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Maackia amurensis

Maackia amurensis - 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 UUID643fd9914cb5b073366438
Scientific name Maackia amurensis
Authority Rupr.
First published in Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg15: 128 (1856)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cladrastis amurenzis (Rupr. & Maxim.) Benth.
Cladrastis amurensis (Rupr.) Benth. ex Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg, sér. 3, 18: 400 (1873)

Common names Top

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Language Common/alternative name
English amur maackia
Belarusian Акатнік амурскі
Belarusian Маакія амурская
Danish amur-maackia
German asiatisches gelbholz
Finnish maakkia
Finnish jokimaakkia
French maackie de l’amour
Japanese イヌエンジュ
Japanese 犬槐
Korean 다릅나무
Norwegian Bokmål amurtre
Russian Акатник амурский
Russian Акация Маака
Russian Кладрастис амурский
Russian Маакия амурская
Chinese 黄色木
Chinese 高丽槐
Chinese 山槐
Chinese 青娘子
Chinese 朝鲜槐
Chinese 山槐花
Chinese 山槐皮
Chinese 山槐枝

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Maackia amurensis var. amurensis Unknown
Maackia amurensis var. stenocarpa Nakai J. Jap. Bot.15: 681 (1939)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
Resents Transplanting: These plants do not tolerate the disturbance of their roots well. It's best to sow these seeds in their final growing location or in a container from which they can be moved without disturbing the root ball.
Requires Darkness: These seeds need to be covered with soil or otherwise kept in the dark to germinate properly. Light inhibits their germination process.
Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
soak in HOT water

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • China
      • China North-central
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
      • Sakhalin
  • Europe
    • Eastern Europe
      • Belarus
      • Central European Russia
      • Krym
      • South European Russia
      • Ukraine

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000186143
Cornell Woody Plants 142
USDA Plants MAAM9
UConn 271
Tropicos 13053277
KEW urn:lsid:ipni.org:names:324545-2
The Plant List ild-32551
Missouri Botanical Garden 280635
PFAF Maackia amurensis
PaleoBotany 122394
Open Tree Of Life 49914
Observations.org 119688
NCBI Taxonomy 37501
IUCN Red List 19892768
IPNI 324545-2
iNaturalist 133358
GBIF 5360278
Freebase /m/03bzzbj
EPPO MCKAM
EOL 643539
USDA GRIN 23023
Wikipedia Maackia_amurensis

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
Lectins as the prominent potential to deliver bioactive metal nanoparticles by recognizing cell surface glycans Bala Subramaniyan S, Veerappan A Heliyon 11-Apr-2024
PMCID:PMC11024627
doi:10.1016/j.heliyon.2024.e29394
Pest categorisation of Eulecanium giganteum Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Akrivou A, Kertesz V, Papachristos D, Sfyra O, MacLeod A EFSA J 03-Apr-2024
PMCID:PMC10988561
doi:10.2903/j.efsa.2024.8666
PMID:38576539
Sialylation on vesicular integrin β1 determined endocytic entry of small extracellular vesicles into recipient cells Lin M, Xu X, Zhou X, Feng H, Wang R, Yang Y, Li J, Fan N, Jiang Y, Li X, Guan F, Tan Z Cell Mol Biol Lett 01-Apr-2024
PMCID:PMC10983696
doi:10.1186/s11658-024-00562-0
PMID:38561669
Construction of an Escherichia coli chassis for efficient biosynthesis of human-like N-linked glycoproteins Bao Z, Gao Y, Song Y, Ding N, Li W, Wu Q, Zhang X, Zheng Y, Li J, Hu X Front Bioeng Biotechnol 20-Mar-2024
PMCID:PMC10987854
doi:10.3389/fbioe.2024.1370685
PMID:38572355
Strain-specific requirements of susceptibility to rhesus enteric calicivirus infection Farkas T, Srivastava V J Virol 14-Feb-2024
PMCID:PMC10949478
doi:10.1128/jvi.01851-23
PMID:38353537
Newcastle disease virus activates diverse signaling pathways via Src to facilitate virus entry into host macrophages Shi Q, Zhao R, Chen L, Liu T, Di T, Zhang C, Zhang Z, Wang F, Han Z, Sun J, Liu S J Virol 09-Feb-2024
PMCID:PMC10949470
doi:10.1128/jvi.01915-23
PMID:38334327
Negative Charge-Carrying Glycans Attached to Exosomes as Novel Liquid Biopsy Marker Kosutova N, Lorencova L, Hires M, Jane E, Orovcik L, Kollar J, Kozics K, Gabelova A, Ukraintsev E, Rezek B, Kasak P, Cernocka H, Ostatna V, Blahutova J, Vikartovska A, Bertok T, Tkac J Sensors (Basel) 08-Feb-2024
PMCID:PMC10892626
doi:10.3390/s24041128
PMID:38400284
Fecal-adherent mucus is a non-invasive source of primary human MUC2 for structural and functional characterization in health and disease Fancy N, Nitin, Kniffen D, Melvin M, Kazemian N, Sadeghi J, Letef CA, D’Aloisio L, Copp AG, Inaba R, Hans G, Jafaripour S, Haskey N, Raman M, Daneshgar P, Chadee K, Ghosh S, Gibson DL, Pakpour S, Zandberg W, Bergstrom KS J Biol Chem 24-Jan-2024
