Bletilla striata - Unknown
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Internal ID UUID643ff27973caf124463994
Scientific name Bletilla striata
Authority Rchb.f.
First published in Bot. Zeitung (Berlin) 36: 75 (1878)

Description Top

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Synonyms Top

Scientific name Authority First published in
Jimensia nervosa Raf. Fl. Tellur. 4: 38 (1838)
Jimensia striata (Thunb.) Garay & R.E.Schult. Bot. Mus. Leafl. 18: 184 (1958)
Limodorum hyacinthinum Donn Hortus Cantabrig. , ed. 4: 201 (1807)
Limodorum striatum Thunb. Syst. Veg. ed. 14 : 816 (1784)
Polytoma inodora Lour. ex Gomes Mem. Acad. Real Sci. Lisboa, 2 Cl. Sci. Moraes , n.s., 4(1): 30 (1872)
Sobralia bletioides Brongn. ex Decne. Rev. Hort. (Paris) , sér. 3, 1: 421 (1847)
Bletia gebina Lindl. J. Hort. Soc. London 2: 307 (1847)
Bletia hyacinthina R.Br. Hortus Kew. 5: 206 (1813)
Bletia striata Druce Rep. Bot. Soc. Exch. Club Brit. Isles 1916: 609 (1917)
Bletilla elegantula (Kraenzl.) Garay & G.A.Romero Harvard Pap. Bot. 3: 53 (1998)
Bletilla gebinae Rchb.f. Fl. Serres Jard. Eur. 8: 246 (1853)
Bletilla striata var. albomarginata Makino J. Jap. Bot. 6: 31. 1929
Bletilla striata f. gebina (Lindl.) Ohwi Bull. Natl. Sci. Mus. Tokyo 33: 70 1953
Bletilla striata var. gebina (Lindl.) Rchb.f. Bot. Zeitung (Berlin) 36: 75. 1878
Calanthe gebina G.Lodd. ex Lindl. Fol. Orchid. 6: 11 (1855)
Coelogyne elegantula Kraenzl. Repert. Spec. Nov. Regni Veg. 17: 111 (1921)
Bletia hyacinthina var. gebina (Lindl.) Blume Coll. Orchid. 17. 1858
Cymbidium hyacinthinum Sm. Exot. Bot. 1: 117 (1805)
Cymbidium striatum Sw. Nova Acta Regiae Soc. Sci. Upsal. 6: 77 (1799)
Epidendrum striatum Thunb. Trans. Linn. Soc. London 2: 327 (1794)
Gyas humilis Salisb. Trans. Hort. Soc. London 1: 300 (1812)
Bletilla hyacinthina (Sm.) Rchb.f. Bot. Zeitung (Berlin) 36: 75 1878

Common names Top

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Language Common/alternative name
English hyacinth orchid
English chinese ground orchid
Spanish orquídea urna
Arabic orchidée
Finnish mikadonkämmen
French orchidée jacinthe
French orchidee jacinthe
Upper Sorbian smužkata bletila
Japanese しらん
Japanese シラン
Japanese 紫蘭
Japanese 白及
Japanese ビャッキュウ
Korean 백급
Korean 자란
lzh 白及
Vietnamese bạch cập
za gobwzgiz
Chinese 連及草
Chinese 苞舌蘭
Chinese 紫蘭根
Chinese 紫蘭
Chinese 白花白芨
Chinese 白給
Chinese 甘根
Chinese 明白芨
Chinese 白芨
Chinese 白哀(白及)
Chinese 白及

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
sow in moist compost as soon as seed is ripe; include soil from an established plant to provide symbiotic fungi

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
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000346630
UNII WV2BSG60EW
Florida Plant Atlas 1895
USDA Plants BLST
Tropicos 23507332
Flora of Italy 8414
KEW urn:lsid:ipni.org:names:617803-1
The Plant List kew-22655
Missouri Botanical Garden 283860
Open Tree Of Life 147334
NCBI Taxonomy 78707
NBN Atlas NHMSYS0000456516
Nature Serve 2.151934
IPNI 617803-1
iNaturalist 131245
GBIF 2808791
Freebase /m/065yhnh
EPPO BLTST
EOL 1124449
USDA GRIN 7270
Wikipedia Bletilla_striata
CMAUP NPO10780

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
Evaluation of Habenaria aitchisonii Reichb. for antioxidant, anti-inflammatory, and antinociceptive effects with in vivo and in silico approaches Asiri SA, Shabnam M, Zafar R, Alshehri OM, Alshehri MA, Sadiq A, Mahnashi MH, Jan MS Front Chem 19-Mar-2024
PMCID:PMC10985259
doi:10.3389/fchem.2024.1351827
PMID:38566899
Integrated management of fruit trees and Bletilla striata: implications for soil nutrient profiles and microbial community structures Xie Q, Xu H, Wen R, Wang L, Yang Y, Zhang H, Su B Front Microbiol 06-Mar-2024
PMCID:PMC10951077
doi:10.3389/fmicb.2024.1307677
PMID:38511009
