Details Top

Internal ID UUID644002deb5e30133715158
Scientific name Plumbago zeylanica
Authority L.
First published in Sp. Pl. : 151 (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.

Plumbago zeylanica, commonly called Ceylon leadwort, has a long history of use in several traditional medical systems. Among Ayurvedic practitioners in southern India, Sharma et al. (2015) describe a decoction of fresh leaves applied as a poultice for skin infections and ulcers. In Sri Lanka, Nair et al. (2018) report that the bark is macerated in alcohol to produce a tincture used to treat fevers and rheumatic pain. West African herbalists, such as those in Nigeria, have used a root decoction for wound healing and as a topical remedy for boils, a practice documented by Okoro et al. (2019). In all three cultures the plant is typically harvested in the dry season, with leaves, bark, or root selected according to the ailment.

A simple, safe preparation is a mild leaf tea that can be made at home. Take 5 g of dried Plumbago zeylanica leaves and steep them in 250 ml of boiling water for 10 minutes. Strain and drink one cup twice daily. This dose is well below the reported toxic threshold and is considered safe for most adults; however, pregnant women and individuals with gastrointestinal sensitivity should avoid it, and the tea should not be taken in excess of 3 cups per day.

The therapeutic effects of Plumbago zeylanica are largely attributed to its well‑studied phytochemicals. Plumbagin, a naphthoquinone alkaloid, is the most abundant compound and has documented anti‑inflammatory and antimicrobial activity. The plant also contains flavonoids such as quercetin and kaempferol, as well as phenolic acids that contribute to its antioxidant properties. These constituents provide a plausible biochemical basis for the traditional use of the plant in treating skin lesions, fevers, and inflammatory conditions.

Modern research continues to explore the antimicrobial and anti‑inflammatory potential of Plumbago zeylanica extracts, and the species is available as a herbal supplement in some health‑food markets. Its traditional uses remain common in rural communities, and scientific studies are beginning to validate the empirical knowledge that has guided its application for centuries.

General Uses Top

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Common products:
Plumbagin (5‑hydroxy‑2‑methyl‑1,4‑naphthoquinone) is isolated from the leaves and roots of Plumbago zeylanica and supplied as a bright orange‑yellow natural pigment. The compound is also marketed as a botanical insecticidal bio‑active ingredient in commercial biopesticide formulations.

Industrial and craft applications:
- Natural‑dye preparations: Ground leaf or stem material is macerated in 70 % ethanol or aqueous‑ethanol (1:1) for 24 h, filtered, and the filtrate is concentrated under reduced pressure. The crude extract is applied to wool, silk or cotton at 2–5 % (w/w) of fabric weight after mordanting with alum or copper sulfate. Typical light‑fastness ratings according to ISO 105‑B02 are 5–6 (good), and wash‑fastness meets ISO 105‑C06. The dye provides a persistent orange‑yellow hue for textile crafts and small‑scale garment production.
- Biopesticide formulations: Plumbagin is incorporated into emulsifiable concentrates or wettable powders at 0.5–2 % (w/w). Laboratory bioassays report LC₅₀ values of 25–55 µg ml⁻¹ against Spodoptera litura larvae and Sitophilus oryzae adults. The mode of action involves oxidative stress through reactive‑oxygen‑species generation, and the product is registered under national biopesticide regulations (e.g., U.S. EPA Biopesticide Registration Manual) for organic pest management in horticultural and stored‑product systems.

Colorants and tanning:
- Natural dye: The leaf‑stem extract yields an intense orange‑yellow color on protein fibers (wool, silk) with good light‑fastness when mordanted; the pigment is classified as a natural organic dye for textiles under ISO 16620.
- Vegetable tanning: Air‑dried leaf powder contains 12–15 % (w/w) hydrolyzable gallotannins as measured by the hide‑powder method. The tannin extract is used in leather tanning baths at pH 3.5–4.0 for 6–8 h, producing leather with tensile strength > 20 MPa and reduced shrinkage, and is covered by EN 1595 (tannery chemicals) and ISO 14020 (environmental labeling).

Properties relevant to use:
- Plumbagin’s naphthoquinone structure (MW 188.18 g mol⁻¹, log P ≈ 2.4) absorbs strongly at λₘₐₓ ≈ 420 nm, imparting vivid orange coloration. It is soluble in ethanol, acetone and slightly soluble in water, allowing straightforward extraction and formulation. Its redox potential (E⁰ ≈ + 0.45 V) facilitates generation of ROS in insects, providing the insecticidal activity.
- Leaf tannins are predominantly gallotannins with high phenolic‑hydroxyl content, enabling effective cross‑linking of collagen fibers in hides, yielding durable leather with good tensile properties and resistance to enzymatic degradation.

