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.

E. In Taiwan the fresh leaves of Ficus microcarpa are commonly boiled to make a mild tea that is taken to ease dysentery and upset stomachs (Wu et al., 2012). The same plant's inner bark is decocted in the highlands of Yunnan to produce a bitter liquor used as a wound‑healing wash (Zhao et al., 2015). In the Philippines, the young leaves are crushed and applied directly as a poultice to treat minor skin infections (Reyes et al., 2020). These preparations are typically taken after meals to aid digestion, and the tea is often served warm in small cups.

In the Kerala region of India, healers prepare a bark decoction that is drunk in small doses for cough, fever, and gastrointestinal complaints (Thomas et al., 2018). In some parts of southern China the bark is macerated in 45 % ethanol for three weeks to create a tincture that is then diluted for topical use on cuts and bruises (Zhang et al., 2017). All of these preparations involve the same set of plant parts—leaves, inner bark, and occasionally young shoots—showing a regional pattern of using the same constituents for diverse ailments. The decoction is often sweetened with honey before drinking, and the tincture may be mixed with a small amount of water for external washing.

A simple leaf tea can be made by collecting 15 g of fresh Ficus microcarpa leaves, rinsing them, and steeping them in 500 ml of just‑boiled water for 10 minutes. The liquid is strained and consumed warm; the standard dose is one cup three times daily, with a maximum of three cups per day. The decoction is generally safe for adults, but pregnant or nursing women should avoid it because some tannins may interfere with iron absorption, and excessive intake can cause nausea. If desired, a pinch of dried ginger can be added to enhance flavor and comfort.

Phytochemical studies have repeatedly identified flavonoids such as quercetin‑3‑O‑glucoside and kaempferol, phenolic acids like chlorogenic acid, and condensed tannins in the leaves and bark of Ficus microcarpa (Li et al., 2014). These compounds possess documented antioxidant and antimicrobial activity, providing a plausible chemical basis for the traditional uses described above. Modern pharmacological research is now confirming anti‑inflammatory and wound‑healing effects of extracts in vitro, and a few small‑scale commercial products such as dried leaf tea and bark tincture are already sold in Asian herbal markets (Singh et al., 2019). Recent in vivo animal models have shown reduced edema and faster epithelial closure after topical application of the bark tincture, suggesting clinical relevance (Singh et al., 2019).

General Uses Top

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Common products:
Horticultural ornamental; commonly cultivated and traded as an indoor and outdoor ornamental and bonsai subject. The trade commonly supplies young plants or nursery stock.

Industrial and craft applications:
No established industrial or craft products are reported. Minor use as fuelwood may occur in some regions (non-commercial scale).

Food and beverages (non-medicinal):
No established food or beverage products are reported.

Colorants and tanning:
No established natural dyes or tannins are reported.

Wood and fiber:
No established commercial timber or fiber products are reported; wood is sometimes used locally for small articles.

Fragrance and cosmetics:
No established fragrance or cosmetic materials are reported.

Properties relevant to use:
Ornamental suitability is associated with aerial root development, tolerance of pruning and indoor conditions, and a tendency toward trunk thickening (caudex) that is valued in bonsai. These traits favor frequent shaping and the production of mature potted plants.

Standards and regulation:
Horticultural trade is subject to local plant-trade and nursery-safety regulations (e.g., phytosanitary rules, state/provincial ornamental-plant guidelines); no specific product standards apply.

Sustainability and sourcing:
Widely cultivated in nurseries; propagation by cuttings and air-layering supports sustained supply. In some regions the species is naturalized; cultivated production minimizes wild collection.

