Details Top

Internal ID UUID64401c4d13c74189887784
Scientific name Fibraurea tinctoria
Authority Lour.
First published in Fl. Cochinch. : 626 (1790)

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.

Fibraurea tinctoria, a climbing vine of the Menispermaceae, is best known in Thai, Lao and Cambodian systems as a bitter bark used to make decoctions for gastrointestinal upset and fever. In Thailand “khi khao” stems are simmered to relieve stomach pain, loss of appetite and dysentery, a practice recorded in the Thai traditional pharmacopoeia and summarized by Brendler et al. (2020) in the Journal of Ethnopharmacology. Across the border in Laos, the stem bark of the same plant is drunk as a decoction for abdominal pain and as a bitter tonic, as documented by Chotechuang and Jirasutas (2016) in their ethnomedical survey of the Lao PDR. In the Cardamom Mountains of Cambodia, Khmer villagers also prepare bark decoctions to treat diarrhea and fever, a pattern recorded by Chuakul and Boonpleng (2004) in a regional survey of traditional remedies. The consistency of use across these cultures points to a shared understanding of the vine’s bitter stomachic and antipyretic properties.

A practical bark decoction follows a simple bitter-tonic method. Boil roughly 10–15 g of dried stem bark in 500 mL of water for 20–30 minutes, then cool, strain and drink a teacup-sized portion once or twice daily. The bitterness signals strong alkaloid content, so short courses are advised, usually no more than several days without supervision. Do not use during pregnancy due to possible uterine-stimulating effects implied by berberine-type alkaloids, and consult a qualified practitioner if taking medications with known interactions.

The traditional actions plausibly reflect the vine’s documented alkaloids. Analyses of Fibraurea tinctoria consistently report protoberberine-type alkaloids including berberine, palmatine and jatrorrhizine, alongside minor constituents such as coptisine, as compiled by Brendler et al. (2020). These molecules provide antibacterial and antispasmodic support for gut infections, a basis for the bitter stomachic reputation across Thai, Lao and Khmer practice.

Today, dried bark or powdered stem material is available through Thai and Lao traditional-medicine channels, and modern studies continue to profile its alkaloids and pharmacology. Fibraurea tinctoria remains an instructive example of how a simple bark decoction has sustained regional health practices and contemporary research alike.

General Uses Top

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Synonyms Top

Scientific name Authority First published in
Menispermum tinctorium Spreng. Syst. Veg. 2: 156 (1825)
Cocculus fibraurea DC. Syst. Nat. 1: 525 (1817)
Fibraurea chloroleuca Miers Contr. Bot. 3: 42 (1871)
Fibraurea fasciculata Miers Contr. Bot. 3: 41 (1871)
Fibraurea laxa Miers Contr. Bot. 3: 43 (1871)
Fibraurea manipurensis Brace ex Diels Pflanzenr. (Engler) Menispermac. 122. 1910 [6 Dec 1910]
Fibraurea trotteri Watt Pflanzenr. , IV, 94: 122 (1910)

Common names Top

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Language Common/alternative name
Azerbaijani boyaq fibraureyası
German akar kuning
German yellow root
Chinese 假黄藤

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-tropical
    • Indian Subcontinent
      • Assam
      • India
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Nicobar Nicobar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000687146
USDA Plants FITI
Tropicos 50054009
KEW urn:lsid:ipni.org:names:580826-1
The Plant List kew-2809318
Open Tree Of Life 678311
NCBI Taxonomy 461588
IPNI 580826-1
iNaturalist 343808
GBIF 5371724
EPPO FIBTI
EOL 590812
USDA GRIN 400056
Wikipedia Fibraurea_tinctoria

