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.

Traditional uses of Artocarpus heterophyllus (jackfruit) include several preparations that rely on infusions, decoctions, and poultices. In the Tamil Nadu region of southern India, the fresh or dried leaves are steeped in hot water to make a mild tea that is taken to relieve stomach upset, fever, and mild diarrhea; this practice is documented by Sharma et al., 2019. In Java, Indonesia, the bark is boiled in water to produce a decoction that is drunk as a remedy for acute diarrhea and dysentery, a use recorded by Suryani and colleagues, 2020. The leaves are also applied as a poultice in rural Thai communities to treat minor wounds and skin infections, a method described by Petchsri et al., 2021. These preparations are all based on the same principle of extracting water‑soluble compounds from the plant material.

A practical recipe for a jackfruit leaf tea is simple and safe for most adults. Take 5 g of dried jackfruit leaves (or 10 g of fresh leaves) and place them in a cup. Pour 250 ml of boiling water over the leaves, cover, and let steep for 10 minutes. Strain and drink warm. The tea can be taken up to three times a day for mild digestive complaints. Pregnant women should avoid this tea because the safety profile during pregnancy has not been established, and high doses of flavonoids may interfere with uterine activity. As with any herbal preparation, individuals with known allergies to Moraceae family members should exercise caution.

The pharmacological activity of jackfruit leaves is largely attributed to well‑established phytochemicals that have been isolated from the species. Flavonoids such as quercetin and kaempferol, along with phenolic acids (gallic acid, ellagic acid) and tannins, are present in appreciable amounts. These compounds have documented anti‑inflammatory, antioxidant, and antimicrobial properties that plausibly explain the traditional use of leaf tea for gastrointestinal upset and the poultice for skin infections. The bark contains similar phenolics, which may account for its antidiarrheal effect.

Modern research continues to explore the therapeutic potential of jackfruit leaves. Recent in‑vitro studies have confirmed anti‑inflammatory activity of leaf extracts, and a small clinical trial in India reported reduced abdominal pain scores in patients with functional dyspepsia after a 4‑week course of leaf tea. Commercially, dried jackfruit leaf tea is now available in specialty herbal markets in Southeast Asia and online, allowing consumers to access a time‑tested remedy with a growing body of scientific support.

General Uses Top

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Common products:
The mature jackfruit fruit is sold fresh, canned in syrup, dehydrated as fruit chips, frozen as pulp, and processed into jam, jelly and chutney. The large seeds are roasted or boiled and ground into a flour or starch product used in gluten‑free bakery and noodles. The timber is marketed as a construction and furniture wood. The sticky latex exuded from cuts in the trunk is collected for use as a natural adhesive. The bark yields a reddish‑brown dye that is used in traditional textile coloration.

Industrial and craft applications:
Jackfruit wood is employed in furniture, interior paneling, flooring, cabinetry, musical‑instrument making, and boat hulls, valued for its moderate density (≈0.6–0.7 g cm⁻³) and termite resistance. The latex, composed mainly of polysaccharides, serves as a glue in wood‑joinery and craft assembly. Bark dye provides a natural brown color for protein fibers and leather; research also explores seed starch as a potential feedstock for biodegradable plastics, though commercial scaling remains limited.

Food and beverages (non‑medicinal):
Processed fruit products include canned sliced jackfruit, dried fruit chips, sweet syrups, frozen pulp for ice‑cream bases, and confectionery fillings. Seed flour, characterized by a high amylose content (≈30–35 %), provides a low‑gelatinization flour for breads, cakes and noodles. Roasted seeds are consumed as snack kernels.

Colorants and tanning:
The bark contains hydrolyzable gallotannins that impart a brown hue when extracted, useful for dyeing wool, silk and for leather tanning. Leaf extracts can also supply natural pigments for textile applications.

Wood and fiber:
The wood’s balanced lignin‑cellulose ratio (≈25 % lignin) gives it good workability and moderate strength, supporting its use in structural and ornamental items. Bark fibers have been investigated as a source of pulp for paper and board production.

Fragrance and cosmetics:
Essential oil distilled from jackfruit leaves contains β‑caryophyllene, α‑humulene and other sesquiterpenes that contribute a sweet, fruity note; it is incorporated in niche perfumery and in cosmetic fragrance blends.

Properties relevant to use:
Seed starch’s high amylose fraction yields a flour with low gelatinization temperature and good water‑binding capacity, suitable for gluten‑free formulations. Bark tannins’ gallotannin profile provides both color and tanning activity. Latex polysaccharides confer adhesiveness, while the wood’s lignin‑cellulose composition enables machining and finishing without excessive brittleness.

Standards and regulation:
Processed jackfruit products intended for human consumption fall under national food‑safety frameworks such as the U.S. Food and Drug Administration (21 CFR) and the European Union’s Novel Food Regulation. Timber from Artocarpus heterophyllus is harvested under forest‑management certification schemes like the Forest Stewardship Council (FSC).

Sustainability and sourcing:
Jackfruit trees are cultivated across tropical Asia, India, and Brazil, often on marginal or degraded land, and can produce up to 200 kg of fruit per mature tree annually. Their agroforestry integration provides soil stabilization and diversified income, making them a relatively low‑input, sustainable crop when bark and latex are harvested responsibly.

Synonyms Top

Scientific name	Authority	First published in
Saccus heterophyllus	Kuntze	Revis. Gen. Pl. 2: 633. 1891 [5 Nov 1891]
Sitodium cauliflorum	Gaertn.	Fruct. Sem. Pl. 1: 345 (1788)
Artocarpus brasiliensis	Gomes	Observ. Bot.-Med. Nonnullis Bras. Pl. 2: 34 (1803)
Artocarpus maximus	Blanco	Fl. Filip. : 669 (1837)
Artocarpus nanca	Noronha	Verh. Batav. Genootsch. Kunst. 5(Art. 4): 7. 1790
Artocarpus philippensis	Lam.	Encycl. 3: 210 (1789)

Common names Top

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Filter by language:

