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Rhododendron dauricum

Rhododendron dauricum - 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 UUID64407c950727c121720798
Scientific name Rhododendron dauricum
Authority L.
First published in Sp. Pl. : 392 (1753)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Rhododendron ledebourii Pojark. Fl. URSS 18: 722 (1952)
Azalea atrovirens (Franch.) (Franch.) Kuntze Revis. Gen. Pl. 2: 387 (1891)
Azalea dahurica K.Koch Dendrologie 2(2): 181. 1873 [Nov 1873]
Azalea daurica (L.) Kuntze Revis. Gen. Pl. 2: 387 (1891)
Rhododendron atrovirens (Ker Gawler) Franch. Bull. Soc. Bot. France 33: 235 (1886)
Rhododendron dauricum subsp. ledebourii (Pojark.) M.S.Alexandrova & P.A.Schmidt Betr. Gehölzk. : 67 (1981 publ. 1982)
Rhododendron dauricum var. atrovirens Ker Gawler Bot. Reg. 3:t.194. (1817)

Common names Top

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Language Common/alternative name
Azerbaijani dauriya rododendronu
Belarusian рададэндран даурскі
Bulgarian даурски рододендрон
Japanese 蝦夷紫躑躅
Japanese エゾムラサキツツジ
Korean 산진달래
Polish różanecznik dahurski
Russian Даурский багульник
Russian Сибирский багульник
Russian Рододендрон даурский
Yakutian Хаскара
Chinese 达子香
Chinese 兴安杜鹃
Chinese 满山红油
Chinese 满山红
Chinese 冬青叶

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
sprinkle seed on 10 cm damp sphagnum moss; cover with clear plastic pop bottle cut in half; transplant seedling to acidic mix in shade outdoors when 5 cm high; protect from rodents and give protection in cold frame first winter

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • West Siberia
      • Yakutskiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000400762
UNII D6T8R3WLWR
Tropicos 12300087
KEW urn:lsid:ipni.org:names:326359-2
The Plant List kew-2419620
Plantarium 31853
Missouri Botanical Garden 279949
Open Tree Of Life 226740
Observations.org 121257
NCBI Taxonomy 880079
IPNI 326359-2
iNaturalist 708691
GBIF 7327670
Freebase /m/010wgp31
EPPO RHODC
EOL 2891271
Elurikkus 588961
USDA GRIN 5069
Wikipedia Rhododendron_dauricum
CMAUP NPO21072

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
Recent developments in the engineered biosynthesis of fungal meroterpenoids Quan Z, Awakawa T Beilstein J Org Chem 13-Mar-2024
PMCID:PMC10949012
doi:10.3762/bjoc.20.50
PMID:38505236
The Diverse Mycorrizal Morphology of Rhododendron dauricum, the Fungal Communities Structure and Dynamics from the Mycorrhizosphere Liu J, Xu Y, Si YJ, Li BQ, Chen P, Wu LL, Guo P, Ji RQ J Fungi (Basel) 14-Jan-2024
PMCID:PMC10817234
doi:10.3390/jof10010065
PMID:38248974
Syringa reticulata potently inhibits the activity of SARS-CoV-2 3CL protease Hao Z, Liu Y, Guan W, Pan J, Li M, Wu J, Liu Y, Kuang H, Yang B Biochem Biophys Rep 26-Dec-2023
PMCID:PMC10873874
doi:10.1016/j.bbrep.2023.101626
PMID:38371528
Landscape Dynamics and Ecological Risk Assessment of Cold Temperate Forest Moose Habitat in the Great Khingan Mountains, China Sun S, Hong Y, Guo J, Zhang N, Zhang M Biology (Basel) 11-Aug-2023
PMCID:PMC10451888
doi:10.3390/biology12081122
PMID:37627006
Targeting oxidative stress as a preventive and therapeutic approach for cardiovascular disease Yan Q, Liu S, Sun Y, Chen C, Yang S, Lin M, Long J, Yao J, Lin Y, Yi F, Meng L, Tan Y, Ai Q, Chen N, Yang Y J Transl Med 02-Aug-2023
PMCID:PMC10394930
doi:10.1186/s12967-023-04361-7
PMID:37533007
Differences in the Suitable Distribution Area between Northern and Southern China Landscape Plants Wang C, Sheng Q, Zhao R, Zhu Z Plants (Basel) 20-Jul-2023
PMCID:PMC10385631
doi:10.3390/plants12142710
PMID:37514324
Natural antioxidants that act against Alzheimer’s disease through modulation of the NRF2 pathway: a focus on their molecular mechanisms of action Sidiropoulou GA, Metaxas A, Kourti M Front Endocrinol (Lausanne) 03-Jul-2023
PMCID:PMC10351420
doi:10.3389/fendo.2023.1217730
