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Artocarpus lacucha

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID64400aeb34e27866823272
Scientific name Artocarpus lacucha
Authority Roxb. ex Buch.-Ham.
First published in Mem. Wern. Nat. Hist. Soc. 5: 333 (1826)

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.

Ethnobotanical Uses

In northern and northeastern India the mature leaves of Artocarpus lacucha are commonly decocted for liver and bile complaints. Among the Tai Ahom of Assam, a decoction of 20–30 fresh leaves is taken daily for jaundice and liver disorders, while the Nepali community in Sikkim uses a leaf decoction in smaller amounts for hepatic complaints. In northeastern India and parts of eastern Nepal, fresh or dried leaf infusions are also drunk as a bitter tonic for gastric upset and loss of appetite. Beyond internal use, poultices of crushed leaves are applied to swellings, bruises, and to speed wound dressing changes; the Karbi community of Assam reports leaf poultices placed over inflammatory swellings. These uses are documented by Sinha (1996) for northeastern India, by Logna Rao et al. (2010) for eastern Nepal, and by Das et al. (2009) in a karbi ethnomedicinal survey of the same region.

A simple recipe that follows these traditions is a mild leaf tea. Place 3–4 g of air‑dried mature leaves in 250 mL of water, bring to a boil, simmer for 10 minutes, and strain. Drink up to one cup daily for up to two weeks; do not exceed this dose or duration without clinical guidance. This preparation reflects the amounts reported for the region and keeps the bitterness tolerable. A bark poultice for topical use can be made by macerating 10–15 g of clean, powdered bark with warm water until a soft paste forms; apply to wounds or bruises and change 2–3 times daily. Do not take decoctions during pregnancy or while breastfeeding; people with known allergies to Moraceae should avoid use, and those on hepatoprotective drugs should seek medical advice before use.

Active constituents reported for this species include flavonoids such as quercetin, kaempferol, and rutin; the stilbenoids oxyresveratrol and trans‑resveratrol; anthocyanins in the fruit; and the triterpene betulinic acid. In vitro studies show antioxidant, anti‑inflammatory, and enzyme‑inhibitory activities that plausibly relate to the hepatoprotective use, although a direct cause‑and‑effect link cannot be assumed from chemistry alone.

Modern relevance

In vitro and animal studies on Artocarpus lacucha leaf and stem bark extracts continue to examine antioxidant and hepatoprotective effects, while leaf and stem bark extracts are marketed by several Indian firms for liver support. Traditional decoctions and infusions remain in use in local markets in northeastern India and neighboring regions, though many commercial products are standardized to total polyphenols rather than to individual stilbenoids.

General Uses Top

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Common products:
Edible fruit (ripe pulp), used as a seasonal food; and sawn timber used locally for light construction and furniture.

Food and beverages (non-medicinal):
The ripe fruit is eaten fresh or occasionally cooked; sweetness varies among accessions. No health claims are implied.

Wood and fiber:
Heartwood is reddish-brown to dark brown, with a pale sapwood; wood is hard and used for light construction, posts, furniture, and tool handles. Due to its density and durability, it is suitable for turnery. Large trees yield logs suitable for sawmilling, producing planks and scantlings for local use.

Properties relevant to use:
Hard, dense timber suitable for structural components and turnery; fruit suitable for consumption when ripe. Properties vary with growth conditions and provenance.

Standards and regulation:
Timber marketed under vernacular and scientific names; no product-specific grading standard cited.

Sustainability and sourcing:
Harvested from natural forest and village trees; limited information on regeneration and trade volumes; exploitable bole size and local availability may constrain supply.

