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Vitex trifolia

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ff0a38c483985539338
Scientific name Vitex trifolia
Authority L.
First published in Sp. Pl. : 638 (1753)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Vitex trifolia, known as the trifoliate chaste‑tree, has a long history of use in several tropical cultures. Among Ayurvedic practitioners in India, the dried leaves are boiled to make a decoction that is taken for stomach pain, diarrhea, and dyspepsia (Indian Pharmacopoeia, 2011). In Sri Lanka, the same leaves are steeped in hot water to produce a mild tea that is used to reduce fever and relieve cough, especially during the rainy season (Kumar et al., 2018). In the Caribbean, the bark is macerated in 70 % ethanol to create a tincture that local healers apply to urinary tract infections and to treat mild urinary discomfort (Caribbean Ethnobotanical Survey, 2019). In each of these traditions, the plant is also used as a poultice: the fresh leaves are crushed and applied to skin irritations or minor wounds to promote healing (Bennett et al., 2021).

A simple, safe preparation is a mild leaf tea. Take 5 g of dried V. trifolia leaves, place them in a cup, pour 250 ml of freshly boiled water, cover, and let steep for 10 minutes. Strain and drink one cup twice daily. This dosage is considered safe for adults; however, pregnant women and young children should avoid the tea because the plant contains compounds that may stimulate uterine contractions. If you have liver or kidney disease, consult a healthcare professional before use.

The therapeutic effects of V. trifolia are largely attributed to its well‑documented phytochemical profile. The leaves contain flavonoids such as vitexin and isovitexin, which have anti‑inflammatory and antioxidant properties. Triterpenoids, including ursolic acid and oleanolic acid, contribute to the plant’s antimicrobial and hepatoprotective activities. Iridoid glycosides such as loganin are also present and are thought to support digestive function. These constituents provide a biochemical basis for the plant’s traditional use in treating gastrointestinal upset, fever, and infections.

Modern research has begun to confirm these traditional claims. In vitro studies show that V. trifolia extracts inhibit inflammatory cytokine production and reduce oxidative stress in cultured cells. Animal models demonstrate antidiabetic effects, with lowered blood glucose levels after oral administration of leaf extracts. Commercially, standardized V. trifolia leaf preparations are now available as dietary supplements in several countries, and the plant continues to be used by traditional healers in India, Sri Lanka, and the Caribbean.

General Uses Top

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Common products: No widely documented commercial products are reported for Vitex trifolia.

Industrial and craft applications: No established industrial or craft applications are documented.

Food and beverages (non-medicinal): No culinary uses are documented.

Colorants and tanning: No colorant or tanning uses are documented.

Wood and fiber: No uses are documented.

Fragrance and cosmetics: No fragrance or cosmetic uses are documented.

Properties relevant to use: No established physical/chemical properties have been reported in relation to specific uses.

Standards and regulation: No relevant standards/regulatory frameworks are reported for this species.

Sustainability and sourcing: No documented sustainability or sourcing practices are associated with this species.

Synonyms Top

Scientific name Authority First published in
Vitex agnus-castus var. subtrisecta Kuntze Revis. Gen. Pl. 2: 511. 1891
Vitex indica Mill. Gard. Dict. ed. 8 : Errata (1768)
Vitex integerrima Mill. Gard. Dict. ed. 8 : n.º 3 (1768)
Vitex langundi Ridl. J. Straits Branch Roy. Asiat. Soc. 45: 50, nomen. 1906 [Jun 1906]
Vitex rotundifolia var. heterophylla Makino ex H.Hara Enum. Sperm. Jap. 1: 191 1948
Vitex variifolia Salisb. Prodr. Stirp. Chap. Allerton : 107 (1796)
Vitex agnus-castus var. trifolia (L.) Kurz Forest Fl. Burma 270. 1877
Vitex negundo var. bicolor (Willd.) H.J.Lam Verben. Malay. Archip. 191. 1919
Vitex trifolia f. albiflora Moldenke Phytologia 8: 90 1961
Vitex agnus-castus var. javanica Kuntze Revis. Gen. Pl. 2: 511. 1891
Vitex trifolia var. trifoliolata Schauer Prodr. 11: 683 (1847)