PMID:37465125
Natural products modulate cell apoptosis: a promising way for treating endometrial cancer Zhou X, Zeng Y, Zheng R, Wang Y, Li T, Song S, Zhang S, Huang J, Ren Y Front Pharmacol 08-Jun-2023
PMCID:PMC10285317
doi:10.3389/fphar.2023.1209412
PMID:37361222
Farrerol directly activates the deubiqutinase UCHL3 to promote DNA repair and reprogramming when mediated by somatic cell nuclear transfer Zhang W, Wang M, Song Z, Fu Q, Chen J, Zhang W, Gao S, Sun X, Yang G, Zhang Q, Yang J, Tang H, Wang H, Kou X, Wang H, Mao Z, Xu X, Gao S, Jiang Y Nat Commun 03-Apr-2023
PMCID:PMC10070447
doi:10.1038/s41467-023-37576-9
PMID:37012254
High-efficient production of mushroom polyketide compounds in a platform host Aspergillus oryzae Han H, Yu C, Qi J, Wang P, Zhao P, Gong W, Xie C, Xia X, Liu C Microb Cell Fact 30-Mar-2023
PMCID:PMC10064546
doi:10.1186/s12934-023-02071-9
PMID:36998045
Silver Nanoparticles Synthesized from Abies alba and Pinus sylvestris Bark Extracts: Characterization, Antioxidant, Cytotoxic, and Antibacterial Effects Macovei I, Luca SV, Skalicka-Woźniak K, Horhogea CE, Rimbu CM, Sacarescu L, Vochita G, Gherghel D, Ivanescu BL, Panainte AD, Nechita C, Corciova A, Miron A Antioxidants (Basel) 24-Mar-2023
PMCID:PMC10135277
doi:10.3390/antiox12040797
PMID:37107172
Extreme temperature events reduced carbon uptake of a boreal forest ecosystem in Northeast China: Evidence from an 11-year eddy covariance observation Yan Y, Zhou L, Zhou G, Wang Y, Song J, Zhang S, Zhou M Front Plant Sci 25-Jan-2023
PMCID:PMC9905745
doi:10.3389/fpls.2023.1119670
PMID:36760633
Understory species composition mediates soil greenhouse gas fluxes by affecting bacterial community diversity in boreal forests Duan B, Xiao R, Cai T, Man X, Ge Z, Gao M, Mencuccini M Front Microbiol 20-Jan-2023
PMCID:PMC9894877
doi:10.3389/fmicb.2022.1090169
PMID:36741883
Natural Active Ingredients and TRPV1 Modulation: Focus on Key Chemical Moieties Involved in Ligand–Target Interaction Andrei C, Zanfirescu A, Nițulescu GM, Olaru OT, Negreș S Plants (Basel) 11-Jan-2023
PMCID:PMC9860573
doi:10.3390/plants12020339
PMID:36679051
Linkages between the molecular composition of dissolved organic matter and soil microbial community in a boreal forest during freeze–thaw cycles Yang Y, Cheng S, Fang H, Guo Y, Li Y, Zhou Y, Shi F, Vancampenhout K Front Microbiol 09-Jan-2023
PMCID:PMC9868181
doi:10.3389/fmicb.2022.1012512
PMID:36699583

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
Benzylacetone 17355 Click to see CC(=O)CCC1=CC=CC=C1 148.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Butyl isobutyl phthalate 28813 Click to see CCCCOC(=O)C1=CC=CC=C1C(=O)OCC(C)C 278.34 unknown via CMAUP database
Dibutyl Phthalate 3026 Click to see CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC 278.34 unknown https://doi.org/10.1016/J.JCHROMB.2004.06.048
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,4-Dihydroxybenzoic acid 1491 Click to see C1=CC(=C(C=C1O)O)C(=O)O 154.12 unknown via CMAUP database
2,5-Dihydroxybenzoic acid 3469 Click to see C1=CC(=C(C=C1O)C(=O)O)O 154.12 unknown https://doi.org/10.1007/S10600-010-9649-7
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1016/S0021-9673(01)01434-0
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1016/S0021-9673(01)01434-0
https://doi.org/10.1007/S10600-010-9649-7
https://doi.org/10.1016/J.JCHROMB.2004.06.048
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4-Dihydroxy-5-methoxybenzoic acid 19829 Click to see COC1=CC(=CC(=C1O)O)C(=O)O 184.15 unknown https://doi.org/10.1007/S10600-010-9649-7
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown https://doi.org/10.1016/S0021-9673(01)01434-0
https://doi.org/10.1007/S10600-010-9649-7
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1007/S10600-010-9649-7
> 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 https://doi.org/10.1016/S0021-9673(01)01434-0