Synonyms Top

Scientific name Authority First published in
Prainea rumphiana Becc. Nelle Forest. Borneo : 636 (1902)
Saccus dadah Kuntze Revis. Gen. Pl. 2: 633. 1891 [5 Nov 1891]
Saccus cumingianus Kuntze Revis. Gen. Pl. 2: 633. 1891 [5 Nov 1891]
Saccus mollis Kuntze Revis. Gen. Pl. 2: 633. 1891 [5 Nov 1891]
Saccus lakoocha Kuntze Revis. Gen. Pl. 2: 633. 1891 [5 Nov 1891]
Antiaris palembanica Miq. Fl. Ned. Ind., Eerste Bijv. : 424 (1861)
Artocarpus acuminatissimus Merr. Philipp. J. Sci. 18: 49 (1921)
Artocarpus benghalensis Roxb. ex Wall. Numer. List [Wallich] sub n. 4655. 1831
Artocarpus cumingianus Trécul Ann. Sci. Nat., Bot. , sér. 3, 8: 119 (1847)
Artocarpus dadah Miq. Fl. Ned. Ind., Eerste Bijv. : 420 (1861)
Artocarpus dasyphyllus Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 212 (1867)
Artocarpus erythrocarpus Korth. ex Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 213. 1867
Artocarpus ficifolius W.T.Wang Acta Phytotax. Sin. 6: 274 (1957)
Artocarpus fretissi Teijsm. & Binn. ex Hassk. Abh. Naturf. Ges. Halle 9: 189 (1866)
Artocarpus inconstantissimus (Miq.) Miq. Ann. Mus. Bot. Lugduno-Batavi 3: 211 (1867)
Artocarpus lakoocha Roxb. Fl. Ind. ed. 1832 , 3: 524 (1832)
Artocarpus lakoocha var. malayanus King Fl. Brit. India 5: 544 1888
Artocarpus leytensis Elmer Leafl. Philipp. Bot. 1: 279 (1908)
Artocarpus mollis Wall. Numer. List [Wallich] n. 4661. 1831
Artocarpus mollis Miq. Fl. Ned. Ind., Eerste Bijv. : 420 (1861)
Artocarpus ovatus Blanco Fl. Filip. : 666 (1837)
Artocarpus paloensis Elmer Leafl. Philipp. Bot. 1: 280 (1908)
Artocarpus peltatus Merr. J. Straits Branch Roy. Asiat. Soc. 85: 166 (1922)
Artocarpus refractus Becc. Nelle Forest. Borneo : 630 (1902)
Artocarpus reniformis Becc. Nelle Forest. Borneo : 631 (1902)
Artocarpus reticulatus B.Heyne ex Wall. Numer. List [Wallich] sub n. 4655. 1831
Artocarpus rufa Miq. Fl. Ned. Ind., Eerste Bijv. : 423 (1861)
Artocarpus rufescens Miq. Fl. Ned. Ind., Eerste Bijv. : 420 (1861)
Artocarpus tampang Miq. Fl. Ned. Ind., Eerste Bijv. : 421 (1861)
Artocarpus yunnanensis Hu Bull. Fan Mem. Inst. Biol. , Bot. 8: 32 (1937)
Ficus inconstantissima Miq. Fl. Ned. Ind., Eerste Bijv. : 431 (1861)
Ficus tampang Miq. Fl. Ned. Ind., Eerste Bijv. : 425 (1861)
Ipo palembanicam Kuntze Revis. Gen. Pl. 2: 629 (1891)

Common names Top

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Language Common/alternative name
English monkey fruit
English monkey jack
English badahar
English barhar
English bohot
English dewa
Assamese বহঁত
Bengali ঢেউফল
Bengali ডেউয়া
Bengali ঢেউয়া
Bengali ডেউফল
Persian میوه میمون
Hindi बड़हल
Kannada ವಾಟೆ
Malayalam കാട്ടുകടപ്ലാവ്, ആരംപുളി, പുളിച്ചക്ക, ചിമ
Malayalam മങ്കീ ജാക്ക്
Malayalam തീറ്റിപ്ലാവ്
Malay pokok keledang beruk
Burmese မျောက်လုပ်
Nepali बडहर
Oriya ଜେଉଟ
Oriya ଜେଉଠ
Punjabi ਢੇਊ
Punjab ڈھیؤ
sat ᱰᱟᱹᱦᱩ
Thai มะหาด
Chinese 野波罗蜜
Chinese 野波羅蜜
Chinese 猴面果
Chinese 野菠萝蜜

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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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000550516
Tropicos 50131993
INPN 993162
KEW urn:lsid:ipni.org:names:927744-1
The Plant List kew-2654005
Open Tree Of Life 702285
NCBI Taxonomy 382341
IPNI 927744-1
iNaturalist 425508
GBIF 3764648
Freebase /m/0j44sd8
USDA GRIN 409385
Wikipedia Artocarpus_lacucha
CMAUP NPO10498

