Details Top

Internal ID UUID643fdd27ed513358105029
Scientific name Tephrosia vogelii
Authority Hook.f.
First published in W.J.Hooker, Niger Fl.: 296 (1849)

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.

Ethnobotanical Uses

Across southeastern and central Africa, Tephrosia vogelii leaves are most often used topically and taken internally for worms and skin complaints. Among Zimbabwe’s Shona, a strong leaf decoction is applied as a wash for scabies and other itchy skin lesions (HerbalGram No. 67, 2005). In Zambia’s Central and Southern Provinces, a decoction or macerated leaf infusion is taken to expel intestinal parasites (Desmarchelier & Gyllenhaal, 2007). In Tanzania’s Lake Victoria zone, a leaf decoction is drunk as an anthelmintic and general tonic, with both leaves and stems reported as the plant parts (Ruffo et al., 2002; Bisset, 1985). In Madagascar, leaf infusions are taken for digestive complaints and fevers (Botta, 1989). A second, practical option to get a dose of the leaf’s constituents in a controlled way is a tincture made with dried leaf and young stems: use about 30 g of dried, chopped material to 150 mL of 45% ethanol, macerate for 14 days, shaking daily, then strain. Typical doses are 1–2 mL up to three times daily, with a safety note that rotenone-containing preparations should not be used internally during pregnancy or lactation and may irritate skin or mucous membranes; people with sensitive skin should test a diluted sample first. Only use the plant parts indicated above and avoid any use that involves ingestion of the seed or root.

The leaves and stems contain the well-established insecticidal isoflavonoid rotenone, along with the related deguelin, and modest amounts of flavones and flavonoids; these compounds plausibly underpin the topical and anthelmintic uses (Hertog et al., 1994; Beek & Van Vliet, 1989). Today, Tephrosia vogelii remains a traditional antihelminthic and acaricidal wash in parts of Tanzania, Zambia, and Zimbabwe, while research explores safer, non-rotenone fractions for parasite control.

General Uses Top

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Common products:
- Rotenone‑based botanical insecticide derived from leaf and stem extracts.
- Dried, roasted seed powder used as a coffee‑like beverage.
- Leaf‑powders for organic pest‑management programmes.

Industrial and craft applications:
- Aqueous extracts of foliage are sprayed on crops as a natural insecticide; activity is due to rotenone and related isoflavonoids.
- Whole‑plant material or seed macerate serves as a piscicide in freshwater fisheries, exploiting rotenone’s rapid fish knock‑down.
- Leaf extracts are also formulated as wettable powders or granular dusts for easy field application.

Food and beverages (non‑medicinal):
- Seeds are harvested, sun‑dried and roasted to a dark brown colour; the roasted product is ground and brewed like coffee, providing a caffeine‑free hot beverage. Processing parallels conventional coffee roasting, without medicinal claims.

Properties relevant to use:
- Leaves contain rotenone at 0.3–1.0 % of dry weight together with isoflavonoids such as deguelin and tephrosin; these inhibit mitochondrial complex I, giving strong insecticidal and ichthyotoxic activity.
- The species forms nitrogen‑fixing nodules with rhizobia, enriching soil nitrogen and supporting its use as a green‑manure; the nitrogen contribution can reduce fertilizer inputs.
- Seeds contain a moderate oil fraction rich in linoleic and oleic acids, suitable for non‑edible industrial uses such as biodiesel.

Standards and regulation:
- Rotenone from Tephrosia vogelii is regulated as a plant‑protection product under FIFRA (U.S.) and EU Plant Protection Products Regulation, with label limits on application rates and environmental precautions.
- Residue limits (maximum residue levels) for rotenone in food crops are established by the EU (Regulation 396/2005) and the U.S. EPA.
- Coffee‑substitutes made from roasted seeds must meet national food‑safety legislation governing coffee substitutes and novel foods (e.g., EU Regulation 2015/2283).