> 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/10.1016/J.JCHROMB.2004.06.048
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-(3-Hydroxybutyl)phenol 97790 Click to see CC(CCC1=CC=C(C=C1)O)O 166.22 unknown via CMAUP database
Rhododendrol 919205 Click to see CC(CCC1=CC=C(C=C1)O)O 166.22 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Hydroquinone 785 Click to see C1=CC(=CC=C1O)O 110.11 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
Orcinol 10436 Click to see CC1=CC(=CC(=C1)O)O 124.14 unknown https://doi.org/10.1021/NP0303916
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hexadecane 11006 Click to see CCCCCCCCCCCCCCCC 226.44 unknown via CMAUP database
Tetradecane 12389 Click to see CCCCCCCCCCCCCC 198.39 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl hexanoate 7824 Click to see CCCCCC(=O)OC 130.18 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E)-(7R,11R)-3,7,11,15-tetramethylhexadec-2-ene-1-ol 145386 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
3,7,11,15-Tetramethyl-2-hexadecen-1-OL 5366244 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
Benzoicacidcyanomethylester 5320547 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
cis-Phytol 6430833 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
Phytol [FHFI] 9018 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Cembrane diterpenoids
(1R,2E,4S,7Z,11E)-1,7,11-trimethyl-4-propan-2-ylcyclotetradeca-2,7,11-trien-1-ol 12444349 Click to see CC1=CCCC(C=CC(CCC(=CCC1)C)C(C)C)(C)O 290.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Grayanoids / Leucothol and grayanotoxane diterpenoids
Andromedotoxin 20842 Click to see CC(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O 412.50 unknown via CMAUP database
Grayanotoxin I 9548612 Click to see CC(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O 412.50 unknown via CMAUP database
Rhodojaponin IV 442083 Click to see CC(=O)OC1CC23CC(C(C2OC(=O)C)CCC3C(C4C1(C(C(C4)O)(C)C)O)(C)O)(C)O 454.60 unknown via CMAUP database
Rhodotoxin 231125 Click to see CC(=O)OC1C2CCC3C1(CC(C4(C(C3(C)O)CC(C4(C)C)O)O)O)CC2(C)O 412.50 unknown https://doi.org/10.1016/J.JCHROMB.2004.06.048
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
5,7,11-Tridecatriene-3,4-diol, 3,8,12-trimethyl- 6437622 Click to see CCC(C)(C(C=CC=C(C)CCC=C(C)C)O)O 252.39 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene 12223113 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(2R)-2-[(3E)-4,8-Dimethyl-3,7-nonadien-1-yl]-2,7-dimethyl-2H-1-benzopyran-5-ol 134843996 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)CCC=C(C)C)O 326.50 unknown https://doi.org/10.1021/NP0303916
(2R)-2-[(3R)-3-hydroxy-8-methyl-4-methylidenenon-7-enyl]-2,7-dimethylchromen-5-ol 162946145 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC(C(=C)CCC=C(C)C)O)O 342.50 unknown https://doi.org/10.1021/NP0303916
(Z)-Daurichromenic acid 101759852 Click to see CC1=CC2=C(C=CC(O2)(C)CCC=C(C)CCC=C(C)C)C(=C1C(=O)O)O 370.50 unknown via CMAUP database
2-(3-Hydroxy-8-methyl-4-methylidenenon-7-enyl)-2,7-dimethylchromen-5-ol 10286747 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC(C(=C)CCC=C(C)C)O)O 342.50 unknown https://doi.org/10.1021/NP0303916
2-(4,8-Dimethylnona-3,7-dienyl)-2,7-dimethylchromen-5-ol 75109426 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)CCC=C(C)C)O 326.50 unknown https://doi.org/10.1021/NP0303916
2-(4,8-Dimethylnona-3,7-dienyl)-5-hydroxy-2,7-dimethylchromene-6-carboxylic acid 70540940 Click to see CC1=CC2=C(C=CC(O2)(C)CCC=C(C)CCC=C(C)C)C(=C1C(=O)O)O 370.50 unknown https://doi.org/10.1016/S0040-4020(00)01144-3
2-(9-Hydroxy-4,8-dimethylnona-3,7-dienyl)-2,7-dimethylchromen-5-ol 85045232 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)CCC=C(C)CO)O 342.50 unknown https://doi.org/10.1021/NP0303916
5-Hydroxy-2-methyl-2-(4,8-dimethyl-3,7-nonadienyl)-7-methyl-2H-1-benzopyran-6-carboxylic acid 11291664 Click to see CC1=CC2=C(C=CC(O2)(C)CCC=C(C)CCC=C(C)C)C(=C1C(=O)O)O 370.50 unknown via CMAUP database
