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Aspalathus linearis

Aspalathus linearis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Aspalathus linearis - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Aspalathus linearis - 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 UUID643fde9292a1f215066275
Scientific name Aspalathus linearis
Authority (Burm.f.) R.Dahlgren
First published in Opera Bot.9: 283 (1963)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Lebeckia candolleana Walp. Linnaea13: 477 (1840)
Aspalathus linearis subsp. linearis (Burm.f.) R.Dahlgren
Aspalathus corymbosa E.Mey. Linnaea7: 159 (1832)
Aspalathus linearis subsp. pinifolia (Marloth) R.Dahlgren Opera Bot.9: 283 (1963)
Borbonia pinifolia Marloth Trans. Roy. Soc. South Africa2: 238 (1912)
Lebeckia linearis (Burm.f.) DC. Prodr.2: 137 (1825)
Aspalathus cognata C.Presl Abh. Königl. Böhm. Ges. Wiss., ser. 5, 3: 556 (1845)
Genista contaminata Poir. J.B.A.M.de Lamarck, Encycl., Suppl. 2: 721 (1812)
Psoralea linearis Burm.f. Fl. Indica, Prodr. Fl. Cap.: 22 (1768)
Aspalathus tenuifolia DC. Prodr.2: 143 (1825)
Achyronia tenuifolia (DC.) Kuntze Revis. Gen. Pl.1: 157 (1891)

Common names Top

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Language Common/alternative name
English rooibos
Spanish rooibos
Afrikaans rooibos
Arabic شاي الشجيرة الحمراء
Arabic رويبوس
Bulgarian ройбос
br te ruz
Catalan rooibos
Czech roibos
Czech rooibos
Danish rooibos
German rooibush
German rooibos
German rotbuschtee
German rooibusch
German rooibostee
German rooibosch
German rooi
German roibosh
German roibos
Esperanto rojbos-arbusto
Estonian rooibos
Estonian tee-punapõõsas
Basque rooibos
Persian راوند
Finnish punapensas
Finnish rooibos
French rooibos
Galician rooibos
Hebrew רויבוש
Hungarian rooibos
Hungarian vörös fokföldirekettye
Indonesian rooibos
Italian rooibos
Japanese ルイボスティー
Japanese ルイボス
Kazakh Ройбұш
Kazakh Ройбос
Korean 루이보스 차
Korean 루이보스
lb rooibos
Lithuanian rooibos
Latvian rooibos tēja
Malay rooibos
Malay roobois
Norwegian Bokmål rooibos
Dutch rooibos
Dutch rooibosthee
Norwegian Nynorsk rooibos
Polish rooibos
Polish czerwonokrzew
Portuguese rooibosch
Portuguese chá de arbusto vermelho
Portuguese arbusto vermelho
Portuguese chá de arbusto
Portuguese chá de rooibos
Portuguese chá vermelho
Portuguese chá vermelho da África do sul
Portuguese roibos
Portuguese rooibos
Romanian rooibos
Russian Ройбос
Russian Ройбуш
Russian Ройбош
Russian Аспалатус линейный
Slovenian roiboos
Slovenian rooibos
Serbian Ројбос
Serbian Рооибос
Serbian Роибос
Swedish roibus
Swedish rooibos
Swedish rött te
Swedish roibos
Thai โรยบอส
Turkish rooibos
Ukrainian Ройбуш
Vietnamese chè rooibos
Chinese 南非茶
Chinese 博士茶
Chinese 路易波士茶
Chinese 南非國寶茶
Chinese 松雀花

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000211610
UNII O17JQA1A9Z
USDA Plants ASLI14
Tropicos 50326573
KEW urn:lsid:ipni.org:names:475647-1
The Plant List ild-6704
Open Tree Of Life 406601
NCBI Taxonomy 155124
IPNI 475647-1
iNaturalist 447656
GBIF 5348220
Freebase /m/013v0m
EPPO ASQLI
EOL 702617
US Library of Congress sh85115345
USDA GRIN 310979
Wikipedia Rooibos
CMAUP NPO27761
PFAF Aspalathus linearis

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
Unleashing the promise of emerging nanomaterials as a sustainable platform to mitigate antimicrobial resistance Rahman S, Sadaf S, Hoque ME, Mishra A, Mubarak NM, Malafaia G, Singh J RSC Adv 01-May-2024
PMCID:PMC11062400
doi:10.1039/d3ra05816f
PMID:38694553
