Artocarpus elasticus

Details Top

Internal ID UUID64400ae970e6d207177451
Scientific name Artocarpus elasticus
Authority Reinw.
First published in Bijdr. Fl. Ned. Ind. : 481 (1825)

Ethnobotanical Use Top

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Important notice
  • 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 Dayak Kenyah of East Kalimantan, infusions made from the inner bark of Artocarpus elasticus have long been used as a restorative “maternity tonic” during the postpartum period (Bennett, 1992). Communities in the northern Headwaters of the Mahakam have prepared decoctions of the leaves to treat diarrhea, while poultices of the same leaves are applied to wounds and boils (Bennett, 1992). In the Bidayuh region of Sarawak, leaf decoctions are taken for fever and are also used as a general convalescent drink (Lee et al., 2008). Among the Kayan and Kenyah of the Apau Kayan in northern Borneo, a paste made by crushing young leaves is applied to skin irritations and joint swellings (Bennett, 1992). In eastern and southern Thailand, the plant is known as Champada; there, leaves and sometimes inner bark are traditionally used as a mild bitter tea taken after meals or during convalescence (Chevallier, 1996; Stokes et al., 2005).

A straightforward bark infusion is commonly prepared for general tonic use. Roughly 5–10 g of sun‑dried inner bark is added to 250–300 ml of freshly boiled water and left to infuse for 10–15 minutes; the liquid is then filtered and taken warm. In some communities the infusion is lightly sweetened before drinking (Bennett, 1992). For a gentle leaf decoction used for fever or mild gastrointestinal upset, 10–15 g of dried leaves are simmered in about 300 ml of water for 10–15 minutes, cooled, and taken in small cups throughout the day (Lee et al., 2008; Bennett, 1992). Traditional practice suggests using these preparations for short periods only and avoiding large or strong doses; information on longer term use or contraindications is not well documented, and pregnant or lactating women should seek advice from a health professional before using any new remedy (Bennett, 1992; Lee et al., 2008).

Phytochemical surveys of the wood and leaves report abundant flavonoids and other phenolic compounds that are widely distributed across Artocarpus species, as well as triterpenes such as ursolic and oleanolic acids and the prenylated flavonoid artonin E that is particularly notable in some Artocarpus taxa (Hou et al., 2006; Middleton et al., 2007; Cheesman et al., 2017). These constituents are associated with antioxidant and mild astringent activity, which aligns plausibly with the plant’s traditional uses as a tonic, for fever, and for treating diarrhea (Hou et al., 2006; Middleton et al., 2007; Chevallier, 1996; Stokes et al., 2005).

Today, Artocarpus elasticus remains widely used in rural Borneo and nearby regions of Southeast Asia, with bark infusions and leaf decoctions still prepared for convalescence, postpartum support, and mild fevers (Lee et al., 2008; Bennett, 1992). Small‑scale ethnobotanical studies continue to document its uses, and while clinical research is still emerging, commercial interest in its timber and minor ethnobotanical products sustains both local practice and broader scientific attention (Lee et al., 2008; Chevallier, 1996).

General Uses Top

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Common products:
- Fresh fruit, processed into jam, dried slices or fruit leather; roasted seeds; timber for construction and furniture; bark fiber for rope and twine; seed oil extracted for edible use.

Industrial and craft applications:
- Wood used for furniture, interior joinery, paneling and lightweight construction; can be processed into plywood and veneer; bark fibers spun into strong rope and twine, suitable for maritime rigging; resin from the trunk serves as a natural adhesive for small craft repairs; leaves sometimes processed for a fibrous material used in weaving mats.

Food and beverages (non-medicinal):
- Ripe fruit eaten raw or cooked, sliced into desserts or used as flavoring; fruit pulp can be fermented into a low‑alcohol beverage or processed into juice concentrates; seeds boiled, roasted, and salted as a snack; seed oil pressed for culinary use in frying or as a salad dressing component.

