Salvadora persica - Unknown
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Internal ID UUID6440038da0d48785928933
Scientific name Salvadora persica
Authority L.
First published in Sp. Pl. : 122 (1753)

Description Top

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Salvadora persica, commonly known as the toothbrush tree, is a small evergreen tree native to the Middle East, Africa and India. Its sticks are traditionally used as a natural toothbrush called miswak and are mentioned by the World Health Organization for oral hygiene use. Other names include arak, jhak, pīlu, and mustard tree. The genus was named by the French botanist Laurent Garcin in 1749 after a Spanish apothecary, Juan Salvador y Bosca. The type specimen was collected in Persia, hence the species name persica. It has a pleasant fragrance, of cress or mustard, as well as a warm and pungent taste. The tree produces small red edible fruits, juicy but pungent, in clusters. Miswak is popular for teeth cleaning throughout the Arabian Peninsula, Iranian Plateau, as well as the wider Muslim world. The fresh leaves can be eaten as part of a salad and are used in traditional medicine. The flowers are small and fragrant and are used as a stimulant and are mildly purgative. The wood of the Salvadora persica can be used for charcoal and firewood. In Namibia, the mustard bush is used as drought-

Synonyms Top

Scientific name Authority First published in
Lauridia multiflora Engl. Bot. Jahrb. Syst. 10: 38 (1888)
Rivina paniculata L. Cent. Pl. II : 9 (1756)
Salvadora wightii Arn. Proc. Roy. Philos. Soc. Glasgow 3: 160 (1851 publ. 1855)
Salvadora crassinervia Hochst. ex T.Anderson J. Proc. Linn. Soc., Bot. 5(Suppl. 1): 30 (1860)
Salvadora paniculata Zucc. Mant. 3: 56 (1827)
Cissus arborea Forssk. Fl. Aegypt.-Arab. : 32 (1775)
Embelia grossularia Retz. Observ. Bot. 4: 24 (1786)
Galenia asiatica Burm.f. Fl. Ind. (N. L. Burman) 88. 1768 [1 Mar-6 Apr 1768]

Common names Top

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Language Common/alternative name
English toothbrush tree
English mustard tree
English tooth brush tree
English peelo fruit
English kikul oil plant
Arabic أراك
Bulgarian персийска салвадора
Bengali পার্সি মেসওয়াক
Czech salvadora perská
German zahnbürstenbaum
Persian اراک (درخت)
Persian درخت مسواک
Persian چوج
Fulah siwaakeehi
Finnish persianhammastikkupuu
Hausa ashuwaki
Hebrew סלוודורה פרסית
Armenian Եղրևանի պարսկական
Kazakh Парсылық Сальвадора
Malayalam ഉകമരം
Dutch tandenborstelboom
Punjabi ਪੀਲੂ
Punjab پیلو
Russian Сальвадора персидская
sd کٻڙ
Serbian Салвадора перзика
Swahili mswaki
Tamil உகாய்
Telugu గున్నంగి
Turkish misvak ağacı
Ukrainian Сальвадора перська
Chinese 亞力
Chinese 阿拉克樹

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Salvadora persica var. cyclophylla (Chiov.) Cufod. ex Verdc. Kew Bull. 19: 152. 1964 (1964)
Salvadora persica var. persica
Salvadora persica var. pubescens Brenan Kew Bull. 4: 90. 1949 (1949)
Salvadora persica var. tuticornica T.A.Rao & Chakraborti Fasc. Fl. India 22: 9 (1996)
Salvadora persica var. wightiana (Planch. ex Thwaites) Verdc. Kew Bull. 19: 150. 1964 (1964)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Djibouti
      • Eritrea
      • Ethiopia
      • Socotra
      • Somalia
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Caprivi Strip
      • Namibia
      • Northern Provinces
    • West Tropical Africa
      • Burkina
      • Mali
      • Mauritania
      • Niger
      • Nigeria
      • Senegal
    • West-central Tropical Africa
      • Cameroon
  • Asia-temperate
    • Arabian Peninsula
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Lebanon-Syria
      • Palestine
      • Sinai