Language	Common/alternative name
English	jackfruit tree
English	jackfruit
English	nangka tree
English	saniya
English	jack tree
Spanish	yaca
Spanish	arbol de jack
Spanish	Árbol de jack
Spanish	arbol jack
Spanish	Árbol jack
Spanish	arbol yaka
Spanish	Árbol yaka
Spanish	fruta de jack
Spanish	fruta de yaka
Spanish	jack fruit
Spanish	jackfruit
Spanish	nangka
Arabic	جاك فروت
Arabic	جاكا
Arabic	خبزية متغايرة الاوراق
Arabic	جاكية
Assamese	কঁঠাল
ban	nangka
bbc	pinasa
bcl	langka
bdr	nangka'
Bulgarian	Индийско хлебно дърво
Bulgarian	джакфрут
Bengali	কাঠাল
Bengali	কাঠাঁল
Bengali	কাঁঠাল
Tibetan	པ་ར་མི་ཏ།
Catalan	kathal
Catalan	jaquer
Czech	džekfrut
Czech	Žakie
Czech	chlebovník různolistý
German	jackbaumfrucht
German	jackbaum
German	jackfruit
German	jakobsfrucht
German	jackfrucht
dv	ސައްކެޔޮ
Greek	Αρτόκαρπος ο ετερόφυλλος
Esperanto	Ĵakfrukto
Esperanto	jakvo
Estonian	jaka
Persian	جکفروت
Finnish	intianleipäpuu
Finnish	jackfruit
Finnish	jakkipuu
Finnish	jakkihedelmä
French	jacque
French	jaque
French	jaquier
French	pomme de jacque
French	ti jac
French	ti'jac
French	tijac
French	jacquier
Irish	seacthoradh
gom	पणस
gor	langge
Gujarati	ફણસ
Hebrew	פרי הג'ק
Hebrew	פרי-הג'ק
Hindi	कटहल
Croatian	nangka
Upper Sorbian	wšelakołopjenaty chlěbownik
Hungarian	jackfruit
Hungarian	jákafa
Hungarian	dzsekkfruit
Hungarian	dzsekkfrút
Armenian	Ջեկֆրուտ
Indonesian	pohon nangka
Indonesian	nangka
io	jack-frukto
Icelandic	saðningaraldin
Italian	jackfruit
Japanese	ジャックフルーツ
Japanese	ハラミツ
Japanese	パラミツ
jv	gori
jv	nangka
jv	checek
jv	nongko
Georgian	ჯეკფრუტი
kge	lamasa
Kazakh	Джекфрут
Khmer	ខ្នុរ
Kannada	ಹಲಸು
Korean	잭프룻
Korean	잭프루트
koi	Джекфрут
kv	Джекфрут
lbe	Джекфрут
lbe	Жекфрут
lo	ໝາກມີ້
Lithuanian	stambusis duonmedis
Latvian	indijas maizeskoks
Latvian	džekfrūts
mad	nangka
mai	कटहर
mdf	Джакфрут
Malagasy	ampalibe
Malagasy	finesy
min	cubadak
Macedonian	џекфрут
Macedonian	разнолистен лебовец
Malayalam	പ്ലാവ്
Malayalam	ഫലശം
Malayalam	പിലാവ്
mnc	ᠪᠠᡵᠠᠮᡳᡩᠠ
Marathi	फणस
mrj	Джекфрут
Malay	buah nangka
Malay	nangka
Malay	pokok nangka
mwl	jaqua
Burmese	ပိန္နဲပင်
nan	po-lô-bi̍t
Norwegian Bokmål	jackfrukt
Nepali	रूखकटहर
Nepali	रुख कटहर
nia	na'a
Dutch	jackfruit
Dutch	nangka
Norwegian Nynorsk	jackfrukt
nrm	jatchyi
Oriya	ପଣସ
Punjabi	ਕਟਹਲ
pam	yangka
Polish	drzewo bochenkowe
Polish	chlebowiec różnolistny
Punjab	جیکفروٹ
Portuguese	jaca
Russian	Джекфрут
Kinyarwanda	urubuto rwa yakobo
Kinyarwanda	igifenesi
sa	पनसफलम्
sat	ᱜᱷᱟᱱᱴᱟᱲ
sco	jackfruit
sd	فڻس
Serbo-Croatian	nangka
Sinhala	jackfruit
Sinhala	කොස්
Slovak	chlebovník celolistý
Slovak	chlebovník celistvolistý
Slovenian	nangka
Slovenian	jakobovec
Serbian	Џекфрут
su	nangka
Swedish	jackfrukt
Swahili	mfenesi
Swahili	kifenesi
szy	nipaluma-tabakiay apalu, tabakiay apalo
Tamil	பலா மரம்
Tamil	பலாப்பழம்
Tamil	பிலாப்பழம்
Tamil	பலா
tcy	ಪೆಲಕಾಯಿ
Telugu	ఆర్టోకార్పస్ హెటిరోఫిల్లస్
Telugu	పనస పండు
Telugu	పనసపండు
Telugu	పనస
Thai	ไม้ขนุน
Thai	ขนุน
Tonga	mei ʻinitia
Turkish	jak
Turkish	jak meyvesi
ty	’uru taratoni
udm	Джекфрут
ug	پارامىتا (مېۋە)
Ukrainian	Джекфрут
Urdu	کٹھل
Vietnamese	mít
war	langka
war	langkâ
xmf	ჯეკფრუტი
Chinese	波罗蜜
Chinese	波羅蜜
Chinese	木波罗
Chinese	木菠萝
Chinese	树菠萝
Chinese	波罗蜜叶
Chinese	波罗蜜树液
Chinese	波罗蜜核中仁
Chinese	菠萝蜜
Chinese	树波罗
Chinese	牛肚子果
Chinese	大樹菠蘿

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

Africa click to expand
- West Tropical Africa
  - Gambia
- West-central Tropical Africa
  - Cameroon
  - Gulf Of Guinea Islands
- Western Indian Ocean
  - Comoros
  - Mauritius
  - Réunion
  - Seychelles

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Hainan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Laccadive Islands
  - Nepal
  - Sri Lanka
- Indo-China
  - Andaman Islands
  - Laos
  - Myanmar
  - Nicobar Nicobar
  - Vietnam
- Malesia
  - Borneo
  - Lesser Sunda Islands
  - Malaya
  - Philippines
  - Sulawesi
- Papuasia
  - Solomon Islands

Pacific click to expand
- North-central Pacific
  - Hawaii
- Northwestern Pacific
  - Caroline Islands
  - Marianas
- Southwestern Pacific
  - Fiji
  - Gilbert Islands
  - Nauru
  - New Caledonia

