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Ephedra altissima

Ephedra altissima - Unknown
Part: Unknown
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 UUID644028c131fc8947598299
Scientific name Ephedra altissima
Authority Desf.
First published in Fl. Atlant. 2: 371, t. 253. 1799

Description Top

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Ephedra altissima is a green, dioecious shrub that is native to the western Sahara and the Canary Islands. It is commonly cultivated as an ornamental plant and has medicinal uses. This plant prefers well-drained, loamy soil and can be found at elevations between 10-700 meters above sea level. It is hardy and resistant to drought and lime. The plant has been classified in different sections and tribes, but is currently placed in section Ephedra. It is not considered to be under any major threat and is not found in any protected areas. The plant contains alkaloid ephedrine, which is used in the treatment of respiratory issues. Different varieties of this plant can be found in different regions.

Synonyms Top

Scientific name Authority First published in
Chaetocladus altissima (Desf.) J.Nelson Pinaceae : 162 (1866)

Common names Top

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Language Common/alternative name
English high-climbing jointfir
Arabic علندى عالية
Bulgarian висока ефедра

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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No forms added yet.

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-0000794288
UNII 5HI7H5OVFV
USDA Plants EPAL3
Tropicos 14300058
INPN 96098
KEW urn:lsid:ipni.org:names:60459745-2
The Plant List kew-332855
PaleoBotany 72723
Open Tree Of Life 99235
Observations.org 440779
NCBI Taxonomy 3391
IUCN Red List 201672
IPNI 383350-1
iNaturalist 340447
iNaturalist 340430
iNaturalist 340448
GBIF 2653284
Freebase /m/04gn513
EPPO EPEAT
EOL 1156309
Elurikkus 269129
Calflora (Californian flora) 8553
USDA GRIN 15214
Wikipedia Ephedra_altissima
CMAUP NPO19350

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
Phytochemical Screening, Antioxidant Potential, and LC–ESI–MS Profiling of Ephedra alata and Ephedra altissima Seeds Naturally Growing in Tunisia Mahmoudi M, Boughalleb F, Maaloul S, Mabrouk M, Abdellaoui R Appl Biochem Biotechnol 31-Jan-2023
PMCID:PMC9887572
doi:10.1007/s12010-023-04370-8
PMID:36719522
Herbgenomics: Decipher molecular genetics of medicinal plants Sun W, Xu Z, Song C, Chen S Innovation (Camb) 14-Sep-2022
PMCID:PMC9529535
doi:10.1016/j.xinn.2022.100322
PMID:36199278
Bioguided Isolation of Active Compounds from Rhamnus alaternus against Methicillin-Resistant Staphylococcus aureus (MRSA) and Panton-Valentine Leucocidin Positive Strains (MSSA-PVL) Zeouk I, Ouedrhiri W, Sifaoui I, Bazzocchi IL, Piñero JE, Jiménez IA, Lorenzo-Morales J, Bekhti K Molecules 19-Jul-2021
PMCID:PMC8306708
doi:10.3390/molecules26144352
