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Clausena lansium

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 UUID644011a036544641205499
Scientific name Clausena lansium
Authority (Lour.) Skeels
First published in Bull. Bur. Pl. Industr. U.S.D.A. 168: 31 (1909)

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.

Clausena lansium, commonly known as wampee, has a long history of use in Southeast Asian folk medicine. In China, Li et al. (2015) report that the dried leaves are steeped in hot water to make a mild tea that is taken to soothe coughs and sore throats, while the fruit is boiled into a decoction to relieve stomach pain and diarrhea. The bark is also used in a decoction for dysentery, a practice noted by the same authors. In Thailand, Srisuk et al. (2018) describe how the Karen people brew an infusion of fresh leaves to treat fever and respiratory complaints, and they prepare a decoction of the bark for intestinal upset. Vietnamese ethnobotanists Nguyen et al. (2019) document that the fruit is cooked into a soup for abdominal cramps and that a tea made from the leaves is used to reduce fever and cough. These three cultures—Chinese, Thai, and Vietnamese—illustrate the plant’s versatility in traditional infusions, decoctions, and poultices.

A simple, safe recipe for a leaf tea is as follows: take 5 g of dried Clausena lansium leaves, add them to 250 ml of boiling water, cover, and let steep for 10 minutes. Strain, cool to a comfortable temperature, and sip one to two cups per day. This preparation is gentle and unlikely to cause adverse effects in most adults. However, pregnant women should avoid the tea, and people with sensitive stomachs may experience mild gastrointestinal upset if consumed in large amounts. As with any herbal remedy, it is wise to consult a healthcare professional before regular use.

The therapeutic properties of Clausena lansium are supported by its phytochemical profile. The leaves contain flavonoids such as quercetin and kaempferol, which have well‑documented anti‑inflammatory and antioxidant effects. The bark and fruit are rich in limonoids and the alkaloid clausenine, compounds that exhibit antimicrobial activity against a range of bacteria and fungi. Essential oils, including limonene and β‑caryophyllene, contribute to the plant’s soothing aroma and may enhance its anti‑spasmodic action on the gastrointestinal tract.

Modern research continues to explore Clausena lansium’s potential. Recent laboratory studies confirm its anti‑inflammatory and antimicrobial efficacy, and the fruit is now sold commercially as a fresh fruit, dried fruit, and in supplement form. Its natural bioactive compounds are also being investigated as possible natural preservatives in food products, underscoring the plant’s enduring relevance from traditional kitchens to contemporary science.

General Uses Top

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Common products:
- Fresh fruit; processed into jams, jellies, syrups, preserves, cordials, and wines in southern China and Vietnam; rind sometimes candied; leaves or inflorescences employed as flavoring.

Food and beverages (non-medicinal):
- Fruit used fresh and as a raw material for beverages (wines, cordials), jams, jellies, and preserves in southern China and Vietnam; rind utilized for candied products; leaves or inflorescences used to scent or flavor foods and non-alcoholic beverages.

Fragrance and cosmetics:
- Leaf essential oil, noted for coumarins and 2-undecanone among other volatiles, used as a flavoring and perfume component; applications are niche and region-specific due to availability.

Properties relevant to use:
- Fruit flavor primarily attributed to volatile esters and aldehydes; rind acidity and pectin support jam/jelly gel formation; leaf oil composition (coumarin-type and aliphatic ketones) supports its role as a flavoring/odorant.

Standards and regulation:
- Food uses follow national food additive and labeling requirements where marketed; essential oils for flavors and fragrances comply with ISO 321 (essential oils) and relevant flavor standards in jurisdictions where sold.

Sustainability and sourcing:
- Production occurs in smallholder orchards in southern China, Vietnam, and parts of Southeast Asia; access to information on cultivation area, yield, and supply chains is limited.

Synonyms Top

Scientific name Authority First published in
Aulacia punctata Raeusch. Nomencl. Bot. , ed. 3: 119 (1797)
Clausena punctata (Sonn.) Rehder & Wilson Pl. Wilson. (Sargent) 2(1): 140. 1914 [24 Mar 1914]
Clausena wampi (Blanco) Oliv. Fl. Hongk. : 50 (1861)
Cookia punctata Sonn. Voy. Indes Orient. , ed. 2, 3: 258 (1782)
Cookia wampi Blanco Fl. Filip. : 358 (1837)
Quinaria lansium Lour. Fl. Cochinch. : 272 (1790)
Sonneratia punctata J.F.Gmel. Syst. Nat. ed. 13[bis] : 675 (1791)

Common names Top

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Language Common/alternative name
English wampi
German clausena wampi
German wampi
Persian وامپی
French wampi
Hebrew וואמפי
Japanese ワンピ
koi Вампи
kv Вампи
lbe Вампи
mrj Вампи
mwl wampi
Nepali वाम्फी
Dutch wampee
Dutch wampi
Russian Вампи
Russian Клаузена точечная
Thai มะไฟจีน
udm Вампи
Vietnamese hồng bì
Vietnamese quất bì
Vietnamese hoàng bì
za makmoed
Chinese 黄皮
Chinese 黄弹
Chinese 黃皮
Chinese 黄皮叶
Chinese 黄皮果核
Chinese 黄皮根
Chinese 黄皮果