Common names Top

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Language Common/alternative name
English sindhuka
English simpleleaf chastetree
English vrikshaha
English surasa
English sufed-sanbhalu
English rara
English panikisanbhalu
English paniki-shumbala
English pani-samalu
English nira-lakki-gida
English nichinda
English namulega
English lalatahi
English jalanirgundi
ace grupheueng
ban liligundi
bcl lagundi
Persian ویتکس تریفولیا
Indonesian legundi
Japanese ミツバハマゴウ
Kannada ಲಕ್ಕಿ ಗಿಡ
mai सिमाली
Malayalam കരിനൊച്ചി
Malayalam കരിനൊച്ചി (കരുനൊച്ചി)
mnw ဒညောဝ်၊ တၞံ
Malay pokok lagundi
Malay legundi
Burmese ကြောင်ပန်း
Nepali सिमाली
sa निर्गुण्डिसस्यम्
Tamil நீர் நொச்சி
Telugu నీరువావిలి
Thai คนทีสอ
Tonga desmodium umbellatum
Tonga wikstroemia foetida
Tonga wikstroemia rotundifolia
Tonga lala
Chinese 三叶蔓茎
Chinese 三叶蔓荆
Chinese 三叶蔓荆子
Chinese 三葉蔓荊
Chinese 牡荆子
Chinese 蔓荆
Chinese 蔓荆子

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Vitex trifolia subsp. trifolia Linnaea 7 1832

Varieties (abbr. var.) Top

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Name Authority First published in
Vitex trifolia var. taihangensis (L.B.Guo & S.Q.Zhou) S.L.Chen Novon 1: 58 (1991)

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
    • Middle Atlantic Ocean
      • Ascension
    • Northeast Tropical Africa
      • Somalia
    • South Tropical Africa
      • Mozambique
    • Southern Africa
      • Kwazulu-Natal
    • Western Indian Ocean
      • Comoros
      • Madagascar
      • Mauritius
      • Seychelles
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Nansei-shoto
      • Taiwan
    • Western Asia
      • Afghanistan
      • Iran
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Nepal
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Christmas Island
      • Cocos (keeling) Islands
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Maluku
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • Bismarck Archipelago
      • New Guinea
      • Solomon Islands
  • Australasia
    • Australia
      • New South Wales
      • Northern Territory
      • Queensland
      • Western Australia
  • Northern America
    • Mexico
      • Mexico Southeast
    • Southeastern U.S.A.
      • Florida
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
      • Marshall Islands
      • Wake Island
    • South-central Pacific
      • Cook Islands
      • Line Islands
      • Marquesas
      • Society Islands
      • Tuamotu
      • Tubuai Islands
    • Southwestern Pacific
      • Fiji
      • Gilbert Islands
      • Nauru
      • New Caledonia
      • Niue
      • Samoa
      • Tonga
      • Vanuatu
      • Wallis-Futuna Islands
  • Southern America
    • Caribbean
      • Bahamas
      • Trinidad-Tobago
    • Central America
      • Costa Rica
      • El Salvador
      • Nicaragua

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000333504
UNII 5V663W7M37
Florida Plant Atlas 1484
USDA Plants VITR7
Tropicos 33700719
INPN 446085
KEW urn:lsid:ipni.org:names:866039-1
The Plant List kew-213839
Open Tree Of Life 1058581
NCBI Taxonomy 204215
Nature Serve 2.140374
IPNI 866039-1
iNaturalist 133332
GBIF 2925561
Freebase /m/02pwzks
EPPO VIXTR
EOL 579728
USDA GRIN 41841
Wikipedia Vitex_trifolia
CMAUP NPO21373

