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Osmanthus heterophyllus

Osmanthus heterophyllus - Unknown
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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 UUID64402b0375add124045043
Scientific name Osmanthus heterophyllus
Authority (G.Don) P.S.Green
First published in Notes Roy. Bot. Gard. Edinburgh 22: 508 (1958)

Description Top

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Synonyms Top

Scientific name Authority First published in
Osmanthus rotundifolius hort. ex Dippel Handb. Laubholzk. i. (1889) 141.
Osmanthus integrifolius Hayata J. Coll. Sci. Imp. Univ. Tokyo 30(1): 191 (1911)
Osmanthus ilicifolius hort. ex Dippel Handb. Laubholzk. i. (1889) 140.
Osmanthus acutus Masam. & Mori J. Jap. Bot. 15: 546 (1939)
Osmanthus aquifolium Siebold ex Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 166 (1846)
Osmanthus bibracteatus Hayata Icon. Pl. Formosan. 9: 71 (1920)
Olea aquifolium var. myrtifolia (G.Nicholson) Dippel Handb. Laubholzk. 1: 141. 1889
Olea aquifolium Siebold & Zucc. Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 166 (1846)
Olea ilicifolia Hassk. Cat. Hort. Bot. Bogor. Alt. : 118 (1844)
Osmanthus heterophyllus var. acutus (Masam. & Mori) T.S.Liu & J.C.Liao Quart. J. Taiwan Mus. 31: 293 (1978)
Osmanthus heterophyllus f. subangustatus (Makino) Murata Acta Phytotax. Geobot. 25: 35 (1972)
Osmanthus heterophyllus var. bibracteatus (Hayata) P.S.Green Notes Roy. Bot. Gard. Edinburgh 22: 516. 1958
Osmanthus aquifolium var. ilicifolius (Hassk.) G.Nicholson Hand-List Trees Shrubs 2: 89. 1896
Osmanthus aquifolium f. subangustatus Makino Bot. Mag. (Tokyo) 23: 14 1909
Osmanthus ilicifolius var. subangustatus (Makino) Makino J. Jap. Bot. 7: 14 1931
Olea aquifolium f. subintegra Miq. Ann. Mus. Bot. Lugduno-Batavi 2: 264 1866
Olea aquifolium var. subintegra (Miq.) Miq. Cat. Mus. Bot. Lugd.-Bat. 57 1870
Olea aquifolium var. ilicifolia (Hassk.) Dippel Handb. Laubholzk. 1: 141. 1889
Osmanthus ilicifolius f. subangustatus (Makino) Makino & Nemoto Fl. Japan ed. 2: 939 1931
Osmanthus ilicifolius var. undulatifolius Makino J. Jap. Bot. 7: 14. 1931
Osmanthus ilicifolius var. aureovariegatus Mouill. Traité Arbr. Arbriss. 2: 982. 1896
Osmanthus ilicifolius var. aureomarginatus Bean Garden (London, 1871-1927) 50: 86. 1896
Osmanthus aquifolium var. aureus C.K.Schneid. Ill. Handb. Laubholzk. 2: 790. 1911
Osmanthus aquifolium var. aureovariegatus (Mouill.) L.H.Bailey Stand. Cycl. Hort. ed. 2, 4: 2412 1917
Osmanthus ilicifolius f. aureus (C.K.Schneid.) Rehder J. Arnold Arbor. 5: 240 1924
Osmanthus ilicifolius var. aureus (C.K.Schneid.) Rehder Man. Cult. Trees 758 1927
Osmanthus ilicifolius f. aureomarginatus (Bean) Rehder Bibl. Cult. Trees 575 1949
Olea aquifolium f. cuneata Miq. Ann. Mus. Bot. Lugduno-Batavi 2: 264 1866
Olea aquifolium var. cuneata (Miq.) Miq. Cat. Mus. Bot. Lugd.-Bat. 57 1870
Olea aquifolium var. rotundifolia H.Jaeger Ziergehloze Gart. Park. ed. 2: 229 1884
Olea rotundifolia (H.Jaeger) Entleutner Immergr. Ziergeh. S.-Tirol 115 1891
Osmanthus aquifolium var. rotundifolius (H.Jaeger) G.Nicholson Hand-List Trees Shrubs 2: 89 1896
Osmanthus ilicifolius var. rotundifolius (H.Jaeger) Rehder Man. Cult. Trees 758 1927
Osmanthus ilicifolius f. rotundifolius (H.Jaeger) Rehder J. Arnold Arbor. 5: 240 1924
Osmanthus myrtifolius Hort.Veitch. ex Dippel Handb. Laubholzk. i. (1889) 141.
