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Chondrodendron tomentosum

Chondrodendron tomentosum - Unknown
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Author: Public Domain - WikiMedia
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Table of Contents

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

Details Top

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

Description Top

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The small, greenish-yellow flowers are borne in axillary clusters. The fruits are large, ovoid drupes, containing a single seed.

Chondrodendron tomentosum is a large tropical liana native to Central and South America. It belongs to the Moonseed family Menispermaceae and is one of six accepted species in the small genus Chondrodendron. It contains highly toxic alkaloids and is one of the sources of the arrow poison curare, specifically 'tube curare'. It has a woody climbing stem that can reach 10 cm in thickness and climb up to 30 metres into the rainforest canopy. The large, glossy, cordate leaves are densely clothed beneath with a silky white pubescence, from which it gets its common name 'Velvet Leaf'. The small, greenish-yellow flowers are borne in axillary clusters and the fruits are large, ovoid drupes, containing a single seed. The generic name is a compound of Greek χόνδρος (chondros) 'cartilage' / 'lump' / 'grain' and δένδρον (dendron) 'tree', while the specific name

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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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
(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 C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown via CMAUP database
Anagyrine 5351589 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown via CMAUP database
Thermospine 638234 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
Caulophylline 670971 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
Mamanine 3085182 Click to see C1CCN2CC(CC(C2C1)CO)C3=CC=CC(=O)N3 262.35 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(+)-12alpha-Hydroxysophocarpine 44408595 Click to see C1CC2CN3C(C4C2N(C1)CCC4)C(C=CC3=O)O 262.35 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 C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4 246.35 unknown via CMAUP database
(5beta,6beta,7beta,11alpha)-Matridin-15-one 638232 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 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 C1CC2C3CC=CC(=O)N3CC4(C2N(C1)CCC4)O 262.35 unknown via CMAUP database
9alpha-Hydroxy-13,14-didehydromatridine-15-one 12133310 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CC(C4)O 262.35 unknown via CMAUP database
9alpha-Hydroxymatrine 15385684 Click to see C1CC2C3CC(CN4C3C(CCC4)CN2C(=O)C1)O 264.36 unknown via CMAUP database
Allomatrine 7000681 Click to see C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 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 C1CC2C3CCCN4C3C(CCC4)CN2C(=O)C1 248.36 unknown via CMAUP database
Sophocarpine 115269 Click to see C1CC2CN3C(CC=CC3=O)C4C2N(C1)CCC4 246.35 unknown via CMAUP database
Sophoranol 12442899 Click to see C1CC2C3CCCN4C3C(CCC4)(CN2C(=O)C1)O 264.36 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 C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 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 CC1C(C(C(C(O1)OC2C(C(C(OC2OC3C(C(C(OC3OC4CCC5(C(C4(C)CO)CCC6(C5CC=C7C6(CCC8(C7CC(CC8OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)CO)O)O)O)(C)C)C)C)C)C)C(=O)OC)O)O)CO)O)O)O)O)O 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 CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(O3)C=C7)N(CCC6=CC(=C5O)OC)C)O)OC 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 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
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 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/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 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/JR9470000936
https://doi.org/10.1039/JR9480001945
Isochondrodendrine 197726 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC=C(O3)C=C7)N(CCC6=CC(=C5O)OC)C)O)OC 594.70 unknown https://doi.org/10.1039/JR9480001945
> Organoheterocyclic compounds / Azoles / Imidazoles
2,4-Dimethylimidazole 70259 Click to see CC1=CN=C(N1)C 96.13 unknown via CMAUP database
4-Methylimidazole 13195 Click to see CC1=CN=CN1 82.10 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Kushecarpin B 10831417 Click to see COC1C2C(C3(CCC(=O)C=C3O1)OC)OC4=CC5=C(C=C24)OCO5 346.30 unknown via CMAUP database
Kushecarpin C 10496772 Click to see COC1C2C(C3(CCC(=O)C=C3O1)O)OC4=CC5=C(C=C24)OCO5 332.30 unknown via CMAUP database
> Organoheterocyclic compounds / Coumarans
Kushecarpin A 10495761 Click to see COC1C2C(C3(CCC(=O)C=C3O1)O)OC4=C2C=CC(=C4)OC 318.32 unknown via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
Sophoramine 169014 Click to see C1CC2CN3C(=O)C=CC=C3C4C2N(C1)CCC4 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
(+)-Isokuraramine 101665417 Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO 222.28 unknown via CMAUP database
(+)-Kuraramine 46187187 Click to see CN1CC(CC(C1)C2=CC=CC(=O)N2)CO 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
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 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 CC(=CCC(CC1=C(C2=C(C=C1O)OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 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 CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3)O)OC)O)C 370.40 unknown via CMAUP database
Kushenol V 10572194 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC(=C(C=C3O)O)OC)O)C 386.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R,3R)-2-(2,4-dihydroxyphenyl)-3,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-prop-1-en-2-ylhexyl]-5-methoxy-2,3-dihydrochromen-4-one 44584091 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
(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 CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 454.50 unknown via CMAUP database
(2S)-2-(2,4-Dihydroxyphenyl)-2,3-dihydro-5,7-dihydroxy-8-[(2R)-5-hydroxy-5-methyl-2-(1-methylethenyl)hexyl]-4H-1-benzopyran-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 CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC(=C(C=C3)O)OC)C 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)-7,2'-dihydroxy-8-lavandulyl-5-methoxyflavanone 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
