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Ethulia conyzoides

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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 UUID643fce3f2b961076978636
Scientific name Ethulia conyzoides
Authority L.f.
First published in Decas Prima Plantarum Rariorum Horti Upsaliensis 1762

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 油棕根
Chinese 都丽菊

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Ethulia conyzoides subsp. conyzoides L.f. 1, t. 1. 1762
Ethulia conyzoides subsp. kraussii (Sch.Bip. ex Walp.) M.G.Gilbert & C.Jeffrey Kew Bull. 43(2): 173 (1988)

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

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000079631
Tropicos 2702466
The Plant List gcc-36207
Open Tree Of Life 1079723
NCBI Taxonomy 434659
IUCN Red List 164429
IPNI 91257-3
iNaturalist 191986
GBIF 3091122
EPPO ETUCO
USDA GRIN 15832
CMAUP NPO9851

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
Anticancer Meroterpenoids from Centrapalus pauciflorus leaves: Chromone- and 2,4-Chromadione-Monoterpene Derivatives Krstić G, Saidu MB, Barta A, Vágvölgyi M, Ali H, Zupkó I, Berkecz R, Gallah US, Rédei D, Hohmann J ACS Omega 16-Aug-2023
PMCID:PMC10468835
doi:10.1021/acsomega.3c03884
PMID:37663471
Antidiabetic, Antioxidant and Anti-Inflammatory Activities of Residual Aqueous Fraction of Ethulia conyzoides in Induced Type 2 Diabetic Rats Okotie HO, Anjuwon TM, Okonkwo OL, Ameh DA, James DB Trop Life Sci Res 31-Mar-2023
PMCID:PMC10093775
doi:10.21315/tlsr2023.34.1.8
PMID:37065804
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Dataset, including a photo-guide, of alien plants sold in traditional medicine markets and healthcare outlets in three South African cities, specifically by traders of Indian, West African, East African, and Chinese origin Williams VL, Burness A, Wojtasik EM, Byrne MJ Data Brief 21-Sep-2021
PMCID:PMC8479245
doi:10.1016/j.dib.2021.107395
PMID:34621926
Molluscicides against the snail-intermediate host of Schistosoma: a review Zheng L, Deng L, Zhong Y, Wang Y, Guo W, Fan X Parasitol Res 06-Sep-2021
PMCID:PMC8418967
doi:10.1007/s00436-021-07288-4
PMID:34486075
Status and consolidated list of threatened medicinal plants of India Gowthami R, Sharma N, Pandey R, Agrawal A Genet Resour Crop Evol 25-May-2021
PMCID:PMC8148398
doi:10.1007/s10722-021-01199-0
PMID:34054223
Effects of extracts and molecules derived from medicinal plants of West Africa in the prevention and treatment of gynecological cancers. A Review Bayala B, Zouré AA, Zohoncon TM, Tinguerie BL, Baron S, Bakri Y, Simpore J, Lobaccaro JM Am J Cancer Res 01-Sep-2020
PMCID:PMC7539771
PMID:33042613
Vernonieae (Asteraceae) of southern Africa: A generic disposition of the species and a study of their pollen Robinson H, Skvarla JJ, Funk VA PhytoKeys 11-Feb-2016
PMCID:PMC4816990
doi:10.3897/phytokeys.60.6734
PMID:27081344
Revisions and key to the Vernonieae (Compositae) of Thailand Bunwong S, Chantaranothai P, Keeley SC PhytoKeys 13-May-2014
PMCID:PMC4023333
doi:10.3897/phytokeys.37.6499
PMID:24843297
