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Ephedra intermedia

Ephedra intermedia - 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 UUID644028c4a0991403997842
Scientific name Ephedra intermedia
Authority Schrenk & C.A.Mey.
First published in Mém. Acad. Imp. Sci. Saint-Pétersbourg, Sér. 6, Sci. Math., Seconde Pt. Sci. Nat. 7(2): 278 (1846)

Description Top

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Ephedra intermedia, also known as Zhong Ma Huang, is a species of plant native to various regions including Siberia, Central Asia, and China. It can be found in a variety of habitats such as deserts, grasslands, and river valleys, and can grow up to 1 meter tall. The plant produces separate male and female strobili, requiring both to produce seeds. It was first described in 1846 and has been classified in different sections and tribes by different botanists. In 1996, it was placed in section Ephedra without a designated tribe by Robert A. Price.

Synonyms Top

Scientific name Authority First published in
Ephedra ferganensis V.A.Nikitin Fl. Tadzhiksk. S.S.R. 1: 504 (1957)
Ephedra intermedia var. persica Stapf Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 56(2): 63. 1889
Ephedra intermedia var. schrenkii Stapf Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 56(2): 62. 1889
Ephedra intermedia var. tibetica Stapf Denkschr. Kaiserl. Akad. Wiss., Wien. Math.-Naturwiss. Kl. 56(2): 63. 1889
Ephedra microsperma V.A.Nikitin Fl. Tadzhiksk. S.S.R. 1: 503 (1957)
Ephedra persica (Stapf) V.A.Nikitin Fl. Tadzhiksk. S.S.R. 1: 504 (1957)
Ephedra tesquorum V.A.Nikitin Fl. Tadzhiksk. S.S.R. 1: 503 (1957)
Ephedra tibetica (Stapf) V.A.Nikitin Fl. Tadzhiksk. S.S.R. 1: 503 (1957)
Ephedra valida V.A.Nikitin Fl. Tadzhiksk. S.S.R. 1: 504 (1957)
Ephedra vulgaris var. submonostachys Boiss. & Buhse Aufz. Transk. Pers. Pfl. Wien 204. 1860

Common names Top

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Language Common/alternative name
Azerbaijani ortaboylu acılıqotu
Bulgarian средна ефедра
Czech chvojník prostřední
Persian ارمک میانه
Finnish siniefedra
Japanese 中麻黄
Japanese チュウマオウ
Kazakh Қызыл тамыр
Russian Хвойник средний
Chinese 中麻黄
Chinese 中麻黄*
Chinese 苡芭菊
Chinese 麻黄
Chinese 麻黄根

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • China
      • Inner Mongolia
      • Tibet
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • West Siberia
    • Western Asia
      • Afghanistan
      • Iran

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000794387
UNII U377004X2E
Tropicos 14300004
KEW urn:lsid:ipni.org:names:383409-1
The Plant List kew-332952
PaleoBotany 51130
Open Tree Of Life 202432
Observations.org 129315
NCBI Taxonomy 173278
IUCN Red List 201664
IPNI 383409-1
iNaturalist 135476
GBIF 2653256
Freebase /m/04gw80v
EPPO EPEIN
EOL 1156332
Elurikkus 269119
USDA GRIN 15229
Wikipedia Ephedra_intermedia
CMAUP NPO21507