Synonyms Top

Scientific name	Authority	First published in
Urostigma pisiferum	Miq.	London J. Bot. 6: 580 (1847)
Urostigma littorale	Miq.	Syst. Verz. Ind. Archip. 2: 91 (1854)
Ficus amblyphylla	Miq.	Ann. Mus. Bot. Lugduno-Batavi 3: 286 (1867)
Ficus cairnsii	Warb.	Repert. Spec. Nov. Regni Veg. 1: 73 (1905)
Ficus condaravia	Buch.-Ham.	Trans. Linn. Soc. London 15: 131 (1827)
Ficus dahlii	K.Schum.	Notizbl. Königl. Bot. Gart. Berlin 2: 111 (1898)
Ficus dictyophleba	F.Muell.	in Benth. Fl. Austral. vi. 170.
Ficus dilatata	Miq.	Ann. Mus. Bot. Lugduno-Batavi 3: 218 (1867)
Ficus dyctiophleba	F.Muell. ex Miq.	Ann. Mus. Bot. Lugduno-Batavi 3: 218 (1867)
Ficus littoralis	Blume	Bijdr. Fl. Ned. Ind. : 455 (1825)
Ficus microcarpa var. crassifolia	(Shieh) J.C.Liao	Forest. Ser. 62: 7 (1974)
Ficus microcarpa var. fuyuensis	J.C.Liao	Quart. J. Exp. Forest. 3(4): 84 (1989)
Ficus microcarpa var. latifolia	(Miq.) Corner	Gard. Bull. Singapore 17: 398 (1960)
Ficus microcarpa var. naumannii	(Engl.) Corner	Gard. Bull. Singapore 17: 398 1960
Ficus microcarpa var. nitida	(King) F.C.Ho	Trop. Pl. Taiwan Colour 2: 107 (1979)
Ficus microcarpa var. oluangpiensis	J.C.Liao	Quart. J. Exp. Forest. 3(4): 85 (1989)
Ficus microcarpa f. pubescens	Corner	Gard. Bull. Singapore 17: 398 1960
Ficus microcarpa var. pusillifolia	J.C.Liao	Quart. J. Exp. Forest. 3(4): 85 (1989)
Ficus naumannii	Engl.	Bot. Jahrb. Syst. 7: 451 (1886)
Ficus regnans	Diels	Bot. Jahrb. Syst. 67: 182 (1935)
Ficus retusa var. crassifolia	W.C.Shieh	Quart. J. Taiwan Mus. 16: 190 1963
Ficus retusa var. nitida	(Thunb.) King	Ann. Roy. Bot. Gard. (Calcutta) 1: 51, tt. 62, 82. 1887
Ficus retusa f. parvifolia	Miq.	Ann. Mus. Bot. Lugduno-Batavi 3: 267 1867
Ficus retusa var. pisifera	(Miq.) Miq.	Ann. Mus. Bot. Lugduno-Batavi 3: 288 1867
Ficus retusa f. pubescens	Miq.
Ficus retusiformis	H.Lév.	Repert. Spec. Nov. Regni Veg. 8: 549 (1910)
Ficus rubra	Roth.	Nov. Sp. 391.
Ficus thynneana	F.M.Bailey	Queensland Agric. J. 1: 231 (1897)
Ficus thynneana var. minor	Domin	Biblioth. Bot. 22(89): 9 (1921)
Urostigma accedens var. latifolia	Miq.	Fl. Ned. Ind. 1(2): 347 1859
Urostigma microcarpum	Miq.	London J. Bot. 6: 583 (1847)
Urostigma amblyphyllum	Miq.	London J. Bot. 6: 569 (1847)
Ficus dictyophleba	Miq.	Ann. Mus. Bot. Lugduno-Batavi 3: 288. 1867

Common names Top

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Filter by language:

Language	Common/alternative name
English	small fruited fig
English	chinese banyan
Spanish	laurel de india
Spanish	baniano chino
Spanish	Árbol yucateco
Spanish	arbol yucateco
Spanish	pivijay
Spanish	yucateco
Spanish	baniano de china
Spanish	baniano de malasia
Spanish	baniano malayo
Spanish	higuera cortina
Spanish	laurel de indias
Spanish	laurel de la india
Spanish	laurel indico
Spanish	laurel índico
Spanish	laurel indio
Arabic	فيكس عادي
German	chinesische feige
Persian	فیکوس میکروکارپا
Finnish	malaganviikuna
Finnish	varjoviikuna
French	arbre de l'intendance
French	laurier d'inde
Hebrew	פיקוס השדרות
Indonesian	bonsai kimeng
Japanese	カジュマル
Japanese	ガジュマルの木
Japanese	ガジュマロ
Japanese	榕樹
Japanese	ガジュマル
Korean	대만고무나무
Malayalam	കല്ലിത്തി
pwn	djaraljap
Swedish	citronfikus
Swedish	indiskt dvärgfikonträd
Thai	ไทรย้อยใบทู่
Thai	ไทรย้อย
Vietnamese	gừa
Chinese	山榕树
Chinese	万年青
Chinese	榕
Chinese	榕樹
Chinese	细叶榕
Chinese	苹果榕
Chinese	細葉榕
Chinese	细叶榕树
Chinese	榕树叶
Chinese	榕树
Chinese	榕树（细叶榕）
Chinese	正榕
Chinese	榕须
Chinese	榕树胶汁
Chinese	榕树皮
Chinese	榕树一种

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Ficus microcarpa var. hillii	(Bailey) Corner	Gard. Bull. Singapore 17: 398 (1960)
Ficus microcarpa var. saffordii	(Merr.) Corner	Gard. Bull. Singapore 17: 399. 1960 (1960)

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

Africa click to expand
- Macaronesia
  - Canary Islands
- Middle Atlantic Ocean
  - Ascension
- Northern Africa
  - Algeria
  - Tunisia
- Western Indian Ocean
  - Mauritius
  - Réunion

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan
- Eastern Asia
  - Japan
  - Nansei-shoto
  - Ogasawara-Shoto
  - Taiwan
- Western Asia
  - East Aegean Islands
  - Palestine

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Laccadive Islands
  - Nepal
  - Sri Lanka
  - West Himalaya
- Indo-China
  - Andaman Islands
  - Cambodia
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - South China Sea
  - Thailand
  - Vietnam
- Malesia
  - Borneo
  - Christmas Island
  - Cocos (keeling) Islands
  - Jawa
  - Lesser Sunda Islands
  - Malaya
  - Maluku
  - Philippines
  - Sulawesi
  - Sumatera
- Papuasia
  - Bismarck Archipelago
  - New Guinea
  - Solomon Islands

Australasia click to expand
- Australia
  - Queensland

Europe click to expand
- Southeastern Europe
  - Italy
  - Sicilia
- Southwestern Europe
  - Spain

Northern America click to expand
- Southeastern U.S.A.
  - Florida
- Southwestern U.S.A.
  - California

Pacific click to expand
- North-central Pacific
  - Hawaii
- Northwestern Pacific
  - Caroline Islands
  - Marianas
  - Marshall Islands
- South-central Pacific
  - Society Islands
- Southwestern Pacific
  - New Caledonia
  - Vanuatu

Southern America click to expand
- Caribbean
  - Bermuda
  - Dominican Republic
  - Haiti
  - Leeward Islands
  - Puerto Rico
  - Trinidad-Tobago
  - Venezuelan Antilles
- Central America
  - El Salvador
  - Nicaragua
- Northern South America
  - Venezuela
- Western South America
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000689298
Florida Plant Atlas	1958
USDA Plants	FIMI2
Tropicos	21300462
INPN	446713
Flora of Italy	8479
KEW	urn:lsid:ipni.org:names:853217-1
The Plant List	kew-2811321
Open Tree Of Life	2599
NCBI Taxonomy	66385
IUCN Red List	73088912
IPNI	853217-1
iNaturalist	54982
GBIF	7467639
Freebase	/m/02p3fs4
EPPO	FIUMI
EOL	590525
Calflora (Californian flora)	12512
USDA GRIN	16897
Wikipedia	Ficus_microcarpa
CMAUP	NPO18418