Afriplex GRTTM extract attenuates hepatic steatosis in an in vitro model of NAFLD Gabuza K, Mabuda TI, Patel O, Khuboni N, van Aarde R, Riedel S, Sangweni NF, Windvogel S, Johnson R, Muller CJ PLoS One 17-Apr-2024
PMCID:PMC11023570
doi:10.1371/journal.pone.0297572
PMID:38630788
Metabolomic profiling of wild rooibos (Aspalathus linearis) ecotypes and their antioxidant-derived phytopharmaceutical potential Wilkinson C, Brooks J, Stander MA, Malgas R, Roodt-Wilding R, Makunga NP Metabolomics 14-Apr-2024
PMCID:PMC11016507
doi:10.1007/s11306-024-02103-4
PMID:38615312
Live yellow mealworm (Tenebrio molitor) larvae: a promising nutritional enrichment for laying quails Dalle Zotte A, Singh Y, Palumbo B, Contiero B, Cullere M Poult Sci 09-Apr-2024
PMCID:PMC11060950
doi:10.1016/j.psj.2024.103759
PMID:38678977
Evaluation of Lippia scaberrima Sond. and Aspalathus linearis (Burm.f.) R. Dahlgren extracts on human CYP enzymes and gold nanoparticle synthesis: implications for drug metabolism and cytotoxicity Kok AM, Juvonen R, Pasanen M, Mandiwana V, Kalombo ML, Ray SS, Rikhotso-Mbungela R, Lall N BMC Complement Med Ther 05-Apr-2024
PMCID:PMC10996199
doi:10.1186/s12906-024-04439-9
PMID:38580936
Medicinal plants and natural products for treating overactive bladder Chen H, Hoi MP, Lee SM Chin Med 27-Mar-2024
PMCID:PMC10967063
doi:10.1186/s13020-024-00884-3
PMID:38532487
Fungal Endophytes: Discovering What Lies within Some of Canada’s Oldest and Most Resilient Grapevines Ali S, Wright AH, Tanney JB, Renaud JB, Sumarah MW J Fungi (Basel) 26-Jan-2024
PMCID:PMC10890244
doi:10.3390/jof10020105
PMID:38392777
Stevens’ Cure (Umckaloabo)—the vindication of a patent medicine Brendler T, Stander MA, van Wyk BE Front Pharmacol 03-Jan-2024
PMCID:PMC10791834
doi:10.3389/fphar.2023.1294997
PMID:38235116
Pyrrolizidine alkaloid contamination of food in Africa: A review of current trends and implications Letsyo E, Madilo FK, Effah-Manu L Heliyon 03-Jan-2024
PMCID:PMC10789634
doi:10.1016/j.heliyon.2024.e24055
PMID:38230234
Preliminary exploration of herbal tea products based on traditional knowledge and hypotheses concerning herbal tea selection: a case study in Southwest Guizhou, China Long X, Ranjitkar S, Waldstein A, Wu H, Li Q, Geng Y J Ethnobiol Ethnomed 02-Jan-2024
PMCID:PMC10763305
doi:10.1186/s13002-023-00645-w
PMID:38169414
Translation of preclinical ethnomedicine data in LMICs: the example of rooibos Pretorius L, Smith C Front Pharmacol 19-Dec-2023
PMCID:PMC10763253
doi:10.3389/fphar.2023.1328828
PMID:38174224
Consumption of herbal infusions/decoctions and tea in Greece: a Planeterranean perspective on the results of Hydria survey Tomou EM, Peppa E, Trichopoulou A J Transl Med 11-Dec-2023
PMCID:PMC10714537
doi:10.1186/s12967-023-04781-5
PMID:38082315
The health benefits of rooibos tea in humans (aspalathus linearis)-a scoping review AFRIFA D, ENGELBRECHT L, EIJNDE BO, TERBLANCHE E J Public Health Afr 01-Dec-2023
PMCID:PMC10774856
doi:10.4081/jphia.2023.2784
PMID:38204815
Content and Yield of L-DOPA and Bioactive Compounds of Broad Bean Plants: Antioxidant and Anti-Inflammatory Activity In Vitro Fuentes-Herrera PB, Herrera-Cabrera BE, Martínez-Ayala AL, Zamilpa A, Delgado-Alvarado A Plants (Basel) 21-Nov-2023
PMCID:PMC10708485
doi:10.3390/plants12233918
PMID:38068555
Iron Oxide Nanoparticles: Green Synthesis and Their Antimicrobial Activity Zúñiga-Miranda J, Guerra J, Mueller A, Mayorga-Ramos A, Carrera-Pacheco SE, Barba-Ostria C, Heredia-Moya J, Guamán LP Nanomaterials (Basel) 08-Nov-2023
PMCID:PMC10674528
doi:10.3390/nano13222919
PMID:37999273

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