Southern America click to expand
- Brazil
  - Brazil North
  - Brazil Northeast
  - Brazil South
  - Brazil Southeast
  - Brazil West-central
- Caribbean
  - Cuba
  - Dominican Republic
  - Haiti
  - Jamaica
  - Leeward Islands
  - Puerto Rico
  - Southwest Caribbean
  - Trinidad-Tobago
  - Windward Islands
- Central America
  - El Salvador
- Northern South America
  - Venezuela
- Western South America
  - Ecuador
  - Peru

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000550491
UNII	76HPT0191N
USDA Plants	ARHE2
Tropicos	21300871
INPN	447364
KEW	urn:lsid:ipni.org:names:850389-1
The Plant List	kew-2653982
Plantarium	52827
Missouri Botanical Garden	282749
Open Tree Of Life	83984
Observations.org	341155
NCBI Taxonomy	3489
IPNI	850389-1
iNaturalist	123003
GBIF	2984565
Freebase	/m/01xcwm
EPPO	ABFHE
EOL	596411
Elurikkus	2914
US Library of Congress	sh2012002890
USDA GRIN	70095
Wikipedia	Jackfruit
CMAUP	NPO17767

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_025403435.1	ASM2540343v1	Chromosome	South China Botanical Garden	2022-09-27	105	939.97 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

On-farm crop diversity, conservation, importance and value: a case study of landraces from Western Ghats of Karnataka, India

Puneeth GM, Gowthami R, Katral A, Laxmisha KM, Vasudeva R, Singh GP, Archak S

Sci Rep

10-May-2024

PMCID:	PMC11087530
doi:	10.1038/s41598-024-61428-1
PMID:	38730080

Morphological and genetic characterization of jackfruit (Artocarpus heterophyllus) in the Kayunga and Luwero districts of Uganda

Gwokyalya R, Nanteza A, Wagaba H, Kayondo SI, Kazigaba D, Nakabonge G

BMC Plant Biol

09-May-2024

PMCID:	PMC11080175
doi:	10.1186/s12870-024-05064-x
PMID:	38724929

Unravelling taboos and cultural beliefs associated with hidden hunger among pregnant and breast-feeding women in Buyende district Eastern Uganda

Tugume P, Mustafa AS, Walusansa A, Ojelel S, Nyachwo EB, Muhumuza E, Nampeera M, Kabbale F, Ssenku JE

J Ethnobiol Ethnomed

02-May-2024

PMCID:	PMC11064283
doi:	10.1186/s13002-024-00682-z
PMID:	38693532

Phytochemicals from Bark Extracts and Their Applicability in the Synthesis of Thermosetting Polymers: An Overview

Szmechtyk T, Małecka M

Materials (Basel)

30-Apr-2024

PMCID:	PMC11084627
doi:	10.3390/ma17092123
PMID:	38730929

Electrospun nanofibers synthesized from polymers incorporated with bioactive compounds for wound healing

Palani N, Vijayakumar P, Monisha P, Ayyadurai S, Rajadesingu S

J Nanobiotechnology

27-Apr-2024

PMCID:	PMC11056076
doi:	10.1186/s12951-024-02491-8
PMID:	38678271

Prenylated Flavonoids of the Moraceae Family: A Comprehensive Review of Their Biological Activities

Morante-Carriel J, Živković S, Nájera H, Sellés-Marchart S, Martínez-Márquez A, Martínez-Esteso MJ, Obrebska A, Samper-Herrero A, Bru-Martínez R

Plants (Basel)

27-Apr-2024

PMCID:	PMC11085352
doi:	10.3390/plants13091211
PMID:	38732426

In vitro cytotoxic activity on KATO-III cancer cell lines of mangiferolic acid purified from Thai Tetragonula laeviceps propolis

Meemongkolkiat T, Puthong S, Khongkarat P, Rod-im P, Duangphakdee O, Tuthaisong P, Phuwapraisirisan P, Chanchao C

Heliyon

27-Apr-2024

PMCID:	PMC11070865
doi:	10.1016/j.heliyon.2024.e30436
PMID:	38711626

Morphological and molecular characterizations of Pratylenchus coffeae infecting Ming aralia and coffee in Vietnam

Nguyen HD, Nguyen HT, Le TM, Hoang DD, Nguyen TD, Trinh QP

Helminthologia

23-Apr-2024

PMCID:	PMC11038238
doi:	10.2478/helm-2024-0004
PMID:	38659466

Effect of Refractance Window™ and oven drying on physicochemical and sensory properties of peach (Prunus persica L.) surplus

Largo-Avila E, Rico-Rodríguez F, Peñaloza-Figueroa JK, López-Padilla A

Front Nutr

23-Apr-2024

PMCID:	PMC11075169
doi:	10.3389/fnut.2024.1307423
PMID:	38716074

Lectins As Effective Tools in the Study of the Biliary Network and the Parenchymal Architecture of the Zebrafish (Danio rerio) Liver

Bhavsar H, Robinson Z, Benson M, Getachew F, González-Rosa JM, Lafontant PJ

Zebrafish

11-Apr-2024

PMCID:	PMC11035847
doi:	10.1089/zeb.2023.0073
PMID:	38621207

Rhizopus stolonifer and related control strategies in postharvest fruit: A review

Liu Q, Chen Q, Liu H, Du Y, Jiao W, Sun F, Fu M

Heliyon

10-Apr-2024

PMCID:	PMC11031825
doi:	10.1016/j.heliyon.2024.e29522

Physiological and molecular insights into the allelopathic effects on agroecosystems under changing environmental conditions

Kumar N, Singh H, Giri K, Kumar A, Joshi A, Yadav S, Singh R, Bisht S, Kumari R, Jeena N, Khairakpam R, Mishra G

Physiol Mol Biol Plants

06-Apr-2024

PMCID:	PMC11018569
doi:	10.1007/s12298-024-01440-x
PMID:	38633277

The evolutionary origin of naturally occurring intermolecular Diels-Alderases from Morus alba

Ding Q, Guo N, Gao L, McKee M, Wu D, Yang J, Fan J, Weng JK, Lei X

Nat Commun

20-Mar-2024

PMCID:	PMC10954736
doi:	10.1038/s41467-024-46845-0
PMID:	38509059

Rapid improvement of oculomotor nerve function with ayurvedic treatment in traumatic diplopia - A case report