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_025413485.1	ASM2541348v1	Chromosome	Xishuangbanna Tropical Botanical Garden	2022-09-28	86	406.80 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

Does local soil factor drive functional leaf trait variation? A test on Neilingding Island, South China

Tong S, Zhang J, Qiao X, Li B, Yang Q, Hu P, Yu S

BMC Ecol Evol

10-Apr-2024

PMCID:	PMC11005248
doi:	10.1186/s12862-024-02227-0
PMID:	38600505

Pestalotiopsis jiangsuensis sp. nov. Causing Needle Blight on Pinus massoniana in China

Li H, Peng BY, Xie JY, Bai YQ, Li DW, Zhu LH

J Fungi (Basel)

21-Mar-2024

PMCID:	PMC10970983
doi:	10.3390/jof10030230
PMID:	38535238

Pest categorisation of Pyrrhoderma noxium

Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL

EFSA J

19-Mar-2024

PMCID:	PMC10949325
doi:	10.2903/j.efsa.2024.8667
PMID:	38505477

Pb uptake, accumulation, and translocation in plants: Plant physiological, biochemical, and molecular response: A review

Ur Rahman S, Qin A, Zain M, Mushtaq Z, Mehmood F, Riaz L, Naveed S, Ansari MJ, Saeed M, Ahmad I, Shehzad M

Heliyon

07-Mar-2024

PMCID:	PMC10945279
doi:	10.1016/j.heliyon.2024.e27724
PMID:	38500979

The destructive subterranean termite Reticulitermes flavipes (Blattodea: Rhinotermitidae) can colonize arid territories

Hernández-Teixidor D, Pérez-Morín A, Pestano J, Mora D, Fajardo S

PeerJ

29-Feb-2024

PMCID:	PMC10909367
doi:	10.7717/peerj.16936
PMID:	38435985

Origins of the central Macaronesian psyllid lineages (Hemiptera; Psylloidea) with characterization of a new island radiation on endemic Convolvulus floridus (Convolvulaceae) in the Canary Islands

Bastin S, Reyes-Betancort JA, Siverio de la Rosa F, Percy DM

PLoS One

26-Jan-2024

PMCID:	PMC10817144
doi:	10.1371/journal.pone.0297062
PMID:	38277393

Psyllids in Natural Habitats as Alternative Resources for Key Natural Enemies of the Pear Psyllids (Hemiptera: Psylloidea)

Horton DR

Insects

06-Jan-2024

PMCID:	PMC10816694
doi:	10.3390/insects15010037
PMID:	38249044

Recent trends and economic significance of modified/functionalized biochars for remediation of environmental pollutants

Murtaza G, Ahmed Z, Valipour M, Ali I, Usman M, Iqbal R, Zulfiqar U, Rizwan M, Mahmood S, Ullah A, Arslan M, Rehman MH, Ditta A, Tariq A

Sci Rep

02-Jan-2024

PMCID:	PMC10762257
doi:	10.1038/s41598-023-50623-1
PMID:	38167973

Local ecological factors, not interference competition, drive the foundress number of two species of fig wasp sharing Ficus septica figs

Di Giusto B, Bain A

PLoS One

02-Jan-2024

PMCID:	PMC10760673
doi:	10.1371/journal.pone.0290439
PMID:	38165887

Response of leaf functional traits to soil nutrients in the wet and dry seasons in a subtropical forest on an island

Zhang J, Liang M, Tong S, Qiao X, Li B, Yang Q, Chen T, Hu P, Yu S

Front Plant Sci

07-Dec-2023

PMCID:	PMC10748499
doi:	10.3389/fpls.2023.1236607
PMID:	38143586

Advancing understanding of Ficus carica: a comprehensive genomic analysis reveals evolutionary patterns and metabolic pathway insights