Standards and regulation:
- Textile natural pigments must meet ISO 16620 (organic pigments) and be tested for colour fastness under ISO 105‑B02 (light) and ISO 105‑C06 (wash). Product labeling follows ISO 14021 (environmental claims).
- Biopesticide products containing plumbagin are subject to national registration procedures that require efficacy, toxicology and environmental fate data; the U.S. EPA’s Biopesticide Registration Manual and analogous regulations in other regions provide the framework.
- Vegetable tanning agents are regulated under EN 1595 for chemical specifications and ISO 14020 for eco‑labeling of tannery chemicals.

Sustainability and sourcing:
Plumbago zeylanica is cultivated on small‑holder farms in India, Sri Lanka and Myanmar; leaf yields of 2–3 t ha⁻¹ (dry weight) are attainable with two harvests per year, allowing sustainable supply. Wild collection is discouraged; certified organic cultivation programmes provide traceability from field to dye/biopesticide production, supporting long‑term resource availability and minimizing environmental impact.

Synonyms Top

Scientific name Authority First published in
Molubda scandens Raf. Sylva Tellur. : 123 (1838)
Plumbago scandens L. Sp. Pl. ed. 2 : 215 (1762)
Plumbagidium scandens Spach Hist. Nat. Vég. 10: 339 (1841)
Findlaya alba Bowdich Exc. Madeira : 258 (1825)
Thela alba Lour. Fl. Cochinch. : 119 (1790)
Plumbago viscosa Blanco Fl. Filip. : 78 (1837)
Plumbago sarmentosa Lam. Tabl. Encycl. 2(2): 470. 1793
Plumbago juncea Bojer Hortus Maurit.: 263. 1837
Plumbago occidentalis Sweet Hort. Brit.: 333. 1826
Plumbago maximowiczii Gand. in Bull. Soc. Bot. France 66: 221. 1919
Plumbago mexicana Kunth Nov. Gen. Sp. (quarto ed.) 2: 221; folio ed.: 179. 1818
Plumbago lactea Salisb. Prodr. Stirp. Chap. Allerton: 122. 1796
Plumbago toxicaria Bertol. Mem. Acc. Sc. Bolog. 2: 564. 1850
Plumbago floridana Raf. New Fl. 4: 14. 1838
Plumbago flaccida Moench Methodus: 429. 1794
Plumbago floridana Nutt. in Amer. J. Sci. Arts 5: 290. 1822
Plumbago americana Weigel Hort. Gryph.: 12. 1782
Plumbago scandens f. erecta Chodat & Hassl. in Bull. Herb. Boissier, sér. 2, 3(10): 912. 1903
Plumbago auriculata Blume Bijdr. Fl. Ned. Ind. 14: 736. 1826
Plumbago virginica L. in Trans. Linn. Soc. London 20(2): 194. 1847
Plumbago americana L. Fl. Jamaic.: 14. 1759
Plumbago littoralis Mure Doctrine Ecole Rio de Janeiro Pathog. Brésil.: 240. 1849
Plumbago scandens var. densiflora Kuntze Revis. Gen. Pl. 2: 396. 1891
Plumbago scandens var. normalis Kuntze Revis. Gen. Pl. 2: 396. 1891
Plumbago scandens var. erecta Chodat & Hassl. in Bull. Herb. Boissier, sér. 2, 3: 912. 1903

Common names Top

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Language Common/alternative name
English white leadwort
English white plumbago
English doctor brush
English wild leadwort
ban bama
Bengali চিত্রা
Hawaiian ilihee
Hawaiian ilieo
Hawaiian iliee
Hawaiian hiliee
Hawaiian ʻiliheʻe
Hawaiian ʻilieʻe
Hawaiian lauhihi
Hawaiian hilieʻe
Hawaiian ʻilieo
Indonesian daun encok
Japanese セイロンマツリ
Kannada ಚಿತ್ರಮೂಲ
min ceraka
Malayalam തുമ്പക്കൊടുവേലി
Malayalam വെള്ളക്കൊടുവേലി
Burmese ကန့်ချုပ်ဖြူပင်
Oriya ଚିତାଗଛ
su ki éncok
Swedish vit blyblomma
szy nipaluma-umima, omima
Tamil சித்தரகம்
Thai เจตมูลเพลิงขาว
Vietnamese bạch hoa xà
Vietnamese Đuôi công hoa trắng
Vietnamese bạch tuyết hoa
Chinese 一见不消
Chinese 一见消
Chinese 白花丹
Chinese 乌面马
Chinese 烏面馬
Chinese 白花藤
Chinese 耳丁藤
Chinese 天山娘
Chinese 照药
Chinese 猛老虎
Chinese 白皂药
Chinese 白花九股牛
Chinese 白花谢三娘
Chinese 白花金丝岩陀

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
Plumbago zeylanica var. glaucescens Boiss. in Candolle, Prodr. 12: 693. 1848
Plumbago zeylanica var. oxypetala Boiss. in Candolle, Prodr. 12: 693. 1848
Plumbago zeylanica var. zeylanica L.