Cytotoxic Activity of Selected Nigerian Plants Sowemimo A, van de Venter M, Baatjies L, Koekemoer T Afr J Tradit Complement Altern Med 03-Jul-2009
PMCID:PMC2816471
doi:10.4314/ajtcam.v6i4.57186
PMID:20606772
The Absolute and Relative Configuration of the Molluscicides Ethuliacoumarin A and Isoethuliacoumarin A. I. Kjøller Larsen, E. Lemmich, S. T. Thiilborg, H. M. Nielsen, Fatima M. Piedade, M. M. Kady, S. Brøgger Christensen Danish Chemical Society 19-Jun-2008
doi:10.3891/ACTA.CHEM.SCAND.46-0750
New 5-methylcoumarins from Ethulia conyzoides Vishnu S. Shukla, Subhash C. Dutta, Robindra N. Baruah, Ram P. Sharma, Gopalakrishna Thyagarajan, Werner Herz, Narendra Kumar, Kinzo Watanabe, John F. Blount Elsevier BV 03-Jan-2008
doi:10.1016/S0031-9422(82)85048-6
Further monoterpene 5-methylcoumarins and an acetophenone derivative from Ethulia conyzoides Ahmed A. Mahmoud, Ahmed A. Ahmed, Munekazu Iinuma, Toshiyuki Tanaka Elsevier BV 30-Apr-2003
doi:10.1016/S0031-9422(97)00907-2
New 5-Methylcoumarin derivatives from Ethulia conyzoides Shafik I. Balbaa, Ahmed F. Halim, Fathi T. Halaweish, Ferdinand Bohlmann Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)80208-1
A 5-methylcoumarin glucoside from Ethulia conyzoides Zeinab F. Mahmoud, Taha M. Sarg, Masouda E. Amer, Saad M. Khafagy, Ferdinand Bohlmann Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)83031-7

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
> Lignans, neolignans and related compounds / Furanoid lignans
(+)-Demethoxyexcelsin 179572 Click to see COC1=CC(=CC2=C1OCO2)C3C4COC(C4CO3)C5=CC6=C(C=C5)OCO6 384.40 unknown via CMAUP database
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
Absinthin 442138 Click to see CC1C2CCC(C3C4C5C=C(C6(C4C(=C3C2OC1=O)C)C5C(CCC7C6OC(=O)C7C)(C)O)C)(C)O 496.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3S)-3abeta,4,5,7,8,9,9abeta,9balpha-Octahydro-3beta,6,9-trimethyl-4beta,7beta,9beta-trihydroxy-8beta-acetoxyazuleno[4,5-b]furan-2(3H)-one 102533402 Click to see CC1C2C(CC(=C3C(C2OC1=O)C(C(C3O)OC(=O)C)(C)O)C)O 340.40 unknown via CMAUP database
Ludartin 14355826 Click to see CC1=C2CC3C(C2C4C(CC1)C(=C)C(=O)O4)(O3)C 246.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(1S,3R,6S,7S,10S,11R)-3,7,12-trimethyl-2,9-dioxatetracyclo[9.3.0.01,3.06,10]tetradec-12-en-8-one 10966851 Click to see CC1C2CCC3(C4(O3)CC=C(C4C2OC1=O)C)C 248.32 unknown via CMAUP database
11alphaH,13-Dihydroestafiatin 15690505 Click to see CC1C2CCC(=C)C3CC4C(C3C2OC1=O)(O4)C 248.32 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lup-20(29)-en-3-ol, (3beta)- 521518 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(80)83031-7
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(80)83031-7
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/0031-9422(80)83031-7
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/0031-9422(80)83031-7
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
10,13-dimethyl-17-(5-propan-2-ylhept-5-en-2-yl)-2,3,4,5,6,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 74059587 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(80)83031-7
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
delta7-Avenasterol 12795736 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/0031-9422(80)83031-7