Traditional Chinese medicine treats ulcerative colitis by regulating gut microbiota, signaling pathway and cytokine: Future novel method option for pharmacotherapy Wang T, Liu X, Zhang W, Wang J, Wang T, Yue W, Ming L, Cheng J, Sun J Heliyon 06-Mar-2024
PMCID:PMC10945194
doi:10.1016/j.heliyon.2024.e27530
PMID:38501018
Identifying potential monkeypox virus inhibitors: an in silico study targeting the A42R protein Ashley CN, Broni E, Wood CM, Okuneye T, Ojukwu MP, Dong Q, Gallagher C, Miller WA III Front Cell Infect Microbiol 04-Mar-2024
PMCID:PMC10945028
doi:10.3389/fcimb.2024.1351737
PMID:38500508
Effect of Crude Polysaccharides from Ecklonia cava Hydrolysate on Cell Proliferation and Differentiation of Hanwoo Muscle Stem Cells for Cultured Meat Production Lee JH, Kim TK, Kang MC, Park MK, Park SH, Choi JS, Choi YS Foods 13-Feb-2024
PMCID:PMC10887812
doi:10.3390/foods13040563
PMID:38397540
Editorial: Multi-omics and computational biology in horticultural plants: from genotype to phenotype, volume II Cao Y, Li X, Song H, Abdullah M, Manzoor MA Front Plant Sci 02-Feb-2024
PMCID:PMC10869615
doi:10.3389/fpls.2024.1368909
PMID:38371409
Nitrogen Addition and Heterotroph Exclusion Affected Plant Species Diversity–Biomass Relationship by Affecting Plant Functional Traits Xu X, Yang L, Shen K, Cao H, Lin Y, Liu J, Han W Plants (Basel) 16-Jan-2024
PMCID:PMC10818353
doi:10.3390/plants13020258
PMID:38256811
Comparative chloroplast genomics of 24 species shed light on the genome evolution and phylogeny of subtribe Coelogyninae (Orchidaceae) Li L, Wu Q, Zhai J, Wu K, Fang L, Li M, Zeng S, Li S BMC Plant Biol 05-Jan-2024
PMCID:PMC10768429
doi:10.1186/s12870-023-04665-2
PMID:38182989
The complete chloroplast genome of Chrysoglossum ornatum (Epidendroideae, Orchidaceae) and its phylogenetic analysis Tan CJ, Yan RR, Yu P, Lu GQ, Wu W, Hu GX Mitochondrial DNA B Resour 03-Jan-2024
PMCID:PMC10769113
doi:10.1080/23802359.2023.2296920
PMID:38187007
Klebsiella michiganensis: a nitrogen-fixing endohyphal bacterium from Ustilago maydis Liang P, Jiang J, Sun Z, Li Y, Yang C, Zhou Y AMB Express 19-Dec-2023
PMCID:PMC10730499
doi:10.1186/s13568-023-01618-8
PMID:38112810
Effect of Bletilla Striata Polysaccharide on the Pasting, Rheological and Adhesive Properties of Wheat Starch Zhao H, Xu Q, Yan T, Zhang H, Yang Y Polymers (Basel) 15-Dec-2023
PMCID:PMC10747244
doi:10.3390/polym15244721
PMID:38139972
The influence of herbal medicine on serum motilin and its effect on human and animal model: a systematic review Cho MS, Park JW, Kim J, Ko SJ Front Pharmacol 14-Dec-2023
PMCID:PMC10755953
doi:10.3389/fphar.2023.1286333
PMID:38161695
Biological Activity of Fermented Plant Extracts for Potential Dermal Applications Herman A, Herman AP Pharmaceutics 14-Dec-2023
PMCID:PMC10748213
doi:10.3390/pharmaceutics15122775
PMID:38140115
Antimicrobial Activity of Stilbenes from Bletilla striata against Cutibacterium acnes and Its Effect on Cell Membrane Yu Q, Sun L, Peng F, Sun C, Xiong F, Sun M, Liu J, Peng C, Zhou Q Microorganisms 11-Dec-2023
PMCID:PMC10746055
doi:10.3390/microorganisms11122958
PMID:38138103
First Report of Colletotrichum fructicola, C. rhizophorae sp. nov. and C. thailandica sp. nov. on Mangrove in Thailand Norphanphoun C, Hyde KD Pathogens 10-Dec-2023
PMCID:PMC10747506
doi:10.3390/pathogens12121436
PMID:38133319

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 / Anthracenes
Anthracene 8418 Click to see C1=CC=C2C=C3C=CC=CC3=CC2=C1 178.23 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585276/
> Benzenoids / Anthracenes / Anthraquinones
Physcione 10639 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC 284.26 unknown https://doi.org/10.1016/0031-9422(91)85139-Q
> Benzenoids / Benzene and substituted derivatives
Benzyl 123147 Click to see [CH2]C1=CC=CC=C1 91.13 unknown via CMAUP database