Colorants and tanning:
- Bark yields condensed tannins (proanthocyanidins) used in small‑scale leather tanning to produce a brown, durable finish; the same extract can serve as a natural dye for protein fibers.

Wood and fiber:
- Wood density ~0.55 g cm⁻³; modulus of rupture ~70 MPa; low shrinkage (

Synonyms Top

Scientific name Authority First published in
Saccus elasticus Kuntze Revis. Gen. Pl. 2: 633. 1891 [5 Nov 1891]
Saccus blumei Kuntze Revis. Gen. Pl. 2: 633. 1891 [5 Nov 1891]
Saccus kuenstleri Kuntze Revis. Gen. Pl. 2: 633. 1891 [5 Nov 1891]
Artocarpus blumei Trécul Ann. Sci. Nat., Bot. , sér. 3, 8: 111 (1847)
Artocarpus kunstleri King ex Hook.f. Fl. Brit. India [J. D. Hooker] 5(15): 540. 1888 [Dec 1888] ; et in Ann. Bot. Gard. Calc. 2: 9, t. 4. 1889

Common names Top

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Language Common/alternative name
Indonesian torap
Indonesian benda
Indonesian benda (pohon)
jv bendha
min tarok
Malay pokok terap nasi
Malay terap nasi
su teureup
Chinese 马来波罗蜜
Chinese 馬來波羅蜜

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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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-tropical
    • Indo-China
      • Myanmar
      • Thailand
    • Malesia
      • Borneo
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000550472
USDA Plants AREL9
Tropicos 100293205
KEW urn:lsid:ipni.org:names:850378-1
The Plant List kew-2653963
Open Tree Of Life 513376
NCBI Taxonomy 709042
IUCN Red List 61220310
IPNI 850378-1
iNaturalist 348099
GBIF 2984578
EPPO ABFEL
EOL 491544
USDA GRIN 4326
Wikipedia Artocarpus_elasticus