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 via CMAUP database
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(1R,2R,5R)-2-[2-(2-hydroxy-6-methylphenyl)-2-oxoethyl]-1,4,4-trimethyl-8-oxabicyclo[3.2.1]octan-6-one 163088925 Click to see CC1=C(C(=CC=C1)O)C(=O)CC2CC(C3C(=O)CC2(O3)C)(C)C 316.40 unknown https://doi.org/10.1016/0031-9422(80)80208-1
(3R)-1-[(2S)-3,3-dimethyloxiran-2-yl]-3-ethenyl-5-(2-hydroxy-6-methylphenyl)-3-methylpentane-1,5-dione 163036072 Click to see CC1=C(C(=CC=C1)O)C(=O)CC(C)(CC(=O)C2C(O2)(C)C)C=C 316.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
(3S)-1-[(2R)-3,3-dimethyloxiran-2-yl]-3-ethenyl-5-(2-hydroxy-6-methylphenyl)-3-methylpentane-1,5-dione 163036071 Click to see CC1=C(C(=CC=C1)O)C(=O)CC(C)(CC(=O)C2C(O2)(C)C)C=C 316.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
1-(2-Hydroxy-6-methylphenyl)ethanone 11159401 Click to see CC1=C(C(=CC=C1)O)C(=O)C 150.17 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
1-(3,3-Dimethyloxiran-2-yl)-3-ethenyl-5-(2-hydroxy-6-methylphenyl)-3-methylpentane-1,5-dione 15378261 Click to see CC1=C(C(=CC=C1)O)C(=O)CC(C)(CC(=O)C2C(O2)(C)C)C=C 316.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
2-[2-(2-Hydroxy-6-methylphenyl)-2-oxoethyl]-1,4,4-trimethyl-8-oxabicyclo[3.2.1]octan-6-one 163088924 Click to see CC1=C(C(=CC=C1)O)C(=O)CC2CC(C3C(=O)CC2(O3)C)(C)C 316.40 unknown https://doi.org/10.1016/0031-9422(80)80208-1
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
(3S,3aS,4R,5R,6aR)-5-ethenyl-3,5,5'-trimethylspiro[3,3a,6,6a-tetrahydrocyclopenta[b]furan-4,3'-chromene]-2,2',4'-trione 162950622 Click to see CC1C2C(CC(C23C(=O)C4=C(C=CC=C4OC3=O)C)(C)C=C)OC1=O 340.40 unknown https://doi.org/10.1016/S0040-4039(00)78261-X
(3S,3aS,5R,6aR)-5-ethenyl-3,5,5'-trimethylspiro[3,3a,6,6a-tetrahydrocyclopenta[b]furan-4,3'-chromene]-2,2',4'-trione 162950620 Click to see CC1C2C(CC(C23C(=O)C4=C(C=CC=C4OC3=O)C)(C)C=C)OC1=O 340.40 unknown https://doi.org/10.1016/S0040-4039(00)78261-X
5-Ethenyl-3,5,5'-trimethylspiro[3,3a,6,6a-tetrahydrocyclopenta[b]furan-4,3'-chromene]-2,2',4'-trione 162950619 Click to see CC1C2C(CC(C23C(=O)C4=C(C=CC=C4OC3=O)C)(C)C=C)OC1=O 340.40 unknown https://doi.org/10.1016/S0040-4039(00)78261-X
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3S)-3abeta,4,5,6,8,9,9abeta,9balpha-Octahydro-3beta,6,9-trimethyl-6alpha,8beta,9beta-trihydroxy-4beta-acetoxyazuleno[4,5-b]furan-2(3H)-one 24011666 Click to see CC1C2C(CC(C3=CC(C(C3C2OC1=O)(C)O)O)(C)O)OC(=O)C 340.40 unknown via CMAUP database
(3S)-4beta-Acetoxy-6alpha,9beta-dihydroxy-3beta,6,9-trimethyl-8beta-methoxy-3abeta,4,5,6,8,9,9abeta,9balpha-octahydroazuleno[4,5-b]furan-2(3H)-one 101044249 Click to see CC1C2C(CC(C3=CC(C(C3C2OC1=O)(C)O)OC)(C)O)OC(=O)C 354.40 unknown via CMAUP database
Artabsin 442146 Click to see CC1C2CCC(C3=CCC(=C3C2OC1=O)C)(C)O 248.32 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
> Phenylpropanoids and polyketides / Coumarins and derivatives
5-methyl-4-[[(2R,3S,4S,5R,6R)-3,4,5,6-tetrahydroxyoxan-2-yl]methoxy]chromen-2-one 162816927 Click to see CC1=C2C(=CC=C1)OC(=O)C=C2OCC3C(C(C(C(O3)O)O)O)O 338.31 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