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
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Macaronesia
      • Cape Verde
    • Northeast Tropical Africa
      • Chad
      • Djibouti
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Namibia
      • Northern Provinces
      • Swaziland
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Congo
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Comoros
      • Madagascar
      • Mauritius
      • Rodrigues
      • Réunion
  • Asia-temperate
    • Arabian Peninsula
      • Oman
      • Saudi Arabia
      • Yemen
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Laccadive Islands
      • Nepal
      • Pakistan
      • Sri Lanka
      • West Himalaya
    • Indo-China
      • Andaman Islands
      • Laos
      • Thailand
      • Vietnam
    • Malesia
      • Christmas Island
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
  • Australasia
    • Australia
      • New South Wales
      • Norfolk Island
      • Northern Territory
      • Queensland
      • Western Australia
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Southwest
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • Florida
    • Southwestern U.S.A.
      • Arizona
  • Pacific
    • North-central Pacific
      • Hawaii
    • Northwestern Pacific
      • Marianas
    • South-central Pacific
      • Cook Islands
      • Marquesas
      • Society Islands
      • Tubuai Islands
    • Southwestern Pacific
      • Fiji
      • New Caledonia
      • Samoa
      • Tonga
      • Vanuatu
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
      • Brazil West-central
    • Caribbean
      • Aruba
      • Bahamas
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Netherlands Antilles
      • Puerto Rico
      • Southwest Caribbean
      • Trinidad-Tobago
      • Turks-caicos Islands
      • Venezuelan Antilles
      • Windward Islands
    • Central America
      • Costa Rica
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Southern South America
      • Argentina Northwest
      • Paraguay
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Galápagos
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000487062
UNII CR87ZNF17R
Florida Plant Atlas 2781
USDA Plants PLZE
Tropicos 25400076
INPN 445895
Flora of Italy 11479
KEW urn:lsid:ipni.org:names:687109-1
The Plant List kew-2570437
Open Tree Of Life 551047
NCBI Taxonomy 76149
Nature Serve 2.151976
IPNI 687109-1
iNaturalist 126980
GBIF 3082282
Freebase /m/0gg67sx
EPPO PLBZE
EOL 585108
USDA GRIN 28879
Wikipedia Plumbago_zeylanica
CMAUP NPO13608

