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Artemisia lactiflora

Artemisia lactiflora - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fd1df6f1ba314627541
Scientific name Artemisia lactiflora
Authority Wall. ex DC.
First published in Prodr. 6: 115 (1838)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Artemisia septemlobata H.Lév. & Vaniot Repert. Spec. Nov. Regni Veg. 7: 22 (1909)

Common names Top

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Language Common/alternative name
Spanish artemisia septemlobata
Spanish artemisia lactiflora var. incisa
Spanish artemisia lactiflora var. taibaishanensis
Spanish artemisia lactiflora f. incisa
Arabic شيح أبيض الزهر
German weißer china-beifuß
German edelraute
Persian برنجاسف سفید
Slovenian beli pelin
Swedish pärlmalört
szy nipaluma-kadamat
Thai จิงจูฉ่าย
Chinese 鸡甜菜
Chinese 秦州菴闾子
Chinese 白花蒿
Chinese 白米蒿
Chinese 广东刘寄奴
Chinese 四季菜
Chinese 角菜
Chinese 白荀蒿(白花嵩）
Chinese 白苞蒿
Chinese 鸭脚艾

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Artemisia lactiflora var. incisa (Pamp.) Ling & Y.R.Ling Bull. Bot. Res., Harbin 8: 42 (1988)
Artemisia lactiflora var. taibaishanensis X.D.Cui Fl. Tsinling. 1(5): 421 (1985)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
    • Indo-China
      • Cambodia
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Jawa

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000118841
UNII EWK54O6568
Canadensys 9870
Tropicos 2745608
KEW urn:lsid:ipni.org:names:179704-1
The Plant List gcc-8015
Open Tree Of Life 606741
NCBI Taxonomy 669127
IPNI 179704-1
iNaturalist 427954
GBIF 3121137
Freebase /m/0lpyct8
USDA GRIN 4288
Wikipedia Artemisia_lactiflora
CMAUP NPO8681

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
Wild and Micropropagated Artemisia eriantha Infusions: In Vitro Digestion Effects on Phenolic Pattern and Antioxidant Activity Rocchi R, Pellegrini M, Pittia P, Pace L Plants (Basel) 27-Dec-2023
PMCID:PMC10780599
doi:10.3390/plants13010085
PMID:38202393
Assessment of Polyphenols Bioaccessibility, Stability, and Antioxidant Activity of White Mugwort (Artemisia lactiflora Wall.) during Static In Vitro Gastrointestinal Digestion Udomwasinakun N, Saha S, Mulet-Cabero AI, Wilde PJ, Pirak T Foods 23-Feb-2023
PMCID:PMC10000887
doi:10.3390/foods12050949
PMID:36900469
A chromosome-scale genome assembly of Artemisia argyi reveals unbiased subgenome evolution and key contributions of gene duplication to volatile terpenoid diversity Chen H, Guo M, Dong S, Wu X, Zhang G, He L, Jiao Y, Chen S, Li L, Luo H Plant Commun 02-Jan-2023
PMCID:PMC10203441
doi:10.1016/j.xplc.2023.100516
PMID:36597358
Artemisia spp.: An Update on Its Chemical Composition, Pharmacological and Toxicological Profiles Sharifi-Rad J, Herrera-Bravo J, Semwal P, Painuli S, Badoni H, Ezzat SM, Farid MM, Merghany RM, Aborehab NM, Salem MA, Sen S, Acharya K, Lapava N, Martorell M, Tynybekov B, Calina D, Cho WC Oxid Med Cell Longev 05-Sep-2022