Osmanthus ilicifolius var. myrtifolius (G.Nicholson) Mouill. Traité Arbr. Arbriss. 2: 982. 1896
Osmanthus aquifolium var. myrtifolius (G.Nicholson) G.Nicholson Hand-List Trees Shrubs 2: 89. 1896
Osmanthus ilicifolius f. myrtifolius (G.Nicholson) Rehder Bibl. Cult. Trees 576 1949
Osmanthus ilicifolius var. purpurascens Bean Garden (London, 1871-1927) 50: 87. 1896
Osmanthus aquifolium var. atropurpureus C.K.Schneid. Ill. Handb. Laubholzk. 2: 790. 1911
Osmanthus aquifolium var. purpureus Bean Trees & Shrubs Brit. Isles 2: 111. 1914
Osmanthus ilicifolius f. purpureus (Bean) Rehder J. Arnold Arbor. 5: 240 1924
Osmanthus ilicifolius var. purpureus (Bean) Rehder Man. Cult. Trees 758 1927
Osmanthus ilicifolius f. purpurascens (Bean) Rehder Bibl. Cult. Trees 575 1949
Osmanthus ilicifolius var. argenteomarginatus Bean Garden (London, 1871-1927) 50: 87. 1896
Osmanthus ilicifolius var. argenteovariegatus Mouill. Traité Arbr. Arbriss. 2: 982. 1896
Osmanthus aquifolium var. argenteus C.K.Schneid. Ill. Handb. Laubholzk. 2: 790. 1911
Osmanthus aquifolium var. argenteomarginatus (Bean) L.H.Bailey Stand. Cycl. Hort. ed. 2, 4: 2412 1917
Osmanthus ilicifolius var. bibracteatus (Hayata) Mori J. Jap. Bot. 15: 552. 1939

Common names Top

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Language Common/alternative name
English holly osmanthus
Danish djævletræ
German stachelblättrige duftblüte
Armenian Օսմանթուս տարատերև
Japanese ひいらぎ
Japanese 柊木
Japanese 疼木
Japanese ヒイラギ
Korean 구골나무
Russian Османтус разнолистный
Russian osmanthus illicifolius variegatus
Thai ฮิอิรากิ
Chinese 异叶木犀
Chinese 圓葉木犀
Chinese 柊树
Chinese 香木菌桂
Chinese 異葉木犀
Chinese 冬树
Chinese 桂花子

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000817131
USDA Plants OSHE
Tropicos 23000777
INPN 611050
KEW urn:lsid:ipni.org:names:610885-1
The Plant List kew-354986
Missouri Botanical Garden 283003
Open Tree Of Life 558202
NCBI Taxonomy 126555
NBN Atlas NHMSYS0000461399
IPNI 610885-1
iNaturalist 404400
GBIF 3172276
Freebase /m/02y_dpf
EPPO OSUHE
EOL 483930
USDA GRIN 26125
Wikipedia Osmanthus_heterophyllus
CMAUP NPO24378

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
Allelopathic Substances of Osmanthus spp. for Developing Sustainable Agriculture Kato-Noguchi H, Hamada Y, Kojima M, Kumagai S, Iwasaki A, Suenaga K Plants (Basel) 13-Jan-2023
PMCID:PMC9861473
doi:10.3390/plants12020376
PMID:36679091
Global ecological niche conservatism and evolution in Olea species Ashraf U, Peterson AT, Chaudhry MN, Cobos ME Saudi J Biol Sci 11-Nov-2022
PMCID:PMC9706617
doi:10.1016/j.sjbs.2022.103500
PMID:36458099
Review on the Pharmacological Properties of Phillyrin Zhou C, Lu M, Cheng J, Rohani ER, Hamezah HS, Han R, Tong X Molecules 07-Jun-2022
PMCID:PMC9231344
doi:10.3390/molecules27123670
PMID:35744798
Plastid genomes reveal evolutionary shifts in elevational range and flowering time of Osmanthus (Oleaceae) Li Y, Li X, Sylvester SP, Zhang M, Wang X, Duan Y Ecol Evol 01-Apr-2022
PMCID:PMC8975774
doi:10.1002/ece3.8777
PMID:35386867
A comprehensive dataset on cultivated and spontaneously growing vascular plants in urban gardens Frey D, Moretti M Data Brief 23-May-2019
PMCID:PMC6545399
doi:10.1016/j.dib.2019.103982
PMID:31194048
The network of plants volatile organic compounds Vivaldo G, Masi E, Taiti C, Caldarelli G, Mancuso S Sci Rep 08-Sep-2017
PMCID:PMC5591229
doi:10.1038/s41598-017-10975-x
PMID:28887468
Host Specificity of Epiplema albida: A Potential Biological Control Agent for Sri Lankan Privet in the Mascarene Islands Shaw RH, Cock MJ Insects 28-Jul-2017
PMCID:PMC5620697
doi:10.3390/insects8030077
PMID:28788086
Dioecious plants are more precocious than cosexual plants: A comparative study of relative sizes at the onset of sexual reproduction in woody species Ohya I, Nanami S, Itoh A Ecol Evol 15-Jun-2017
PMCID:PMC5551102
doi:10.1002/ece3.3117
PMID:28808545
Studies on the Constituents of Osmanthus Species. III. On the Components of the Leaves of Osmanthus ilicifolius (HASSK.) MOUILLEFERT MASAO KIKUCHI, YOKO YAMAUCHI Pharmaceutical Society of Japan 20-Apr-2017
doi:10.1248/YAKUSHI1947.105.5_442
Rapid, Effective DNA Isolation from Osmanthus via Modified Alkaline Lysis Alexander L J Biomol Tech 18-Jan-2016
