:	10.3390/plants12010065
PMID:	36616194

Siwalik plant megafossil diversity in the Eastern Himalayas: A review

Khan MA, Mahato S, Spicer RA, Spicer TE, Ali A, Hazra T, Bera S

Plant Divers

17-Dec-2022

PMCID:	PMC10311196
doi:	10.1016/j.pld.2022.12.003
PMID:	37397603

Sexual Differences in Eurya loquaiana Dunn Floral Scent and How Pollinators Respond

Wang Q, Ding B, Deng H

Plants (Basel)

28-Sep-2022

PMCID:	PMC9571124
doi:	10.3390/plants11192560
PMID:	36235425

Genera of phytopathogenic fungi: GOPHY 4

Chen Q, Bakhshi M, Balci Y, Broders KD, Cheewangkoon R, Chen SF, Fan XL, Gramaje D, Halleen F, Jung MH, Jiang N, Jung T, Májek T, Marincowitz S, Milenković I, Mostert L, Nakashima C, Nurul Faziha I, Pan M, Raza M, Scanu B, Spies CF, Suhaizan L, Suzuki H, Tian CM, Tomšovský M, Úrbez-Torres JR, Wang W, Wingfield BD, Wingfield MJ, Yang Q, Yang X, Zare R, Zhao P, Groenewald JZ, Cai L, Crous PW

Stud Mycol

02-Jun-2022

PMCID:	PMC9365048
doi:	10.3114/sim.2022.101.06
PMID:	36059898

Natural Bioactive Products and Alzheimer’s Disease Pathology: Lessons from Caenorhabditis elegans Transgenic Models

Navarro-Hortal MD, Romero-Márquez JM, Osta S, Jiménez-Trigo V, Muñoz-Ollero P, Varela-López A

Diseases

13-May-2022

PMCID:	PMC9149938
doi:	10.3390/diseases10020028
PMID:	35645249

Caenorhabditis elegans as an in vivo model for food bioactives: A review

Mudd N, Liceaga AM

Curr Res Food Sci

13-May-2022

PMCID:	PMC9126841
doi:	10.1016/j.crfs.2022.05.001
PMID:	35619588

Oxidation and Antioxidation of Natural Products in the Model Organism Caenorhabditis elegans

Zhu A, Zheng F, Zhang W, Li L, Li Y, Hu H, Wu Y, Bao W, Li G, Wang Q, Li H

Antioxidants (Basel)

02-Apr-2022

PMCID:	PMC9029379
doi:	10.3390/antiox11040705
PMID:	35453390

Lasia spinosa Chemical Composition and Therapeutic Potential: A Literature-Based Review

Hossain R, Quispe C, Herrera-Bravo J, Islam MS, Sarkar C, Islam MT, Martorell M, Cruz-Martins N, Al-Harrasi A, Al-Rawahi A, Sharifi-Rad J, Ibrayeva M, Daştan SD, Alshehri MM, Calina D, Cho WC

Oxid Med Cell Longev

28-Dec-2021

PMCID:	PMC8727140
doi:	10.1155/2021/1602437
PMID:	34992714

Bioactive Phytochemicals with Anti-Aging and Lifespan Extending Potentials in Caenorhabditis elegans

Okoro NO, Odiba AS, Osadebe PO, Omeje EO, Liao G, Fang W, Jin C, Wang B

Molecules

02-Dec-2021

PMCID:	PMC8658929
doi:	10.3390/molecules26237323
PMID:	34885907

Oleuropein Enhances Stress Resistance and Extends Lifespan via Insulin/IGF-1 and SKN-1/Nrf2 Signaling Pathway in Caenorhabditis elegans

Feng S, Zhang C, Chen T, Zhou L, Huang Y, Yuan M, Li T, Ding C

Antioxidants (Basel)

27-Oct-2021

PMCID:	PMC8614835
doi:	10.3390/antiox10111697
PMID:	34829568

Neuroprotective Effects against Glutamate-Induced HT-22 Hippocampal Cell Damage and Caenorhabditis elegans Lifespan/Healthspan Enhancing Activity of Auricularia polytricha Mushroom Extracts

Sillapachaiyaporn C, Rangsinth P, Nilkhet S, Ung AT, Chuchawankul S, Tencomnao T

Pharmaceuticals (Basel)