Methyl phenylacetate 7559 Click to see COC(=O)CC1=CC=CC=C1 150.17 unknown https://doi.org/10.1021/JF00062A024
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1021/JF00062A024
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Methyl benzoate 7150 Click to see COC(=O)C1=CC=CC=C1 136.15 unknown https://doi.org/10.1021/JF00062A024
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters / o-Hydroxybenzoic acid esters
Methyl Salicylate 4133 Click to see COC(=O)C1=CC=CC=C1O 152.15 unknown https://doi.org/10.1021/JF00062A024
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see C1=CC(=C(C=C1O)C(=O)O)O 154.12 unknown via CMAUP database
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/S0031-9422(00)86894-6
3,5-Dihydroxybenzoic acid 7424 Click to see C1=C(C=C(C=C1O)O)C(=O)O 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1016/S0031-9422(00)86894-6
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> 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/BF02858780
> 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/S0031-9422(00)86894-6
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see C1=CC=C(C(=C1)C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methylbenzaldehyde 7725 Click to see CC1=CC=C(C=C1)C=O 120.15 unknown https://doi.org/10.1021/JF00062A024
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown https://doi.org/10.1021/JF00062A024
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
Benzyl Alcohol 244 Click to see C1=CC=C(C=C1)CO 108.14 unknown https://doi.org/10.1021/JF00062A024
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde 998 Click to see C1=CC=C(C=C1)CC=O 120.15 unknown https://doi.org/10.1021/JF00062A024
> Benzenoids / Naphthalenes
1-Methylnaphthalene 7002 Click to see CC1=CC=CC2=CC=CC=C12 142.20 unknown https://doi.org/10.1021/JF00062A024
2-Methylnaphthalene 7055 Click to see CC1=CC2=CC=CC=C2C=C1 142.20 unknown https://doi.org/10.1021/JF00062A024
Naphthalene 931 Click to see C1=CC=C2C=CC=CC2=C1 128.17 unknown https://doi.org/10.1021/JF00062A024
> Benzenoids / Phenols / 1-hydroxy-2-unsubstituted benzenoids
4-Ethylphenol 31242 Click to see CCC1=CC=C(C=C1)O 122.16 unknown https://doi.org/10.1021/JF00062A024
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Phenol 996 Click to see C1=CC=C(C=C1)O 94.11 unknown https://doi.org/10.1021/JF00062A024
> Benzenoids / Phenols / Cresols / Para cresols
P-Cresol 2879 Click to see CC1=CC=C(C=C1)O 108.14 unknown https://doi.org/10.1021/JF00062A024
> Benzenoids / Phenols / Methoxyphenols
1,2-Ethanediol, 1-(4-hydroxy-3-methoxyphenyl)-, (R)- 688030 Click to see COC1=C(C=CC(=C1)C(CO)O)O 184.19 unknown via CMAUP database
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1021/JF00062A024
Guaiacol 460 Click to see COC1=CC=CC=C1O 124.14 unknown https://doi.org/10.1021/JF00062A024
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see C1=CC(=CC=C1CCO)O 138.16 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
gamma-Terpinene 7461 Click to see CC1=CCC(=CC1)C(C)C 136.23 unknown https://doi.org/10.1021/JF00062A024
> Lignans, neolignans and related compounds / Dibenzylbutane lignans / Dibenzylbutanediol lignans
(+)-Secoisolariciresinol 6336781 Click to see COC1=C(C=CC(=C1)CC(CO)C(CC2=CC(=C(C=C2)O)OC)CO)O 362.40 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 https://doi.org/10.1021/JF00062A024
Methyl Octanoate 8091 Click to see CCCCCCCC(=O)OC 158.24 unknown https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
