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Solanum lyratum

Solanum lyratum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Solanum lyratum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Solanum lyratum - 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 UUID644041c04684b365958437
Scientific name Solanum lyratum
Authority Thunb.
First published in Fl. Jap. (Thunberg) 92. 1784.

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Solanum cathayanum C.Y.Wu & S.C.Huang Fl. Reipubl. Popul. Sin. 67(1): 84. 1978.
Solanum dichotomum Lour. Fl. Cochinch. 129. 1790.
Solanum dulcamara var. chinense Dunal Prodr. [A. P. de Candolle] 13(1): 79. 1852
Solanum dulcamara var. lyratum (Thunb.) Bonati
Solanum dulcamara var. pubescens Blume Bijdr. Fl. Ned. Ind. 13: 698. 1825
Solanum kayamae T.Yamaz. J. Jap. Bot. 68: 339. 1993.
Solanum lyratum Thunb. Syst. Veg., ed. 14 (J. A. Murray). 224. 1784 [May-Jun 1784]
Solanum lyratum var. filamentaceum Hayashi J. Geobot. 22: 4. 1974.
Solanum lyratum var. glabratum Maxim.
Solanum septemlobum var. indutum Hand.-Mazz. Oesterr. Bot. Z. 83: 234. 1934
Solanum lyratum f. purpuratum Konta & Katsuy. Bull. Natl. Sci. Mus. 31(1): 23. 2005.

Common names Top

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Language Common/alternative name
Japanese ヒヨドリジョウゴ
Korean 배풍등
lzh 白英
Chinese 北风藤
Chinese 白英 (植物)
Chinese 蔓茄
Chinese 白荚
Chinese 生毛鸡屎藤
Chinese 山甜菜
Chinese 千年不烂心
Chinese 鬼目
Chinese 蜀羊泉
Chinese 白英（排风藤）
Chinese 白英
Chinese 白毛藤
Chinese 排风藤
Chinese 苦茄

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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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
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
      • Tibet
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001029226
Tropicos 29604522
KEW urn:lsid:ipni.org:names:927300-1
The Plant List tro-29604522
Open Tree Of Life 693272
NCBI Taxonomy 230192
IPNI 927300-1
iNaturalist 367802
GBIF 2930006
Freebase /m/0nbdbpq
EPPO SOLLR
USDA GRIN 459142
Wikipedia Solanum_lyratum

