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Stachyurus himalaicus

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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 UUID64402354a0503896763816
Scientific name Stachyurus himalaicus
Authority Hook.f. & Thomson ex Benth.
First published in J. Proc. Linn. Soc., Bot. 5: 55 (1860)

Description Top

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Synonyms Top

Scientific name Authority First published in
Stachyurus chinensis var. brachystachyus C.Y.Wu & S.K.Chen Acta Bot. Yunnan. 3(2): 132. 1981
Stachyurus chinensis subsp. brachystachyus (C.Y.Wu & S.K.Chen) Y.C.Tang & Y.L.Cao Acta Phytotax. Sin. 21: 246 (1983)
Stachyurus himalaicus var. alatipes C.Y.Wu Fl. Yunnan. 3: 343 (1983).
Stachyurus himalaicus var. microphyllus C.Y.Wu Fl. Yunnan. 3: 344 (1983).
Stachyurus himalaicus var. dasyrachis C.Y.Wu Fl. Yunnan. 3: 344 (1983).
Stachyurus brachystachyus (C.Y.Wu & S.K.Chen) Y.C.Tang & Y.L.Cao Acta Bot. Yunnan. 10: 349 (1988)
Stachyurus himalaicus subsp. purpureus Y.P.Zhu & Zhi Y.Zhang Acta Phytotax. Sin. 42: 465 (2004)

Common names Top

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Language Common/alternative name
Chinese 小通草
Chinese 小通草叶
Chinese 小通草根
Chinese 西域旌节花
Chinese 西域旌节花（喜马山旌节花）
Chinese 通條樹
Chinese 喜马山旌节花
Chinese 空藤杆
Chinese 通条树

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-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • Nepal
    • Indo-China
      • Myanmar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000747135
Tropicos 50039727
KEW urn:lsid:ipni.org:names:829502-1
The Plant List kew-2900656
Open Tree Of Life 1015897
NCBI Taxonomy 167472
IUCN Red List 147377251
IPNI 829502-1
iNaturalist 490991
GBIF 3701709
EPPO STWHI
EOL 2889959
CMAUP NPO244

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
Climbing strategies of Taiwan climbers Chen PH, Chung AC, Lin HC, Yang SZ Bot Stud 22-Sep-2023
PMCID:PMC10516820
doi:10.1186/s40529-023-00399-4
PMID:37736799
Differences of oribatid mite community and trophic structure between karst caves and surface different moss habitats Gong T, Yin X, Liu W, Chen H, Shi Z PLoS One 17-Aug-2023
PMCID:PMC10434907
doi:10.1371/journal.pone.0290144
PMID:37590253
Pharmaceutical Potential of High-Altitude Plants for Fatigue-Related Disorders: A Review Zhu H, Liu C, Qian H Plants (Basel) 31-Jul-2022
PMCID:PMC9370126
doi:10.3390/plants11152004
PMID:35956482
Current progress and future prospects in phylofloristics Li R, Qian L, Sun H Plant Divers 17-Jul-2018
PMCID:PMC6137264
doi:10.1016/j.pld.2018.07.003
PMID:30740558
An integrated system for identifying the hidden assassins in traditional medicines containing aristolochic acids Wu L, Sun W, Wang B, Zhao H, Li Y, Cai S, Xiang L, Zhu Y, Yao H, Song J, Cheng YC, Chen S Sci Rep 13-Aug-2015
PMCID:PMC4535178
doi:10.1038/srep11318
PMID:26270958
Revision of the genus Dercetina from Taiwan and their similar species, with description of a new species from Myanmar (Insecta, Chrysomelidae, Galerucinae) Lee CF, Bezděk J Zookeys 13-Aug-2013
PMCID:PMC3760291
doi:10.3897/zookeys.323.5195
PMID:24003313
Chinese Herbal Medicine: A Safe Alternative Therapy for Urinary Tract infection in Patients with Renal Insufficiency Tong Y, Leng Y, Bai J Afr J Tradit Complement Altern Med 29-Dec-2011
PMCID:PMC3746634
doi:10.4314/ajtcam.v9i2.13
PMID:23983345
Fluoroquinolone-Resistant Uncomplicated Urinary Tract Infections, Chinese Herbal Medicine May Provide Help Tong Y, Jing Y, Zhao D, Zhang L, Zeng S Afr J Tradit Complement Altern Med 03-Jul-2011
PMCID:PMC3252729
doi:10.4314/ajtcam.v8i5S.18
PMID:22754063
Flavonoids from leaves and twigs of Stachyurus himalaicus VAR. himalaicus Jing-Hua Yang, Hao Lu, Rong Huang, Yun-Song Wang Springer Science and Business Media LLC 05-Apr-2011
doi:10.1007/S10600-011-9847-Y
In Vitro Screening of Tumoricidal Properties of International Medicinal Herbs: Part II Mazzio EA, Soliman KF Phytother Res 01-Dec-2010
PMCID:PMC2957567
doi:10.1002/ptr.3191
PMID:20564497
Effects of Chinese Herbs on the Hemagglutination and Adhesion of Escherichia Coli Strain In Vitro Tong Y, Wu Q, Zhao D, Liu Y, Cao M, Zhang L, Zeng S Afr J Tradit Complement Altern Med 02-Oct-2010
PMCID:PMC3218435
doi:10.4314/ajtcam.v8i1.60530
PMID:22238488
Triterpenes from Stachyurus himalaicus var. himalaicus Hook. f. et Thoms. ex Benth. Wang YS, Huang R, Li NZ, Xu HY, Yang JH Molecules 24-Mar-2010
PMCID:PMC6257289
doi:10.3390/MOLECULES15042096
PMID:20428029
Triterpenes from Stachyurus himalaicus var. himalaicus Hook. f. et Thoms. ex Benth Wang YS, Huang R, Li NZ, Xu HY, Yang JH Molecules 24-Mar-2010
PMCID:PMC6257289
doi:10.3390/molecules15042096
PMID:20428029
New cytotoxic steroid from Stachyurus imalaicus var. himalaicus. Wang YS, Yang JH, Luo SD, Zhang HB, Li L Molecules 17-Mar-2007
PMCID:PMC6149339
doi:10.3390/12030536
PMID:17851408
New Cytotoxic Steroid from Stachyurus himalaicus var. himalaicus Wang YS, Yang JH, Luo SD, Zhang HB, Li L Molecules 17-Mar-2007
PMCID:PMC6149339
doi:10.3390/12030536
PMID:17851408

