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Saussurea salicifolia

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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 UUID643fcb4a0a9aa132476862
Scientific name Saussurea salicifolia
Authority DC.
First published in Ann. Mus. Natl. Hist. Nat. xvi. (1810) 200.

Description Top

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Synonyms Top

Scientific name Authority First published in
Serratula salicifolia L. Sp. Pl. : 817 (1753)
Serratula salicifolia Lepech. It. 1: 262 1795
Theodorea salicifolia Kuntze Revis. Gen. Pl. 1: 368. 1891 [5 Nov 1891]
Heterotrichum leptophyllum M.Bieb. ex DC. Prodr. [A. P. de Candolle] 6: 533. 1838 [1837 publ. early Jan 1838]

Common names Top

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Language Common/alternative name
Chinese 柳叶风毛菊
Chinese 柳葉風毛菊

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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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
      • Inner Mongolia
      • Manchuria
      • Xinjiang
    • Mongolia
      • Mongolia
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • Yakutskiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000045075
Tropicos 2732156
KEW urn:lsid:ipni.org:names:242619-1
The Plant List gcc-143595
Open Tree Of Life 289582
Observations.org 142275
NCBI Taxonomy 446849
IPNI 242619-1
iNaturalist 779252
GBIF 5404376
EOL 6211493
USDA GRIN 413675
CMAUP NPO22375

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
Immunomodulatory Activity of Polysaccharides Isolated from Saussurea salicifolia L. and Saussurea frolovii Ledeb Schepetkin IA, Danilets MG, Ligacheva AA, Trofimova ES, Selivanova NS, Sherstoboev EY, Krivoshchekov SV, Gulina EI, Brazovskii KS, Kirpotina LN, Quinn MT, Belousov MV Molecules 16-Sep-2023
PMCID:PMC10536955
doi:10.3390/molecules28186655
PMID:37764432
Fecal Microbiota and Diet Composition of Buryatian Horses Grazing Warm- and Cold-Season Grass Pastures Zaitseva S, Dagurova O, Radnagurueva A, Kozlova A, Izotova A, Krylova A, Noskov S, Begmatov S, Patutina E, Barkhutova DD Microorganisms 30-Jul-2023
PMCID:PMC10459317
doi:10.3390/microorganisms11081947
PMID:37630507
The complete chloroplast genome sequence of Centaurea cyanus (Asteraceae) Zhang N, Xie P, Huang K, Yin H, Mo P, Wang Y Mitochondrial DNA B Resour 13-Mar-2023
PMCID:PMC10013558
doi:10.1080/23802359.2023.2185470
PMID:36926644
Preclinical evidence of polyherbal formulations on wound healing: A systematic review on research trends and perspectives Dubey S, Dixit AK J Ayurveda Integr Med 24-Feb-2023
PMCID:PMC9988554
doi:10.1016/j.jaim.2023.100688
PMID:36841194
Health Benefits and Pharmacological Aspects of Chrysoeriol Aboulaghras S, Sahib N, Bakrim S, Benali T, Charfi S, Guaouguaou FE, Omari NE, Gallo M, Montesano D, Zengin G, Taghzouti K, Bouyahya A Pharmaceuticals (Basel) 07-Aug-2022
PMCID:PMC9415049
doi:10.3390/ph15080973
PMID:36015121
Lignans: a versatile source of anticancer drugs Mukhija M, Joshi BC, Bairy PS, Bhargava A, Sah AN Beni Suef Univ J Basic Appl Sci 04-Jun-2022
PMCID:PMC9166195
doi:10.1186/s43088-022-00256-6
PMID:35694188
The complete chloroplast genome sequence of Tussilago farfara (Asteraceae) Yizhong D, Lu K, Zhongyu D, Shen Y Mitochondrial DNA B Resour 25-Mar-2022
PMCID:PMC8959504
doi:10.1080/23802359.2021.2005494
PMID:35356793
Opportunities to integrate herders’ indicators into formal rangeland monitoring: an example from Mongolia Jamsranjav C, Fernández‐Giménez ME, Reid RS, Adya B Ecol Appl 17-May-2019
PMCID:PMC6851969
doi:10.1002/eap.1899
PMID:31020715
Overview of the anti-inflammatory effects, pharmacokinetic properties and clinical efficacies of arctigenin and arctiin from Arctium lappa L Gao Q, Yang M, Zuo Z Acta Pharmacol Sin 26-Apr-2018
PMCID:PMC5943914
doi:10.1038/aps.2018.32
PMID:29698388
Cynaropicrin: A Comprehensive Research Review and Therapeutic Potential As an Anti-Hepatitis C Virus Agent Elsebai MF, Mocan A, Atanasov AG Front Pharmacol 08-Dec-2016
PMCID:PMC5143615
doi:10.3389/fphar.2016.00472
PMID:28008316
Lignans inhibit cell growth via regulation of Wnt/beta-catenin signaling. Yoo JH, Lee HJ, Kang K, Jho EH, Kim CY, Baturen D, Tunsag J, Nho CW Food Chem Toxicol 01-Aug-2010
doi:10.1016/J.FCT.2010.05.056
PMID:20510325
In Vitro Ultramorphological Assessment of Apoptosis Induced by Zerumbone on (HeLa) Abdel Wahab SI, Abdul AB, Alzubairi AS, Mohamed Elhassan M, Mohan S J Biomed Biotechnol 25-Mar-2009
PMCID:PMC2661117
doi:10.1155/2009/769568
PMID:19343171
The chemopreventive effects of Saussurea salicifolia through induction of apoptosis and phase II detoxification enzyme. Kang K, Lee HJ, Kim CY, Lee SB, Tunsag J, Batsuren D, Nho CW Biol Pharm Bull 01-Dec-2007
doi:10.1248/BPB.30.2352
PMID:18057725
A sesquiterpene lactone fromSaussurea salicifolia V. V. Dudko, K. S. Rybalko Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00579663
Further guaianolides from Hymenopappus species F. Eid, J. Jakupovic, F. Bohlmann, L. Watson, J.R. Estes Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80612-5

