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Kunzea ambigua

Kunzea ambigua - 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 UUID643fe029dbcb7779398935
Scientific name Kunzea ambigua
Authority Druce
First published in Rep. Bot. Soc. Exch. Club Brit. Isles 1916: 629 (1917)

Description Top

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Synonyms Top

Scientific name Authority First published in
Kunzea corifolia (Vent.) Schauer Pl. Preiss. 1: 124 (1844)
Kunzea pelagia Miq. Ned. Kruidk. Arch. 4: 145 (1856)
Leptospermum ambiguum Sm. Trans. Linn. Soc. London 3: 264 (1797)
Metrosideros abietina Hoffmanns. Verz. Pfl.-Kult. : 80 (1824)
Metrosideros corifolia Vent. Jard. Malmaison : 46 (1804)
Stenospermum corifolium (Vent.) Sweet ex Heynh. Nom. Bot. Hort. : 787 (1841)
Callistemon corifolius (Vent.) Mouill.

Common names Top

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Language Common/alternative name
English tickbush
Arabic كونزية ملتبسة
Croatian tik-tak grm
Chinese 含糊雪茶木

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
  • Australasia
    • Australia
      • New South Wales
      • South Australia
      • Tasmania
      • Victoria

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000221558
USDA Plants KUAM2
Tropicos 100211808
KEW urn:lsid:ipni.org:names:597187-1
The Plant List kew-106525
Open Tree Of Life 102661
NCBI Taxonomy 106041
IPNI 597187-1
iNaturalist 321043
GBIF 5420044
Freebase /m/03w9hp6
EOL 5457095
USDA GRIN 403670
Wikipedia Kunzea_ambigua