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000492914
UNII QY11DDA752
Tropicos 28400008
KEW urn:lsid:ipni.org:names:779348-1
The Plant List kew-2581806
PaleoBotany 91848
Open Tree Of Life 1012296
NCBI Taxonomy 4326
IUCN Red List 138472280
IPNI 779348-1
iNaturalist 197082
GBIF 5580727
Freebase /m/06zxxl
EPPO SVDPE
EOL 2900520
USDA GRIN 32819
Wikipedia Salvadora_persica
CMAUP NPO6621

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
Integration of local knowledge in the secondary school chemistry curriculum - A few examples of ethno-chemistry from Zambia Chibuye B, Singh IS Heliyon 08-Apr-2024
PMCID:PMC11021971
doi:10.1016/j.heliyon.2024.e29174
PMID:38633622
An Alarming Decline in the Nutritional Quality of Foods: The Biggest Challenge for Future Generations’ Health Bhardwaj RL, Parashar A, Parewa HP, Vyas L Foods 14-Mar-2024
PMCID:PMC10969708
doi:10.3390/foods13060877
PMID:38540869
Folk Knowledge and Perceptions about the Use of Wild Fruits and Vegetables–Cross-Cultural Knowledge in the Pipli Pahar Reserved Forest of Okara, Pakistan Jabeen S, Arshad F, Harun N, Waheed M, Alamri S, Haq SM, Vitasović-Kosić I, Fatima K, Chaudhry AS, Bussmann RW Plants (Basel) 14-Mar-2024
PMCID:PMC10974405
doi:10.3390/plants13060832
PMID:38592859
Efficacy of Various Herbal Preparations Against Oral Candida: A Lab-Based Study Karni PA, Muraleedharan A, Bhandary S, Mujoo S, Maini AP, Chaturvedi M J Pharm Bioallied Sci 29-Feb-2024
PMCID:PMC11000960
doi:10.4103/jpbs.jpbs_486_23
PMID:38595550
Transcriptomics, proteomics, and metabolomics interventions prompt crop improvement against metal(loid) toxicity Raza A, Salehi H, Bashir S, Tabassum J, Jamla M, Charagh S, Barmukh R, Mir RA, Bhat BA, Javed MA, Guan DX, Mir RR, Siddique KH, Varshney RK Plant Cell Rep 27-Feb-2024
PMCID:PMC10899315
doi:10.1007/s00299-024-03153-7
PMID:38411713
The sustainable use of diverse plants accustomed by different ethnic groups in Sibi District, Balochistan, Pakistan Maria B, Saeed S, Ahmed A, Ahmed M, Rehman A PLoS One 21-Feb-2024
PMCID:PMC10880983
doi:10.1371/journal.pone.0294989
PMID:38381718
Using participatory epidemiology to investigate the causes of cattle abortion in Southwest Ethiopia Robi DT, Bogale A, Temteme S, Aleme M, Urge B Heliyon 14-Feb-2024
PMCID:PMC10881556
doi:10.1016/j.heliyon.2024.e25726
PMID:38390138
Even low levels of tree cover improve dietary quality in West Africa den Braber B, Hall C, Brandt M, Reiner F, Mugabowindekwe M, Rasmussen LV PNAS Nexus 09-Feb-2024
PMCID:PMC10890828
doi:10.1093/pnasnexus/pgae067
PMID:38404357
The Potential of Cochlospermum tinctorium, Flueggea virosa, and Waltheria indica Traditional Plants From Burkina Faso in Treating Periodontitis: A Systematic Review Diarra A, Agossa K, Youl EN Cureus 17-Jan-2024
PMCID:PMC10873538
doi:10.7759/cureus.52471
PMID:38371022
Efficacy of a Eucalyptus oil-based dentifrice in reducing plaque and gingival bleeding scores – A randomized clinical crossover study Osman FA, Sarhan LA, Eladl NE, Desai V, Narayanan J, Thangavelu L, Varma SR J Adv Pharm Technol Res 15-Jan-2024
PMCID:PMC10880914
doi:10.4103/JAPTR.JAPTR_103_23
PMID:38389967
Formulation of Quercetin Mouthwash and Anti-microbial Potential Against Critical Pathogens: An In-Vitro Evaluation L A, Krishna Kumar J, Shanmugam R Cureus 05-Jan-2024
PMCID:PMC10838391
doi:10.7759/cureus.51688
PMID:38314006
Microbiological Evaluation of Herbal Extracts against Candida albicans in Early Childhood Caries Patients: An In Vitro Study Siddaiah SB, Sinha S, Archana B Int J Clin Pediatr Dent 01-Jan-2024
PMCID:PMC10978517
doi:10.5005/jp-journals-10005-2733
PMID:38559866
Silvicultural Practices for Diversity Conservation and Invasive Species Suppression in Forest Ecosystems of the Bundala National Park, Sri Lanka Suraweera C, Gallo J, Vacek Z, Cukor J, Vacek S, Baláš M Plants (Basel) 31-Dec-2023
PMCID:PMC10780521
doi:10.3390/plants13010121
PMID:38202429
Mucoadhesive Pharmacology: Latest Clinical Technology in Antiseptic Gels Baus-Domínguez M, Aguilera FR, Vivancos-Cuadras F, Ferra-Domingo L, Torres-Lagares D, Gutiérrez-Pérez JL, Pereira-Riveros T, Vinuesa T, Serrera-Figallo MÁ Gels 26-Dec-2023
PMCID:PMC10815608
doi:10.3390/gels10010023
PMID:38247746
Diversity, Distribution, and applications of arbuscular mycorrhizal fungi in the Arabian Peninsula Alrajhi K, Bibi S, Abu-Dieyeh M Saudi J Biol Sci 25-Dec-2023
PMCID:PMC10805673
doi:10.1016/j.sjbs.2023.103911
PMID:38268781

