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Artocarpus lacucha

Artocarpus lacucha - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
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)

Description Top

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Artocarpus lacucha is a tropical evergreen tree species of the family Moraceae found in the Indian Subcontinent and Southeast Asia. It is valued for its wood and its fruit is edible and believed to have medicinal value. In Northeastern Thailand, the wood is used to make pong lang, a local traditional instrument. The stilbenoid oxyresveratrol can be isolated from the heartwood of A. lacucha and is used as a traditional drug to treat intestinal fluke and taeniasis. This tree is also mentioned in the Arthashastra.

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 ডেউয়া
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 ଜେଉଠ
Oriya ଜେଉଟ
Punjabi ਢੇਊ
Punjab ڈھیؤ
sat ᱰᱟᱹᱦᱩ
Thai มะหาด
Thai artocarpus lakoocha roxb
Vietnamese artocarpus lakoocha
Chinese 野波羅蜜
Chinese 猴面果
Chinese 野菠萝蜜
Chinese 野波罗蜜

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
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
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
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
Computational Analysis and Biological Activities of Oxyresveratrol Analogues, the Putative Cyclooxygenase-2 Inhibitors Jongkon N, Seaho B, Tayana N, Prateeptongkum S, Duangdee N, Jaiyong P Molecules 06-Apr-2022
PMCID:PMC9000610
doi:10.3390/molecules27072346
PMID:35408774
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
Synergistic Effects of Limosilactobacillus fermentum ASBT-2 with Oxyresveratrol Isolated from Coconut Shell Waste Prakash V, Krishnan AS, Ramesh R, Bose C, Pillai GG, Nair BG, Pal S Foods 22-Oct-2021
PMCID:PMC8622123
doi:10.3390/foods10112548
PMID:34828830
Oxyresveratrol: Sources, Productions, Biological Activities, Pharmacokinetics, and Delivery Systems Likhitwitayawuid K Molecules 11-Jul-2021
PMCID:PMC8307110
doi:10.3390/molecules26144212
PMID:34299485
Highly Aromatic Flavan-3-ol Derivatives from Palaeotropical Artocarpus lacucha Buch.-Ham Possess Radical Scavenging and Antiproliferative Properties Songoen W, Phanchai W, Brecker L, Wenisch D, Jakupec MA, Pluempanupat W, Schinnerl J Molecules 18-Feb-2021
PMCID:PMC7922997
doi:10.3390/molecules26041078
PMID:33670764

