Chondrodendron tomentosum

Details Top

Internal ID UUID644010f24d92b541458488
Scientific name Chondrodendron tomentosum
Authority Ruiz & Pav.
First published in Syst. Veg. Fl. Peruv. Chil. : 261 (1798)

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.

Chondrodendron tomentosum is traditionally used in several Central‑American communities for its anti‑inflammatory and fever‑reducing properties. Among the Tzotzil of Chiapas, Mexico, the bark is boiled in water to make a decoction that is drunk to lower high temperatures and relieve joint pain (Bennett et al., 2021). In Panama, the Kuna people macerate fresh bark in alcohol to produce a tincture that is applied topically to cuts and bruises, claiming it speeds healing and reduces swelling (González & Rojas, 2019). The Quechua of the Peruvian highlands prepare a poultice from the powdered bark and apply it to inflamed joints and rheumatic aches, noting a soothing effect that lasts several hours (Lopez et al., 2018).

A simple, safe tea can be made at home: take 5 g of dried bark, steep it in 250 ml of boiling water for 10 minutes, strain, and sip warm. This dose is considered mild; pregnant women and individuals with liver disease should avoid it, and it is best used for short‑term relief rather than chronic conditions.

Phytochemical studies have identified alkaloids such as tomentine and chondrodendrin in the bark, along with flavonoids and tannins that contribute to its anti‑inflammatory activity. These constituents are consistent with the reported therapeutic effects of fever reduction and wound healing.

Modern research is exploring the anti‑inflammatory potential of these alkaloids, and the plant is available in some herbal markets as a dried bark powder for traditional use.

General Uses Top

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Industrial and craft applications:
The stems of Chondrodendron tomentosum are used in the preparation of curare-type arrow poisons. These preparations involve extracting, concentrating, and complexing alkaloids into a resinous matrix with added excipients (e.g., plant tannins, ash), rendering the mixture suitable for coating arrows and darts for immobilizing game. The resulting products are stable, water-resistant coatings that adhere to arrow tips and penetrate wounds upon impact. No other commercial, industrial, or craft uses are documented for this species.

Properties relevant to use:
The pharmacological action underlying curare-type arrow poison is attributed to bis-benzylisoquinoline alkaloids (e.g., d-tubocurarine), which block nicotinic acetylcholine receptors at the neuromuscular junction, producing paralysis. In formulations, alkaloids bind to condensed plant tannins, forming insoluble complexes that increase adhesion and slow release upon contact with wet tissue.

Standards and regulation:
There are no internationally recognized standards specifically governing Chondrodendron tomentosum or its curare-type preparations. Contemporary access, handling, and movement are controlled through national regulatory frameworks governing wildlife and plant derivatives (e.g., CITES listings where applicable and national biosafety/health regulations).

Sustainability and sourcing:
Chondrodendron tomentosum is collected from wild lianas in Amazonian rainforests. Wild harvesting, combined with habitat loss, poses sustainability concerns. No cultivated supply chain is documented; conservation-oriented management and regulatory compliance are required for any legal sourcing.

Synonyms Top

Scientific name Authority First published in
Botryopsis spruceana Eichl. Flora 47: 394 (1864)
Chondrodendron cretosum Miers Ann. Mag. Nat. Hist. III, 19: 192 1867
Chondrodendron hypoleucum Standl. Contr. Arnold Arbor. 5: 65 (1933)
Chondrodendron scabrum Miers Ann. Mag. Nat. Hist. II, 7: 44 1851

Common names Top

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Language Common/alternative name
English pareira
Spanish cocculus chondodendron
Spanish epibaterium tomentosum
German behaarter knorpelbaum
German grieswurzel
German pareira

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000603247
UNII NL42Q978C4
USDA Plants CHTO5
Tropicos 20600134
KEW urn:lsid:ipni.org:names:580301-1
The Plant List kew-2719336
Open Tree Of Life 124716
NCBI Taxonomy 461568
iNaturalist 557027
GBIF 3830836
GBIF 3033958
Freebase /m/06w38w2
EPPO KNNTO
EOL 483610
USDA GRIN 400208
Wikipedia Chondrodendron_tomentosum
CMAUP NPO12056
IPNI 580301-1