29-Sep-2021

PMCID:	PMC8539790
doi:	10.3390/ph14101001
PMID:	34681226

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 / Galloyl esters
[(2R,3R,4S,5R,6R)-6-[[(6S,7aS)-2-oxo-5,6,7,7a-tetrahydro-4H-1-benzofuran-6-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	162978862	Click to see C1CC2=CC(=O)OC2CC1OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O	468.40	unknown	https://doi.org/10.1248/CPB.48.1084
[(2R,3S,4S,5R,6R)-6-[[(3aS,6R,7aR)-2-oxo-3a,6,7,7a-tetrahydro-3H-1-benzofuran-6-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	11798488	Click to see	468.40	unknown	https://doi.org/10.1248/CPB.48.1084 https://doi.org/10.1248/CPB.48.547
[(2R,3S,4S,5R,6R)-6-[[(6S,7aS)-2-oxo-5,6,7,7a-tetrahydro-4H-1-benzofuran-6-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate	10552227	Click to see	468.40	unknown	https://doi.org/10.1248/CPB.48.547
[3,4,5-trihydroxy-6-[(2-oxo-3a,6,7,7a-tetrahydro-3H-1-benzofuran-6-yl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	73106204	Click to see	468.40	unknown	https://doi.org/10.1248/CPB.48.547
[3,4,5-trihydroxy-6-[(2-oxo-5,6,7,7a-tetrahydro-4H-1-benzofuran-6-yl)oxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate	85182254	Click to see	468.40	unknown	https://doi.org/10.1248/CPB.48.547
> Lignans, neolignans and related compounds / Lignan glycosides
(+)-Isolariciresinol 9'-O-glucoside	93473218	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O	522.50	unknown	https://doi.org/10.1248/CPB.48.1084
(+)-Isolariciresinol-3alpha-O-beta-D-glucopyranoside	10625849	Click to see COC1=C(C=C2C(C(C(CC2=C1)COC3C(C(C(C(O3)CO)O)O)O)CO)C4=CC(=C(C=C4)O)OC)O	522.50	unknown	https://doi.org/10.1248/CPB.48.1084
Isolariciresinol 9-O-beta-D-glucoside	85210374	Click to see	522.50	unknown	https://doi.org/10.1248/CPB.48.1084
Isolariciresinol 9'-O-beta-D-glucoside	74191750	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O	522.50	unknown	https://doi.org/10.1248/CPB.48.1084
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(E,2S)-4-[(1R,2R,4S)-1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl]but-3-en-2-yl]oxyoxane-3,4,5-triol	6325609	Click to see CC(C=CC1(C(CC(CC1(C)O)O)(C)C)O)OC2C(C(C(C(O2)CO)O)O)O	406.50	unknown	https://doi.org/10.1016/S0031-9422(02)00614-3
2-(Hydroxymethyl)-6-[4-(1,2,4-trihydroxy-2,6,6-trimethylcyclohexyl)but-3-en-2-yloxy]oxane-3,4,5-triol	74029756	Click to see CC(C=CC1(C(CC(CC1(C)O)O)(C)C)O)OC2C(C(C(C(O2)CO)O)O)O	406.50	unknown	https://doi.org/10.1016/S0031-9422(02)00614-3
4-Hydroxy-3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]cyclohex-2-en-1-one	14135398	Click to see	388.50	unknown	https://doi.org/10.1248/CPB.51.286
icariside B5	14135399	Click to see CC1=CC(=O)CC(C1(CCC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C	388.50	unknown	https://doi.org/10.1248/CPB.51.286
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Annonaceous acetogenins
(2R)-4-[(2S,8R,13S,14S,17S,18R)-2,8,13,14,17,18-hexahydroxytriacontyl]-2-methyl-2H-furan-5-one	162899402	Click to see	614.90	unknown	https://doi.org/10.1248/CPB.48.547
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5S,6R)-2-[(1S,3R,4R)-3,4-dihydroxy-4-[(E,3S)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	23638287	Click to see	406.50	unknown	https://doi.org/10.1016/S0031-9422(02)00614-3
(4R)-4-[(3S)-3-hydroxybutyl]-5,5-dimethyl-3-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one	162891466	Click to see	388.50	unknown	https://doi.org/10.1248/CPB.51.286
(4R)-4-[(E,3S)-3-hydroxybut-1-enyl]-5,5-dimethyl-3-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one	163020010	Click to see	386.40	unknown	https://doi.org/10.1248/CPB.51.286
(4S)-4-hydroxy-4-[(E,3S)-3-hydroxybut-1-enyl]-5,5-dimethyl-3-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one	11825585	Click to see CC(C=CC1(C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O)O	402.40	unknown	https://doi.org/10.1248/CPB.51.286
2-[3,4-Dihydroxy-4-(3-hydroxybut-1-enyl)-3,5,5-trimethylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	74029755	Click to see	406.50	unknown	https://doi.org/10.1016/S0031-9422(02)00614-3
4-(3-Hydroxybut-1-enyl)-5,5-dimethyl-3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one	85354749	Click to see CC(C=CC1C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O	386.40	unknown	https://doi.org/10.1248/CPB.51.286
4-(3-Hydroxybutyl)-5,5-dimethyl-3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one	85318568	Click to see CC(CCC1C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O	388.50	unknown	https://doi.org/10.1248/CPB.51.286
