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Ligustrum obtusifolium

Ligustrum obtusifolium - Unknown
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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 UUID64402ae952d54975270122
Scientific name Ligustrum obtusifolium
Authority Siebold & Zucc.
First published in Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 168 (1846)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ligustrum ibota var. suave Kitag. Bot. Mag. (Tokyo) 48: 612. 1934
Ligustrum obtusifolium subsp. suave (Kitag.) Kitag. J. Jap. Bot. 40: 134. 1965 (1965)
Ligustrum ibota var. angustifolium Blume Mus. Bot. 1: 312. 1851
Ligustrum ibota var. obovatum Blume Mus. Bot. 1: 312. 1851
Ligustrum ciliatum var. spathulatum Blume Mus. Bot. 1: 312. 1851
Ligustrum ibota var. tschonoskii Nakai Fl. Kor. 2: 89. 1911
Ligustrum ibota f. tschonoskii (Nakai) Nakai Bot. Mag. (Tokyo) 32: 124 1918
Ligustrum ibota f. angustifolium (Blume) Nakai Bot. Mag. (Tokyo) 32: 123 1918
Ligustrum ibota f. obtusifolium (Siebold & Zucc.) Koidz. Bot. Mag. (Tokyo) 40: 342 1926
Ligustrum obtusifolium var. regelianum (Koehne) Rehder Möller's Deutsche Gärtn.-Zeitung 14: 218 1899
Ligustrum ibota var. regelianum (Koehne) Siebold ex Beissn., Schelle & Zabel Handb. Laubholzben. 418 1903
Ligustrum ibota var. diabolicum Koidz. Bot. Mag. (Tokyo) 30: 82. 1916
Ligustrum ibota var. amurense (Carrière) Mansf. Beibl. Bot. Jahrb. Syst. 132: 65. 1924
Ligustrum obtusifolium f. leiocalyx (Nakai) Murata Acta Phytotax. Geobot. 19: 71 1962
Ligustrum obtusifolium f. velutinum (Blume) Murata Acta Phytotax. Geobot. 19: 72 1962
Ligustrum tschonoskii var. leiocalyx Nakai Trees Shrubs Japan 276. 1922
Ligustrum obtusifolium var. leiocalyx (Nakai) H.Hara J. Jap. Bot. 20: 329 1944
Ligustrum ibota var. velutinum Blume Mus. Bot. 1: 312. 1851
Ligustrum obtusifolium var. velutinum (Blume) H.Hara J. Jap. Bot. 20: 329 1944
Ligustrum ibota var. obtusifolium (Siebold & Zucc.) Koidz. Bot. Mag. (Tokyo) 40(474): 342 1926
Ligustrum obtusifolium var. amurense (Carrière) Mansf. Abh. Bayer. Akad. Wiss., Math.-Naturwiss. Abt. 4(3): 167 1846

Common names Top

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Language Common/alternative name
English border privet
Czech ptačí zob tupolistý
Danish butbladet liguster
German stumpfblättriger liguster
Japanese イボタノキ
Korean 검정알나무
Korean 쥐똥나무
Russian Бирючина туполистная
Swedish japansk liguster
Chinese 水蜡树
Chinese 水腊树
Chinese 辽东水蜡树
Chinese 水蜡
Chinese 水蠟

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Ligustrum obtusifolium subsp. microphyllum (Nakai) P.S.Green Kew Bull. 50: 385 (1995)
Ligustrum obtusifolium subsp. obtusifolium Unknown

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
  • Northern America
    • North-central U.S.A.
      • Illinois
    • Northeastern U.S.A.
      • New York
      • Vermont
    • Southeastern U.S.A.
      • Alabama
      • Kentucky
      • Maryland
      • Tennessee

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000816339
UNII OX2H1D0H32
Flora of Alabama 2727
Cornell Woody Plants 328
USDA Plants LIOB
UConn 254
Tropicos 23000161
KEW urn:lsid:ipni.org:names:610053-1
The Plant List kew-354228
Missouri Botanical Garden 282945
Open Tree Of Life 11345
NCBI Taxonomy 178760
Nature Serve 2.153017
IPNI 610053-1
iNaturalist 204160
GBIF 3172296
Freebase /m/02q_qj8
EPPO LIGOB
EOL 579171
USDA GRIN 22087
Wikipedia Ligustrum_obtusifolium
CMAUP NPO5384

