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Maclura cochinchinensis

Maclura cochinchinensis - Unknown
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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 UUID643ffde711208396228966
Scientific name Maclura cochinchinensis
Authority (Lour.) Corner
First published in Gard. Bull. Singapore 19: 239 (1962)

Description Top

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Synonyms Top

Scientific name Authority First published in
Vanieria alternifolia Stokes Bot. Mat. Med. 4: 381 (1812)
Vanieria cochinchinensis Lour. Fl. Cochinch. : 565 (1790)
Maclura timorensis Blume Mus. Bot. 2: 84 (1856)
Maclura gerontogea Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 220 (1846)
Maclura cochinchinensis var. gerontogea (Siebold & Zucc.) S.S.Ying Colour. Illustr. Pl. Taiwan, Pt. 3; Colour. Illustr. Ligneous Pl. Taiwan 1: 382 (1987):.
Trophis fruticosa Hook. & Arn. Bot. Beechey Voy. : 215 (1837)
Procris cochinchinensis Spreng. Syst. Veg. 3: 846 (1826)
Plecospermum cuneifolium Thwaites Hooker's J. Bot. Kew Gard. Misc. 6: 303 (1854)
Cudrania cochinchinensis var. gerontogea (Siebold & Zucc.) Kudô & Masam. Rep. (Annual) Taihoku Bot. Gard. 2: 27 1932
Vanieria cochinchinensis var. gerontogea (Siebold & Zucc.) Nakai Bot. Mag. (Tokyo) 41: 516 1927
Boehmeria cochinchinensis Pers. Syn. Pl. 2: 557 (1807)
Cudrania amboinensis Miq. Fl. Ned. Ind. 1(2): 290 (1859)
Cudrania cambodiana Gagnep. Bull. Soc. Bot. France 72: 808 (1925 publ. 1926)
Cudrania cochinchinensis (Lour.) Yakuro Kudo & Masam. Rep. (Annual) Taihoku Bot. Gard. 2: 27 (1932)
Cudrania fruticosa Wight ex Kurz Forest Fl. Burma 2: 434 (1877)
Cudrania grandifolia Merr. Philipp. J. Sci. 18: 52 (1921)
Cudrania integra F.T.Wang & Tang Acta Phytotax. 1: 127 (1951)
Cudrania javanensis Trécul Ann. Sci. Nat., Bot. , sér. 3, 8: 123 (1847)
Cudrania javanensis var. bancroftii F.M.Bailey Syn. Queensl. Fl. : 491 (1883)
Cudrania jinghongensis S.S.Chang Acta Phytotax. Sin. 22: 64 (1984)
Cudrania obovata Trécul Ann. Sci. Nat., Bot. , sér. 3, 8: 126 (1847)
Cudrania pubescens Trécul Ann. Sci. Nat., Bot. , sér. 3, 8: 125 (1847)
Cudrania rectispina Hance J. Bot. 14: 365 (1876)
Cudrania rumphii Thwaites Enum. Pl. Zeyl. : 262 (1861)
Cudrania thorelii Gagnep. Bull. Soc. Bot. France 72: 810 (1925 publ. 1926)
Cudrania spinosus Kuntze Revis. Gen. Pl. 2: 623. 1891 (1891)
Vanieria fruticosa (Roxb.) Chun J. Arnold Arbor. 8: 21 (1927)
Vanieria pubescens (Trécul) Chun J. Arnold Arbor. 8: 21 (1927)
Cudrania jingdongensis S.S.Chang Acta Phytotax. Sin. 22(1): 64. 1984 [18 Feb 1984]
Maclura cochinchinensis var. pubescens (Trécul) Corner Gard. Bull. Singapore 19(2): 239 1962
Maclura amboinensis Blume Mus. Bot. 2: 84 (1856)
Maclura thorelii (Gagnep.) Corner Gard. Bull. Singapore 19: 240 (1962)
Maclura pubescens (Trécul) Z.K.Zhou & M.G.Gilbert Fl. China 5: 36 (2003)
Maclura cochinchinensis var. bancroftii (Bailey) Corner Gard. Bull. Singapore 19: 239 (1962)

Common names Top

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Language Common/alternative name
Persian ماکلورا کوشینشیننسیس
Indonesian sisir/kaliage
nan n̂g-kim-kuì
Thai แกแล
Vietnamese vàng lồ
Chinese 葨芝
Chinese 黃金桂
Chinese 枸棘
Chinese 大丁癀
Chinese 穿破石
Chinese 桃南瓜
Chinese 柘樹
Chinese 构棘（葨芝）
Chinese 构棘
Chinese 山荔枝果
Chinese 奴拓刺
Chinese 刺格

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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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-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
      • Tibet
    • Eastern Asia
      • Japan
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • Nepal
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Christmas Island
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000448071
Tropicos 21300009
INPN 671201
KEW urn:lsid:ipni.org:names:584314-1
The Plant List kew-2501635
PFAF Maclura cochinchinensis
Open Tree Of Life 368912
NCBI Taxonomy 194324
IPNI 584314-1
iNaturalist 370175
GBIF 7262552
Freebase /m/0c41lr3
USDA GRIN 416047
Wikipedia Maclura_cochinchinensis
CMAUP NPO23156

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