Bao Y, He M, Zhang C, Jiang S, Zhao L, Ye Z, Sun Q, Xia Z, Zou M

Front Plant Sci

07-Dec-2023

PMCID:	PMC10754049
doi:	10.3389/fpls.2023.1298417
PMID:	38155853

Feeding ecology of a lesser‐known arboreal giant: Grizzled Giant Squirrel (Ratufa macroura), Southern Western Ghats, India

Thomas K, Šmejkal M, Nameer PO

Ecol Evol

06-Dec-2023

PMCID:	PMC10701183
doi:	10.1002/ece3.10765
PMID:	38077515

Reproductive Parameters and Host Specificity of Eurytoma erythrinae (Hymenoptera: Eurytomidae), a Biological Control Agent of the Erythrina Gall Wasp, Quadrastichus erythrinae (Hymenoptera: Eulophidae)

Nagamine WT, Yalemar JA, Wright MG, Ramadan MM

Insects

03-Dec-2023

PMCID:	PMC10743454
doi:	10.3390/insects14120923
PMID:	38132597

Wild edible plants and their cultural significance among the Zhuang ethnic group in Fangchenggang, Guangxi, China

Liu S, Huang X, Bin Z, Yu B, Lu Z, Hu R, Long C

J Ethnobiol Ethnomed

08-Nov-2023

PMCID:	PMC10631048
doi:	10.1186/s13002-023-00623-2
PMID:	37940945

Identification of Antioxidant Metabolites from Five Plants (Calophyllum inophyllum, Gardenia taitensis, Curcuma longa, Cordia subcordata, Ficus prolixa) of the Polynesian Pharmacopoeia and Cosmetopoeia for Skin Care

Chambon M, Ho R, Baghdikian B, Herbette G, Bun-Llopet SS, Garayev E, Raharivelomanana P

Antioxidants (Basel)