CID 5150539 5150539 Click to see CC1=CC=C[C-]=C1 91.13 unknown via CMAUP database
> 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/10.1016/0031-9422(83)85044-4
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1016/0031-9422(83)85044-4
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see C1=CC=C(C(=C1)C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
4-Hydroxybenzyl alcohol 125 Click to see C1=CC(=CC=C1CO)O 124.14 unknown https://doi.org/10.1016/0031-9422(83)85044-4
> Benzenoids / Benzene and substituted derivatives / Phenethylamines / Amphetamines and derivatives
2-Propanol,1-chloro-3-[(phenylmethyl)amino]- 15228166 Click to see C1=CC=C(C=C1)CC(C(CCl)O)N 199.68 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
2,3,4,7-Tetramethoxyphenanthrene 11437978 Click to see COC1=CC2=C(C=C1)C3=C(C(=C(C=C3C=C2)OC)OC)OC 298.30 unknown https://doi.org/10.1016/0031-9422(91)85139-Q
2,4,7-Trimethoxyphenanthrene 15693458 Click to see COC1=CC2=C(C=C1)C3=C(C=C(C=C3C=C2)OC)OC 268.31 unknown https://doi.org/10.1016/0031-9422(91)85139-Q
Biphenanthrene 21709721 Click to see C1=CC=C2C(=C1)C=CC3=C2C=CC=C3C4=CC=CC5=C4C=CC6=CC=CC=C65 354.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585276/
Phenanthrene 995 Click to see C1=CC=C2C(=C1)C=CC3=CC=CC=C32 178.23 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
(2,7-Dihydroxy-4-methoxy-9,10-dihydrophenanthren-1-yl)-(4-hydroxyphenyl)methanone 129686646 Click to see COC1=C2C(=C(C(=C1)O)C(=O)C3=CC=C(C=C3)O)CCC4=C2C=CC(=C4)O 362.40 unknown https://doi.org/10.1016/0031-9422(93)85115-8
1-(4-Hydroxybenzyl)-2-methoxy-9,10-dihydrophenanthrene-4,7-diol 44392570 Click to see COC1=C(C2=C(C3=C(CC2)C=C(C=C3)O)C(=C1)O)CC4=CC=C(C=C4)O 348.40 unknown https://doi.org/10.1016/0031-9422(83)85044-4
https://doi.org/10.1016/J.BMCL.2004.12.026
1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol 11163864 Click to see COC1=C2C(=C(C(=C1)O)CC3=CC=C(C=C3)O)CCC4=C2C=CC(=C4)O 348.40 unknown via CMAUP database
1,2-Dihydrophenanthrene 148774 Click to see C1CC2=C(C=C1)C3=CC=CC=C3C=C2 180.24 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585276/
1,6-Bis(4-hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol 14630663 Click to see COC1=C2C(=C(C(=C1)O)CC3=CC=C(C=C3)O)CCC4=CC(=C(C=C42)CC5=CC=C(C=C5)O)O 454.50 unknown https://doi.org/10.1016/0031-9422(90)83053-4
2,4,7-Trimethoxy-9,10-dihydrophenanthrene 15693459 Click to see COC1=CC2=C(C=C1)C3=C(CC2)C=C(C=C3OC)OC 270.32 unknown https://doi.org/10.1016/0031-9422(91)85139-Q
4-Methoxy-3-(4-hydroxybenzyl)-9,10-dihydrophenanthrene-2,7-diol 14630662 Click to see COC1=C2C(=CC(=C1CC3=CC=C(C=C3)O)O)CCC4=C2C=CC(=C4)O 348.40 unknown https://doi.org/10.1016/0031-9422(90)83053-4
7-Methoxy-9,10-dihydrophenanthrene-2,5-diol 442702 Click to see COC1=CC2=C(C3=C(CC2)C=C(C=C3)O)C(=C1)O 242.27 unknown https://doi.org/10.1016/0031-9422(83)85044-4
Blestrianol A 14863073 Click to see COC1=C2C(=C(C(=C1)O)C3=C(C=C4CCC5=C(C4=C3OC)C=CC(=C5)O)O)CCC6=C2C=CC(=C6)O 482.50 unknown https://doi.org/10.1016/J.BMCL.2004.12.026
https://doi.org/10.1016/0031-9422(91)85133-K
https://doi.org/10.1016/0031-9422(90)85437-K
Blestrianol B 14863075 Click to see COC1=C2C(=C(C(=C1)O)CC3=CC=C(C=C3)O)CCC4=CC(=C(C=C42)C5=C6CCC7=C(C6=C(C=C5O)OC)C=CC(=C7)O)O 588.60 unknown https://doi.org/10.1016/0031-9422(91)85133-K
https://doi.org/10.1016/0031-9422(90)85437-K
Blestriarene A 11317652 Click to see COC1=C2C(=C(C(=C1)O)C3=C4CCC5=C(C4=C(C=C3O)OC)C=CC(=C5)O)CCC6=C2C=CC(=C6)O 482.50 unknown https://doi.org/10.1016/0031-9422(89)80373-5
Blestrin A 14583570 Click to see COC1=CC(=CC2=C1C3=C(CC2)C=C(C=C3)O)OC4=C5CCC6=C(C5=C(C=C4O)OC)C=CC(=C6)O 482.50 unknown https://doi.org/10.1016/0031-9422(90)85437-K
Blestrin B 14583572 Click to see COC1=CC2=C(C3=C(CC2)C=C(C=C3)OC4=C5CCC6=C(C5=C(C=C4O)OC)C=CC(=C6)O)C(=C1)O 482.50 unknown https://doi.org/10.1016/0031-9422(90)85437-K