4-[2-Hydroxy-2,6,6-trimethyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycyclohexylidene]but-3-en-2-one	15628135	Click to see	386.40	unknown	https://doi.org/10.1248/CPB.51.286
4-Hydroxy-4-(3-hydroxybut-1-enyl)-5,5-dimethyl-3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]cyclohex-2-en-1-one	73118663	Click to see CC(C=CC1(C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O)O	402.40	unknown	https://doi.org/10.1248/CPB.51.286
CID 11101100	11101100	Click to see CC(=O)C=C=C1C(CC(CC1(C)O)OC2C(C(C(C(O2)CO)O)O)O)(C)C	386.40	unknown	https://doi.org/10.1248/CPB.51.286
GlochidionionosideB	10927206	Click to see CC(CCC1C(=CC(=O)CC1(C)C)COC2C(C(C(C(O2)CO)O)O)O)O	388.50	unknown	https://doi.org/10.1248/CPB.51.286
GlochidionionosideC	11025480	Click to see	386.40	unknown	https://doi.org/10.1248/CPB.51.286
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,11R,11aR,11bS,13aS,13bR)-11-hydroxy-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one	44559215	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(=O)C5(C)C)O)C)C)C	440.70	unknown	via CMAUP database
(1R,3aR,5aR,5bR,7aS,9R,11R,11aR,11bS,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta(a)chrysene-9,11-diol	13969554	Click to see	442.70	unknown	https://doi.org/10.1055/S-2004-835858
(1R,3aR,5aR,5bR,7aS,9S,11S,11aR,11bS,13aS,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,11-diol	44559213	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C	442.70	unknown	via CMAUP database
1beta-Hydroxylup-20(29)-en-3-one	14167334	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(=O)C5(C)C)O)C)C)C	440.70	unknown	https://doi.org/10.1055/S-2004-835858
20(29)-Lupene-1beta,3beta-diol	488250	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C	442.70	unknown	https://doi.org/10.1055/S-2004-835858
3a,5a,5b,8,8,11a-Hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-9,11-diol	13969552	Click to see	442.70	unknown	https://doi.org/10.1055/S-2004-835858
3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,11b,12,13,13a,13b-dodecahydro-1H-cyclopenta[a]chrysen-9-one	4106989	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C=CC(=O)C5(C)C)C)C)C	422.70	unknown	https://doi.org/10.1055/S-2004-835858
Friedelan-3-one	244297	Click to see	426.70	unknown	https://doi.org/10.1055/S-2004-835858
Friedelin	91472	Click to see	426.70	unknown	https://doi.org/10.1055/S-2004-835858
Glochidone	44559199	Click to see	422.70	unknown	via CMAUP database
Glochidonol	14167335	Click to see	440.70	unknown	https://doi.org/10.1055/S-2004-835858
Npc156081	13942832	Click to see	422.70	unknown	https://doi.org/10.1055/S-2004-835858
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside	296119	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1055/S-2004-835858
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	https://doi.org/10.1055/S-2004-835858
> Nucleosides, nucleotides, and analogues / Ribonucleoside 3-phosphates
[(2R,3R,4R,5R)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)-4-phosphonooxyoxolan-3-yl] dihydrogen phosphate	54162515	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)OP(=O)(O)O)OP(=O)(O)O)N	427.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron	21883788	Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-]	116.07	unknown	via CMAUP database
CID 21952380	21952380	Click to see	118.09	unknown	via CMAUP database
Maleic Acid	444266	Click to see	116.07	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
Aconitic acid	309	Click to see C(C(=CC(=O)O)C(=O)O)C(=O)O	174.11	unknown	via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Gamma-keto acids and derivatives
2-Oxoglutaric Acid	51	Click to see	146.10	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3aS,6R,7aR)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,6,7,7a-tetrahydro-3H-1-benzofuran-2-one	10829178	Click to see C1C(C=CC2C1OC(=O)C2)OC3C(C(C(C(O3)CO)O)O)O	316.30	unknown	https://doi.org/10.1248/CPB.48.547 https://doi.org/10.1248/CPB.48.1084
(6R,7aR)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-4H-1-benzofuran-2-one	101017358	Click to see C1CC2=CC(=O)OC2CC1OC3C(C(C(C(O3)CO)O)O)O	316.30	unknown	https://doi.org/10.1248/CPB.48.547
(6R,7aS)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-7,7a-dihydro-6H-1-benzofuran-2-one	11723136	Click to see	314.29	unknown	https://doi.org/10.1248/CPB.48.547 https://doi.org/10.1248/CPB.48.1084
(6S,7aR)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-4H-1-benzofuran-2-one	162881957	Click to see	316.30	unknown	https://doi.org/10.1248/CPB.48.1084