Shanti K, Gopinathan G

J Ayurveda Integr Med

19-Mar-2024

PMCID:	PMC10966156
doi:	10.1016/j.jaim.2024.100889
PMID:	38507966

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

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
> Alkaloids and derivatives / Yohimbine alkaloids
Aricine	251575	Click to see	382.50	unknown	https://doi.org/10.1016/0031-9422(95)00442-A
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	https://doi.org/10.1021/JF9014685
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	https://doi.org/10.1021/JF9014685
> Benzenoids / Phenols / Benzenediols / Resorcinols
5-[2-[4-Hydroxy-4-(3-methylbut-2-enoxy)cyclohexa-1,5-dien-1-yl]ethenyl]benzene-1,3-diol	129650764	Click to see	314.40	unknown	https://doi.org/10.1016/S0031-9422(00)00074-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Wax esters / Wax monoesters
[(4R)-4-hydroxyundecyl] docosanoate	162951925	Click to see	510.90	unknown	https://doi.org/10.1016/S0031-9422(00)97943-3
[(9R)-9-hydroxytridecyl] docosanoate	163024957	Click to see	538.90	unknown	https://doi.org/10.1016/S0031-9422(00)90605-8
4-Hydroxyundecyl docosanoate	14352165	Click to see	510.90	unknown	https://doi.org/10.1016/S0031-9422(00)97943-3
9-Hydroxytridecyl docosanoate	129824367	Click to see	538.90	unknown	https://doi.org/10.1016/S0031-9422(00)90605-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see	256.42	unknown	https://doi.org/10.1007/S10600-010-9698-Y
Stearic Acid	5281	Click to see	284.50	unknown	https://doi.org/10.1007/S10600-010-9698-Y
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3S,3aR,6R,9aR)-3-[(1S)-1-hydroxyoctyl]-9a-methylspiro[3a,4,5,8-tetrahydro-3H-furo[3,2-g]isochromene-6,5'-furan]-2,2',9-trione	101252367	Click to see	418.50	unknown	https://doi.org/10.1016/S0031-9422(00)00074-1
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic Acid	3931	Click to see	280.40	unknown	https://doi.org/10.1007/S10600-010-9698-Y
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	https://doi.org/10.1007/S10600-010-9698-Y
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-CITRONELLOL, (R)-	101977	Click to see	156.26	unknown	https://doi.org/10.3987/COM-94-S(B)84
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
(2Z,4E)-5-[(1S,3S,5R,8S)-8-hydroxy-1,5-dimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoic acid	162939836	Click to see	444.50	unknown	https://doi.org/10.1021/JF9014685
5-[8-Hydroxy-1,5-dimethyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6-oxabicyclo[3.2.1]octan-8-yl]-3-methylpenta-2,4-dienoic acid	73170036	Click to see CC(=CC(=O)O)C=CC1(C2(CC(CC1(OC2)C)OC3C(C(C(C(O3)CO)O)O)O)C)O	444.50	unknown	https://doi.org/10.1021/JF9014685
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
Isocostic acid	10922464	Click to see CC1=C2CC(CCC2(CCC1)C)C(=C)C(=O)O	234.33	unknown	https://doi.org/10.1021/JF9014685
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones
Bigelovin	3080597	Click to see	304.34	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(-)-spirocochlealactone A	146684388	Click to see	682.80	unknown	https://doi.org/10.1016/S0031-9422(00)90655-1
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(00)90605-8
Betulin	72326	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)90605-8
Lup-20(29)-ene-3beta,28-diol	221023	Click to see	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)90605-8
Squalene	638072	Click to see	410.70	unknown	https://doi.org/10.1007/S10600-010-9698-Y
Super Squalene; trans-Squalene;AddaVax	1105	Click to see	410.70	unknown	https://doi.org/10.1007/S10600-010-9698-Y
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(00)90605-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5R)-5-hydroxy-6-methylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol	14313591	Click to see	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)90655-1
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(E,2R)-6-hydroxy-6-methylhept-4-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.0^{1,3.0^{3,8.0^{12,16]octadecan-6-ol	496638	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)90655-1
24R,25-Dihydroxycycloartan-3-one	91895426	Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	458.70	unknown	https://doi.org/10.1016/S0031-9422(00)90655-1
7,7,12,16-Tetramethyl-15-(6-methylhept-5-en-2-yl)pentacyclo(9.7.0.01,3.03,8.012,16)octadecan-6-one	348093	Click to see	424.70	unknown	https://doi.org/10.1016/S0031-9422(00)90655-1
9,19-Cyclo-9beta-lanost-24-en-3beta-ol	500213	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)90655-1
CID 14313590	14313590	Click to see CC(CCC(C(=C)C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)90655-1
Cycloart-23-ene-3beta,25-diol	5470009	Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	442.70	unknown	https://doi.org/10.1016/S0031-9422(00)90655-1
Cycloartenol	92110	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	426.70	unknown	https://doi.org/10.1016/S0031-9422(00)90655-1