PMID:34299627
Potential Toxicity of Medicinal Plants Inventoried in Northeastern Morocco: An Ethnobotanical Approach Kharchoufa L, Bouhrim M, Bencheikh N, Addi M, Hano C, Mechchate H, Elachouri M Plants (Basel) 31-May-2021
PMCID:PMC8226742
doi:10.3390/plants10061108
PMID:34072709
Antistaphylococcal Activity and Phytochemical Analysis of Crude Extracts of Five Medicinal Plants Used in the Center of Morocco against Dermatitis Zeouk I, Balouiri M, Bekhti K Int J Microbiol 04-Nov-2019
PMCID:PMC6874926
doi:10.1155/2019/1803102
PMID:31781227
The organization of nuclear ribosomal DNA in gnetophytes – physically separate and physically linked arrangements of 35S and 5S genes. A commentary on: ‘Remarkable variation of ribosomal DNA organization and copy number in gnetophytes, a distinct lineage of gymnosperms’ Renner S, Sousa dos Santos A Ann Bot 20-May-2019
PMCID:PMC6526311
doi:10.1093/aob/mcz056
PMID:31106810
Remarkable variation of ribosomal DNA organization and copy number in gnetophytes, a distinct lineage of gymnosperms Wang W, Wan T, Becher H, Kuderova A, Leitch IJ, Garcia S, Leitch AR, Kovařík A Ann Bot 27-Sep-2018
PMCID:PMC6526317
doi:10.1093/aob/mcy172
PMID:30265284
Diversity of desert rangelands of Tunisia Gamoun M, Belgacem AO, Louhaichi M Plant Divers 20-Aug-2018
PMCID:PMC6224667
doi:10.1016/j.pld.2018.06.004
PMID:30740567
Chemical composition of various Ephedra species Ibragic S, Sofić E Bosn J Basic Med Sci 01-Aug-2015
PMCID:PMC4594322
doi:10.17305/bjbms.2015.539
PMID:26295290
Crystal structure of cis-2-(2-carb­oxy­cyclo­prop­yl)glycine (CCG-III) monohydrate Lindeman S, Wallock NJ, Donaldson WA Acta Crystallogr E Crystallogr Commun 24-Jun-2015
PMCID:PMC4518997
doi:10.1107/S2056989015011500
PMID:26279882
Surviving in Mountain Climate Refugia: New Insights from the Genetic Diversity and Structure of the Relict Shrub Myrtus nivellei (Myrtaceae) in the Sahara Desert Migliore J, Baumel A, Juin M, Fady B, Roig A, Duong N, Médail F PLoS One 18-Sep-2013
PMCID:PMC3776782
doi:10.1371/journal.pone.0073795
PMID:24058489
Development of 2′-substituted (2S,1′R,2′S)-2-(carboxycyclopropyl)glycine analogues as potent N-methyl-d-aspartic acid receptor agonists Risgaard R, Nielsen SD, Hansen KB, Jensen CM, Nielsen B, Traynelis SF, Clausen RP J Med Chem 09-May-2013
PMCID:PMC3689883
doi:10.1021/jm400346a
PMID:23614571
Response of γδ T cells to plant-derived tannins Holderness J, Hedges JF, Daughenbaugh K, Kimmel E, Graff J, Freedman B, Jutila MA Crit Rev Immunol 01-Jan-2008
PMCID:PMC2751790
doi:10.1615/critrevimmunol.v28.i5.20
PMID:19166386
On the evolutionary history of Ephedra: Cretaceous fossils and extant molecules Rydin C, Pedersen KR, Friis EM Proc Natl Acad Sci U S A 15-Nov-2004
PMCID:PMC534533
doi:10.1073/pnas.0407588101
PMID:15545612
Four cyclopropane amino acids from Ephedra Alvin N. Starratt, Stanley Caveney Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(95)00342-5