PMCID:PMC10891339
doi:10.1016/j.jbc.2024.105675
PMID:38272223
Proteome Analysis of Serum Purified Using Solanum tuberosum and Lycopersicon esculentum Lectins Nakajima D, Konno R, Miyashita Y, Ishikawa M, Ohara O, Kawashima Y Int J Mol Sci 21-Jan-2024
PMCID:PMC10816257
doi:10.3390/ijms25021315
PMID:38279312
Novel GNE missense variants impair de novo sialylation and cause defective angiogenesis in the developing brain in mice Huang L, Kondo Y, Cao L, Han J, Li T, Zuo B, Yang F, Li Y, Ma Z, Bai X, Jiang M, Ruan C, Xia L Blood Adv 20-Jan-2024
PMCID:PMC10879683
doi:10.1182/bloodadvances.2023011490
PMID:38237079
Challenges for Field-Effect-Transistor-Based Graphene Biosensors Ono T, Okuda S, Ushiba S, Kanai Y, Matsumoto K Materials (Basel) 09-Jan-2024
PMCID:PMC10817696
doi:10.3390/ma17020333
PMID:38255502
Antioxidant potential of chlorogenic acid in Age‐Related eye diseases Tang Y, Fang C, Shi J, Chen H, Chen X, Yao X Pharmacol Res Perspect 08-Jan-2024
PMCID:PMC10772849
doi:10.1002/prp2.1162
PMID:38189160
The avian influenza A virus receptor SA-α2,3-Gal is expressed in the porcine nasal mucosa sustaining the pig as a mixing vessel for new influenza viruses Kristensen C, Larsen LE, Trebbien R, Jensen HE Virus Res 03-Jan-2024
PMCID:PMC10793167
doi:10.1016/j.virusres.2023.199304
PMID:38142890
Enrichment of sweat-derived extracellular vesicles of human and bacterial origin for biomarker identification Zhyvolozhnyi A, Samoylenko A, Bart G, Kaisanlahti A, Hekkala J, Makieieva O, Pratiwi F, Miinalainen I, Kaakinen M, Bergman U, Singh P, Nurmi T, Khosrowbadi E, Abdelrady E, Kellokumpu S, Kosamo S, Reunanen J, Röning J, Hiltunen J, Vainio SJ Nanotheranostics 01-Jan-2024
PMCID:PMC10750121
doi:10.7150/ntno.87822
PMID:38164498
Development and characterization of an immortalized swine respiratory cell line for influenza A virus research Neasham PJ, Pliasas VC, North JF, Johnson C, Tompkins SM, Kyriakis CS Front Vet Sci 18-Dec-2023
PMCID:PMC10765598
doi:10.3389/fvets.2023.1258269
PMID:38179335

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
> Alkaloids and derivatives / Lupin alkaloids / Anagyrine-type alkaloids
(+)-Thermopsine 682648 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1248/CPB.34.3982
(1S,9S,10R,12S)-12-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4-dien-6-one 131676079 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1248/CPB.34.3982
Anagyrine 5351589 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/S0031-9422(00)98029-4
https://doi.org/10.1248/CPB.48.641
CID 10246 10246 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1016/S0031-9422(00)98029-4
https://doi.org/10.1248/CPB.48.641
Epibaptifoline 91747695 Click to see C1CN2CC3CC(C2CC1O)CN4C3=CC=CC4=O 260.33 unknown https://doi.org/10.1248/CPB.48.641
Thermopsine 92768 Click to see C1CCN2CC3CC(C2C1)CN4C3=CC=CC4=O 244.33 unknown https://doi.org/10.1248/CPB.48.641
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(-)-Cytisine 22407 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1248/CPB.48.641
(1R,5S)-1,2,3,4,5,6-Hexahydro-3-[[(1R,5S)-1,5,6,8-tetrahydro-8-oxo-1,5-methano-2H-pyrido[1,2-a][1,5]diazocin-3(4H)-yl]methyl]-1,5-methano-8H-pyrido[1,2-a][1,5]diazocin-8-one 6351029 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)CN4CC5CC(C4)C6=CC=CC(=O)N6C5 392.50 unknown https://doi.org/10.1248/CPB.48.641
(1R,5S)-3-(3-Oxo-butyl)-1,2,3,4,5,6-hexahydro-1,5-methano-pyrido[1,2-a][1,5]diazocin-8-one 44398032 Click to see CC(=O)CCN1CC2CC(C1)C3=CC=CC(=O)N3C2 260.33 unknown https://doi.org/10.1248/CPB.48.641
(1R,9R)-11-methyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 1747617 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1016/S0031-9422(00)98029-4
https://doi.org/10.1248/CPB.48.641
(1R,9R)-6-oxo-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-diene-11-carbaldehyde 7067491 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown https://doi.org/10.1248/CPB.48.641
(1S,5R)-3,4,5,6-tetrahydro-1H-1,5-methanopyrido[1,2-a][1,5]diazocin-8(2H)-one 6713952 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1016/S0031-9422(00)98029-4
https://doi.org/10.1248/CPB.48.641
(1S,9R)-11-but-3-enyl-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 7067420 Click to see C=CCCN1CC2CC(C1)C3=CC=CC(=O)N3C2 244.33 unknown https://doi.org/10.1248/CPB.48.641
1,5-Methano-8H-pyrido[1,2-a][1,5]diazocin-8-one, 3-(3-butenyl)-1,2,3,4,5,6-hexahydro-, (1R)- 547355 Click to see C=CCCN1CC2CC(C1)C3=CC=CC(=O)N3C2 244.33 unknown https://doi.org/10.1016/S0031-9422(00)98029-4
https://doi.org/10.1248/CPB.48.641