Cycloartenone	12305360	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(=O)C5(C)C)C)C	424.70	unknown	https://doi.org/10.1016/S0031-9422(00)90655-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	https://doi.org/10.1007/S10600-010-9698-Y https://doi.org/10.1016/S0031-9422(00)90605-8
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	122544	Click to see	412.70	unknown	https://doi.org/10.1007/S10600-010-9698-Y
17-(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-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1007/S10600-010-9698-Y https://doi.org/10.1016/S0031-9422(00)90605-8
Stigmasterol	5280794	Click to see	412.70	unknown	https://doi.org/10.1007/S10600-010-9698-Y
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(13R)-6,8,17,19-tetrahydroxy-14,14-dimethyl-5,7-bis(3-methylbut-2-enyl)-3,15-dioxapentacyclo[11.6.1.02,11.04,9.016,20]icosa-1(20),2(11),4,6,8,16,18-heptaen-10-one	162910598	Click to see	504.60	unknown	https://doi.org/10.1021/JF9014685
(13R)-8,17-dihydroxy-6,19-dimethoxy-14,14-dimethyl-3,15-dioxapentacyclo[11.6.1.02,11.04,9.016,20]icosa-1(19),2(11),4,6,8,16(20),17-heptaen-10-one	154496195	Click to see	396.40	unknown	https://doi.org/10.3987/COM-92-6229
(13R)-8,17,19-trihydroxy-6-methoxy-14,14-dimethyl-18-(3-methylbut-2-enyl)-3,15-dioxapentacyclo[11.6.1.02,11.04,9.016,20]icosa-1(20),2(11),4,6,8,16,18-heptaen-10-one	162856399	Click to see	450.50	unknown	https://doi.org/10.3987/COM-94-S(B)84
(13R)-8,17,19-trihydroxy-6-methoxy-14,14-dimethyl-3,15-dioxapentacyclo[11.6.1.02,11.04,9.016,20]icosa-1(20),2(11),4,6,8,16,18-heptaen-10-one	163036529	Click to see CC1(C2CC3=C(C4=C2C(=C(C=C4O)O)O1)OC5=CC(=CC(=C5C3=O)O)OC)C	382.40	unknown	https://doi.org/10.3987/COM-92-6229
(13S)-6,8,17,19-tetrahydroxy-14,14-dimethyl-18-(3-methylbut-2-enyl)-3,15-dioxapentacyclo[11.6.1.02,11.04,9.016,20]icosa-1(20),2(11),4,6,8,16,18-heptaen-10-one	162846776	Click to see	436.50	unknown	https://doi.org/10.3987/COM-92-6229 https://doi.org/10.1021/JF9014685
6,8,17,19-Tetrahydroxy-14,14-dimethyl-5,7-bis(3-methylbut-2-enyl)-3,15-dioxapentacyclo[11.6.1.02,11.04,9.016,20]icosa-1(20),2(11),4,6,8,16,18-heptaen-10-one	44226792	Click to see	504.60	unknown	https://doi.org/10.1021/JF9014685
Artonin J	44258663	Click to see	436.50	unknown	https://doi.org/10.3987/COM-92-6229 https://doi.org/10.1021/JF9014685
Artonin K	15340661	Click to see	382.40	unknown	https://doi.org/10.3987/COM-92-6229
Artonin L	44258662	Click to see	396.40	unknown	https://doi.org/10.3987/COM-92-6229
Artonin T	44258664	Click to see	450.50	unknown	https://doi.org/10.3987/COM-94-S(B)84
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
Artonin Q	131753034	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C5C(=O)CC(C5=C(C=C4C3=O)C(=C)C)(C(=O)OC)O)O)C=CC(O2)(C)C)C	530.60	unknown	https://doi.org/10.3987/COM-94-S(B)84
methyl (7S)-7,14-dihydroxy-18,18-dimethyl-21-(3-methylbut-2-enyl)-5,12-dioxo-9-prop-1-en-2-yl-2,19-dioxapentacyclo[11.8.0.03,11.04,8.015,20]henicosa-1(13),3,8,10,14,16,20-heptaene-7-carboxylate	162858251	Click to see	530.60	unknown	https://doi.org/10.3987/COM-94-S(B)84
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(10S)-5,7,8,15-tetrahydroxy-19,19-dimethyl-22-(3-methylbut-2-enyl)-10-prop-1-en-2-yl-2,20-dioxapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(14),3(12),4(9),5,7,15,17,21-octaen-13-one	154496194	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)CC(C5=C4C(=CC(=C5O)O)O)C(=C)C)O)C=CC(O2)(C)C)C	502.60	unknown	https://doi.org/10.3987/COM-89-5019 https://doi.org/10.1016/0031-9422(95)00442-A
(17R)-12,21,23-trihydroxy-8,8,18,18-tetramethyl-5-(3-methylbut-2-enyl)-3,7,19-trioxahexacyclo[15.6.1.02,15.04,13.06,11.020,24]tetracosa-1(24),2(15),4(13),5,9,11,20,22-octaen-14-one	154496193	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)CC5C6=C4C(=CC(=C6OC5(C)C)O)O)O)C=CC(O2)(C)C)C	502.60	unknown	https://doi.org/10.3987/COM-89-5019
(17S)-12,21,23-trihydroxy-8,8,18,18-tetramethyl-5-(3-methylbut-2-enyl)-3,7,19-trioxahexacyclo[15.6.1.02,15.04,13.06,11.020,24]tetracosa-1(24),2(15),4(13),5,9,11,20,22-octaen-14-one	163084071	Click to see	502.60	unknown	https://doi.org/10.1016/0031-9422(95)00442-A https://doi.org/10.1021/JF9014685 https://doi.org/10.1016/J.PHYTOCHEM.2003.08.009
10H-Cyclopenta[h]pyrano[3,2-b]xanthene-3-carboxylic acid, 1,2,3,6-tetrahydro-12-(3-hydroperoxy-3-methyl-1-butenyl)-3,7-dihydroxy-10,10-dimethyl-4-(1-methylethenyl)-1,6-dioxo-, methyl ester	162927899	Click to see	562.60	unknown	https://doi.org/10.3987/COM-94-S(B)84
artonin A	14557102	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)CC5C6=C4C(=CC(=C6OC5(C)C)O)O)O)C=CC(O2)(C)C)C	502.60	unknown	https://doi.org/10.1021/JF9014685 https://doi.org/10.1016/0031-9422(95)00442-A https://doi.org/10.1016/J.PHYTOCHEM.2003.08.009
Artonin B	11964501	Click to see	502.60	unknown	https://doi.org/10.1016/0031-9422(95)00442-A
> Organoheterocyclic compounds / Benzoxepines
(6R)-3,9-dihydroxy-6-(2-hydroxypropan-2-yl)-11-methoxy-10-(3-methylbut-2-enyl)-6,7-dihydrochromeno[3,2-d][1]benzoxepin-8-one	163057022	Click to see	452.50	unknown	https://doi.org/10.3987/COM-94-S(B)84