Ethnobotany and phytochemistry of plants used to treat musculoskeletal disorders among Skaw Karen, Thailand Kantasrila R, Pandith H, Balslev H, Wangpakapattanawong P, Panyadee P, Inta A Pharm Biol 22-Dec-2023
PMCID:PMC10763916
doi:10.1080/13880209.2023.2292261
PMID:38131672
Climbing strategies of Taiwan climbers Chen PH, Chung AC, Lin HC, Yang SZ Bot Stud 22-Sep-2023
PMCID:PMC10516820
doi:10.1186/s40529-023-00399-4
PMID:37736799
In vitro evaluation of the anti‑breast cancer properties and gene expression profiles of Thai traditional formulary medicine extracts Khamwut A, Klomkliew P, Jumpathong W, Kaewsapsak P, Chanchaem P, Sivapornnukul P, Chantanakat K, T-Thienprasert NP, Payungporn S Biomed Rep 30-Aug-2023
PMCID:PMC10502604
doi:10.3892/br.2023.1652
PMID:37719681
A Review of Classification, Biosynthesis, Biological Activities and Potential Applications of Flavonoids Chen S, Wang X, Cheng Y, Gao H, Chen X Molecules 25-Jun-2023
PMCID:PMC10343696
doi:10.3390/molecules28134982
PMID:37446644
Biological activities of extracts and compounds from Thai Kae-Lae (Maclura cochinchinensis (Lour.) Corner) Rueankham L, Panyajai P, Saiai A, Rungrojsakul M, Tima S, Chiampanichayakul S, Yeerong K, Somwongin S, Chaiyana W, Dejkriengkraikul P, Okonogi S, Katekunlaphan T, Anuchapreeda S BMC Complement Med Ther 09-Jun-2023
PMCID:PMC10257291
doi:10.1186/s12906-023-03979-w
PMID:37296375
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Potential of natural flavonols and flavanones in the treatment of ulcerative colitis Li C, Tang Y, Ye Y, Zuo M, Lu Q Front Pharmacol 03-Mar-2023
PMCID:PMC10020211
doi:10.3389/fphar.2023.1120616
PMID:36937890
Changes in homegardens in relocation villages, a case study in the Baiku Yao area in Southern China Hu R, Xu C, Nong Y, Luo B J Ethnobiol Ethnomed 27-Feb-2023
PMCID:PMC9972620
doi:10.1186/s13002-023-00578-4
PMID:36849896
Xanthones: Biosynthesis and Trafficking in Plants, Fungi and Lichens Badiali C, Petruccelli V, Brasili E, Pasqua G Plants (Basel) 04-Feb-2023
PMCID:PMC9967055
doi:10.3390/plants12040694
PMID:36840041
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Ethnobotanical study of Hakka traditional medicine in Ganzhou, China and their antibacterial, antifungal, and cytotoxic assessments Hu H, Yang Y, Aissa A, Tekin V, Li J, Panda SK, Huang H, Luyten W BMC Complement Med Ther 19-Sep-2022
PMCID:PMC9484230
doi:10.1186/s12906-022-03712-z
PMID:36123737
Model yeast as a versatile tool to examine the antioxidant and anti-ageing potential of flavonoids, extracted from medicinal plants Zahoor H, Watchaputi K, Hata J, Pabuprapap W, Suksamrarn A, Chua LS, Soontorngun N Front Pharmacol 02-Sep-2022
PMCID:PMC9479101
doi:10.3389/fphar.2022.980066
PMID:36120300
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
Pharmacologically Active Phytomolecules Isolated from Traditional Antidiabetic Plants and Their Therapeutic Role for the Management of Diabetes Mellitus Ansari P, Akther S, Hannan JM, Seidel V, Nujat NJ, Abdel-Wahab YH Molecules 03-Jul-2022
PMCID:PMC9268530
doi:10.3390/molecules27134278
PMID:35807526
Commodity risk assessment of Acer palmatum plants grafted on Acer davidii from China Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 12-May-2022
PMCID:PMC9096882
doi:10.2903/j.efsa.2022.7298
PMID:35592020

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1002/JPS.2600601135
> 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/10.1002/JPS.2600601135
> Benzenoids / Benzene and substituted derivatives / Benzophenones
(5,7-Dihydroxy-2,2-dimethyl-chromen-8-yl)-[3,5-dihydroxy-2-(3-methylbut-2-enyl)phenyl]methanone 509242 Click to see CC(=CCC1=C(C=C(C=C1O)O)C(=O)C2=C(C=C(C3=C2OC(C=C3)(C)C)O)O)C 396.40 unknown https://doi.org/10.1021/NP000406P
(5,7-Dihydroxy-2,2-dimethylchromen-8-yl)-[3-hydroxy-2-(3-methylbut-2-enyl)phenyl]methanone 10523817 Click to see CC(=CCC1=C(C=CC=C1O)C(=O)C2=C(C=C(C3=C2OC(C=C3)(C)C)O)O)C 380.40 unknown https://doi.org/10.1021/NP000406P
[2,4-Dihydroxy-5-(3-methylbut-2-enyl)phenyl]-[3,5-dihydroxy-2-(3-methylbut-2-enyl)phenyl]methanone 509241 Click to see CC(=CCC1=CC(=C(C=C1O)O)C(=O)C2=C(C(=CC(=C2)O)O)CC=C(C)C)C 382.40 unknown https://doi.org/10.1021/NP000406P
Cudranone 191694 Click to see CC(=CCC1=C(C=CC=C1O)C(=O)C2=C(C=C(C=C2O)OC)O)C 328.40 unknown https://doi.org/10.1021/NP000406P