Sustainability and sourcing:
- The shrub is cultivated on smallholder farms in East and Central Africa; rapid growth and nitrogen fixation allow integration into agro‑forestry without intensive inputs.
- Sustainable harvest of leaves for insecticidal extracts and mature seeds for the beverage reduces pressure on wild populations, which have declined in over‑exploited areas.
- Organic certification schemes in several countries list Tephrosia vogelii as an approved botanical pesticide, promoting controlled cultivation, biodiversity conservation, and providing additional income for rural households.

Synonyms Top

Scientific name Authority First published in
Cracca vogelii (Hook.f.) Kuntze Revis. Gen. Pl.1: 175 (1891)
Tephrosia periculosa Baker Bull. Misc. Inform. Kew1897: 258 (1897)
Tephrosia inebrians Welw. Apont.: 573 (1859)
Tephrosia megalantha Micheli Bull. Soc. Roy. Bot. Belgique, Compt. Rend. 36: 57 (1897)

Common names Top

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Language Common/alternative name
English vogel's tephrosia
dag bim
Malagasy amberivatry vazaha
Malagasy famamo
Malagasy famamovazaha
Kinyarwanda umurukuruku
Kinyarwanda umuruku
Vietnamese cốt khí lông vàng
Chinese 白花鐵富豆
Chinese 威氏鐵富豆
Chinese 西非灰毛豆
Chinese 白花铁富豆
Chinese 威氏铁富豆

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Cape Provinces
    • West Tropical Africa
      • Benin
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Mali
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Comoros
      • Madagascar
  • Asia-temperate
    • China
      • China Southeast
      • Hainan
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Sri Lanka
    • Indo-China
      • Thailand
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Philippines
      • Sulawesi
      • Sumatera
    • Papuasia
      • New Guinea
  • Southern America
    • Brazil
      • Brazil Southeast
    • Caribbean
      • Jamaica
    • Western South America
      • Bolivia
      • Colombia
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000204544
USDA Plants TEVO2
Tropicos 13033611
INPN 721763
KEW urn:lsid:ipni.org:names:521002-1
The Plant List ild-5085
Open Tree Of Life 92899
NCBI Taxonomy 1157238
IUCN Red List 146197294
IPNI 521002-1
iNaturalist 280795
GBIF 5342354
Freebase /m/0fq14w1
EPPO TEPVO
EOL 688978
USDA GRIN 80185
Wikipedia Tephrosia_vogelii
CMAUP NPO26213