Coelonin 11390848 Click to see COC1=CC(=CC2=C1C3=C(CC2)C=C(C=C3)O)O 242.27 unknown https://doi.org/10.1080/10286020.2018.1516212
Flavanthrin 102004681 Click to see COC1=CC2=C(C=C1)C3=C(CC2)C(=C(C=C3O)O)C4=C(C=C(C5=C4CCC6=C5C=CC(=C6)O)O)OC 482.50 unknown https://doi.org/10.1016/0031-9422(89)80373-5
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
(3R)-6,7'-dihydroxy-10'-methoxyspiro[1,2-dihydroindene-3,3'-naphtho[2,1-e][1]benzofuran]-2'-one 162988438 Click to see COC1=C2C3=C(C=CC2=C4C(=C1)OC(=O)C45CCC6=C5C=CC(=C6)O)C=C(C=C3)O 398.40 unknown https://doi.org/10.1016/0031-9422(93)85119-C
1-(2-Hydroxy-4,7-dimethoxyphenanthren-1-yl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol 122178805 Click to see COC1=CC2=C(C=C1)C3=C(C=C(C(=C3C=C2)C4=C5CCC6=C(C5=C(C=C4O)OC)C=CC(=C6)O)O)OC 494.50 unknown https://doi.org/10.1021/NP501012N
1-(2-Hydroxy-4,7-dimethoxyphenanthren-1-yl)-5-methoxy-9,10-dihydrophenanthrene-2,7-diol 122178806 Click to see COC1=CC2=C(C=C1)C3=C(C=C(C(=C3C=C2)C4=C(C=CC5=C4CCC6=C5C(=CC(=C6)O)OC)O)O)OC 494.50 unknown https://doi.org/10.1021/NP501012N
1-(4-Hydroxybenzyl)-4,8-dimethoxyphenanthrene-2,7-diol 44392553 Click to see COC1=C2C3=C(C=CC2=C(C(=C1)O)CC4=CC=C(C=C4)O)C(=C(C=C3)O)OC 376.40 unknown https://doi.org/10.1016/J.BMCL.2004.12.026
1-(7-Hydroxy-3,5-dimethoxy-9,10-dihydrophenanthren-2-yl)-4,7-dimethoxyphenanthren-2-ol 122178803 Click to see COC1=CC2=C(C=C1)C3=C(C=C(C(=C3C=C2)C4=C(C=C5C(=C4)CCC6=C5C(=CC(=C6)O)OC)OC)O)OC 508.60 unknown https://doi.org/10.1021/NP501012N
1-(7-Hydroxy-5-methoxyphenanthren-2-yl)oxy-4-methoxyphenanthrene-2,7-diol 101634591 Click to see COC1=C2C(=CC(=C1)O)C=CC3=C2C=CC(=C3)OC4=C5C=CC6=C(C5=C(C=C4O)OC)C=CC(=C6)O 478.50 unknown https://doi.org/10.1016/S0031-9422(00)97568-X
1-[(4-Hydroxyphenyl)methyl]-4-methoxyphenanthrene-2,7-diol 14630664 Click to see COC1=C2C3=C(C=CC2=C(C(=C1)O)CC4=CC=C(C=C4)O)C=C(C=C3)O 346.40 unknown https://doi.org/10.1016/0031-9422(90)83053-4
1-[(7-Hydroxy-4-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-4-methoxyphenanthrene-2,7-diol 163008939 Click to see COC1=CC(=CC2=C1C3=C(CC2)C=C(C=C3)O)OC4=C5C=CC6=C(C5=C(C=C4O)OC)C=CC(=C6)O 480.50 unknown https://doi.org/10.1016/S0031-9422(00)97568-X
1,8-Bis(4-hydroxybenzyl)-4-methoxyphenanthrene-2,7-diol 14863079 Click to see COC1=C2C3=C(C=CC2=C(C(=C1)O)CC4=CC=C(C=C4)O)C(=C(C=C3)O)CC5=CC=C(C=C5)O 452.50 unknown https://doi.org/10.1016/0031-9422(91)85133-K
2,6-Phenanthrenediol, 5,7-dimethoxy- 10445823 Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C=CC(=C3)O)OC)O 270.28 unknown https://doi.org/10.1002/HLCA.200890056
2,7-Phenanthrenediol, 3,4-dimethoxy- 158975 Click to see COC1=C(C=C2C=CC3=C(C2=C1OC)C=CC(=C3)O)O 270.28 unknown https://doi.org/10.1002/HLCA.200890056
3-(2-Hydroxy-4,7-dimethoxyphenanthren-1-yl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol 122178804 Click to see COC1=CC2=C(C=C1)C3=C(C=C(C(=C3C=C2)C4=C(C=C5CCC6=C(C5=C4)C(=CC(=C6)OC)O)O)O)OC 494.50 unknown https://doi.org/10.1021/NP501012N
4,4',8,8'-Tetramethoxy[1,1'-biphenanthrene]-2,2',7,7'-tetrol 14104273 Click to see COC1=C2C3=C(C=CC2=C(C(=C1)O)C4=C5C=CC6=C(C5=C(C=C4O)OC)C=CC(=C6OC)O)C(=C(C=C3)O)OC 538.50 unknown https://doi.org/10.1021/NP501012N
Blespirol 102440970 Click to see COC1=C2C3=C(C=CC2=C4C(=C1)OC(=O)C45CCC6=C5C=CC(=C6)O)C=C(C=C3)O 398.40 unknown https://doi.org/10.1016/0031-9422(93)85119-C
Blestrianol C 14863077 Click to see COC1=C2C(=C(C(=C1)O)CC3=CC=C(C=C3)O)CCC4=CC(=C(C=C42)C5=C6C=CC7=C(C6=C(C=C5O)OC)C=CC(=C7)O)O 586.60 unknown https://doi.org/10.1016/0031-9422(91)85133-K
https://doi.org/10.1016/0031-9422(90)85437-K
Blestriarene B 442695 Click to see COC1=C2C(=C(C(=C1)O)C3=C4C=CC5=C(C4=C(C=C3O)OC)C=CC(=C5)O)CCC6=C2C=CC(=C6)O 480.50 unknown https://doi.org/10.1016/J.BMCL.2004.12.026
https://doi.org/10.1016/0031-9422(89)80373-5