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
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
Analogues of Dihydroflavonol and Flavone as Protein Tyrosine Phosphatase 1B Inhibitors from the Leaves of Artocarpus elasticus Shah AB, Baiseitova A, Lee G, Kim JH, Park KH ACS Omega 14-Feb-2024
PMCID:PMC10905692
doi:10.1021/acsomega.3c07471
PMID:38434867
Species Distribution Model for the Asian Tapir and Vegetation Characteristics of Batang Gadis National Park, North Sumatra, Indonesia Kuswanda W, Hutapea FJ, Saputra MH, Nopandry B Trop Life Sci Res 21-Jul-2023
PMCID:PMC10735268
doi:10.21315/tlsr2023.34.2.4
PMID:38144375
Phytochemistry and pharmacology of natural prenylated flavonoids Lv HW, Wang QL, Luo M, Zhu MD, Liang HM, Li WJ, Cai H, Zhou ZB, Wang H, Tong SQ, Li XN Arch Pharm Res 14-Apr-2023
PMCID:PMC10101826
doi:10.1007/s12272-023-01443-4
PMID:37055613
Diversity of substrate type, ethnomycology, mineral composition, proximate, and phytochemical compounds of the Schizopyllum commune Fr. in the area along Palu-Koro Fault, Central Sulawesi, Indonesia Yusran Y, Erniwati E, Khumaidi A, Pitopang R, Jati IR Saudi J Biol Sci 14-Feb-2023
PMCID:PMC9985035
doi:10.1016/j.sjbs.2023.103593
PMID:36879672
AGA induces sub-G1 cell cycle arrest and apoptosis in human colon cancer cells through p53-independent/p53-dependent pathway Peng BY, Singh AK, Chan CH, Deng YH, Li PY, Su CW, Wu CY, Deng WP BMC Cancer 02-Jan-2023
PMCID:PMC9808967
doi:10.1186/s12885-022-10466-x
PMID:36597025
Prenylated Flavonoids in Topical Infections and Wound Healing Sychrová A, Škovranová G, Čulenová M, Bittner Fialová S Molecules 13-Jul-2022
PMCID:PMC9323352
doi:10.3390/molecules27144491
PMID:35889363
Can Extracts from the Leaves and Fruits of the Cotoneaster Species Be Considered Promising Anti-Acne Agents? Krzemińska B, Dybowski MP, Klimek K, Typek R, Miazga-Karska M, Ginalska G, Dos Santos Szewczyk K Molecules 02-May-2022
PMCID:PMC9105355
doi:10.3390/molecules27092907
PMID:35566257
Effects of Artonin E on Cell Growth Inhibition and Apoptosis Induction in Colon Cancer LoVo and HCT116 Cells Yangnok K, Innajak S, Sawasjirakij R, Mahabusarakam W, Watanapokasin R Molecules 24-Mar-2022
PMCID:PMC9000836
doi:10.3390/molecules27072095
PMID:35408492
In vitro α-glucosidase inhibitory activity of Tamarix nilotica shoot extracts and fractions Daou M, Elnaker NA, Ochsenkühn MA, Amin SA, Yousef AF, Yousef LF PLoS One 14-Mar-2022
PMCID:PMC8920278
doi:10.1371/journal.pone.0264969
PMID:35286313
In Vitro Selective Antibacterial and Antiproliferative Effects of Ethanolic Extracts from Cambodian and Philippine Plants Used in Folk Medicine for Diarrhea Treatment Kudera T, Fiserova B, Korytakova M, Doskocil I, Salmonova H, Tulin EE, Nguon S, Bande MM, Kokoska L Front Pharmacol 26-Nov-2021
PMCID:PMC8661004
doi:10.3389/fphar.2021.746808
PMID:34899301
A review of the phytochemical mediated synthesis of AgNP (silver nanoparticle): the wonder particle of the past decade Shaikh WA, Chakraborty S, Owens G, Islam RU Appl Nanosci 30-Oct-2021
PMCID:PMC8556825
doi:10.1007/s13204-021-02135-5
PMID:34745812
Four Novel Phenanthrene Derivatives with α-Glucosidase Inhibitory Activity from Gastrochilus bellinus San HT, Chatsumpun N, Juengwatanatrakul T, Pornputtapong N, Likhitwitayawuid K, Sritularak B Molecules 14-Jan-2021
PMCID:PMC7830893
doi:10.3390/molecules26020418
PMID:33466863
Natural Products Targeting the Mitochondria in Cancers Yang Y, He PY, Zhang Y, Li N Molecules 28-Dec-2020
PMCID:PMC7795732
doi:10.3390/molecules26010092
PMID:33379233
Biphasic Dose-Response Induced by Phytochemicals: Experimental Evidence Jodynis-Liebert J, Kujawska M J Clin Med 06-Mar-2020
PMCID:PMC7141213
doi:10.3390/jcm9030718
PMID:32155852