11-(3-Oxobutyl)-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 56674705 Click to see CC(=O)CCN1CC2CC(C1)C3=CC=CC(=O)N3C2 260.33 unknown https://doi.org/10.1248/CPB.48.641
11-[(6-Oxo-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-11-yl)methyl]-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one 3669400 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)CN4CC5CC(C4)C6=CC=CC(=O)N6C5 392.50 unknown https://doi.org/10.1248/CPB.48.641
Caulophylline 670971 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1248/CPB.48.641
Cytisine, N-formyl- 589870 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown https://doi.org/10.1248/CPB.48.641
Cytisinicline 10235 Click to see C1C2CNCC1C3=CC=CC(=O)N3C2 190.24 unknown https://doi.org/10.1248/CPB.48.641
N-Formylcytisine 179619 Click to see C1C2CN(CC1C3=CC=CC(=O)N3C2)C=O 218.25 unknown https://doi.org/10.1248/CPB.48.641
N-Methylcytisine 234566 Click to see CN1CC2CC(C1)C3=CC=CC(=O)N3C2 204.27 unknown https://doi.org/10.1248/CPB.48.641
> Alkaloids and derivatives / Lupin alkaloids / Leontidine-type alkaloids
(1R,2S,9S,10R)-7,14-diazatetracyclo[7.6.1.02,7.010,14]hexadecan-6-one 15060884 Click to see C1CC2C3CC(CN2C(=O)C1)C4CCCN4C3 234.34 unknown https://doi.org/10.1248/CPB.48.641
7,14-Diazatetracyclo[7.6.1.02,7.010,14]hexadecan-6-one 163035900 Click to see C1CC2C3CC(CN2C(=O)C1)C4CCCN4C3 234.34 unknown https://doi.org/10.1248/CPB.48.641
https://doi.org/10.1016/S0031-9422(00)98029-4
> Alkaloids and derivatives / Lupin alkaloids / Lupinine-type alkaloids
6-[(1S,3R,8R,9aR)-8-hydroxy-1-(hydroxymethyl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-3-yl]-1H-pyridin-2-one 21636115 Click to see C1CN2CC(CC(C2CC1O)CO)C3=CC=CC(=O)N3 278.35 unknown https://doi.org/10.1248/CPB.34.3982
6-[8-hydroxy-1-(hydroxymethyl)-2,3,4,6,7,8,9,9a-octahydro-1H-quinolizin-3-yl]-1H-pyridin-2-one 14274653 Click to see C1CN2CC(CC(C2CC1O)CO)C3=CC=CC(=O)N3 278.35 unknown https://doi.org/10.1248/CPB.34.3982
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(+)-Sparteine 7014 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/S0031-9422(00)98029-4
(1R,2R,3R,9R,10R)-2-hydroxy-3-[[(1R,9S)-6-oxo-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-11-yl]methyl]-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 10837946 Click to see C1CCN2CC3CC(C2C1)CN4C3(C(CCC4=O)CN5CC6CC(C5)C7=CC=CC(=O)N7C6)O 466.60 unknown https://doi.org/10.1248/CPB.48.641
(1R,2R,9R,10R)-2-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 162939756 Click to see C1CCN2CC3CC(C2C1)CN4C3(CCCC4=O)O 264.36 unknown https://doi.org/10.1248/CPB.48.641
(1R,2R,9R,10R)-2-methoxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 10707743 Click to see COC12CCCC(=O)N1CC3CC2CN4C3CCCC4 278.39 unknown https://doi.org/10.1248/CPB.48.641
(1R,9R,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-6-one 14379239 Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O 246.35 unknown https://doi.org/10.1248/CPB.48.641
(1S,9S,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane 5320360 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4 234.38 unknown https://doi.org/10.1016/S0031-9422(00)98029-4
2-Hydroxy-3-[(6-oxo-7,11-diazatricyclo[7.3.1.02,7]trideca-2,4-dien-11-yl)methyl]-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 73200985 Click to see C1CCN2CC3CC(C2C1)CN4C3(C(CCC4=O)CN5CC6CC(C5)C7=CC=CC(=O)N7C6)O 466.60 unknown https://doi.org/10.1248/CPB.48.641
2-Hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 73201047 Click to see C1CCN2CC3CC(C2C1)CN4C3(CCCC4=O)O 264.36 unknown https://doi.org/10.1248/CPB.48.641
2-Methoxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecan-6-one 73201091 Click to see COC12CCCC(=O)N1CC3CC2CN4C3CCCC4 278.39 unknown https://doi.org/10.1248/CPB.48.641
5,6-Dehydrolupanine 520559 Click to see C1CCN2CC3CC(C2C1)CN4C3=CCCC4=O 246.35 unknown https://doi.org/10.1248/CPB.48.641
alpha-Isolupanine 119201 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1248/CPB.48.641
Hydrorhombinine 7018997 Click to see C1CCN2CC3CC(C2C1)CN4C3CCCC4=O 248.36 unknown https://doi.org/10.1248/CPB.48.641
https://doi.org/10.1016/S0031-9422(00)98029-4
> Benzenoids / Phenols / Methoxyphenols
(1S,3aR,4S,8bR)-1-(3,4-dihydroxyphenyl)-4-(4-hydroxy-3,5-dimethoxyphenyl)-3,3a,4,8b-tetrahydro-1H-indeno[1,2-c]furan-5,7-diol 163013872 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3C4=C2C(=CC(=C4)O)O)C5=CC(=C(C=C5)O)O 452.50 unknown https://doi.org/10.1016/0031-9422(95)00270-H
> Lignans, neolignans and related compounds / Stilbenolignans