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
Exploring the immune-inflammatory mechanism of Maxing Shigan Decoction in treating influenza virus A-induced pneumonia based on an integrated strategy of single-cell transcriptomics and systems biology Zhang S, Li B, Zeng L, Yang K, Jiang J, Lu F, Li L, Li W Eur J Med Res 15-Apr-2024
PMCID:PMC11017673
doi:10.1186/s40001-024-01777-9
PMID:38622728
Distribution Pattern of Suitable Areas and Corridor Identification of Endangered Ephedra Species in China Zhang H, Li J, Zou H, Wang Z, Zhu X, Zhang Y, Liu Z Plants (Basel) 20-Mar-2024
PMCID:PMC10975542
doi:10.3390/plants13060890
PMID:38592953
Assessing the efficacy and safety of Yinqiao powder-maxing Ganshi decoction in the treatment of the major symptoms of mild and moderate COVID-19 by telemedicine–study protocol for a randomized, double-blind, placebo-controlled trial Sum CH, Li TW, Zhang H, Hung HY, Fong BY, Lin WL, Chow TY, Leung KC, Lo CW, Chia CP, Chan KL, Lin ZX Front Pharmacol 08-Jan-2024
PMCID:PMC10800621
doi:10.3389/fphar.2023.1261338
PMID:38259270
Exploring the potential of Crotalaria juncea flower extracts as a source of antioxidants, antimicrobials, and cytoprotective agents for biomedical applications Mahasawat P, Boukaew S, Prasertsan P BioTechnologia (Pozn) 21-Dec-2023
PMCID:PMC10777724
doi:10.5114/bta.2023.132772
PMID:38213478
Essential Oils in Cervical Cancer: Narrative Review on Current Insights and Future Prospects Abd Rashid N, Mohamad Najib NH, Abdul Jalil NA, Teoh SL Antioxidants (Basel) 13-Dec-2023
PMCID:PMC10740549
doi:10.3390/antiox12122109
PMID:38136228
Distribution Patterns of Gymnosperm Species along Elevations on the Qinghai–Tibet Plateau: Effects of Climatic Seasonality, Energy–Water, and Physical Tolerance Variables Umair M, Hu X, Cheng Q, Ali S, Ni J Plants (Basel) 04-Dec-2023
PMCID:PMC10708526
doi:10.3390/plants12234066
PMID:38068701
The Distribution Characteristics of Vegetation in the Subrange of the Altai Mountains, Xinjiang Cao Q, Wei Y, Li W, Feng Y, Abduraimov OS Plants (Basel) 20-Nov-2023
PMCID:PMC10675357
doi:10.3390/plants12223915
PMID:38005812
Could Natural Products Help in the Control of Obesity? Current Insights and Future Perspectives Park J, Nurkolis F, Won H, Yang J, Oh D, Jo H, Choi J, Chung S, Kurniawan R, Kim B Molecules 13-Sep-2023
PMCID:PMC10534927
doi:10.3390/molecules28186604
PMID:37764380
Relationship among Chinese herb polysaccharide (CHP), gut microbiota, and chronic diarrhea and impact of CHP on chronic diarrhea Xue H, Mei C, Wang F, Tang X Food Sci Nutr 06-Aug-2023
PMCID:PMC10563694
doi:10.1002/fsn3.3596
PMID:37823142
Potential herb–drug interactions between anti-COVID-19 drugs and traditional Chinese medicine Ye L, Fan S, Zhao P, Wu C, Liu M, Hu S, Wang P, Wang H, Bi H Acta Pharm Sin B 05-Jun-2023
PMCID:PMC10239737
doi:10.1016/j.apsb.2023.06.001
PMID:37360014
Study on wild medicinal plant resources and their applied ethnology in multiethnic areas of the Gansu–Ningxia–Inner Mongolia intersection zone Xie J, Luo C, Yang X, Ren Y, Zhang X, Chen H, Zhao Y, Liu S, Wu F J Ethnobiol Ethnomed 20-May-2023
PMCID:PMC10199607
doi:10.1186/s13002-023-00585-5
PMID:37210577
The use of Ephedra herbs in the treatment of COVID-19 Sadeghi Dousari A, Karimian Amroabadi M, Soofi Neyestani Z, Taati Moghadam M, Satarzadeh N Avicenna J Phytomed 01-May-2023
PMCID:PMC10465882
doi:10.22038/AJP.2022.21607
PMID:37654998
Modeling for Predicting the Potential Geographical Distribution of Three Ephedra Herbs in China Guo L, Gao Y, He P, He Y, Meng F Plants (Basel) 09-Feb-2023
PMCID:PMC9963152
doi:10.3390/plants12040787
PMID:36840134
Interaction between Chinese medicine and digoxin: Clinical and research update Zhuang W, He T, Jia BB, Wang ZZ, Zhang L, Dong XZ, Xi SY Front Pharmacol 07-Feb-2023
PMCID:PMC9941676
doi:10.3389/fphar.2023.1040778
PMID:36825153
Disadvantaged Economic Conditions and Stricter Border Rules Shape Afghan Refugees’ Ethnobotany: Insights from Kohat District, NW Pakistan Shah AA, Badshah L, Khalid N, Shah MA, Manduzai AK, Faiz A, De Chiara M, Mattalia G, Sõukand R, Pieroni A Plants (Basel) 28-Jan-2023
PMCID:PMC9918957
doi:10.3390/plants12030574
PMID:36771658