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
Chitosan-Based Nanoencapsulated Essential Oils: Potential Leads against Breast Cancer Cells in Preclinical Studies Tan WN, Samling BA, Tong WY, Chear NJ, Yusof SR, Lim JW, Tchamgoue J, Leong CR, Ramanathan S Polymers (Basel) 08-Feb-2024
PMCID:PMC10891598
doi:10.3390/polym16040478
PMID:38399856
Exploring the Antimicrobial Properties of 99 Natural Flavour and Fragrance Raw Materials against Pathogenic Bacteria: A Comparative Study with Antibiotics Bacińska Z, Baberowska K, Surowiak AK, Balcerzak L, Strub DJ Plants (Basel) 06-Nov-2023
PMCID:PMC10648197
doi:10.3390/plants12213777
PMID:37960133
Structure modelling of odorant receptor from Aedes aegypti and identification of potential repellent molecules Tiwari V, Sowdhamini R Comput Struct Biotechnol J 06-Mar-2023
PMCID:PMC10066510
doi:10.1016/j.csbj.2023.03.005
PMID:37013002
The Effect of the Height of Coppicing and Harvest Season on the Yield and Quality of the Essential Oil of Kunzea ambigua Park C, Garland SM, Close DC Plants (Basel) 20-Dec-2022
PMCID:PMC9824379
doi:10.3390/plants12010020
PMID:36616149
Essential Oils as Novel Anthelmintic Drug Candidates Panda SK, Daemen M, Sahoo G, Luyten W Molecules 29-Nov-2022
PMCID:PMC9735941
doi:10.3390/molecules27238327
PMID:36500419
Recent Advances on Natural Aryl-C-glycoside Scaffolds: Structure, Bioactivities, and Synthesis—A Comprehensive Review Liu CF Molecules 01-Nov-2022
PMCID:PMC9654268
doi:10.3390/molecules27217439
PMID:36364266
Fusarium and allied fusarioid taxa (FUSA). 1 Crous PW, Sandoval-Denis M, Costa MM, Groenewald JZ, van Iperen AL, Starink-Willemse M, Hernández-Restrepo M, Kandemir H, Ulaszewski B, de Boer W, Abdel-Azeem AM, Abdollahzadeh J, Akulov A, Bakhshi M, Bezerra JD, Bhunjun CS, Câmara MP, Chaverri P, Vieira WA, Decock CA, Gaya E, Gené J, Guarro J, Gramaje D, Grube M, Gupta VK, Guarnaccia V, Hill R, Hirooka Y, Hyde KD, Jayawardena RS, Jeewon R, Jurjević Ž, Korsten L, Lamprecht SC, Lombard L, Maharachchikumbura SS, Polizzi G, Rajeshkumar KC, Salgado-Salazar C, Shang QJ, Shivas RG, Summerbell RC, Sun GY, Swart WJ, Tan YP, Vizzini A, Xia JW, Zare R, González CD, Iturriaga T, Savary O, Coton M, Coton E, Jany JL, Liu C, Zeng ZQ, Zhuang WY, Yu ZH, Thines M Fungal Syst Evol 23-Jun-2022
PMCID:PMC9355104
doi:10.3114/fuse.2022.09.08
PMID:35978986
Exploring the Roles of Dietary Herbal Essential Oils in Aquaculture: A Review Dawood MA, El Basuini MF, Yilmaz S, Abdel-Latif HM, Alagawany M, Kari ZA, Abdul Razab MK, Hamid NK, Moonmanee T, Van Doan H Animals (Basel) 24-Mar-2022
PMCID:PMC8996993
doi:10.3390/ani12070823
PMID:35405814
Naturally Occurring Chromone Glycosides: Sources, Bioactivities, and Spectroscopic Features Amen Y, Elsbaey M, Othman A, Sallam M, Shimizu K Molecules 16-Dec-2021
PMCID:PMC8704703
doi:10.3390/molecules26247646
PMID:34946728
Geranium and Lemon Essential Oils and Their Active Compounds Downregulate Angiotensin-Converting Enzyme 2 (ACE2), a SARS-CoV-2 Spike Receptor-Binding Domain, in Epithelial Cells Senthil Kumar KJ, Gokila Vani M, Wang CS, Chen CC, Chen YC, Lu LP, Huang CH, Lai CS, Wang SY Plants (Basel) 19-Jun-2020
PMCID:PMC7355681
doi:10.3390/plants9060770
PMID:32575476
Topical and device‐based treatments for fungal infections of the toenails Foley K, Gupta AK, Versteeg S, Mays R, Villanueva E, John D Cochrane Database Syst Rev 16-Jan-2020
PMCID:PMC6984586
doi:10.1002/14651858.CD012093.pub2
PMID:31978269
Bigger Data Approach to Analysis of Essential Oils and Their Antifungal Activity against Aspergillus niger, Candida albicans, and Cryptococcus neoformans Powers CN, Satyal P, Mayo JA, McFeeters H, McFeeters RL Molecules 07-Aug-2019
PMCID:PMC6718987
doi:10.3390/molecules24162868
PMID:31394798
Myrtaceae Plant Essential Oils and their β-Triketone Components as Insecticides against Drosophila suzukii Park CG, Jang M, Shin E, Kim J Molecules 24-Jun-2017
PMCID:PMC6152387
doi:10.3390/molecules22071050
PMID:28672824
Chemical Characterization and in Vitro Antibacterial Activity of Myrcianthes hallii (O. Berg) McVaugh (Myrtaceae), a Traditional Plant Growing in Ecuador Chavez Carvajal P, Coppo E, Di Lorenzo A, Gozzini D, Bracco F, Zanoni G, Nabavi SM, Marchese A, Arciola CR, Daglia M Materials (Basel) 07-Jun-2016
PMCID:PMC5456788
doi:10.3390/ma9060454
PMID:28773577
Foliar Essential Oil Glands of Eucalyptus Subgenus Eucalyptus (Myrtaceae) Are a Rich Source of Flavonoids and Related Non-Volatile Constituents Goodger JQ, Seneratne SL, Nicolle D, Woodrow IE PLoS One 15-Mar-2016
PMCID:PMC4792381
doi:10.1371/journal.pone.0151432
PMID:26977933