PMCID:PMC4719223
doi:10.7171/jbt.16-2702-001
PMID:26816495
Disturbance regimes, gap‐demanding trees and seed mass related to tree height in warm temperate rain forests worldwide Grubb PJ, Bellingham PJ, Kohyama TS, Piper FI, Valido A Biol Rev Camb Philos Soc 19-Mar-2013
PMCID:PMC7161821
doi:10.1111/brv.12029
PMID:23506298
Population Genetic Analysis Infers Migration Pathways of Phytophthora ramorum in US Nurseries Goss EM, Larsen M, Chastagner GA, Givens DR, Grünwald NJ PLoS Pathog 18-Sep-2009
PMCID:PMC2736564
doi:10.1371/journal.ppat.1000583
PMID:19774068
Phylogenetics of Olea (Oleaceae) based on plastid and nuclear ribosomal DNA sequences: Tertiary climatic shifts and lineage differentiation times Besnard G, Rubio de Casas R, Christin PA, Vargas P Ann Bot 25-May-2009
PMCID:PMC2706730
doi:10.1093/aob/mcp105
PMID:19465750
Ilicifoliosides A and B, Bis-Secoiridoid Glycosides from Osmanthus ilicifolius Masao Kikuchi, Shigeaki Sakamoto, Koichi Machida The Japan Institute of Heterocyclic Chemistry 02-Mar-2009
doi:10.3987/COM-07-S(W)9
Secoiridoid Di-glycosides from Osmanthus ilicifolius Masao Kikuchi, Koichi Machida, Shigeaki Sakamoto The Japan Institute of Heterocyclic Chemistry 19-Feb-2009
doi:10.3987/COM-08-S(F)3

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Phenol ethers / Anisoles
1,2,3-Trimethoxybenzene 12462 Click to see COC1=C(C(=CC=C1)OC)OC 168.19 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-(1-Hydroxyethyl)phenol 102803 Click to see CC(C1=CC=C(C=C1)O)O 138.16 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
> Benzenoids / Phenols / Tyrosols and derivatives
2-(4-Hydroxyphenyl)ethyl acetate 637753 Click to see CC(=O)OCCC1=CC=C(C=C1)O 180.20 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
> Lignans, neolignans and related compounds / Lignan glycosides
(2R,3R,4S,5S,6R)-2-[(2R,3S)-3-hydroxy-3-(4-hydroxy-3-methoxyphenyl)-2-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163191425 Click to see COC1=CC(=CC(=C1OC(COC2C(C(C(C(O2)CO)O)O)O)C(C3=CC(=C(C=C3)O)OC)O)OC)C=CCO 568.60 unknown https://doi.org/10.1002/MRC.2292
(2R,3R,4S,5S,6R)-2-[(2R,3S)-3-hydroxy-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163188533 Click to see COC1=CC(=CC(=C1OC(COC2C(C(C(C(O2)CO)O)O)O)C(C3=CC(=C(C(=C3)OC)O)OC)O)OC)C=CCO 598.60 unknown https://doi.org/10.1002/MRC.2292
(2R,3R,4S,5S,6R)-2-[(2S,3R)-3-hydroxy-3-(4-hydroxy-3-methoxyphenyl)-2-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163190710 Click to see COC1=CC(=CC(=C1OC(COC2C(C(C(C(O2)CO)O)O)O)C(C3=CC(=C(C=C3)O)OC)O)OC)C=CCO 568.60 unknown https://doi.org/10.1002/MRC.2292
(2R,3R,4S,5S,6R)-2-[(2S,3R)-3-hydroxy-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163190629 Click to see COC1=CC(=CC(=C1OC(COC2C(C(C(C(O2)CO)O)O)O)C(C3=CC(=C(C(=C3)OC)O)OC)O)OC)C=CCO 598.60 unknown https://doi.org/10.1002/MRC.2292
(2S,3R,4S,5R,6S)-2-[4-[(3R,3aR,6S,6aR)-3-(3,4-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162976050 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC)OC 534.60 unknown https://doi.org/10.1007/S11418-008-0247-Y
(2S,3R,4S,5R,6S)-2-[4-[(3S,3aR,6S,6aR)-3-(4-hydroxy-3,5-dimethoxyphenyl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 161481407 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 580.60 unknown https://doi.org/10.1007/S11418-008-0247-Y
(2S,3S,4S,5S,6R)-2-[4-[(3S,3aR,6S,6aR)-6-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 154496911 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.1007/S11418-008-0247-Y
2-[3-Hydroxy-3-(4-hydroxy-3-methoxyphenyl)-2-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162897585 Click to see COC1=CC(=CC(=C1OC(COC2C(C(C(C(O2)CO)O)O)O)C(C3=CC(=C(C=C3)O)OC)O)OC)C=CCO 568.60 unknown https://doi.org/10.1002/MRC.2292
2-[3-Hydroxy-3-(4-hydroxy-3,5-dimethoxyphenyl)-2-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]propoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163019414 Click to see COC1=CC(=CC(=C1OC(COC2C(C(C(C(O2)CO)O)O)O)C(C3=CC(=C(C(=C3)OC)O)OC)O)OC)C=CCO 598.60 unknown https://doi.org/10.1002/MRC.2292