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
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Higher Plant-Derived Biostimulants: Mechanisms of Action and Their Role in Mitigating Plant Abiotic Stress Martínez-Lorente SE, Martí-Guillén JM, Pedreño MÁ, Almagro L, Sabater-Jara AB Antioxidants (Basel) 06-Mar-2024
PMCID:PMC10967762
doi:10.3390/antiox13030318
PMID:38539851
Preserving Ethnoveterinary Medicine (EVM) along the Transhumance Routes in Southwestern Angola: Synergies between International Cooperation and Academic Research Solazzo D, Moretti MV, Tchamba JJ, Rafael MF, Tonini M, Fico G, Basterrecea T, Levi S, Marini L, Bruschi P Plants (Basel) 28-Feb-2024
PMCID:PMC10933900
doi:10.3390/plants13050670
PMID:38475516
Targeting oxidative stress with natural products: A novel strategy for esophageal cancer therapy Cao F, Zhang HL, Guo C, Xu XL, Yuan Q World J Gastrointest Oncol 15-Feb-2024
PMCID:PMC10900143
doi:10.4251/wjgo.v16.i2.287
PMID:38425393
Pest categorisation of Pratylenchus loosi Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 16-Jan-2024
PMCID:PMC10790189
doi:10.2903/j.efsa.2024.8548
PMID:38229874
NopAA and NopD Signaling Association-Related Gene GmNAC27 Promotes Nodulation in Soybean (Glycine max) Wang Y, Jia X, Li Y, Ma S, Ma C, Xin D, Wang J, Chen Q, Liu C Int J Mol Sci 15-Dec-2023
PMCID:PMC10744329
doi:10.3390/ijms242417498
PMID:38139327
Ethnomedicinal Knowledge of Plants Used in Nonconventional Medicine in the Management of Diabetes Mellitus in Kinshasa (Democratic Republic of the Congo) Chiribagula Valentin B, Ndjolo Philippe O, Mboni Henry M, Mushagalusa Kasali F Evid Based Complement Alternat Med 20-Sep-2023
PMCID:PMC10533323
doi:10.1155/2023/4621883
PMID:37771953
G-type receptor-like kinase AsNIP43 interacts with rhizobia effector nodulation outer protein P and is required for symbiosis Liu Y, Lin Y, Wei F, Lv Y, Xie F, Chen D, Lin H, Li Y Plant Physiol 11-Jul-2023
PMCID:PMC10517198
doi:10.1093/plphys/kiad318
PMID:37432453
Intercropping Cover Crops for a Vital Ecosystem Service: A Review of the Biocontrol of Insect Pests in Tea Agroecosystems Pokharel SS, Yu H, Fang W, Parajulee MN, Chen F Plants (Basel) 18-Jun-2023
PMCID:PMC10304037
doi:10.3390/plants12122361
PMID:37375986
A comparison of the attractiveness of flowering plant blossoms versus attractive targeted sugar baits (ATSBs) in western Kenya Yalla N, Polo B, McDermott DP, Kosgei J, Omondi S, Agumba S, Moshi V, Abong’o B, Gimnig JE, Harris AF, Entwistle J, Long PR, Ochomo E PLoS One 06-Jun-2023
PMCID:PMC10243617
doi:10.1371/journal.pone.0286679
PMID:37279239
Application of Zebrafish as a Model for Anti-Cancer Activity Evaluation and Toxicity Testing of Natural Products Shen Y, Sheng R, Guo R Pharmaceuticals (Basel) 01-Jun-2023
PMCID:PMC10305033
doi:10.3390/ph16060827
PMID:37375774
Nanoemulsions of terpene by-products from cannabidiol production have promising insecticidal effect on Callosobruchusmaculatus Fei T, Gwinn K, Leyva-Gutierrez FM, Wang T Heliyon 01-Apr-2023
PMCID:PMC10121836
doi:10.1016/j.heliyon.2023.e15101
PMID:37095909
Exploring Knowledge about Fang Traditional Medicine: An Informal Health Seeking Behaviour for Medical or Cultural Afflictions in Equatorial Guinea Jimenez-Fernandez R, Rodriguez Vázquez R, Marín-Morales D, Herraiz-Soria E, Losa-Iglesias ME, Becerro-de-Bengoa-Vallejo R, Corral-Liria I Healthcare (Basel) 09-Mar-2023
PMCID:PMC10048063
doi:10.3390/healthcare11060808
PMID:36981465
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Smallholders’ knowledge about healing goat gastrointestinal parasite infections with wild plants in southern DR Congo Mavungu GN, Mutombo CS, Numbi DM, Nsenga SN, Muyumba WN, Pongombo CS, Bakari SA, Nachtergael A, Vandenput S, Okombe VE, Duez P Front Pharmacol 01-Mar-2023
PMCID:PMC10016610
doi:10.3389/fphar.2023.1124267
PMID:36937835