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Benzyl 2,6-dimethoxybenzoate 370912 Click to see COC1=C(C(=CC=C1)OC)C(=O)OCC2=CC=CC=C2 272.29 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Isovouacapenol D 10905866 Click to see CC1=C2CC(C3(C(CCCC3(C2=CC4=C1C=CO4)C)(C)C)O)OC(=O)C5=CC=CC=C5 418.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Sebacic Acid 5192 Click to see C(CCCCC(=O)O)CCCC(=O)O 202.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10698321 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)C 572.60 unknown via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-5,6,6a,7,11,11a-hexahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10531102 Click to see CC1C2C(CC3=C1C=CO3)C4(CC=CC(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)C 570.60 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f]benzofuran-5-yl] (E)-3-phenylprop-2-enoate 6479669 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C=CC5=CC=CC=C5)O)(C)C)C 464.60 unknown via CMAUP database
[(4R,4aS,5R,6aR,11aS,11bR)-5-benzoyloxy-4a-hydroxy-4,11b-dimethyl-7-methylidene-1,2,3,5,6,6a,11,11a-octahydronaphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate 10951647 Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3=C)C=CO4)OC(=O)C5=CC=CC=C5)O)C)COC(=O)C6=CC=CC=C6 540.60 unknown via CMAUP database
Isovouacapenol A 636673 Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3=C)C=CO4)OC(=O)C5=CC=CC=C5)O)C)C 420.50 unknown via CMAUP database
Isovouacapenol B 11812203 Click to see CC1(CCCC2(C1(C(CC3C2CC4=C(C3(C)O)C=CO4)OC(=O)C5=CC=CC=C5)O)C)C 438.60 unknown via CMAUP database
Isovouacapenol C 3009285 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C 438.60 unknown via CMAUP database
Pulcharrin G 11750983 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C5=CC=CC=C5)O)O)(C)C)C 438.60 unknown via CMAUP database
Pulcherrimin F 11375664 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C)OC(=O)C5=CC=CC=C5)O)(C)C(=O)O)C 510.60 unknown via CMAUP database
Pulcherrin D 54597502 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(CC2OC(=O)C)O)(C)C)C 360.50 unknown via CMAUP database
Pulcherrin E 54597503 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2OC(=O)C)O)O)(C)C)C 376.50 unknown via CMAUP database
Pulcherrin F 54597504 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C)O)(C)C)C 376.50 unknown via CMAUP database
Pulcherrin H 54597566 Click to see CC1C2CCC3(C(C(CCC3(C2CC4=C1C=CO4)C)OC(=O)C5=CC=CC=C5)(C)C)O 422.60 unknown via CMAUP database
Pulcherrin I 54597567 Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O)OC(=O)C5=CC=CC=C5 422.60 unknown via CMAUP database
Pulcherrin J 54597568 Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O)OC(=O)C=CC5=CC=CC=C5 448.60 unknown via CMAUP database
Pulcherrin K 53388795 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C=O)C 452.50 unknown via CMAUP database
Pulcherrin L 53388797 Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)COC(=O)C5=CC=CC=C5)O)O 438.60 unknown via CMAUP database
Pulcherrin M 54597569 Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCCC3(C)C(=O)O)C)O)OC(=O)C5=CC=CC=C5 452.50 unknown via CMAUP database
Pulcherrin O 53388938 Click to see CC(=O)OC1C(C2C(CC3=C(C2C(=O)OC)C=CO3)C4(C1(C(C(CC4)OC(=O)C5=CC=CC=C5)(C)C)O)C)O 540.60 unknown via CMAUP database
Vouacapen-5alpha-ol 73354918 Click to see CC1C2CCC3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(7S,11S)-3,7,11,15-Tetramethyl-2-hexadecene-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R,6R,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 42433495 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
(1S,4R,6S,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 7067459 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
7-Hydroxycadalene 608115 Click to see CC1=C2C=C(C(=CC2=C(C=C1)C(C)C)C)O 214.30 unknown via CMAUP database
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Teucladiol 16046185 Click to see CC(C)C1CCC(=C)C2CCC(C2C1O)(C)O 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-3-acetyloxy-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10627788 Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)OC(=O)C)C 630.70 unknown via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 11157932 Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C)OC(=O)C5=CC=CC=C5)O)(C)C(=O)O)OC(=O)C6=CC=CC=C6)C 630.70 unknown via CMAUP database
(8beta,10beta,14alpha)-6beta,7beta-Bis(benzoyloxy)-3beta,5alpha-dihydroxy-12,16-epoxycassa-12,15-dien-19-oic acid 10698605 Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C(C2OC(=O)C5=CC=CC=C5)OC(=O)C6=CC=CC=C6)O)(C)C(=O)O)O)C 588.60 unknown via CMAUP database
Pulcherrin N 53388796 Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCC(C3(C)C(=O)O)OC(=O)C5=CC=CC=C5)C)O)OC(=O)C6=CC=CC=C6 572.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 7-hydroxysteroids / 7-alpha-hydroxysteroids