https://doi.org/10.1016/0031-9422(80)83031-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
5-Methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 14427391 Click to see CC1=C2C(=CC=C1)OC(=O)C=C2OC3C(C(C(C(O3)CO)O)O)O 338.31 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
https://doi.org/10.1016/0031-9422(80)83031-7
Gerberinside 196468 Click to see CC1=C2C(=CC=C1)OC(=O)C=C2OC3C(C(C(C(O3)CO)O)O)O 338.31 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
https://doi.org/10.1016/0031-9422(80)83031-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(1R,4R,4'R,5R)-4'-ethenyl-1,4',10'-trimethylspiro[3,6-dioxabicyclo[3.1.0]hexane-4,2'-3H-pyrano[3,2-c]chromene]-5'-one 23983654 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC4(CC3(C)C=C)C5C(O5)(CO4)C 340.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
(1S,4R,4'R,5S)-4'-ethenyl-1,4',10'-trimethylspiro[3,6-dioxabicyclo[3.1.0]hexane-4,2'-3H-pyrano[3,2-c]chromene]-5'-one 163006949 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC4(CC3(C)C=C)C5C(O5)(CO4)C 340.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
(2R,3'R,4R)-4-ethenyl-3'-hydroxy-4,4',4',10-tetramethylspiro[3H-pyrano[3,2-c]chromene-2,2'-oxetane]-5-one 163009369 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC4(CC3(C)C=C)C(C(O4)(C)C)O 342.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
(2R,3'S,4R)-4-ethenyl-3'-hydroxy-4,4',4',10-tetramethylspiro[3H-pyrano[3,2-c]chromene-2,2'-oxetane]-5-one 163009370 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC4(CC3(C)C=C)C(C(O4)(C)C)O 342.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
(2R,4R)-2-[(1R)-1,2-dihydroxy-2-methylpropyl]-4-ethenyl-2-hydroxy-4,10-dimethyl-3H-pyrano[3,2-c]chromen-5-one 162938129 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(CC3(C)C=C)(C(C(C)(C)O)O)O 360.40 unknown https://doi.org/10.1016/0031-9422(81)85246-6
(2R,4R)-4-ethenyl-2-hydroxy-2-(1-hydroxy-2-methylprop-2-enyl)-4,10-dimethyl-3H-pyrano[3,2-c]chromen-5-one 102316533 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(CC3(C)C=C)(C(C(=C)C)O)O 342.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
(2R,4R)-4-ethenyl-2-hydroxy-2-[(1S)-1-hydroxy-2-methylprop-2-enyl]-4,10-dimethyl-3H-pyrano[3,2-c]chromen-5-one 162932417 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(CC3(C)C=C)(C(C(=C)C)O)O 342.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
(2R,4S)-2-[(2R)-3,3-dimethyloxiran-2-yl]-4-ethenyl-2-hydroxy-4,10-dimethyl-3H-pyrano[3,2-c]chromen-5-one 14464539 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(CC3(C)C=C)(C4C(O4)(C)C)O 342.40 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.46-0750
(2R,4S)-4-ethenyl-2-hydroxy-2-[(1R)-1-hydroxy-2-methylprop-2-enyl]-4,10-dimethyl-3H-pyrano[3,2-c]chromen-5-one 162932418 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(CC3(C)C=C)(C(C(=C)C)O)O 342.40 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.46-0750
(2S,3'R,4R)-4-ethenyl-3'-hydroxy-4,4',4',10-tetramethylspiro[3H-pyrano[3,2-c]chromene-2,2'-oxetane]-5-one 102316532 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC4(CC3(C)C=C)C(C(O4)(C)C)O 342.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