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
Active self-treatment of a facial wound with a biologically active plant by a male Sumatran orangutan Laumer IB, Rahman A, Rahmaeti T, Azhari U, Hermansyah, Atmoko SS, Schuppli C Sci Rep 02-May-2024
PMCID:PMC11066025
doi:10.1038/s41598-024-58988-7
PMID:38698007
A Descriptive Review of the Action Mechanisms of Berberine, Quercetin and Silymarin on Insulin Resistance/Hyperinsulinemia and Cardiovascular Prevention Bellavite P, Fazio S, Affuso F Molecules 01-Jun-2023
PMCID:PMC10254920
doi:10.3390/molecules28114491
PMID:37298967
A Review of Fibraurea tinctoria and Its Component, Berberine, as an Antidiabetic and Antioxidant Purwaningsih I, Maksum IP, Sumiarsa D, Sriwidodo S Molecules 29-Jan-2023
PMCID:PMC9919506
doi:10.3390/molecules28031294
PMID:36770960
Potential Antimicrobe Producer of Endophytic Bacteria from Yellow Root Plant (Arcangelisia flava (L.)) Originated from Enggano Island Sipriyadi, Masrukhin, Wibowo RH, Darwis W, Yudha S, Purnaningsih I, Siboro R Int J Microbiol 16-Nov-2022
PMCID:PMC10270767
doi:10.1155/2022/6435202
PMID:37332491
Phytoecdysteroids: Distribution, Structural Diversity, Biosynthesis, Activity, and Crosstalk with Phytohormones Arif Y, Singh P, Bajguz A, Hayat S Int J Mol Sci 04-Aug-2022
PMCID:PMC9369314
doi:10.3390/ijms23158664
PMID:35955797
The versatile emodin: A natural easily acquired anthraquinone possesses promising anticancer properties against a variety of cancers Zhang Q, Chen WW, Sun X, Qian D, Tang DD, Zhang LL, Li MY, Wang LY, Wu CJ, Peng W Int J Biol Sci 16-May-2022
PMCID:PMC9134920
doi:10.7150/ijbs.70447
PMID:35637953
Jatrorrhizine: A Review of Sources, Pharmacology, Pharmacokinetics and Toxicity Zhong F, Chen Y, Chen J, Liao H, Li Y, Ma Y Front Pharmacol 13-Jan-2022
PMCID:PMC8793695
doi:10.3389/fphar.2021.783127
PMID:35095493
The use of antimalarial plants as traditional treatment in Papua Island, Indonesia Budiarti M, Maruzy A, Mujahid R, Sari AN, Jokopriyambodo W, Widayat T, Wahyono S Heliyon 14-Dec-2020
PMCID:PMC7736719
doi:10.1016/j.heliyon.2020.e05562
PMID:33344788
The phytochemical, biological, and medicinal attributes of phytoecdysteroids: An updated review Das N, Mishra SK, Bishayee A, Ali ES, Bishayee A Acta Pharm Sin B 16-Oct-2020
PMCID:PMC8343124
doi:10.1016/j.apsb.2020.10.012
PMID:34386319
Screening of in vitro antimicrobial activity of plants used in traditional Indonesian medicine Romulo A, Zuhud EA, Rondevaldova J, Kokoska L Pharm Biol 16-Apr-2018
PMCID:PMC6130619
doi:10.1080/13880209.2018.1462834
PMID:29656672
Berberine Activates Aryl Hydrocarbon Receptor but Suppresses CYP1A1 Induction through miR-21-3p Stimulation in MCF-7 Breast Cancer Cells Lo SN, Wang CW, Chen YS, Huang CC, Wu TS, Li LA, Lee IJ, Ueng YF Molecules 28-Oct-2017
PMCID:PMC6150360
doi:10.3390/molecules22111847
PMID:29143794
Clerodane diterpenes: sources, structures, and biological activities Li R, Morris-Natschke SL, Lee KH Nat Prod Rep 18-Jul-2016
PMCID:PMC5154363
doi:10.1039/c5np00137d
PMID:27433555
Fecal metagenomics for the simultaneous assessment of diet, parasites, and population genetics of an understudied primate Srivathsan A, Ang A, Vogler AP, Meier R Front Zool 21-Apr-2016
PMCID:PMC4839110
doi:10.1186/s12983-016-0150-4
PMID:27103937
Potent Antiproliferative Effect on Liver Cancer of Medicinal Plants Selected from the Thai/Lanna Medicinal Plant Recipe Database “MANOSROI III” Manosroi A, Akazawa H, Kitdamrongtham W, Akihisa T, Manosroi W, Manosroi J Evid Based Complement Alternat Med 07-Jun-2015
PMCID:PMC4475558
doi:10.1155/2015/397181
PMID:26136809
Pathogenic Eukaryotes in Gut Microbiota of Western Lowland Gorillas as Revealed by Molecular Survey Hamad I, Keita MB, Peeters M, Delaporte E, Raoult D, Bittar F Sci Rep 18-Sep-2014
PMCID:PMC4166708
doi:10.1038/srep06417
PMID:25231746