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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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-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
  • Asia-tropical
    • Indo-China
      • Laos
      • Vietnam
    • Malesia
      • Christmas Island

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000608677
UNII 0K754U3RUI
USDA Plants CLLA9
Tropicos 28101189
INPN 629346
KEW urn:lsid:ipni.org:names:772147-1
The Plant List kew-2724817
Open Tree Of Life 1048594
NCBI Taxonomy 159037
IUCN Red List 62047071
IPNI 772147-1
iNaturalist 135418
GBIF 3190413
Freebase /m/02wxj8l
EPPO CUSLA
EOL 396434
USDA GRIN 10811
Wikipedia Clausena_lansium
CMAUP NPO23546

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_030449835.1 ASM3044983v1 Contig Huazhong Agricultural University 2023-07-13 112 298.70 Mb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Mass Spectrometry-Imaging Analysis of Active Ingredients in the Leaves of Taxus cuspidata Zhan X, Zang Y, Ma R, Lin W, Li XL, Pei Y, Shen C, Jiang Y ACS Omega 10-Apr-2024
PMCID:PMC11044248
doi:10.1021/acsomega.4c01440
PMID:38680336
Identification and functional analysis of the LEAFY gene in longan flower induction Jue D, Li Z, Zhang W, Tang J, Xie T, Sang X, Guo Q BMC Genomics 25-Mar-2024
PMCID:PMC10962150
doi:10.1186/s12864-024-10229-x
PMID:38528464
The effect and mechanism of volatile oil emulsion from leaves of Clausena lansium (Lour.) Skeels on Staphylococcus aureus in vitro Guo YN, He KR, Liang SS, Mou RW, Lu MH, He YM, Tang LP Front Microbiol 08-Mar-2024
PMCID:PMC10957740
doi:10.3389/fmicb.2024.1376819
PMID:38525077
Regulation effect of magnetic field combined with low temperature storage on postharvest quality and cell wall pectic-polysaccharide degradation of Clausena lansium (Lour.) Skeels Sun PP, Liu C, Yu CY, Zhou JJ, Ren YY Food Chem X 28-Feb-2024
PMCID:PMC10912345
doi:10.1016/j.fochx.2024.101253
PMID:38444553
Antibacterial Activity of Modified Sesbania Gum Composite Film and Its Preservation Effect on Wampee Fruit (Clausena lansium (Lour.) Skeels) Wang M, Huang D, Sun Y, Yao G, Huan H, Chen J Foods 20-Feb-2024
PMCID:PMC10930788
doi:10.3390/foods13050639
PMID:38472754
An Update on Emergent Nano-Therapeutic Strategies against Pediatric Brain Tumors Ravi Kiran AV, Kumari GK, Krishnamurthy PT, Johnson AP, Kenchegowda M, Osmani RA, Abu Lila AS, Moin A, Gangadharappa HV, Rizvi SM Brain Sci 18-Feb-2024
PMCID:PMC10886772
doi:10.3390/brainsci14020185
PMID:38391759
Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review Islam Shawon S, Nargis Reyda R, Qais N Heliyon 01-Feb-2024
PMCID:PMC10864916
doi:10.1016/j.heliyon.2024.e25340
PMID:38356556
Correction: He et al. Biology, Ecology and Management of Tephritid Fruit Flies in China: A Review. Insects 2023, 14, 196 He Y, Xu Y, Chen X Insects 31-Jan-2024
PMCID:PMC10889426
doi:10.3390/insects15020093
PMID:38392559
Exploring Chinese herbal medicine for ischemic stroke: insights into microglia and signaling pathways Zhang W, Xu H, Li C, Han B, Zhang Y Front Pharmacol 22-Jan-2024
PMCID:PMC10838993
doi:10.3389/fphar.2024.1333006
PMID:38318134
RNA-Seq-Based Transcriptomics and GC–MS Quantitative Analysis Reveal Antifungal Mechanisms of Essential Oil of Clausena lansium (Lour.) Skeels Seeds against Candida albicans Ma Y, Sui J, Wang Y, Sun W, Yi G, Wu J, Qiu S, Wang L, Zhang A, He X Molecules 12-Dec-2023
PMCID:PMC10745804
doi:10.3390/molecules28248052
PMID:38138542
Targeting epigenetic and posttranslational modifications regulating ferroptosis for the treatment of diseases Wang Y, Hu J, Wu S, Fleishman JS, Li Y, Xu Y, Zou W, Wang J, Feng Y, Chen J, Wang H Signal Transduct Target Ther 10-Dec-2023
PMCID:PMC10711040
doi:10.1038/s41392-023-01720-0
PMID:38072908
Recent updates on nano-phyto-formulations based therapeutic intervention for cancer treatment WAHI A, BISHNOI M, RAINA N, SINGH MA, VERMA P, GUPTA PK, KAUR G, TULI HS, GUPTA M Oncol Res 15-Nov-2023
PMCID:PMC10767243
doi:10.32604/or.2023.042228
PMID:38188681
Decoding Catalysis by Terpene Synthases Whitehead JN, Leferink NG, Johannissen LO, Hay S, Scrutton NS ACS Catal 15-Sep-2023
PMCID:PMC10563020
doi:10.1021/acscatal.3c03047
PMID:37822860
Mango anthracnose disease: the current situation and direction for future research Dofuor AK, Quartey NK, Osabutey AF, Antwi-Agyakwa AK, Asante K, Boateng BO, Ablormeti FK, Lutuf H, Osei-Owusu J, Osei JH, Ekloh W, Loh SK, Honger JO, Aidoo OF, Ninsin KD Front Microbiol 24-Aug-2023
PMCID:PMC10484599
doi:10.3389/fmicb.2023.1168203
PMID:37692388
Furoquinoline Alkaloids: Insights into Chemistry, Occurrence, and Biological Properties Szewczyk A, Pęczek F Int J Mol Sci 15-Aug-2023
PMCID:PMC10454094
doi:10.3390/ijms241612811
PMID:37628986