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
> Benzenoids / Benzene and substituted derivatives / Phenylpropanes
(-)-Ephedrinium 6922965 Click to see CC(C(C1=CC=CC=C1)O)[NH2+]C 166.24 unknown via CMAUP database
(-)-Pseudoephedrine 62946 Click to see CC(C(C1=CC=CC=C1)O)NC 165.23 unknown https://doi.org/10.1248/CPB.28.2900
(+)-N-Methylephedrine 102023 Click to see CC(C(C1=CC=CC=C1)O)N(C)C 179.26 unknown via CMAUP database
(+)-N-Methylpseudoephedrine 7059596 Click to see CC(C(C1=CC=CC=C1)O)N(C)C 179.26 unknown https://doi.org/10.1248/CPB.51.1382
(1R,2R)-2-(dimethylamino)-1-phenylpropan-1-ol 5706040 Click to see CC(C(C1=CC=CC=C1)O)N(C)C 179.26 unknown via CMAUP database
(1r,2s)-n-Methylephedrine 6918907 Click to see CC(C(C1=CC=CC=C1)O)[NH+](C)C 180.27 unknown via CMAUP database
(1S,2S)-(+)-norpseudoephedrine 6918945 Click to see CC(C(C1=CC=CC=C1)O)[NH3+] 152.21 unknown via CMAUP database
(1S)-1-Phenyl-2-(methylamino)-1-propanol 11972440 Click to see CC(C(C1=CC=CC=C1)O)NC 165.23 unknown via CMAUP database
(2S)-2-amino-1-((1,2,3,4,5,6-14C6)cyclohexatrienyl)propan-1-ol 10080695 Click to see CC(C(C1=CC=CC=C1)O)N 163.16 unknown via CMAUP database
[(1R,2S)-1-hydroxy-1-phenylpropan-2-yl]-dimethylazanium;chloride 11954231 Click to see CC(C(C1=CC=CC=C1)O)[NH+](C)C.[Cl-] 215.72 unknown via CMAUP database
1-Phenyl-1,2-propanedione 11363 Click to see CC(=O)C(=O)C1=CC=CC=C1 148.16 unknown via CMAUP database
2-Amino-1-phenyl-1-propanol 4786 Click to see CC(C(C1=CC=CC=C1)O)N 151.21 unknown via CMAUP database
Cathine 441457 Click to see CC(C(C1=CC=CC=C1)O)N 151.21 unknown via CMAUP database
d-Ephedrine 9457 Click to see CC(C(C1=CC=CC=C1)O)NC 165.23 unknown via CMAUP database
DL-Methylephedrine saccharinate 9851505 Click to see CC(C(C1=CC=CC=C1)O)N(C)C 179.26 unknown https://doi.org/10.1055/S-2006-962342
Ephedrine 9294 Click to see CC(C(C1=CC=CC=C1)O)NC 165.23 unknown https://doi.org/10.1248/CPB.51.1382
https://doi.org/10.1055/S-2006-962342
hydron;(1S,2S)-2-(methylamino)-1-phenylpropan-1-ol;chloride 25137849 Click to see [H+].CC(C(C1=CC=CC=C1)O)NC.[Cl-] 201.69 unknown via CMAUP database
Methylephedrine 64782 Click to see CC(C(C1=CC=CC=C1)O)N(C)C 179.26 unknown https://doi.org/10.1248/CPB.51.1382
N-Methylephedrine 4374 Click to see CC(C(C1=CC=CC=C1)O)N(C)C 179.26 unknown via CMAUP database
Norephedrine 26934 Click to see CC(C(C1=CC=CC=C1)O)N 151.21 unknown https://doi.org/10.1055/S-2006-962342
Norpseudoephedrine 162265 Click to see CC(C(C1=CC=CC=C1)O)N 151.21 unknown via CMAUP database
Phenylpropanolamine 10297 Click to see CC(C(C1=CC=CC=C1)O)N 151.21 unknown via CMAUP database
Pseudoephedrine 7028 Click to see CC(C(C1=CC=CC=C1)O)NC 165.23 unknown https://doi.org/10.1248/CPB.51.1382
Racephedrine 5032 Click to see CC(C(C1=CC=CC=C1)O)NC 165.23 unknown https://doi.org/10.1248/CPB.28.2900
> Benzenoids / Phenol ethers / Anisoles
4-Methoxystyrene 12507 Click to see COC1=CC=C(C=C1)C=C 134.17 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