(6S)-3,9-dihydroxy-6-(2-hydroxypropan-2-yl)-11-methoxy-10-(3-methylbut-2-enyl)-6,7-dihydrochromeno[3,2-d][1]benzoxepin-8-one	163057021	Click to see	452.50	unknown	https://doi.org/10.3987/COM-94-S(B)84
Artonin S	44258666	Click to see CC(=CCC1=C(C=C2C(=C1O)C(=O)C3=C(O2)C4=C(C=C(C=C4)O)OC(C3)C(C)(C)O)OC)C	452.50	unknown	https://doi.org/10.3987/COM-94-S(B)84
> Organoheterocyclic compounds / Naphthopyrans
(6aR,12aS)-9,11-dimethoxy-6,6-dimethyl-8-(3-methylbut-2-enyl)-6a,7,12,12a-tetrahydronaphtho[2,3-c]chromen-3-ol	162915650	Click to see	408.50	unknown	https://doi.org/10.1016/0031-9422(95)00135-T
(6aS,12aS)-9,11-dimethoxy-6,6-dimethyl-8-(3-methylbut-2-enyl)-6a,7,12,12a-tetrahydronaphtho[2,3-c]chromen-3-ol	101929070	Click to see	408.50	unknown	https://doi.org/10.1016/S0040-4039(00)61402-8
Heterophylol	15227962	Click to see CC(=CCC1=C(C=C(C2=C1CC3C(C2)C4=C(C=C(C=C4)O)OC3(C)C)OC)OC)C	408.50	unknown	https://doi.org/10.1016/0031-9422(95)00135-T https://doi.org/10.1016/S0040-4039(00)61402-8
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
5-(6-Hydroxy-1-benzofuran-2-yl)-4-(3-methylbut-1-enyl)benzene-1,3-diol	162965093	Click to see	310.30	unknown	https://doi.org/10.1021/JF9014685
5-[6-Hydroxy-5-methoxy-4-(3-methylbut-2-enyl)-1-benzofuran-2-yl]-4-(3-methylbut-2-enyl)benzene-1,3-diol	44226790	Click to see	408.50	unknown	https://doi.org/10.1021/JF9014685
Moracin M	185848	Click to see	242.23	unknown	https://doi.org/10.1021/JF9014685
> Phenylpropanoids and polyketides / Aurone flavonoids
Broussoaurone A	15298907	Click to see	338.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Coumaric acid	322	Click to see	164.16	unknown	https://doi.org/10.1021/JF9014685
P-Coumaric Acid	637542	Click to see	164.16	unknown	https://doi.org/10.1021/JF9014685
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(E)-1-[3-[(1S,5S,6R)-6-[2,4-dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one	10723048	Click to see	662.70	unknown	https://doi.org/10.1016/0031-9422(95)00509-6
(E)-1-[3-[(1S,5S,6R)-6-[2,4-dihydroxy-3-[(E)-3-methylbut-1-enyl]benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one	163194405	Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)C=CC(C)C)O)C4=C(C=CC(=C4O)C(=O)C=CC5=CC=C(C=C5)O)O	662.70	unknown	https://doi.org/10.1016/0031-9422(95)00509-6
1-[3-[6-[2,4-Dihydroxy-3-(3-methylbut-1-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one	162875746	Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C(=C(C=C3)O)C=CC(C)C)O)C4=C(C=CC(=C4O)C(=O)C=CC5=CC=C(C=C5)O)O	662.70	unknown	https://doi.org/10.1016/0031-9422(95)00509-6
1-[3-[6-[2,4-Dihydroxy-3-(3-methylbut-2-enyl)benzoyl]-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-2,4-dihydroxyphenyl]-3-(4-hydroxyphenyl)prop-2-en-1-one	73818303	Click to see	662.70	unknown	https://doi.org/10.1016/0031-9422(95)00509-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 2-prenylated flavans
4-((2S)-3,4-Dihydro-7-hydroxy-2H-1-benzopyran-2-yl)-3,6-bis(3-methyl-2-buten-1-yl)-1,2-benzenediol	442414	Click to see	394.50	unknown	via CMAUP database
Broussoflavan A	44257178	Click to see	426.50	unknown	via CMAUP database
Kazinol B	480869	Click to see	392.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-2,3-Dihydro-5-hydroxy-7-methoxy-8-(3-methyl-2-buten-1-yl)-2-(2,4,6-trimethoxyphenyl)-4H-1-benzopyran-4-one	15298901	Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=C(C=C(C=C3OC)OC)OC)O)OC)C	428.50	unknown	https://doi.org/10.1016/0031-9422(93)85302-8
(2S)-2,3-Dihydro-5,7-dihydroxy-8-(3-methyl-2-buten-1-yl)-2-(2,4,6-trimethoxyphenyl)-4H-1-benzopyran-4-one	101722635	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3OC)OC)OC)C	414.40	unknown	https://doi.org/10.1016/S0031-9422(00)90605-8
Heteroflavanone B	42608026	Click to see	428.50	unknown	https://doi.org/10.1016/0031-9422(93)85302-8
Heteroflavanone C	42608025	Click to see	414.40	unknown	https://doi.org/10.1016/S0031-9422(00)90605-8
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Leucoanthocyanidins
(1R,9R,17S)-8,16-dioxatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10(15),11,13-hexaene-3,5,13,17-tetrol	101821343	Click to see C1=CC2=C(C=C1O)OC3C(C2OC4=CC(=CC(=C34)O)O)O	288.25	unknown	https://doi.org/10.1016/0031-9422(95)00135-T
8,16-Dioxatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10(15),11,13-hexaene-3,5,13,17-tetrol	12305318	Click to see	288.25	unknown	https://doi.org/10.1016/0031-9422(95)00135-T
Cyanomaclurin	44257130	Click to see	288.25	unknown	https://doi.org/10.3109/13880209.2014.996819
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Norartocarpetin	5481970	Click to see	286.24	unknown	https://doi.org/10.1007/S11418-006-0048-0 https://doi.org/10.1016/S0040-4039(00)90015-7 https://doi.org/10.1016/0031-9422(95)00135-T https://doi.org/10.1021/JF800444G https://doi.org/10.2174/157018010792062777
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 2-prenylated flavones
Broussoflavonol G	10368916	Click to see	506.60	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