[2-acetyloxy-4-[(2R,3R)-3-(3,5-diacetyloxyphenyl)-6-[(E)-2-(3,5-diacetyloxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-2-yl]phenyl] acetate 163187173 Click to see CC(=O)OC1=C(C=C(C=C1)C2C(OC3=C(O2)C=CC(=C3)C=CC4=CC(=CC(=C4)OC(=O)C)OC(=O)C)C5=CC(=CC(=C5)OC(=O)C)OC(=O)C)OC(=O)C 738.70 unknown https://doi.org/10.1007/BF00630640
[2-Acetyloxy-4-[3-(3,5-diacetyloxyphenyl)-6-[2-(3,5-diacetyloxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-2-yl]phenyl] acetate 73816196 Click to see CC(=O)OC1=C(C=C(C=C1)C2C(OC3=C(O2)C=CC(=C3)C=CC4=CC(=CC(=C4)OC(=O)C)OC(=O)C)C5=CC(=CC(=C5)OC(=O)C)OC(=O)C)OC(=O)C 738.70 unknown https://doi.org/10.1007/BF00630640
4-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-[(Z)-2-(3,5-dihydroxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-2-yl]benzene-1,2-diol 163190490 Click to see C1=CC2=C(C=C1C=CC3=CC(=CC(=C3)O)O)OC(C(O2)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O 486.50 unknown https://doi.org/10.1007/BF02323300
4-[3-(3,5-Dihydroxyphenyl)-6-[2-(3,5-dihydroxyphenyl)ethenyl]-2,3-dihydro-1,4-benzodioxin-2-yl]benzene-1,2-diol 73816195 Click to see C1=CC2=C(C=C1C=CC3=CC(=CC(=C3)O)O)OC(C(O2)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O 486.50 unknown https://doi.org/10.1007/BF02323300
https://doi.org/10.1007/BF00630640
Maackin 56666152 Click to see C1=CC2=C(C=C1C=CC3=CC(=CC(=C3)O)O)OC(C(O2)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O 486.50 unknown https://doi.org/10.1007/BF00630640
> 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 https://doi.org/10.1007/BF00576208
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown https://doi.org/10.1007/BF00576208
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic acid 3931 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1007/BF00576208
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1007/BF00576208
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(3,7,10-Triacetyloxy-9-hydroxy-12,12-dimethyl-6-methylidene-17-oxapentacyclo[7.6.2.15,8.01,11.02,8]octadecan-15-yl) acetate 14106501 Click to see CC(=O)OC1CCC(C2C13COC(C2OC(=O)C)(C45C3C(CC(C4)C(=C)C5OC(=O)C)OC(=O)C)O)(C)C 534.60 unknown https://doi.org/10.1016/0031-9422(95)00270-H
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1007/BF00576208
Super Squalene; trans-Squalene;AddaVax 1105 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1007/BF00576208
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
[(1S,2S,6S,9S,10S,11R,12R,13S,14S,15S,16R,18S,19S,22S,23S,25R)-16-acetyloxy-10,12,14,23-tetrahydroxy-6,10,19-trimethyl-13-[(Z)-2-methylbut-2-enoyl]oxy-24-oxa-4-azaheptacyclo[12.12.0.02,11.04,9.015,25.018,23.019,25]hexacosan-22-yl] (Z)-2-methylbut-2-enoate 101835363 Click to see CC=C(C)C(=O)OC1CCC2(C3C1(OC24CC5C6CN7CC(CCC7C(C6C(C(C5(C4C(C3)OC(=O)C)O)OC(=O)C(=CC)C)O)(C)O)C)O)C 715.90 unknown https://doi.org/10.1007/BF00630640
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(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 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00576208
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00576208
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00576208
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
Aculene C 139586350 Click to see CCC1=CC(=O)C2(C1=CC=C(CC2O)C)C 218.29 unknown https://doi.org/10.1007/BF02323300
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Cytosine 597 Click to see C1=C(NC(=O)N=C1)N 111.10 unknown https://doi.org/10.2307/4117899
> Organoheterocyclic compounds / Indolizidines
N-(2,3,5,6,7,8a-hexahydro-1H-indolizin-8-ylidenemethyl)acetamide 73812410 Click to see CC(=O)NC=C1CCCN2C1CCC2 194.27 unknown https://doi.org/10.1248/CPB.48.641
N-[(E)-[(8aR)-2,3,5,6,7,8a-hexahydro-1H-indolizin-8-ylidene]methyl]acetamide 21599262 Click to see CC(=O)NC=C1CCCN2C1CCC2 194.27 unknown https://doi.org/10.1248/CPB.48.641
> Organoheterocyclic compounds / Naphthofurans
Arbusclin D 3035762 Click to see CC12CCCC(C1C3C(=C(C(=O)O3)CO)CC2)(C)O 266.33 unknown https://doi.org/10.1007/BF00630640
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
1-[5-[(2R)-pyrrolidin-2-yl]-3,4-dihydro-2H-pyridin-1-yl]ethanone 14413772 Click to see CC(=O)N1CCCC(=C1)C2CCCN2 194.27 unknown https://doi.org/10.1248/CPB.48.641
https://doi.org/10.1016/S0031-9422(00)98029-4
Ammodendrine 442625 Click to see CC(=O)N1CCCC(=C1)C2CCCCN2 208.30 unknown https://doi.org/10.1016/S0031-9422(00)98029-4
https://doi.org/10.1248/CPB.48.641
Pyridine, 1-acetyl-1,2,3,4-tetrahydro-5-(2-piperidinyl)- 108191 Click to see CC(=O)N1CCCC(=C1)C2CCCCN2 208.30 unknown https://doi.org/10.1248/CPB.48.641
https://doi.org/10.1016/S0031-9422(00)98029-4
Pyridine, 1-acetyl-1,2,3,4-tetrahydro-5-(2-pyrrolidinyl)- 606526 Click to see CC(=O)N1CCCC(=C1)C2CCCN2 194.27 unknown https://doi.org/10.1248/CPB.48.641
https://doi.org/10.1016/S0031-9422(00)98029-4