Cudraphenone A 11793144 Click to see CC(=CCC1=C(C=CC=C1O)C(=O)C2=C(C=C3C(=C2)C=CC(O3)(C)C)O)C 364.40 unknown https://doi.org/10.1021/NP000406P
Cudraphenone B 11793280 Click to see CC(=CCC1=CC(=C(C=C1O)O)C(=O)C2=C(C(=CC=C2)O)CC=C(C)C)C 366.40 unknown https://doi.org/10.1021/NP000406P
Cudraphenone D 509243 Click to see CC(=CCC1=C(C=CC=C1O)C(=O)C2=C(C=C(C(=C2O)CC=C(C)C)O)O)C 382.40 unknown https://doi.org/10.1021/NP000406P
https://doi.org/10.1021/NP030024U
> Lignans, neolignans and related compounds / Lignan glycosides
9-(1,3-benzodioxol-5-yl)-4-[(2S,3R,4R)-3-[(2R,3S,4R,5R)-4-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxyoxan-2-yl]oxy-4-hydroxy-4-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxolan-2-yl]oxy-6,7-dimethoxy-3H-benzo[f][2]benzofuran-1-one 44559772 Click to see COC1=C(C=C2C(=C1)C(=C3C(=C2OC4C(C(CO4)(COC5C(C(C(CO5)O)O)O)O)OC6C(C(C(CO6)O)OC7C(C(CO7)(CO)O)O)O)COC3=O)C8=CC9=C(C=C8)OCO9)OC 908.80 unknown https://doi.org/10.1016/S0031-9422(00)98098-1
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Meleic acid monomethyl ester 61799 Click to see COC(=O)C=CC(=O)O 130.10 unknown https://doi.org/10.1002/JPS.2600601135
Monomethyl Fumarate 5369209 Click to see COC(=O)C=CC(=O)O 130.10 unknown https://doi.org/10.1002/JPS.2600601135
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl linoleate 5284421 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown https://doi.org/10.1016/0031-9422(88)84133-5
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Panduratin H 24864449 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)OC)C2=CC=CC=C2 298.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
[(2R)-7-Hydroxy-5-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-8-yl][(1R,2S,6R)-3-methyl-2-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexenyl]methanone 101855692 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 540.70 unknown via CMAUP database
[(2S)-7-Hydroxy-5-methoxy-2-methyl-2-(4-methyl-3-pentenyl)-2H-1-benzopyran-8-yl][(1R,2S,6R)-3-methyl-2-(3-methyl-2-butenyl)-6-phenyl-3-cyclohexenyl]methanone 101855694 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)CCC=C(C)C)C4=CC=CC=C4 540.70 unknown via CMAUP database
Panduratin D 24864268 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CO3)C4=CC=CC=C4 430.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(5S,5aS,7R,8aR,9S)-7-(hydroxymethyl)-5,7-dimethyl-4,5a,6,8,8a,9-hexahydroazuleno[5,6-c]furan-5,9-diol 14488477 Click to see CC1(CC2C(C1)C(CC3=COC=C3C2O)(C)O)CO 266.33 unknown via CMAUP database
Mitissimols C 15939741 Click to see CC1=CC(C(C=CC(=O)C(=CC(C1)O)C)(C)C)O 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(1S,5S,5aS,8aR,9S)-1,5,9-trihydroxy-5,7,7-trimethyl-4,5a,6,8,8a,9-hexahydro-1H-azuleno[5,6-c]furan-3-one 95049893 Click to see CC1(CC2C(C1)C(CC3=C(C2O)C(OC3=O)O)(C)O)C 282.33 unknown via CMAUP database
4,4abeta,5,6,7,7abeta,8,9-Octahydro-4beta,8beta-dihydroxy-6beta-(hydroxymethyl)-6,8-dimethylazuleno[5,6-c]furan-1(3H)-one 14488475 Click to see CC1(CC2C(C1)C(CC3=C(C2O)COC3=O)(C)O)CO 282.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
Dehydrocostus lactone, (-)- 73174 Click to see C=C1CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1016/0031-9422(88)84133-5
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,10R,13R,14R,17R)-4,4,10,13,14-pentamethyl-17-[(2R)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 102004740 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(95)00277-E
(3S,5R,10R,13S,14S)-17-[(1R)-1,5-dimethylhex-4-enyl]-4,4,10,13,14-pentamethyl-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 472759 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(95)00277-E
[(3S,5R,9R,10R,13S,14S,17R)-4,4,10,13,14-pentamethyl-17-[(2S)-6-methylhept-5-en-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 162979286 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)90178-X
[4,4,10,13,14-pentamethyl-17-(6-methylhept-5-en-2-yl)-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-yl] acetate 14286764 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)90178-X
Butyrospermol acetate 6427349 Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(95)00277-E