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(Z)-methyl 4-(2-(3,4-dihydroxyphenethoxy)-2-oxoethyl)-3-ethylidene-2-((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yloxy)-3,4-dihydro-2H-pyran-5-carboxylate 134688908 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 540.50 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
10-Acetoxyligustroside 131751686 Click to see CC(=O)OCC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC=C(C=C3)O 582.50 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
10-Acetoxyoleuropein 131751685 Click to see CC(=O)OCC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 598.50 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
10-Hydroxyligstroside 14756316 Click to see COC(=O)C1=COC(C(=CCO)C1CC(=O)OCCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O 540.50 unknown https://doi.org/10.3987/COM-08-S(F)3
https://doi.org/10.1248/YAKUSHI1947.105.5_442
10-Hydroxyoleuropein 6440747 Click to see COC(=O)C1=COC(C(=CCO)C1CC(=O)OCCC2=CC(=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 556.50 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
2H-Pyran-4-acetic acid, 3-ethylidene-2-(beta-D-glucopyranosyloxy)-3,4-dihydro-5-(methoxycarbonyl)-, 2-(4-hydroxyphenyl)ethyl ester, [2S-(2alpha,3E,4beta)]-; Ligstroside 72727933 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC=C(C=C3)O 524.50 unknown https://doi.org/10.3987/COM-08-S(F)3
CID 102117098 102117098 Click to see CC(=O)OCC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC=C(C=C3)O 582.50 unknown https://doi.org/10.3987/COM-08-S(F)3
Ligustroside 14136859 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC=C(C=C3)O 524.50 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl (4S,5E,6R)-5-ethylidene-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 75492723 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC=C(C=C3)O 524.50 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
methyl (4S,5E,6S)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 3789874 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 540.50 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl (4S,5E,6S)-5-(2-acetyloxyethylidene)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 102117099 Click to see CC(=O)OCC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 598.50 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl (4S,5E,6S)-5-(2-acetyloxyethylidene)-6-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-4H-pyran-3-carboxylate 102031348 Click to see CC(=O)OCC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)OC3C(C(C(C(O3)CO)O)O)O)O)C(=O)OC)CC(=O)OCCC4=CC(=C(C=C4)O)O 760.70 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl (4S,5E,6S)-5-(2-acetyloxyethylidene)-6-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-4H-pyran-3-carboxylate 102031344 Click to see CC(=O)OCC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)OC3C(C(C(C(O3)CO)O)O)O)O)C(=O)OC)CC(=O)OCCC4=CC=C(C=C4)O 744.70 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl (4S,5E,6S)-6-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-4H-pyran-3-carboxylate 102031346 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)OC3C(C(C(C(O3)CO)O)O)O)O)C(=O)OC)CC(=O)OCCC4=CC(=C(C=C4)O)O 702.70 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl (4S,5E,6S)-6-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-(2-hydroxyethylidene)-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-4H-pyran-3-carboxylate 102031347 Click to see COC(=O)C1=COC(C(=CCO)C1CC(=O)OCCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O 702.70 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl (4S,5E,6S)-6-[(2S,3R,4S,5R,6R)-3,5-dihydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-ethylidene-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-4H-pyran-3-carboxylate 102031345 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)OC3C(C(C(C(O3)CO)O)O)O)O)C(=O)OC)CC(=O)OCCC4=CC=C(C=C4)O 686.70 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl 5-(2-acetyloxyethylidene)-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163014037 Click to see CC(=O)OCC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 598.50 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl 5-(2-acetyloxyethylidene)-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 75110895 Click to see CC(=O)OCC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC=C(C=C3)O 