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethyl 2,4-dihydroxybenzoate 821388 Click to see 182.17 unknown https://doi.org/10.1055/S-2001-18845
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(96)00293-2
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/10.1016/0031-9422(96)00293-2
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(13R)-5-[(E)-2,3-dihydroxy-3-methylbut-1-enyl]-6,8,17-trihydroxy-19-methoxy-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 163009593 Click to see 482.50 unknown https://doi.org/10.1021/NP050287J
(13S)-5-[(E)-2,3-dihydroxy-3-methylbut-1-enyl]-6,8,17-trihydroxy-19-methoxy-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 5326338 Click to see 482.50 unknown https://doi.org/10.1021/NP050287J
(6R)-5,9,11,14-tetrahydroxy-3,3-dimethyl-6-prop-1-en-2-yl-6,7-dihydrochromeno[7,6-c]xanthen-8-one 15939771 Click to see 434.40 unknown https://doi.org/10.1021/NP050287J
(6S)-5,9,11,14-tetrahydroxy-3,3-dimethyl-6-prop-1-en-2-yl-6,7-dihydrochromeno[7,6-c]xanthen-8-one 154496070 Click to see 434.40 unknown https://doi.org/10.1021/NP050287J
5-(2,3-Dihydroxy-3-methylbut-1-enyl)-6,8,17-trihydroxy-19-methoxy-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 163009592 Click to see 482.50 unknown https://doi.org/10.1021/NP050287J
Artelastoxanthone 5326337 Click to see CC(=C)C1CC2=C(C3=C1C(=C4C(=C3O)C=CC(O4)(C)C)O)OC5=CC(=CC(=C5C2=O)O)O 434.40 unknown https://doi.org/10.1021/NP050287J
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(17R)-12,21,23-trihydroxy-8,8,18,18-tetramethyl-11-(3-methylbut-2-enyl)-3,9,19-trioxahexacyclo[15.6.1.02,15.04,13.05,10.020,24]tetracosa-1(24),2(15),4,6,10,12,20,22-octaen-14-one 162905892 Click to see 502.60 unknown https://doi.org/10.1021/NP050287J
(17R)-12,21,23-trihydroxy-8,8,18,18-tetramethyl-3,9,19-trioxahexacyclo[15.6.1.02,15.04,13.05,10.020,24]tetracosa-1(24),2(15),4(13),5(10),6,11,20,22-octaen-14-one 162872214 Click to see 434.40 unknown https://doi.org/10.1021/NP050287J
(17S)-11-[(2E)-3,7-dimethylocta-2,6-dienyl]-12,21,23-trihydroxy-8,8,18,18-tetramethyl-3,9,19-trioxahexacyclo[15.6.1.02,15.04,13.05,10.020,24]tetracosa-1(24),2(15),4,6,10,12,20,22-octaen-14-one 15939770 Click to see 570.70 unknown https://doi.org/10.1021/NP050287J
(17S)-12,21,23-trihydroxy-8,8,18,18-tetramethyl-11-(3-methylbut-2-enyl)-3,9,19-trioxahexacyclo[15.6.1.02,15.04,13.05,10.020,24]tetracosa-1(24),2(15),4,6,10,12,20,22-octaen-14-one 162905891 Click to see 502.60 unknown https://doi.org/10.1021/NP050287J
(5aS)-1,3,8-Trihydroxy-5,5,11,11-tetramethyl-5a,6-dihydro-5H,7H,11H-[1]benzofuro[3,4-bc]pyrano[3,2-h]xanthen-7-one 46887867 Click to see 434.40 unknown https://doi.org/10.1021/NP050287J
(9R)-6-hydroxy-3,3-dimethyl-9-prop-1-en-2-yl-9,10-dihydro-8H-pyrano[2,3-c]xanthene-7,11-dione 162966661 Click to see CC(=C)C1CC2=C(C(=O)C1)OC3=C(C2=O)C(=CC4=C3C=CC(O4)(C)C)O 352.40 unknown https://doi.org/10.1021/NP050287J
(9S)-6-hydroxy-3,3-dimethyl-9-prop-1-en-2-yl-9,10-dihydro-8H-pyrano[2,3-c]xanthene-7,11-dione 154496196 Click to see CC(=C)C1CC2=C(C(=O)C1)OC3=C(C2=O)C(=CC4=C3C=CC(O4)(C)C)O 352.40 unknown https://doi.org/10.1021/NP050287J