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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(88)84133-5
24-Ethylcholest-5-en-3beta-ol 22012 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(88)84133-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Acyloins
Mitissimol G 102380141 Click to see CC1(C=CC(=O)C(CC(CC2(C(C1O)O2)C)O)(C)O)C 284.35 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Aspidinol 122841 Click to see CCCC(=O)C1=C(C(=C(C=C1O)OC)C)O 224.25 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Panduratin E 24864269 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C3C(=C(C=C2O)OC)C=CC(O3)(C)C)C4=CC=CC=C4 472.60 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
(2R)-4,8,9-trihydroxy-2-(2-hydroxypropan-2-yl)-11-(2-methylbut-3-en-2-yl)-2,3-dihydrofuro[3,2-b]xanthen-5-one 163013970 Click to see CC(C)(C=C)C1=C2C(=C(C3=C1OC4=C(C3=O)C=CC(=C4O)O)O)CC(O2)C(C)(C)O 412.40 unknown https://doi.org/10.1021/NP000406P
(2R)-4,8,9-trihydroxy-2,3,3-trimethyl-2H-furo[3,2-b]xanthen-5-one 163040073 Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)(C)C 328.30 unknown https://doi.org/10.1021/NP030024U
(2S)-4,8,9-trihydroxy-11-methoxy-2,3,3-trimethyl-2H-furo[3,2-b]xanthen-5-one 163029215 Click to see CC1C(C2=C(O1)C(=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)OC)(C)C 358.30 unknown https://doi.org/10.1016/0031-9422(89)80058-5
(2S)-4,8,9-trihydroxy-2,3,3-trimethyl-2H-furo[3,2-b]xanthen-5-one 163040074 Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)(C)C 328.30 unknown https://doi.org/10.1021/NP030024U
(2S)-5,9,10-trihydroxy-1,1,2-trimethyl-2H-furo[2,3-c]xanthen-6-one 163021269 Click to see CC1C(C2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC(=C4O)O)O)(C)C 328.30 unknown https://doi.org/10.1248/CPB.45.1615
1,2,5,7-Tetrahydroxyxanthen-9-one 162909448 Click to see C1=CC2=C(C(=C1O)O)C(=O)C3=C(O2)C(=CC(=C3)O)O 260.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
1,3,5-Trihydroxyxanthone 5281663 Click to see C1=CC2=C(C(=C1)O)OC3=CC(=CC(=C3C2=O)O)O 244.20 unknown https://doi.org/10.1248/CPB.45.1615
1,3,5,6-Tetrahydroxyxanthone 5479774 Click to see C1=CC(=C(C2=C1C(=O)C3=C(C=C(C=C3O2)O)O)O)O 260.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
1,3,6-Trihydroxy-5-methoxyxanthone 5493675 Click to see COC1=C(C=CC2=C1OC3=CC(=CC(=C3C2=O)O)O)O 274.22 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
1,5,6-Trihydroxy-3-methoxy-2-(2-methylbut-3-en-2-yl)xanthen-9-one 14412273 Click to see CC(C)(C=C)C1=C(C=C2C(=C1O)C(=O)C3=C(O2)C(=C(C=C3)O)O)OC 342.30 unknown https://doi.org/10.1016/S0031-9422(00)98098-1
2,5,7-Trihydroxy-1-methoxyxanthen-9-one 11579945 Click to see COC1=C(C=CC2=C1C(=O)C3=C(O2)C(=CC(=C3)O)O)O 274.22 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
4,8,9-trihydroxy-11-methoxy-2,3,3-trimethyl-2H-furo[3,2-b]xanthen-5-one 14259060 Click to see CC1C(C2=C(O1)C(=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)OC)(C)C 358.30 unknown https://doi.org/10.1016/0031-9422(89)80058-5
5,9,10-trihydroxy-1,1,2-trimethyl-2H-furo[2,3-c]xanthen-6-one 10336602 Click to see CC1C(C2=C(O1)C=C(C3=C2OC4=C(C3=O)C=CC(=C4O)O)O)(C)C 328.30 unknown https://doi.org/10.1248/CPB.45.1615
8,9-dihydroxy-4-methoxy-2,3,3-trimethyl-2H-furo[3,2-b]xanthen-5-one 15223507 Click to see CC1C(C2=C(O1)C=C3C(=C2OC)C(=O)C4=C(O3)C(=C(C=C4)O)O)(C)C 342.30 unknown https://doi.org/10.1016/0031-9422(95)00277-E
Cudraxanthone P 10644437 Click to see CC(=CCOC1=C(C2=C(C=C1)C(=O)C3=C(O2)C=C(C(=C3O)C(C)(C)C=C)O)O)C 396.40 unknown https://doi.org/10.1021/NP000406P
Cudraxanthone R 10716607 Click to see CC(C)(C=C)C1=C2C(=C(C3=C1OC4=C(C3=O)C=CC(=C4O)O)O)CC(O2)C(C)(C)O 412.40 unknown https://doi.org/10.1021/NP000406P
Cudraxanthone S 5495918 Click to see CC(C)(C=C)C1=C(C2=C(C=C1O)OC3=C(C2=O)C=CC(=C3O)O)O 328.30 unknown https://doi.org/10.1021/NP030024U
isocudraniaxanthone A 10687703 Click to see CC(C)(C=C)C1=C(C=C(C2=C1OC3=C(C2=O)C=CC(=C3O)O)O)O 328.30 unknown https://doi.org/10.1248/CPB.45.1615
isocudraniaxanthone B 10831150 Click to see CC(C)(C=C)C1=C(C=C(C2=C1OC3=C(C2=O)C=CC(=C3O)O)O)OC 342.30 unknown https://doi.org/10.1248/CPB.45.1615
Lancerin 5281645 Click to see C1=CC2=C(C=C1O)C(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O 406.30 unknown https://doi.org/10.1016/0378-8741(94)90072-8