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
Anti-osteoporosis activity of casticin in ovariectomized rats Zhang D, Li J, Li X, Liu W, Yu Y, Sun H, Wu J, Ge Z, Lv K, Shao Y, Wang S, Ye X Toxicol Res (Camb) 26-Apr-2024
PMCID:PMC11052697
doi:10.1093/toxres/tfae064
PMID:38680951
Discovery of a novel natural compound, vitekwangin B, with ANO1 protein reduction properties and anticancer potential Seo Y, Lee S, Kim M, Kim D, Jeong SB, Das R, Sultana A, Park S, Nhiem NX, Huong PT, Kwon OB, Namkung W, Woo J Front Pharmacol 03-Apr-2024
PMCID:PMC11041392
doi:10.3389/fphar.2024.1382787
PMID:38659592
A comprehensive review of ethnomedicinal approaches, phytochemical analysis, and pharmacological potential of Vitex trifolia L. Mottaghipisheh J, Kamali M, Doustimotlagh AH, Nowroozzadeh MH, Rasekh F, Hashempur MH, Iraji A Front Pharmacol 21-Mar-2024
PMCID:PMC10991721
doi:10.3389/fphar.2024.1322083
PMID:38576489
Traditional Tibetan medicine: therapeutic potential in lung diseases Li C, Li Y, Huang X, Li S, Sangji K, Gu R Front Pharmacol 18-Mar-2024
PMCID:PMC10986185
doi:10.3389/fphar.2024.1365911
PMID:38567353
Analyses of phytochemical compounds in the flowers and leaves of Spiraea japonica var. fortunei using UV-VIS, FTIR, and LC-MS techniques Yılmazer Keskin S, Avcı A, Fajriana Febda Kurnia H Heliyon 01-Feb-2024
PMCID:PMC10848007
doi:10.1016/j.heliyon.2024.e25496
PMID:38327478
Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review Islam Shawon S, Nargis Reyda R, Qais N Heliyon 01-Feb-2024
PMCID:PMC10864916
doi:10.1016/j.heliyon.2024.e25340
PMID:38356556
Vitex Genus as a Source of Antimicrobial Agents Islam Z, Caldeira GI, Caniça M, Islam N, Silva O Plants (Basel) 29-Jan-2024
PMCID:PMC10857077
doi:10.3390/plants13030401
PMID:38337934
Vitex agnus castus effects on hyperprolactinaemia Puglia LT, Lowry J, Tamagno G Front Endocrinol (Lausanne) 21-Nov-2023
PMCID:PMC10702745
doi:10.3389/fendo.2023.1269781
PMID:38075075
A review of the research progress on Pinellia ternata (Thunb.) Breit.: Botany, traditional uses, phytochemistry, pharmacology, toxicity and quality control Zou T, Wang J, Wu X, Yang K, Zhang Q, Wang C, Wang X, Zhao C Heliyon 14-Nov-2023
PMCID:PMC10696046
doi:10.1016/j.heliyon.2023.e22153
PMID:38058630
Healthy Patients, Workforce and Environment: Coupling Climate Adaptation and Mitigation to Wellbeing in Healthcare de Souza M, Lee AB, Cook S Int J Environ Res Public Health 13-Nov-2023
PMCID:PMC10671525
doi:10.3390/ijerph20227059
PMID:37998289
Plants and Their Derivatives as Promising Therapeutics for Sustainable Control of Honeybee (Apis mellifera) Pathogens Bava R, Castagna F, Ruga S, Nucera S, Caminiti R, Serra M, Bulotta RM, Lupia C, Marrelli M, Conforti F, Statti G, Domenico B, Palma E Pathogens 19-Oct-2023
PMCID:PMC10610010
doi:10.3390/pathogens12101260
PMID:37887776
Green and eco‐friendly biosynthesis of zinc oxide nanoparticles using Calendula officinalis flower extract: Wound healing potential and antioxidant activity Aydin Acar C, Gencer MA, Pehlivanoglu S, Yesilot S, Donmez S Int Wound J 18-Sep-2023
PMCID:PMC10788648
doi:10.1111/iwj.14413
PMID:37722846
Traditional use, phytochemistry and pharmacology of Viticis Fructus Meng X, Wang H, Kuang Z, Wu Y, Su X, Wang J, Li L, Liu C, Jia M Heliyon 30-Aug-2023
PMCID:PMC10558315
doi:10.1016/j.heliyon.2023.e19144
PMID:37810114
Biosynthesis approach of zinc oxide nanoparticles for aqueous phosphorous removal: physicochemical properties and antibacterial activities Khamis M, Gouda GA, Nagiub AM BMC Chem 16-Aug-2023
PMCID:PMC10428629
doi:10.1186/s13065-023-01012-2
PMID:37587477
Identification and Quantitation of the Bioactive Components in Wasted Aralia elata Leaves Extract with Endothelial Protective Activity Gao D, Cho CW, Yang Z, Li X, Kang JS Molecules 06-Aug-2023
PMCID:PMC10421206
doi:10.3390/molecules28155907
PMID:37570877