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
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
Antibacterial and antioxidant activities in various parts of Artocarpus lacucha Buch. Ham. ethanolic extract Pertiwi D, Hartati R, Julianti E, Fidrianny I Biomed Rep 23-Feb-2024
PMCID:PMC10928476
doi:10.3892/br.2024.1755
PMID:38476607
Oxyresveratrol attenuates bone resorption by inhibiting the mitogen-activated protein kinase pathway in ovariectomized rats Lee YJ, Ahn JC, Oh CH Nutr Metab (Lond) 19-Jan-2024
PMCID:PMC10799353
doi:10.1186/s12986-024-00781-4
PMID:38243227
Assessment of Carbon Sequestration in Private Forests across Two Different Physiographic Regions of Nepal: Implications for Conservation and Climate Change Mitigation Joshi R, Shrestha TK, Mishra B, Gautam J, Maharjan B, Gosai KR, Maraseni T, Neupane B Scientifica (Cairo) 04-Dec-2023
PMCID:PMC10713251
doi:10.1155/2023/6599067
PMID:38089447
The presence of wild edible plants and determinants influencing their harvest, consumption, and conservation in south eastern Bhutan Bajgai RC, Bajgai Y, Johnson SB PLoS One 10-Oct-2023
PMCID:PMC10564141
doi:10.1371/journal.pone.0285936
PMID:37816046
Bioactivity and nutritional quality of nutgall (Rhus semialata Murray), an underutilized fruit of Manipur Singh TS, Kshetri P, Devi AK, Langamba P, Tamreihao K, Singh HN, Akoijam R, Chongtham T, Devi CP, Singh TB, Chongtham S, Devi YP, Kuna A, Singh SG, Sharma SK, Das A, Roy SS Front Nutr 05-Jun-2023
PMCID:PMC10277484
doi:10.3389/fnut.2023.1133576
PMID:37342546
Potentiality of homestead agroforestry for achieving sustainable development goals: Bangladesh perspectives Ruba UB, Talucder MS Heliyon 13-Mar-2023
PMCID:PMC10036652
doi:10.1016/j.heliyon.2023.e14541
PMID:36967908
Screening of Antioxidant, Antibacterial, Anti-Adipogenic, and Anti-Inflammatory Activities of Five Selected Medicinal Plants of Nepal Lamichhane G, Sharma G, Sapkota B, Adhikari M, Ghimire S, Poudel P, Jung HJ J Exp Pharmacol 02-Mar-2023
PMCID:PMC9987241
doi:10.2147/JEP.S388968
PMID:36891159
Chemical Constituents from Streblus taxoides Wood with Their Antibacterial and Antityrosinase Activities Plus in Silico Study Parndaeng K, Pitakbut T, Wattanapiromsakul C, Hwang JS, Udomuksorn W, Dej-adisai S Antibiotics (Basel) 03-Feb-2023
PMCID:PMC9952338
doi:10.3390/antibiotics12020319
PMID:36830230
In Vitro, In Vivo, and In Silico Analyses of Molecular Anti-Pigmentation Mechanisms of Selected Thai Rejuvenating Remedy and Bioactive Metabolites Dej-adisai S, Koyphokaisawan N, Wattanapiromsakul C, Nuankaew W, Kang TH, Pitakbut T Molecules 18-Jan-2023
PMCID:PMC9920523
doi:10.3390/molecules28030958
PMID:36770624
Arbutin: Occurrence in Plants, and Its Potential as an Anticancer Agent Nahar L, Al-Groshi A, Kumar A, Sarker SD Molecules 11-Dec-2022
PMCID:PMC9787540
doi:10.3390/molecules27248786
PMID:36557918
Assessing the Cooling and Air Pollution Tolerance among Urban Tree Species in a Tropical Climate Yarnvudhi A, Leksungnoen N, Andriyas T, Tor-Ngern P, Premashthira A, Wachrinrat C, Marod D, Hermhuk S, Pattanakiat S, Nakashizuka T, Kjelgren R Plants (Basel) 13-Nov-2022
PMCID:PMC9698331
doi:10.3390/plants11223074
PMID:36432803
A Literature Review of Artocarpus lacucha Focusing on the Phytochemical Constituents and Pharmacological Properties of the Plant Sitorus P, Keliat JM, Asfianti V, Muhammad M, Satria D Molecules 16-Oct-2022
PMCID:PMC9610210
doi:10.3390/molecules27206940
PMID:36296532
The Modulation of Melanogenesis in B16 Cells Upon Treatment with Plant Extracts and Isolated Plant Compounds Merecz-Sadowska A, Sitarek P, Kowalczyk T, Zajdel K, Kucharska E, Zajdel R Molecules 07-Jul-2022
PMCID:PMC9324663
doi:10.3390/molecules27144360
PMID:35889231
Review of unique ophthalmic formulations in Vaidya Manorama: A traditional Kerala Ayurveda literature Balakrishnan P, Ajayan S, Mukkudakkattu S, Nechiyil K, Nambi N J Ayurveda Integr Med 02-Jun-2022
PMCID:PMC9168494
doi:10.1016/j.jaim.2022.100576
PMID:35661934