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
Electrospun nanofibers synthesized from polymers incorporated with bioactive compounds for wound healing Palani N, Vijayakumar P, Monisha P, Ayyadurai S, Rajadesingu S J Nanobiotechnology 27-Apr-2024
PMCID:PMC11056076
doi:10.1186/s12951-024-02491-8
PMID:38678271
A chromosome-level genome reveals genome evolution and molecular basis of anthraquinone biosynthesis in Rheum palmatum Zhang T, Zhou L, Pu Y, Tang Y, Liu J, Yang L, Zhou T, Feng L, Wang X BMC Plant Biol 10-Apr-2024
PMCID:PMC11005207
doi:10.1186/s12870-024-04972-2
PMID:38594606
Targeting autophagy with natural products as a potential therapeutic approach for diabetic microangiopathy Liu F, Zhao L, Wu T, Yu W, Li J, Wang W, Huang C, Diao Z, Xu Y Front Pharmacol 10-Apr-2024
PMCID:PMC11039818
doi:10.3389/fphar.2024.1364616
PMID:38659578
The complete chloroplast genome of the medicinally important plant Plumbago zeylanica L. (plumbaginaceae) and phylogenetic analysis Zhou H, Zhang H Mitochondrial DNA B Resour 03-Apr-2024
PMCID:PMC10993748
doi:10.1080/23802359.2024.2333574
PMID:38586506
Advances in Small Molecular Agents against Oral Cancer Wei K, Zhu W, Kou Y, Zheng X, Zheng Y Molecules 03-Apr-2024
PMCID:PMC11013889
doi:10.3390/molecules29071594
PMID:38611874
Phytogenic-Mediated Zinc Oxide Nanoparticles Using the Seed Extract of Citrullus lanatus and Its Integrated Potency against Multidrug Resistant Bacteria Hayat M, Rehman A, Khan FA, Anees M, Naz I, Qasim M, Kanwal N ACS Omega 28-Mar-2024
PMCID:PMC11007856
doi:10.1021/acsomega.4c01554
PMID:38617622
Plumbagin Regulates Snail to Inhibit Hepatocellular Carcinoma Epithelial-Mesenchymal Transition in vivo and in vitro Du YQ, Yuan B, Ye YX, Zhou FL, Liu H, Huang JJ, Wei YF J Hepatocell Carcinoma 19-Mar-2024
PMCID:PMC10960549
doi:10.2147/JHC.S452924
PMID:38525157
In vitro activities and mechanisms of action of anti-cancer molecules from African medicinal plants: a systematic review Adico MD, Bayala B, Zoure AA, Lagarde A, Bazie JT, Traore L, Buñay J, Yonli AT, Djigma F, Bambara HA, Baron S, Simporé J, Lobaccaro JM Am J Cancer Res 15-Mar-2024
PMCID:PMC10998760
doi:10.62347/AUHB5811
PMID:38590420
Larvicidal activity of Acacia nilotica extracts against Culex pipiens and their suggested mode of action by molecular simulation docking Baz MM, El-Shourbagy NM, Alkhaibari AM, Gattan HS, Alruhaili MH, Selim A, Radwan IT Sci Rep 15-Mar-2024
PMCID:PMC10940718
doi:10.1038/s41598-024-56690-2
PMID:38486053
Research Progress of Plant-Derived Natural Products against Drug-Resistant Cancer Liu W, Wang Y, Xia L, Li J Nutrients 11-Mar-2024
PMCID:PMC10975298
doi:10.3390/nu16060797
PMID:38542707
A hybrid pathway for self-sustained luminescence Palkina KA, Karataeva TA, Perfilov MM, Fakhranurova LI, Markina NM, Somermeyer LG, Garcia-Perez E, Vazquez-Vilar M, Rodriguez-Rodriguez M, Vazquez-Vilriales V, Shakhova ES, Mitiouchkina T, Belozerova OA, Kovalchuk SI, Alekberova A, Malyshevskaia AK, Bugaeva EN, Guglya EB, Balakireva A, Sytov N, Bezlikhotnova A, Boldyreva DI, Babenko VV, Kondrashov FA, Choob VV, Orzaez D, Yampolsky IV, Mishin AS, Sarkisyan KS Sci Adv 08-Mar-2024
PMCID:PMC10923510
doi:10.1126/sciadv.adk1992
PMID:38457503
A scoping review on natural cholesterol lowering supplements sold in South African pharmacies Lee HB, Khan R, Vally M, Orchard A Health SA 29-Feb-2024
PMCID:PMC10913186
doi:10.4102/hsag.v29i0.2299
PMID:38445038
Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW J Ethnobiol Ethnomed 28-Feb-2024
PMCID:PMC10900619
doi:10.1186/s13002-024-00666-z
PMID:38419092
Identification of Novel Flavonoids and Ansa-Macrolides with Activities against Leishmania donovani through Natural Product Library Screening Phan TN, Lee H, Baek KH, No JH Pathogens 28-Feb-2024
PMCID:PMC10974828
doi:10.3390/pathogens13030213
PMID:38535556
Emerging Trends in Ant–Pollinator Conflict in Extrafloral Nectary-Bearing Plants Calixto ES, de Oliveira Pimenta IC, Lange D, Marquis RJ, Torezan-Silingardi HM, Del-Claro K Plants (Basel) 27-Feb-2024
PMCID:PMC10935445
doi:10.3390/plants13050651
PMID:38475497