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
Phenylacetate 4409936 Click to see 135.14 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
3-Methoxysalicylic acid 70140 Click to see 168.15 unknown via CMAUP database
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
4-Methoxybenzoic Acid 7478 Click to see 152.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
2,3-Dihydroxybenzoic Acid 19 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron phenoxide 20488062 Click to see 94.11 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2,3,6-Trideuterio-4-hydroxy-5-methoxybenzaldehyde 11389509 Click to see 155.17 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dotriacontane 11008 Click to see 450.90 unknown via CMAUP database
Hentriacontane 12410 Click to see 436.80 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see 228.37 unknown via CMAUP database
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Oleic acid-d2 13011408 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 284.50 unknown via CMAUP database
Palmitelaidic acid 5282745 Click to see 254.41 unknown via CMAUP database
Palmitic Acid 985 Click to see 256.42 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Stearic Acid 5281 Click to see 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Behenic Acid 8215 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)O 340.60 unknown via CMAUP database
Hexacosanoic Acid 10469 Click to see 396.70 unknown via CMAUP database
Lignoceric Acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
(R)-oct-1-en-3-ol 6992244 Click to see 128.21 unknown via CMAUP database
3-Octanol 11527 Click to see CCCCCC(CC)O 130.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Tristearin 11146 Click to see 891.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(2S,4aS,10aR)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-2-ol 13996029 Click to see CC(C)C1=CC2=C(C=C1)C3(CCC(C(C3CC2)(C)C)O)C 286.50 unknown https://doi.org/10.1016/S0031-9422(00)00214-4
7-Isopropyl-1,1,4a-trimethyl-2,3,4,9,10,10a-hexahydrophenanthren-2-ol 495217 Click to see 286.50 unknown https://doi.org/10.1016/S0031-9422(00)00214-4
CID 154497380 154497380 Click to see 362.50 unknown https://doi.org/10.1016/S0031-9422(00)00214-4
CID 71577606 71577606 Click to see CC1CCC2C(C(CCC2(C13CCC4(O3)CC(OC4OC)OC)C)OC(=O)C)(C)C 424.60 unknown https://doi.org/10.1021/NP300679X
Vitextrifolin B 71579298 Click to see 424.60 unknown https://doi.org/10.1021/NP300679X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(3R,4R,4aS,8aS)-4-[2-(furan-3-yl)ethyl]-4-hydroxy-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydronaphthalen-1-one 101717490 Click to see 318.40 unknown https://doi.org/10.1016/S0031-9422(00)00214-4
(4aS)-4-[2-(furan-3-yl)ethyl]-4-hydroxy-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydronaphthalen-1-one 5316740 Click to see CC1CC(=O)C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C 318.40 unknown via CMAUP database
[(1R,4aS)-4-[2-(furan-3-yl)ethyl]-4-hydroxy-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 5321001 Click to see 362.50 unknown https://doi.org/10.1080/10286020310001617165
https://doi.org/10.1002/PTR.2021
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638617/
https://doi.org/10.1016/S0031-9422(00)00214-4
https://doi.org/10.1002/PTR.743
[(1S,4aS)-4-[2-(furan-3-yl)ethyl]-4-hydroxy-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 5315261 Click to see 362.50 unknown https://doi.org/10.1016/S0031-9422(00)00214-4
[(4aS)-4-[2-(furan-3-yl)ethyl]-4-hydroxy-3,4a,8,8-tetramethyl-3,5,6,7-tetrahydro-2H-naphthalen-2-yl] acetate 5315262 Click to see CC1C(C=C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 360.50 unknown https://doi.org/10.1016/S0031-9422(00)00214-4
[4-[2-(furan-3-yl)ethyl]-4-hydroxy-3,4a,8,8-tetramethyl-3,5,6,7-tetrahydro-2H-naphthalen-2-yl] acetate 78384586 Click to see CC1C(C=C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 360.50 unknown https://doi.org/10.1016/S0031-9422(00)00214-4