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
Camphene 6616 Click to see CC1(C2CCC(C2)C1=C)C 136.23 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
Confluentin 10381750 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)CCC=C(C)C)O 326.50 unknown https://doi.org/10.1021/NP0303916
Daurichromene B 10043034 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC(C(=C)CCC=C(C)C)O)O 342.50 unknown https://doi.org/10.1021/NP0303916
Daurichromene D 10427504 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)CCC=C(C)CO)O 342.50 unknown https://doi.org/10.1021/NP0303916
Daurichromenic acid 6475854 Click to see CC1=CC2=C(C=CC(O2)(C)CCC=C(C)CCC=C(C)C)C(=C1C(=O)O)O 370.50 unknown https://doi.org/10.1016/S0040-4020(00)01144-3
https://doi.org/10.1016/J.JCHROMB.2004.06.048
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Isolongifolene 11127402 Click to see CC1(CCC=C2C13CCC(C3)C2(C)C)C 204.35 unknown via CMAUP database
(+)-delta-Cadinene 441005 Click to see CC1=CC2C(CCC(=C2CC1)C)C(C)C 204.35 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
(1S,2R)-1,3-dimethyl-8-propan-2-yltricyclo[4.4.0.02,7]dec-3-ene 145994486 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
(1Z,4E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene 45115091 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown via CMAUP database
(3R,6E)-nerolidol 11241545 Click to see CC(=CCCC(=CCCC(C)(C=C)O)C)C 222.37 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
1,3-Benzenediol, 5-methyl-2-(3,7,11-trimethyl-2,6,10-dodecatrienyl)- 586192 Click to see CC1=CC(=C(C(=C1)O)CC=C(C)CCC=C(C)CCC=C(C)C)O 328.50 unknown https://doi.org/10.1021/NP0303916
3-Hydroxy-5,9,13-trimethyl-13-(4-methylpent-3-enyl)-8-oxatetracyclo[7.4.1.02,7.012,14]tetradeca-2(7),3,5-triene-4-carboxylic acid 73200932 Click to see CC1=CC2=C(C3C4C(C3(C)CCC=C(C)C)CCC4(O2)C)C(=C1C(=O)O)O 370.50 unknown https://doi.org/10.1016/S0040-4020(00)01144-3
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
Alpha-Farnesene 5281516 Click to see CC(=CCCC(=CCC=C(C)C=C)C)C 204.35 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
alpha-Santalene 94164 Click to see CC(=CCCC1(C2CC3C1(C3C2)C)C)C 204.35 unknown via CMAUP database
Ar-Curcumene 3083834 Click to see CC1=CC=C(C=C1)C(C)CCC=C(C)C 202.33 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
beta-Elemenone 10955018 Click to see CC(=C1CC(C(CC1=O)(C)C=C)C(=C)C)C 218.33 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
Bisabolol 1549992 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81225-X
https://doi.org/10.1007/978-0-85729-323-7_1048
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)81225-X
cis-beta-Copaene 87529 Click to see CC(C)C1CCC2(C3C1C2C(=C)CC3)C 204.35 unknown via CMAUP database
Copaene 19725 Click to see CC1=CCC2C3C1C2(CCC3C(C)C)C 204.35 unknown via CMAUP database
delta-Guaiene 94275 Click to see CC1CCC2=C(CCC(CC12)C(=C)C)C 204.35 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
gamma-Bisabolene, (Z)- 3033866 Click to see CC1=CCC(=C(C)CCC=C(C)C)CC1 204.35 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
gamma-Selinene 521334 Click to see CC(=C1CCC2(CCCC(=C)C2C1)C)C 204.35 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
Grifolin 5372312 Click to see CC1=CC(=C(C(=C1)O)CC=C(C)CCC=C(C)CCC=C(C)C)O 328.50 unknown https://doi.org/10.1021/NP0303916
Humulane 5318100 Click to see CC1CCCC(CCC(CCC1)(C)C)C 210.40 unknown via CMAUP database
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
Juniper camphor 521214 Click to see CC(=C1CCC2(CCCC(C2C1)(C)O)C)C 222.37 unknown https://doi.org/10.1007/978-0-85729-323-7_1048
Levomenol 442343 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown via CMAUP database
Rhododaurichromanic acid A 483509 Click to see CC1=CC2=C(C3C4C(C3(C)CCC=C(C)C)CCC4(O2)C)C(=C1C(=O)O)O 370.50 unknown https://doi.org/10.1016/S0040-4020(00)01144-3