PMCID:PMC9467740
doi:10.1155/2022/5628601
PMID:36105486
Comparative analysis of the plastid and mitochondrial genomes of Artemisia giraldii Pamp. Yue J, Lu Q, Ni Y, Chen P, Liu C Sci Rep 17-Aug-2022
PMCID:PMC9385723
doi:10.1038/s41598-022-18387-2
PMID:35978085
Sequence Characteristics and Phylogenetic Analysis of the Artemisia argyi Chloroplast Genome Chen C, Miao Y, Luo D, Li J, Wang Z, Luo M, Zhao T, Liu D Front Plant Sci 20-Jun-2022
PMCID:PMC9252292
doi:10.3389/fpls.2022.906725
PMID:35795352
Effect of chicken manure and chemical fertilizer on the yield and qualities of white mugwort at dissimilar harvesting times Thepsilvisut O, Chutimanukul P, Sae-Tan S, Ehara H PLoS One 26-Apr-2022
PMCID:PMC9041803
doi:10.1371/journal.pone.0266190
PMID:35472063
Artemisia lactiflora Extracts Prevent Inflammatory Responses of Human Macrophages Stimulated with Charcoal Pyrolysis Smoke Kooltheat N, Chujit K, Nuangnong K, Nokkaew N, Bunluepuech K, Yamasaki K, Chatatikun M J Evid Based Integr Med 23-Dec-2021
PMCID:PMC8725217
doi:10.1177/2515690X211068837
PMID:34939447
Phytochemical screening, antimalarial activities, and genetic relationship of 16 indigenous Thai Asteraceae medicinal plants: A combinatorial approach using phylogeny and ethnobotanical bioprospecting in antimalarial drug discovery Liana D, Rungsihirunrat K J Adv Pharm Technol Res 16-Jul-2021
PMCID:PMC8300331
doi:10.4103/japtr.JAPTR_238_21
PMID:34345604
Screening of Native Plants Growing on a Pb/Zn Mining Area in Eastern Morocco: Perspectives for Phytoremediation Hasnaoui SE, Fahr M, Keller C, Levard C, Angeletti B, Chaurand P, Triqui ZE, Guedira A, Rhazi L, Colin F, Smouni A Plants (Basel) 29-Oct-2020
PMCID:PMC7693513
doi:10.3390/plants9111458
PMID:33137928
Effects of Litterfall on the Accumulation of Extracted Soil Humic Substances in Subalpine Forests Wei X, Yang Y, Shen Y, Chen Z, Dong Y, Wu F, Zhang L Front Plant Sci 05-Mar-2020
PMCID:PMC7066323
doi:10.3389/fpls.2020.00254
PMID:32194612
Exotic Plants Used by the Hmong in Thailand Nguanchoo V, Wangpakapattanawong P, Balslev H, Inta A Plants (Basel) 14-Nov-2019
PMCID:PMC6918319
doi:10.3390/plants8110500
PMID:31739420
Endophytic Fungi in Species of Artemisia Cosoveanu A, Cabrera R J Fungi (Basel) 01-May-2018
PMCID:PMC6023322
doi:10.3390/jof4020053
PMID:29724011
Fungi as Endophytes in Artemisia thuscula: Juxtaposed Elements of Diversity and Phylogeny Cosoveanu A, Rodriguez Sabina S, Cabrera R J Fungi (Basel) 27-Jan-2018
PMCID:PMC5872320
doi:10.3390/jof4010017
PMID:29382076
Three-Dimensional Evaluation on Ecotypic Diversity of Traditional Chinese Medicine: A Case Study of Artemisia annua L. Li L, Josef BA, Liu B, Zheng S, Huang L, Chen S Front Plant Sci 11-Jul-2017
PMCID:PMC5504922
doi:10.3389/fpls.2017.01225
PMID:28744301