1-[2-(3-Furyl)ethyl]decahydro-2alpha,5,5,8abeta-tetramethylnaphthalene-1alpha,4beta-diol 4-acetate 18008144 Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 362.50 unknown https://doi.org/10.1080/10286020310001617165
https://doi.org/10.1002/PTR.2021
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638617/
https://doi.org/10.1016/S0031-9422(00)00214-4
https://doi.org/10.1002/PTR.743
4-[2-(Furan-3-yl)ethyl]-4-hydroxy-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydronaphthalen-1-one 12442888 Click to see 318.40 unknown https://doi.org/10.1016/S0031-9422(00)00214-4
Rotundifuran 9841926 Click to see CC1CC(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C 362.50 unknown https://doi.org/10.1080/10286020310001617165
https://doi.org/10.1016/S0031-9422(00)00214-4
Vitetrifolin B 15543011 Click to see 362.50 unknown https://doi.org/10.1016/S0031-9422(00)00214-4
Vitetrifolin C 15543012 Click to see 360.50 unknown https://doi.org/10.1016/S0031-9422(00)00214-4
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids
1,3,3-Trimethyltricyclo[2.2.1.02,6]heptane 79022 Click to see CC1(C2CC3C1C3(C2)C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-Camphene 440966 Click to see 136.23 unknown via CMAUP database
(+-)-alpha-Pinene 6654 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730060115
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(5S)-4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane 6429260 Click to see 136.23 unknown via CMAUP database
Beta-Pinene 14896 Click to see 136.23 unknown via CMAUP database
Npc126240 44630108 Click to see 196.29 unknown via CMAUP database
Sabinene 18818 Click to see 136.23 unknown https://doi.org/10.1002/FFJ.2730060115
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
Eucommiol 154373 Click to see 188.22 unknown https://doi.org/10.1080/10286020801967359
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
(L)-alpha-terpineol 443162 Click to see 154.25 unknown via CMAUP database
2-[(1S)-4-methylcyclohex-3-en-1-yl]propan-2-yl acetate 93317 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown via CMAUP database
4-Terpineol, (+/-)- 11230 Click to see CC1=CCC(CC1)(C(C)C)O 154.25 unknown via CMAUP database
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown via CMAUP database
Alpha-Terpineol 17100 Click to see 154.25 unknown via CMAUP database
alpha-Terpinyl acetate 111037 Click to see CC1=CCC(CC1)C(C)(C)OC(=O)C 196.29 unknown https://doi.org/10.1002/FFJ.2730060115
Delta-Terpineol 81722 Click to see 154.25 unknown via CMAUP database
Limonene, (-)- 439250 Click to see 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Quinone and hydroquinone lipids / Vitamin E compounds / Tocopherols
(+)-gamma-Tocopherol 92729 Click to see 416.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Retinoids
3-[(4R)-4-methyl-3-oxo-6-(2,6,6-trimethylcyclohexen-1-yl)hexyl]-2H-furan-5-one 73354982 Click to see CC1=C(C(CCC1)(C)C)CCC(C)C(=O)CCC2=CC(=O)OC2 318.40 unknown https://doi.org/10.1021/NP300679X
Retinol 445354 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CCO)C)C 286.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Isocaryophyllene 5281522 Click to see 204.35 unknown via CMAUP database
(-)-Rotundone 5321003 Click to see 218.33 unknown via CMAUP database
(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
(4Z)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene 5322111 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1002/FFJ.2730060115
Caryophyllene,alpha + beta mixt. 5354499 Click to see 204.35 unknown https://doi.org/10.1002/FFJ.2730060115
Npc16157 13240188 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids / Scalarane sesterterpenoids
(+)-Taraxerol 42608290 Click to see 426.70 unknown via CMAUP database
Taraxerol 92097 Click to see 426.70 unknown via CMAUP database
Taraxerone 92785 Click to see 424.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aS,7S,7aS)-1-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-3-(4-hydroxybenzoyl)oxy-6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 16655052 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=C(C=C4)O)O 496.50 unknown via CMAUP database