Toxyloxanthone C 5495919 Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)(C)C 328.30 unknown https://doi.org/10.1021/NP000406P
https://doi.org/10.1021/NP030024U
Xanthone 7020 Click to see C1=CC=C2C(=C1)C(=O)C3=CC=CC=C3O2 196.20 unknown https://doi.org/10.1016/S0031-9422(00)98098-1
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 2-prenylated xanthones
(2R)-4,8-dihydroxy-9-methoxy-2,3,3-trimethyl-7-(3-methylbut-2-enyl)-2H-furo[3,2-b]xanthen-5-one 163035098 Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C(=C4)CC=C(C)C)O)OC)(C)C 410.50 unknown https://doi.org/10.1016/S0031-9422(00)98098-1
(2S)-4,8,9-trihydroxy-2,3,3-trimethyl-7-(3-methylbut-2-enyl)-2H-furo[3,2-b]xanthen-5-one 101673615 Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C(=C4)CC=C(C)C)O)O)(C)C 396.40 unknown https://doi.org/10.1016/S0031-9422(00)98098-1
1,3,7-Trihydroxy-2-prenylxanthone 5495920 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C=C(C=C3)O)O)C 312.30 unknown https://doi.org/10.1021/NP030024U
https://doi.org/10.1021/NP000406P
gerontoxanthone G 14412268 Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C(C(=C4)CC=C(C)C)O)O)(C)C 396.40 unknown https://doi.org/10.1016/S0031-9422(00)98098-1
https://doi.org/10.1021/NP000406P
gerontoxanthone I 14412270 Click to see CC(=CCC1=C(C2=C(C(=C1O)C(C)(C)C=C)OC3=C(C2=O)C=CC(=C3O)O)O)C 396.40 unknown https://doi.org/10.1021/NP000406P
https://doi.org/10.1016/S0031-9422(00)98098-1
Isoalvaxanthone 10596886 Click to see CC(=CCC1=CC2=C(C(=C1O)O)OC3=C(C2=O)C(=C(C(=C3)O)C(C)(C)C=C)O)C 396.40 unknown https://doi.org/10.1021/NP000406P
https://doi.org/10.1248/CPB.45.1615
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
(2R)-4,8,9-trihydroxy-2,3,3-trimethyl-11-(3-methylbut-2-enyl)-2H-furo[3,2-b]xanthen-5-one 163022891 Click to see CC1C(C2=C(O1)C(=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)CC=C(C)C)(C)C 396.40 unknown https://doi.org/10.1016/0031-9422(89)80058-5
1,3,5-Trihydroxy-4-(3-methylbut-2-en-1-yl)-9H-xanthen-9-one 10335672 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C(=CC=C3)O)C 312.30 unknown https://doi.org/10.1248/CPB.45.1615
brasixanthone B 10362269 Click to see CC(=CCC1=C2C(=C(C3=C1OC4=C(C3=O)C=C(C=C4)O)O)C=CC(O2)(C)C)C 378.40 unknown https://doi.org/10.1021/NP000406P
Gerontoxanthone C 14259059 Click to see CC1C(C2=C(O1)C(=C3C(=C2O)C(=O)C4=C(O3)C(=C(C=C4)O)O)CC=C(C)C)(C)C 396.40 unknown https://doi.org/10.1016/0031-9422(89)80058-5
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 8-prenylated xanthones
6,9-Dihydroxy-3,3-dimethyl-8-(3-methylbut-2-enyl)pyrano[2,3-c]xanthen-7-one 86276176 Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(O2)C4=C(C=C3O)OC(C=C4)(C)C)O)C 378.40 unknown https://doi.org/10.1016/0378-8741(94)90072-8
https://doi.org/10.1016/J.BMCL.2015.02.075
Alvaxanthone 12305823 Click to see CC(=CCC1=CC(=C(C2=C1C(=O)C3=C(O2)C=C(C(=C3O)C(C)(C)C=C)O)O)O)C 396.40 unknown https://doi.org/10.1021/NP000406P
https://doi.org/10.1248/CPB.45.1615
gerontoxanthone H 11211194 Click to see CC(=CCC1=C(C=CC2=C1C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)C 380.40 unknown https://doi.org/10.1021/NP000406P
https://doi.org/10.1016/J.BMCL.2015.02.075
https://doi.org/10.1016/S0031-9422(00)98098-1
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / Pyranoxanthones
(7S)-10,21-dihydroxy-7,8,8,18,18-pentamethyl-2,6,19-trioxapentacyclo[11.8.0.03,11.05,9.015,20]henicosa-1(13),3,5(9),10,14,16,20-heptaen-12-one 163046372 Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C5C(=C4)C=CC(O5)(C)C)O)(C)C 394.40 unknown https://doi.org/10.1016/0031-9422(89)80058-5
11-Hydroxy-7,7,18,18-tetramethyl-2,8,19-trioxapentacyclo[12.8.0.03,12.04,9.015,20]docosa-1(14),3(12),4(9),5,10,15(20),16,21-octaen-13-one 14259061 Click to see CC1(C=CC2=C(O1)C=CC3=C2C(=O)C4=C(O3)C5=C(C=C4O)OC(C=C5)(C)C)C 376.40 unknown https://doi.org/10.1016/0031-9422(89)80058-5
21-Hydroxy-6-(2-hydroxypropan-2-yl)-17,17-dimethyl-7,12,18-trioxapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-1(13),3(11),4(8),9,14(19),15,20-heptaen-2-one 101616167 Click to see CC1(C=CC2=C(O1)C=C(C3=C2OC4=C(C3=O)C5=C(C=C4)OC(C5)C(C)(C)O)O)C 394.40 unknown https://doi.org/10.1016/J.BMCL.2015.02.075