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
> Lignans, neolignans and related compounds
[(E)-3-[4-[(1R,2S)-1-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxypropan-2-yl]oxy-3,5-dimethoxyphenyl]prop-2-enyl] (E)-3-(4-hydroxyphenyl)prop-2-enoate 636951 Click to see 698.70 unknown https://doi.org/10.1021/NP010451C
3-[4-[1-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-[3-(4-hydroxyphenyl)prop-2-enoyloxy]propan-2-yl]oxy-3-methoxyphenyl]prop-2-enyl 3-(4-hydroxyphenyl)prop-2-enoate 85415541 Click to see 668.70 unknown https://doi.org/10.1021/NP010451C
3-[4-[1-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-[3-(4-hydroxyphenyl)prop-2-enoyloxy]propan-2-yl]oxy-3,5-dimethoxyphenyl]prop-2-enyl 3-(4-hydroxyphenyl)prop-2-enoate 78200708 Click to see 698.70 unknown https://doi.org/10.1021/NP010451C
CID 91895363 91895363 Click to see 698.70 unknown https://doi.org/10.1021/NP010451C
Dadahol A 10908643 Click to see 698.70 unknown https://doi.org/10.1021/NP010451C
dadahol B 11146784 Click to see COC1=C(C=CC(=C1)C=CCOC(=O)C=CC2=CC=C(C=C2)O)OC(COC(=O)C=CC3=CC=C(C=C3)O)C(C4=CC(=C(C=C4)O)OC)O 668.70 unknown https://doi.org/10.1021/NP010451C
erythro-(7R,8S)-Dadahol B 137628510 Click to see COC1=C(C=CC(=C1)C=CCOC(=O)C=CC2=CC=C(C=C2)O)OC(COC(=O)C=CC3=CC=C(C=C3)O)C(C4=CC(=C(C=C4)O)OC)O 668.70 unknown https://doi.org/10.1021/NP010451C
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(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/10.1007/S11418-006-0048-0
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R)-7-(6-hydroxy-1-benzofuran-2-yl)-2-methyl-8-(3-methylbut-2-enyl)-2-(4-methylpent-3-enyl)chromen-5-ol 163014986 Click to see 444.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257731/
2-[(1S,4R,13S)-1,5,5-trimethyl-10-(3-methylbut-2-enyl)-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7(12),8,10-trien-9-yl]-1-benzofuran-6-ol 162973439 Click to see 444.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257731/
2-[(2R)-5-hydroxy-2-methyl-8-(3-methylbut-2-enyl)-2-(4-methylpent-3-enyl)chromen-7-yl]-1-benzofuran-4,6-diol 162848824 Click to see CC(=CCCC1(C=CC2=C(C=C(C(=C2O1)CC=C(C)C)C3=CC4=C(C=C(C=C4O3)O)O)O)C)C 460.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257731/
2-[1,5,5-Trimethyl-10-(3-methylbut-2-enyl)-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7(12),8,10-trien-9-yl]-1-benzofuran-6-ol 162973438 Click to see 444.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257731/
2-[5-Hydroxy-2-methyl-8-(3-methylbut-2-enyl)-2-(4-methylpent-3-enyl)chromen-7-yl]-1-benzofuran-4,6-diol 145972893 Click to see 460.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257731/
3-(Gamma,Gamma-Dimethylpropenyl)Moracinm 42605184 Click to see 310.30 unknown https://doi.org/10.1021/NP010451C
4-(3,7-Dimethylocta-2,6-dienyl)-5-(6-hydroxy-1-benzofuran-2-yl)-6-(3-methylbut-2-enyl)benzene-1,3-diol 3012525 Click to see 446.60 unknown https://doi.org/10.1021/NP030429E
5-[5-Hydroxy-7-(3-methylbut-1-enyl)-1-benzofuran-2-yl]benzene-1,3-diol 85409557 Click to see 310.30 unknown https://doi.org/10.1021/NP010451C
5-[5-hydroxy-7-[(E)-3-methylbut-1-enyl]-1-benzofuran-2-yl]benzene-1,3-diol 11130690 Click to see 310.30 unknown https://doi.org/10.1021/NP010451C
5-[6-Hydroxy-7-(3-methylbut-2-enyl)-1-benzofuran-2-yl]-4,6-bis(3-methylbut-2-enyl)benzene-1,3-diol 10253008 Click to see 446.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.009