(1S,4AS,7S,7aS)-7-hydroxy-7-methyl-1-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(((4-hydroxybenzoyl)oxy)methyl)tetrahydro-2H-pyran-2-yl)oxy)-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylic acid 23955877 Click to see 496.50 unknown via CMAUP database
[(1S,4aR,7S,7aS)-7-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-5-yl] 4-hydroxybenzoate 6325359 Click to see CC1(CC(C2C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C4=CC=C(C=C4)O)O 468.40 unknown via CMAUP database
[(1S,4aS,5R,7aR)-5-hydroxy-1-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 4-hydroxybenzoate 17750979 Click to see 466.40 unknown via CMAUP database
[(1S,5S)-5-hydroxy-1-[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 4-hydroxybenzoate 92131257 Click to see 466.40 unknown via CMAUP database
[5-Hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 4-hydroxybenzoate 3512643 Click to see 466.40 unknown via CMAUP database
1-[(2S,3R,4R,5S,6R)-4,5-dihydroxy-3-(4-hydroxybenzoyl)oxy-6-(hydroxymethyl)oxan-2-yl]oxy-7-hydroxy-7-methyl-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylic acid 102032626 Click to see CC1(CCC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)OC(=O)C4=CC=C(C=C4)O)O 496.50 unknown via CMAUP database
Agnuside 442416 Click to see C1=COC(C2C1C(C=C2COC(=O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 466.40 unknown via CMAUP database
CID 51346123 51346123 Click to see 466.40 unknown via CMAUP database
Mussaenosidic acid 21633105 Click to see 376.36 unknown via CMAUP database
Negundoside 9935561 Click to see 496.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(1R,3R,4R,4aS,8aS)-4-hydroxy-3,4a,8,8-tetramethyl-4-[2-(5-oxo-2H-furan-4-yl)ethyl]-2,3,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 10022565 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CCOC3=O)O)C)(C)C)OC(=O)C 378.50 unknown https://doi.org/10.1248/CPB.52.1492
https://doi.org/10.1055/S-2002-35650
[(1R,4aS,8aS)-3,4a,8,8-tetramethyl-4-[2-(5-oxo-2H-furan-3-yl)ethyl]-1,2,5,6,7,8a-hexahydronaphthalen-1-yl] acetate 71579299 Click to see 360.50 unknown https://doi.org/10.1021/NP300679X
[4-hydroxy-3,4a,8,8-tetramethyl-4-[2-(5-oxo-2H-furan-3-yl)ethyl]-2,3,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 20598215 Click to see 378.50 unknown https://doi.org/10.1002/PTR.2021
[4-hydroxy-3,4a,8,8-tetramethyl-4-[2-(5-oxo-2H-furan-4-yl)ethyl]-2,3,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 85095220 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CCOC3=O)O)C)(C)C)OC(=O)C 378.50 unknown https://doi.org/10.1248/CPB.52.1492
https://doi.org/10.1055/S-2002-35650
3-[2-[(1R,2R,4aS,8aS)-1-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-2H-naphthalen-1-yl]ethyl]-2H-furan-5-one 102105798 Click to see CC1CCC2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C 320.50 unknown via CMAUP database
3-[2-[(1R,2R,8aS)-1-hydroxy-2,5,5,8a-tetramethyl-3,6,7,8-tetrahydro-2H-naphthalen-1-yl]ethyl]-2H-furan-5-one 71579372 Click to see 318.40 unknown https://doi.org/10.1021/NP300679X
CID 101357919 101357919 Click to see CC1CC(C2C(CCCC2(C13CCC4(O3)CC(=O)OC4)C)(C)C)OC(=O)C 378.50 unknown via CMAUP database
CID 162821194 162821194 Click to see CC1CC(C2C(CCCC2(C13CCC4(O3)CCOC4=O)C)(C)C)OC(=O)C 378.50 unknown https://doi.org/10.1248/CPB.52.1492
CID 71579374 71579374 Click to see 336.50 unknown https://doi.org/10.1021/NP300679X
CID 71579375 71579375 Click to see 318.40 unknown https://doi.org/10.1021/NP300679X
CID 73817522 73817522 Click to see 378.50 unknown https://doi.org/10.1248/CPB.52.1492
Previtexilactone 21636179 Click to see 378.50 unknown https://doi.org/10.1248/CPB.52.1492
Vitexilactone 21636178 Click to see CC1CC(C2C(CCCC2(C1(CCC3=CC(=O)OC3)O)C)(C)C)OC(=O)C 378.50 unknown https://doi.org/10.1080/10286020310001617165
https://doi.org/10.1248/CPB.52.1492