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 / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4aR,7S,7aR,7bR)-1,1-dimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[h]azulen-7-ol 162945400 Click to see CC1(C2C1C3C(CCC3O)C(=C)CC2)C 206.32 unknown https://doi.org/10.1016/J.TET.2004.08.027
(1aR,4aR,7S,7aS,7bR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 13854258 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/J.TET.2004.08.027
(1aR,4R,4aR,7R,7aR,7bS)-1,1,4,7-tetramethyl-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulen-4-ol 124305339 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/J.TET.2004.08.027
(7aR)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 5321422 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/J.TET.2004.08.027
1,1-dimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[h]azulen-7-ol 162945399 Click to see CC1(C2C1C3C(CCC3O)C(=C)CC2)C 206.32 unknown https://doi.org/10.1016/J.TET.2004.08.027
Globulol 12304985 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/J.TET.2004.08.027
Globulol 101716 Click to see CC1CCC2C1C3C(C3(C)C)CCC2(C)O 222.37 unknown https://doi.org/10.1016/J.TET.2004.08.027
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1R,2S,4S,7R,9R,12S,13R)-3,3,7,12,16,16,18,18-octamethyl-13-(2-methylpropyl)-8,20-dioxapentacyclo[10.8.0.02,4.07,9.014,19]icos-14(19)-ene-15,17-dione 162903283 Click to see CC(C)CC1C2=C(C(C(=O)C(C2=O)(C)C)(C)C)OC3C1(CCC4C(O4)(CCC5C3C5(C)C)C)C 470.70 unknown https://doi.org/10.1016/J.TET.2004.08.027
(1S,2S,4S,7R,9R,12S,13R)-3,3,7,12,16,16,18,18-octamethyl-13-(2-methylpropyl)-8,20-dioxapentacyclo[10.8.0.02,4.07,9.014,19]icos-14(19)-ene-15,17-dione 101356486 Click to see CC(C)CC1C2=C(C(C(=O)C(C2=O)(C)C)(C)C)OC3C1(CCC4C(O4)(CCC5C3C5(C)C)C)C 470.70 unknown https://doi.org/10.1016/J.TET.2004.08.027
3,3,7,12,16,16,18,18-Octamethyl-13-(2-methylpropyl)-8,20-dioxapentacyclo[10.8.0.02,4.07,9.014,19]icos-14(19)-ene-15,17-dione 72773280 Click to see CC(C)CC1C2=C(C(C(=O)C(C2=O)(C)C)(C)C)OC3C1(CCC4C(O4)(CCC5C3C5(C)C)C)C 470.70 unknown https://doi.org/10.1016/J.TET.2004.08.027
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
trans-5-O-(4-coumaroyl)-D-quinic acid 6441280 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC=C(C=C2)O)O)O 338.31 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
methyl (1S,3S,6S,7S,7aR)-6-hydroxy-3-methoxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,3,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 101085901 Click to see CC1C(CC2=C(C(OC(C12)OC3C(C(C(C(O3)CO)O)O)O)OC)C(=O)OC)O 420.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R)-1-[2-hydroxy-3,5-dimethyl-4,6-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]phenyl]-2-methylbutan-1-one 163068230 Click to see CCC(C)C(=O)C1=C(C(=C(C(=C1O)C)OC2C(C(C(C(O2)CO)O)O)O)C)OC3C(C(C(C(O3)CO)O)O)O 562.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
(2S)-1-[2,4-dihydroxy-3-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2-methylbutan-1-one 163104161 Click to see CCC(C)C(=O)C1=C(C=C(C(=C1O)C2C(C(C(C(O2)CO)O)O)O)O)OC3C(C(C(C(O3)CO)O)O)O 534.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
[(2R,3S,4R,5R,6S)-6-[2,6-dihydroxy-3-[(2R)-2-methylbutanoyl]-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-2-yl]oxyphenyl]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 163105136 Click to see CCC(C)C(=O)C1=C(C=C(C(=C1O)C2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O 838.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[3-hydroxy-2,6-dimethyl-4-[(2R)-2-methylbutanoyl]-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]oxan-2-yl]methyl 3,4,5-trihydroxybenzoate 163104433 Click to see CCC(C)C(=O)C1=C(C(=C(C(=C1O)C)OC2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)O)C)OC4C(C(C(C(O4)CO)O)O)O 714.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
[(2R,3S,4S,5R,6S)-6-[4-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxy-6-[(3,4,5-trihydroxybenzoyl)oxymethyl]oxan-2-yl]-3,5-dihydroxy-2-[(2S)-2-methylbutanoyl]phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 163106915 Click to see CCC(C)C(=O)C1=C(C=C(C(=C1O)C2C(C(C(C(O2)COC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)OC5C(C(C(C(O5)COC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)O 990.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
[(2S,3R,4S,5S,6R)-2-(5,7-dihydroxy-2-methyl-4-oxochromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 21576255 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O 506.40 unknown https://doi.org/10.1021/NP030367S