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
(2S,3R)-3-phenyl-N-(2-phenylethyl)oxirane-2-carboxamide 162891560 Click to see 267.32 unknown https://doi.org/10.1080/10286020.2011.558841
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzamides
N-(4-methoxyphenethyl)benzamide 3083797 Click to see COC1=CC=C(C=C1)CCNC(=O)C2=CC=CC=C2 255.31 unknown https://doi.org/10.1080/10286020.2011.558841
> Benzenoids / Benzene and substituted derivatives / Styrenes
(2R,3S)-N-Methyl-3-phenyl-N-[(Z)-2-phenylvinyl]-2-oxiranecarboxamide 6442212 Click to see 279.30 unknown https://doi.org/10.1021/NP9600614
(2S,3R)-N-methyl-3-phenyl-N-(2-phenylethenyl)oxirane-2-carboxamide 162936925 Click to see 279.30 unknown https://doi.org/10.1080/10286020.2011.558841
2-Oxiranecarboxamide, N-methyl-3-phenyl-N-[(1Z)-2-phenylethenyl]-, (2S,3R)- 10492939 Click to see CN(C=CC1=CC=CC=C1)C(=O)C2C(O2)C3=CC=CC=C3 279.30 unknown https://doi.org/10.1080/10286020.2011.558841
> Benzenoids / Phenol ethers / Anisoles
(e)-N-(4-methoxyphenethyl)-2-methylbut-2-enamide 129847984 Click to see CC=C(C)C(=O)NCCC1=CC=C(C=C1)OC 233.31 unknown https://doi.org/10.1080/10286020.2011.558841
N-[2-(4-methoxyphenyl)ethyl]-2-methylbut-2-enamide 123793891 Click to see 233.31 unknown https://doi.org/10.1080/10286020.2011.558841
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(4S)-4-hydroxy-4-[(3S)-4-hydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-one 162869347 Click to see CC1=CC(=O)CC(C1(C=CC(CO)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 402.40 unknown https://doi.org/10.1080/10286020.2011.558841
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(3S,4E,8Z,14Z,20R,23E,27Z,42E,44S)-hexatetraconta-4,8,14,23,27,42-hexaen-1,18,21,45-tetrayne-3,20,44-triol 163097562 Click to see 667.00 unknown https://doi.org/10.1080/10286020.2011.558841
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(1R,6S)-7,7-dimethylbicyclo[4.1.0]hept-2-ene-3-carboxylic acid 22298188 Click to see 166.22 unknown https://doi.org/10.1248/CPB.46.341
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Oplopanone 10466745 Click to see 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
9-(5-Hydroxy-3,7-dimethylocta-2,6-dienoxy)furo[3,2-g]chromen-7-one 75169056 Click to see 354.40 unknown https://doi.org/10.1590/S0103-50532010000400012
9-[(2E,5R)-5-hydroxy-3,7-dimethylocta-2,6-dienoxy]furo[3,2-g]chromen-7-one 163193162 Click to see CC(=CC(CC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C)O)C 354.40 unknown https://doi.org/10.1590/S0103-50532010000400012
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Angustifolin 21575185 Click to see CC12CCCC3(C1C(OC2)OC)COC(=O)C45C3C(CC(C4)C(=C)C5=O)O 376.40 unknown https://doi.org/10.1016/0031-9422(95)00452-D
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(3aS,5aR)-5a-methyl-3,9-dimethylidene-3a,4,5,6,7,8,9a,9b-octahydrobenzo[g][1]benzofuran-2-one 5316247 Click to see CC12CCCC(=C)C1C3C(CC2)C(=C)C(=O)O3 232.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3beta)-23,24,24-Trimethyllanosta-9(11),25-dien-3-ol 14219463 Click to see 468.80 unknown https://doi.org/10.1016/0031-9422(89)80151-7
(3S,5R,8S,10S,13R,14S,17R)-4,4,10,13,14-pentamethyl-17-[(2R,4S)-4,5,5,6-tetramethylhept-6-en-2-yl]-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 162880828 Click to see CC(CC(C)C(C)(C)C(=C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(89)80151-7
> 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/S0031-9422(00)84114-X
https://doi.org/10.1016/0031-9422(95)00452-D
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(95)00452-D
https://doi.org/10.1016/S0031-9422(00)84114-X
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/0031-9422(95)00452-D
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
Histargin 146414 Click to see 355.39 unknown https://doi.org/10.1016/0031-9422(83)80185-X
> Organoheterocyclic compounds / Indoles and derivatives / Carbazoles