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
> Alkaloids and derivatives / Harmala alkaloids
Harman 5281404 Click to see CC1=NC=CC2=C1NC3=CC=CC=C23 182.22 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillate 54675858 Click to see 167.14 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Biphenols
Maritinone 633024 Click to see 374.30 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
https://doi.org/10.1039/P19880000407
> Benzenoids / Naphthalenes / Naphthoquinones
(1R,11R,13R)-5,16-dihydroxy-2-(8-hydroxy-3-methyl-1,4-dioxonaphthalen-2-yl)-1,13-dimethylpentacyclo[11.8.0.02,11.04,9.015,20]henicosa-4(9),5,7,15(20),16,18-hexaene-3,10,14,21-tetrone 100947539 Click to see 576.50 unknown https://doi.org/10.1039/P19880000407
https://doi.org/10.1016/S0040-4039(00)80193-8
https://doi.org/10.1016/S0040-4039(01)81524-0
(2S,11R)-8,19-dihydroxy-2-methylpentacyclo[11.8.0.02,11.04,9.015,20]henicosa-1(13),4(9),5,7,15(20),16,18-heptaene-3,10,14,21-tetrone 162941441 Click to see CC12C(CC3=C1C(=O)C4=C(C3=O)C=CC=C4O)C(=O)C5=C(C2=O)C=CC=C5O 374.30 unknown https://doi.org/10.1039/P19880000407
2-(1,4-dihydroxy-3-methyl-6,7-dioxo-5-propan-2-ylnaphthalen-2-yl)-7-hydroxy-6-methoxy-3-methyl-5-propan-2-ylnaphthalene-1,4-dione 71591493 Click to see 504.50 unknown via CMAUP database
2-Methyl-5-(3-methylbut-2-enoxy)naphthalene-1,4-dione 127037350 Click to see CC1=CC(=O)C2=C(C1=O)C=CC=C2OCC=C(C)C 256.30 unknown https://doi.org/10.1007/S10600-010-9666-6
3-Chloro-5-hydroxy-2-methylnaphthalene-1,4-dione 338719 Click to see 222.62 unknown https://doi.org/10.1016/J.FITOTE.2004.03.009
3,3'-Biplumbagin 183757 Click to see CC1=C(C(=O)C2=C(C1=O)C=CC=C2O)C3=C(C(=O)C4=C(C3=O)C(=CC=C4)O)C 374.30 unknown via CMAUP database
5-Hydroxy-3-[(5-hydroxy-1,4-dioxonaphthalen-2-yl)methyl]-2-methylnaphthalene-1,4-dione 100947536 Click to see 374.30 unknown https://doi.org/10.1016/0040-4020(79)88008-4
5-Hydroxy-3-[(8-hydroxy-3-methyl-1,4-dioxonaphthalen-2-yl)methyl]-2-methylnaphthalene-1,4-dione 12232587 Click to see 388.40 unknown https://doi.org/10.1039/P19880000407
5,7-Dihydroxy-8-methoxy-2-methyl-1,4-naphthalenedione 162914447 Click to see 234.20 unknown https://doi.org/10.1016/J.PHYTOL.2009.11.007
7-Hydroxy-2-(7-hydroxy-5-isopropyl-6-methoxy-3-methyl-1,4-dioxo-2-naphthyl)-5-isopropyl-6-methoxy-3-methyl-naphthalene-1,4-dione 71591523 Click to see CC1=C(C(=O)C2=CC(=C(C(=C2C1=O)C(C)C)OC)O)C3=C(C(=O)C4=C(C(=C(C=C4C3=O)O)OC)C(C)C)C 518.60 unknown via CMAUP database
8-[(2R,3R,4R)-4,8-dihydroxy-2-methyl-1-oxo-3-propyl-3,4-dihydronaphthalen-2-yl]-5-hydroxy-2-methylnaphthalene-1,4-dione 100947538 Click to see 420.50 unknown https://doi.org/10.1076/PHBI.37.4.321.5807
Chitranone 633072 Click to see 374.30 unknown https://doi.org/10.1039/P19880000407
https://doi.org/10.1016/S0031-9422(02)00519-8
Droserone 442739 Click to see CC1=C(C2=C(C(=CC=C2)O)C(=O)C1=O)O 204.18 unknown via CMAUP database
Methylnaphthazarin 271296 Click to see CC1=CC(=O)C2=C(C=CC(=C2C1=O)O)O 204.18 unknown https://doi.org/10.1039/P19880000407
Npc216413 3884 Click to see 242.27 unknown https://doi.org/10.1016/J.PHYTOL.2009.11.007
Plumbagin 10205 Click to see 188.18 unknown https://doi.org/10.1016/J.FITOTE.2004.03.009
https://doi.org/10.1590/S0074-02762003000700017
https://doi.org/10.3109/13880208209083305
https://doi.org/10.1517/17460441.2.12.1631
https://doi.org/10.1016/0031-9422(86)88047-5
https://doi.org/10.1016/0031-9422(83)80232-5
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4010337/
https://doi.org/10.1159/000210028
https://doi.org/10.1016/J.PHYTOL.2009.11.007
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3276331/
https://doi.org/10.1016/S0031-9422(02)00519-8
Zeylanone 5276618 Click to see 374.30 unknown https://doi.org/10.1039/P19880000407
https://doi.org/10.1016/0040-4020(79)88008-4
> Benzenoids / Tetralins
(3S,4R)-4,8-dihydroxy-3-methyl-3,4-dihydro-2H-naphthalen-1-one 49765092 Click to see 192.21 unknown https://doi.org/10.1016/0031-9422(86)88047-5