[(2S,3R,4S,5S,6R)-2-(5,7-dihydroxy-2-methyl-4-oxochromen-8-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 21576257 Click to see CC1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 506.40 unknown https://doi.org/10.1021/NP030367S
[(2S,3S,4S,5R,6R)-2-(5,7-dihydroxy-2-methyl-4-oxochromen-6-yl)-5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate 21576256 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 658.50 unknown https://doi.org/10.1021/NP030367S
[(2S,3S,4S,5R,6R)-2-(5,7-dihydroxy-2-methyl-4-oxochromen-8-yl)-5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate 21576258 Click to see CC1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3C(C(C(C(O3)CO)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 658.50 unknown https://doi.org/10.1021/NP030367S
[(2S,3S,4S,5R,6R)-2-(5,7-dihydroxy-4-oxo-2-propan-2-ylchromen-6-yl)-5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate 21576253 Click to see CC(C)C1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 686.60 unknown https://doi.org/10.1021/NP030367S
[(2S,3S,4S,5R,6R)-2-(5,7-dihydroxy-4-oxo-2-propan-2-ylchromen-8-yl)-5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate 21576254 Click to see CC(C)C1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3C(C(C(C(O3)CO)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 686.60 unknown https://doi.org/10.1021/NP030367S
[2-(5,7-Dihydroxy-2-methyl-4-oxochromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 73802528 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O 506.40 unknown https://doi.org/10.1021/NP030367S
[2-(5,7-Dihydroxy-2-methyl-4-oxochromen-6-yl)-5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate 73802529 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 658.50 unknown https://doi.org/10.1021/NP030367S
[2-(5,7-Dihydroxy-2-methyl-4-oxochromen-8-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 73802530 Click to see CC1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 506.40 unknown https://doi.org/10.1021/NP030367S
[2-(5,7-Dihydroxy-2-methyl-4-oxochromen-8-yl)-5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate 73802531 Click to see CC1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3C(C(C(C(O3)CO)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 658.50 unknown https://doi.org/10.1021/NP030367S
[2-(5,7-Dihydroxy-4-oxo-2-propan-2-ylchromen-6-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 73981588 Click to see CC(C)C1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O 534.50 unknown https://doi.org/10.1021/NP030367S
[2-(5,7-Dihydroxy-4-oxo-2-propan-2-ylchromen-6-yl)-5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate 73802526 Click to see CC(C)C1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O 686.60 unknown https://doi.org/10.1021/NP030367S
[2-(5,7-Dihydroxy-4-oxo-2-propan-2-ylchromen-8-yl)-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl] 3,4,5-trihydroxybenzoate 73981589 Click to see CC(C)C1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 534.50 unknown https://doi.org/10.1021/NP030367S
[2-(5,7-Dihydroxy-4-oxo-2-propan-2-ylchromen-8-yl)-5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxybenzoyl)oxyoxan-4-yl] 3,4,5-trihydroxybenzoate 73802527 Click to see CC(C)C1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3C(C(C(C(O3)CO)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 686.60 unknown https://doi.org/10.1021/NP030367S
1-[2-hydroxy-3,5-dimethyl-4,6-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]phenyl]-2-methylpropan-1-one 102033043 Click to see CC1=C(C(=C(C(=C1OC2C(C(C(C(O2)CO)O)O)O)C)OC3C(C(C(C(O3)CO)O)O)O)C(=O)C(C)C)O 548.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
1,5-Anhydro-1-(5,7-dihydroxy-2-methyl-4-oxo-4H-1-benzopyran-6-yl)hexitol 5087647 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O 354.31 unknown https://doi.org/10.1021/NP030367S
4'-O-beta-D-glucosyl-cis-p-coumaric acid 10604651 Click to see C1=CC(=CC=C1C=CC(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
5,7-Dihydroxy-2-propan-2-yl-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 78384983 Click to see CC(C)C1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O 382.40 unknown https://doi.org/10.1021/NP030367S
5,7-Dihydroxy-2-propan-2-yl-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 73981595 Click to see CC(C)C1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3C(C(C(C(O3)CO)O)O)O 382.40 unknown https://doi.org/10.1021/NP030367S
6-(2-O-Galloyl-beta-D-glucopyranosyl)-5,7-dihydroxy-2-isopropylchromone 5317461 Click to see CC(C)C1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O 534.50 unknown https://doi.org/10.1021/NP030367S