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
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown via CMAUP database
> Benzenoids / Tetralins
(4S)-10-Nor-calamenen-10-one 73350586 Click to see CC1=CC2=C(C=C1)C(=O)CCC2C(C)C 202.29 unknown via CMAUP database
Oxyphyllenotriol A 51041015 Click to see CC(C)C1=C2C(C(CCC2=C(C=C1)O)(C)O)O 236.31 unknown via CMAUP database
Oxyphyllone G 51041016 Click to see CC1=C(C2=C(C=C1)C(=O)CCC2C(C)C)O 218.29 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans / Dibenzylbutyrolactone lignans
3,4-Bis[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-2-one 345761 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)O 358.40 unknown https://doi.org/10.1016/J.FCT.2010.05.056
Arctigenin 64981 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown https://doi.org/10.1016/J.FCT.2010.05.056
https://doi.org/10.1016/0031-9422(88)80612-5
l-Arctigenin 230232 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)OC 372.40 unknown https://doi.org/10.1016/J.FCT.2010.05.056
Matairesinol 119205 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)O)OC)O 358.40 unknown https://doi.org/10.1016/0031-9422(88)80612-5
https://doi.org/10.1016/J.FCT.2010.05.056
Trachelogenin 452855 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2(CC3=CC(=C(C=C3)O)OC)O)OC 388.40 unknown https://doi.org/10.1016/0031-9422(88)80612-5
> Lignans, neolignans and related compounds / Lignan glycosides
Arctii;NSC 315527;Arctigenin-4-glucoside 3660596 Click to see COC1=C(C=C(C=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)OC 534.60 unknown https://doi.org/10.1016/J.FCT.2010.05.056
Matairesinoside 486612 Click to see COC1=C(C=CC(=C1)CC2COC(=O)C2CC3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O 520.50 unknown https://doi.org/10.1248/BPB.30.2352
> 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 via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Labda-8(17),12-diene-15,16-dial 11077520 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C(CC=O)C=O)C)C 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1r,2r)-p-Menth-3-en-1,2-diol 71423340 Click to see CC(C)C1=CC(C(CC1)(C)O)O 170.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1aR,4aR,7R,8aR)-7-hydroxy-1a,4a-dimethyl-7-prop-1-en-2-yl-4,5,6,8-tetrahydro-3H-naphtho[1,8a-b]oxiren-2-one 51041018 Click to see CC(=C)C1(CCC2(CCC(=O)C3(C2(C1)O3)C)C)O 250.33 unknown via CMAUP database
(1R,2R,3R,6S,7S)-1-hydroxy-3,7-dimethyl-10-propan-2-yl-11-oxatricyclo[5.3.1.02,6]undec-9-en-8-one 76285513 Click to see CC1CCC2C1C3(C(=CC(=O)C2(O3)C)C(C)C)O 250.33 unknown via CMAUP database
Oxyphyllanene D 57396910 Click to see CC(=C)C1(CCC2(CCC(=O)C3(C2(C1)O3)C)C)O 250.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(11S)-Nootkatone-11,12-diol 15601439 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(C)(CO)O)C 252.35 unknown via CMAUP database
(1S,4R,4aS,6R)-4,4a-dimethyl-6-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalen-1-ol 44576208 Click to see CC1CCC(C2=CCC(CC12C)C(=C)C)O 220.35 unknown via CMAUP database
(3S,4aS,5R)-4a,5-dimethyl-3-prop-1-en-2-yl-3,4,5,6-tetrahydro-2H-naphthalene-1,7-dione 72715093 Click to see CC1CC(=O)C=C2C1(CC(CC2=O)C(=C)C)C 232.32 unknown via CMAUP database
(4R,4aR)-6-acetyl-4,4a-dimethyl-3,4,7,8-tetrahydronaphthalen-2-one 117654813 Click to see CC1CC(=O)C=C2C1(C=C(CC2)C(=O)C)C 218.29 unknown via CMAUP database