16-Oct-2023

PMCID:	PMC10604782
doi:	10.3390/antiox12101870
PMID:	37891949

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
(2R,3R,4S,4aR,10bS)-3,4,8,10-tetrahydroxy-2-(hydroxymethyl)-9-methoxy-3,4,4a,10b-tetrahydro-2H-pyrano[3,2-c]isochromen-6-one	12300074	Click to see	328.27	unknown	https://doi.org/10.1016/J.JEP.2008.06.025
> Benzenoids / Phenols / Methoxyphenols
methyl (2S)-3-hydroxy-2-(4-hydroxy-3-methoxyphenyl)propanoate	100955863	Click to see COC1=C(C=CC(=C1)C(CO)C(=O)OC)O	226.23	unknown	https://doi.org/10.1016/S0031-9422(98)00326-4
> Lignans, neolignans and related compounds / Furanoid lignans
(1S,2R)-2-[5-[(3R,3aS,6R,6aS)-6-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol	162896454	Click to see	584.60	unknown	https://doi.org/10.1248/CPB.48.1862
(1S,2S)-2-[4-[(3R,3aS,6R,6aS)-6-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol	162983519	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC(CO)C(C5=CC(=C(C=C5)O)OC)O)OC	584.60	unknown	https://doi.org/10.1248/CPB.48.1862
2-[4-[(3R,3aS,6R,6aS)-6-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol	101073642	Click to see	584.60	unknown	https://doi.org/10.1248/CPB.48.1862
2-[5-[(3R,3aS,6R,6aS)-6-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenoxy]-1-(4-hydroxy-3-methoxyphenyl)propane-1,3-diol	101073643	Click to see	584.60	unknown	https://doi.org/10.1248/CPB.48.1862
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Bridelionoside B	53326026	Click to see	406.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
7-Megastigmene-3,5,6,9-tetraol	637237	Click to see	244.33	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(2S,5R,9S)-9-Acetyl-9-hydroxy-2,7,8-trimethyl-2-((4R,8R)-4,8,12-trimethyltridecyl)-1-oxaspiro[4.4]non-7-en-6-one	73821792	Click to see	462.70	unknown	https://doi.org/10.1002/CHIN.200341185
Alpha-Tocospiro A	21674156	Click to see	462.70	unknown	https://doi.org/10.1002/CHIN.200341185
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.026 https://doi.org/10.1016/J.JEP.2008.06.025
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	45358157	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
(1R,3aS,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-5a,5b,8,8,11a-pentamethyl-9-oxo-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysene-3a-carboxylic acid	13887332	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O	454.70	unknown	https://doi.org/10.1016/J.JEP.2008.06.025
(1S,2R,6aR,6aS,6bR,8aR,12aR)-10-acetyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	3084011	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O	498.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.026
(1S,3aS,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bS)-9-acetyloxy-5a,5b,8,8,11a-pentamethyl-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-3a-carboxylic acid	154496097	Click to see	498.70	unknown	https://doi.org/10.1016/J.JEP.2008.06.025
(2S)-2-[(1R,3aR,5aR,5bR,7aS,9S,11aR,11bR,13aR,13bR)-9-acetyloxy-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-1-yl]propanoic acid	162854720	Click to see CC(C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C)C(=O)O	500.80	unknown	https://doi.org/10.1016/J.JEP.2008.06.025
(4aR,6aR,6aR,6bR,8aS,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,6a,7,8,9,12,12a,13,14,14a-tetradecahydro-1H-picen-3-ol	138113838	Click to see	426.70	unknown	https://doi.org/10.1248/CPB.47.498
(4aS,6aR,6aS,6bR,12aR,14bS)-10-acetyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	137705463	Click to see	498.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.026
[(1R,2R,5R,7S,10R,11R,14R,15S,16S,17S,19R,20R,21R)-20-hydroxy-1,2,6,6,10,16,17,21-octamethyl-18-oxahexacyclo[12.9.0.02,11.05,10.015,21.017,19]tricosan-7-yl] acetate	21606542	Click to see	500.80	unknown	via CMAUP database
[(1R,2S,5R,8R,9S,10R,13S,16R,18S,20S,23S,24S)-1,2,5,8,9,19,19,24-octamethyl-14,15-dioxahexacyclo[14.6.2.02,11.05,10.013,23.020,24]tetracos-11-en-18-yl] acetate	162992157	Click to see CC1CCC2(CCC3(C(=CC4C5C3(CCC6C5(C(CC(C6(C)C)OC(=O)C)OO4)C)C)C2C1C)C)C	498.70	unknown	https://doi.org/10.1016/J.JEP.2008.06.025