6-beta-D-Glucopyranosyl-5,7-dihydroxy-2-isopropylchromone 5317687 Click to see CC(C)C1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O 382.40 unknown https://doi.org/10.1021/NP030367S
8-(2-O-Galloyl-beta-D-glucopyranosyl)-5,7-dihydroxy-2-isopropylchromone 5317462 Click to see CC(C)C1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 534.50 unknown https://doi.org/10.1021/NP030367S
8-Glucosyl-5,7-dihydroxy-2-isopropylchromone 5317688 Click to see CC(C)C1=CC(=O)C2=C(O1)C(=C(C=C2O)O)C3C(C(C(C(O3)CO)O)O)O 382.40 unknown https://doi.org/10.1021/NP030367S
Biflorin 441959 Click to see CC1=CC(=O)C2=C(O1)C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O 354.31 unknown https://doi.org/10.1021/NP030367S
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Rhexifoline 185301 Click to see CC1CC(C2=C(C=NC=C12)C(=O)OC)O 207.23 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2S,6R)-5-hydroxy-8,8,10,10,12-pentamethyl-6-(2-methylpropyl)-2-phenyl-3,6-dihydro-2H-chromeno[3,2-g]chromene-4,7,9-trione 11477598 Click to see CC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=CC=C4)O)C(C5=C(O2)C(C(=O)C(C5=O)(C)C)(C)C)CC(C)C 502.60 unknown https://doi.org/10.1016/J.TET.2004.08.027
(2S,6S)-5-hydroxy-8,8,10,10,12-pentamethyl-6-(2-methylpropyl)-2-phenyl-3,6-dihydro-2H-chromeno[3,2-g]chromene-4,7,9-trione 11785364 Click to see CC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=CC=C4)O)C(C5=C(O2)C(C(=O)C(C5=O)(C)C)(C)C)CC(C)C 502.60 unknown https://doi.org/10.1016/J.TET.2004.08.027
5-hydroxy-8,8,10,10,12-pentamethyl-6-(2-methylpropyl)-2-phenyl-3,6-dihydro-2H-chromeno[3,2-g]chromene-4,7,9-trione 72976789 Click to see CC1=C2C(=C(C3=C1OC(CC3=O)C4=CC=CC=C4)O)C(C5=C(O2)C(C(=O)C(C5=O)(C)C)(C)C)CC(C)C 502.60 unknown https://doi.org/10.1016/J.TET.2004.08.027
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-Dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone 6453244 Click to see CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3 270.28 unknown https://doi.org/10.1016/J.TET.2004.08.027
Cryptostrobin 15953986 Click to see CC1=C2C(=C(C=C1O)O)C(=O)CC(O2)C3=CC=CC=C3 270.28 unknown https://doi.org/10.1016/J.TET.2004.08.027
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Pinoquercetin 5281679 Click to see CC1=C(C2=C(C=C1O)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1021/NP030367S
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-8-[[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-6-yl]methyl]-5,7-dihydroxy-6-methyl-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one 85427171 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=C(C(=C3)O)CC4=C5C(=C(C(=C4O)C)O)C(=O)C(=C(O5)C6=CC(=C(C=C6)O)O)OC7C(C(C(C(O7)C)O)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O 922.80 unknown https://doi.org/10.1021/NP030367S
2-(3,4-dihydroxyphenyl)-8-[[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxo-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-6-yl]methyl]-5,7-dihydroxy-6-methyl-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 163047784 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=C(C(=C3)O)CC4=C5C(=C(C(=C4O)C)O)C(=O)C(=C(O5)C6=CC(=C(C=C6)O)O)OC7C(C(C(C(O7)C)O)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O 922.80 unknown https://doi.org/10.1021/NP030367S
Kunzeagin A 11182168 Click to see CC1C(C(C(C(O1)OC2=C(OC3=C(C2=O)C(=C(C(=C3)O)CC4=C5C(=C(C(=C4O)C)O)C(=O)C(=C(O5)C6=CC(=C(C=C6)O)O)OC7C(C(C(C(O7)C)O)O)O)O)C8=CC(=C(C=C8)O)O)O)O)O 922.80 unknown https://doi.org/10.1021/NP030367S
Myricetin 3-beta-D-glucopyranoside 12311099 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1021/NP030367S
Myricetin 3-galactoside 5491408 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1021/NP030367S
Quercetin 3-O-rhamnoside 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/10.1021/NP030367S
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/10.1021/NP030367S
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11S)-10-[(14R,15R,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 159610769 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
3,3'-Di-O-methylellagic acid 5488919 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)OC)O)O 330.24 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
beta-Pedunculagin 5320441 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
Casuarinin 442673 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O 936.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003
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/10.1016/J.PHYTOCHEM.2008.03.003
Pedunculagin 442688 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.03.003

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