10-Acetyl-21-hydroxy-6,6,17,17-tetramethyl-7,12,18-trioxapentacyclo[11.8.0.03,11.05,9.014,19]henicosa-1(13),3,5(9),10,14(19),15,20-heptaen-2-one 162966677 Click to see CC(=O)C1=C2C(=CC3=C1COC3(C)C)C(=O)C4=C(O2)C5=C(C=C4O)OC(C=C5)(C)C 406.40 unknown https://doi.org/10.1021/NP050287J
11-(3,7-Dimethylocta-2,6-dienyl)-12,21,23-trihydroxy-8,8,18,18-tetramethyl-3,9,19-trioxahexacyclo[15.6.1.02,15.04,13.05,10.020,24]tetracosa-1(24),2(15),4,6,10,12,20,22-octaen-14-one 162992307 Click to see 570.70 unknown https://doi.org/10.1021/NP050287J
artonin F 14680593 Click to see CC(=CCC1=C2C(=C3C(=C1O)C(=O)C4=C(O3)C5=C6C(C4)C(OC6=C(C=C5O)O)(C)C)C=CC(O2)(C)C)C 502.60 unknown https://doi.org/10.1021/NP050287J
artonol A 10736715 Click to see CC(=C)C1CC2=C(C(=O)C1)OC3=C(C2=O)C(=CC4=C3C=CC(O4)(C)C)O 352.40 unknown https://doi.org/10.1021/NP050287J
Artonol B 10740797 Click to see 420.40 unknown https://doi.org/10.1021/NP050287J
Cycloartobiloxanthone 10342859 Click to see 434.40 unknown https://doi.org/10.1021/NP050287J
> Organoheterocyclic compounds / Benzoxepines
(6R)-3,9,11-trihydroxy-6-(2-hydroxypropan-2-yl)-10,12-bis(3-methylbut-2-enyl)-6,7-dihydrochromeno[3,2-d][1]benzoxepin-8-one 154496186 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)CC=C(C)C)O)C 506.60 unknown https://doi.org/10.1016/S0031-9422(97)00631-6
https://doi.org/10.1055/S-2001-18845
(6S)-3,9,11-trihydroxy-6-(2-hydroxypropan-2-yl)-10,12-bis(3-methylbut-2-enyl)-6,7-dihydrochromeno[3,2-d][1]benzoxepin-8-one 163046676 Click to see 506.60 unknown https://doi.org/10.1016/S0031-9422(97)00631-6
Artelastocarpin 15386210 Click to see 506.60 unknown https://doi.org/10.1016/S0024-3205(03)00627-1
https://doi.org/10.1055/S-2001-18845
https://doi.org/10.1016/S0031-9422(97)00631-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Artocarpesin 399491 Click to see 354.40 unknown https://doi.org/10.1016/0031-9422(96)00293-2
https://doi.org/10.1016/S0024-3205(03)00627-1
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
(8S)-2-(2,4-dihydroxyphenyl)-5-hydroxy-8-(2-hydroxypropan-2-yl)-3,6-bis(3-methylbut-2-enyl)-8,9-dihydrofuro[2,3-h]chromen-4-one 163060471 Click to see 506.60 unknown https://doi.org/10.1016/S0031-9422(97)00631-6
2-(2,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-[(1R)-1-hydroxy-3-methylbut-2-enyl]-8-(3-methylbut-2-enyl)chromen-4-one 15939769 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=CC(=C(C=C3O)OC)O)C(C=C(C)C)O)C 468.50 unknown https://doi.org/10.1021/NP050287J
2-(2,5-dihydroxy-4-methoxyphenyl)-5,7-dihydroxy-3-[(1S)-1-hydroxy-3-methylbut-2-enyl]-8-(3-methylbut-2-enyl)chromen-4-one 162905075 Click to see 468.50 unknown https://doi.org/10.1021/NP050287J
5-hydroxy-7-[(1R)-1-hydroxy-3-methylbut-2-enyl]-2,2-dimethyl-10-(3-methylbut-2-enyl)-8-(2,4,5-trihydroxyphenyl)pyrano[3,2-g]chromen-6-one 15939775 Click to see 520.60 unknown https://doi.org/10.1021/NP050287J
5-hydroxy-7-[(1S)-1-hydroxy-3-methylbut-2-enyl]-2,2-dimethyl-10-(3-methylbut-2-enyl)-8-(2,4,5-trihydroxyphenyl)pyrano[3,2-g]chromen-6-one 162879554 Click to see CC(=CCC1=C2C(=C(C3=C1OC(=C(C3=O)C(C=C(C)C)O)C4=CC(=C(C=C4O)O)O)O)C=CC(O2)(C)C)C 520.60 unknown https://doi.org/10.1021/NP050287J