(4R,4aS,6R)-6-(2-hydroxypropan-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 89960876 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(C)(C)O)C 236.35 unknown via CMAUP database
(4R,4aS,6R)-6-(3-hydroxyprop-1-en-2-yl)-4,4a-dimethyl-3,4,5,6,7,8-hexahydronaphthalen-2-one 53249021 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)CO)C 234.33 unknown via CMAUP database
(4R,4aS,6S,8S)-8-hydroxy-4,4a-dimethyl-6-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one 11651584 Click to see CC1CC(=O)C=C2C1(CC(CC2O)C(=C)C)C 234.33 unknown via CMAUP database
Nootkatene 25200342 Click to see CC1CC=CC2=CCC(CC12C)C(=C)C 202.33 unknown via CMAUP database
Nootkatol 182645 Click to see CC1CC(C=C2C1(CC(CC2)C(=C)C)C)O 220.35 unknown via CMAUP database
Nootkatone 1268142 Click to see CC1CC(=O)C=C2C1(CC(CC2)C(=C)C)C 218.33 unknown via CMAUP database
oxyphyllol C 10857540 Click to see CC1CCC(C2(C1(CC(CC2)C(=C)C)C)O)O 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,4aR,7R,8aS)-1,4a-dimethyl-7-prop-1-en-2-yl-2,3,4,5,6,7,8,8a-octahydronaphthalen-1-ol 15560338 Click to see CC(=C)C1CCC2(CCCC(C2C1)(C)O)C 222.37 unknown via CMAUP database
(2R,4aS,7R,8aR)-4a-Methyl-1-methylidene-7-(prop-1-en-2-yl)decahydronaphthalen-2-ol 14076604 Click to see CC(=C)C1CCC2(CCC(C(=C)C2C1)O)C 220.35 unknown via CMAUP database
(4aS,7S,8R)-8-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-3,4,5,6,7,8-hexahydronaphthalen-2-one 57393410 Click to see CC1=C2C(C(CCC2(CCC1=O)C)C(=C)C)O 234.33 unknown via CMAUP database
(4aS,7S)-7-hydroxy-1,4a-dimethyl-7-prop-1-en-2-yl-4,5,6,8-tetrahydro-3H-naphthalen-2-one 57335617 Click to see CC1=C2CC(CCC2(CCC1=O)C)(C(=C)C)O 234.33 unknown via CMAUP database
7-Epi-Teucrenone B 57393409 Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C 234.33 unknown via CMAUP database
Ligucyperonol 14681770 Click to see CC1=C2CC(CCC2(C(CC1=O)O)C)C(=C)C 234.33 unknown via CMAUP database
Oxyphyllol A 637451 Click to see CC(=C)C1CCC2(CCCC(C2=C1)(C)O)C 220.35 unknown via CMAUP database
Rel-Oxyphyllanene E 57400339 Click to see CC(=C)C1(CCC2(CCC(C(=C)C2C1)O)C)O 236.35 unknown via CMAUP database
Teucrenone 10105443 Click to see CC1=CC(=O)CC2(C1CC(CC2)(C(=C)C)O)C 234.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
(4aS,8aR,9aR)-3,5,8a-trimethyl-4a,8,9,9a-tetrahydro-4H-benzo[f][1]benzofuran-2,7-dione 71681246 Click to see CC1=CC(=O)CC2(C1CC3=C(C(=O)OC3C2)C)C 246.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(8-Hydroxy-3,6-dimethylidene-2-oxospiro[3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-9,2'-oxirane]-4-yl) 2-methylprop-2-enoate 15628198 Click to see CC(=C)C(=O)OC1CC(=C)C2CC(C3(C2C4C1C(=C)C(=O)O4)CO3)O 346.40 unknown https://doi.org/10.1016/0031-9422(88)80612-5
[(3aS,4R,6aS,8R,9aS,9bS)-8-hydroxy-3,6,9-trimethylidene-2-oxo-3a,4,5,6a,7,8,9a,9b-octahydroazuleno[4,5-b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 163019222 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO 346.40 unknown https://doi.org/10.1007/BF00579663
Cynaropicrin 119093 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO 346.40 unknown https://doi.org/10.1007/BF00579663
https://doi.org/10.1016/0031-9422(88)80612-5
Deacyljanerin 176588 Click to see C=C1CC(C2C(C3C1CC(C34CO4)O)OC(=O)C2=C)O 278.30 unknown https://doi.org/10.1016/0031-9422(88)80612-5