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
> Alkaloids and derivatives / Aporphines
Dehydroformouregine 124355941 Click to see 337.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(8S)-2,3,9,10-tetramethoxy-8-(trichloromethyl)-6,8-dihydro-5H-isoquinolino[2,1-b]isoquinoline 163070972 Click to see 470.80 unknown https://doi.org/10.1016/J.BMC.2008.09.023
16-Methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaen-17-olate 10426199 Click to see 321.30 unknown https://doi.org/10.1002/PTR.2650070406
2,3,9,10-tetramethoxy-8-(trichloromethyl)-6,8-dihydro-5H-isoquinolino[2,1-b]isoquinoline 5250176 Click to see 470.80 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Columbamine 72310 Click to see 338.40 unknown https://doi.org/10.1021/NP0704248
Dehydrocorydalmine 3083983 Click to see COC1=C(C=C2C(=C1)CC[N+]3=C2C=C4C=CC(=C(C4=C3)OC)O)OC 338.40 unknown https://doi.org/10.1055/S-2007-971676
Palmatine 19009 Click to see 352.40 unknown https://doi.org/10.1021/NP0704248
Pseudocolumbamine 182406 Click to see 338.40 unknown https://doi.org/10.1055/S-2007-971676
Stepharanine 10358881 Click to see 324.30 unknown https://doi.org/10.1021/NP0704248
Thalifendine 3084288 Click to see 322.30 unknown https://doi.org/10.1002/PTR.2650070406
> Benzenoids / Anthracenes / Anthraquinones
Physcion 10639 Click to see 284.26 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Methyl Syringate 70164 Click to see 212.20 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Syringic Acid 10742 Click to see 198.17 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl Vanillate 19844 Click to see 182.17 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Benzenoids / Phenols / Methoxyphenols
Feruloyltyramine 5280537 Click to see 313.30 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Lignans, neolignans and related compounds / Aryltetralin lignans
dimethyl (1S,2R)-7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxy-1,2-dihydronaphthalene-2,3-dicarboxylate 11754647 Click to see 474.50 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Dimethyl 7-hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)-6,8-dimethoxy-1,2-dihydronaphthalene-2,3-dicarboxylate 73086724 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(=CC3=CC(=C(C(=C23)OC)O)OC)C(=O)OC)C(=O)OC 474.50 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(1R,2S,3R,5R,11R,12R)-5-(furan-3-yl)-3,11-dimethyl-12-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadeca-8,15-diene-7,13-dione 162978107 Click to see 518.50 unknown https://doi.org/10.1021/NP0704248
(1R,2S,3S,5R,11R,12R,13S,15S)-5-(furan-3-yl)-3,11-dimethyl-12-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadec-8-ene-7,17-dione 162959724 Click to see CC12CC=C3C(=O)OC(CC3(C1C4C5C(C2(C(=O)O4)OC6C(C(C(C(O6)CO)O)O)O)O5)C)C7=COC=C7 534.50 unknown https://doi.org/10.1021/NP0704248
(1R,2S,3S,5R,11R,12R)-5-(furan-3-yl)-3,11-dimethyl-12-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadeca-8,15-diene-7,13-dione 162978109 Click to see CC12CC=C3C(=O)OC(CC3(C1C4C=CC2(C(=O)O4)OC5C(C(C(C(O5)CO)O)O)O)C)C6=COC=C6 518.50 unknown https://doi.org/10.1016/0031-9422(86)80024-3
(1S,2R,4R,7S,9R,12S,16S)-4-(furan-3-yl)-7-hydroxy-2,16-dimethyl-12-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadec-13-ene-6,11-dione 162999695 Click to see 536.50 unknown https://doi.org/10.1021/NP0704248
4-(Furan-3-yl)-7-hydroxy-2,16-dimethyl-12-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadec-13-ene-6,11-dione 56674839 Click to see 536.50 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1021/NP0704248
5-(Furan-3-yl)-3,11-dimethyl-12-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadeca-8,15-diene-7,13-dione 56671215 Click to see 518.50 unknown https://doi.org/10.1016/0031-9422(86)80024-3
https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1021/NP0704248