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
Scopoletin: a review of its pharmacology, pharmacokinetics, and toxicity Gao XY, Li XY, Zhang CY, Bai CY Front Pharmacol 23-Feb-2024
PMCID:PMC10923241
doi:10.3389/fphar.2024.1268464
PMID:38464713
Traditional and contemporary herbal medicines in management of cancer: A scoping review Imtiaz I, Schloss J, Bugarcic A J Ayurveda Integr Med 23-Feb-2024
PMCID:PMC10901831
doi:10.1016/j.jaim.2024.100904
PMID:38395014
Antiherpetic Activity of a Root Exudate from Solanum lycopersicum Bajetto G, Arnodo D, Biolatti M, Trifirò L, Albano C, Pasquero S, Gugliesi F, Campo E, Spyrakis F, Prandi C, De Andrea M, Dell’Oste V, Visentin I, Blangetti M Microorganisms 11-Feb-2024
PMCID:PMC10892521
doi:10.3390/microorganisms12020373
PMID:38399777
Effects of Traditional Chinese Medicine “Fuzheng Qingdu Decoction” on Autonomic Function and Cancer-Related Symptoms in Patients with Advanced Gastric Cancer undergoing Chemotherapy: A Controlled Trial Yuan C, Wu S, Wu Y, Tian C, Wang Z, Zhang X Integr Cancer Ther 07-Feb-2024
PMCID:PMC10851715
doi:10.1177/15347354241229414
PMID:38323452
Isocorydine Exerts Anticancer Activity by Disrupting the Energy Metabolism and Filamentous Actin Structures of Oral Squamous Carcinoma Cells Zhou Q, Zhang Q, Liao L, Li Q, Qu H, Wang X, Zhou Y, Zhang G, Sun M, Zhang K, Zhang B Curr Issues Mol Biol 09-Jan-2024
PMCID:PMC10814041
doi:10.3390/cimb46010042
PMID:38248344
A real-world study and network pharmacology analysis of EGFR-TKIs combined with ZLJT to delay drug resistance in advanced lung adenocarcinoma Han X, Liang L, He C, Ren Q, Su J, Cao L, Zheng J BMC Complement Med Ther 21-Nov-2023
PMCID:PMC10664478
doi:10.1186/s12906-023-04213-3
PMID:37990309
Toxicity, arsenic speciation and characteristics of hyphenated techniques used for arsenic determination in vegetables. A review Sadee BA, Galali Y, Zebari SM RSC Adv 23-Oct-2023
PMCID:PMC10591994
doi:10.1039/d3ra05770d
PMID:37876652
Potential targets of natural medicines: preventing lung cancer pre-metastatic niche formation by regulating exosomes Zhu XY, Li J Front Oncol 28-Aug-2023
PMCID:PMC10493872
doi:10.3389/fonc.2023.1137007
PMID:37700835
Yao-Shan of traditional Chinese medicine: an old story for metabolic health Yang S, Yang H, Zhang Y Front Pharmacol 16-Aug-2023
PMCID:PMC10468577
doi:10.3389/fphar.2023.1194026
PMID:37663255
Elucidation of the anti-lung cancer mechanism of Juan-Liu-San-Jie prescription based on network pharmacology and experimental validation Wang Y, Pan Y, Luo Y, Wu J, Fang Z, Teng W, Guan Y, Li Y Heliyon 23-Jul-2023
PMCID:PMC10407049
doi:10.1016/j.heliyon.2023.e18298
PMID:37560652
Ginseng-containing traditional medicine preparations in combination with fluoropyrimidine-based chemotherapy for advanced gastric cancer: A systematic review and meta-analysis Hu J, Cheng M, Li Y, Shi B, He S, Yao Z, Jiang J, Yu H, He Z, Zhao Y, Zheng H, Hua B, Liu R PLoS One 17-Apr-2023
PMCID:PMC10109524
doi:10.1371/journal.pone.0284398
PMID:37068063
Fuzheng Nizeng Decoction regulated ferroptosis and endoplasmic reticulum stress in the treatment of gastric precancerous lesions: A mechanistic study based on metabolomics coupled with transcriptomics Chu YM, Wang TX, Jia XF, Yang Y, Shi ZM, Cui GH, Huang QY, Ye H, Zhang XZ Front Pharmacol 23-Nov-2022
PMCID:PMC9727497
doi:10.3389/fphar.2022.1066244
PMID:36506541
Phytochemical and pharmacological studies on Solanum lyratum: a review Zhao Y, Gao WK, Wang XD, Zhang LH, Yu HY, Wu HH Nat Prod Bioprospect 09-Nov-2022
PMCID:PMC9643311
doi:10.1007/s13659-022-00361-0
PMID:36348127
Stem cambial variants of Taiwan lianas Yang SZ, Chen PH, Chen JJ Bot Stud 24-Sep-2022
PMCID:PMC9509506
doi:10.1186/s40529-022-00358-5
PMID:36153445
Antitumor effects of Chinese herbal medicine compounds and their nano-formulations on regulating the immune system microenvironment Sun K, Wu L, Wang S, Deng W Front Oncol 23-Sep-2022
PMCID:PMC9540406
doi:10.3389/fonc.2022.949332
PMID:36212483