(-)-Synephrine 854067 Click to see CNCC(C1=CC=C(C=C1)O)O 167.20 unknown via CMAUP database
(+)-Synephrine 667452 Click to see CNCC(C1=CC=C(C=C1)O)O 167.20 unknown via CMAUP database
(R)-synephrine 6951208 Click to see C[NH2+]CC(C1=CC=C(C=C1)O)O 168.21 unknown via CMAUP database
Synephrine 7172 Click to see CNCC(C1=CC=C(C=C1)O)O 167.20 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonacosane 12409 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCC 408.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Nonacosanol 243696 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCO 424.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
13-Pentacosanol 14926689 Click to see CCCCCCCCCCCCC(CCCCCCCCCCCC)O 368.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,4-Cineole 10106 Click to see CC(C)C12CCC(O1)(CC2)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-alpha-Terpineol 443162 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3R,4R,5R,6S)-2-[(2R,3S,4R,5R,6R)-6-[[3,12-dihydroxy-17-[(5R)-5-(2-hydroxypropan-2-yl)-2-methyloxolan-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-6-yl]oxy]-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 6325857 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3CC4(C(CC(C5C4(CCC5C6(CCC(O6)C(C)(C)O)C)C)O)C7(C3C(C(CC7)O)(C)C)C)C)CO)O)O)O 801.00 unknown via CMAUP database
(4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2R,3R,4S,5S,6S)-3,4,5-trihydroxy-6-methoxycarbonyloxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 21626559 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)C(=O)OC)O)O)O)C)C(=O)O)C 662.80 unknown via CMAUP database
CID 102004874 102004874 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C(=O)O)C 634.80 unknown via CMAUP database
Ecliptasaponin A 476537 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C(=O)O)C 634.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
methyl 6-[(10S,13R,17R)-7,15-dihydroxy-4,4,10,13,14-pentamethyl-3,11-dioxo-2,5,6,7,12,15,16,17-octahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methyl-4-oxoheptanoate 5319630 Click to see CC(CC(=O)CC(C)C(=O)OC)C1CC(C2(C1(CC(=O)C3=C2C(CC4C3(CCC(=O)C4(C)C)C)O)C)C)O 530.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 6-hydroxysteroids
2-(methylamino)ethyl (2E)-2-(8-formyl-7,10-dihydroxy-1,4b,8-trimethyl-3,4,4a,5,6,7,8a,9,10,10a-decahydro-1H-phenanthren-2-ylidene)acetate 5476322 Click to see CC1C2C(CCC1=CC(=O)OCCNC)C3(CCC(C(C3CC2O)(C)C=O)O)C 407.50 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Tertiary amines / Trialkylamines
N,N-Dimethylisopropylamine 70452 Click to see CC(C)N(C)C 87.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
Ethanol 702 Click to see CCO 46.07 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
Nonacosan-10-one 441490 Click to see CCCCCCCCCCCCCCCCCCCC(=O)CCCCCCCCC 422.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(+)-Cathinone 149798 Click to see CC(C(=O)C1=CC=CC=C1)N 149.19 unknown via CMAUP database