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
Four new species of Phyllosticta from China based on morphological and phylogenetic characterization Sui XN, Guo MJ, Zhou H, Hou CL Mycology 04-Jul-2023
PMCID:PMC10424619
doi:10.1080/21501203.2023.2225552
PMID:37583457
Bioactive compounds and biomedical applications of endophytic fungi: a recent review Hashem AH, Attia MS, Kandil EK, Fawzi MM, Abdelrahman AS, Khader MS, Khodaira MA, Emam AE, Goma MA, Abdelaziz AM Microb Cell Fact 06-Jun-2023
PMCID:PMC10243280
doi:10.1186/s12934-023-02118-x
PMID:37280587
The influence of climate warming on flowering phenology in relation to historical annual and seasonal temperatures and plant functional traits Geissler C, Davidson A, Niesenbaum RA PeerJ 21-Apr-2023
PMCID:PMC10124540
doi:10.7717/peerj.15188
PMID:37101791
Metabolites extracted from microorganisms as potential inhibitors of glycosidases (α-glucosidase and α-amylase): A review Wang X, Li J, Shang J, Bai J, Wu K, Liu J, Yang Z, Ou H, Shao L Front Microbiol 17-Nov-2022
PMCID:PMC9712454
doi:10.3389/fmicb.2022.1050869
PMID:36466660
Succession of the Abandoned Rice Fields Restores the Riparian Forest Lim BS, Seol J, Kim AR, An JH, Lim CH, Lee CS Int J Environ Res Public Health 21-Aug-2022
PMCID:PMC9407847
doi:10.3390/ijerph191610416
PMID:36012049
Functional Characterization of Genes Coding for Novel β-D-Glucosidases Involved in the Initial Step of Secoiridoid Glucosides Catabolism in Centaurium erythraea Rafn Božunović J, Milutinović M, Aničić N, Skorić M, Matekalo D, Živković S, Dragićević M, Filipović B, Banjanac T, Petrović L, Mišić D Front Plant Sci 23-Jun-2022
PMCID:PMC9260424
doi:10.3389/fpls.2022.914138
PMID:35812935
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, 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, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
Growth Suppression of a Gingivitis and Skin Pathogen Cutibacterium (Propionibacterium) acnes by Medicinal Plant Extracts Choi HA, Ahn SO, Lim HD, Kim GJ Antibiotics (Basel) 09-Sep-2021
PMCID:PMC8465884
doi:10.3390/antibiotics10091092
PMID:34572674
Nitric Oxide as a Target for Phytochemicals in Anti-Neuroinflammatory Prevention Therapy Subedi L, Gaire BP, Kim SY, Parveen A Int J Mol Sci 30-Apr-2021
PMCID:PMC8124914
doi:10.3390/ijms22094771
PMID:33946349
Habitat Elevation Shapes Microbial Community Composition and Alter the Metabolic Functions in Wild Sable (Martes zibellina) Guts Su L, Liu X, Jin G, Ma Y, Tan H, Khalid M, Romantschuk M, Yin S, Hui N Animals (Basel) 18-Mar-2021
PMCID:PMC8002971
doi:10.3390/ani11030865
PMID:33803658
Host Suitability for Crapemyrtle Bark Scale (Acanthococcus lagerstroemiae) Differed Significantly among Crapemyrtle Species Wu B, Xie R, Knox GW, Qin H, Gu M Insects 23-Dec-2020
PMCID:PMC7823534
doi:10.3390/insects12010006
PMID:33374734
Taxonomy and phylogeny of the Erysiphe lonicerae complex (Helotiales, Erysiphaceae) on Lonicera spp. Bradshaw M, Braun U, Götz M, Takamatsu S Fungal Syst Evol 26-Nov-2020
PMCID:PMC8165964
doi:10.3114/fuse.2021.07.03
PMID:34124617
Phylogenetic and functional distinctiveness explain alien plant population responses to competition Levin SC, Crandall RM, Pokoski T, Stein C, Knight TM Proc Biol Sci 01-Jul-2020
PMCID:PMC7423470
doi:10.1098/rspb.2020.1070
PMID:32605513
Feeding Preference of Crapemyrtle Bark Scale (Acanthococcus lagerstroemiae) on Different Species Xie R, Wu B, Dou H, Liu C, Knox GW, Qin H, Gu M Insects 28-Jun-2020
PMCID:PMC7412028
doi:10.3390/insects11070399
PMID:32605244
The arrangement of lateral veins along the midvein of leaves is not related to leaf phyllotaxis Koyama K, Masuda T Sci Rep 06-Nov-2018
PMCID:PMC6219558
doi:10.1038/s41598-018-34772-2
PMID:30401940