https://doi.org/10.1016/J.JCHROMB.2004.06.048
Rhododaurichromanic acid B 483510 Click to see CC1=CC2=C(C3C4C(C3(C)CCC=C(C)C)CCC4(O2)C)C(=C1C(=O)O)O 370.50 unknown https://doi.org/10.1016/S0040-4020(00)01144-3
https://doi.org/10.1016/J.JCHROMB.2004.06.048
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(+)-Aromadendrene 11095734 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown via CMAUP database
(1aS,4aS,7aS,7bR)-1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene 91746456 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown via CMAUP database
Aromadendrene 91354 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown via CMAUP database
beta-Diploalbicene 177445 Click to see CC1CCC2C1C3C(C3(C)C)CCC2=C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(8aS)-4a,8,8a-trimethyl-2-prop-1-en-2-yl-1,2,3,4,5,6-hexahydronaphthalene 5321227 Click to see CC1=CCCC2(C1(CC(CC2)C(=C)C)C)C 218.38 unknown via CMAUP database
1alpha-Angeloyloxy-6beta-acetoxy-9-oxo-10alphaH-furanoeremophilane 101596866 Click to see CC=C(C)C(=O)OC1CCC(C2(C1C(=O)C3=C(C2OC(=O)C)C(=CO3)C)C)C 388.50 unknown via CMAUP database
Isobutyric acid [(4S)-4,4a,5,6,7,9-hexahydro-3,4abeta,5beta-trimethylnaphtho[2,3-b]furan]-4beta-yl ester 101938831 Click to see CC1CCC=C2C1(C(C3=C(C2)OC=C3C)OC(=O)C(C)C)C 302.40 unknown via CMAUP database
NCGC00180744-03_C19H24O6_Naphtho[2,3-b]furan-9(4H)-one, 4,8-bis(acetyloxy)-4a,5,6,7,8,8a-hexahydro-3,4a,5-trimethyl-, (4S,4aR,5S,8S,8aS)- 23843927 Click to see CC1CCC(C2C1(C(C3=C(C2=O)OC=C3C)OC(=O)C)C)OC(=O)C 348.40 unknown via CMAUP database
Neoadenostylone 6442373 Click to see CC=C(C)C(=O)OC1C2=C(C(=O)C3=CCCC(C13C)C)OC=C2C 328.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
Germacrone 6436348 Click to see CC1=CCC(=C(C)C)C(=O)CC(=CCC1)C 218.33 unknown https://doi.org/10.1016/S0031-9422(00)81225-X
https://doi.org/10.1007/978-0-85729-323-7_1048
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
(1R,4R,5S,10R,12R,13S,16R,17R)-13-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-1,5,16-trimethyl-4-prop-1-en-2-yl-9-oxatetracyclo[8.6.1.05,17.012,16]heptadecan-8-one 10718641 Click to see CC(=CCCC(C)(C1CCC2(C1CC3C4C2(CCC(C4(CCC(=O)O3)C)C(=C)C)C)C)O)C 456.70 unknown https://doi.org/10.1021/NP0303916
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Subspicatin K 101548940 Click to see CC=C(C)C(=O)OC1CCC(C2(C1CC3C(=C(C(=O)O3)C)C2)C)C 332.40 unknown via CMAUP database
Subspicatin L 101548941 Click to see CC=C(C)C(=O)OC1CCC(C2(C1CC3(C(=C(C(=O)O3)C)C2)O)C)C 348.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones
Fastigilin B 442241 Click to see CC1C2C=CC(=O)C2(C(C3C(C(=O)OC3C1O)C)OC(=O)C=C(C)C)C 362.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,6aR,6bR,8aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,6a,7,8,9,10,13,14,14a-tetradecahydropicen-3-ol 11611623 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C)C)C 426.70 unknown via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 45483610 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 via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1007/BF00564187
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 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/10.1007/BF00564187
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 21-hydroxysteroids
Flucort 3381 Click to see CC1(OC2CC3C4CC(C5=CC(=O)C=CC5(C4(C(CC3(C2(O1)C(=O)CO)C)O)F)C)F)C 452.50 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 via CMAUP database
cis-Chlorogenic acid 1794425 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 via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Arbutin 440936 Click to see C1=CC(=CC=C1O)OC2C(C(C(C(O2)CO)O)O)O 272.25 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
3-(Hydroxymethyl)furan-2-carbaldehyde 16730373 Click to see C1=COC(=C1CO)C=O 126.11 unknown https://doi.org/10.1016/J.JCHROMB.2004.06.048