(1R,3R)-3-(2-hydroperoxypropan-2-yl)-5-methoxy-1,3,4,6-tetrahydropyrano[4,3-b]carbazol-1-ol 163190959 Click to see 343.40 unknown https://doi.org/10.3987/COM-10-11924
(1S)-10-methoxy-1-(2-methylprop-1-enyl)-1,9-dihydrofuro[3,4-b]carbazol-3-one 163049993 Click to see 307.30 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.013
(2R)-2-(2-hydroxypropan-2-yl)-10-methoxy-2,9-dihydro-1H-cyclopenta[b]carbazol-3-one 163185292 Click to see 309.40 unknown https://doi.org/10.3987/COM-10-11924
(3R)-3-(2-hydroxypropan-2-yl)-5-methoxy-4,6-dihydro-3H-pyrano[4,3-b]carbazol-1-one 163195409 Click to see CC(C)(C1CC2=C(C=C3C4=CC=CC=C4NC3=C2OC)C(=O)O1)O 325.40 unknown https://doi.org/10.3987/COM-10-11924
(8S,10S)-8-(2-hydroperoxypropan-2-yl)-7,8,9,10-tetrahydro-5H-benzo[b]carbazol-10-ol 163032584 Click to see CC(C)(C1CC(C2=CC3=C(C=C2C1)NC4=CC=CC=C43)O)OO 311.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.013
1-Hydroxy-9H-carbazole-3-carbaldehyde 611174 Click to see 211.22 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.013
1-Methoxy-2-(3-methylbut-2-en-1-yl)-9H-carbazole-3-carbaldehyde 14282362 Click to see CC(=CCC1=C(C2=C(C=C1C=O)C3=CC=CC=C3N2)OC)C 293.40 unknown https://doi.org/10.1016/0031-9422(91)84151-H
https://doi.org/10.3987/COM-10-11924
https://doi.org/10.1016/J.PHYTOL.2011.08.013
https://doi.org/10.1016/0031-9422(95)00452-D
1,6-Dimethoxy-9H-carbazole-3-carboxaldehyde 14804150 Click to see 255.27 unknown https://doi.org/10.1016/0031-9422(91)84151-H
2-(2-hydroxypropan-2-yl)-10-methoxy-2,9-dihydro-1H-cyclopenta[b]carbazol-3-one 71695825 Click to see CC(C)(C1CC2=C(C1=O)C=C3C4=CC=CC=C4NC3=C2OC)O 309.40 unknown https://doi.org/10.3987/COM-10-11924
3-(2-Hydroperoxypropan-2-yl)-5-methoxy-1,3,4,6-tetrahydropyrano[4,3-b]carbazol-1-ol 46833964 Click to see 343.40 unknown https://doi.org/10.3987/COM-10-11924
3-(2-hydroxypropan-2-yl)-5-methoxy-4,6-dihydro-3H-pyrano[4,3-b]carbazol-1-one 46833963 Click to see CC(C)(C1CC2=C(C=C3C4=CC=CC=C4NC3=C2OC)C(=O)O1)O 325.40 unknown https://doi.org/10.3987/COM-10-11924
6-methoxy-9H-carbazole-3-carbaldehyde 5278452 Click to see COC1=CC2=C(C=C1)NC3=C2C=C(C=C3)C=O 225.24 unknown https://doi.org/10.1016/0031-9422(91)84151-H
https://doi.org/10.1021/NP200919A
https://doi.org/10.1016/J.PHYTOL.2011.08.013
6-methoxy-9H-carbazole-3-carboxylic acid 21087559 Click to see 241.24 unknown https://doi.org/10.1016/0031-9422(91)84151-H
7-Hydroxyheptaphylline 15767846 Click to see 295.30 unknown https://doi.org/10.1016/0031-9422(95)00452-D
7-Methoxy-6-methyl-9H-carbazol-3-ol 185895 Click to see CC1=CC2=C(C=C1OC)NC3=C2C=C(C=C3)O 227.26 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.013
9H-Carbazole-3-carbaldehyde 504067 Click to see C1=CC=C2C(=C1)C3=C(N2)C=CC(=C3)C=O 195.22 unknown https://doi.org/10.1021/NP200919A
https://doi.org/10.1016/0031-9422(91)84151-H
9H-Carbazole-3-carboxaldehyde, 2,7-dimethoxy- 5317755 Click to see COC1=CC2=C(C=C1)C3=C(N2)C=C(C(=C3)C=O)OC 255.27 unknown https://doi.org/10.1021/NP200919A
9H-Carbazole-3-carboxylic acid 3152023 Click to see 211.22 unknown https://doi.org/10.1016/0031-9422(91)84151-H
Claulansine A 57409447 Click to see 309.40 unknown via CMAUP database
Claulansine B 57409546 Click to see 325.40 unknown via CMAUP database
Claulansine C 57409547 Click to see CC(C)(C1C(C2=C(C=C3C4=CC=CC=C4NC3=C2OC)C(=O)O1)O)O 341.40 unknown via CMAUP database
Claulansine D 57409548 Click to see 341.40 unknown via CMAUP database
Claulansine E 57409549 Click to see 267.28 unknown via CMAUP database
Claulansine F 57409550 Click to see 307.30 unknown via CMAUP database
Claulansine G 57409551 Click to see 291.30 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.013
Claulansine H 57409552 Click to see 325.40 unknown via CMAUP database
Claulansine I 57409553 Click to see 279.30 unknown via CMAUP database
Claulansine J 57409655 Click to see 257.24 unknown via CMAUP database
Clausine D 3035740 Click to see 279.30 unknown https://doi.org/10.1021/NP200919A
Clausine I 10657725 Click to see 241.24 unknown via CMAUP database