582.50 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl 5-(2-acetyloxyethylidene)-6-[3,5-dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-4H-pyran-3-carboxylate 162921369 Click to see CC(=O)OCC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)OC3C(C(C(C(O3)CO)O)O)O)O)C(=O)OC)CC(=O)OCCC4=CC(=C(C=C4)O)O 760.70 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl 5-(2-acetyloxyethylidene)-6-[3,5-dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-4H-pyran-3-carboxylate 163036984 Click to see CC(=O)OCC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)OC3C(C(C(C(O3)CO)O)O)O)O)C(=O)OC)CC(=O)OCCC4=CC=C(C=C4)O 744.70 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl 5-(2-hydroxyethylidene)-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 74184139 Click to see COC(=O)C1=COC(C(=CCO)C1CC(=O)OCCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)O)O 540.50 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl 6-[3,5-dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4-[2-[2-(3,4-dihydroxyphenyl)ethoxy]-2-oxoethyl]-5-ethylidene-4H-pyran-3-carboxylate 163060877 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)OC3C(C(C(C(O3)CO)O)O)O)O)C(=O)OC)CC(=O)OCCC4=CC(=C(C=C4)O)O 702.70 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl 6-[3,5-dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-(2-hydroxyethylidene)-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-4H-pyran-3-carboxylate 162993177 Click to see COC(=O)C1=COC(C(=CCO)C1CC(=O)OCCC2=CC=C(C=C2)O)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O 702.70 unknown https://doi.org/10.3987/COM-08-S(F)3
methyl 6-[3,5-dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-ethylidene-4-[2-[2-(4-hydroxyphenyl)ethoxy]-2-oxoethyl]-4H-pyran-3-carboxylate 75614578 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)OC3C(C(C(C(O3)CO)O)O)O)O)C(=O)OC)CC(=O)OCCC4=CC=C(C=C4)O 686.70 unknown https://doi.org/10.3987/COM-08-S(F)3
Oleuropein 5281544 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCCC3=CC(=C(C=C3)O)O 540.50 unknown https://doi.org/10.3987/COM-08-S(F)3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
3beta-(2-O-beta-D-Galactopyranosyl-beta-D-glucurono pyranosyloxy)olean-12-en-28-oic acid 101923141 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)O)C 795.00 unknown via CMAUP database
Araloside A 10079497 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 927.10 unknown via CMAUP database
Calenduloside E 176079 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 632.80 unknown via CMAUP database
Calenduloside F 13909684 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 795.00 unknown via CMAUP database
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylate 21669007 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)OC)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 971.10 unknown via CMAUP database
Narcissiflorine 162878 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C 764.90 unknown via CMAUP database
Papyrioside LE 11803947 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CCC7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O 941.10 unknown via CMAUP database
Papyrioside LF 10819773 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CCC7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)COC(=O)C)O)O)O 983.10 unknown via CMAUP database
Scheffleraside II 101720880 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(C(O9)C(=O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1103.20 unknown via CMAUP database
Udosaponin B 21635582 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 957.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 13878127 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)O)C 588.80 unknown via CMAUP database
3-Epipapyriogenin C 16112782 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)O)C)C 468.70 unknown via CMAUP database
3-O-alpha-L-Arabinopyranosylechinocystic acid 15379012 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(CO6)O)O)O)C)C(=O)O)C 604.80 unknown via CMAUP database
3alpha,21beta,22alpha-Trihydroxyoleana-11,13(18)-diene-28-oic acid 16112781 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1O)O)C(=O)O)C)C)(C)C)O)C)C 486.70 unknown via CMAUP database