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4R,5R,10R,11R,14R,15S,18S,23S)-4-hydroxy-2,7,7,10,14,15,21,21-octamethyl-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene-18-carboxylic acid 102491166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C6C5(COC(O6)(C)C)C)O)C)C)C2C1)C)C(=O)O)C 528.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257289/
(1R,2R,4R,5S,10R,11R,14R,15S,18R,21R,23S)-4-hydroxy-21-(hydroxymethyl)-2,7,7,10,14,15,21-heptamethyl-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene-18-carboxylic acid 102153700 Click to see CC1(OCC2(C3CCC4(C(C3(CC(C2O1)O)C)CC=C5C4(CCC6(C5CC(CC6)(C)CO)C(=O)O)C)C)C)C 544.80 unknown https://doi.org/10.1002/HLCA.200690254
(1R,2R,5S,10R,11R,14R,15S,18S,23S)-2,7,7,10,14,15,21,21-octamethyl-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene-18-carboxylic acid 162669810 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC6C5(COC(O6)(C)C)C)C)C)C2C1)C)C(=O)O)C 512.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257289/
(2R,4aR,6aR,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 16095123 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)CO 504.70 unknown https://doi.org/10.1002/HLCA.200690254
10,11-Dihydroxy-2,9-bis(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162919040 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)CO 504.70 unknown https://doi.org/10.1002/HLCA.200690254
10,11-Dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 5320146 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257289/
2,7,7,10,14,15,21,21-Octamethyl-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene-18-carboxylic acid 4314143 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC6C5(COC(O6)(C)C)C)C)C)C2C1)C)C(=O)O)C 512.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257289/
4-Hydroxy-2,7,7,10,14,15,21,21-octamethyl-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene-18-carboxylic acid 163033184 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C6C5(COC(O6)(C)C)C)O)C)C)C2C1)C)C(=O)O)C 528.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257289/
4-Hydroxy-21-(hydroxymethyl)-2,7,7,10,14,15,21-heptamethyl-6,8-dioxahexacyclo[12.12.0.02,11.05,10.015,24.018,23]hexacos-24-ene-18-carboxylic acid 162876802 Click to see CC1(OCC2(C3CCC4(C(C3(CC(C2O1)O)C)CC=C5C4(CCC6(C5CC(CC6)(C)CO)C(=O)O)C)C)C)C 544.80 unknown https://doi.org/10.1002/HLCA.200690254
alpha-Hederagenin 258538 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257289/
Arjunolic acid 73641 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1)C)C(=O)O)C 488.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257289/
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257289/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives
2,3,14-trihydroxy-10,13-dimethyl-17-(2,3,6-trihydroxy-6-methylheptan-2-yl)-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 271605 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 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149339/
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 https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149339/
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
(2S,3R,5S,9S,10R,13S,14R,17S)-2,3,5-trihydroxy-17-[(4R,5R)-5-(3-hydroxy-3-methylbutyl)-2,2,4-trimethyl-1,3-dioxolan-4-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 162931247 Click to see CC1(OC(C(O1)(C)C2CCC3C2(CCC4C3=CC(=O)C5(C4(CC(C(C5)O)O)C)O)C)CCC(C)(C)O)C 520.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149339/
17-(2,6-Dihydroxy-6-methylheptan-2-yl)-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-one 77915993 Click to see CC12CCC3C(C1CCC2C(C)(CCCC(C)(C)O)O)CCC4=CC(=O)CCC34C 416.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149339/
2,3,14-trihydroxy-17-[5-(3-hydroxy-3-methylbutyl)-2,2,4-trimethyl-1,3-dioxolan-4-yl]-10,13-dimethyl-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 3808392 Click to see CC1(OC(C(O1)(C)C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)CCC(C)(C)O)C 520.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149339/