(2S)-7,4'-dihydroxy-8-lavandulyl-5-methoxyflavanone 42608062 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=C(C=C3)O)C(=C)C)C 422.50 unknown via CMAUP database
(2S)-euchrenone a7 44593508 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=C(C=C(C=C3)O)O)O)C 340.40 unknown via CMAUP database
(2S)-Isoxanthohumol 9928523 Click to see CC(=CCC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=CC=C(C=C3)O)C 354.40 unknown via CMAUP database
7,2',4'-Trihydroxy-8-lavandulyl-5-methoxyflavanone 11982640 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
8-Prenylnaringenin 480764 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=C(C=C3)O)C 340.40 unknown 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
Flavenochromane A 11351168 Click to see CC1(CCC2=CC(=C(C=C2O1)O)C3C(C(=O)C4=C(O3)C5=C(C=C4O)OC(CC5)(C)C)O)C 440.50 unknown via CMAUP database
Isobavachin 193679 Click to see CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C 324.40 unknown via CMAUP database
Kurarinol 44563198 Click to see CC(=C)C(CCC(C)(C)O)CC1=C2C(=C(C=C1O)OC)C(=O)CC(O2)C3=C(C=C(C=C3)O)O 456.50 unknown via CMAUP database
Kushenol A 44563121 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O)C(=C)C)C 408.50 unknown via CMAUP database
Kushenol E 127234 Click to see CC(=CCC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)CC=C(C)C)O)C 424.50 unknown via CMAUP database
Kushenol I 20832634 Click to see CC(=CCC(CC1=C2C(=C(C=C1O)OC)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 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 S 10854625 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3O)C 340.40 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 CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)OC)C(=C)C)C 438.50 unknown via CMAUP database
Leachianone G 5275227 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=C(C=C(C=C3)O)O)C 356.40 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 CC(=CCC1=C(C2=C(C=C1O)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)C 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
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
Flavenochromane B 11327657 Click to see CC1(CCC2=C3C(=C4C(=C2O1)CCC(O4)(C)C)C(=O)C(=C(O3)C5=CC=C(C=C5)O)O)C 422.50 unknown via CMAUP database
Flavenochromane C 11451469 Click to see CC1(CCC2=C3C(=C(C=C2O1)OC)C(=O)C(=C(O3)C4=CC=C(C=C4)O)O)C 368.40 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 CC(=CCC(CC1=C2C(=C(C=C1O)O)C(=O)C(=C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 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 C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 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 COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C=C(C=C3)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 562.50 unknown via CMAUP database
7-(alpha-D-Glucopyranosyloxy)-5-hydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one 12304095 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Furanoisoflavonoids / Pterocarpans
(-)-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
(-)-Variabilin 442828 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
(+)-Maackiain 161298 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown via CMAUP database
(+)-Medicarpin 73067 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 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 COC1=CC2=C(C=C1)C3C(CO2)C4=CC(=C(C=C4O3)O)O 286.28 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
(6aS,12aS)-6abeta,12abeta-Dihydro-3-methoxy-6H-[1,3]dioxolo[5,6]benzofuro[3,2-c][1]benzopyran 373519 Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5 298.29 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
Maackiain 91510 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown via CMAUP database
Pterocarpin 1715306 Click to see COC1=CC2=C(C=C1)C3C(CO2)C4=CC5=C(C=C4O3)OCO5 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 C1=CC(=C(C=C1C2=COC3=C(C2=O)C=CC(=C3)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
Flavescenone A 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
Alpinumisoflavone 5490139 Click to see CC1(C=CC2=C(O1)C=C3C(=C2O)C(=O)C(=CO3)C4=CC=C(C=C4)O)C 336.30 unknown via CMAUP database
Flavescenone B 101238024 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC4=C(C=C3O)OCO4)O)C 382.40 unknown via CMAUP database
Lupalbigenin 10001388 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C(C2=O)C(=C(C(=C3)O)CC=C(C)C)O)O)C 406.50 unknown via CMAUP database
Luteone 5281797 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=C(C=C(C=C3)O)O)O)C 354.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3'-Hydroxy-4'-methoxy-7-(6-O-(beta-D-xylopyranosyl)-beta-D-glucopyranosyloxy)isoflavone 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
3'-Hydroxy-4'-methoxy-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone 73603978 Click to see COC1=C(C=C(C=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
3'-Hydroxydaidzin 68607439 Click to see C1=CC(=C(C=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
3'-Methoxy-4'-hydroxy-7-(6-O-(beta-D-xylopyranosyl)-beta-D-glucopyranosyloxy)isoflavone 73603979 Click to see COC1=C(C=CC(=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
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
3',4'-(Epoxymethanoxy)-7-(6-O-(D-apio-beta-D-furanosyl)-beta-D-glucopyranosyloxy)isoflavone 102131643 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C(=CO4)C5=CC6=C(C=C5)OCO6)O)O)O)O)(CO)O 576.50 unknown via CMAUP database
Ambonin 20055730 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C3)C(=O)C(=CO4)C5=CC=C(C=C5)O)O)O)O)O)(CO)O 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 COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O)O 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 COC1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O 284.26 unknown via CMAUP database
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Kuraridine 44428631 Click to see CC(=CCC(CC1=C(C(=C(C=C1O)OC)C(=O)C=CC2=C(C=C(C=C2)O)O)O)C(=C)C)C 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
Sophodibenzoside A 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
Sophodibenzoside B 73603972 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(C(CO4)O)O)O)O)O)O)O)O 582.50 unknown via CMAUP database

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