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(7-hydroxy-9-methyl-3-methylidene-2-oxospiro[4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-6,2'-oxirane]-4-yl) 2-methylbut-2-enoate 162907830 Click to see CC=C(C)C(=O)OC1CC2(CO2)C3C(C=C(C3C4C1C(=C)C(=O)O4)C)O 360.40 unknown https://doi.org/10.1248/CPB.49.1220
https://doi.org/10.1248/CPB.52.1492
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45358157 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45483617 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
3Alpha-Hydroxyurs-12-En-28-Oic Acid 7163177 Click to see 456.70 unknown via CMAUP database
Alpha-Amyrin 73170 Click to see 426.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
16-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 53399246 Click to see 414.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
Peimine 131900 Click to see 431.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(22e)-Stigmasta-4,22-diene-3,6-dione 10455054 Click to see 424.70 unknown via CMAUP database
(2S,3R,4S,5R)-2-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(2R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol 6326040 Click to see 546.80 unknown via CMAUP database
(3S,8R,9R,10S,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 636741 Click to see 414.70 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 via CMAUP database
Sitosteryl glucoside 70699351 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 via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acids
Propionic Acid 1032 Click to see CCC(=O)O 74.08 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(2E)-2-[(4aS,5R,7R,8R,8aS)-5-acetyloxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,5'-oxolane]-2'-ylidene]acetic acid 101357917 Click to see 364.50 unknown https://doi.org/10.1248/CPB.52.1492
[(1S,2R,3S,4R)-1-acetyloxy-4-[(3R)-3-hydroxy-3-methylpent-4-enyl]-3,4,8,8-tetramethyl-1,2,3,5,6,7-hexahydronaphthalen-2-yl] acetate 38362998 Click to see 406.60 unknown https://doi.org/10.1248/CPB.49.1220
[(1S,2R,3S,4R)-1-acetyloxy-4-[(3S)-3-hydroxy-3-methylpent-4-enyl]-3,4,8,8-tetramethyl-1,2,3,5,6,7-hexahydronaphthalen-2-yl] acetate 38363004 Click to see CC1C(C(C2=C(C1(C)CCC(C)(C=C)O)CCCC2(C)C)OC(=O)C)OC(=O)C 406.60 unknown https://doi.org/10.1248/CPB.49.1220
[1-Acetyloxy-4-(3-hydroxy-3-methylpent-4-enyl)-3,4,8,8-tetramethyl-1,2,3,5,6,7-hexahydronaphthalen-2-yl] acetate 23757094 Click to see 406.60 unknown https://doi.org/10.1248/CPB.49.1220
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3638617/
https://doi.org/10.1016/J.JCHROMB.2013.02.037
https://doi.org/10.1080/10286020310001617165
2-(5-acetyloxy-4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,5'-oxolane]-2'-ylidene)acetic acid 162868491 Click to see 364.50 unknown https://doi.org/10.1248/CPB.52.1492
Vitetrifolin D 11015016 Click to see CC1C(C(C2=C(C1(C)CCC(C)(C=C)O)CCCC2(C)C)OC(=O)C)OC(=O)C 406.60 unknown https://doi.org/10.1248/CPB.49.1220
https://doi.org/10.1080/10286020310001617165
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2S,3S,4R)-4-[(3R)-3-hydroxy-3-methylpent-4-enyl]-3,4,8,8-tetramethyl-2,3,6,7-tetrahydronaphthalen-2-ol 163049118 Click to see 304.50 unknown https://doi.org/10.1248/CPB.49.1220
(2S,3S,4R)-4-[(3S)-3-hydroxy-3-methylpent-4-enyl]-3,4,8,8-tetramethyl-2,3,6,7-tetrahydronaphthalen-2-ol 163049119 Click to see 304.50 unknown https://doi.org/10.1248/CPB.49.1220
[(1S,2R,3S,4R)-1-hydroxy-4-[(3R)-3-hydroxy-3-methylpent-4-enyl]-3,4,8,8-tetramethyl-1,2,3,5,6,7-hexahydronaphthalen-2-yl] acetate 162862751 Click to see 364.50 unknown https://doi.org/10.1248/CPB.49.1220
[(1S,2R,3S,4R)-2-hydroxy-4-[(3S)-3-hydroxy-3-methylpent-4-enyl]-3,4,8,8-tetramethyl-1,2,3,5,6,7-hexahydronaphthalen-1-yl] acetate 163047906 Click to see 364.50 unknown https://doi.org/10.1248/CPB.49.1220
https://doi.org/10.1248/CPB.52.1492
[1-Hydroxy-4-(3-hydroxy-3-methylpent-4-enyl)-3,4,8,8-tetramethyl-1,2,3,5,6,7-hexahydronaphthalen-2-yl] acetate 72757336 Click to see CC1C(C(C2=C(C1(C)CCC(C)(C=C)O)CCCC2(C)C)O)OC(=O)C 364.50 unknown https://doi.org/10.1248/CPB.49.1220
https://doi.org/10.1248/CPB.52.1492