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 / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
4-Hydroxy-2-methoxybenzoic acid 12695575 Click to see COC1=C(C=CC(=C1)O)C(=O)O 168.15 unknown via CMAUP database
> Benzenoids / Indanes / Indanones
(2R-trans)-2,3-Dihydro-3-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-1H-inden-1-one 169729 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)O 234.29 unknown via CMAUP database
(2R)-2-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-3H-inden-1-one 46849571 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)O 234.29 unknown via CMAUP database
(2S-trans)-6-(2-Chloroethyl)-2,3-dihydro-3-hydroxy-2,5,7-trimethyl-1H-inden-1-one 148419 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCCl)C)O 252.73 unknown via CMAUP database
(2S,3R)-3-hydroxy-6-(2-hydroxyethyl)-2,5,7-trimethyl-2,3-dihydroinden-1-one 46850078 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)O 234.29 unknown via CMAUP database
(2S)-6-(2-hydroxyethyl)-2,5,7-trimethyl-2,3-dihydroinden-1-one 12314748 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCO)C 218.29 unknown via CMAUP database
(3R)-6-(2-chloroethyl)-3-hydroxy-2,2,5,7-tetramethyl-3H-inden-1-one 23260004 Click to see CC1=CC2=C(C(=C1CCCl)C)C(=O)C(C2O)(C)C 266.76 unknown via CMAUP database
(3S)-3-hydroxy-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-3H-inden-1-one 71361396 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)C 248.32 unknown via CMAUP database
(S)-2,3-Dihydro-2-(hydroxymethyl)-6-(2-methoxyethyl)-2,5,7-trimethyl-1H-inden-1-one 134443 Click to see CC1=CC2=C(C(=C1CCOC)C)C(=O)C(C2)(C)CO 262.34 unknown via CMAUP database
(S)-2,3-Dihydro-6-(2-hydroxyethyl)-2-(hydroxymethyl)-5,7-dimethyl-1H-inden-1-one 169739 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)CO 234.29 unknown via CMAUP database
(S)-2,3-Dihydro-6-(2-hydroxyethyl)-5-(hydroxymethyl)-2,7-dimethyl-1H-inden-1-one 151323 Click to see CC1CC2=CC(=C(C(=C2C1=O)C)CCO)CO 234.29 unknown via CMAUP database
1-Indanone 6735 Click to see C1CC(=O)C2=CC=CC=C21 132.16 unknown via CMAUP database
2S,3S-acetylpterosin C 21122778 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC(=O)C)C)O 276.33 unknown via CMAUP database
Epipterosin L 46848746 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)CO 264.32 unknown via CMAUP database
Pterosin A 135017 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)CO 248.32 unknown via CMAUP database
Pterosin B 115049 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCO)C 218.29 unknown via CMAUP database
Pterosin C 186209 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)O 234.29 unknown via CMAUP database
Pterosin D 147559 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)C 248.32 unknown via CMAUP database
Pterosin E 148588 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CC(=O)O)C 232.27 unknown via CMAUP database
Pterosin H 135029 Click to see CC1=CC2=C(C(=C1CCCl)C)C(=O)C(C2)(C)C 250.76 unknown via CMAUP database
Pterosin I 161891 Click to see CC1=CC2=C(C(=C1CCOC)C)C(=O)C(C2)(C)C 246.34 unknown via CMAUP database
Pterosin K 148420 Click to see CC1=CC2=C(C(=C1CCCl)C)C(=O)C(C2)(C)CO 266.76 unknown via CMAUP database
Pterosin L 21633068 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2O)(C)CO 264.32 unknown via CMAUP database
Pterosin O 135255 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCOC)C 232.32 unknown via CMAUP database
Pterosin Z 134977 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2)(C)C 232.32 unknown via CMAUP database
Pterosinf 46849741 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCCl)C 236.73 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(2-Penta-1,3-diynoxyspiro[6-oxabicyclo[3.1.0]hex-2-ene-4,6'-oxane]-3'-yl) 3-methylbutanoate 5318915 Click to see CC#CC#COC1=CC2(CCC(CO2)OC(=O)CC(C)C)C3C1O3 330.40 unknown via CMAUP database
(3-Chloro-2-hexa-2,4-diynylidene-4-hydroxy-1,10-dioxaspiro[4.5]decan-8-yl) 3-methylbutanoate 85282968 Click to see CC#CC#CC=C1C(C(C2(O1)CCC(CO2)OC(=O)CC(C)C)O)Cl 366.80 unknown https://doi.org/10.1021/JF980521U
[(2E,3R,4S,5R,8S)-3-chloro-2-hexa-2,4-diynylidene-4-hydroxy-1,10-dioxaspiro[4.5]decan-8-yl] 3-methylbutanoate 100959956 Click to see CC#CC#CC=C1C(C(C2(O1)CCC(CO2)OC(=O)CC(C)C)O)Cl 366.80 unknown https://doi.org/10.1021/JF980521U
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Pteridicacid A 11013967 Click to see CCC1C=CC2(C(C(C(C(O2)C(C)C=CC=CC(=O)O)C)O)C)OC1C 364.50 unknown via CMAUP database
Pteridicacid B 10883014 Click to see CCC1C=CC2(C(C(C(C(O2)C(C)C=CC=CC(=O)O)C)O)C)OC1C 364.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Tripalmitin 11147 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCC 807.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Lactiflorenol 102113807 Click to see CC(C)C1=CC2C(CCC2(C)O)C(=C)CC1 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Ptaquiloside Z 101242525 Click to see CC1=CC2(CC(C(=O)C2C(C13CC3)(C)O)(C)C)OC4C(C(C(C(O4)CO)O)O)O 412.50 unknown via CMAUP database
Pteridanoside 11795946 Click to see CC1(CC2C(C1=O)C3(CCC3=C(C2O)COC4C(C(C(C(O4)CO)O)O)O)C)C 412.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[(3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-12-methyl-14-oxo-2,7,9,13-tetraoxapentacyclo[8.7.0.01,15.03,8.012,16]heptadecan-15-yl]methyl benzoate 5318917 Click to see CC12CC3C4(CC1C4(C(=O)O2)COC(=O)C5=CC=CC=C5)OC6C(C(C(OC6O3)CO)O)O 462.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
20-Hydroxyecdysone 5459840 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
3alpha-Hydroxyecdysone 70686927 Click to see CC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O 480.60 unknown via CMAUP database
Pterosterone 441836 Click to see CC(C)C(CC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O)O 480.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
3-Epiecdysone 23724769 Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)O 464.60 unknown via CMAUP database