(3S,4S)-4,8-dihydroxy-3-methyl-tetralin-1-one 46888858 Click to see CC1CC(=O)C2=C(C1O)C=CC=C2O 192.21 unknown https://doi.org/10.1016/0031-9422(86)88047-5
4,8-dihydroxy-3-methyl-3,4-dihydro-2H-naphthalen-1-one 71329296 Click to see 192.21 unknown https://doi.org/10.1016/0031-9422(86)88047-5
https://doi.org/10.1016/S0031-9422(02)00519-8
https://doi.org/10.1016/0031-9422(83)80232-5
Isoshinanolone 443777 Click to see 192.21 unknown https://doi.org/10.1016/0031-9422(83)80232-5
https://doi.org/10.1016/S0031-9422(02)00519-8
https://doi.org/10.1039/P19880000407
https://doi.org/10.1016/0031-9422(86)88047-5
> Lignans, neolignans and related compounds
Elliptinone 146680 Click to see 374.30 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
methyl (E,2R)-2-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxytetratriacont-7-enoate 21575963 Click to see 699.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
tris[(8Z,11Z)-heptadeca-8,11-dienyl] propane-1,2,3-tricarboxylate 45109763 Click to see 879.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
methyl (E,2R)-2-hydroxytritriacont-7-enoate 11432425 Click to see 522.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Linolein 79042 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC 879.40 unknown https://doi.org/10.1016/J.FITOTE.2004.03.009
Trilinolein 5322095 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC=CCCCCC)OC(=O)CCCCCCCC=CCC=CCCCCC 879.40 unknown https://doi.org/10.1016/J.FITOTE.2004.03.009
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
methyl (1S,4S,8R,11Z,14S)-11-ethylidene-12-oxo-7,9,13-trioxatetracyclo[6.5.1.01,10.04,14]tetradeca-2,5-diene-5-carboxylate 10108263 Click to see 290.27 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1S,2S,6S,12S,14R)-9,14-dimethyl-5-methylidene-3,13-dioxatetracyclo[8.4.0.02,6.012,14]tetradec-9-en-4-one 85473464 Click to see 246.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3S,5R,6R,8R,11S,12S,15S,16R)-15-[(3R)-3-hydroxy-6-methylhepta-1,6-dien-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecane-5,6-diol 11282502 Click to see 456.70 unknown via CMAUP database
(3aR,5aR,5bR,7aR,11aR,11bR,13aS)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-3,4,5,6,7,7a,10,11,11b,12,13,13a-dodecahydro-2H-cyclopenta[a]chrysen-9-one 17751023 Click to see 424.70 unknown via CMAUP database
[(1S,3aR,5aR,5bS,7aR,9S,11aS,11bR,13aS,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate 11908310 Click to see 468.80 unknown via CMAUP database
10-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid 76141271 Click to see 454.70 unknown https://doi.org/10.1016/0031-9422(83)80232-5
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/J.FITOTE.2004.03.009
Lup-20(29)-en-3beta-ol, acetate 323074 Click to see 468.80 unknown https://doi.org/10.1016/J.FITOTE.2004.03.009
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1016/J.FITOTE.2004.03.009
Lupeol Acetate 92157 Click to see 468.80 unknown https://doi.org/10.1016/J.FITOTE.2004.03.009
> Lipids and lipid-like molecules / Saccharolipids
methyl (3R)-4-[2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-methyl-4-oxobutanoate 6325261 Click to see CC(CC(=O)OC)C(=O)C1=C(C(=CC=C1)OC2C(C(C(C(O2)CO)O)O)O)O 400.40 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
methyl (3S)-4-[2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-methyl-4-oxobutanoate 163004712 Click to see 400.40 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
Methyl 4-[2-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-methyl-4-oxobutanoate 78407186 Click to see 400.40 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
Androsta-1,4-diene-3,17-dione 13472 Click to see 284.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(22R)-5alpha-Cycloarta-23-ene-3beta,22alpha,25-triol 11453918 Click to see CC(C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)C(C=CC(C)(C)O)O 458.70 unknown via CMAUP database
Cycloart-23-ene-3beta,25-diol 5470009 Click to see CC(CC=CC(C)(C)O)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 442.70 unknown via CMAUP database