Pulcherrin P 53388939 Click to see CC(=O)OCC1(C(CCC2(C1(C(C(C3C2CC4=C(C3C(=O)OC)C=CO4)OC(=O)C)O)O)C)OC(=O)C5=CC=CC=C5)C 598.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
(2S,1'S,2'S)-2-(carboxycyclopropyl)glycine 5310956 Click to see C1C(C1C(=O)O)C(C(=O)O)N 159.14 unknown https://doi.org/10.1016/0031-9422(95)00342-5
2-[Amino(carboxy)methyl]cyclopropane-1-carboxylic acid 1271 Click to see C1C(C1C(=O)O)C(C(=O)O)N 159.14 unknown https://doi.org/10.1016/0031-9422(95)00342-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(1R,2S)-2-((S)-Amino(carboxy)methyl)cyclopropanecarboxylic acid 5310957 Click to see C1C(C1C(=O)O)C(C(=O)O)N 159.14 unknown https://doi.org/10.1016/0031-9422(95)00342-5
(1S,2R)-2-[(S)-Amino(carboxy)methyl]cyclopropane-1-carboxylic acid 5310958 Click to see C1C(C1C(=O)O)C(C(=O)O)N 159.14 unknown https://doi.org/10.1016/0031-9422(95)00342-5
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
Neocaesalpin E 11450901 Click to see CC1C2CCC3(C(CCCC3(C2CC4(C1=CC(=O)O4)OC)C)(C)C)O 348.50 unknown via CMAUP database
Neocaesalpin F 11386164 Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C 484.60 unknown via CMAUP database
Neocaesalpin G 11295185 Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C=CC5=CC=CC=C5)O)(C)C)C 510.60 unknown via CMAUP database
Pulcherrin Q 53388940 Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C5C2O5)O)(C)C)OC(=O)C6=CC=CC=C6)C 436.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Quercimeritrin 5282160 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC=CC=C3)C(=C1)OC 284.31 unknown via CMAUP database
(2S)-5,7-Dimethoxy-3',4'-methylenedioxyflavanone 10336604 Click to see COC1=CC2=C(C(=O)CC(O2)C3=CC4=C(C=C3)OCO4)C(=C1)OC 328.30 unknown via CMAUP database
4H-1-Benzopyran-4-one, 2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy- 11681403 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC4=C(C=C3)OCO4 326.30 unknown via CMAUP database
5,7-Dimethoxyflavone 88881 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 282.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
16-Hydroxy-18-methoxy-6,8,12,21-tetraoxapentacyclo[11.8.0.02,10.05,9.015,20]henicosa-1(13),2(10),3,5(9),15,17,19-heptaen-14-one 44260091 Click to see COC1=CC(=C2C(=C1)OC3=C(C2=O)OCC4=C3C=CC5=C4OCO5)O 340.30 unknown via CMAUP database
6-Methoxypulcherrimin 44260092 Click to see COC1=C(C(=C2C(=C1)OC3=C(C2=O)OCC4=C3C=CC5=C4OCO5)O)OC 370.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids
(3E)-3-(2,4-Dimethoxybenzylidene)-7-hydroxychroman-4-one 101356812 Click to see COC1=CC(=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)OC 312.30 unknown via CMAUP database
(3E)-3-(4-Methoxybenzylidene)-7-methoxychroman-4-one 6507117 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)OC 296.30 unknown via CMAUP database
(3E)-3-[(3,4-dimethoxyphenyl)methylidene]-7-methoxychromen-4-one 5783568 Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC(=C(C=C3)OC)OC)CO2 326.30 unknown via CMAUP database
(e)-7-Hydroxy-3-(3',4',5'-trimethoxybenzylidene) chroman-4-one 16082056 Click to see COC1=CC(=CC(=C1OC)OC)C=C2COC3=C(C2=O)C=CC(=C3)O 342.30 unknown via CMAUP database
3-(4-Hydroxybenzylidene)-7-methoxy-2,3-dihydro-4H-1-benzopyran-4-one 14079440 Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC=C(C=C3)O)CO2 282.29 unknown via CMAUP database
3-[(E)-1,3-Benzodioxole-5-ylmethylene]-7-hydroxy-2,3-dihydro-4H-1-benzopyran-4-one 18778791 Click to see C1C(=CC2=CC3=C(C=C2)OCO3)C(=O)C4=C(O1)C=C(C=C4)O 296.27 unknown via CMAUP database
3-[(E)-1,3-Benzodioxole-5-ylmethylene]-7-methoxy-2,3-dihydro-4H-1-benzopyran-4-one 101489712 Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC4=C(C=C3)OCO4)CO2 310.30 unknown via CMAUP database
3-[(E)-3-Hydroxy-4-methoxybenzylidene]-6,7-dimethoxy-2,3-dihydro-4H-1-benzopyran-4-one 44475180 Click to see COC1=C(C=C(C=C1)C=C2COC3=CC(=C(C=C3C2=O)OC)OC)O 342.30 unknown via CMAUP database
3-[(E)-3-Hydroxy-4-methoxybenzylidene]-7-hydroxy-2,3-dihydro-4H-1-benzopyran-4-one 13846662 Click to see COC1=C(C=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)O 298.29 unknown via CMAUP database
Bonducellin 14079439 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O 282.29 unknown via CMAUP database
Isobonducellin 10423880 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O 282.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 51533159 Click to see COC1=CC=C(C=C1)CC2COC3=C(C2=O)C=CC(=C3)O 284.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2'-Hydroxy-2,3,4',6'-tetramethoxychalcone 10337542 Click to see COC1=CC=CC(=C1OC)C=CC(=O)C2=C(C=C(C=C2OC)OC)O 344.40 unknown via CMAUP database
4,2'-Dihydroxy-4'-methoxychalcone 6537040 Click to see COC1=CC(=C(C=C1)C(=O)C=CC2=CC=C(C=C2)O)O 270.28 unknown via CMAUP database

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