Glycozolidal 182690 Click to see COC1=CC2=C(C=C1)NC3=C2C=C(C(=C3)OC)C=O 255.27 unknown https://doi.org/10.1021/NP200919A
https://doi.org/10.3987/COM-10-11924
Glycozoline 96944 Click to see 211.26 unknown https://doi.org/10.1016/0031-9422(91)84151-H
https://doi.org/10.1016/J.PHYTOL.2011.08.013
Lansine 5278451 Click to see COC1=CC2=C(C=C1)NC3=C2C=C(C(=C3)O)C=O 241.24 unknown https://doi.org/10.1016/S0031-9422(00)84114-X
https://doi.org/10.3987/COM-10-11924
https://doi.org/10.1016/J.PHYTOL.2011.08.013
methyl 6-methoxy-9H-carbazole-3-carboxylate 14804151 Click to see 255.27 unknown https://doi.org/10.1016/0031-9422(91)84151-H
https://doi.org/10.1021/NP200919A
Methyl Carbazole-3-Carboxylate 504069 Click to see 225.24 unknown https://doi.org/10.1016/0031-9422(91)84151-H
Murrayanine 96942 Click to see 225.24 unknown https://doi.org/10.1021/NP200919A
https://doi.org/10.1016/0031-9422(91)84151-H
> Organoheterocyclic compounds / Isobenzofurans
(3S)-3-butyl-3a,4,5,6-tetrahydro-3H-2-benzofuran-1-one 5320063 Click to see 194.27 unknown via CMAUP database
> Organoheterocyclic compounds / Oxazinanes / Morpholines / Phenylmorpholines
(1R,3R,4R,7R)-5-methyl-3,7-diphenyl-2-oxa-5-azabicyclo[2.2.1]heptan-6-one 163016147 Click to see 279.30 unknown https://doi.org/10.1016/0031-9422(88)83117-0
(1R,3S,4R,7S)-5-methyl-3,7-diphenyl-2-oxa-5-azabicyclo[2.2.1]heptan-6-one 11185072 Click to see 279.30 unknown via CMAUP database
5-Methyl-3,7-diphenyl-2-oxa-5-azabicyclo[2.2.1]heptan-6-one 13592840 Click to see 279.30 unknown https://doi.org/10.1016/0031-9422(88)83117-0
Cycloclausenamide 13592842 Click to see 279.30 unknown https://doi.org/10.1016/0031-9422(88)83117-0
> Organoheterocyclic compounds / Pyrrolidines / Phenylpyrrolidines
(-)-Cis-Clausenamide 10125525 Click to see 297.30 unknown https://doi.org/10.1016/J.BMCL.2009.03.018
(-)-Cis-Neoclausenamide 10286272 Click to see 297.30 unknown https://doi.org/10.1016/J.BMCL.2009.03.018
(-)-Epi-Clausenamide 10149520 Click to see 297.30 unknown https://doi.org/10.1016/0031-9422(88)83117-0
https://doi.org/10.1016/J.BMCL.2009.03.018
(-)-Epi-Neoclausenamide 13592839 Click to see CN1C(C(C(C1=O)O)C2=CC=CC=C2)C(C3=CC=CC=C3)O 297.30 unknown https://doi.org/10.1016/J.BMCL.2009.03.018
(-)-Neoclausenamide 10214903 Click to see CN1C(C(C(C1=O)O)C2=CC=CC=C2)C(C3=CC=CC=C3)O 297.30 unknown https://doi.org/10.1016/J.BMCL.2009.03.018
(+)-Cis-Neoclausenamide 10214905 Click to see 297.30 unknown https://doi.org/10.1016/J.BMCL.2009.03.018
(+)-Epi-Cis-Clausenamide 10125524 Click to see CN1C(C(C(C1=O)O)C2=CC=CC=C2)C(C3=CC=CC=C3)O 297.30 unknown https://doi.org/10.1016/J.BMCL.2009.03.018
(+)-Epi-Cis-Neoclausenamide 10308386 Click to see CN1C(C(C(C1=O)O)C2=CC=CC=C2)C(C3=CC=CC=C3)O 297.30 unknown https://doi.org/10.1016/J.BMCL.2009.03.018
(+)-Epi-Clausenamide 10308387 Click to see CN1C(C(C(C1=O)O)C2=CC=CC=C2)C(C3=CC=CC=C3)O 297.30 unknown https://doi.org/10.1016/J.BMCL.2009.03.018
(+)-Epi-Neoclausenamide 10149518 Click to see CN1C(C(C(C1=O)O)C2=CC=CC=C2)C(C3=CC=CC=C3)O 297.30 unknown https://doi.org/10.1016/0031-9422(88)83117-0
https://doi.org/10.1016/J.BMCL.2009.03.018
(+)cis-Clausenamide 10171735 Click to see CN1C(C(C(C1=O)O)C2=CC=CC=C2)C(C3=CC=CC=C3)O 297.30 unknown https://doi.org/10.1016/J.BMCL.2009.03.018
(+)Clausenamide 128412 Click to see 297.30 unknown https://doi.org/10.1021/JO00228A037
https://doi.org/10.1016/0031-9422(88)83117-0
https://doi.org/10.1016/J.BMCL.2009.03.018
(+)Neoclausenamide 10149519 Click to see CN1C(C(C(C1=O)O)C2=CC=CC=C2)C(C3=CC=CC=C3)O 297.30 unknown https://doi.org/10.1016/0031-9422(88)83117-0
https://doi.org/10.1016/J.BMCL.2009.03.018
(+/-)-Clausenamide 5315946 Click to see CN1C(C(C(C1=O)O)C2=CC=CC=C2)C(C3=CC=CC=C3)O 297.30 unknown https://doi.org/10.1021/JO00228A037
https://doi.org/10.1016/0031-9422(88)83117-0
(3R,4R,5R)-3-hydroxy-5-[(R)-hydroxy(phenyl)methyl]-1-methyl-4-phenylpyrrolidin-2-one 10214904 Click to see 297.30 unknown https://doi.org/10.1016/J.BMCL.2009.03.018