6-Deoxyjacareubin 5281629 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=CC=C4)O)C 310.30 unknown https://doi.org/10.1021/NP000406P
https://doi.org/10.1021/NP030024U
gerontoxanthone A 11948658 Click to see CC1C(C2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C(=C5C(=C4)C=CC(O5)(C)C)O)(C)C 394.40 unknown https://doi.org/10.1016/0031-9422(89)80058-5
https://doi.org/10.1021/NP000406P
https://doi.org/10.1016/J.BMCL.2015.02.075
gerontoxanthone B 14259057 Click to see CC1(C=CC2=CC3=C(C(=C2O1)O)OC4=C(C3=O)C(=C(C(=C4)O)C(C)(C)C=C)O)C 394.40 unknown https://doi.org/10.1016/0031-9422(89)80058-5
https://doi.org/10.1021/NP000406P
https://doi.org/10.1016/J.BMCL.2015.02.075
Macluraxanthone 5281646 Click to see CC1(C=CC2=C(C3=C(C(=C2O1)C(C)(C)C=C)OC4=C(C3=O)C=CC(=C4O)O)O)C 394.40 unknown https://doi.org/10.1021/NP000406P
Osajaxanthone 6064803 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)C=CC(=C4)O)C 310.30 unknown https://doi.org/10.1002/JPS.2600601135
https://doi.org/10.1016/0031-9422(89)80058-5
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1021/NP000406P
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(-)-nicolaioidesin B 637029 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)OC)O 406.50 unknown via CMAUP database
(1'R,2'S,6'R)-2-Hydroxyisopanduratin A 23656472 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3O)O)O 392.50 unknown via CMAUP database
(2-hydroxy-4,6-dimethoxyphenyl)-[(1R,2S,6R)-3-methyl-2-(3-methylbut-2-enyl)-6-phenylcyclohex-3-en-1-yl]methanone 44444916 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)OC)O)C3=CC=CC=C3 420.50 unknown via CMAUP database
2,6-Dihydroxy-4-methoxyphenyl[2beta-(3-methyl-2-butenyl)-3-methyl-6alpha-phenyl-3-cyclohexene-1beta-yl]methanone 25023021 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
4-hydroxypanduratin A 636530 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)O)O)C3=CC=CC=C3 392.50 unknown via CMAUP database
Isopanduratin A 10069916 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
Isopanduratin A1 44444913 Click to see CC1=CCC(C(C1CC=C(C)C)C2=CC=CC=C2)C(=O)C3=C(C=C(C=C3OC)O)O 406.50 unknown via CMAUP database
Panduratin A 6483648 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2O)OC)O)C3=CC=CC=C3 406.50 unknown via CMAUP database
Panduratin C 6483647 Click to see CC1=CCC(C(C1CC=C(C)C)C(=O)C2=C(C=C(C=C2OC)O)O)C3=CC=C(C=C3)O 422.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 102004723 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C 356.40 unknown https://doi.org/10.1021/NP030024U
(2S)-6-geranylpinostrobin 44444914 Click to see CC(=CCCC(=CCC1=C(C=C2C(=C1O)C(=O)CC(O2)C3=CC=CC=C3)OC)C)C 406.50 unknown via CMAUP database
2alpha-Phenyl-6-[(E)-3,7-dimethyl-2,6-octadienyl]-2,3-dihydro-5,7-dihydroxy-4H-1-benzopyran-4-one 44444915 Click to see CC(=CCCC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=CC=C3)O)C)C 392.50 unknown via CMAUP database
Cudraflavanone B 509244 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C 356.40 unknown https://doi.org/10.1021/NP030024U
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R)-8-geranylpinostrobin 23656470 Click to see CC(=CCCC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=CC=C3)O)OC)C)C 406.50 unknown via CMAUP database
8-Prenylnaringenin 480764 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C 340.40 unknown https://doi.org/10.1021/NP000406P
Sophoraflavanone B 509245 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C 340.40 unknown https://doi.org/10.1021/NP000406P
sophoraflavanone B(1-) 25200892 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)[O-])C 339.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<13::AID-PTR764>3.0.CO;2-1
https://doi.org/10.1016/0031-9422(95)00277-E
https://doi.org/10.1021/NP000406P
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<13::AID-PTR764>3.0.CO;2-1
https://doi.org/10.1016/0031-9422(95)00277-E
https://doi.org/10.1021/NP000406P
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1021/NP000406P
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin 471 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
(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/10.1016/J.PHYTOCHEM.2005.09.015