> Organoheterocyclic compounds / Quinolizines
Lusitanine 6452371 Click to see CC(=O)NC=C1CCCN2C1CCCC2 208.30 unknown https://doi.org/10.1016/S0031-9422(00)98029-4
https://doi.org/10.1248/CPB.48.641
N-(2,3,4,6,7,8,9,9a-octahydroquinolizin-1-ylidenemethyl)acetamide 78410938 Click to see CC(=O)NC=C1CCCN2C1CCCC2 208.30 unknown https://doi.org/10.1248/CPB.48.641
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3R)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2,3-dihydronaphtho[2,1-e][1]benzofuran-7,8,10-triol 101631691 Click to see C1=CC(=C(C=C1C2C(C3=C(O2)C=C(C4=C3C=CC5=CC(=C(C=C54)O)O)O)C6=CC(=CC(=C6)O)O)O)O 484.50 unknown https://doi.org/10.1007/BF02323300
[2-acetyloxy-4-[(E)-2-[(2R,3R)-6-acetyloxy-2-(3,4-diacetyloxyphenyl)-3-(3,5-diacetyloxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]ethenyl]phenyl] acetate 163193716 Click to see CC(=O)OC1=C(C=C(C=C1)C=CC2=C3C(C(OC3=CC(=C2)OC(=O)C)C4=CC(=C(C=C4)OC(=O)C)OC(=O)C)C5=CC(=CC(=C5)OC(=O)C)OC(=O)C)OC(=O)C 780.70 unknown https://doi.org/10.1007/BF00630640
[4-[(E)-2-[(2R,3R)-6-acetyloxy-2-(3,4-diacetyloxyphenyl)-3-(3,5-diacetyloxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]ethenyl]phenyl] acetate 163188119 Click to see CC(=O)OC1=CC=C(C=C1)C=CC2=C3C(C(OC3=CC(=C2)OC(=O)C)C4=CC(=C(C=C4)OC(=O)C)OC(=O)C)C5=CC(=CC(=C5)OC(=O)C)OC(=O)C 722.70 unknown https://doi.org/10.1007/BF00630640
[4-[2-[6-Acetyloxy-2-(3,4-diacetyloxyphenyl)-3-(3,5-diacetyloxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]ethenyl]phenyl] acetate 73816194 Click to see CC(=O)OC1=CC=C(C=C1)C=CC2=C3C(C(OC3=CC(=C2)OC(=O)C)C4=CC(=C(C=C4)OC(=O)C)OC(=O)C)C5=CC(=CC(=C5)OC(=O)C)OC(=O)C 722.70 unknown https://doi.org/10.1007/BF00630640
2-(3,4-Dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-2,3-dihydronaphtho[2,1-e][1]benzofuran-7,8,10-triol 162898483 Click to see C1=CC(=C(C=C1C2C(C3=C(O2)C=C(C4=C3C=CC5=CC(=C(C=C54)O)O)O)C6=CC(=CC(=C6)O)O)O)O 484.50 unknown https://doi.org/10.1007/BF02323300
4-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-4-[(E)-2-(4-hydroxyphenyl)vinyl]-2,3-dihydrobenzofuran-2-yl]benzene-1,2-diol 5279244 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 470.50 unknown https://doi.org/10.1007/BF00630640
4-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-4-[(Z)-2-(4-hydroxyphenyl)vinyl]-2,3-dihydrobenzofuran-2-yl]benzene-1,2-diol 5279245 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 470.50 unknown https://doi.org/10.1007/BF02323300
4-[(2S,3S)-3-(3,5-dihydroxyphenyl)-5-[(E)-2-(3,5-dihydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-2-yl]benzene-1,2-diol 163189558 Click to see C1=CC2=C(C=C1C=CC3=CC(=CC(=C3)O)O)C(C(O2)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O 470.50 unknown https://doi.org/10.1007/BF02323300
4-[(E)-2-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2,3-dihydrobenzofuran-4-yl]vinyl]benzene-1,2-diol 5279247 Click to see C1=CC(=C(C=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O)O 486.50 unknown https://doi.org/10.1007/BF00630640
4-[(Z)-2-[(2R,3R)-2-(3,4-dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2,3-dihydro-1-benzofuran-4-yl]ethenyl]benzene-1,2-diol 163187406 Click to see C1=CC(=C(C=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O)O 486.50 unknown https://doi.org/10.1007/BF02323300
4-[2-[2-(3,4-Dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2,3-dihydro-1-benzofuran-4-yl]ethenyl]benzene-1,2-diol 155287 Click to see C1=CC(=C(C=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O)O 486.50 unknown https://doi.org/10.1007/BF02323300
https://doi.org/10.1007/BF00630640
4-[3-(3,5-Dihydroxyphenyl)-5-[2-(3,5-dihydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-2-yl]benzene-1,2-diol 162937746 Click to see C1=CC2=C(C=C1C=CC3=CC(=CC(=C3)O)O)C(C(O2)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O 470.50 unknown https://doi.org/10.1007/BF02323300
4-[3-(3,5-Dihydroxyphenyl)-6-hydroxy-4-[2-(4-hydroxyphenyl)ethenyl]-2,3-dihydro-1-benzofuran-2-yl]benzene-1,2-diol 155288 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 470.50 unknown https://doi.org/10.1007/BF02323300
https://doi.org/10.1007/BF00630640
Scirpusin A 5458896 Click to see C1=CC(=CC=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O 470.50 unknown https://doi.org/10.1007/BF00630640
Scirpusin B 5458999 Click to see C1=CC(=C(C=C1C=CC2=C3C(C(OC3=CC(=C2)O)C4=CC(=C(C=C4)O)O)C5=CC(=CC(=C5)O)O)O)O 486.50 unknown https://doi.org/10.1007/BF00630640
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
abyssinone II 10064832 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C=C3)O)O)C 324.40 unknown https://doi.org/10.1248/CPB.57.302