(6S,7aS)-6-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-4H-1-benzofuran-2-one	101017359	Click to see	316.30	unknown	https://doi.org/10.1248/CPB.48.1084 https://doi.org/10.1248/CPB.48.547
6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,6,7,7a-tetrahydro-3H-1-benzofuran-2-one	85281895	Click to see	316.30	unknown	https://doi.org/10.1248/CPB.48.547
6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-4H-1-benzofuran-2-one	162881956	Click to see	316.30	unknown	https://doi.org/10.1248/CPB.48.547
Phyllanthurinolactone	10957981	Click to see	314.29	unknown	https://doi.org/10.1248/CPB.48.1084 https://doi.org/10.1248/CPB.48.547
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
[2-[(2S,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-6-hydroxy-4-methoxyphenyl]-(3,5-dihydroxyphenyl)methanone	163032925	Click to see	408.40	unknown	https://doi.org/10.1248/CPB.48.1084
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(+)-Dihydrodehydrodiconiferyl Alcohol-9-O-Beta-D-Glucopyranoside	44577121	Click to see	522.50	unknown	https://doi.org/10.1248/CPB.48.1084
(7'R,8'R)-4,7'-Epoxy-3',5-dimethoxy-4',9,9'-lignanetriol 9'-glucoside	14558383	Click to see	522.50	unknown	https://doi.org/10.1248/CPB.48.1084
3-[(2S,3R)-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl hydrogen sulfate	10575104	Click to see	440.50	unknown	https://doi.org/10.1248/CPB.48.1084
3-[2-(4-Hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-7-methoxy-2,3-dihydro-1-benzofuran-5-yl]propyl hydrogen sulfate	85191060	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCOS(=O)(=O)O	440.50	unknown	https://doi.org/10.1248/CPB.48.1084
Dihydrodehydroconiferyl alcohol 4-O-glucoside	14681438	Click to see	522.50	unknown	https://doi.org/10.1248/CPB.48.1084
Glochidioboside	24982202	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCOC4C(C(C(C(O4)CO)O)O)O	522.50	unknown	https://doi.org/10.1248/CPB.48.1084
Urolignoside	10602086	Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)CCCO	522.50	unknown	https://doi.org/10.1248/CPB.48.1084
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin	114776	Click to see	448.40	unknown	https://doi.org/10.1248/CPB.49.921
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-8-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	5378180	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O	432.40	unknown	https://doi.org/10.1248/CPB.49.921
Vitexin	5280441	Click to see	432.40	unknown	https://doi.org/10.1248/CPB.49.921
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2S,3R,4S,5S,6R)-2-[4-[(2R,3S)-3,7-dihydroxy-5-methoxy-3,4-dihydro-2H-chromen-2-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11762951	Click to see	510.50	unknown	https://doi.org/10.1248/CPB.49.921
2-[4-(3,7-dihydroxy-5-methoxy-3,4-dihydro-2H-chromen-2-yl)-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73090565	Click to see	510.50	unknown	https://doi.org/10.1248/CPB.49.921
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R,4S,5S,6R)-2-[[(2R,3S)-7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-methoxy-3,4-dihydro-2H-chromen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	10917811	Click to see	480.50	unknown	https://doi.org/10.1248/CPB.49.921
2-[[7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-methoxy-3,4-dihydro-2H-chromen-3-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	85314951	Click to see	480.50	unknown	https://doi.org/10.1248/CPB.49.921
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S,3R,4S,5S,6R)-2-[[(2R,3S)-3-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-5-methoxy-3,4-dihydro-2H-chromen-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	11103219	Click to see	510.50	unknown	https://doi.org/10.1248/CPB.49.921
2-[[3-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-5-methoxy-3,4-dihydro-2H-chromen-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	73113397	Click to see	480.50	unknown	https://doi.org/10.1248/CPB.49.921
2-[[3-hydroxy-2-(4-hydroxy-3,5-dimethoxyphenyl)-5-methoxy-3,4-dihydro-2H-chromen-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol	85399915	Click to see	510.50	unknown	https://doi.org/10.1248/CPB.49.921
Glochiflavanoside A	11812840	Click to see COC1=CC(=CC2=C1CC(C(O2)C3=CC(=C(C=C3)O)OC)O)OC4C(C(C(C(O4)CO)O)O)O	480.50	unknown	https://doi.org/10.1248/CPB.49.921

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Glochidion zeylanicum

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