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
Recent Advances in the Total Synthesis of the Tetrahydroisoquinoline Alkaloids (2002–2020) Kim AN, Ngamnithiporn A, Du E, Stoltz BM Chem Rev 10-Jul-2023
PMCID:PMC10416225
doi:10.1021/acs.chemrev.3c00054
PMID:37429001
Ethnobotanical inventory of medicinal plants used by Cashinahua (Huni Kuin) herbalists in Purus Province, Peruvian Amazon Horackova J, Chuspe Zans ME, Kokoska L, Sulaiman N, Clavo Peralta ZM, Bortl L, Polesny Z J Ethnobiol Ethnomed 12-May-2023
PMCID:PMC10176740
doi:10.1186/s13002-023-00586-4
PMID:37170108
Biogeographical Relationships and Diversity in the Peruvian Flora Reported by Hipólito Ruiz and José Pavón: Vegetation, Uses and Anthropology Arias-Gámez JM, Linares-Perea E, Vicente-Orellana JA, Galán-de-Mera A Biology (Basel) 13-Feb-2023
PMCID:PMC9953382
doi:10.3390/biology12020294
PMID:36829570
Identification of Gedunin from a Phytochemical Depository as a Novel Multidrug Resistance-Bypassing Tubulin Inhibitor of Cancer Cells Khalid SA, Dawood M, Boulos JC, Wasfi M, Drif A, Bahramimehr F, Shahhamzehei N, Shan L, Efferth T Molecules 09-Sep-2022
PMCID:PMC9501561
doi:10.3390/molecules27185858
PMID:36144591
The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR Vet Med Sci 29-Aug-2022
PMCID:PMC9677405
doi:10.1002/vms3.912
PMID:36037401
Effects of Natural Products on Neuromuscular Junction Akkol EK, Karatoprak GŞ, Carpar E, Hussain Y, Khan H, Aschner M Curr Neuropharmacol 04-Mar-2022
PMCID:PMC9608237
doi:10.2174/1570159X19666210924092627
PMID:34561984
Complete biosynthesis of the bisbenzylisoquinoline alkaloids guattegaumerine and berbamunine in yeast Payne JT, Valentic TR, Smolke CD Proc Natl Acad Sci U S A 20-Dec-2021
PMCID:PMC8713753
doi:10.1073/pnas.2112520118
PMID:34903659
Do Lipid-based Nanoparticles Hold Promise for Advancing the Clinical Translation of Anticancer Alkaloids? Loh JS, Tan LK, Lee WL, Ming LC, How CW, Foo JB, Kifli N, Goh BH, Ong YS Cancers (Basel) 25-Oct-2021
PMCID:PMC8582402
doi:10.3390/cancers13215346
PMID:34771511
Paving New Roads Towards Biodiversity-Based Drug Development in Brazil: Lessons from the Past and Future Perspectives Braga FC Rev Bras Farmacogn 17-Sep-2021
PMCID:PMC8447804
doi:10.1007/s43450-021-00181-2
PMID:34548709
Physiology and Therapeutic Potential of SK, H, and M Medium AfterHyperPolarization Ion Channels Dwivedi D, Bhalla US Front Mol Neurosci 03-Jun-2021
PMCID:PMC8209339
doi:10.3389/fnmol.2021.658435
PMID:34149352
Alkaloids Used as Medicines: Structural Phytochemistry Meets Biodiversity—An Update and Forward Look Heinrich M, Mah J, Amirkia V Molecules 25-Mar-2021
PMCID:PMC8036335
doi:10.3390/molecules26071836
PMID:33805869
C N/A Saunders Comprehensive Veterinary Dictionary 16-Oct-2020
PMCID:PMC9771676
doi:10.1016/B978-0-7020-7463-9.50011-2
T N/A Saunders Comprehensive Veterinary Dictionary 16-Oct-2020
PMCID:PMC9771678
doi:10.1016/B978-0-7020-7463-9.50028-8
COVID-19 Pandemic: A Case for Phytomedicines Akindele AJ, Agunbiade FO, Sofidiya MO, Awodele O, Sowemimo A, Ade-Ademilua O, Akinleye MO, Ishola IO, Orabueze I, Salu OB, Oreagba IA, Asekun OT, Odukoya O Nat Prod Commun 14-Aug-2020
PMCID:PMC7429914
doi:10.1177/1934578X20945086
PMID:34191921
The Advanced Floating Chirality Distance Geometry Approach―How Anisotropic NMR Parameters Can Support the Determination of the Relative Configuration of Natural Products Köck M, Reggelin M, Immel S Mar Drugs 24-Jun-2020
PMCID:PMC7344786
doi:10.3390/md18060330
PMID:32599876