Abyssinone V 442153 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(C=C(C=C3O2)O)O)C 408.50 unknown https://doi.org/10.1248/CPB.57.302
abyssinone-IV 7330513 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(O2)C=C(C=C3)O)C 392.50 unknown https://doi.org/10.1248/CPB.57.302
Sigmoidin E 195173 Click to see CC(=CCC1=CC(=CC2=C1OC(C=C2)(C)C)C3CC(=O)C4=C(C=C(C=C4O3)O)O)C 406.50 unknown https://doi.org/10.1248/CPB.57.302
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-5,7-dihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 124355984 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)C 476.60 unknown https://doi.org/10.1023/B:CONC.0000018120.22592.36
https://doi.org/10.1248/CPB.57.302
https://doi.org/10.1016/S0031-9422(00)97051-1
CID 124355910 124355910 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2CC(=O)C3=C(O2)C(=C(C=C3O)OC)CC=C(C)C)C 438.50 unknown https://doi.org/10.1016/S0031-9422(00)97051-1
Hydroxysophoranone 42607927 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)C 476.60 unknown https://doi.org/10.1023/B:CONC.0000018120.22592.36
Maackiaflavanone 42608032 Click to see CC(=CCC1=CC(=C(C=C1O)O)C2CC(=O)C3=C(O2)C(=C(C=C3O)OC)CC=C(C)C)C 438.50 unknown https://doi.org/10.1248/CPB.57.302
https://doi.org/10.1016/S0031-9422(00)97051-1
Maackiaflavanone A 25231267 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=C(C=C4C(=C3)C=CC(O4)(C)C)O)O)OC)C 436.50 unknown https://doi.org/10.1248/CPB.57.302
Maackiaflavanone B 25224569 Click to see CC(=CCC1=CC(=CC2=C1OC(C=C2)(C)C)C3CC(=O)C4=C(C=C(C(=C4O3)CC=C(C)C)O)O)C 474.60 unknown https://doi.org/10.1248/CPB.57.302
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
4H-1-Benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)- 1889 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1007/S10600-009-9195-3
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1007/S10600-009-9195-3
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown https://doi.org/10.1007/S10600-009-9195-3
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1007/S10600-009-9195-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown https://doi.org/10.1007/BF00598182
https://doi.org/10.1007/BF00576208
https://doi.org/10.1016/S0367-326X(00)00129-5
https://doi.org/10.1007/BF00574576
> Phenylpropanoids and polyketides / Isoflavonoids
3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[[(12S)-5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-1(20),2,4(8),9,13(18),14,16-heptaen-16-yl]oxy]oxan-2-yl]methoxy]propanoic acid 163188204 Click to see C1OC2=C(O1)C=C3C(=C2)C4=COC5=C(C4O3)C=CC(=C5)OC6C(C(C(C(O6)COC(=O)CC(=O)O)O)O)O 530.40 unknown https://doi.org/10.1021/JF801227Q
3-Oxo-3-[[3,4,5-trihydroxy-6-(5,7,11,19-tetraoxapentacyclo[10.8.0.02,10.04,8.013,18]icosa-1(20),2,4(8),9,13(18),14,16-heptaen-16-yloxy)oxan-2-yl]methoxy]propanoic acid 163072437 Click to see C1OC2=C(O1)C=C3C(=C2)C4=COC5=C(C4O3)C=CC(=C5)OC6C(C(C(C(O6)COC(=O)CC(=O)O)O)O)O 530.40 unknown https://doi.org/10.1021/JF801227Q
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Medicagol 5319322 Click to see C1OC2=C(O1)C=C3C(=C2)C4=C(O3)C5=C(C=C(C=C5)O)OC4=O 296.23 unknown https://doi.org/10.1002/JPS.2600640504
> 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 https://doi.org/10.1021/JF801227Q
(+)-Maackiain 161298 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown https://doi.org/10.1248/CPB.57.302
(+)-Medicarpin 73067 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1248/CPB.57.302
3-Hydroxy-8,9-methylenedioxypterocarpane 363863 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown https://doi.org/10.1021/JF801227Q
https://doi.org/10.1016/S0367-326X(00)00129-5
https://doi.org/10.1023/B:CONC.0000018120.22592.36
https://doi.org/10.1016/S0031-9422(00)97051-1
6'-Malonyltrifolirhizin 14841223 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 https://doi.org/10.1021/JF801227Q
9-Methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-3-ol 623060 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1023/B:CONC.0000018120.22592.36
https://doi.org/10.1021/JF801227Q
Maackiain 91510 Click to see C1C2C(C3=C(O1)C=C(C=C3)O)OC4=CC5=C(C=C24)OCO5 284.26 unknown https://doi.org/10.1021/JF801227Q
https://doi.org/10.1023/B:CONC.0000018120.22592.36
Maackiapterocarpan A 25231270 Click to see CC1(CCC2=C(O1)C(=CC3=C2C4C(CO3)C5=CC6=C(C=C5O4)OCO6)O)C 368.40 unknown https://doi.org/10.1248/CPB.57.302
Maackiapterocarpan B 25231269 Click to see CC1(C=CC2=C(O1)C(=CC3=C2C4C(CO3)C5=CC6=C(C=C5O4)OCO6)O)C 366.40 unknown https://doi.org/10.1248/CPB.57.302
Medicarpin 336327 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)O 270.28 unknown https://doi.org/10.1021/JF801227Q
https://doi.org/10.1016/S0367-326X(00)00129-5
https://doi.org/10.1023/B:CONC.0000018120.22592.36