Blestrin C 101636138 Click to see COC1=C2C(=CC(=C1)C3=C4C=CC5=C(C4=C(C=C3O)OC)C=CC(=C5)O)C=CC6=C2C=CC(=C6)O 462.50 unknown https://doi.org/10.1016/S0031-9422(00)97568-X
Blestrin D 162930850 Click to see COC1=CC(=CC2=C1C3=C(CC2)C=C(C=C3)OC4=C5C=CC6=C(C5=C(C=C4O)OC)C=CC(=C6)O)O 480.50 unknown https://doi.org/10.1016/S0031-9422(00)97568-X
Cirrhopetalanthin 9982511 Click to see COC1=C2C3=C(C=CC2=C(C(=C1)O)C4=C5C=CC6=C(C5=C(C=C4O)OC)C=CC(=C6)O)C=C(C=C3)O 478.50 unknown https://doi.org/10.1016/J.BMCL.2004.12.026
https://doi.org/10.1021/NP501012N
https://doi.org/10.1016/0031-9422(89)80373-5
Flavanthrinin 14777892 Click to see COC1=C2C(=CC(=C1)O)C=CC3=C2C=CC(=C3)O 240.25 unknown https://doi.org/10.1002/HLCA.200890056
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
10-O-Caffeoylaucubin 101667548 Click to see C1=COC(C2C1C(C=C2COC(=O)C=CC3=CC(=C(C=C3)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 508.50 unknown via CMAUP database
6-O-Cumaroylaucubin 101667549 Click to see C1=COC(C2C1C(C=C2CO)OC(=O)C=CC3=CC=C(C=C3)O)OC4C(C(C(C(O4)CO)O)O)O 492.50 unknown via CMAUP database
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown via CMAUP database
Eurostoside 20839507 Click to see C1=COC(C2C1C(C=C2COC(=O)C=CC3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 492.50 unknown via CMAUP database
Mussaenosidic acid 21633105 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Glycol Dimethacrylate 7355 Click to see CC(=C)C(=O)OCCOC(=O)C(=C)C 198.22 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585276/
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3R,4S,5S,6R)-2-(7-hydroxy-4-methoxyphenanthren-2-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162931425 Click to see COC1=C2C(=CC(=C1)OC3C(C(C(C(O3)CO)O)O)O)C=CC4=C2C=CC(=C4)O 402.40 unknown https://doi.org/10.1016/0031-9422(93)80041-P
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[5-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenanthren-2-yl]oxyoxane-3,4,5-triol 162933387 Click to see COC1=C2C(=CC(=C1)OC3C(C(C(C(O3)CO)O)O)O)C=CC4=C2C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(93)80041-P
(2S,3R,4R,5R,6R)-2-(7-hydroxy-4-methoxy-9,10-dihydrophenanthren-2-yl)-6-(hydroxymethyl)oxane-3,4,5-triol 163090640 Click to see COC1=CC(=CC2=C1C3=C(CC2)C=C(C=C3)O)C4C(C(C(C(O4)CO)O)O)O 388.40 unknown https://doi.org/10.1016/0031-9422(93)80041-P
(2S,3R,4S,5R,6R)-2-[4-[(2,7-dihydroxy-4-methoxy-9,10-dihydrophenanthren-1-yl)methyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162961559 Click to see COC1=C2C(=C(C(=C1)O)CC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)CCC5=C2C=CC(=C5)O 510.50 unknown https://doi.org/10.1016/0031-9422(93)80041-P
(2S,3R,4S,5S,6R)-2-(7-hydroxy-2,4-dimethoxyphenanthren-3-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162946675 Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C=CC(=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(93)80041-P
(2S,3R,4S,5S,6R)-2-(7-hydroxy-4-methoxyphenanthren-2-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162931424 Click to see COC1=C2C(=CC(=C1)OC3C(C(C(C(O3)CO)O)O)O)C=CC4=C2C=CC(=C4)O 402.40 unknown https://doi.org/10.1016/0031-9422(93)80041-P
(2S,3R,4S,5S,6R)-2-[4-[(2,7-dihydroxy-4-methoxy-9,10-dihydrophenanthren-1-yl)methyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162961558 Click to see COC1=C2C(=C(C(=C1)O)CC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)CCC5=C2C=CC(=C5)O 510.50 unknown https://doi.org/10.1016/0031-9422(93)80041-P
(2S,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[5-methoxy-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenanthren-2-yl]oxyoxane-3,4,5-triol 162933388 Click to see COC1=C2C(=CC(=C1)OC3C(C(C(C(O3)CO)O)O)O)C=CC4=C2C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(93)80041-P