5-Hydroxymethylfurfural 237332 Click to see C1=C(OC(=C1)C=O)CO 126.11 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
CID 15560170 15560170 Click to see CC1(CCCC2(C13CC3C(=O)C=C2)C)C 204.31 unknown via CMAUP database
Mayurone 538435 Click to see CC1(CCCC2(C13CC3C(=O)C=C2)C)C 204.31 unknown https://doi.org/10.1016/J.JCHROMB.2004.06.048
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(+)-Mayurone 13154078 Click to see CC1(CCCC2(C13CC3C(=O)CC2)C)C 206.32 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone 7469 Click to see CC(=O)C1=CC=C(C=C1)O 136.15 unknown via CMAUP database
> Organohalogen compounds / Organochlorides
3-Chloro-1-heptene 534251 Click to see CCCCC(C=C)Cl 132.63 unknown https://doi.org/10.1016/J.JCHROMB.2004.06.048
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(2R)-2-(7-hydroxy-4,8-dimethylnona-3,8-dienyl)-2,7-dimethylchromen-5-ol 91409377 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)CCC(C(=C)C)O)O 342.50 unknown https://doi.org/10.1021/NP0303916
(2R)-2-(8-hydroxy-4,8-dimethylnona-3,6-dienyl)-2,7-dimethylchromen-5-ol 91285391 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)CC=CC(C)(C)O)O 342.50 unknown https://doi.org/10.1021/NP0303916
(2R)-2-[(3E,7R)-7-hydroxy-4,8-dimethylnona-3,8-dienyl]-2,7-dimethylchromen-5-ol 163194657 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)CCC(C(=C)C)O)O 342.50 unknown https://doi.org/10.1021/NP0303916
2-(7-Hydroxy-4,8-dimethylnona-3,8-dienyl)-2,7-dimethylchromen-5-ol 85101739 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)CCC(C(=C)C)O)O 342.50 unknown https://doi.org/10.1021/NP0303916
2-(8-Hydroxy-4,8-dimethylnona-3,6-dienyl)-2,7-dimethylchromen-5-ol 73311029 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)CC=CC(C)(C)O)O 342.50 unknown https://doi.org/10.1021/NP0303916
Daurichromene A 10043035 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)CCC(C(=C)C)O)O 342.50 unknown https://doi.org/10.1021/NP0303916
Daurichromene C 10450086 Click to see CC1=CC(=C2C=CC(OC2=C1)(C)CCC=C(C)CC=CC(C)(C)O)O 342.50 unknown https://doi.org/10.1021/NP0303916
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
cis-Cinnamic acid 5372954 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid 639655 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown via CMAUP database
Caffeic acid phenethyl ester 5281787 Click to see C1=CC=C(C=C1)CCOC(=O)C=CC2=CC(=C(C=C2)O)O 284.31 unknown via CMAUP database
Rosmarinic acid 5281792 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
2-Hydroxycinnamic acid, (2E)- 637540 Click to see C1=CC=C(C(=C1)C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/J.JCHROMB.2004.06.048
3'-Hydroxycinnamic acid 637541 Click to see C1=CC(=CC(=C1)O)C=CC(=O)O 164.16 unknown via CMAUP database
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
cis-p-Coumaric acid 1549106 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown via CMAUP database
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Isoimperatorin 68081 Click to see CC(=CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)C 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-hydroxypsoralens
Demethylfuropinnarin 5316520 Click to see CC(C)(C=C)C1=C2C(=C(C3=C1OC=C3)O)C=CC(=O)O2 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1007/S10600-010-9649-7
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/S10600-010-9649-7
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Endotelon 130556 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1007/S10600-010-9649-7
Procyanidin B1 11250133 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=CC(=CC(=C34)O)O)C5=CC(=C(C=C5)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O 578.50 unknown https://doi.org/10.1007/S10600-010-9649-7
> 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/S10600-010-9649-7