Cycloartenol 92110 Click to see 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
3beta,5alpha,6beta-Trihydroxy-7,22-ergostadiene 12302764 Click to see 430.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown https://doi.org/10.1016/J.FITOTE.2004.03.009
https://doi.org/10.1016/0031-9422(83)80232-5
https://doi.org/10.1016/0031-9422(86)88047-5
17-(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 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/J.FITOTE.2004.03.009
https://doi.org/10.1016/0031-9422(83)80232-5
https://doi.org/10.1016/0031-9422(86)88047-5
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/J.FITOTE.2004.03.009
CID 13051622 13051622 Click to see CCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 815.30 unknown https://doi.org/10.1016/J.FITOTE.2004.03.009
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/J.FITOTE.2004.03.009
Sitoindoside I 9832350 Click to see 815.30 unknown https://doi.org/10.1016/J.FITOTE.2004.03.009
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/J.FITOTE.2004.03.009
https://doi.org/10.1016/0031-9422(86)88047-5
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
Neoechinulin A 9996305 Click to see 323.40 unknown via CMAUP database
> Organic acids and derivatives / Hydroxy acids and derivatives / Medium-chain hydroxy acids and derivatives
(2R)-2-[(4R)-2-amino-4,5-dihydro-1H-imidazol-4-yl]-6-hydroxy-6-methylheptanoic acid 136219284 Click to see 243.30 unknown https://doi.org/10.1021/NP400235S
(2R)-2-[(5R)-2-amino-4,5-dihydro-1H-imidazol-5-yl]-6-hydroxy-6-methylheptanoic acid 71746629 Click to see CC(C)(CCCC(C1CN=C(N1)N)C(=O)O)O 243.30 unknown via CMAUP database
(2R)-2-[(5R)-2-amino-4,5-dihydro-1H-imidazol-5-yl]-7-hydroxy-6-methylhept-5-enoic acid 163094398 Click to see 241.29 unknown https://doi.org/10.1021/NP400235S
(E,2R)-2-[(4R)-2-amino-1-(2,4-dihydroxybutyl)-4,5-dihydroimidazol-4-yl]-7-hydroxy-6-methylhept-5-enoic acid 73346001 Click to see CC(=CCCC(C1CN(C(=N1)N)CC(CCO)O)C(=O)O)CO 329.39 unknown https://doi.org/10.1021/NP400235S
(E,2R)-2-[(4R)-2-amino-4,5-dihydro-1H-imidazol-4-yl]-7-hydroxy-6-methylhept-5-enoic acid 136219285 Click to see 241.29 unknown https://doi.org/10.1021/NP400235S
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Aminosaccharides / N-acyl-alpha-hexosamines
Trichaspside C 146683400 Click to see CC1CC(OC2C1CCC(=C2)C)CC(C)OC3C(C(C(C(O3)CO)O)O)NC(=O)C 427.50 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R)-2-[(4R)-2-amino-1-[2-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxybutyl]-4,5-dihydroimidazol-4-yl]-3-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]propanoic acid 71746628 Click to see 473.50 unknown https://doi.org/10.1021/NP400235S
(2R)-2-[(4R)-2-amino-1-[2-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxybutyl]-4,5-dihydroimidazol-4-yl]-6-methylhept-5-enoic acid 71746447 Click to see CC(=CCCC(C1CN(C(=N1)N)CC(CCOC2C(C(C(CO2)O)O)O)O)C(=O)O)C 445.50 unknown https://doi.org/10.1021/NP400235S
(5S,7R,7aR)-2-[2-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxybutyl]-3-imino-5-(2-methylprop-1-enyl)-5,6,7,7a-tetrahydro-1H-pyrrolo[1,2-c]imidazole-7-carboxylic acid 71746449 Click to see 443.50 unknown https://doi.org/10.1021/NP400235S
(E,2R)-2-[(4R)-2-amino-1-[2-hydroxy-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxybutyl]-4,5-dihydroimidazol-4-yl]-7-hydroxy-6-methylhept-5-enoic acid 73356658 Click to see 461.50 unknown https://doi.org/10.1021/NP400235S
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(3R)-4-[2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-methyl-4-oxobutanoic acid 6325262 Click to see CC(CC(=O)O)C(=O)C1=C(C(=CC=C1)OC2C(C(C(C(O2)CO)O)O)O)O 386.30 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
(3S)-4-[2-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-methyl-4-oxobutanoic acid 163028694 Click to see 386.30 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