(3r)-5-Methyl-3-[(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]methoxycarbonyl]hexanoic acid 10555851 Click to see CC(C)CC(CC(=O)O)(C(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC3C(C(C(C(O3)CO)O)O)O 620.60 unknown https://doi.org/10.1002/HLCA.200890056
2-(7-Hydroxy-2,4-dimethoxyphenanthren-3-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162946674 Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C=CC(=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O 432.40 unknown https://doi.org/10.1016/0031-9422(93)80041-P
2-(7-Hydroxy-4-methoxyphenanthren-2-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162931423 Click to see COC1=C2C(=CC(=C1)OC3C(C(C(C(O3)CO)O)O)O)C=CC4=C2C=CC(=C4)O 402.40 unknown https://doi.org/10.1016/0031-9422(93)80041-P
2-(Hydroxymethyl)-6-[5-methoxy-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenanthren-2-yl]oxyoxane-3,4,5-triol 162933386 Click to see COC1=C2C(=CC(=C1)OC3C(C(C(C(O3)CO)O)O)O)C=CC4=C2C=CC(=C4)OC5C(C(C(C(O5)CO)O)O)O 564.50 unknown https://doi.org/10.1016/0031-9422(93)80041-P
2-[4-[(2,7-Dihydroxy-4-methoxy-9,10-dihydrophenanthren-1-yl)methyl]phenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162961557 Click to see COC1=C2C(=C(C(=C1)O)CC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)CCC5=C2C=CC(=C5)O 510.50 unknown https://doi.org/10.1016/0031-9422(93)80041-P
2-Hydroxy-4-methyl-2-[2-oxo-2-[[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxy]ethyl]pentanoic acid 73031675 Click to see CC(C)CC(CC(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)(C(=O)O)O 458.50 unknown https://doi.org/10.1002/HLCA.200890056
3-Hydroxy-5-methyl-3-[[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxycarbonyl]hexanoic acid 73038926 Click to see CC(C)CC(CC(=O)O)(C(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)O 458.50 unknown https://doi.org/10.1002/HLCA.200890056
5-Methyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxycarbonyl]hexanoic acid 9986365 Click to see CC(C)CC(CC(=O)O)(C(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)OC3C(C(C(C(O3)CO)O)O)O 620.60 unknown https://doi.org/10.1002/HLCA.200890056
Bis[[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methyl] 2-(2-methylpropyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanedioate 85279153 Click to see CC(C)CC(CC(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 888.90 unknown https://doi.org/10.1002/HLCA.200890056
Dactylorhin A 10819499 Click to see CC(C)CC(CC(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 888.90 unknown https://doi.org/10.1002/HLCA.200890056
Gymnoside 11641120 Click to see CC(C)CC(CC(=O)O)(C(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)O 458.50 unknown https://doi.org/10.1002/HLCA.200890056
Gymnoside II 11619501 Click to see CC(C)CC(CC(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)(C(=O)O)O 458.50 unknown https://doi.org/10.1002/HLCA.200890056
Gymnoside IX 11651021 Click to see CC(C)CC(CC(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)COC(=O)C)OC(=O)C=CC6=CC=CC=C6)O)O 1061.00 unknown via CMAUP database
Gymnoside V 11693717 Click to see CC(C)CC(CC(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)OC(=O)C=CC6=CC=CC=C6)O)O 1019.00 unknown via CMAUP database
Militarine 171638 Click to see CC(C)CC(CC(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O 726.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Amylum 24836924 Click to see CC1C(C(C(C(O1)CO)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)OC)O)O)OC4C(C(C(C(O4)CO)OC)O)O)O)O)O)O 692.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown https://doi.org/10.1080/10286020.2018.1516212
https://doi.org/10.1016/0031-9422(83)85044-4
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1016/0031-9422(83)85044-4
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1016/0031-9422(83)85044-4
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