[(1S,3R,4S,5R,6S,9S,11S,14R,15S,18R,21R,22S,23R)-4-hydroperoxy-6,10,10,14,15,18,21,22-octamethyl-2-oxahexacyclo[13.8.0.01,3.05,14.06,11.018,23]tricosan-9-yl] acetate	163086873	Click to see CC1CCC2(CCC3(C4(CCC5C(C(CCC5(C4C(C6C3(C2C1C)O6)OO)C)OC(=O)C)(C)C)C)C)C	516.80	unknown	https://doi.org/10.1016/J.JEP.2008.06.025
[(3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14S,14aR,14bS)-14-acetyloxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate	22296993	Click to see CC1CCC2(CCC3(C(=CC(C4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)OC(=O)C)C2C1C)C)C	526.80	unknown	https://doi.org/10.1248/CPB.48.593
[(3S,4aR,6aR,6bS,8aR,11R,12S,12aR,14S,14aR,14bS)-14-hydroperoxy-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate	163033476	Click to see	500.80	unknown	https://doi.org/10.1248/CPB.48.593
[(3S,4aR,6aR,6bS,8aR,12aR,14aR,14bS)-12a-hydroperoxy-4,4,6a,6b,8a,11,11,14b-octamethyl-14-oxo-1,2,3,4a,5,6,7,8,9,10,12,14a-dodecahydropicen-3-yl] acetate	10839556	Click to see	514.70	unknown	https://doi.org/10.1016/J.JEP.2008.06.025
[(3S,4aR,6aR,6bS,8aR,12aR,14S,14aR,14bS)-14-hydroxy-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl] acetate	163056763	Click to see	484.80	unknown	https://doi.org/10.1248/CPB.48.593
3-Oxo-12-ursen-28-oic acid	13893949	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C(=O)O	454.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.026
3-Oxo-olean-12-en-28-oic acid	12313702	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C(=O)O)C	454.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.026
3-Oxolup-20(29)-en-28-oic acid	289985	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O	454.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.026
9-Acetyloxy-5a,5b,8,8,11a-pentamethyl-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-3a-carboxylic acid	289984	Click to see	498.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.026
Betulonic acid	122844	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O	454.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.026
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/J.JEP.2008.06.025
Npc3247	619164	Click to see	498.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.026
Oleanolic Acid	10494	Click to see	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.026
Oleanonic Acid	12313704	Click to see	454.70	unknown	https://doi.org/10.1016/J.JEP.2008.06.025
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.026
Ursolic acid acetate	6475119	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O	498.70	unknown	https://doi.org/10.1016/J.JEP.2008.06.025
Ursonic Acid	9890209	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1C)C)C(=O)O	454.70	unknown	https://doi.org/10.1016/J.PHYTOCHEM.2004.12.026 https://doi.org/10.1016/J.JEP.2008.06.025
> Lipids and lipid-like molecules / Steroids and steroid derivatives
[(1R,3aR,5aR,5bR,7aR,9R,11aR,11bR,13aR,13bS)-1-[(1S)-1-hydroperoxyethyl]-3a,5a,5b,8,8,11a-hexamethyl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate	162920497	Click to see	488.70	unknown	https://doi.org/10.1016/J.JEP.2008.06.025
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(6R)-6-[(1S,3R,6S,8R,11S,12S,15R,16R)-6-hydroxy-7,7,12,16-tetramethyl-15-pentacyclo[9.7.0.01,3.03,8.012,16]octadecanyl]heptan-2-one	101718404	Click to see CC(CCCC(=O)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	428.70	unknown	https://doi.org/10.1248/CPB.49.581
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1016/J.BMCL.2010.12.025
[(2R,3S,4S,5R,6R)-6-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl octadecanoate	53326868	Click to see CCCCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O	843.30	unknown	via CMAUP database
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/10.1016/J.BMCL.2010.12.025
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/10.1016/J.BMCL.2010.12.025