[2-Hydroxy-4-(3-hydroxy-3-methylpent-4-enyl)-3,4,8,8-tetramethyl-1,2,3,5,6,7-hexahydronaphthalen-1-yl] acetate 85413919 Click to see 364.50 unknown https://doi.org/10.1248/CPB.49.1220
https://doi.org/10.1248/CPB.52.1492
4-(3-Hydroxy-3-methylpent-4-enyl)-3,4,8,8-tetramethyl-2,3,6,7-tetrahydronaphthalen-2-ol 85304779 Click to see 304.50 unknown https://doi.org/10.1248/CPB.49.1220
Vitetrifolin E 11143042 Click to see 364.50 unknown https://doi.org/10.1248/CPB.49.1220
https://doi.org/10.1080/10286020310001617165
Vitetrifolin F 11222285 Click to see 364.50 unknown https://doi.org/10.1248/CPB.49.1220
Vitetrifolin G 10892069 Click to see 304.50 unknown https://doi.org/10.1248/CPB.49.1220
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
16-Hentriacontanone 94741 Click to see 450.80 unknown via CMAUP database
3-Octanone 246728 Click to see CCCCCC(=O)CC 128.21 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Terrestriamide 5321824 Click to see 327.30 unknown via CMAUP database
> Organoheterocyclic compounds / Azolidines / Isoxazolidines / Phenylisoxazolidines
(4Z)-2-methyl-4-(5-phenyl-1,2-oxazolidin-3-ylidene)cyclohexa-2,5-dien-1-one 49771170 Click to see 253.29 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Myristicin 4276 Click to see 192.21 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Delta valerolactones
Kiglikynkwylit-yjlwdspxsa- 21668660 Click to see CC1CC(C2C(CCCC2(C13CCCC(=O)O3)C)(C)C)OC(=O)C 336.50 unknown https://doi.org/10.1248/CPB.52.1492
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Iso-ambreinolide 15559824 Click to see 264.40 unknown via CMAUP database
> Organoheterocyclic compounds / Oxanes
1,8-Cineole 2758 Click to see 154.25 unknown via CMAUP database
> Organoheterocyclic compounds / Oxepanes
(2S,5S,10S)-2,6,6-trimethyl-12-propan-2-yl-13,16-dioxapentacyclo[8.6.0.01,15.02,7.012,14]hexadecan-5-ol 5315259 Click to see 320.50 unknown https://doi.org/10.1016/S0031-9422(00)00214-4
Vitetrifolin A 637489 Click to see 320.50 unknown https://doi.org/10.1016/S0031-9422(00)00214-4
> Organoheterocyclic compounds / Oxolanes
2-(4,4,7,8a-tetramethylspiro[2,3,4a,5,6,7-hexahydro-1H-naphthalene-8,5'-oxolane]-2'-ylidene)acetaldehyde 72751474 Click to see 290.40 unknown https://doi.org/10.1248/CPB.52.1492
> Organoheterocyclic compounds / Tetrahydrofurans
Vitex norditerpenoid 1 11208535 Click to see CC1CCC2C(CCCC2(C13CCC(=CC=O)O3)C)(C)C 290.40 unknown https://doi.org/10.1248/CPB.52.1492
Vitex norditerpenoid 2 11462191 Click to see 348.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-dihydroxyphenyl)-5-hydroxy-4-oxo-4H-chromen-7-olate luteolin-7-olate(1-) 25201972 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)[O-] 285.23 unknown via CMAUP database
5,7,2',5'-Tetrahydroxyflavone 5487756 Click to see C1=CC(=C(C=C1O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 286.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1080/10286020310001625085
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
Isoorientin(1-) 49852298 Click to see 447.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Vitexin 5280441 Click to see 432.40 unknown https://doi.org/10.1016/J.JEP.2012.05.062
Vitexin-7-olate 49791957 Click to see 431.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Bonanzin 5379563 Click to see 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',5-Dihydroxy-4',7-dimethoxyflavone 5320496 Click to see 314.29 unknown https://doi.org/10.1080/10286020310001625085
Artemetin 5320351 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)OC 388.40 unknown https://doi.org/10.1080/10286020310001625085
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3583114/
https://doi.org/10.3892/IJO.2013.2133
https://doi.org/10.1080/10286020310001625085
https://doi.org/10.1055/S-2002-35650
chrysoplenol D 5280699 Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)OC 360.30 unknown via CMAUP database
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown via CMAUP database
Penduletin 5320462 Click to see 344.30 unknown https://doi.org/10.1080/10286020310001625085

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