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
7-Methoxy-2H-1,3-benzodioxole-5-carboxylic acid 607309 Click to see COC1=CC(=CC2=C1OCO2)C(=O)O 196.16 unknown via CMAUP database
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
(aR,7R)-Dihydroisosubamol 71620318 Click to see COC1=C(C=C2C3=C(CCC(C2=C1)CO)C=C(C=C3)O)O 286.32 unknown via CMAUP database
9,12-di-O-methylsubamol 71461983 Click to see COCC1=CCC2=C(C=CC(=C2)OC)C3=CC(=C(C=C13)OC)O 312.40 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown via CMAUP database
Syringaldehyde 8655 Click to see COC1=CC(=CC(=C1O)OC)C=O 182.17 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown https://doi.org/10.1248/YAKUSHI1947.104.4_390
https://doi.org/10.1248/YAKUSHI1947.103.3_360
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Syringaresinol 11604108 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC 418.40 unknown via CMAUP database
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[[3-hydroxy-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 5320285 Click to see COC1=C(C=CC(=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)OC)O)OC4C(C(C(C(O4)CO)O)O)O 538.50 unknown https://doi.org/10.1248/YAKUSHI1947.104.4_390
https://doi.org/10.1248/YAKUSHI1947.108.7_647
Acanthoside B 443024 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/10.1248/YAKUSHI1947.108.7_647
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-hex-3-enoxy-6-(hydroxymethyl)oxane-3,4,5-triol 125625 Click to see CCC=CCCOC1C(C(C(C(O1)CO)O)O)O 262.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Secosubamolide 16104910 Click to see CCCCCCCCCCCCCC=C(C(C(=O)C)O)C(=O)OC 340.50 unknown via CMAUP database
Secosubamolide A 24795973 Click to see CCCCCCCCCCCCCCCC=C(C(C(=O)C)O)C(=O)OC 368.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Polyprenols
Ficaprenol 10 12866490 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C 699.20 unknown via CMAUP database
Ficaprenol 11 11411688 Click to see CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C)C)C)C)C)C)C)C 767.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Gibberodione 11586727 Click to see CC1CCC(=CC(=O)C1CCC(=O)C)C(C)C 236.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Abscisic acids and derivatives
Abscisic acid 5280896 Click to see CC1=CC(=O)CC(C1(C=CC(=CC(=O)O)C)O)(C)C 264.32 unknown via CMAUP database
> 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/YAKUSHI1947.104.4_390
https://doi.org/10.1248/YAKUSHI1947.108.7_647
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/10.1248/YAKUSHI1947.104.4_390
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/YAKUSHI1947.108.7_647
https://doi.org/10.1248/YAKUSHI1947.104.4_390
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/YAKUSHI1947.104.4_390
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4aS,6aR,6aS,6bR,10S,12aR,14bS)-10-acetyloxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 15917992 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1248/YAKUSHI1947.103.3_360
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1248/YAKUSHI1947.108.7_647
https://doi.org/10.1248/YAKUSHI1947.103.3_360
https://doi.org/10.1248/YAKUSHI1947.104.4_390
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://doi.org/10.1248/YAKUSHI1947.108.7_647
https://doi.org/10.1248/YAKUSHI1947.104.4_390
https://doi.org/10.1248/YAKUSHI1947.103.3_360
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/YAKUSHI1947.103.3_360
https://doi.org/10.1248/YAKUSHI1947.104.4_390
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1248/YAKUSHI1947.108.7_647
Ursolic acid acetate 6475119 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O 498.70 unknown https://doi.org/10.1248/YAKUSHI1947.104.4_390
> Lipids and lipid-like molecules / Saccharolipids