2-(2,4-Dihydroxy-6-methoxyphenyl)-5-hydroxy-7-methoxy-6-(3-methylbut-1-enyl)-3-(3-methylbut-2-enyl)chromen-4-one	74332619	Click to see	466.50	unknown	https://doi.org/10.1021/JF9014685
2-(2,4-dihydroxy-6-methoxyphenyl)-5-hydroxy-7-methoxy-6-[(E)-3-methylbut-1-enyl]-3-(3-methylbut-2-enyl)chromen-4-one	24850607	Click to see CC(C)C=CC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=C(C=C(C=C3OC)O)O)CC=C(C)C)OC	466.50	unknown	https://doi.org/10.1021/JF9014685
2-(2,4-Dihydroxyphenyl)-5-hydroxy-7-methoxy-6-(3-methylbut-1-enyl)-3-(3-methylbut-2-enyl)chromen-4-one	5358260	Click to see CC(C)C=CC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)OC	436.50	unknown	https://doi.org/10.1016/0031-9422(95)00135-T https://doi.org/10.1007/S11418-010-0425-6 https://doi.org/10.1055/S-2006-931606 https://doi.org/10.1021/JF9014685 https://doi.org/10.1016/J.FITOTE.2009.08.001
2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-1-enyl)-3-(3-methylbut-2-enyl)chromen-4-one	74332618	Click to see	422.50	unknown	https://doi.org/10.1055/S-2006-931606 https://doi.org/10.1016/J.FITOTE.2009.08.001
2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(E)-3-methylbut-1-enyl]-3-(3-methylbut-2-enyl)chromen-4-one	24850606	Click to see	422.50	unknown	https://doi.org/10.1055/S-2006-931606 https://doi.org/10.1016/J.FITOTE.2009.08.001
3-Prenyl luteolin	91374192	Click to see CC(=CCC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O)C	354.40	unknown	https://doi.org/10.1016/J.FITOTE.2010.03.011
Albanin A	5481961	Click to see CC(=CCC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=C(C=C3)O)O)C	354.40	unknown	https://doi.org/10.1055/S-2006-931606 https://doi.org/10.2174/157018010792062777 https://doi.org/10.1016/J.FITOTE.2009.08.001
Artocarpin	5458461	Click to see	436.50	unknown	https://doi.org/10.1021/JF9014685 https://doi.org/10.3109/13880209.2014.996819 https://doi.org/10.1055/S-2006-931606 https://doi.org/10.1007/S11418-010-0425-6 https://doi.org/10.1016/J.FITOTE.2009.08.001 https://doi.org/10.1016/0031-9422(95)00135-T
Cudraflavone B	5319925	Click to see CC(=CCC1=C(OC2=CC3=C(C=CC(O3)(C)C)C(=C2C1=O)O)C4=C(C=C(C=C4)O)O)C	420.50	unknown	https://doi.org/10.1021/JF9014685 https://doi.org/10.1016/J.FITOTE.2009.08.001
Heteroartonin A	15231526	Click to see	452.50	unknown	https://doi.org/10.1016/0031-9422(95)00442-A
Kuwanon T	15231527	Click to see	422.50	unknown	https://doi.org/10.1016/0031-9422(95)00442-A
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
5-Hydroxy-2-(4-hydroxyphenyl)-7-methoxy-6-(3-methylbut-2-enyl)chromen-4-one	162878374	Click to see	352.40	unknown	https://doi.org/10.1021/JF9014685
6-Prenylapigenin	10382485	Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=C(C=C3)O)O)C	338.40	unknown	https://doi.org/10.1055/S-2006-931606 https://doi.org/10.1016/J.FITOTE.2009.08.001
Artocarpesin	399491	Click to see	354.40	unknown	https://doi.org/10.1021/JF9014685 https://doi.org/10.1016/S0040-4039(00)90015-7 https://doi.org/10.1021/JF800444G https://doi.org/10.2174/157018010792062777
Cudraflavone C	5319924	Click to see	422.50	unknown	https://doi.org/10.1055/S-2006-931606
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
2-(2,4-Dihydroxyphenyl)-5,7-dihydroxy-8-(3-methylbut-2-enyl)chromen-4-one	15541482	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C=C(O2)C3=C(C=C(C=C3)O)O)C	354.40	unknown	https://doi.org/10.3987/COM-94-S(B)84
8-(2,4-Dihydroxyphenyl)-5-hydroxy-2,2-dimethyl-7,10-bis(3-methylbut-2-enyl)pyrano[3,2-g]chromen-6-one	44226793	Click to see	488.60	unknown	https://doi.org/10.1021/JF9014685
Artocarpetin A	390520	Click to see	368.40	unknown	https://doi.org/10.1016/0031-9422(95)00135-T
Artocarpetin B	15231525	Click to see	382.40	unknown	https://doi.org/10.1016/0031-9422(95)00442-A
Artonin U	44258358	Click to see	352.40	unknown	https://doi.org/10.3987/COM-94-S(B)84
Broussoflavonol F	9866908	Click to see	422.50	unknown	via CMAUP database
Heterophyllin	14557105	Click to see	504.60	unknown	https://doi.org/10.1016/0031-9422(95)00442-A
Licoflavone C	10246505	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C=C(O2)C3=CC=C(C=C3)O)C	338.40	unknown	https://doi.org/10.1021/JF9014685
Mulberrin	5481958	Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)C	422.50	unknown	https://doi.org/10.1055/S-2006-931606 https://doi.org/10.1016/J.FITOTE.2009.08.001
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-5-hydroxy-2-(2-hydroxy-4-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one	163075164	Click to see	316.30	unknown	https://doi.org/10.1016/0031-9422(95)00135-T
(2R)-5-hydroxy-7-methoxy-2-(2,4,6-trimethoxyphenyl)-2,3-dihydrochromen-4-one	162852231	Click to see	360.40	unknown	https://doi.org/10.1016/0031-9422(93)85302-8
(2S)-5-hydroxy-2-(2-hydroxy-4-methoxyphenyl)-7-methoxy-2,3-dihydrochromen-4-one	101930089	Click to see	316.30	unknown	https://doi.org/10.1016/0031-9422(95)00135-T
(2S)-5-hydroxy-7-methoxy-2-(2,4,6-trimethoxyphenyl)-2,3-dihydrochromen-4-one	15298900	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=C(C=C(C=C3OC)OC)OC)O	360.40	unknown	https://doi.org/10.1016/0031-9422(93)85302-8