2-Aminopropiophenone 107786 Click to see CC(C(=O)C1=CC=CC=C1)N 149.19 unknown via CMAUP database
Cathinone 62258 Click to see CC(C(=O)C1=CC=CC=C1)N 149.19 unknown via CMAUP database
> Organoheterocyclic compounds / Azolidines / Oxazolidines / Oxazolidinones
3,4-Dimethyl-5-phenyl-1,3-oxazolidin-2-one 237192 Click to see CC1C(OC(=O)N1C)C2=CC=CC=C2 191.23 unknown via CMAUP database
Ephedroxane 161171 Click to see CC1C(OC(=O)N1C)C2=CC=CC=C2 191.23 unknown via CMAUP database
> Organoheterocyclic compounds / Bi- and oligothiophenes
[5-(5-But-3-en-1-ynylthiophen-2-yl)thiophen-2-yl]methyl acetate 5315563 Click to see CC(=O)OCC1=CC=C(S1)C2=CC=C(S2)C#CC=C 288.40 unknown via CMAUP database
[5-(5-Thiophen-2-ylthiophen-2-yl)thiophen-2-yl]methyl acetate 5321832 Click to see CC(=O)OCC1=CC=C(S1)C2=CC=C(S2)C3=CC=CS3 320.50 unknown via CMAUP database
2,2':5',2''-Terthiophene 65067 Click to see C1=CSC(=C1)C2=CC=C(S2)C3=CC=CS3 248.40 unknown via CMAUP database
alpha-Terthienylmethanol 454740 Click to see C1=CSC(=C1)C2=CC=C(S2)C3=CC=C(S3)CO 278.40 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrazines
2,3,5,6-Tetramethylpyrazine 14296 Click to see CC1=C(N=C(C(=N1)C)C)C 136.19 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
5,6,8-trihydroxy-2-methylbenzo[g]chromen-4-one 5320218 Click to see CC1=CC(=O)C2=C(C3=C(C=C(C=C3C=C2O1)O)O)O 258.23 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyrrolidinylpyridines
Nicotine 89594 Click to see CN1CCCC1C2=CN=CC=C2 162.23 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Dihydrofuranoquinolines
O-Methylptelefolonium 148759 Click to see CC(=C)C1CC2=C(C3=C(C(=CC(=C3)OC)OC)[N+](=C2O1)C)OC 316.40 unknown via CMAUP database
> Organoheterocyclic compounds / Thiophenes / 2,5-disubstituted thiophenes
(2S)-1-chloro-4-(5-penta-1,3-diynylthiophen-2-yl)but-3-yn-2-ol 86310851 Click to see CC#CC#CC1=CC=C(S1)C#CC(CCl)O 248.73 unknown via CMAUP database
2-(1,3-Butadiynyl)-5-(3-butene-1-ynyl)thiophene 5315560 Click to see C=CC#CC1=CC=C(S1)C#CC#C 182.24 unknown via CMAUP database
> Organosulfur compounds / Thioethers / Aryl thioethers
Gs-39783 6604928 Click to see CSC1=NC(=C(C(=N1)NC2CCCC2)[N+](=O)[O-])NC3CCCC3 337.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
(-)-Epiafzelechin 443639 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC=C(C=C3)O)O 274.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,8,9-trihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-[1]benzofuro[3,2-c]chromen-6-one 6325048 Click to see C1=C(C=C2C(=C1O)C3=C(C4=CC(=C(C=C4O3)O)O)C(=O)O2)OC5C(C(C(C(O5)CO)O)O)O 462.40 unknown via CMAUP database
Demethylwedelolactone 5489605 Click to see C1=C(C=C2C(=C1O)C3=C(C4=CC(=C(C=C4O3)O)O)C(=O)O2)O 300.22 unknown via CMAUP database
Isodemethylwedelolactone 5318547 Click to see C1=C(C=C(C2=C1C3=C(C4=CC(=C(C=C4O3)O)O)C(=O)O2)O)O 300.22 unknown via CMAUP database
Wedelolactone 5281813 Click to see COC1=CC(=C2C(=C1)OC(=O)C3=C2OC4=CC(=C(C=C43)O)O)O 314.25 unknown via CMAUP database

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