methyl 5-ethylidene-4-[2-[[5-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3,4-dihydroxy-6-[2-(4-hydroxyphenyl)ethoxy]oxan-2-yl]methoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 74191743 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)OCCC4=CC=C(C=C4)O)OC(=O)CC5C(=COC(C5=CC)OC6C(C(C(C(O6)CO)O)O)O)C(=O)OC)O)O 1073.00 unknown https://doi.org/10.1248/YAKUSHI1947.109.7_460
> 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/YAKUSHI1947.103.3_360
https://doi.org/10.1248/YAKUSHI1947.108.7_647
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/YAKUSHI1947.108.7_647
https://doi.org/10.1248/YAKUSHI1947.104.4_390
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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/YAKUSHI1947.108.7_647
https://doi.org/10.1248/YAKUSHI1947.104.4_390
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/YAKUSHI1947.108.7_647
https://doi.org/10.1248/YAKUSHI1947.103.3_360
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasterol glucoside 6602508 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown https://doi.org/10.1248/YAKUSHI1947.108.7_647
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
3-Methoxy-5-(beta-D-glucopyranosyloxymethyl)-7H-dibenzo[a,c]cycloheptene-2,9-diol 102345052 Click to see COC1=C(C=C2C3=C(CC=C(C2=C1)COC4C(C(C(C(O4)CO)O)O)O)C=C(C=C3)O)O 446.40 unknown via CMAUP database
3,9-Dimethoxy-5-(beta-D-glucopyranosyloxymethyl)-7H-dibenzo[a,c]cycloheptene-2-ol 71620321 Click to see COC1=CC2=C(C=C1)C3=CC(=C(C=C3C(=CC2)COC4C(C(C(C(O4)CO)O)O)O)OC)O 460.50 unknown via CMAUP database
Methyl alpha-D-galactopyranoside 76935 Click to see COC1C(C(C(C(O1)CO)O)O)O 194.18 unknown https://doi.org/10.1248/YAKUSHI1947.104.4_390
Subavenoside A 71453067 Click to see COC1=C(C=C2C3=CC=CC=C3CC=C(C2=C1)COC4C(C(C(C(O4)CO)O)O)O)O 430.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(alpha-L-Rhamnopyranosyloxy)-3-methoxy-5-(hydroxymethyl)-7H-dibenzo[a,c]cycloheptene-9-ol 102345053 Click to see CC1C(C(C(C(O1)OC2=C(C=C3C(=CCC4=C(C3=C2)C=CC(=C4)O)CO)OC)O)O)O 430.40 unknown via CMAUP database
2,4,6-Trihydroxy1butyrophenone 2-O-beta-D-glucopyranoside 51357548 Click to see CCCC(=O)C1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)O)O 358.34 unknown via CMAUP database
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/YAKUSHI1947.108.7_647
Furcatin 442789 Click to see C=CCC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 428.40 unknown via CMAUP database
Ibotanolide B 6442827 Click to see C1=CC(=C(C=C1CCO)O)OC2C(C(C(C(O2)COC(=O)C=CC3=CC(=C(C=C3)O)O)O)O)O 478.40 unknown https://doi.org/10.1248/YAKUSHI1947.109.7_496
Subavenoside D 71461984 Click to see COC1=C(C=C2C3=CC=CC=C3CC=C(C2=C1)CO)OC4C(C(C(C(O4)CO)O)O)O 430.40 unknown via CMAUP database
Subavenoside E 71451248 Click to see COCC1=CCC2=C(C=CC(=C2)OC)C3=CC(=C(C=C13)OC)OC4C(C(C(C(O4)CO)O)O)O 474.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2S,3R,4S,5R,6R)-6-(hydroxymethyl)-2-methyloxane-2,3,4,5-tetrol 17751028 Click to see CC1(C(C(C(C(O1)CO)O)O)O)O 194.18 unknown https://doi.org/10.1248/YAKUSHI1947.104.4_390
> 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/YAKUSHI1947.104.4_390
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
Oxyphyllenodiol A 10082923 Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O 238.32 unknown via CMAUP database
Oxyphyllenodiol B 5279294 Click to see CC(C)C1CCC(=O)C2=C1C(C(CC2)(C)O)O 238.32 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
Subamolide A 16104909 Click to see CCCCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 340.50 unknown via CMAUP database
Subamolide B 16104907 Click to see CCCCCCCCCCCCCC=C1C(C(OC1=O)(C)OC)O 340.50 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Myristicin 4276 Click to see COC1=CC(=CC2=C1OCO2)CC=C 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Oxolanes