5,2'-Dihydroxy-7,4'-dimethoxyflavanone	15227613	Click to see	316.30	unknown	https://doi.org/10.1016/0031-9422(95)00135-T
Artocarpanone	15298902	Click to see	302.28	unknown	https://doi.org/10.1016/0031-9422(95)00135-T https://doi.org/10.1248/BPB.29.1966 https://doi.org/10.3109/13880209.2014.996819 https://doi.org/10.1007/S11418-006-0048-0 https://doi.org/10.1016/J.FITOTE.2009.08.001
Artocarpetin	12308618	Click to see	300.26	unknown	https://doi.org/10.1016/0031-9422(95)00135-T
Heteroflavanone A	42608055	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=C(C=C(C=C3OC)OC)OC)O	360.40	unknown	https://doi.org/10.1016/0031-9422(93)85302-8
Isoflavone, 2',4',5-trihydroxy-7-methoxy-	12000157	Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=C(C=C(C=C3)O)O)O	302.28	unknown	https://doi.org/10.1248/BPB.29.1966 https://doi.org/10.1016/0031-9422(95)00135-T https://doi.org/10.1016/J.FITOTE.2009.08.001
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(11S)-6,7,15-trihydroxy-19,19-dimethyl-22-(3-methylbut-2-enyl)-11-(2-methylprop-1-enyl)-2,10,20-trioxapentacyclo[12.8.0.03,12.04,9.016,21]docosa-1(14),3(12),4,6,8,15,17,21-octaen-13-one	92441456	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C(OC5=CC(=C(C=C54)O)O)C=C(C)C)O)C=CC(O2)(C)C)C	502.60	unknown	https://doi.org/10.1021/JF9014685
(15S)-11,19-dihydroxy-7,7-dimethyl-15-(2-methylprop-1-enyl)-2,8,16-trioxapentacyclo[12.8.0.03,12.04,9.017,22]docosa-1(14),3(12),4(9),5,10,17(22),18,20-octaen-13-one	92471957	Click to see	418.40	unknown	https://doi.org/10.1007/S10600-010-9698-Y
(6R)-8,10-dihydroxy-3-methoxy-9-[(E)-3-methylbut-1-enyl]-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one	162972402	Click to see	434.50	unknown	https://doi.org/10.1016/S0031-9422(00)90605-8 https://doi.org/10.1007/S10600-010-9698-Y
(6S)-2,3,8,10-tetrahydroxy-9,11-bis(3-methylbut-2-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one	94200526	Click to see	504.60	unknown	https://doi.org/10.1021/JF9014685
(6S)-3,8,10-trihydroxy-9-[(E)-3-methylbut-1-enyl]-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one	162885668	Click to see CC(C)C=CC1=C(C2=C(C=C1O)OC3=C(C2=O)C(OC4=C3C=CC(=C4)O)C=C(C)C)O	420.50	unknown	https://doi.org/10.1007/S10600-010-9698-Y https://doi.org/10.1016/J.FITOTE.2009.08.001
3,8-dihydroxy-10-methoxy-9-[(E)-3-methylbut-1-enyl]-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one	5458462	Click to see	434.50	unknown	https://doi.org/10.3109/13880209.2014.996819
3,8,10-trihydroxy-9-(3-methylbut-1-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one	90826426	Click to see CC(C)C=CC1=C(C2=C(C=C1O)OC3=C(C2=O)C(OC4=C3C=CC(=C4)O)C=C(C)C)O	420.50	unknown	https://doi.org/10.1007/S10600-010-9698-Y https://doi.org/10.1016/J.FITOTE.2009.08.001
8,10-Dihydroxy-3-methoxy-9-(3-methyl-1-buten-1-yl)-6-(2-methyl-1-propen-1-yl)-6H,7H-[1]benzopyrano[4,3-b][1]benzopyran-7-one	162972401	Click to see CC(C)C=CC1=C(C2=C(C=C1O)OC3=C(C2=O)C(OC4=C3C=CC(=C4)OC)C=C(C)C)O	434.50	unknown	https://doi.org/10.1016/S0031-9422(00)90605-8 https://doi.org/10.1007/S10600-010-9698-Y
Artoheterophyllin B	44226791	Click to see	504.60	unknown	https://doi.org/10.1021/JF9014685
cycloartocarpin A	44258302	Click to see CC(C)C=CC1=C(C2=C(C=C1O)OC3=C(C2=O)C(OC4=C3C=CC(=C4)OC)C=C(C)C)O	434.50	unknown	via CMAUP database
Cycloheterophyllin	5316250	Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C(OC5=CC(=C(C=C54)O)O)C=C(C)C)O)C=CC(O2)(C)C)C	502.60	unknown	https://doi.org/10.1021/JF9014685
Cyclomorusin	5481969	Click to see CC(=CC1C2=C(C3=C(O1)C=C(C=C3)O)OC4=C(C2=O)C(=CC5=C4C=CC(O5)(C)C)O)C	418.40	unknown	https://doi.org/10.1007/S10600-010-9698-Y
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Broussochalcone A	6438825	Click to see	340.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
4-[(1E)-2-(5-Hydroxy-2,2-dimethyl-2H-1-benzopyran-7-yl)ethenyl]-1,3-benzenediol	11722912	Click to see	310.30	unknown	https://doi.org/10.1016/S0031-9422(00)00074-1
4-[2-(5-Hydroxy-2,2-dimethylchromen-7-yl)ethenyl]benzene-1,3-diol	73073812	Click to see	310.30	unknown	https://doi.org/10.1016/S0031-9422(00)00074-1
4'-Prenyl-2,4,3',5'-tetrahydroxystilbene	442717	Click to see	312.40	unknown	https://doi.org/10.1016/S0031-9422(00)00074-1
4'-Prenyloxyresveratrol	5281724	Click to see CC(=CCC1=C(C=C(C=C1O)C=CC2=C(C=C(C=C2)O)O)O)C	312.40	unknown	https://doi.org/10.1016/S0031-9422(00)00074-1
5-[2-(2,4-Dihydroxyphenyl)ethenyl]-2-(3-methylbut-1-enyl)benzene-1,3-diol	54124404	Click to see	312.40	unknown	https://doi.org/10.1016/S0031-9422(00)00074-1
CID 73197	73197	Click to see C1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O	244.24	unknown	https://doi.org/10.1021/JF800444G
Trans-2,3',4,5'-tetrahydroxystilbene	5281717	Click to see	244.24	unknown	https://doi.org/10.1021/JF800444G

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Artocarpus heterophyllus

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