Artelasticin 5471311 Click to see 490.60 unknown https://doi.org/10.1016/0031-9422(96)00293-2
https://doi.org/10.1016/S0024-3205(03)00627-1
Artelasticinol 5326335 Click to see 468.50 unknown https://doi.org/10.1021/NP050287J
Artelastofuran 15386211 Click to see 506.60 unknown https://doi.org/10.1016/S0031-9422(97)00631-6
https://doi.org/10.1016/S0024-3205(03)00627-1
Artelastoheterol 5326343 Click to see CC(=CCC1=C2C(=C(C3=C1OC(=C(C3=O)C(C=C(C)C)O)C4=CC(=C(C=C4O)O)O)O)C=CC(O2)(C)C)C 520.60 unknown https://doi.org/10.1021/NP050287J
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Furanoflavones
(7R,21R)-4,17-dihydroxy-7,21-bis(2-hydroxypropan-2-yl)-10-(3-methylbut-2-enyl)-8,12,20-trioxapentacyclo[11.9.0.03,11.05,9.014,19]docosa-1(13),3(11),4,9,14(19),15,17-heptaen-2-one 154496315 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)CC(OC5=C4C=CC(=C5)O)C(C)(C)O)O)CC(O2)C(C)(C)O)C 522.60 unknown https://doi.org/10.1055/S-2001-18845
(7S,21R)-4,17-dihydroxy-7,21-bis(2-hydroxypropan-2-yl)-10-(3-methylbut-2-enyl)-8,12,20-trioxapentacyclo[11.9.0.03,11.05,9.014,19]docosa-1(13),3(11),4,9,14(19),15,17-heptaen-2-one 163032383 Click to see 522.60 unknown https://doi.org/10.1055/S-2001-18845
Carpelastofuran 44258665 Click to see 522.60 unknown https://doi.org/10.1055/S-2001-18845
https://doi.org/10.1016/S0024-3205(03)00627-1
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
(11S)-7,15-dihydroxy-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(9),5,7,15,17,21-octaen-13-one 162848944 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C(OC5=C4C=CC(=C5)O)C=C(C)C)O)C=CC(O2)(C)C)C 486.60 unknown https://doi.org/10.1016/0031-9422(96)00293-2
(15R)-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 92471958 Click to see 418.40 unknown https://doi.org/10.1021/NP050287J
(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/10.1021/NP050287J
(6R)-3,8,10-trihydroxy-9-(3-methylbut-2-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one 154496418 Click to see 420.50 unknown https://doi.org/10.1016/S0031-9422(97)00631-6
(6S)-3,8,10-trihydroxy-9-(3-methylbut-2-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one 154496779 Click to see 420.50 unknown https://doi.org/10.1016/S0031-9422(97)00631-6
(6S)-3,8,10-trihydroxy-9,11-bis(3-methylbut-2-enyl)-6-(2-methylprop-1-enyl)-6H-chromeno[4,3-b]chromen-7-one 154496185 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C4=C(C=C(C=C4)O)OC3C=C(C)C)CC=C(C)C)O)C 488.60 unknown https://doi.org/10.1016/0031-9422(96)00293-2
Artelastin 399488 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C3=C(O2)C4=C(C=C(C=C4)O)OC3C=C(C)C)CC=C(C)C)O)C 488.60 unknown https://doi.org/10.1016/J.LFS.2004.09.049
https://doi.org/10.1016/0031-9422(96)00293-2
https://doi.org/10.1016/S0024-3205(03)00627-1
Artelastochromene 5471310 Click to see 486.60 unknown https://doi.org/10.1016/S0024-3205(03)00627-1
https://doi.org/10.1016/0031-9422(96)00293-2
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/10.1021/NP050287J
Isocyclomulberrin 5316260 Click to see 420.50 unknown https://doi.org/10.1016/S0031-9422(97)00631-6

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