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
[(7R,8R)-7-[(2R)-2-methylbutanoyl]oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2R)-2,3-dihydroxy-2-[(1S)-1-hydroxyethyl]-3-methylbutanoate 163021335 Click to see CCC(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)O)(C(C)(C)O)O 399.50 unknown https://doi.org/10.1007/S10600-014-0827-X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1007/BF02974274
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1007/BF02974274
> Benzenoids / Phenols / Cresols / Meta cresols
4-[(4-Hydroxy-2,6-dimethylphenyl)methyl]-5,5-dimethyloxolan-2-one 74817673 Click to see CC1=CC(=CC(=C1CC2CC(=O)OC2(C)C)C)O 248.32 unknown https://doi.org/10.1248/CPB.57.408
Lyratol D 42604343 Click to see CC1=CC(=CC(=C1CC2CC(=O)OC2(C)C)C)O 248.32 unknown https://doi.org/10.1248/CPB.57.408
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
4-Hydroxy-3,5,5-trimethyl-4-(3-oxo-1-butenyl)-2-cyclohexen-1-one 440265 Click to see CC1=CC(=O)CC(C1(C=CC(=O)C)O)(C)C 222.28 unknown https://doi.org/10.1248/CPB.57.408
4-Hydroxy-4-(3-hydroxybut-1-enyl)-3,5,5-trimethylcyclohex-2-en-1-one 440244 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown https://doi.org/10.1248/CPB.57.408
Dehydrovomifoliol 688492 Click to see CC1=CC(=O)CC(C1(C=CC(=O)C)O)(C)C 222.28 unknown https://doi.org/10.1248/CPB.57.408
Vomifoliol 5280462 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown https://doi.org/10.1248/CPB.57.408
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,2R,4aR,6S,8aS)-6-[(2S)-1,2-dihydroxypropan-2-yl]-8a-methyl-4-methylidene-1,2,3,4a,5,6,7,8-octahydronaphthalene-1,2-diol 70697932 Click to see CC12CCC(CC1C(=C)CC(C2O)O)C(C)(CO)O 270.36 unknown https://doi.org/10.1248/CPB.57.408
(4aS,7R)-7-(2-hydroxypropan-2-yl)-1,4a-dimethyl-5,6,7,8-tetrahydronaphthalen-2-one 10868238 Click to see CC1=C2CC(CCC2(C=CC1=O)C)C(C)(C)O 234.33 unknown https://doi.org/10.1007/BF02978238
6-(1,2-Dihydroxypropan-2-yl)-8a-methyl-4-methylidene-1,2,3,4a,5,6,7,8-octahydronaphthalene-1,2-diol 74817672 Click to see CC12CCC(CC1C(=C)CC(C2O)O)C(C)(CO)O 270.36 unknown https://doi.org/10.1248/CPB.57.408
Lyratol C 42604342 Click to see CC12CCC(CC1C(=C)CC(C2O)O)C(C)(CO)O 270.36 unknown https://doi.org/10.1248/CPB.57.408
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids
(1S,2S,5S,6R,9S,10R,15S)-5-(5,6-dimethylhept-3-en-2-yl)-6,10-dimethyl-16,17-dioxapentacyclo[13.2.2.01,9.02,6.010,15]nonadec-18-en-13-ol 129316892 Click to see CC(C)C(C)C=CC(C)C1CCC2C1(CCC3C24C=CC5(C3(CCC(C5)O)C)OO4)C 428.60 unknown https://doi.org/10.1007/BF02978238
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
16-Dehydropregnenolone 92871 Click to see CC(=O)C1=CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 314.50 unknown https://doi.org/10.1007/BF02974274
3beta-Hydroxy-5alpha-pregn-16-en-20-one 1775252 Click to see CC(=O)C1=CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C 316.50 unknown https://doi.org/10.1007/BF02974274
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroid glucuronide conjugates
(2S,3S,4S,5R,6R)-6-[[(3S,8S,9S,10R,13S,14S,16S,17R)-17-[(2S,3R,6R)-3,7-dihydroxy-6-methylheptan-2-yl]-16-hydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxane-2-carboxylic acid 162883500 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6(C(C5CC=C4C3)CC(C6C(C)C(CCC(C)CO)O)O)C)C)C(=O)O)O)O)O)O)O 756.90 unknown https://doi.org/10.1248/CPB.37.1802
6-[[17-(3,7-dihydroxy-6-methylheptan-2-yl)-16-hydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-3,4-dihydroxy-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxane-2-carboxylic acid 14769366 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6(C(C5CC=C4C3)CC(C6C(C)C(CCC(C)CO)O)O)C)C)C(=O)O)O)O)O)O)O 756.90 unknown https://doi.org/10.1248/CPB.37.1802
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3R,4S,5S,6R)-2-[(2R)-4-[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-16-[(2R,3R,4S,5R,6R)-5-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methoxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163012979 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)OC 1227.30 unknown https://doi.org/10.1016/S0031-9422(00)80717-7