1,3-Bis(4-hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol 44392564 Click to see COC1=C2C(=C(C(=C1CC3=CC=C(C=C3)O)O)CC4=CC=C(C=C4)O)CCC5=C2C=CC(=C5)O 454.50 unknown https://doi.org/10.1016/J.BMCL.2004.12.026
https://doi.org/10.1016/0031-9422(93)85115-8
2,6-Bis[(4-hydroxyphenyl)methyl]-3-methoxy-5-[2-(3-methoxyphenyl)ethyl]phenol 141467282 Click to see COC1=CC=CC(=C1)CCC2=CC(=C(C(=C2CC3=CC=C(C=C3)O)O)CC4=CC=C(C=C4)O)OC 470.60 unknown https://doi.org/10.1002/HLCA.200890056
Arundinin 102316541 Click to see COC1=CC(=CC(=C1CC2=CC=C(C=C2)O)O)CCC3=CC(=CC=C3)O 350.40 unknown https://doi.org/10.1016/0031-9422(93)85115-8
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
2,4-Bis(4-hydroxybenzyl)-3-(3-hydroxyphenethyl)-5-methoxyphenol 11282492 Click to see COC1=C(C(=C(C(=C1)O)CC2=CC=C(C=C2)O)CCC3=CC(=CC=C3)O)CC4=CC=C(C=C4)O 456.50 unknown https://doi.org/10.1016/0031-9422(83)85044-4
https://doi.org/10.1016/J.BMCL.2004.12.026
2,4-Bis[(4-hydroxyphenyl)methyl]-5-methoxy-3-[2-(3-methoxyphenyl)ethyl]phenol 87579315 Click to see COC1=CC=CC(=C1)CCC2=C(C(=CC(=C2CC3=CC=C(C=C3)O)OC)O)CC4=CC=C(C=C4)O 470.60 unknown https://doi.org/10.1016/0031-9422(83)85044-4
3,3'-Dihydroxy-5-methoxy-2,5',6-tris-(p-hydroxybenzyl)bibenzyl 87579595 Click to see COC1=C(C(=C(C(=C1)O)CC2=CC=C(C=C2)O)CCC3=CC(=CC(=C3)O)CC4=CC=C(C=C4)O)CC5=CC=C(C=C5)O 562.60 unknown https://doi.org/10.1016/0031-9422(83)85044-4
Blestritin A 101845671 Click to see COC1=CC=CC(=C1)CCC2=C(C(=C(C(=C2CC3=CC=C(C=C3)O)OC)CC4=CC=C(C=C4)O)O)CC5=CC=C(C=C5)O 576.70 unknown https://doi.org/10.1002/HLCA.200890056
Blestritin B 101845672 Click to see COC1=C(C=CC(=C1)CCC2=C(C(=CC(=C2CC3=CC=C(C=C3)O)OC)O)CC4=CC=C(C=C4)O)O 486.60 unknown https://doi.org/10.1002/HLCA.200890056
Blestritin C 101845673 Click to see COC1=C(C(=C(C(=C1)O)CC2=CC=C(C=C2)O)CCC3=CC(=C(C=C3)CC4=CC=C(C=C4)O)O)CC5=CC=C(C=C5)O 562.60 unknown https://doi.org/10.1002/HLCA.200890056
Bulbocodin[bibenzyl] 102316538 Click to see COC1=C(C(=C(C(=C1)O)CC2=CC=C(C=C2)O)CCC3=C(C=CC(=C3)CC4=CC=C(C=C4)O)O)CC5=CC=C(C=C5)O 562.60 unknown https://doi.org/10.1002/HLCA.200890056
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 7-O-p-coumaroyl glycosides / Anthocyanidin 7-O-6-p-coumaroyl glycosides
3-[[(2R,3S,4R,5S,6S)-6-[7-[(2S,3S,4S,5S,6R)-6-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-[3-hydroxy-4-[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-enoyl]oxymethyl]oxan-2-yl]oxyphenyl]chromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid 163192092 Click to see C1=CC(=C(C=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C=C(C(=[O+]C4=C3)C5=CC(=C(C=C5)O)OC6C(C(C(C(O6)COC(=O)C=CC7=CC(=C(C=C7)OC8C(C(C(C(O8)COC(=O)C=CC9=CC(=C(C=C9)OC1C(C(C(C(O1)CO)O)O)O)O)O)O)O)O)O)O)O)OC1C(C(C(C(O1)COC(=O)CC(=O)O)O)O)O)O)O)O)O)O)O 1670.40 unknown https://doi.org/10.1016/0031-9422(95)00479-Q
3-oxo-3-[[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-2-[4-hydroxy-3-[(2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyl]oxymethyl]oxan-2-yl]oxyphenyl]prop-2-enoyl]oxymethyl]oxan-2-yl]oxyphenyl]-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[3-(4-hydroxyphenyl)prop-2-enoyloxymethyl]oxan-2-yl]oxychromenylium-3-yl]oxyoxan-2-yl]methoxy]propanoic acid 163192089 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC(=C4C=C(C(=[O+]C4=C3)C5=CC(=C(C=C5)O)OC6C(C(C(C(O6)COC(=O)C=CC7=CC=C(C=C7)OC8C(C(C(C(O8)COC(=O)C=CC9=CC=C(C=C9)OC1C(C(C(C(O1)CO)O)O)O)O)O)O)O)O)O)OC1C(C(C(C(O1)COC(=O)CC(=O)O)O)O)O)O)O)O)O)O 1622.40 unknown https://doi.org/10.1016/0031-9422(95)00479-Q
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids
[(10R,11R)-3-hydroxy-10-(4-hydroxy-3-methoxyphenyl)-1-methoxy-6,9,10,11-tetrahydro-5H-naphtho[1,2-g]chromen-11-yl] acetate 163057784 Click to see CC(=O)OC1C(COC2=C1C=C3C(=C2)CCC4=C3C(=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC 462.50 unknown https://doi.org/10.1016/S0031-9422(00)95008-8