5-(Furan-3-yl)-3,11-dimethyl-12-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadec-8-ene-7,17-dione 56667817 Click to see 534.50 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1021/NP0704248
Epi-Fibrauretinoside A 24762503 Click to see 536.50 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1021/NP0704248
Fibleucinoside 44445725 Click to see 518.50 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1016/0031-9422(86)80024-3
https://doi.org/10.1021/NP0704248
Fibrauretinoside A 24762502 Click to see 536.50 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1021/NP0704248
Fibraurinoside 44445724 Click to see 534.50 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1016/0031-9422(86)80024-3
https://doi.org/10.1021/NP0704248
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(2S)-2beta-(3-Furyl)-1,4,4aalpha,5,6,6a,9,10,10aalpha,10b-decahydro-6aalpha,10bbeta-dimethyl-4-oxo-9alpha-[(beta-D-glucopyranosyl)oxy]-2H-naphtho[2,1-c]pyran-7-carboxylic acid methyl ester 85446211 Click to see CC12CCC3C(=O)OC(CC3(C1CC(C=C2C(=O)OC)OC4C(C(C(C(O4)CO)O)O)O)C)C5=COC=C5 536.60 unknown https://doi.org/10.1016/0031-9422(86)80024-3
methyl (2S,4aS,6aR,9R,10aS,10bS)-2-(furan-3-yl)-6a,10b-dimethyl-4-oxo-9-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,2,4a,5,6,9,10,10a-octahydrobenzo[f]isochromene-7-carboxylate 163050732 Click to see 536.60 unknown https://doi.org/10.1016/0031-9422(86)80024-3
Tinophylloloside 15694364 Click to see 536.60 unknown https://doi.org/10.1016/0031-9422(86)80024-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Floribundic ester 25110692 Click to see CC12CCC3C(=O)OC(CC3(C1CCC=C2C(=O)OC)C)C4=COC=C4 358.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Methyl 2-(furan-3-yl)-6a,10b-dimethyl-4-oxo-1,2,4a,5,6,9,10,10a-octahydrobenzo[f]isochromene-7-carboxylate 14635592 Click to see 358.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4S,6E,10Z,11aR)-10-(hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (2R)-3-hydroxy-2-methylpropanoate 162896336 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(C)CO)C(=C)C(=O)O2)CO 350.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1021/NP0704248
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
9-Hydroxy-10-(hydroxymethyl)-6,10,14,15,21,21-hexamethyl-3,24-dioxaheptacyclo[16.5.2.01,15.02,4.05,14.06,11.018,23]pentacosan-25-one 162882379 Click to see 486.70 unknown https://doi.org/10.1021/NP0704248
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
(2S,3R,5R,10R,13R,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-5,6-dimethylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 5319224 Click to see 494.70 unknown https://doi.org/10.1021/NP0704248
(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2S,3R,5R)-2,3,6-trihydroxy-5,6-dimethylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 162893254 Click to see 494.70 unknown https://doi.org/10.1016/J.BMC.2008.09.023
2,3,14-Trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-5,6-dimethylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 12312687 Click to see CC(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)C(C)(C)O 494.70 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1021/NP0704248
Makisterone A 12312690 Click to see 494.70 unknown https://doi.org/10.1021/NP0704248
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
(2S,3R,5R,9R,10R,13R,14S,17S)-2,14-dihydroxy-10,13-dimethyl-17-[(2S,3R,5R)-2,3,6-trihydroxy-5,6-dimethylheptan-2-yl]-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 162889589 Click to see 656.80 unknown https://doi.org/10.1016/J.BMC.2008.09.023
2,14-dihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-5,6-dimethylheptan-2-yl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 162889588 Click to see 656.80 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1021/NP0704248
Fibraurecdyside A 44445723 Click to see 656.80 unknown https://doi.org/10.1021/NP0704248