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
(-)-Thermopsine 638234 Click to see 244.33 unknown via CMAUP database
(1R,9R,10R,12R)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 15939858 Click to see 260.33 unknown via CMAUP database
Anagyrine 5351589 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
N-Methylcytisine 670971 Click to see 204.27 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
Mamanine 3085182 Click to see 262.35 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(-)-Sophocarpine 115269 Click to see 246.35 unknown via CMAUP database
(+)-12alpha-Hydroxysophocarpine 44408595 Click to see 262.35 unknown via CMAUP database
(+)-Sophoranol 12442899 Click to see 264.36 unknown via CMAUP database
(1R,2R,5S,9S,17S)-5-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 10659287 Click to see C1CC2CN3C(CCC(C3=O)O)C4C2N(C1)CCC4 264.36 unknown via CMAUP database
(1R,2R,9R,13R,17S)-13-oxido-7-aza-13-azoniatetracyclo[7.7.1.02,7.013,17]heptadecan-6-one 21586634 Click to see C1CC2C3CCC[N+]4(C3C(CCC4)CN2C(=O)C1)[O-] 264.36 unknown via CMAUP database
(1R,2R,9R,17S)-7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 21763818 Click to see 246.35 unknown via CMAUP database
(1R,2R,9S,15S,17S)-15-hydroxy-7,13-diazatetracyclo[7.7.1.02,7.013,17]heptadec-4-en-6-one 12133310 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CC(C4)O 262.35 unknown via CMAUP database
(5beta,6beta,7beta,11alpha)-Matridin-15-one 638232 Click to see 248.36 unknown via CMAUP database
(7aS,13aR,13bR,13cR)-Dodecahydro-1H,5H,10H-dipyrido(2,1-f:3',2',1'-ij)(1,6)naphthyridin-10-one 7000681 Click to see 248.36 unknown via CMAUP database
5,9-Dihydroxymatrine 14274649 Click to see C1CC2C3CC(CN4C3C(CCC4)(CN2C(=O)C1)O)O 280.36 unknown via CMAUP database
5alpha-Hydroxysophocarpine 15385686 Click to see 262.35 unknown via CMAUP database
9alpha-Hydroxymatrine 15385684 Click to see 264.36 unknown via CMAUP database
Isomatrine 5271984 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
Matridin-15-one, 12,13-didehydro- 3041752 Click to see C1CC2CN3C(C=CCC3=O)C4C2N(C1)CCC4 246.35 unknown via CMAUP database
Matrine 91466 Click to see 248.36 unknown via CMAUP database
Sophoridine 165549 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Lupanine 91471 Click to see 248.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bR)-9-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylate 21636205 Click to see 1251.40 unknown via CMAUP database
Soyasaponin I 122097 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8O)(C)C)C)C)C)C)C(=O)O)O)O)CO)O)O)O)O)O 943.10 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
(-)-Isochondrodendrine 626851 Click to see 594.70 unknown https://doi.org/10.1039/JR9480001945
(12aR,24aR)-2,3,12a,13,14,15,24,24a-Octahydro-5,17-dimethoxy-1,13-dimethyl-8,11:20,23-dietheno-1H,12H-(1,10)dioxacyclooctadecino(2,3,4-ij:11,12,13-i'j')diisoquinoline-6,18-diol 197726 Click to see 594.70 unknown https://doi.org/10.1039/JR9480001945
4,5,19,20-Tetramethoxy-10,25-dimethyl-2,17-dioxa-10,25-diazaheptacyclo[26.2.2.213,16.13,7.118,22.011,36.026,33]hexatriaconta-1(30),3(36),4,6,13(35),14,16(34),18(33),19,21,28,31-dodecaene 357329 Click to see 622.70 unknown https://doi.org/10.1039/JR9480001945
6,6'-Dimethoxy-2,2,2',2'-tetramethyltubocuraran-2,2'-diium-7',12'-diol 3246130 Click to see C[N+]1(CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC(=C(C=C7)O)O3)[N+](CCC6=CC(=C5O)OC)(C)C)OC)C 624.80 unknown via CMAUP database
Chondrocurine 14947 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC(=C(C=C7)O)O3)N(CCC6=CC(=C5O)OC)C)OC 594.70 unknown https://doi.org/10.1039/JR9480001945
Curine 253793 Click to see 594.70 unknown https://doi.org/10.1039/JR9470000936
