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Salsola collina

Salsola collina - 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 UUID643ffcbe2552d016470309
Scientific name Salsola collina
Authority Pall.
First published in Ill. Pl. : 34 (1803)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Salsola kali subsp. collina (Pall.) O.Bolòs & Vigo Butl. Inst. Catalana Hist. Nat., Secc. Bot. 38(1): 89 (1974)
Salsola chinensis Gand. Bull. Soc. Bot. France 60: 421 (1913)

Common names Top

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Language Common/alternative name
English slender russian thistle
Czech slanobýl chlumní
German hügel-salzkraut
Estonian kink-ogamalts
Finnish tähkäotakilokki
Kazakh Қаңбақ сораң
Lithuanian Šlaitinė druskė
mn Толгодын бударгана
Chinese 猪毛菜

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
    • Caucasus
      • Transcaucasus
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
      • Xinjiang
    • Eastern Asia
      • Korea
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya
    • Western Asia
      • Afghanistan
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • Krym
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Czechoslovakia
      • Hungary
      • Poland
    • Southwestern Europe
      • Spain
  • Northern America
    • Eastern Canada
      • Ontario
    • North-central U.S.A.
      • Illinois
      • Iowa
      • Kansas
      • Minnesota
      • Missouri
      • Nebraska
      • North Dakota
      • Oklahoma
      • South Dakota
    • Northeastern U.S.A.
      • Michigan
      • New Hampshire
      • New York
      • Vermont
    • Northwestern U.S.A.
      • Colorado
      • Montana
    • South-central U.S.A.
      • New Mexico
      • Texas
    • Southeastern U.S.A.
      • Kentucky
    • Southwestern U.S.A.
      • Arizona
      • Utah
    • Western Canada
      • Saskatchewan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000436079
Canadensys 4560
USDA Plants SACO8
Tropicos 7200273
INPN 120590
KEW urn:lsid:ipni.org:names:166737-1
The Plant List kew-2481563
Plantarium 33338
PaleoBotany 30469
Open Tree Of Life 544741
Observations.org 121704
NCBI Taxonomy 525237
NBN Atlas NHMSYS0000463180
Nature Serve 2.136139
IPNI 166737-1
iNaturalist 168371
GBIF 3083953
WisFlora 7622
EPPO SASCO
EOL 585946
Elurikkus 7042
USDA GRIN 316815