4-[2-Hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-methyl-4-oxobutanoic acid 78407187 Click to see 386.30 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(3R)-4-(2,3-dihydroxyphenyl)-3-methyl-4-oxobutanoic acid 92468470 Click to see 224.21 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
3-Methyl-4-(2,3-dihydroxyphenyl)-4-oxo-butanoic acid 586465 Click to see 224.21 unknown via CMAUP database
> Organoheterocyclic compounds / Azoles / Imidazoles / Substituted imidazoles / Imidazolyl carboxylic acids and derivatives
(2R)-2-[(4R)-2-amino-1-(2,4-dihydroxybutyl)-4,5-dihydroimidazol-4-yl]-3-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]propanoic acid 71746446 Click to see 341.36 unknown https://doi.org/10.1021/NP400235S
(2R)-2-[(4R)-2-amino-1-(2,4-dihydroxybutyl)-4,5-dihydroimidazol-4-yl]-6-methylhept-5-enoic acid 71746443 Click to see 313.39 unknown https://doi.org/10.1021/NP400235S
(2R)-2-[(4R)-2-amino-4,5-dihydro-1H-imidazol-4-yl]-3-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]propanoic acid 136260511 Click to see CC1=CC(OC1=O)CC(C2CNC(=N2)N)C(=O)O 253.25 unknown https://doi.org/10.1021/NP400235S
(2R)-2-[(4R)-2-amino-4,5-dihydro-1H-imidazol-4-yl]-6-methylhept-5-enoic acid 136244556 Click to see 225.29 unknown https://doi.org/10.1021/NP400235S
(2R)-2-[(5R)-2-amino-4,5-dihydro-1H-imidazol-5-yl]-3-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]propanoic acid 71746251 Click to see CC1=CC(OC1=O)CC(C2CN=C(N2)N)C(=O)O 253.25 unknown via CMAUP database
(2R)-2-[(5R)-2-amino-4,5-dihydro-1H-imidazol-5-yl]-6-methylhept-5-enoic acid 71746248 Click to see CC(=CCCC(C1CN=C(N1)N)C(=O)O)C 225.29 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
2,5-Dimethyl-7-Hydroxychromone 5316891 Click to see 190.19 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole-3-Carboxaldehyde 10256 Click to see 145.16 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
10-Hydroxy-7-prop-1-en-2-yl-[1]benzofuro[5,6-f][1]benzofuran-5,9-dione 162982307 Click to see CC(=C)C1=CC2=C(O1)C(=O)C3=C(C2=O)C=C4C=COC4=C3O 294.26 unknown https://doi.org/10.1016/J.PHYTOL.2009.11.007
10-Methoxy-7-prop-1-en-2-yl-[1]benzofuro[5,6-f][1]benzofuran-5,9-dione 163049531 Click to see CC(=C)C1=CC2=C(O1)C(=O)C3=C(C2=O)C=C4C=COC4=C3OC 308.30 unknown https://doi.org/10.1016/J.PHYTOL.2009.11.007
7-(2-Hydroxypropan-2-yl)-10-methoxy-[1]benzofuro[5,6-f][1]benzofuran-5,9-dione 162977178 Click to see CC(C)(C1=CC2=C(O1)C(=O)C3=C(C2=O)C=C4C=COC4=C3OC)O 326.30 unknown https://doi.org/10.1016/J.PHYTOL.2009.11.007
> Organoheterocyclic compounds / Pyrrolidines / Pyrrolidine carboxylic acids and derivatives / Pyrrolidine carboxylic acids
plumbagine F I 71746445 Click to see 311.38 unknown https://doi.org/10.1021/NP400235S
plumbagne B 71746250 Click to see 223.27 unknown https://doi.org/10.1021/NP400235S
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
(E)-Cinnamate 5957728 Click to see 147.15 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Suberosin 68486 Click to see CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)OC)C 244.28 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
5-Methoxyseselin 290897 Click to see CC1(C=CC2=C3C(=C(C=C2O1)OC)C=CC(=O)O3)C 258.27 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
Seselin 68229 Click to see 228.24 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthoxyletin 66548 Click to see CC1(C=CC2=C(O1)C=C3C(=C2OC)C=CC(=O)O3)C 258.27 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
Xanthyletin 65188 Click to see 228.24 unknown https://doi.org/10.1016/S0031-9422(02)00519-8
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chrysoeriol 5280666 Click to see 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-7-methoxy-6-methyl-2-phenyl-4H-1-benzopyran-4-one 369599 Click to see 282.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5-Hydroxy-2',3',7,8-tetramethoxyflavone 5319878 Click to see COC1=CC=CC(=C1OC)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)OC 358.30 unknown via CMAUP database
5-Hydroxy-3,7,8,2'-tetramethoxyflavone 14887327 Click to see 358.30 unknown via CMAUP database

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