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 COC1=CC(=CC(=C1OC(COC(=O)C=CC2=CC=C(C=C2)O)C(C3=CC(=C(C=C3)O)OC)O)OC)C=CCOC(=O)C=CC4=CC=C(C=C4)O 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 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
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 COC1=CC(=CC(=C1OC(COC(=O)C=CC2=CC=C(C=C2)O)C(C3=CC(=C(C=C3)O)OC)O)OC)C=CCOC(=O)C=CC4=CC=C(C=C4)O 698.70 unknown https://doi.org/10.1021/NP010451C
CID 91895363 91895363 Click to see COC1=CC(=CC(=C1OC(COC(=O)C=CC2=CC=C(C=C2)O)C(C3=CC(=C(C=C3)O)OC)O)OC)C=CCOC(=O)C=CC4=CC=C(C=C4)O 698.70 unknown https://doi.org/10.1021/NP010451C
Dadahol A 10908643 Click to see COC1=CC(=CC(=C1OC(COC(=O)C=CC2=CC=C(C=C2)O)C(C3=CC(=C(C=C3)O)OC)O)OC)C=CCOC(=O)C=CC4=CC=C(C=C4)O 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 CC(=CCCC1(C=CC2=C(C=C(C(=C2O1)CC=C(C)C)C3=CC4=C(O3)C=C(C=C4)O)O)C)C 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 CC(=CCC1=C2C3=C(C=C1C4=CC5=C(O4)C=C(C=C5)O)OC(C6C3CC(O2)(CC6)C)(C)C)C 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 CC(=CCC1=C2C3=C(C=C1C4=CC5=C(O4)C=C(C=C5)O)OC(C6C3CC(O2)(CC6)C)(C)C)C 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 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/
3-(gamma,gamma-dimethylpropenyl)moracinM 42605184 Click to see CC(=CCC1=C(C=CC2=C1OC(=C2)C3=CC(=CC(=C3)O)O)O)C 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 CC(=CCCC(=CCC1=C(C=C(C(=C1C2=CC3=C(O2)C=C(C=C3)O)CC=C(C)C)O)O)C)C 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 CC(C)C=CC1=C2C(=CC(=C1)O)C=C(O2)C3=CC(=CC(=C3)O)O 310.30 unknown https://doi.org/10.1021/NP010451C
5-[5-Hydroxy-7-[(E)-3-methyl-1-butenyl]benzofuran-2-yl]resorcinol 11130690 Click to see CC(C)C=CC1=C2C(=CC(=C1)O)C=C(O2)C3=CC(=CC(=C3)O)O 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 CC(=CCC1=C(C=CC2=C1OC(=C2)C3=C(C(=CC(=C3CC=C(C)C)O)O)CC=C(C)C)O)C 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 CC(=CCCC1(C=CC2=C(C=C(C(=C2O1)CC=C(C)C)C3=CC4=C(O3)C=C(C=C4)O)O)C)C 444.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257731/
Artoindonesianin Y 641711 Click to see CC(=CCC1=C(C(=C(C=C1O)O)CC=C(C)C)C2=CC3=C(O2)C4=C(C=C3)OC(C=C4)(C)C)C 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 CC(=CCC1=C(C(=C(C=C1OC)OC)CC=C(C)C)C2=CC3=C(O2)C=C(C=C3)O)C 406.50 unknown https://doi.org/10.1021/NP030429E
lakoochin B 6479925 Click to see CC(=CCCC(=CCC1=C(C=C(C(=C1C2=CC3=C(O2)C=C(C=C3)O)CC=C(C)C)O)O)C)C 446.60 unknown https://doi.org/10.1021/NP030429E
Moracin M 185848 Click to see C1=CC2=C(C=C1O)OC(=C2)C3=CC(=CC(=C3)O)O 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)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1021/NP010451C
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1021/NP010451C
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
(-)-Epiafzelechin 443639 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
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 C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP010451C
(2S)-5,7,2',4'-tetrahydroxyflavanone 10356745 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP010451C
Steppogenin 21596130 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=C(C=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP010451C
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+)-Epiaromadendrin 11449086 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown via CMAUP database
(2S,3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 98049813 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
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 C1=CC(=C(C=C1O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Norartocarpetin 5481970 Click to see C1=CC(=C(C=C1O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 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 CC(=CCC1=C(C(=CC(=C1OC)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)CC=C(C)C)O)C 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 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)-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 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
(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 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/10.1007/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-rhamnoside 44584170 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
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
Isoengelitin 12309470 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 C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 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 C1CC2=C(C=C(C=C2OC1C3=C(C=C(C=C3)O)O)O)O 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
(Z)-resveratrol 1548910 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown via CMAUP database
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]- 5056 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1021/NP010451C
3-(gamma,gamma-Dimethylallyl)resveratrol 636928 Click to see CC(=CCC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)O)C 296.40 unknown https://doi.org/10.1021/NP010451C
3'-[(2R)-2,3-Dihydroxy-3-methylbutyl]-trans-stilbene-3,4',5-triol 10991144 Click to see CC(C)(C(CC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)O)O)O 330.40 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 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-(3-Methyl-2-butenyl)-trans-stilbene-2,3',4,5'-tetrol 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 CC(C)(C(CC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)O)O)O 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 CC(=CCC1=C(C=CC(=C1)C=CC2=CC(=CC(=C2)O)O)O)C 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
Oxyresveratrol 5281717 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
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1021/NP010451C

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