Cianidanol 9064 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/S10600-010-9649-7
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/S10600-010-9649-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate 107905 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1007/S10600-010-9649-7
(-)-Epicatechingallate 367141 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 442.40 unknown https://doi.org/10.1007/S10600-010-9649-7
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Dihydromyricetin 12306070 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 via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
4H-1-Benzopyran-4-one, 2,3-dihydro-5,7-dihydroxy-2-phenyl-, (2R)- 667544 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxyphenyl)-6,8-dimethylchroman-4-one 91144 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)C)O 300.30 unknown https://doi.org/10.1021/NP100778K
https://doi.org/10.1007/S10600-010-9649-7
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
Farrerol 442396 Click to see CC1=C(C(=C2C(=C1O)C(=O)CC(O2)C3=CC=C(C=C3)O)C)O 300.30 unknown https://doi.org/10.1016/J.JCHROMB.2004.06.048
https://doi.org/10.1016/S0021-9673(01)01434-0
https://doi.org/10.1007/S10600-010-9649-7
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown via CMAUP database
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1016/J.JCHROMB.2004.06.048
Poriol 301798 Click to see CC1=C(C2=C(C=C1O)OC(CC2=O)C3=CC=C(C=C3)O)O 286.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Epitaxifolin 712318 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
(-)-Taxifolin 712316 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
(+/-)-Taxifolin 471 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
(2r)-2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-2,3-dihydro-4h-chromen-4-one 10185 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
Pinobanksin 73202 Click to see C1=CC=C(C=C1)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 272.25 unknown https://doi.org/10.1016/J.JCHROMB.2004.06.048
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 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
Chrysin 5281607 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 254.24 unknown https://doi.org/10.1016/J.JCHROMB.2004.06.048
Kaempferol oxoanion 25202062 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O 285.23 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
Quercetin-7-olate 46906036 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)[O-])O)O 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Azaleatin 5281604 Click to see COC1=CC(=CC2=C1C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)O 316.26 unknown https://doi.org/10.1016/J.JCHROMB.2004.06.048
Galangin 5281616 Click to see C1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Gossypetin 5280647 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)O)O)O 318.23 unknown via CMAUP database
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/S10600-010-9649-7
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1007/BF02329610
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/10.1016/S0021-9673(01)01434-0
https://doi.org/10.1007/BF02329610
https://doi.org/10.1007/S10600-010-9649-7
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 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)O 448.40 unknown https://doi.org/10.1007/S10600-010-9649-7
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/S10600-010-9649-7
3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 12308704 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown https://doi.org/10.1007/S10600-010-9649-7
3-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxy-chromen-4-one 49766656 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(O3)CO)O)O)C4=CC(=C(C=C4)O)O)O 448.40 unknown via CMAUP database