(2S,3R,4S,5R)-2-[(2S,3R,4S,5S,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13S,16S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-piperidine]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 101711963 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(CO9)O)O)O)O)O)C)C)C)NC1 872.00 unknown https://doi.org/10.1007/S10600-014-0827-X
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5R,6R)-5-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162868584 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)C)C)C)OC1 1033.20 unknown https://doi.org/10.1016/S0031-9422(00)80717-7
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5R,6R)-2-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(9S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 6325867 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)C)OC1 1033.20 unknown https://doi.org/10.1016/S0031-9422(00)80717-7
2-[2-[4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,6R,8S,9S,12R,13S,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 138115302 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)C)OC1 1035.20 unknown https://doi.org/10.1016/S0305-1978(00)00061-2
2-[4-[16-[5-[3,5-Dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-6-methoxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163012978 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(CO8)O)O)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)OC 1227.30 unknown https://doi.org/10.1016/S0031-9422(00)80717-7
2-[5-[3,5-Dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4-hydroxy-6-(hydroxymethyl)-2-(5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl)oxyoxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162868583 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)C)C)C)OC1 1033.20 unknown https://doi.org/10.1016/S0031-9422(00)80717-7
Aspidistrin 21670028 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(CO9)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)C)C)C)OC1 1033.20 unknown https://doi.org/10.1016/S0031-9422(00)80717-7
> Organoheterocyclic compounds / Naphthofurans
Atractylenolide I 5321018 Click to see CC1=C2CC3C(=C)CCCC3(C=C2OC1=O)C 230.30 unknown https://doi.org/10.1007/BF02978238
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1007/BF02974274
> 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 https://doi.org/10.1007/BF02974274
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanols
(3R,4S)-3-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-3,4-dihydro-2H-chromene-4,7-diol 46861704 Click to see CC(=CCC1=C(C=CC(=C1O)C2COC3=C(C2O)C=CC(=C3)O)O)C 342.40 unknown https://doi.org/10.1248/CPB.58.840
3-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-3,4-dihydro-2H-chromene-4,7-diol 75216075 Click to see CC(=CCC1=C(C=CC(=C1O)C2COC3=C(C2O)C=CC(=C3)O)O)C 342.40 unknown https://doi.org/10.1248/CPB.58.840
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3R,4S)-3-(2-hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-chromene-4,7-diol 46861702 Click to see COC1=CC(=C(C=C1)C2COC3=C(C2O)C=CC(=C3)O)O 288.29 unknown https://doi.org/10.1248/CPB.58.840
3-(2-Hydroxy-4-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-4,7-diol 74089773 Click to see COC1=CC(=C(C=C1)C2COC3=C(C2O)C=CC(=C3)O)O 288.29 unknown https://doi.org/10.1248/CPB.58.840
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
(3R,4S)-3-(5-hydroxy-2,2-dimethylchromen-6-yl)-3,4-dihydro-2H-chromene-4,7-diol 46861703 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C3COC4=C(C3O)C=CC(=C4)O)C 340.40 unknown https://doi.org/10.1248/CPB.58.840
(3R)-6-[(3R,4S)-4,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl]-2,2-dimethyl-3,4-dihydrochromene-3,5-diol 162998245 Click to see CC1(C(CC2=C(O1)C=CC(=C2O)C3COC4=C(C3O)C=CC(=C4)O)O)C 358.40 unknown https://doi.org/10.1248/CPB.58.840
3-(5-hydroxy-2,2-dimethylchromen-6-yl)-3,4-dihydro-2H-chromene-4,7-diol 75214730 Click to see CC1(C=CC2=C(O1)C=CC(=C2O)C3COC4=C(C3O)C=CC(=C4)O)C 340.40 unknown https://doi.org/10.1248/CPB.58.840
6-(4,7-dihydroxy-3,4-dihydro-2H-chromen-3-yl)-2,2-dimethyl-3,4-dihydrochromene-3,5-diol 75214731 Click to see CC1(C(CC2=C(O1)C=CC(=C2O)C3COC4=C(C3O)C=CC(=C4)O)O)C 358.40 unknown https://doi.org/10.1248/CPB.58.840

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