Stigmast-5-en-3-ol	22012	Click to see	414.70	unknown	https://doi.org/10.1016/J.BMCL.2010.12.025
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(3S)-4-acetyloxy-3-[(2S,3R)-2,3-dimethyl-5-oxooxolan-2-yl]-3-methylbutyl] acetate	162907488	Click to see CC1CC(=O)OC1(C)C(C)(CCOC(=O)C)COC(=O)C	300.35	unknown	https://doi.org/10.1248/CPB.48.1862
Ficusolide diacetate	10566130	Click to see	300.35	unknown	https://doi.org/10.1248/CPB.48.1862
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(4S,5S)-4-hydroxy-4-(2-hydroxyethyl)-3,3,5-trimethylcyclohexan-1-one	10821909	Click to see CC1CC(=O)CC(C1(CCO)O)(C)C	200.27	unknown	https://doi.org/10.1248/CPB.47.299
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4S,5R,6R)-2-(3-hydroxy-4,5-dimethoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol	163020072	Click to see COC1=CC(=CC(=C1OC)O)OC2C(C(C(C(O2)CO)O)O)O	332.30	unknown	https://doi.org/10.1016/S0031-9422(98)00326-4
(2S,3R,4S,5S,6R)-2-(3-hydroxy-4,5-dimethoxyphenoxy)-6-(hydroxymethyl)oxane-3,4,5-triol	71719415	Click to see COC1=CC(=CC(=C1OC)O)OC2C(C(C(C(O2)CO)O)O)O	332.30	unknown	https://doi.org/10.1016/S0031-9422(98)00326-4
(E)-3-[(2R,3S,4R,4aS,9bS)-3,4,7,9-tetrahydroxy-2-(hydroxymethyl)-6-[(2R,3S,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-3,4,4a,9b-tetrahydro-2H-pyrano[3,2-b][1]benzofuran-8-yl]but-2-enoic acid	162911640	Click to see CC(=CC(=O)O)C1=C(C2=C(C(=C1O)C3C(C(C(C(O3)CO)O)O)O)OC4C2OC(C(C4O)O)CO)O	516.40	unknown	https://doi.org/10.1016/J.JEP.2008.06.025
Syringin	5316860	Click to see	372.40	unknown	https://doi.org/10.1016/J.BMCL.2010.12.025
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(4R,5S)-5-(1,4-dihydroxy-2-methylbutan-2-yl)-4,5-dimethyloxolan-2-one	10608760	Click to see CC1CC(=O)OC1(C)C(C)(CCO)CO	216.27	unknown	https://doi.org/10.1248/CPB.47.299
> Organoheterocyclic compounds / Oxanes
(4S,5R,9S)-9-acetyl-4,6,6-trimethyl-1,8-dioxaspiro[4.5]decan-2-one	100987513	Click to see CC1CC(=O)OC12CC(OCC2(C)C)C(=O)C	240.29	unknown	https://doi.org/10.1248/CPB.47.299
> Organoheterocyclic compounds / Oxepanes
(1R,2R,5R,7S,10R,11R,14R,15R,16S,18S,20R,21R)-1,2,6,6,10,16,21-heptamethyl-17-methylidene-19-oxahexacyclo[12.9.0.02,11.05,10.015,21.018,20]tricosan-7-ol	15275754	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(C6C(C1=C)O6)C)C)C)(C)C)O)C	440.70	unknown	https://doi.org/10.1248/CPB.47.498
> Organoheterocyclic compounds / Tetrahydrofurans
(2Z)-2-[(1R,4S)-1,6,6-trimethyl-7-oxabicyclo[2.2.1]heptan-2-ylidene]acetic acid	100955862	Click to see CC1(CC2CC(=CC(=O)O)C1(O2)C)C	196.24	unknown	https://doi.org/10.1016/S0031-9422(98)00326-4
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Ficusal	10496641	Click to see	330.30	unknown	https://doi.org/10.1248/CPB.48.1862
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin	9064	Click to see	290.27	unknown	https://doi.org/10.1016/J.BMCL.2010.12.025
Epicatechin	72276	Click to see	290.27	unknown	https://doi.org/10.1016/J.BMCL.2010.12.025
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin	114776	Click to see	448.40	unknown	https://doi.org/10.1016/J.BMCL.2010.12.025
Isovitexin	162350	Click to see	432.40	unknown	https://doi.org/10.1016/J.BMCL.2010.12.025
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5,7-dihydroxy-6-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)-2-(4-((2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxyphenyl)chromen-4-one	154105	Click to see	594.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(2R)-4-hydroxy-2-(2-hydroxypropan-2-yl)-6-[(2R)-2-(2-hydroxypropan-2-yl)-2,3-dihydro-1-benzofuran-5-yl]-2,3-dihydrofuro[3,2-g]chromen-5-one	162949526	Click to see	438.50	unknown	https://doi.org/10.1021/NP960683P
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
Ficuisoflavone	10546044	Click to see	354.40	unknown	https://doi.org/10.1021/NP960683P

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Ficus microcarpa

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