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/10.1016/J.PHYTOCHEM.2005.09.015
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1248/CPB.45.1615
https://doi.org/10.1021/NP030024U
https://doi.org/10.1016/0031-9422(95)00277-E
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1248/CPB.45.1615
https://doi.org/10.1021/NP030024U
https://doi.org/10.1016/0031-9422(95)00277-E
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol oxoanion 25202062 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O 285.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
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/10.1016/0031-9422(95)00277-E
Artocarpesin 399491 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(=CC2=O)C3=C(C=C(C=C3)O)O)O)C 354.40 unknown https://doi.org/10.1016/0031-9422(95)00277-E
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
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/10.1016/0031-9422(95)00277-E
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,7-Dihydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxychromen-4-one 11709692 Click to see COC1=CC(=CC2=C1C(=O)C(=C(O2)C3=C(C=C(C=C3)O)OC)O)O 330.29 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/0031-9422(95)00277-E
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
Morin 5281670 Click to see C1=CC(=C(C=C1O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 302.23 unknown https://doi.org/10.1016/S0944-7113(00)80069-0
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S,3R)-3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 11155141 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 25203835 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 14282776 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 450.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
5-Hydroxy-2-(4-hydroxyphenyl)-3,7-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]chromen-4-one 13647408 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
Kaempferol 3,7-diglucoside 6325460 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
kaempferol 7-O-glucoside 10095180 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/0031-9422(95)00277-E
https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<13::AID-PTR764>3.0.CO;2-1
Kaempferol-7-o-glucoside 5480982 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 5-O-methylated flavonoids
(2R,3R)-3,7-dihydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxy-2,3-dihydrochromen-4-one 11500888 Click to see COC1=CC(=CC2=C1C(=O)C(C(O2)C3=C(C=C(C=C3)O)OC)O)O 332.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
3,7-Dihydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxy-2,3-dihydrochromen-4-one 72985981 Click to see COC1=CC(=CC2=C1C(=O)C(C(O2)C3=C(C=C(C=C3)O)OC)O)O 332.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
5-O-Methylnaringenin 182315 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
Alpinetin 154279 Click to see COC1=CC(=CC2=C1C(=O)CC(O2)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2R)-5,7-Dimethoxyflavanone 689012 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
3,5,7-Trimethoxyflavone 117900 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C(=C(O2)C3=CC=CC=C3)OC 312.30 unknown via CMAUP database
3',4',5,7-Tetramethoxyflavone 631170 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
4H-1-Benzopyran-4-one, 5-hydroxy-3,7-dimethoxy-2-phenyl- 5748697 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=CC=C3)O 298.29 unknown via CMAUP database
5-Hydroxy-7-methoxy-2-phenylchroman-4-one 73201 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
5,7-Dimethoxyflavone 88881 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 282.29 unknown via CMAUP database
Apigenin 7,4'-dimethyl ether 5281601 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC)O 298.29 unknown via CMAUP database
Apigenin trimethyl ether 79730 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3OC)OC 312.30 unknown via CMAUP database
Kaempferol 3,7,4'-trimethyl ether 5468749 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC 328.30 unknown via CMAUP database
Pinostrobin 6950539 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