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
Patterns and environmental drivers of C, N, and P stoichiometry in the leaf‐litter‐soil system associated with Mongolian pine forests Ren Y, Gao G, Ding G, Zhang Y, Zhao P Ecol Evol 20-Mar-2024
PMCID:PMC10954427
doi:10.1002/ece3.11172
PMID:38516573
Effect of grazing and climatic factors on biodiversity-ecosystem functioning relationships in grassland ecosystems - a case study of typical steppe in Inner Mongolia, China Zhang Y, Wuriliga, Liu P, Fan R, Guo J, Liu L, Ding Y Front Plant Sci 22-Dec-2023
PMCID:PMC10770857
doi:10.3389/fpls.2023.1297061
PMID:38186605
The complete chloroplast genome of a halophyte glasswort Salicornia europaea Liu T, Zuo Z, He Y, Miao J, Yu J, Qu C Mitochondrial DNA B Resour 30-Oct-2023
PMCID:PMC10769547
doi:10.1080/23802359.2023.2275833
PMID:38188438
Temporal approach to identifying ectomycorrhizal community associated with Mongolian pine in a desert environment, northern China Ren Y, Gao G, Ding G, Zhang Y, Zhao P, Wang J Microbiol Spectr 14-Sep-2023
PMCID:PMC10580992
doi:10.1128/spectrum.02026-23
PMID:37707453
Secondary succession of shrub-herb communities in the hilly area of Taihang Mountain Liu X, Zhou W, Li X, Zhang Y, Dong W Front Plant Sci 08-Sep-2023
PMCID:PMC10514918
doi:10.3389/fpls.2023.1194083
PMID:37746017
Phytochemical profiling of Salsola tetragona Delile by LC-HR/MS and investigation of the antioxidant, anti-inflammatory, cytotoxic, antibacterial and anti-SARS-CoV-2 activities Cherrada N, Elkhalifa Chemsa A, Erol E, Günaydın Akyildiz A, Oyku Dinc H, Gheraissa N, Ghemam Amara D, Rebiai A, Abdel-Kader MS, Messaoudi M Saudi Pharm J 05-Aug-2023
PMCID:PMC10448174
doi:10.1016/j.jsps.2023.101731
PMID:37638223
Effects of Spring Drought and Nitrogen Addition on Productivity and Community Composition of Degraded Grasslands Li S, Lu S, Li X, Hou X, Zhao X, Xu X, Zhao N Plants (Basel) 31-Jul-2023
PMCID:PMC10421370
doi:10.3390/plants12152836
PMID:37570989
Insights into the nutritional properties and molecular basis of biosynthesis of amino acids and vitamins of Gastrodia elata offered by metabolomic and transcriptomic analysis Wang Y, Shahid MQ Front Plant Sci 26-Jun-2023
PMCID:PMC10331839
doi:10.3389/fpls.2023.1183139
PMID:37434605
Soil habitat condition shapes Tamarix chinensis community diversity in the coastal saline-alkali soils Yu Q, Suo L, Qi J, Wang Y, Hu Q, Shan Y, Zhao Y Front Plant Sci 26-Apr-2023
PMCID:PMC10169711
doi:10.3389/fpls.2023.1156297
PMID:37180386
Addressing the Relationship between Leaf Nitrogen and Carbon Isotope Discrimination from the Three Levels of Community, Population and Individual Wang S, Han Y, Jia Y, Chen Z, Wang G Plants (Basel) 04-Apr-2023
PMCID:PMC10097192
doi:10.3390/plants12071551
PMID:37050177
Variation and association of leaf traits for desert plants in the arid area, northwest China Wang H, Yang J, Xie T, Ma L, Niu F, He C, Shan L Ecol Evol 24-Mar-2023
PMCID:PMC10037433
doi:10.1002/ece3.9946
PMID:36969926
Different Responses of Growing Season Ecosystem CO2 Fluxes to Rain Addition in a Desert Ecosystem Xu X, Wu B, Bao F, Gao Y, Li X, Cao Y, Lu Q, Gao J, Xin Z, Liu M Plants (Basel) 03-Mar-2023
PMCID:PMC10005604
doi:10.3390/plants12051158
PMID:36904018
Effects of warming seasonal rotational grazing on plant communities' structure and diversity in desert steppe Li W, Su T, Shen Y, Ma H, Zhou Y, Lu Q, Wang G, Liu Z, Li J Ecol Evol 19-Jan-2023
PMCID:PMC9852940
doi:10.1002/ece3.9748
PMID:36699569
15N Natural Abundance of C3 and C4 Herbaceous Plants and Its Response to Climatic Factors along an Agro-Pastoral Zone of Northern China Liu X, Li Y, Zhang Y, Su Q, Feng T, Song Y Plants (Basel) 14-Dec-2022
PMCID:PMC9784019
doi:10.3390/plants11243526
PMID:36559638
Positive legacies of severe droughts in the Inner Mongolia grassland Sun J, Liu W, Pan Q, Zhang B, Lv Y, Huang J, Han X Sci Adv 23-Nov-2022
PMCID:PMC9683728
doi:10.1126/sciadv.add6249
PMID:36417538