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Ethylparaben 8434 Click to see CCOC(=O)C1=CC=C(C=C1)O 166.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Benzaldehyde 240 Click to see C1=CC=C(C=C1)C=O 106.12 unknown via CMAUP database
p-Anisaldehyde 31244 Click to see COC1=CC=C(C=C1)C=O 136.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl cyanides
Phenylacetonitrile 8794 Click to see C1=CC=C(C=C1)CC#N 117.15 unknown https://doi.org/10.1080/1057563021000040790
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown https://doi.org/10.1080/1057563021000040790
Isovanillin 12127 Click to see COC1=C(C=C(C=C1)C=O)O 152.15 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(1S,3aS,4S,6aS)-1-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3,3,6,6-tetramethyl-1,3a,4,6a-tetrahydrofuro[3,4-c]furan-4-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163028601 Click to see CC1(C2C(C(O1)C3=CC(=C(C(=C3)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)C(OC2C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC)(C)C)C 798.80 unknown https://doi.org/10.1016/0031-9422(92)83301-E
(2S,3R,4S,5S,6R)-2-[4-[[(3R,4R,5S)-5-[3,5-dimethoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-4-(hydroxymethyl)oxolan-3-yl]methyl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101630443 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CC3COC(C3CO)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 744.70 unknown https://doi.org/10.1016/0031-9422(92)83301-E
2-[4-[(3aR,6aS)-6-[3,5-dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 138107782 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.1016/0031-9422(92)83301-E
2-[4-[1-[3,5-Dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3,3,6,6-tetramethyl-1,3a,4,6a-tetrahydrofuro[3,4-c]furan-4-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163028600 Click to see CC1(C2C(C(O1)C3=CC(=C(C(=C3)OC)OC4C(C(C(C(O4)CO)O)O)O)OC)C(OC2C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC)(C)C)C 798.80 unknown https://doi.org/10.1016/0031-9422(92)83301-E
Liriodendrin 226371 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C3C4COC(C4CO3)C5=CC(=C(C(=C5)OC)OC6C(C(C(C(O6)CO)O)O)O)OC 742.70 unknown https://doi.org/10.1016/0031-9422(92)83301-E
Salvadoraside 162343330 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)CC3COC(C3CO)C4=CC(=C(C(=C4)OC)OC5C(C(C(C(O5)CO)O)O)O)OC 744.70 unknown https://doi.org/10.1016/0031-9422(92)83301-E
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(4Z,7Z,10Z,13Z)-hexadeca-4,7,10,13-tetraenoic acid 5312433 Click to see CCC=CCC=CCC=CCC=CCCC(=O)O 248.36 unknown via CMAUP database
(R)-2-hydroxypalmitic acid 11065598 Click to see CCCCCCCCCCCCCCC(C(=O)O)O 272.42 unknown via CMAUP database
2-Keto palmitic acid 5282996 Click to see CCCCCCCCCCCCCCC(=O)C(=O)O 270.41 unknown via CMAUP database
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://doi.org/10.1039/JR9390001015
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Capric Acid 2969 Click to see CCCCCCCCCC(=O)O 172.26 unknown https://doi.org/10.1039/JR9390001015
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
Valeric acid 7991 Click to see CCCCC(=O)O 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty aldehydes
(8Z,11Z,14Z)-Heptadecatrienal 6430107 Click to see CCC=CCC=CCC=CCCCCCCC=O 248.40 unknown via CMAUP database