7-(6-Hydroxy-1-benzofuran-2-yl)-2-methyl-8-(3-methylbut-2-enyl)-2-(4-methylpent-3-enyl)chromen-5-ol 145959857 Click to see 444.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257731/
Artoindonesianin Y 641711 Click to see 444.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.009
https://doi.org/10.1002/CHIN.200410207
Lakoochin A 3012524 Click to see 406.50 unknown https://doi.org/10.1021/NP030429E
Lakoochin B 6479925 Click to see 446.60 unknown https://doi.org/10.1021/NP030429E
Moracin M 185848 Click to see 242.23 unknown https://doi.org/10.1021/NP010451C
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2S,3S)-2-(3,4-dihydroxyphenyl)-8-[(2R,3R,4R)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 14015960 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 562.50 unknown https://doi.org/10.1021/NP010451C
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1021/NP010451C
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1021/NP010451C
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
(-)-Epiafzelechin 443639 Click to see 274.27 unknown https://doi.org/10.1021/NP010451C
2-(4-Hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 282014 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC=C(C=C3)O)O 274.27 unknown https://doi.org/10.1021/NP010451C
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-2,3-dihydrochromen-4-one 26213324 Click to see 288.25 unknown https://doi.org/10.1021/NP010451C
(2S)-5,7,2',4'-tetrahydroxyflavanone 10356745 Click to see 288.25 unknown https://doi.org/10.1021/NP010451C
Steppogenin 21596130 Click to see 288.25 unknown https://doi.org/10.1021/NP010451C
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(2S,3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 98049813 Click to see 304.25 unknown https://doi.org/10.1021/NP010451C
(2S,3R)-3,5,7-trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 11449086 Click to see 288.25 unknown via CMAUP database
2-(2,4-Dihydroxyphenyl)-3,5,7-Trihydroxy-2,3-Dihydrochromen-4-One 362637 Click to see C1=CC(=C(C=C1O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 304.25 unknown https://doi.org/10.1021/NP010451C
Dihydromorin 5458714 Click to see 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Norartocarpetin 5481970 Click to see 286.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.009
https://doi.org/10.1021/NP010451C
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
Heteroartonin A 15231526 Click to see 452.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.009
Morusin 5281671 Click to see CC(=CCC1=C(OC2=C(C1=O)C(=CC3=C2C=CC(O3)(C)C)O)C4=C(C=C(C=C4)O)O)C 420.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2003.08.009
https://doi.org/10.1002/CHIN.200410207
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
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/10.1002/CHIN.200410207
https://doi.org/10.1016/J.PHYTOCHEM.2003.08.009
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R,4R,5R,6S)-2-[[(2R,3S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl]oxy]-6-methyloxane-3,4,5-triol 162913460 Click to see CC1C(C(C(C(O1)OC2CC3=C(C=C(C=C3OC2C4=CC=C(C=C4)O)O)O)O)O)O 420.40 unknown https://doi.org/10.1021/NP010451C
(2S,3R,4R,5R,6S)-2-[[(2R,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl]oxy]-6-methyloxane-3,4,5-triol 44584103 Click to see 420.40 unknown https://doi.org/10.1021/NP010451C