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 https://doi.org/10.1007/S10600-011-9896-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
p-Anisic acid 7478 Click to see COC1=CC=C(C=C1)C(=O)O 152.15 unknown https://doi.org/10.1007/S10600-011-9896-2
> Benzenoids / Phenols / Methoxyphenols
(E)-N-[(2R)-2-hydroxy-2-(4-hydroxy-3-methoxyphenyl)ethyl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide 163185762 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCC(C2=CC(=C(C=C2)O)OC)O)O 359.40 unknown https://doi.org/10.1007/S10600-011-9896-2
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1007/S10600-011-9896-2
> Lipids and lipid-like molecules / Endocannabinoids
1,3-Dihydroxypropan-2-yl 3,8-diacetyloxyicosanoate 163021367 Click to see CCCCCCCCCCCCC(CCCCC(CC(=O)OC(CO)CO)OC(=O)C)OC(=O)C 502.70 unknown https://doi.org/10.1007/BF00630328
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown https://doi.org/10.1007/BF00598098
https://doi.org/10.1007/BF00574357
Palmitic Acid 985 Click to see CCCCCCCCCCCCCCCC(=O)O 256.42 unknown https://doi.org/10.1007/BF00574357
https://doi.org/10.1007/BF00598098
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1007/BF00598098
https://doi.org/10.1007/BF00574357
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
4-Hydroxy-3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one 73815023 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1007/S10600-011-9896-2
Corchoionoside C 10317980 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1007/S10600-011-9896-2
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
2,15-Dimethyl-14-(6-methylheptan-2-yl)tetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-7-en-5-ol 304 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1007/BF00574357
Cholesta-5,24-dien-3beta-ol 313036 Click to see CC(CCC=C(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 384.60 unknown https://doi.org/10.1007/BF00574357
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1007/BF00598098
https://doi.org/10.1007/BF00574357
Desmosterol 439577 Click to see CC(CCC=C(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 384.60 unknown https://doi.org/10.1007/BF00574357
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1007/BF00598098
https://doi.org/10.1007/BF00630448
https://doi.org/10.1007/BF00574357
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1007/BF00574357
https://doi.org/10.1007/BF00598098
https://doi.org/10.1007/BF00630448
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1007/BF00630448
https://doi.org/10.1007/BF00574357
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1007/BF00630448
https://doi.org/10.1007/BF00574357
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol 6743 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C 416.70 unknown https://doi.org/10.1007/BF00630448
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00630448
https://doi.org/10.1007/BF00574357
https://doi.org/10.1007/BF00598098
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00630448
https://doi.org/10.1007/BF00598098
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00630448
https://doi.org/10.1007/BF00574357
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/10.1007/BF00598098
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/10.1007/BF00598098
Stigmastanol 241572 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C 416.70 unknown https://doi.org/10.1007/BF00630448
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1007/BF00598098
https://doi.org/10.1007/BF00574357
https://doi.org/10.1007/BF00630448
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine 6029 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown https://doi.org/10.1007/S10600-011-9896-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
Betaine 247 Click to see C[N+](C)(C)CC(=O)[O-] 117.15 unknown https://doi.org/10.1007/BF00630448
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / N-acyl-alpha amino acids
N-Acetyl-DL-tryptophan 2002 Click to see CC(=O)NC(CC1=CNC2=CC=CC=C21)C(=O)O 246.26 unknown https://doi.org/10.1007/S10600-011-9896-2
N-Acetyl-L-tryptophan 700653 Click to see CC(=O)NC(CC1=CNC2=CC=CC=C21)C(=O)O 246.26 unknown https://doi.org/10.1007/S10600-011-9896-2
> Organic acids and derivatives / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
[(2S,3S,4R)-4-methoxy-6-oxo-2-[(E,3S,5R,6S)-3,5,6-triacetyloxyhept-1-enyl]oxan-3-yl] acetate 101267306 Click to see CC(C(CC(C=CC1C(C(CC(=O)O1)OC)OC(=O)C)OC(=O)C)OC(=O)C)OC(=O)C 458.50 unknown https://doi.org/10.1007/S10600-011-9896-2
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Inositol 892 Click to see C1(C(C(C(C(C1O)O)O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00630328
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Ethyl glucoside 428040 Click to see CCOC1C(C(C(C(O1)CO)O)O)O 208.21 unknown https://doi.org/10.1007/BF00630328
Sucrose 5988 Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O 342.30 unknown https://doi.org/10.1007/BF00630328
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose 5984 Click to see C(C(C(C(C(=O)CO)O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00630328
D-Fructose 2723872 Click to see C1C(C(C(C(O1)(CO)O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00630328
> 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/10.1007/BF00630328
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1007/BF00630328
> 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/10.1007/BF00630328