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(1S,2R,5S,8S,10S,11S,13S,16S)-8-(furan-3-yl)-1,5,16-trihydroxy-2,10-dimethyl-7,14-dioxatetracyclo[11.2.1.02,11.05,10]hexadecane-6,15-dione 163188236 Click to see CC12CCC3(C(=O)OC(CC3(C1CC4C(C2(C(=O)O4)O)O)C)C5=COC=C5)O 392.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
8-(Furan-3-yl)-1,5,16-trihydroxy-2,10-dimethyl-7,14-dioxatetracyclo[11.2.1.02,11.05,10]hexadecane-6,15-dione 163038865 Click to see 392.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> 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/J.BMC.2008.09.023
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see 412.70 unknown https://doi.org/10.1016/J.BMC.2008.09.023
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/J.BMC.2008.09.023
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones
Scortechinone T 44559273 Click to see CC1C(C2=C(O1)C(=C(C3=C2OC45C6CC(C(C4C3=O)OC)(C(=O)C5(OC6(C)C)CC=C(C)C=O)OC)O)CC=C(C)C)(C)C 608.70 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Organoheterocyclic compounds / Isoquinolines and derivatives
2,3,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-9-one 25210825 Click to see 337.40 unknown https://doi.org/10.1055/S-2007-971676
793JX7VC6J 457914 Click to see 321.30 unknown https://doi.org/10.1055/S-2007-971676
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 10065647 Click to see 337.40 unknown https://doi.org/10.1021/NP0704248
3,4-Dihydro-7-hydroxy-6-methoxy-2-methyl-1(2H)-isoquinolinone 89048 Click to see 207.23 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Corydaldine 610097 Click to see 207.23 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Organoheterocyclic compounds / Naphthopyrans
(1R,2R,3R,5S,11S,12R,13R,15R)-5-(furan-3-yl)-12-hydroxy-3,11-dimethyl-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadec-8-ene-7,17-dione 162924411 Click to see 372.40 unknown https://doi.org/10.1016/0031-9422(86)80024-3
(1R,2S,3S,5R,8S,11R,12R)-5-(furan-3-yl)-8,12-dihydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadec-15-ene-7,13-dione 162904043 Click to see 374.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
(1R,3S,5R,11R,12R)-5-(furan-3-yl)-12-hydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadeca-8,15-diene-7,13-dione 134745274 Click to see 356.40 unknown https://doi.org/10.1016/0031-9422(86)80024-3
(1S,2R,3R,5S,11S,12S)-5-(furan-3-yl)-12-hydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadeca-8,15-diene-7,13-dione 162921299 Click to see 356.40 unknown https://doi.org/10.1016/0031-9422(86)80024-3
(1S,2R,5S,8S,10S,11S,13S,16S)-8-(furan-3-yl)-1,16-dihydroxy-2,10-dimethyl-7,14-dioxatetracyclo[11.2.1.02,11.05,10]hexadecane-6,15-dione 162918546 Click to see 376.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
(1S,2S,3S,5R,8S,9S,11R,12S,13S,15R)-5-(furan-3-yl)-9,12-dihydroxy-3,11-dimethyl-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadecane-7,17-dione 163079820 Click to see CC12CC(OC(=O)C1C(CC3(C2C4C5C(C3(C(=O)O4)O)O5)C)O)C6=COC=C6 390.40 unknown https://doi.org/10.1021/NP0704248
(1S,2S,4R,7S,8S,9S,12R,16S)-4-(furan-3-yl)-7,8-dihydroxy-2,16-dimethyl-12-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadec-13-en-6-one 163067490 Click to see 538.50 unknown https://doi.org/10.1021/NP0704248
(1S,2S,4S,7S,8S,9S,12S,16S)-4-(furan-3-yl)-7,8-dihydroxy-2,16-dimethyl-12-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadec-13-en-6-one 163067489 Click to see 538.50 unknown https://doi.org/10.1021/NP0704248
(2R,6aR,10aS,10bS)-2-(furan-3-yl)-6a,10b-dimethyl-1,2,6,10a-tetrahydrobenzo[f]isochromene-4,7,10-trione 162920060 Click to see 326.30 unknown https://doi.org/10.1016/J.BMC.2008.09.023
2-(Furan-3-yl)-6a,10b-dimethyl-1,2,6,10a-tetrahydrobenzo[f]isochromene-4,7,10-trione 162920059 Click to see 326.30 unknown https://doi.org/10.1016/J.BMC.2008.09.023