(8z,11z)-8,11-Heptadecadienal 14543488 Click to see CCCCCC=CCC=CCCCCCCC=O 250.40 unknown via CMAUP database
(8Z,11Z)-Heptadecadienal 6430322 Click to see CCCCCC=CCC=CCCCCCCC=O 250.40 unknown via CMAUP database
(Z)-8-heptadecenal 6430106 Click to see CCCCCCCCC=CCCCCCCC=O 252.40 unknown via CMAUP database
7,10,13-Hexadecatrienenal 14543490 Click to see CCC=CCC=CCC=CCCCCCC=O 234.38 unknown via CMAUP database
8-Heptadecenal 14543489 Click to see CCCCCCCCC=CCCCCCCC=O 252.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
9,12-Octadecadienoic acid 3931 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Glycosylglycerols / Sulfoquinovosylmonoacylglycerols / Sulfoquinovosyl 1-monoacylglycerols
[(2S,3S,4S,5R,6S)-6-[(2R)-3-hexadecanoyloxy-2-hydroxypropoxy]-3,4,5-trihydroxyoxan-2-yl]methanesulfonic acid 102201401 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COC1C(C(C(C(O1)CS(=O)(=O)O)O)O)O)O 556.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(R)-(+)-Citronellal 75427 Click to see CC(CCC=C(C)C)CC=O 154.25 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 via CMAUP database
Thymol 6989 Click to see CC1=CC(=C(C=C1)C(C)C)O 150.22 unknown https://doi.org/10.1080/1057563021000040790
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Isoterpinolene 102443 Click to see CC1CCC(=C(C)C)C=C1 136.23 unknown https://doi.org/10.1080/1057563021000040790
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(-)-alpha-Tocopherol 1742129 Click to see CC1=C(C2=C(CCC(O2)(C)CCCC(C)CCCC(C)CCCC(C)C)C(=C1O)C)C 430.70 unknown via CMAUP database
(2R)-2,8-Dimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydrochromen-6-ol 12444418 Click to see CC1=CC(=CC2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)O 402.70 unknown via CMAUP database
(2S)-2,5,8-Trimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydro-2H-1-benzopyran-6-ol 76959905 Click to see CC1=CC(=C(C2=C1OC(CC2)(C)CCCC(C)CCCC(C)CCCC(C)C)C)O 416.70 unknown via CMAUP database
(S)-2,7,8-Trimethyl-2-[(4S,8S)-4,8,12-trimethyltridecyl]-3,4-dihydro-2H-1-benzopyran-6-ol 73416557 Click to see CC1=C(C=C2CCC(OC2=C1C)(C)CCCC(C)CCCC(C)CCCC(C)C)O 416.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1080/1057563021000040790
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(24E)-24-N-Propylidenecholesterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/0031-9422(92)83301-E
Fucosterol 5281326 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/0031-9422(92)83301-E
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6802 Click to see C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N 283.24 unknown via CMAUP database
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine 6029 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Acrylic acids and derivatives / Acrylic acids
Acrylic acid 6581 Click to see C=CC(=O)O 72.06 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
(3S,6S)-3-Isopropyl-6-methylpiperazine-2,5-dione 13783106 Click to see CC1C(=O)NC(C(=O)N1)C(C)C 170.21 unknown via CMAUP database
(3S,8aS)-3-Isobutylhexahydropyrrolo[1,2-a]pyrazine-1,4-dione 7074739 Click to see CC(C)CC1C(=O)N2CCCC2C(=O)N1 210.27 unknown via CMAUP database
cyclo(L-Pro-L-Val) 6992261 Click to see CC(C)C1C(=O)N2CCCC2C(=O)N1 196.25 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Dipeptides