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Protocatechualdehyde 8768 Click to see C1=CC(=C(C=C1C=O)O)O 138.12 unknown https://doi.org/10.1007/S10600-011-9896-2
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
Ethyl b-D-fructopyranoside 14425699 Click to see CCOC1(C(C(C(CO1)O)O)O)CO 208.21 unknown https://doi.org/10.1007/BF00630328
Ethyl beta-fructopyranoside 6325163 Click to see CCOC1(C(C(C(CO1)O)O)O)CO 208.21 unknown https://doi.org/10.1007/BF00630328
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see C1=CNC(=O)NC1=O 112.09 unknown https://doi.org/10.1007/S10600-011-9896-2
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
6,7-dihydroxy-3,4-dihydro-2H-isoquinolin-1-one 11030394 Click to see C1CNC(=O)C2=CC(=C(C=C21)O)O 179.17 unknown https://doi.org/10.1007/S10600-011-9896-2
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3E,5R)-3-[(5S)-5-ethyloxolan-2-ylidene]-5-methyloxolane-2,4-dione 21151019 Click to see CCC1CCC(=C2C(=O)C(OC2=O)C)O1 210.23 unknown https://doi.org/10.1007/S10600-011-9896-2
3-(5-Ethyloxolan-2-ylidene)-5-methyloxolane-2,4-dione 73744855 Click to see CCC1CCC(=C2C(=O)C(OC2=O)C)O1 210.23 unknown https://doi.org/10.1007/S10600-011-9896-2
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(10bS)-8,9-dihydroxy-2,5,6,10b-tetrahydro-1H-pyrrolo[2,1-a]isoquinolin-3-one 11160309 Click to see C1CC(=O)N2C1C3=CC(=C(C=C3CC2)O)O 219.24 unknown https://doi.org/10.1007/S10600-011-9896-2
8,9-Dihydroxy-1,5,6,10B-tetrahydropyrrolo[2,1-A]isoquinolin-3(2H)-one 21574476 Click to see C1CC(=O)N2C1C3=CC(=C(C=C3CC2)O)O 219.24 unknown https://doi.org/10.1007/S10600-011-9896-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
(R)-N-trans-Feruloyloctopamine 11151622 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCC(C2=CC=C(C=C2)O)O)O 329.30 unknown https://doi.org/10.1007/S10600-011-9896-2
N-[2-hydroxy-2-(4-hydroxy-3-methoxyphenyl)ethyl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide 162863275 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCC(C2=CC(=C(C=C2)O)OC)O)O 359.40 unknown https://doi.org/10.1007/S10600-011-9896-2
N-[2-hydroxy-2-(4-hydroxyphenyl)ethyl]-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide 74178121 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCC(C2=CC=C(C=C2)O)O)O 329.30 unknown https://doi.org/10.1007/S10600-011-9896-2
N-feruloyltyramine; Moupinamide 125213 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1007/S10600-011-9896-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1007/S10600-011-9896-2
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1007/S10600-011-9896-2
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1007/S10600-011-9896-2
https://doi.org/10.1007/BF00598093
https://doi.org/10.1016/B978-0-08-028853-6.50009-7
https://doi.org/10.1007/BF00630448
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/10.1007/BF00630448
https://doi.org/10.1016/B978-0-08-028853-6.50009-7
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/10.1007/S10600-011-9896-2
https://doi.org/10.1007/BF00630448
https://doi.org/10.1016/B978-0-08-028853-6.50009-7
> 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/10.1016/B978-0-08-028853-6.50009-7
https://doi.org/10.1007/BF00630448
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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/10.1007/BF00630448
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one 5320020 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)OC)O)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1007/BF00598093
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 https://doi.org/10.1007/BF00598093
https://doi.org/10.1007/BF00630448
Narcissin 5481663 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)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.1007/BF00598093
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/10.1016/B978-0-08-028853-6.50009-7
https://doi.org/10.1007/S10600-011-9896-2
https://doi.org/10.1007/BF00630448
Vitamin P 5293655 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/10.1007/S10600-011-9896-2
https://doi.org/10.1007/BF00630448
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Tricin 7-glucoside 5322022 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 492.40 unknown https://doi.org/10.1007/BF00598093
https://doi.org/10.1007/S10600-011-9896-2
Tricin 7-O-glucoside 13984469 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 492.40 unknown https://doi.org/10.1007/S10600-011-9896-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
(-)-(7''R,8''S)-4'',5,7-trihydroxy-3',3'',5'-trimethoxy-4',8''-oxyflavonolignan-7'',9''-diol 5323535 Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3=CC(=O)C4=C(C=C(C=C4O3)O)O 526.50 unknown https://doi.org/10.1007/BF00630164
(-)-(7''S,8''S)-4'',5,7-trihydroxy-3',3'',5'-trimethoxy-4',8''-oxyflavonolignan-7'',9''-diol 21575482 Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3=CC(=O)C4=C(C=C(C=C4O3)O)O 526.50 unknown https://doi.org/10.1007/BF00630164
Flavone base + 3O, 2MeO, O-guaiacylglycerol 21159153 Click to see COC1=CC(=CC(=C1OC(CO)C(C2=CC(=C(C=C2)O)OC)O)OC)C3=CC(=O)C4=C(C=C(C=C4O3)O)O 526.50 unknown https://doi.org/10.1007/BF00630164
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown https://doi.org/10.1007/S10600-011-9896-2
https://doi.org/10.1007/BF00598093
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Irisone B 5387194 Click to see C1OC2=C(O1)C(=C3C(=C2)OC=C(C3=O)C4=CC=CC=C4O)O 298.25 unknown https://doi.org/10.1007/S10600-011-9896-2

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