3-[(2S,3S,4R,5S)-5-(1,2-dihydroxyethyl)-3,4-dihydroxyoxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 10226724 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(CO)O)O)O)O)O 464.40 unknown via CMAUP database
3-[(2S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 44144273 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown via CMAUP database
4-[5,7-dihydroxy-4-oxo-3-[(3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-yl]-2-hydroxyphenolate 54758589 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-] 463.40 unknown via CMAUP database
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown https://doi.org/10.1007/BF02329610
https://doi.org/10.1007/S10600-010-9649-7
https://doi.org/10.1016/J.JCHROMB.2004.06.048
Hyperoside 5281643 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/S10600-010-9649-7
Isohyperoside 5748375 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)C(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 https://doi.org/10.1016/J.JCHROMB.2004.06.048
Quercitrin 5280459 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)O 448.40 unknown https://doi.org/10.1007/S10600-010-9649-7
https://doi.org/10.1007/BF02977686
Quercitrin-7-olate 49792009 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)O 447.40 unknown via CMAUP database
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2S)-7-[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-6,8-dimethyl-2,3-dihydrochromen-4-one 11093171 Click to see CC1=C(C2=C(C(=C1OC3C(C(C(C(O3)COC4C(C(CO4)(CO)O)O)O)O)O)C)OC(CC2=O)C5=CC=C(C=C5)O)O 594.60 unknown via CMAUP database
(2S)-7-[[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyl-2-oxanyl]oxy]-2-oxanyl]oxy]-5-hydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one 6710627 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database
(2S)-7-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 5351463 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database
4H-1-Benzopyran-4-one, 7-((2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl)oxy)-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-, (S)- 5284651 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database
4H-1-Benzopyran-4-one, 7-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-, (2S)- 4441 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database
4H-1-Benzopyran-4-one, 7-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-, (S)- 91740219 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database
7-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 45358136 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database
7-[(2S,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 74787988 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database
7-[[2-O-(6-deoxy-alpha-l-mannopyranosyl)-beta-d-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(4-hydroxyphenyl)-4h-1-benzopyran-4-one 25075 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database
Naringin 442428 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database
Naringin [10236-47-2] 45933923 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC=C(C=C5)O)O)CO)O)O)O)O)O 580.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 11968523 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)O)O)O 804.70 unknown via CMAUP database
Gossypin 5281621 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 480.40 unknown https://doi.org/10.1016/J.JCHROMB.2004.06.048
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Hesperetin 72281 Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanols
(2S,3R)-3-(3,4-dihydroxyphenyl)-2,6,8-trihydroxy-2,3-dihydrochromen-4-one 57336522 Click to see C1=CC(=C(C=C1C2C(OC3=C(C2=O)C=C(C=C3O)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Dihydroresveratrol 185914 Click to see C1=CC(=CC=C1CCC2=CC(=CC(=C2)O)O)O 230.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown https://doi.org/10.1007/S10600-010-9649-7

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