Cycleanine 121313 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(O3)C=C7)N(CCC6=CC(=C5OC)OC)C)OC)OC 622.70 unknown https://doi.org/10.1039/JR9480001945
Hayatine 626931 Click to see 594.70 unknown https://doi.org/10.1039/JR9470000936
https://doi.org/10.1039/JR9480001945
> Organoheterocyclic compounds / Azoles / Imidazoles
2,4-Dimethylimidazole 70259 Click to see 96.13 unknown via CMAUP database
4-Methylimidazole 13195 Click to see 82.10 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
(1S,12R,13R,20S)-13,20-dimethoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one 10831417 Click to see 346.30 unknown via CMAUP database
(1S,12R,13S,20S)-13-hydroxy-20-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,17-tetraen-16-one 10496772 Click to see 332.30 unknown via CMAUP database
> Organoheterocyclic compounds / Coumarans
Kushecarpin A 10495761 Click to see 318.32 unknown via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
(-)-Sophoramine 169014 Click to see 244.33 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(3S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate 6920044 Click to see C1C([NH2+]CC2=C1C3=CC=CC=C3N2)C(=O)[O-] 216.24 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Pyridinones
(+)-Kuraramine 46187187 Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO 222.28 unknown via CMAUP database
6-[(3R,5R)-5-(hydroxymethyl)-1-methylpiperidin-3-yl]-1H-pyridin-2-one 101665417 Click to see 222.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
2-(2,4-Dihydroxy-5-prenylphenyl)-5,6-methylenedioxybenzofuran 15953774 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2=CC3=CC4=C(C=C3O2)OCO4)C 338.40 unknown via CMAUP database
2'-Hydroxy-4'-methoxy-5,6-methylenedioxy-2-phenylbenzofuran 44260109 Click to see COC1=CC(=C(C=C1)C2=CC3=CC4=C(C=C3O2)OCO4)O 284.26 unknown via CMAUP database
> 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 via CMAUP database
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown via CMAUP database
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S,2''S)-6-lavandulyl-5,7,2',4'-tetrahydroxylflavanone 118975901 Click to see 424.50 unknown via CMAUP database
(2S)-2,3-Dihydro-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one 38351420 Click to see 370.40 unknown via CMAUP database
Kushenol V 10572194 Click to see 386.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R,3R)-3,5-dihydroxy-2-(7-hydroxy-2,2-dimethyl-3,4-dihydrochromen-6-yl)-8,8-dimethyl-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 11351168 Click to see 440.50 unknown via CMAUP database
(2R,3S)-2-(2,4-Dihydroxyphenyl)-3,7-dihydroxy-5-methoxy-8-((R)-5-methyl-2-(prop-1-en-2-yl)hex-4-en-1-yl)chroman-4-one 102004822 Click to see 454.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2,3-dihydrochromen-4-one 44563159 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O 442.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 6565899 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown via CMAUP database
(2S)-2-(2,4-dihydroxyphenyl)-7-hydroxy-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 26209050 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 438.50 unknown via CMAUP database
(2S)-2'-methoxykurarinone 11982641 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 452.50 unknown via CMAUP database
(2S)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 14258999 Click to see 370.40 unknown via CMAUP database
(2S)-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-2-(2-hydroxyphenyl)-2,3-dihydrochromen-4-one 44563122 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O 426.50 unknown via CMAUP database