[(10R,11S)-3-hydroxy-10-(4-hydroxy-3-methoxyphenyl)-1-methoxy-6,9,10,11-tetrahydro-5H-naphtho[1,2-g]chromen-11-yl] acetate 163057786 Click to see CC(=O)OC1C(COC2=C1C=C3C(=C2)CCC4=C3C(=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC 462.50 unknown https://doi.org/10.1016/S0031-9422(00)95008-8
Bletilol C 102121478 Click to see CC(=O)OC1C(COC2=C1C=C3C(=C2)CCC4=C3C(=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC 462.50 unknown https://doi.org/10.1016/S0031-9422(00)95008-8
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids
[(3S,4R)-8-hydroxy-3-(4-hydroxy-3-methoxyphenyl)-11-methoxy-3,4,5,6-tetrahydro-2H-naphtho[2,1-f]chromen-4-yl] acetate 162954315 Click to see CC(=O)OC1C(COC2=CC(=C3C(=C12)CCC4=C3C=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC 462.50 unknown https://doi.org/10.1016/S0031-9422(00)95008-8
[8-hydroxy-3-(4-hydroxy-3-methoxyphenyl)-11-methoxy-3,4,5,6-tetrahydro-2H-naphtho[2,1-f]chromen-4-yl] acetate 162642271 Click to see CC(=O)OC1C(COC2=CC(=C3C(=C12)CCC4=C3C=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC 462.50 unknown https://doi.org/10.1016/S0031-9422(00)95008-8
[8-hydroxy-3-(4-hydroxy-3,5-dimethoxyphenyl)-11-methoxy-3,4,5,6-tetrahydro-2H-naphtho[2,1-f]chromen-4-yl] acetate 162938370 Click to see CC(=O)OC1C(COC2=CC(=C3C(=C12)CCC4=C3C=CC(=C4)O)OC)C5=CC(=C(C(=C5)OC)O)OC 492.50 unknown https://doi.org/10.1016/S0031-9422(00)95008-8
Bletilol A 102121477 Click to see CC(=O)OC1C(COC2=CC(=C3C(=C12)CCC4=C3C=CC(=C4)O)OC)C5=CC(=C(C(=C5)OC)O)OC 492.50 unknown https://doi.org/10.1016/S0031-9422(00)95008-8
Bletilol B 146075490 Click to see CC(=O)OC1C(COC2=CC(=C3C(=C12)CCC4=C3C=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC 462.50 unknown https://doi.org/10.1016/S0031-9422(00)95008-8
CID 101688453 101688453 Click to see CC(=O)OC1C(COC2=CC(=C3C(=C12)CCC4=C3C=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC 462.50 unknown https://doi.org/10.1016/S0031-9422(00)95008-8
> Phenylpropanoids and polyketides / Stilbenes
2-(p-Hydroxybenzyl)-3-(m-methoxyphenethyl)5-methoxyphenol 11428499 Click to see COC1=CC=CC(=C1)CCC2=C(C(=CC(=C2)OC)O)CC3=CC=C(C=C3)O 364.40 unknown https://doi.org/10.1002/HLCA.200890056
3,3',5-Trimethoxybibenzyl 15693460 Click to see COC1=CC=CC(=C1)CCC2=CC(=CC(=C2)OC)OC 272.34 unknown https://doi.org/10.1016/0031-9422(91)85139-Q
https://doi.org/10.1016/0031-9422(93)85115-8
3'-O-Methylbatatasin III 442711 Click to see COC1=CC=CC(=C1)CCC2=CC(=CC(=C2)OC)O 258.31 unknown https://doi.org/10.1002/HLCA.200890056
https://doi.org/10.1016/0031-9422(89)80373-5
3',5-Dihydroxy-2-(4-hydroxybenzyl)3-methoxybibenzyl 11187204 Click to see COC1=CC(=CC(=C1CC2=CC=C(C=C2)O)CCC3=CC(=CC=C3)O)O 350.40 unknown https://doi.org/10.1016/J.BMCL.2004.12.026
https://doi.org/10.1016/0031-9422(93)85115-8
batatasin III 10466989 Click to see COC1=CC(=CC(=C1)O)CCC2=CC(=CC=C2)O 244.28 unknown https://doi.org/10.1016/0031-9422(89)80373-5
https://doi.org/10.1002/HLCA.200890056
Benzene, 1,3-dimethoxy-5-(2-phenylethyl)- 10538117 Click to see COC1=CC(=CC(=C1)CCC2=CC=CC=C2)OC 242.31 unknown https://doi.org/10.1016/0031-9422(91)85139-Q
https://doi.org/10.1016/0031-9422(93)85115-8
Bibenzyl 7647 Click to see C1=CC=C(C=C1)CCC2=CC=CC=C2 182.26 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3585276/
Gigantol 3085362 Click to see COC1=C(C=C(C=C1)CCC2=CC(=CC(=C2)OC)O)O 274.31 unknown https://doi.org/10.1002/HLCA.200890056
Isoarundinin II 91542987 Click to see COC1=CC(=C(C(=C1)O)CC2=CC=C(C=C2)O)CCC3=CC(=CC=C3)O 350.40 unknown https://doi.org/10.1016/0031-9422(93)85115-8
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Schizandrin 23915 Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3CC1(C)O)OC)OC)OC)OC)OC)OC 432.50 unknown via CMAUP database

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