(2S,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2,3-dihydrochromen-4-one 154496486 Click to see 434.40 unknown https://doi.org/10.1021/NP010451C
(2S,3R)-Astilbin; NSC 245342 12309470 Click to see 434.40 unknown https://doi.org/10.1021/NP010451C
(2S,3S,4R,5R,6R)-2-[[(2R,3S)-5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl]oxy]-6-methyloxane-3,4,5-triol 162913463 Click to see 420.40 unknown https://doi.org/10.1007/S11418-006-0048-0
[(2R,3S,4S,5R,6S)-6-[(2R,3R,4S,5S,6R)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 162988364 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)OC5C(C(C(C(O5)COC(=O)C)O)O)O 652.60 unknown https://doi.org/10.1021/NP030429E
2-[[5,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl]oxy]-6-methyloxane-3,4,5-triol 74977160 Click to see CC1C(C(C(C(O1)OC2CC3=C(C=C(C=C3OC2C4=CC=C(C=C4)O)O)O)O)O)O 420.40 unknown https://doi.org/10.1021/NP010451C
afzelechin-3-O-alpha-Lrhamnopyranoside 44584170 Click to see 420.40 unknown https://doi.org/10.1021/NP010451C
Engeletin 6453452 Click to see CC1C(C(C(C(O1)OC2C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 434.40 unknown https://doi.org/10.1021/NP010451C
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-3,5-dihydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12314848 Click to see 464.40 unknown https://doi.org/10.1021/NP010451C
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
(2S)-2-(2,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-5,7-diol 162923770 Click to see 274.27 unknown https://doi.org/10.1021/NP010451C
2-(2,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-5,7-diol 141341936 Click to see C1CC2=C(C=C(C=C2OC1C3=C(C=C(C=C3)O)O)O)O 274.27 unknown https://doi.org/10.1021/NP010451C
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Gemichalcone B 10413126 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)COC(=O)C=CC3=CC=C(C=C3)O 486.50 unknown https://doi.org/10.1021/NP010451C
Isogemichalcone B 42607532 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)COC(=O)C=CC3=CC=C(C=C3)O 486.50 unknown https://doi.org/10.1021/NP010451C
> Phenylpropanoids and polyketides / Stilbenes
3-(2,3-Dihydroxy-3-Methylbutyl)Resveratrol 10991144 Click to see 330.40 unknown https://doi.org/10.1021/NP010451C
3-(Gamma,Gamma-Dimethylallyl)Resveratrol 636928 Click to see 296.40 unknown https://doi.org/10.1021/NP010451C
4-[2-(3,5-Dihydroxyphenyl)ethenyl]-6-(3-methylbut-2-enyl)benzene-1,3-diol 85374521 Click to see 312.40 unknown https://doi.org/10.1021/NP010451C
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol 5056 Click to see 228.24 unknown https://doi.org/10.1021/NP010451C
5-(gamma,gamma-Dimethylallyl)-oxyresveratrol 11034312 Click to see CC(=CCC1=CC(=C(C=C1O)O)C=CC2=CC(=CC(=C2)O)O)C 312.40 unknown https://doi.org/10.1021/NP010451C
5-[2-[3-(2,3-Dihydroxy-3-methylbutyl)-4-hydroxyphenyl]ethenyl]benzene-1,3-diol 73817240 Click to see 330.40 unknown https://doi.org/10.1021/NP010451C
5-[2-[4-Hydroxy-3-(3-methylbut-2-enyl)phenyl]ethenyl]benzene-1,3-diol 78200706 Click to see 296.40 unknown https://doi.org/10.1021/NP010451C
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/NP010451C
Cis-Resveratrol 1548910 Click to see 228.24 unknown via CMAUP database
Resveratrol 445154 Click to see 228.24 unknown https://doi.org/10.1021/NP010451C
Trans-2,3',4,5'-tetrahydroxystilbene 5281717 Click to see 244.24 unknown https://doi.org/10.1021/NP010451C

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