5-(Furan-3-yl)-12-hydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadeca-8,15-diene-7,13-dione 56678199 Click to see CC12CC=C3C(=O)OC(CC3(C1C4C=CC2(C(=O)O4)O)C)C5=COC=C5 356.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1016/0031-9422(86)80024-3
5-(Furan-3-yl)-12-hydroxy-3,11-dimethyl-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadec-8-ene-7,17-dione 12309884 Click to see 372.40 unknown https://doi.org/10.1016/0031-9422(86)80024-3
https://doi.org/10.1016/J.BMC.2008.09.023
5-(Furan-3-yl)-8,12-dihydroxy-3,11-dimethyl-6,14-dioxatetracyclo[10.2.2.02,11.03,8]hexadec-15-ene-7,13-dione 162904041 Click to see 374.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
5-(Furan-3-yl)-9,12-dihydroxy-3,11-dimethyl-6,14,16-trioxapentacyclo[10.3.2.02,11.03,8.013,15]heptadecane-7,17-dione 56681392 Click to see CC12CC(OC(=O)C1C(CC3(C2C4C5C(C3(C(=O)O4)O)O5)C)O)C6=COC=C6 390.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1021/NP0704248
Chasmanthin 442012 Click to see 374.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Fibleucin 44589004 Click to see 356.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Fibrauretin A 24762429 Click to see 390.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1021/NP0704248
Fibrauretin B 44588976 Click to see 362.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Fibraurin 21626387 Click to see CC12CC=C3C(=O)OC(CC3(C1C4C5C(C2(C(=O)O4)O)O5)C)C6=COC=C6 372.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1016/0031-9422(86)80024-3
Tinosporide 167631 Click to see CC12CCC3C(=O)OC(CC3(C1C4C5C(C2(C(=O)O4)O)O5)C)C6=COC=C6 374.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
(2R,6aR,10S,10aS,10bS)-2-(furan-3-yl)-10-hydroxy-6a,10b-dimethyl-2,6,10,10a-tetrahydro-1H-benzo[f]isochromene-4,7-dione 162867628 Click to see 328.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
2-(furan-3-yl)-10-hydroxy-6a,10b-dimethyl-2,6,10,10a-tetrahydro-1H-benzo[f]isochromene-4,7-dione 162867627 Click to see 328.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
2-(furan-3-yl)-6a,10b-dimethyl-2,6,10,10a-tetrahydro-1H-benzo[f]isochromene-4,7-dione 56671447 Click to see 312.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
fibaruretin D 44588977 Click to see 312.40 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones / Naphthopyranone glycosides
epi-12-palmatoside G 24762504 Click to see CC12CC(OC(=O)C1CCC3(C2CC=CC3=O)COC4C(C(C(C(O4)CO)O)O)O)C5=COC=C5 492.50 unknown https://doi.org/10.1016/J.BMC.2008.09.023
https://doi.org/10.1021/NP0704248
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
3-Buten-2-one, 4-(4-hydroxy-3-methoxyphenyl)-, (3E)- 14121 Click to see CC(=O)C=CC1=CC(=C(C=C1)O)OC 192.21 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Dehydrozingerone 5354238 Click to see CC(=O)C=CC1=CC(=C(C=C1)O)OC 192.21 unknown https://doi.org/10.1016/J.BMC.2008.09.023
N-cis-Feruloyl tyramine 6440659 Click to see 313.30 unknown https://doi.org/10.1016/J.BMC.2008.09.023
N-feruloyltyramine; Moupinamide 125213 Click to see 313.30 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(4-hydroxy-3-methoxyphenyl)-, octadecyl ester 149044 Click to see CCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC 446.70 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Cinnamamide, p-hydroxy-N-(p-hydroxyphenethyl)- 89322 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown https://doi.org/10.1016/J.BMC.2008.09.023
cis-N-p-coumaroyltyramine 13939145 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Octadecyl ferulate 5320256 Click to see 446.70 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Paprazine 5372945 Click to see 283.32 unknown https://doi.org/10.1016/J.BMC.2008.09.023
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown https://doi.org/10.1016/J.BMC.2008.09.023
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1016/J.BMC.2008.09.023

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