Medicarpin 3-O-(6'-malonylgluclside) 44257430 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)COC(=O)CC(=O)O)O)O)O 518.50 unknown https://doi.org/10.1021/JF801227Q
Medicarpin 3-O-glucoside-6'-malonate 23724665 Click to see COC1=CC2=C(C=C1)C3COC4=C(C3O2)C=CC(=C4)OC5C(C(C(C(O5)COC(=O)CC(=O)O)O)O)O 518.50 unknown https://doi.org/10.1021/JF801227Q
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 https://doi.org/10.1016/S0031-9422(00)97051-1
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
5,7-Dihydroxyisoflavone 5377381 Click to see C1=CC=C(C=C1)C2=COC3=CC(=CC(=C3C2=O)O)O 254.24 unknown https://doi.org/10.1007/BF00576208
Daidzein 5281708 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)O)O 254.24 unknown https://doi.org/10.1021/JF801227Q
https://doi.org/10.1016/S0367-326X(00)00129-5
https://doi.org/10.1016/S0031-9422(00)97051-1
Genistein 5280961 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O 270.24 unknown https://doi.org/10.1248/CPB.20.2488
https://doi.org/10.1007/BF00598182
https://doi.org/10.1021/JF801227Q
https://doi.org/10.1007/BF00630020
https://doi.org/10.1007/BF00576208
https://doi.org/10.1016/S0367-326X(00)00129-5
Orobol 5281801 Click to see C1=CC(=C(C=C1C2=COC3=CC(=CC(=C3C2=O)O)O)O)O 286.24 unknown https://doi.org/10.1023/B:CONC.0000018120.22592.36
Pseudobaptigenin 5281805 Click to see C1OC2=C(O1)C=C(C=C2)C3=COC4=C(C3=O)C=CC(=C4)O 282.25 unknown https://doi.org/10.1021/JF801227Q
Tectorigenin 5281811 Click to see COC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)O)O 300.26 unknown https://doi.org/10.1023/B:CONC.0000018120.22592.36
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
5-Hydroxy-3-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-8,8-dimethyl-6-(3-methylbut-2-enyl)pyrano[2,3-h]chromen-4-one 25231268 Click to see CC(=CCC1=C(C=CC(=C1)C2=COC3=C4C=CC(OC4=C(C(=C3C2=O)O)CC=C(C)C)(C)C)O)C 472.60 unknown https://doi.org/10.1248/CPB.57.302
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 8-prenylated isoflavanones
(3S)-5,7-dihydroxy-3-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 163060831 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2COC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C 476.60 unknown https://doi.org/10.1016/S0031-9422(00)97051-1
5,7-Dihydroxy-3-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 163060830 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2COC3=C(C(=CC(=C3C2=O)O)O)CC=C(C)C)C 476.60 unknown https://doi.org/10.1016/S0031-9422(00)97051-1
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
3-(4-methoxyphenyl)-7-[(2S,4S,5R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44257215 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1007/BF00630020
https://doi.org/10.1016/S0031-9422(00)97051-1
3-(4-Methoxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 3733033 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1016/S0031-9422(00)97051-1
https://doi.org/10.1007/BF00630020
https://doi.org/10.1021/JF801227Q
3'-Methoxydaidzin 10527347 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1021/JF801227Q
4H-1-Benzopyran-4-one, 7-(beta-D-glucopyranosyloxy)-3-(4-hydroxyphenyl)- 4183640 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1021/JF801227Q
4H-1-Benzopyran-4-one,7-(b-D-glucopyranosyloxy)-3-(4-hydroxy-3-methoxyphenyl)- 13629778 Click to see COC1=C(C=CC(=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1021/JF801227Q
6''-O-Malonylgenistin 131750882 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O 518.40 unknown https://doi.org/10.1021/JF801227Q
7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 171292 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 578.50 unknown https://doi.org/10.1021/JF801227Q
Calycosin 7-galactoside 91973796 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1021/JF801227Q
CALYCOSIN 7-O-beta-D-GLUCOSIDE 5318267 Click to see COC1=C(C=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1021/JF801227Q
Daidzein-4,7-diglucoside 131751509 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 578.50 unknown https://doi.org/10.1021/JF801227Q
Daidzin 107971 Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O)O 416.40 unknown https://doi.org/10.1021/JF801227Q
Formononetin 7-(6''-malonylglucoside) 131750877 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O 516.40 unknown https://doi.org/10.1021/JF801227Q
Formononetin 7-O-glucoside-6''-O-malonate 23724663 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O 516.40 unknown https://doi.org/10.1021/JF801227Q
Genistein 7-O-beta-D-glucoside 5284639 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1007/BF00630020
https://doi.org/10.1021/JF801227Q