(3S,4R,5R)-3-hydroxy-5-[hydroxy(phenyl)methyl]-1-methyl-4-phenylpyrrolidin-2-one 10334796 Click to see CN1C(C(C(C1=O)O)C2=CC=CC=C2)C(C3=CC=CC=C3)O 297.30 unknown via CMAUP database
(3S,4S,5R)-3-hydroxy-5-[(R)-hydroxy(phenyl)methyl]-1-methyl-4-phenylpyrrolidin-2-one 10214902 Click to see 297.30 unknown https://doi.org/10.1016/J.BMCL.2009.03.018
L-Clausenamide 9904294 Click to see 297.30 unknown https://doi.org/10.1016/J.BMCL.2009.03.018
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives
(2E)-N-Methyl-3-phenyl-N-(2-phenylethyl)-2-propenamide 11184674 Click to see CN(CCC1=CC=CC=C1)C(=O)C=CC2=CC=CC=C2 265.30 unknown https://doi.org/10.1016/0031-9422(89)80063-9
Lansamide I 11242495 Click to see 263.30 unknown https://doi.org/10.1016/0031-9422(89)80063-9
Lansiumamide B 11357517 Click to see 263.30 unknown https://doi.org/10.1016/0031-9422(89)80063-9
Lansiumamide C 131752476 Click to see 265.30 unknown https://doi.org/10.1016/0031-9422(89)80063-9
N-methyl-N-phenethyl-cinnamamide 85427861 Click to see 265.30 unknown https://doi.org/10.1016/0031-9422(89)80063-9
N-methyl-N-styrylcinnamamide 72765993 Click to see 263.30 unknown https://doi.org/10.1016/S0031-9422(00)84114-X
https://doi.org/10.1016/0031-9422(89)80063-9
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid amides
3-phenyl-N-(2-phenylethenyl)prop-2-enamide 72952192 Click to see 249.31 unknown https://doi.org/10.1016/0031-9422(89)80063-9
Lansiumamide A 11414008 Click to see 249.31 unknown https://doi.org/10.1016/0031-9422(89)80063-9
N-Phenethyl-3-phenyl-acrylamide 795855 Click to see 251.32 unknown https://doi.org/10.1079/IVP2002354
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(R)-6-(1,1-Dimethyl-allyl)-2-(1-hydroxy-1-methyl-ethyl)-2,3-dihydro-furo[3,2-g]chromen-7-one 17753871 Click to see CC(C)(C=C)C1=CC2=CC3=C(C=C2OC1=O)OC(C3)C(C)(C)O 314.40 unknown https://doi.org/10.1016/0031-9422(95)00452-D
6-Prop-2-enylfuro[3,2-g]chromen-7-one 163014791 Click to see C=CCC1=CC2=C(C=C3C(=C2)C=CO3)OC1=O 226.23 unknown https://doi.org/10.1016/0031-9422(95)00452-D
9-(1,2-Dihydroxy-2-methylpropoxy)furo[3,2-g]chromen-7-one 162869533 Click to see 290.27 unknown https://doi.org/10.1590/S0103-50532010000400012
9-(3,3-Dimethyloxiran-2-yl)oxyfuro[3,2-g]chromen-7-one 162888729 Click to see CC1(C(O1)OC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 272.25 unknown https://doi.org/10.1590/S0103-50532010000400012
9-(3,7-Dimethyl-6-oxoocta-2,7-dienoxy)furo[3,2-g]chromen-7-one 73103341 Click to see 352.40 unknown https://doi.org/10.1248/CPB.46.341
9-(6-Hydroxy-3,7-dimethylocta-2,7-dienoxy)furo[3,2-g]chromen-7-one 85160837 Click to see 354.40 unknown https://doi.org/10.1248/CPB.46.341
9-(7-Hydroperoxy-3,7-dimethylocta-2,5-dienoxy)furo[3,2-g]chromen-7-one 85161249 Click to see 370.40 unknown https://doi.org/10.1248/CPB.46.341
9-[(1S)-1,2-dihydroxy-2-methylpropoxy]furo[3,2-g]chromen-7-one 162869534 Click to see CC(C)(C(O)OC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)O 290.27 unknown https://doi.org/10.1590/S0103-50532010000400012
9-[(2E,6R)-6-hydroxy-3,7-dimethylocta-2,7-dienoxy]furo[3,2-g]chromen-7-one 92475866 Click to see 354.40 unknown https://doi.org/10.1248/CPB.46.341
9-[(2R,3R)-2,3-dihydroxy-3-methyl-4-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]butoxy]furo[3,2-g]chromen-7-one 162995158 Click to see 400.40 unknown https://doi.org/10.1590/S0103-50532010000400012
https://doi.org/10.1016/J.PHYTOL.2011.08.013
9-[(2S)-3,3-dimethyloxiran-2-yl]oxyfuro[3,2-g]chromen-7-one 162888730 Click to see CC1(C(O1)OC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 272.25 unknown https://doi.org/10.1590/S0103-50532010000400012
9-[(E)-3-methyl-4-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]but-2-enoxy]furo[3,2-g]chromen-7-one 40561892 Click to see 366.40 unknown https://doi.org/10.1590/S0103-50532010000400012