Guaianin N 10395290 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C 751.00 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
Papyriogenin A 3081523 Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)C)C 466.70 unknown via CMAUP database
Papyriogenin C 3081568 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)O)C)C 468.70 unknown via CMAUP database
Papyriogenin D 101277260 Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)C)C 468.70 unknown via CMAUP database
Papyriogenin E 101277261 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)O)C)C 470.70 unknown via CMAUP database
Papyriogenin F 102239749 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)O)C)C 470.70 unknown via CMAUP database
Papyrioside LG 10605857 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CC=C7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O 939.10 unknown via CMAUP database
Papyrioside LH 10748397 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CC=C7C6(CCC8C7(CCC(=O)C8(C)C)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O 937.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids
methyl (4S,5E,6S)-5-ethylidene-4-[2-[(2S,3R,4S,5S,6R)-2-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 101458329 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OC3C(C(C(OC3OC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)CO)O)O 952.90 unknown https://doi.org/10.3987/COM-07-S(W)9
methyl (4S,5E,6S)-5-ethylidene-4-[2-[[(2R,3S,4S,5R,6S)-6-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 101458328 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)O)O)O 952.90 unknown https://doi.org/10.3987/COM-07-S(W)9
methyl 5-ethylidene-4-[2-[[6-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163049530 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)O)O)O 952.90 unknown https://doi.org/10.3987/COM-07-S(W)9
methyl 5-ethylidene-4-[2-[2-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163030464 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OC3C(C(C(OC3OC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)CO)O)O 952.90 unknown https://doi.org/10.3987/COM-07-S(W)9
> 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/10.1248/YAKUSHI1947.105.5_442
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/10.1248/YAKUSHI1947.105.5_442
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
28-Noroleana-11,13(18),17(22)-triene-3,21-dione 102588576 Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2=CC1=O)C)C)(C)C)C)C 420.60 unknown via CMAUP database
3alpha-Hydroxy-28-noroleana-11,13(18),17(22)-triene-21-one 102588575 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2=CC1=O)C)C)(C)C)O)C)C 422.60 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
1-Benzofuran-5-carbaldehyde 2773875 Click to see C1=CC2=C(C=CO2)C=C1C=O 146.14 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Beta propiolactones
Papyriogenin G 101967008 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC26C(C1O)OC6=O)C)C)(C)C)O)C)C 468.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
3,4-Dihydrocoumarin 660 Click to see C1CC(=O)OC2=CC=CC=C21 148.16 unknown via CMAUP database
> 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/10.1248/YAKUSHI1947.105.5_442
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Phenylallyl alcohol 308 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
Kaempferol 3,4',7-triacetate 44584293 Click to see CC(=O)OC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC(=O)C)O)OC(=O)C 412.30 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Luteolin 5-glucoside 5317471 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigetrin 5280704 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442
kaempferol 7-O-(2-E-p-coumaroyl-alpha-L-rhamnopyranoside) 11678667 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)O)O 578.50 unknown via CMAUP database
kaempferol 7-O-(2,3-di-E-p-coumaroyl-alpha-L-rhamnopyranoside) 11607311 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O)O 724.70 unknown via CMAUP database
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1248/YAKUSHI1947.105.5_442

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