alpha-(beta-D-Glucopyranosyloxy)-trans-cinnamic acid 53385591 Click to see C1=CC=C(C=C1)C=C(C(=O)O)OC2C(C(C(C(O2)CO)O)O)O 326.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Neryl acetate 1549025 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Heptanol 8129 Click to see CCCCCCCO 116.20 unknown https://doi.org/10.1021/JF00062A024
1-Hexanol 8103 Click to see CCCCCCO 102.17 unknown https://doi.org/10.1021/JF00062A024
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown https://doi.org/10.1021/JF00062A024
1-Octen-3-Ol 18827 Click to see CCCCCC(C=C)O 128.21 unknown https://doi.org/10.1021/JF00062A024
2-Heptanol 10976 Click to see CCCCCC(C)O 116.20 unknown https://doi.org/10.1021/JF00062A024
2-Octanol 20083 Click to see CCCCCCC(C)O 130.23 unknown https://doi.org/10.1021/JF00062A024
Hept-2-en-1-ol 36504 Click to see CCCCC=CCO 114.19 unknown https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (+/-)- 6549 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown https://doi.org/10.1021/JF00062A024
Myrcene 31253 Click to see CC(=CCCC(=C)C=C)C 136.23 unknown https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-ol 64685 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/JF00062A024
CID 44630107 44630107 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1021/JF00062A024
Alpha-Terpineol 17100 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown https://doi.org/10.1021/JF00062A024
beta-Terpineol 8748 Click to see CC(=C)C1CCC(CC1)(C)O 154.25 unknown https://doi.org/10.1021/JF00062A024
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown https://doi.org/10.1021/JF00062A024
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
Emericolin A 6480207 Click to see CC1CC(C2C1CC3(CCC4(CCC(C4C3CC=C2C=O)C(=C)C)C)C)O 370.60 unknown https://doi.org/10.1016/J.MRGENTOX.2007.03.009
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Hexyl Acetate 8908 Click to see CCCCCCOC(=O)C 144.21 unknown https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organic oxides
beta-Cyclocitral 9895 Click to see CC1=C(C(CCC1)(C)C)C=O 152.23 unknown https://doi.org/10.1021/JF00062A024
Safranal 61041 Click to see CC1=C(C(CC=C1)(C)C)C=O 150.22 unknown https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 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 / Alcohols and polyols / Secondary alcohols
1-Hepten-3-OL 21057 Click to see CCCCC(C=C)O 114.19 unknown https://doi.org/10.1021/JF00062A024
3-Heptanol 11520 Click to see CCCCC(CC)O 116.20 unknown https://doi.org/10.1021/JF00062A024
4-Heptanol 11513 Click to see CCCC(CCC)O 116.20 unknown https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
Linalool, oxide 102611 Click to see CC(=CCCC(C)(C1CO1)O)C 170.25 unknown https://doi.org/10.1021/JF00062A024
> 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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Hepten-1-al 17167 Click to see CCCCC=CC=O 112.17 unknown https://doi.org/10.1021/JF00062A024
2-Octenal 5283324 Click to see CCCCCC=CC=O 126.20 unknown https://doi.org/10.1021/JF00062A024
4-Heptenal, (4Z)- 71590 Click to see CCC=CCCC=O 112.17 unknown https://doi.org/10.1021/JF00062A024
Dodecanal 8194 Click to see CCCCCCCCCCCC=O 184.32 unknown https://doi.org/10.1021/JF00062A024
Heptanal 8130 Click to see CCCCCCC=O 114.19 unknown https://doi.org/10.1021/JF00062A024
Non-2-enal 17166 Click to see CCCCCCC=CC=O 140.22 unknown https://doi.org/10.1021/JF00062A024
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown https://doi.org/10.1021/JF00062A024
Oct-2-enal 16900 Click to see CCCCCC=CC=O 126.20 unknown https://doi.org/10.1021/JF00062A024