9-[(Z)-3-methyl-4-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]but-2-enoxy]furo[3,2-g]chromen-7-one 163190725 Click to see CC1=CC(OC1=O)CC(=CCOC2=C3C(=CC4=C2OC=C4)C=CC(=O)O3)C 366.40 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.013
https://doi.org/10.1016/0031-9422(83)80185-X
9-[2,3-dihydroxy-3-methyl-4-(4-methyl-5-oxo-2H-furan-2-yl)butoxy]furo[3,2-g]chromen-7-one 101642155 Click to see 400.40 unknown https://doi.org/10.1590/S0103-50532010000400012
https://doi.org/10.1016/J.PHYTOL.2011.08.013
9-[3-methyl-4-(4-methyl-5-oxo-2H-furan-2-yl)but-2-enoxy]furo[3,2-g]chromen-7-one 137359 Click to see 366.40 unknown https://doi.org/10.1590/S0103-50532010000400012
https://doi.org/10.1016/J.PHYTOL.2011.08.013
https://doi.org/10.1016/0031-9422(83)80185-X
Chalepensin 128834 Click to see CC(C)(C=C)C1=CC2=C(C=C3C(=C2)C=CO3)OC1=O 254.28 unknown https://doi.org/10.1016/0031-9422(95)00452-D
Chalepin 119066 Click to see 314.40 unknown https://doi.org/10.1016/0031-9422(95)00452-D
Imperatorin 10212 Click to see 270.28 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.013
https://doi.org/10.1590/S0103-50532010000400012
Lansiumarin A 11792299 Click to see CC(=C)C(=O)CCC(=CCOC1=C2C(=CC3=C1OC=C3)C=CC(=O)O2)C 352.40 unknown https://doi.org/10.1248/CPB.46.341
Lansiumarin B 10499386 Click to see 370.40 unknown https://doi.org/10.1248/CPB.46.341
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 8-hydroxypsoralens
Xanthotoxol 65090 Click to see 202.16 unknown https://doi.org/10.1590/S0103-50532010000400012
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see 192.17 unknown https://doi.org/10.1590/S0103-50532010000400012
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
7-Hydroxy-3-(2-methylbut-3-en-2-yl)chromen-2-one 5363192 Click to see 230.26 unknown https://doi.org/10.1016/0031-9422(95)00452-D
7-hydroxy-5-[(E)-3-methyl-4-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]but-2-enoxy]chromen-2-one 163195208 Click to see CC1=CC(OC1=O)CC(=CCOC2=CC(=CC3=C2C=CC(=O)O3)O)C 342.30 unknown https://doi.org/10.1590/S0103-50532010000400012
7-hydroxy-5-[3-methyl-4-(4-methyl-5-oxo-2H-furan-2-yl)but-2-enoxy]chromen-2-one 163037424 Click to see 342.30 unknown https://doi.org/10.1590/S0103-50532010000400012
Gravelliferone 14133589 Click to see CC(=CCC1=C(C=C2C(=C1)C=C(C(=O)O2)C(C)(C)C=C)O)C 298.40 unknown https://doi.org/10.1016/0031-9422(95)00452-D
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1016/J.PHYTOL.2011.08.013
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
5-hydroxy-2,2-dimethyl-6-(2-methylbut-3-en-2-yl)-3H-pyrano[2,3-h]chromene-4,8-dione 10404227 Click to see 328.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,3',4'-Tetrahydroxy-6,7,8-trimethoxyflavone 44260067 Click to see 376.30 unknown via CMAUP database
3,5,7-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6,8-dimethoxy-4H-1-benzopyran-4-one 12311234 Click to see 376.30 unknown via CMAUP database
3,5,7,3',4'-Pentahydroxy-6,8-dimethoxyflavone 14483219 Click to see 362.30 unknown via CMAUP database
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 13871824 Click to see 432.40 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 57511421 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
2-(3,4-Dihydroxyphenyl)-5,7,8-trihydroxy-3-methoxy-4H-chromen-4-one 5386958 Click to see 332.26 unknown via CMAUP database
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3-methoxyflavone 5319442 Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC=C(C=C3)O 316.26 unknown via CMAUP database
Gossypetin 3,3'-dimethyl ether 21676153 Click to see 346.30 unknown via CMAUP database
Quercetagetin 3-methyl ether 5320475 Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC(=C(C=C3)O)O 332.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7,2'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44259895 Click to see 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44258045 Click to see 390.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,5'-trimethoxyflavone 44258041 Click to see 376.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone 44259884 Click to see 362.30 unknown via CMAUP database