Arginyl-Glutamine 7019985 Click to see C(CC(C(=O)NC(CCC(=O)N)C(=O)O)N)CN=C(N)N 302.33 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-phenylmethoxyoxan-3-yl] hydrogen sulfate 178723 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)OS(=O)(=O)O 350.34 unknown https://doi.org/10.1016/0031-9422(92)83301-E
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1016/0031-9422(92)83301-E
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1016/0031-9422(92)83301-E
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
Furfural 7362 Click to see C1=COC(=C1)C=O 96.08 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see C1=CNC(=O)NC1=O 112.09 unknown via CMAUP database
> Organoheterocyclic compounds / Isoindoles and derivatives / Isoindolines / Isoindolones
Chaetoglobosin Fex 71768077 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(C(=O)C(=C1)C)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 530.70 unknown via CMAUP database
Cytoglobosin A 46209792 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CC4C1C(=C(C4=O)O)C)C(=O)NC3CC5=CNC6=CC=CC=C65)C)O 528.60 unknown via CMAUP database
Cytoglobosin B 46209793 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)C=CC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 530.70 unknown via CMAUP database
Cytoglobosin C 44610809 Click to see CC1CC=CC2C(C(=C(C3C2(C(=O)C=CC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)C)O 530.70 unknown via CMAUP database
Cytoglobosin D 46209919 Click to see CC1CC=CC2C=C(C(C3C2(C(=O)C=CC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)C 514.70 unknown via CMAUP database
Cytoglobosin E 46209920 Click to see CC1CC=CC2C=C(C(C3C2(C(=O)CCC(=O)C(=O)C(=C1)C)C(=O)NC3CC4=CNC5=CC=CC=C54)C)CO 528.60 unknown via CMAUP database
Cytoglobosin F 46209921 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(=O)C(C(=C1)C)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 530.70 unknown via CMAUP database
Cytoglobosin G 46209922 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(C(C(=C1)C)O)O)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 532.70 unknown via CMAUP database
isochaetoglobosin D 23259926 Click to see CC1CC=CC2C(C(=C)C(C3C2(C(=O)CCC(=O)C(=O)C(=C1)C)C(=O)NC3CC4=CNC5=CC=CC=C54)C)O 528.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde 637511 Click to see C1=CC=C(C=C1)C=CC=O 132.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,5R,6R)-4,5-dihydroxy-3-[(2S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,4S,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 44391816 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)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 740.70 unknown https://doi.org/10.21608/BFSA.1997.68759
5,7-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-((((2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-4H-chromen-4-one 5320020 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)OC)O)O)O)O)O)O)O 624.50 unknown https://doi.org/10.21608/BFSA.1997.68759
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.21608/BFSA.1997.68759
Biorobin 15944778 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 594.50 unknown https://doi.org/10.21608/BFSA.1997.68759
Kaempferol-3-O-rutinoside 5318767 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 594.50 unknown https://doi.org/10.21608/BFSA.1997.68759
Narcissin 5481663 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)OC)O)O)O)O)O)O 624.50 unknown https://doi.org/10.21608/BFSA.1997.68759

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