Genistein 7,4'-di-O-beta-D-glucopyranoside 91431845 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 594.50 unknown https://doi.org/10.1021/JF801227Q
Genistein7,4'-di-O-beta-D-glucopyranoside 13338930 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 594.50 unknown https://doi.org/10.1021/JF801227Q
Genistin 5281377 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1021/JF801227Q
https://doi.org/10.1007/BF00630020
Malonylgenistin 15934091 Click to see C1=CC(=CC=C1C2=COC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O 518.40 unknown https://doi.org/10.1021/JF801227Q
Ononin 442813 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown https://doi.org/10.1007/BF00630020
https://doi.org/10.1021/JF801227Q
https://doi.org/10.1016/S0031-9422(00)97051-1
Tectoridin 5281810 Click to see COC1=C(C=C2C(=C1O)C(=O)C(=CO2)C3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 462.40 unknown https://doi.org/10.1016/J.PHYMED.2013.10.022
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids
(3R)-4'-Methoxy-2',3',7-trihydroxyisoflavanone 66728616 Click to see COC1=CC(=C(C=C1)C2(COC3=C(C2=O)C=CC(=C3)O)O)O 302.28 unknown https://doi.org/10.1023/B:CONC.0000018120.22592.36
4'-Methoxy-2',3,7-trihydroxyisoflavanone 77181160 Click to see COC1=CC(=C(C=C1)C2(COC3=C(C2=O)C=CC(=C3)O)O)O 302.28 unknown https://doi.org/10.1023/B:CONC.0000018120.22592.36
Vestitol 92503 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown https://doi.org/10.1023/B:CONC.0000018120.22592.36
Vestitol, (-)- 182259 Click to see COC1=CC(=C(C=C1)C2CC3=C(C=C(C=C3)O)OC2)O 272.29 unknown https://doi.org/10.1023/B:CONC.0000018120.22592.36
> 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 https://doi.org/10.1007/S10600-009-9195-3
https://doi.org/10.1021/JF801227Q
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 4-O-methylisoflavones
2-(3,4-Dihydroxyphenyl)-3-(3,5-dihydroxyphenyl)-8-(4-methoxyphenyl)-2,3-dihydropyrano[3,2-h][1,4]benzodioxin-7-one 162880579 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC4=C3OC(C(O4)C5=CC(=CC(=C5)O)O)C6=CC(=C(C=C6)O)O 526.50 unknown https://doi.org/10.1007/BF00598182
https://doi.org/10.1007/BF00574576
7,8-Dihydroxy-4'-methoxyisoflavone 5481240 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3O)O 284.26 unknown https://doi.org/10.1007/BF00576208
Formononetin 5280378 Click to see COC1=CC=C(C=C1)C2=COC3=C(C2=O)C=CC(=C3)O 268.26 unknown https://doi.org/10.1248/CPB.20.2488
https://doi.org/10.1007/BF00598182
https://doi.org/10.1021/JF801227Q
https://doi.org/10.1007/BF00630020
https://doi.org/10.1007/BF00576208
https://doi.org/10.1023/B:CONC.0000018120.22592.36
https://doi.org/10.1016/S0367-326X(00)00129-5
https://doi.org/10.1016/S0031-9422(00)97051-1
> Phenylpropanoids and polyketides / Isoflavonoids / Pyranoisoflavonoids
ulexone A 14583600 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(=CO2)C3=CC4=C(C=C3)OC(C=C4)(C)C)C 404.50 unknown https://doi.org/10.1248/CPB.57.302
Ulexone B 14583601 Click to see CC1(C=CC2=C(O1)C=CC(=C2)C3=COC4=C(C3=O)C(=CC5=C4C=CC(O5)(C)C)O)C 402.40 unknown https://doi.org/10.1248/CPB.57.302
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
(2S)-1-(2,4-dihydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one 44446908 Click to see C1=CC(=CC=C1CC(C(=O)C2=C(C=C(C=C2)O)O)O)O 274.27 unknown https://doi.org/10.1007/S10600-009-9195-3
1-(2,4-Dihydroxyphenyl)-2-hydroxy-3-(4-hydroxyphenyl)propan-1-one 14632192 Click to see C1=CC(=CC=C1CC(C(=O)C2=C(C=C(C=C2)O)O)O)O 274.27 unknown https://doi.org/10.1007/S10600-009-9195-3
> Phenylpropanoids and polyketides / Neoflavonoids / Neoflavones
5,7-Dimethoxy-4-phenylchromen-2-one 701671 Click to see COC1=CC2=C(C(=CC(=O)O2)C3=CC=CC=C3)C(=C1)OC 282.29 unknown https://doi.org/10.1021/JF801227Q
> Phenylpropanoids and polyketides / Stilbenes
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]- 5056 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1007/BF00598182
https://doi.org/10.1007/BF00576208
https://doi.org/10.1016/S0367-326X(00)00129-5
4-[2-(3,5-Dihydroxyphenyl)ethenyl]benzene-1,2-diol 4813 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://doi.org/10.1007/BF00576208
Dihydroresveratrol 185914 Click to see C1=CC(=CC=C1CCC2=CC(=CC(=C2)O)O)O 230.26 unknown https://doi.org/10.1007/S10600-009-9195-3
Piceatannol 667639 Click to see C1=CC(=C(C=C1C=CC2=CC(=CC(=C2)O)O)O)O 244.24 unknown https://doi.org/10.1016/S0367-326X(00)00129-5
https://doi.org/10.1007/BF00576208
Resveratrol 445154 Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O 228.24 unknown https://doi.org/10.1007/BF00598182
https://doi.org/10.1007/BF00576208
https://doi.org/10.1016/S0367-326X(00)00129-5

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