Janerin 14021480 Click to see C=C1CC(C2C(C3C1CC(C34CO4)O)OC(=O)C2=C)OC(=O)C(=C)CO 362.40 unknown https://doi.org/10.1016/0031-9422(88)80612-5
Saupirin 181128 Click to see C=C1CC(C2C(C3C1CC(C3=C)O)OC(=O)C2=C)OC(=O)C(=C)CO 346.40 unknown https://doi.org/10.1007/BF00579663
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
beta-Sitosteryl palmitate 9852570 Click to see CCCCCCCCCCCCCCCC(=O)OC1CCC2(C3CCC4(C(C3CC=C2C1)CCC4C(C)CCC(CC)C(C)C)C)C 653.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
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 via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
Pubescone 102054514 Click to see CC(C)C1C2C(C2CCC(=O)C)CCC1=O 222.32 unknown via CMAUP database
Spiro[4.4]nonan-2-one 549163 Click to see C1CCC2(C1)CCC(=O)C2 138.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(1aR,7R,7bS)-1a-methyl-7-propan-2-yl-2,3,5,6,7,7b-hexahydronaphtho[1,2-b]oxiren-4-one 44255203 Click to see CC(C)C1CCC(=O)C2=C1C3C(O3)(CC2)C 220.31 unknown via CMAUP database
(4aR,6S,8aS)-6-acetyl-4a-hydroxy-4,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-2-one 71681103 Click to see CC1=CC(=O)CC2(C1(CC(CC2)C(=O)C)O)C 236.31 unknown via CMAUP database
(4aR)-7-acetyl-1,4a-dimethyl-3,4,5,6-tetrahydronaphthalen-2-one 71681245 Click to see CC1=C2C=C(CCC2(CCC1=O)C)C(=O)C 218.29 unknown via CMAUP database
(4aS,8aR)-4a,8-dimethyl-3,4,5,8a-tetrahydro-1H-naphthalene-2,6-dione 122402647 Click to see CC1=CC(=O)CC2(C1CC(=O)CC2)C 192.25 unknown via CMAUP database
4-Hydroxy-11,12,13-trinor-5-eudesmen-7-one 15153217 Click to see CC12CCCC(C1=CC(=O)CC2)(C)O 194.27 unknown via CMAUP database
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
Oxyphyllenone A 10262534 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Oxyphyllenone B 44310512 Click to see CC12CCC(C(C1=CC(=O)CC2)(C)O)O 210.27 unknown via CMAUP database
Teuhetenone A 15153216 Click to see CC12CCCC(C1=CC(=O)CC2)(C)O 194.27 unknown via CMAUP database
> Organoheterocyclic compounds / Epoxides
(1S,4S,6S,8E,12S)-1,6,10,10-tetramethyl-5,13-dioxatricyclo[10.1.0.04,6]tridec-8-ene 12014673 Click to see CC1(CC2C(O2)(CCC3C(O3)(CC=C1)C)C)C 236.35 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
Oxyphyllanene C 57335616 Click to see CC1=C2C3C(O3)(CCC2(CCC1=O)C)C(=O)C 234.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(1E)-1-(4-Hydroxy-3-methoxyphenyl)-7-phenyl-1-hepten-3-one 6440365 Click to see COC1=C(C=CC(=C1)C=CC(=O)CCCCC2=CC=CC=C2)O 310.40 unknown via CMAUP database
1-(2,4-Dihydroxy-3-methoxyphenyl)-7-(4-methoxyphenyl)heptan-3-one 72708396 Click to see COC1=CC=C(C=C1)CCCCC(=O)CCC2=C(C(=C(C=C2)O)OC)O 358.40 unknown via CMAUP database
1-(3,5-Dihydroxy-4-methoxyphenyl)-7-phenylheptan-3-one 72708395 Click to see COC1=C(C=C(C=C1O)CCC(=O)CCCCC2=CC=CC=C2)O 328.40 unknown via CMAUP database
Yakuchinone-A 133145 Click to see COC1=C(C=CC(=C1)CCC(=O)CCCCC2=CC=CC=C2)O 312.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5-Dihydroxy-7-methoxy-2-(4-methoxyphenyl)-4H-chromen-4-one 5378823 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)O 314.29 unknown via CMAUP database
Izalpinin 5318691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
Kaempferide 5281666 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin 5281954 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=CC=C3)O 268.26 unknown via CMAUP database

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