Quercetin pentamethyl ether 97332 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC)OC 372.40 unknown via CMAUP database
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown via CMAUP database
Sakuranetin 73571 Click to see COC1=CC(=C2C(=O)CC(OC2=C1)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown via CMAUP database
Tetramethylkaempferol 631095 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C=C3OC)OC)OC 342.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
Carpachromene 10449654 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C=C(O3)C4=CC=C(C=C4)O)C 336.30 unknown https://doi.org/10.1021/NP000406P
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
https://doi.org/10.1016/0031-9422(95)00277-E
Orobol 5281801 Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O 286.24 unknown https://doi.org/10.1016/0031-9422(95)00277-E
https://doi.org/10.1016/J.PHYTOCHEM.2005.09.015
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones / 2-prenylated isoflavones
7-[3,6-Dihydroxy-2-(3-methylbut-2-enyl)phenyl]-5-hydroxy-2,2-dimethylpyrano[3,2-g]chromen-6-one 5386667 Click to see CC(=CCC1=C(C=CC(=C1C2=COC3=CC4=C(C=CC(O4)(C)C)C(=C3C2=O)O)O)O)C 420.50 unknown https://doi.org/10.1016/0031-9422(88)84133-5
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
6-Prenyl-5,7,4'-trihydroxyisoflavone 25245294 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)[O-])C 337.30 unknown via CMAUP database
Alpinumisoflavone 5490139 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C 336.30 unknown https://doi.org/10.1021/NP000406P
Lupalbigenin 10001388 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)C 406.50 unknown https://doi.org/10.1002/CHIN.200947195
Wighteone 5281814 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O)C 338.40 unknown https://doi.org/10.1002/(SICI)1099-1573(199602)10:1<13::AID-PTR764>3.0.CO;2-1
https://doi.org/10.1021/NP000406P
https://doi.org/10.1016/0031-9422(95)00277-E
https://doi.org/10.1021/NP030024U
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids / 3-O-methylisoflavones
3'-O-Methylorobol 5319744 Click to see COC1=C(C=CC(=C1)C2=COC3=CC(=CC(=C3C2=O)O)O)O 300.26 unknown https://doi.org/10.1021/NP000406P
https://doi.org/10.1021/NP030024U
https://doi.org/10.1016/0031-9422(88)84133-5
Gerontoisoflavone A 15223506 Click to see COC1=CC(=CC2=C1C(=O)C(=CO2)C3=CC(=C(C=C3)O)OC)O 314.29 unknown https://doi.org/10.1016/0031-9422(95)00277-E
> Phenylpropanoids and polyketides / Kavalactones
2H-Pyran-2-one, 4-methoxy-6-(2-phenylethyl)- 160673 Click to see COC1=CC(=O)OC(=C1)CCC2=CC=CC=C2 230.26 unknown via CMAUP database
Demethoxyyangonin 5273621 Click to see COC1=CC(=O)OC(=C1)C=CC2=CC=CC=C2 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
4,2',4'-Trihydroxy-6'-methoxydihydrochalcone 42607705 Click to see COC1=CC(=CC(=C1C(=O)CCC2=CC=C(C=C2)O)O)O 288.29 unknown via CMAUP database
Phloretin 4788 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2O)O)O)O 274.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
(E)-1-[(1R,4S,13R)-9-hydroxy-1,5,5-trimethyl-6,15-dioxatetracyclo[9.3.1.04,13.07,12]pentadeca-7,9,11-trien-8-yl]-3-phenylprop-2-en-1-one 101306880 Click to see CC1(C2CCC3(CC2C4=C(O3)C=C(C(=C4O1)C(=O)C=CC5=CC=CC=C5)O)C)C 390.50 unknown via CMAUP database
2',4-Dihydroxy-4',6'-dimethoxychalcone 6293081 Click to see COC1=CC(=C(C(=C1)OC)C(=O)C=CC2=CC=C(C=C2)O)O 300.30 unknown via CMAUP database
Cardamonin 641785 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=CC=C2)O)O 270.28 unknown via CMAUP database
CID 460718 460718 Click to see C1=CC=C(C=C1)C=CC(=O)C2=C(C=C(C=C2O)O)O 256.25 unknown via CMAUP database
Helichrysetin 6253344 Click to see COC1=CC(=CC(=C1C(=O)C=CC2=CC=C(C=C2)O)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
2',4'-Dihydroxy-3'-[(2E)-3,7-dimethyl-2,6-octadienyl]-6'-methoxychalcone 23656471 Click to see CC(=CCCC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=CC=C2)O)C)C 406.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
2,4-Dihydroxy-6-phenethylbenzoic acid (2E)-3,7-dimethyl-2,6-octadienyl ester 23656469 Click to see CC(=CCCC(=CCOC(=O)C1=C(C=C(C=C1O)O)CCC2=CC=CC=C2)C)C 394.50 unknown via CMAUP database

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