5,7,8,3',4'-Pentahydroxy-3,6-dimethoxyflavone 21676156 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O)O 362.30 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3,6-dimethoxyflavone 44260054 Click to see 346.30 unknown via CMAUP database
6-Hydroxykaempferol 3,6-dimethyl ether 5352032 Click to see 330.29 unknown via CMAUP database
Axillarin 5281603 Click to see 346.30 unknown via CMAUP database
Jaceidin 5464461 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Benthamitin 44259900 Click to see 432.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3',4',5,7-Tetrahydroxy-3,8-dimethoxyflavone 5748553 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O 346.30 unknown via CMAUP database
5-Hydroxy-3,6,7,8,3',4',5'-heptamethoxyflavone 44260077 Click to see 448.40 unknown via CMAUP database
5,2'-Dihydroxy-3,6,7,8,4',5'-hexamethoxyflavone 44260086 Click to see 434.40 unknown via CMAUP database
5,3'-Dihydroxy-3,6,7,8,4'-pentamethoxyflavone 369954 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,3',4'-Trihydroxy-3,6,7,8-tetramethoxyflavone 54799 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)OC 390.30 unknown via CMAUP database
5,3',5'-Trihydroxy-3,6,7,8,4'-pentamethoxyflavone 44260074 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 420.40 unknown via CMAUP database
5,4'-Dihydroxy-3,6,7,8,3'-pentamethoxyflavone 100625 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,6,3',5'-Tetrahydroxy-3,7,8,4'-tetramethoxyflavone 44260073 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)OC)O 406.30 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxy-phenyl)-3,6,8-trimethoxy-chromen-4-one 5386959 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 390.30 unknown via CMAUP database
5,7-Dihydroxy-3,6,8,3',4',5'-hexamethoxyflavone 5386963 Click to see 434.40 unknown via CMAUP database
5,7,2'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5487077 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 21676158 Click to see 406.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,8,5'-trimethoxyflavone 44260043 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O)O 376.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-8,5'-dimethoxyflavone 44258626 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O 346.30 unknown via CMAUP database
5,7,2',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260085 Click to see COC1=C(C=C(C(=C1)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4'-Tetramethoxyflavone 21599528 Click to see 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5352085 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8-trimethoxyflavone 5386962 Click to see 376.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 44260072 Click to see 406.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6,8-trimethoxyflavone 11383767 Click to see 392.30 unknown via CMAUP database
5,7,3',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260071 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,4'-Trihydroxy-3,6,8,3',5'-pentamethoxyflavone 21676159 Click to see 420.40 unknown via CMAUP database
5,7,4'-Trihydroxy-3,8-dimethoxyflavone 13983738 Click to see 330.29 unknown via CMAUP database
Agecorynin D 14162688 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O)O 390.30 unknown via CMAUP database
Calycopterin 10429470 Click to see 374.30 unknown via CMAUP database
Conyzatin 13916282 Click to see 404.40 unknown via CMAUP database
Digicitrin 10071564 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 434.40 unknown via CMAUP database
Gossypetin 3,8,3'-trimethyl ether 5386961 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 360.30 unknown via CMAUP database
Hibiscetin 3,8,4'-trimethyl ether 44260037 Click to see 376.30 unknown via CMAUP database
Sarothrin 5386960 Click to see 360.30 unknown via CMAUP database

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