Undecanal 8186 Click to see CCCCCCCCCCC=O 170.29 unknown https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha,beta-unsaturated ketones / Enones
2-Methyl-2-hepten-4-one 31138 Click to see CCCC(=O)C=C(C)C 126.20 unknown https://doi.org/10.1021/JF00062A024
Damascenone 5366074 Click to see CC=CC(=O)C1=C(C=CCC1(C)C)C 190.28 unknown https://doi.org/10.1021/JF00062A024
Oct-3-en-2-one 15475 Click to see CCCCC=CC(=O)C 126.20 unknown https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
Salicylaldehyde 6998 Click to see C1=CC=C(C(=C1)C=O)O 122.12 unknown https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Heptanone 8051 Click to see CCCCCC(=O)C 114.19 unknown https://doi.org/10.1021/JF00062A024
2-Nonanone 13187 Click to see CCCCCCCC(=O)C 142.24 unknown https://doi.org/10.1021/JF00062A024
2-Octanone 8093 Click to see CCCCCCC(=O)C 128.21 unknown https://doi.org/10.1021/JF00062A024
3-Heptanone 7802 Click to see CCCCC(=O)CC 114.19 unknown https://doi.org/10.1021/JF00062A024
4-Heptanone 31246 Click to see CCCC(=O)CCC 114.19 unknown https://doi.org/10.1021/JF00062A024
6-Methyl-5-hepten-2-one 9862 Click to see CC(=CCCC(=O)C)C 126.20 unknown https://doi.org/10.1021/JF00062A024
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Methylacetophenone 8500 Click to see CC1=CC=C(C=C1)C(=O)C 134.17 unknown https://doi.org/10.1021/JF00062A024
Acetophenone 7410 Click to see CC(=O)C1=CC=CC=C1 120.15 unknown https://doi.org/10.1021/JF00062A024
> Organoheterocyclic compounds / Benzothiazoles
Benzothiazole 7222 Click to see C1=CC=C2C(=C1)N=CS2 135.19 unknown https://doi.org/10.1021/JF00062A024
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
Ascorbic Acid 54670067 Click to see C(C(C1C(=C(C(=O)O1)O)O)O)O 176.12 unknown https://doi.org/10.1007/BF02858780
> Organoheterocyclic compounds / Heteroaromatic compounds
2-Pentylfuran 19602 Click to see CCCCCC1=CC=CO1 138.21 unknown https://doi.org/10.1021/JF00062A024
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Xanthines
Caffeine 2519 Click to see CN1C=NC2=C1C(=O)N(C(=O)N2C)C 194.19 unknown https://doi.org/10.1007/BF02858780
> Organoheterocyclic compounds / Lactones / Delta valerolactones
delta-Valerolactone 10953 Click to see C1CCOC(=O)C1 100.12 unknown https://doi.org/10.1021/JF00062A024
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(S)-4-Nonanolide 441574 Click to see CCCCCC1CCC(=O)O1 156.22 unknown https://doi.org/10.1021/JF00062A024
Gamma-nonalactone 7710 Click to see CCCCCC1CCC(=O)O1 156.22 unknown https://doi.org/10.1021/JF00062A024
gamma-Octalactone 7704 Click to see CCCCC1CCC(=O)O1 142.20 unknown https://doi.org/10.1021/JF00062A024
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dihydrodehydroconiferyl alcohol, (7R,8S)-(-)- 5274623 Click to see COC1=CC(=CC2=C1OC(C2CO)C3=CC(=C(C=C3)O)OC)CCCO 360.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)86894-6
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/S0031-9422(00)86894-6
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/S0031-9422(00)86894-6
Sinapinic acid 637775 Click to see COC1=CC(=CC(=C1O)OC)C=CC(=O)O 224.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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 https://doi.org/10.1021/JF0347721
https://doi.org/10.1016/0027-5107(95)00116-6
https://doi.org/10.1016/S0031-9422(00)86894-6
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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/S0031-9422(00)86894-6
https://doi.org/10.1021/JF0347721
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
(2R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 45271033 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