https://doi.org/10.1016/0031-9422(80)80208-1
(2S,3'S,4R)-4-ethenyl-3'-hydroxy-4,4',4',10-tetramethylspiro[3H-pyrano[3,2-c]chromene-2,2'-oxetane]-5-one 15376404 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC4(CC3(C)C=C)C(C(O4)(C)C)O 342.40 unknown https://doi.org/10.1016/S0031-9422(00)82113-5
https://doi.org/10.1016/S0031-9422(97)00907-2
(2S,3'S,5S)-3'-ethenyl-2-hydroxy-3,3',10'-trimethylspiro[2H-furan-5,2'-4H-pyrano[3,2-c]chromene]-5'-one 163096516 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC4(C=C(C(O4)O)C)C(C3)(C)C=C 340.40 unknown https://doi.org/10.1016/S0031-9422(82)85048-6
(2S,4R)-2-[(2S)-3,3-dimethyloxiran-2-yl]-4-ethenyl-2-hydroxy-4,10-dimethyl-3H-pyrano[3,2-c]chromen-5-one 101642675 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(CC3(C)C=C)(C4C(O4)(C)C)O 342.40 unknown https://doi.org/10.1016/0031-9422(80)80208-1
https://doi.org/10.1016/S0031-9422(00)82113-5
https://doi.org/10.1016/0031-9422(80)83031-7
https://doi.org/10.1016/S0031-9422(97)00907-2
(2S,4R)-4-ethenyl-2-hydroxy-2-[(1R)-1-hydroxy-2-methylprop-2-enyl]-4,10-dimethyl-3H-pyrano[3,2-c]chromen-5-one 162932416 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(CC3(C)C=C)(C(C(=C)C)O)O 342.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
(2S,4R)-4-ethenyl-2-hydroxy-2-[(1S)-1-hydroxy-2-methylprop-2-enyl]-4,10-dimethyl-3H-pyrano[3,2-c]chromen-5-one 101642676 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(CC3(C)C=C)(C(C(=C)C)O)O 342.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
https://doi.org/10.1055/S-2006-961479
https://doi.org/10.1016/S0031-9422(00)82113-5
https://doi.org/10.1016/0031-9422(80)80208-1
(4R,4'R)-4'-ethenyl-1,4',10'-trimethylspiro[3,6-dioxabicyclo[3.1.0]hexane-4,2'-3H-pyrano[3,2-c]chromene]-5'-one 102316529 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC4(CC3(C)C=C)C5C(O5)(CO4)C 340.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
(4R)-2-(1,2-dihydroxy-2-methylpropyl)-4-ethenyl-2-hydroxy-4,10-dimethyl-3H-pyrano[3,2-c]chromen-5-one 162938130 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(CC3(C)C=C)(C(C(C)(C)O)O)O 360.40 unknown https://doi.org/10.1016/0031-9422(81)85246-6
(4R)-4-ethenyl-4,10-dimethyl-3H-pyrano[3,2-c]chromene-2,5-dione 162939230 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(=O)CC3(C)C=C 270.28 unknown https://doi.org/10.1016/S0031-9422(00)82113-5
(4S)-2-(1,2-dihydroxy-2-methylpropyl)-4-ethenyl-4,10-dimethylpyrano[3,2-c]chromen-5-one 162946146 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(=CC3(C)C=C)C(C(C)(C)O)O 342.40 unknown https://doi.org/10.1016/S0031-9422(00)82113-5
(4S)-2-[(1R)-1,2-dihydroxy-2-methylpropyl]-4-ethenyl-4,10-dimethylpyrano[3,2-c]chromen-5-one 162946147 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(=CC3(C)C=C)C(C(C)(C)O)O 342.40 unknown https://doi.org/10.1016/0031-9422(80)80208-1
(E)-3-[(2R,3S)-3-ethenyl-3,10-dimethyl-5-oxo-2,4-dihydropyrano[3,2-c]chromen-2-yl]-2-methylprop-2-enoic acid 163193732 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(C(C3)(C)C=C)C=C(C)C(=O)O 340.40 unknown https://doi.org/10.1016/S0031-9422(82)85048-6