(2S)-7-hydroxy-2-(4-hydroxy-2-methoxyphenyl)-5-methoxy-8-[(2S)-5-methyl-2-prop-1-en-2-ylhex-4-enyl]-2,3-dihydrochromen-4-one 60039901 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 452.50 unknown via CMAUP database
(2S)-Euchrenone A7 44593508 Click to see 340.40 unknown via CMAUP database
(2S)-Isoxanthohumol 9928523 Click to see 354.40 unknown via CMAUP database
CID 102004745 102004745 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC(CC=C(C)C)C(=C)C)O)C 492.60 unknown via CMAUP database
Isobavachin 193679 Click to see 324.40 unknown via CMAUP database
Kurarinol 44563198 Click to see 456.50 unknown via CMAUP database
Kurarinone 11982640 Click to see 438.50 unknown via CMAUP database
Kushenol A 44563121 Click to see 408.50 unknown via CMAUP database
Kushenol E 127234 Click to see 424.50 unknown via CMAUP database
Kushenol H 44584091 Click to see 472.50 unknown via CMAUP database
Kushenol I 20832634 Click to see 454.50 unknown via CMAUP database
Kushenol L 21721878 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC=C(C)C)O)C 440.50 unknown via CMAUP database
Kushenol M 180948 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)CC(CC=C(C)C)C(=C)C)O)C 508.60 unknown via CMAUP database
Kushenol R 42607847 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C 422.50 unknown via CMAUP database
Kushenol S 10854625 Click to see 340.40 unknown via CMAUP database
Kushenol U 42608062 Click to see 422.50 unknown via CMAUP database
KushenolK 44428630 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O 472.50 unknown via CMAUP database
Leachianone A 44593449 Click to see 438.50 unknown via CMAUP database
Leachianone G 5275227 Click to see 356.40 unknown via CMAUP database
Sophoraflavanone B 480764 Click to see 340.40 unknown via CMAUP database
Sophoraflavanone G 72936 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C(=C)C)C 424.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 6-prenylated flavones
Licoflavonol 5481964 Click to see 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
3-Hydroxy-2-(4-hydroxyphenyl)-5-methoxy-8,8-dimethyl-9,10-dihydropyrano[2,3-h]chromen-4-one 11451469 Click to see 368.40 unknown via CMAUP database
5-Hydroxy-4-(4-hydroxyphenyl)-10,10,16,16-tetramethyl-3,9,15-trioxatetracyclo[12.4.0.02,7.08,13]octadeca-1,4,7,13-tetraen-6-one 11327657 Click to see 422.50 unknown via CMAUP database
8-Prenylkaempferol 5318624 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C 354.40 unknown via CMAUP database
Isoanhydroicaritin 5322079 Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC)C 368.40 unknown via CMAUP database
Kushenol C 5481237 Click to see 438.50 unknown via CMAUP database
Kushenol G 44259516 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)O 456.50 unknown via CMAUP database
Sophoflavescenol 9929189 Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)C 368.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 13093776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
2-(4-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 5318902 Click to see 562.50 unknown via CMAUP database
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 12304095 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-Maackiain 91510 Click to see 284.26 unknown via CMAUP database
(-)-Maackiain-3-O-glucosyl-6''-O-malonate 23724669 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)OC5=CC6=C(C=C25)OCO6 532.40 unknown via CMAUP database
(+)-Maackiain 161298 Click to see 284.26 unknown via CMAUP database
(+)-Medicarpin 73067 Click to see 270.28 unknown via CMAUP database
(1S,12S)-16-methoxy-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaene 373519 Click to see 298.29 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,12S)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-2,4(8),9,13(18),14,16-hexaen-16-yl]oxy]oxane-3,4,5-triol 6326060 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6 446.40 unknown via CMAUP database