Ecdysone 19212 Click to see CC(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)C(CCC(C)(C)O)O 464.60 unknown via CMAUP database
Ponasterone A 115127 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O 464.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
Ponasteroside A 12314455 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)OC5C(C(C(C(O5)CO)O)O)O)O)C)C)O)O)O 626.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron 21883788 Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-] 116.07 unknown via CMAUP database
Butanedioate;hydron 21952380 Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-] 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3R)-3-hydroxy-2,5,7-trimethyl-6-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-2,3-dihydroinden-1-one 46848577 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C)O 396.40 unknown via CMAUP database
(2S,3S)-6-(2-hydroxyethyl)-2,5,7-trimethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydroinden-1-one 23260007 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)OC3C(C(C(C(O3)CO)O)O)O 396.40 unknown via CMAUP database
(2S)-2,5,7-trimethyl-6-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-2,3-dihydroinden-1-one 46848576 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C 380.40 unknown via CMAUP database
(3R)-6-(2-hydroxyethyl)-2,2,5,7-tetramethyl-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3H-inden-1-one 46848743 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2OC3C(C(C(C(O3)CO)O)O)O)(C)C 410.50 unknown via CMAUP database
Ptaquiloside 13962857 Click to see CC1CC2(C=C(C3(CC3)C(C2C1=O)(C)O)C)OC4C(C(C(C(O4)CO)O)O)O 398.40 unknown via CMAUP database
Pteroside A 169727 Click to see CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2)(C)CO 410.50 unknown via CMAUP database
Pteroside B 134279 Click to see CC1CC2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C 380.40 unknown via CMAUP database
Pteroside C 169728 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C)O 396.40 unknown via CMAUP database
Pteroside D 169738 Click to see CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2O)(C)C 410.50 unknown via CMAUP database
Pteroside P 148715 Click to see CC1CC2=CC(=C(C(=C2C1=O)C)CCOC3C(C(C(C(O3)CO)O)O)O)CO 396.40 unknown via CMAUP database
Pteroside Z 169737 Click to see CC1=CC2=C(C(=C1CCOC3C(C(C(C(O3)CO)O)O)O)C)C(=O)C(C2)(C)C 394.50 unknown via CMAUP database
pterosin C 3-O-glucoside 44201982 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C)O 396.40 unknown via CMAUP database
Pterosin D 3-O-glucoside 21670079 Click to see CC1=CC2=C(C(=C1CCO)C)C(=O)C(C2OC3C(C(C(C(O3)CO)O)O)O)(C)C 410.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-Ethenylphenyl beta-D-glucopyranoside 182338 Click to see C=CC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 282.29 unknown via CMAUP database
beta-D-Glucopyranoside, 4-ethenylphenyl 6-O-beta-D-xylopyranosyl- 185053 Click to see C=CC1=CC=C(C=C1)OC2C(C(C(C(O2)COC3C(C(C(CO3)O)O)O)O)O)O 414.40 unknown via CMAUP database
Ptelatoside b 130179 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC=C(C=C3)C=C)CO)O)O)O)O)O 428.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2E,3S,4R,5R)-3-chloro-2-hexa-2,4-diynylidene-1,10-dioxaspiro[4.5]decan-4-ol 10706900 Click to see CC#CC#CC=C1C(C(C2(O1)CCCCO2)O)Cl 266.72 unknown https://doi.org/10.1021/JF980521U
3-Chloro-2-hexa-2,4-diynylidene-1,10-dioxaspiro[4.5]decan-4-ol 85239938 Click to see CC#CC#CC=C1C(C(C2(O1)CCCCO2)O)Cl 266.72 unknown https://doi.org/10.1021/JF980521U
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidones / Pyrrolidine-2-ones
(5R)-5-methoxypyrrolidin-2-one 643445 Click to see COC1CCC(=O)N1 115.13 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
5-Caffeoylshikimic acid 5281762 Click to see C1C(C(C(C=C1C(=O)O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O 336.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
7-Methoxycoumarin 10748 Click to see COC1=CC2=C(C=C1)C=CC(=O)O2 176.17 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 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 via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
kaempferol 3-O-(6"-O-feruloyl)-glucoside 23265189 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O 624.50 unknown via CMAUP database
Tiliroside 5320686 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
kaempferol 5-O-beta-L-glucopyranoside 72551435 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(O2)C=C(C=C3OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(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-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxychromen-4-one 101714010 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC(=C(C=C5)O)O)O 640.50 unknown via CMAUP database
3-[(3-O-beta-D-Glucopyranosyl-beta-D-glucopyranosyl)oxy]-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-4H-1-benzopyran-4-one 101683505 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 640.50 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
Isoquercetin 5280804 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 via CMAUP database
Isoquercitin 10813969 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 via CMAUP database
kaempferol 3-O-beta-L-glucopyranoside 9911508 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
Quercetin 3-laminaribioside 101683504 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)OC5C(C(C(C(O5)CO)O)O)O)O)O)O 626.50 unknown via CMAUP database
Trifolin 5282149 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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Kaempferol 7-O-alpha-L-rhamnopyranoside-4'-O-beta-D-glucopyranoside 101949540 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)O)O)O)O 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Hesperetin(1-) 49859576 Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)[O-])O 301.27 unknown via CMAUP database

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