(4R)-3-[(E)-Undecylidene]-4beta-hydroxy-5-methylenetetrahydrofuran-2-one 24757906 Click to see CCCCCCCCCCC=C1C(C(=C)OC1=O)O 266.38 unknown via CMAUP database
Isolinderanolide B 53308122 Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 308.50 unknown via CMAUP database
Isooblusilactonc A 6442493 Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 308.50 unknown via CMAUP database
Obtusilactone A 6442492 Click to see CCCCCCCCCCCCCC=C1C(C(=C)OC1=O)O 308.50 unknown via CMAUP database
Subamolide D 24757907 Click to see CCCCCCCCCCC=C1C(C(=C)OC1=O)O 266.38 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
[[(2R,3R)-2,3-Dihydro-2-(4-hydroxy-3-methoxyphenyl)-5-(3-hydroxypropyl)-7-methoxybenzofuran-3-yl]methyl]beta-D-glucopyranoside 95223221 Click to see COC1=CC(=CC2=C1OC(C2COC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)CCCO 522.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-(3,4-Dihydroxyphenyl)ethyl 3-O-(6-Deoxy-alpha-L-mannopyranosyl)-4-O-[(2E)-3-(3,4-dihydroxyphenyl)-2-propenoyl]-beta-D-glucopyranoside 132274946 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown https://doi.org/10.1248/YAKUSHI1947.104.4_390
Ibotalactone B 6442829 Click to see CC1C2C(CC(=O)O1)C(=COC2OC3C(C(C(C(O3)COC(=O)C=CC4=CC(=C(C=C4)O)O)O)O)O)C(=O)O 552.50 unknown https://doi.org/10.1248/YAKUSHI1947.109.7_460
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Ibotalactone A 6442828 Click to see CC1C2C(CC(=O)O1)C(=COC2OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)O)C(=O)O 536.50 unknown https://doi.org/10.1248/YAKUSHI1947.109.7_460
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
1-Caffeoyl-beta-D-glucose 5281761 Click to see C1=CC(=C(C=C1C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O)O 342.30 unknown https://doi.org/10.1248/YAKUSHI1947.108.7_647
1-O-feruloyl-beta-D-glucose 13962928 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O 356.32 unknown https://doi.org/10.1248/YAKUSHI1947.108.7_647
> 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/YAKUSHI1947.108.7_647
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1248/YAKUSHI1947.108.7_647
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1248/YAKUSHI1947.108.7_647
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3,4-Methylenedioxy-5-methoxycinnamyl alcohol 85441832 Click to see COC1=CC(=CC2=C1OCO2)C=CCO 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Aescultitannin B 10010849 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown via CMAUP database
Cinnamtannin D1 46173958 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC5=C4C6C(C(O5)(OC7=CC(=CC(=C67)O)O)C8=CC(=C(C=C8)O)O)O)O)C9=CC(=C(C=C9)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 864.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> 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/YAKUSHI1947.108.7_647
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/YAKUSHI1947.108.7_647
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(2R)-7-hydroxy-2-(4-hydroxyphenyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 3083618 Click to see C1C(OC2=C(C1=O)C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database
Helichrysin A 15559669 Click to see C1C(OC2=C(C1=O)C(=CC(=C2)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database
Phlorizin 6072 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C=C2OC3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1248/YAKUSHI1947.108.7_647
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 https://doi.org/10.1248/YAKUSHI1947.108.7_647
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/YAKUSHI1947.108.7_647
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/YAKUSHI1947.108.7_647
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Prunin 92794 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database

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