2,3,5-trihydroxy-17-[5-(3-hydroxy-3-methylbutyl)-2,2,4-trimethyl-1,3-dioxolan-4-yl]-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one 162931246 Click to see CC1(OC(C(O1)(C)C2CCC3C2(CCC4C3=CC(=O)C5(C4(CC(C(C5)O)O)C)O)C)CCC(C)(C)O)C 520.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149339/
Ecdysterone 20,22-monoacetonide 11060391 Click to see CC1(OC(C(O1)(C)C2CCC3(C2(CCC4C3=CC(=O)C5C4(CC(C(C5)O)O)C)C)O)CCC(C)(C)O)C 520.70 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149339/
Stachsterol 70697813 Click to see CC12CCC3C(C1CCC2C(C)(CCCC(C)(C)O)O)CCC4=CC(=O)CCC34C 416.60 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149339/
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
{[2-Hydroxy-1,1-bis(hydroxymethyl)ethyl]ammonio}acetate 6992779 Click to see C(C(=O)[O-])[NH2+]C(CO)(CO)CO 179.17 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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives
1-(3-(6,7-Dimethoxyisoquinolin-1-yl)propyl)guanidine 10062645 Click to see COC1=C(C=C2C(=C1)C=CN=C2CCCN=C(N)N)OC 288.34 unknown via CMAUP database
Crispine B 10105261 Click to see COC1=C(C=C2C3=[N+](CCC3)C=CC2=C1)OC 230.28 unknown via CMAUP database
Crispine D 10069639 Click to see COC1=C(C=C2C(=C1)C(=CN=C2CCCN=C(N)N)CCCCN=C(N)N)OC 401.50 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(+)-Crispine A 11673094 Click to see COC1=C(C=C2C3CCCN3CCC2=C1)OC 233.31 unknown via CMAUP database
2-[3-[(1S)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolin-1-yl]propyl]guanidine 24823534 Click to see COC1=C(C=C2C(NCCC2=C1)CCCN=C(N)N)OC 292.38 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol 1203 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1007/S10600-011-9847-Y
Epicatechin 72276 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1007/S10600-011-9847-Y
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)chroman-4-one 5153580 Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 320.25 unknown https://doi.org/10.1007/S10600-011-9847-Y
Dihydromyricetin 161557 Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 320.25 unknown https://doi.org/10.1007/S10600-011-9847-Y
> 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
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown 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/10.1007/S10600-011-9847-Y
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
2-[3-(6-Deoxy-alpha-L-mannopyranosyloxy)-4-hydroxyphenyl]-5,7-dihydroxy-4H-1-benzopyran-4-one 21721958 Click to see CC1C(C(C(C(O1)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)O 432.40 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,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/S10600-011-9847-Y
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 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/10.1007/S10600-011-9847-Y
6''-O-Acetylastragalin 10435673 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 490.40 unknown https://doi.org/10.1007/S10600-011-9847-Y
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/10.1007/S10600-011-9847-Y
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/S10600-011-9847-Y
Kaempferol 3-(6-acetylgalactoside) 74978029 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 490.40 unknown https://doi.org/10.1007/S10600-011-9847-Y
Quercetin 3-O-(6''-acetyl-glucoside) 10006384 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 506.40 unknown https://doi.org/10.1007/S10600-011-9847-Y
Quercetin-3-O-glucosyl-6''-acetate 15596585 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 506.40 unknown https://doi.org/10.1007/S10600-011-9847-Y
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-2-[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl]oxy-6-(hydroxymethyl)oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate 11377340 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)OC)O)CO)O)O)O)O)O 666.60 unknown via CMAUP database
Linariifolioside 5492485 Click to see CC(=O)OCC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)O)O 652.60 unknown via CMAUP database

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