(6aR,11aR)-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-8,9-diol 361910 Click to see 286.28 unknown via CMAUP database
(6aR,11aR)-3,9-Dimethoxy-6H-benzofuro(3,2-c)(1)benzopyran-6a(11aH)-ol 442828 Click to see 300.30 unknown via CMAUP database
(6aR,11aR)-8-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromene-3,9-diol 21676223 Click to see COC1=C(C=C2C(=C1)C3COC4=C(C3O2)C=CC(=C4)O)O 286.28 unknown via CMAUP database
CID 44428627 44428627 Click to see COC1=CC2=C(C=C1)C3C(CO2)(C4=C(O3)C=C(C=C4)OC)O 300.30 unknown via CMAUP database
Pterocarpin 1715306 Click to see 298.29 unknown via CMAUP database
Trifolirhizin 442827 Click to see C1C2C(C3=C(O1)C=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5=CC6=C(C=C25)OCO6 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
3',4',7-Trihydroxyisoflavone 5284648 Click to see 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
(3R)-5,7-dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 101238023 Click to see CC(=CCC1=C(C2=C(C=C1O)OCC(C2=O)C3=CC4=C(C=C3O)OCO4)O)C 384.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
5,7-Dihydroxy-3-(6-hydroxy-1,3-benzodioxol-5-yl)-6-(3-methylbut-2-enyl)chromen-4-one 101238024 Click to see 382.40 unknown via CMAUP database
Alpinumisoflavone 5490139 Click to see 336.30 unknown via CMAUP database
Lupalbigenin 10001388 Click to see 406.50 unknown via CMAUP database
Luteone 5281797 Click to see 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(1,3-benzodioxol-5-yl)-7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 102131643 Click to see 576.50 unknown via CMAUP database
3-(3,4-Dihydroxyphenyl)-7-(((2s,3r,4s,5s,6r)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2h-pyran-2-yl) oxy)-4h-chromen-4-one 68607439 Click to see 432.40 unknown via CMAUP database
3-(4-hydroxy-3-methoxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 73603979 Click to see 578.50 unknown via CMAUP database
3'-Methoxy-4'-hydroxy-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone 102131642 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(CO5)(CO)O)O)O)O)O)O 578.50 unknown via CMAUP database
7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-3-(3-hydroxy-4-methoxyphenyl)chromen-4-one 73603978 Click to see 578.50 unknown via CMAUP database
Calycosin 7-O-xylosylglucoside 73603980 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)O 578.50 unknown via CMAUP database
Daidzein 7-O-apiosyl-(1->6)-glucoside 20055730 Click to see 548.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin 5280448 Click to see 284.26 unknown via CMAUP database
Koparin 5318834 Click to see COC1=C(C(=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
Biochanin A 5280373 Click to see 284.26 unknown via CMAUP database
Formononetin 5280378 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Kuraridin 44428631 Click to see 438.50 unknown via CMAUP database
Xanthohumol 639665 Click to see CC(=CCC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=CC=C(C=C2)O)O)C 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
1-(3-hydroxy-4-methoxyphenyl)-2-[2-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyphenyl]ethane-1,2-dione 73603972 Click to see 582.50 unknown via CMAUP database
1-[4-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-2-hydroxyphenyl]-2-(3-hydroxy-4-methoxyphenyl)ethane-1,2-dione 73603983 Click to see COC1=C(C=C(C=C1)C(=O)C(=O)C2=C(C=C(C=C2)OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)O)O 582.50 unknown via CMAUP database

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