(Z)-3-[(2R,3S)-3-ethenyl-3,10-dimethyl-5-oxo-2,4-dihydropyrano[3,2-c]chromen-2-yl]-2-methylprop-2-enoic acid 163193733 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(C(C3)(C)C=C)C=C(C)C(=O)O 340.40 unknown https://doi.org/10.1016/S0031-9422(82)85048-6
2-(1,2-dihydroxy-2-methylpropyl)-4-ethenyl-2-hydroxy-4,10-dimethyl-3H-pyrano[3,2-c]chromen-5-one 162938128 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(CC3(C)C=C)(C(C(C)(C)O)O)O 360.40 unknown https://doi.org/10.1016/0031-9422(81)85246-6
2-(1,2-Dihydroxy-2-methylpropyl)-4-ethenyl-4,10-dimethylpyrano[3,2-c]chromen-5-one 14464543 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(=CC3(C)C=C)C(C(C)(C)O)O 342.40 unknown https://doi.org/10.1016/0031-9422(80)80208-1
2-(3,3-dimethyloxiran-2-yl)-4-ethenyl-2-hydroxy-4,10-dimethyl-3H-pyrano[3,2-c]chromen-5-one 14464536 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(CC3(C)C=C)(C4C(O4)(C)C)O 342.40 unknown https://doi.org/10.3891/ACTA.CHEM.SCAND.46-0750
https://doi.org/10.1016/0031-9422(80)80208-1
https://doi.org/10.1016/0031-9422(80)83031-7
https://doi.org/10.1016/S0031-9422(97)00907-2
3-(3-Ethenyl-3,10-dimethyl-5-oxo-2,4-dihydropyrano[3,2-c]chromen-2-yl)-2-methylprop-2-enoic acid 162891315 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(C(C3)(C)C=C)C=C(C)C(=O)O 340.40 unknown https://doi.org/10.1016/S0031-9422(82)85048-6
3'-ethenyl-2-hydroxy-3,3',10'-trimethylspiro[2H-furan-5,2'-4H-pyrano[3,2-c]chromene]-5'-one 163096515 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC4(C=C(C(O4)O)C)C(C3)(C)C=C 340.40 unknown https://doi.org/10.1016/S0031-9422(82)85048-6
4-ethenyl-2-hydroxy-2-(1-hydroxy-2-methylprop-2-enyl)-4,10-dimethyl-3H-pyrano[3,2-c]chromen-5-one 14464540 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC(CC3(C)C=C)(C(C(=C)C)O)O 342.40 unknown https://doi.org/10.1016/0031-9422(80)80208-1
https://doi.org/10.1016/0031-9422(80)83031-7
https://doi.org/10.1016/S0031-9422(97)00907-2
https://doi.org/10.3891/ACTA.CHEM.SCAND.46-0750
4-ethenyl-3'-hydroxy-4,4',4',10-tetramethylspiro[3H-pyrano[3,2-c]chromene-2,2'-oxetane]-5-one 163009368 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC4(CC3(C)C=C)C(C(O4)(C)C)O 342.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
https://doi.org/10.1016/0031-9422(80)80208-1
4'-ethenyl-1,4',10'-trimethylspiro[3,6-dioxabicyclo[3.1.0]hexane-4,2'-3H-pyrano[3,2-c]chromene]-5'-one 74151535 Click to see CC1=C2C(=CC=C1)OC(=O)C3=C2OC4(CC3(C)C=C)C5C(O5)(CO4)C 340.40 unknown https://doi.org/10.1016/S0031-9422(97)00907-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown via CMAUP database
Chrysosplenetin 5281608 Click to see COC1=C(C=CC(=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 / Tannins / Hydrolyzable tannins
[(1R,18S,19S,21S,22S)-6,7,8,11,12,13,22-heptahydroxy-21-(hydroxymethyl)-3,16-dioxo-2,17,20-trioxatetracyclo[16.3.1.04,9.010,15]docosa-4,6,8,10,12,14-hexaen-19-yl] 3,4,5-trihydroxybenzoate 159801914 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C3C(C(C(O2)CO)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)O 634.50 unknown https://doi.org/10.1016/0031-9422(80)83031-7

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