(2R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 162904319 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1016/S0031-9422(00)00182-5
(2S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-6-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 162904320 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1016/S0031-9422(00)00182-5
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-2,3-dihydrochromen-4-one 44715644 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1016/S0031-9422(00)00182-5
Eriodictyol-6-glucoside 102370911 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown https://doi.org/10.1016/S0031-9422(00)00182-5
Hemiphloin 160711 Click to see C1C(OC2=C(C1=O)C(=C(C(=C2)O)C3C(C(C(C(O3)CO)O)O)O)O)C4=CC=C(C=C4)O 434.40 unknown via CMAUP database
Isoorientin 114776 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF0347721
Isovitexin 162350 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown https://doi.org/10.1021/JF0347721
https://doi.org/10.1016/S0031-9422(00)86894-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Eriodictyol-8-glucoside 122221847 Click to see C1C(OC2=C(C(=CC(=C2C1=O)O)O)C3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)O 450.40 unknown via CMAUP database
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown https://doi.org/10.1021/JF0347721
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown https://doi.org/10.1021/JF0347721
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 102467789 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C(=C(C=C2O)O)OC3C(C(C(C(O3)CO)O)O)O)O)O 452.40 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,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1021/JF0347721
https://doi.org/10.1016/S0031-9422(00)86894-6
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/10.1021/JF0347721
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 via CMAUP database
Quercetin 3-O-robinobioside 10371536 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
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown https://doi.org/10.1021/JF0347721
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1021/JF0347721
https://doi.org/10.1016/S0031-9422(00)86894-6
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
3-(3,4-Dihydroxyphenyl)-1-(3-beta-D-glucopyranosyl-2,4,6-trihydroxyphenyl)-1-propanone 16752601 Click to see C1=CC(=C(C=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O)O 452.40 unknown https://doi.org/10.1016/J.PHYMED.2008.11.009
https://doi.org/10.1016/S0031-9422(00)86894-6
https://doi.org/10.1021/JF0347721
https://doi.org/10.1016/J.MRGENTOX.2007.03.009
https://doi.org/10.1016/0308-8146(95)00166-2
3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl]propan-1-one 133562015 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/0308-8146(95)00166-2
3-(4-hydroxyphenyl)-1-[2,4,6-trihydroxy-3-[(2S,3S,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]phenyl]propan-1-one 154497759 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/S0031-9422(00)00182-5
3'-C-glucosylphloretin 73830082 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown https://doi.org/10.1016/J.MRGENTOX.2007.03.009
Aspalathin 11282394 Click to see C1=CC(=C(C=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O)O 452.40 unknown https://doi.org/10.1016/J.MRGENTOX.2007.03.009
Nothofagin 21722188 Click to see C1=CC(=CC=C1CCC(=O)C2=C(C=C(C(=C2O)C3C(C(C(C(O3)CO)O)O)O)O)O)O 436.40 unknown via CMAUP database

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