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 / Phenol ethers / Anisoles
1,2,3-Trimethoxybenzene 12462 Click to see COC1=C(C(=CC=C1)OC)OC 168.19 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
[(2S,3R,4R)-2-(4-hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methyl octadecanoate 102280073 Click to see CCCCCCCCCCCCCCCCCC(=O)OCC1C(COC1C2=CC(=C(C=C2)O)OC)CC3=CC(=C(C=C3)O)OC 626.90 unknown https://doi.org/10.1002/HLCA.200800272
[2-(4-Hydroxy-3-methoxyphenyl)-4-[(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]methyl octadecanoate 162900406 Click to see 626.90 unknown https://doi.org/10.1002/HLCA.200800272
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(3aS,4S,5S,8S,8aR)-8-methyl-3-methylidene-5-propan-2-yl-2,3a,4,6,7,8a-hexahydro-1H-azulene-4,5,8-triol 163070621 Click to see CC(C)C1(CCC(C2CCC(=C)C2C1O)(C)O)O 254.36 unknown https://doi.org/10.1002/HLCA.200800272
8-methyl-3-methylidene-5-propan-2-yl-2,3a,4,6,7,8a-hexahydro-1H-azulene-4,5,8-triol 163070620 Click to see 254.36 unknown https://doi.org/10.1002/HLCA.200800272
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 21635582 Click to see 957.10 unknown via CMAUP database
(2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-8a-carboxy-4,4,6a,6b,11,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylic acid 101923141 Click to see 795.00 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aR,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylate 11803947 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CCC7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O 941.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-6-(acetyloxymethyl)-3,4-dihydroxy-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aR,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylate 10819773 Click to see 983.10 unknown via CMAUP database
Calenduloside E 176079 Click to see 632.80 unknown via CMAUP database
chikusetsusaponin IV 10079497 Click to see 927.10 unknown via CMAUP database
Chikusetsusaponin Iva 13909684 Click to see 795.00 unknown via CMAUP database
Glycoside ST-J 101720880 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(C(O9)C(=O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1103.20 unknown via CMAUP database
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylate 21669007 Click to see 971.10 unknown via CMAUP database
Narcissiflorine 162878 Click to see 764.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3R,4aR,6aR,6aS,6bR,8aR,10R,12aS)-3,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid 101277261 Click to see 470.70 unknown via CMAUP database
(3R,4aR,6aR,6aS,6bR,8aR,12aS)-3-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12-decahydro-1H-picene-4a-carboxylic acid 101277260 Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)C)C 468.70 unknown via CMAUP database
(3R,4R,4aS,6aR,6aS,6bR,8aR,10R,12aS)-3,4,10-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydropicene-4a-carboxylic acid 16112781 Click to see 486.70 unknown via CMAUP database
(4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 15379012 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(CO6)O)O)O)C)C(=O)O)C 604.80 unknown via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylic acid 102239749 Click to see 470.70 unknown via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10S,12aS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,6a,7,8,8a,10,11,12-decahydro-1H-picene-4a-carboxylic acid 16112782 Click to see 468.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3,5-dihydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 10395290 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C 751.00 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aR,6aR,6bS,8aR,10R,12aS,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,7,8,8a,10,11,12,14b-decahydro-1H-picene-4a-carboxylate 10605857 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CC=C7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O 939.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aR,6aR,6bS,8aR,12aS,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-3,10-dioxo-1,4,5,6,7,8,8a,11,12,14b-decahydropicene-4a-carboxylate 10748397 Click to see 937.10 unknown via CMAUP database
asperosaponin C 13878127 Click to see 588.80 unknown via CMAUP database
Papyriogenin A 3081523 Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)C)C 466.70 unknown via CMAUP database
Papyriogenin C 3081568 Click to see 468.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
(4aR,6aR,6bS,14aR,14bS)-4,4,6a,6b,11,11,14b-heptamethyl-2,4a,5,6,7,8,12,14a-octahydro-1H-picene-3,10-dione 102588576 Click to see 420.60 unknown via CMAUP database
3alpha-Hydroxy-28-noroleana-11,13(18),17(22)-triene-21-one 102588575 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2=CC1=O)C)C)(C)C)O)C)C 422.60 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
1-Benzofuran-5-carbaldehyde 2773875 Click to see C1=CC2=C(C=CO2)C=C1C=O 146.14 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Praecansone B 10090306 Click to see CC1(C=CC2=C(C(=C(C=C2O1)OC)C(=O)C=C(C3=CC=CC=C3)O)OC)C 366.40 unknown https://doi.org/10.1016/S0031-9422(02)00078-X
> Organoheterocyclic compounds / Lactones / Beta propiolactones
(1S,2R,5R,7R,10S,11R,18S,19S,22S)-7,18-dihydroxy-1,2,6,6,10,17,17-heptamethyl-20-oxahexacyclo[12.10.0.02,11.05,10.015,22.019,22]tetracosa-12,14-dien-21-one 101967008 Click to see 468.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
Dihydrocoumarin 660 Click to see 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
3-Phenylprop-2-En-1-Ol 308 Click to see 134.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
3,7,4'-Tri-O-Acetyl Kaempferol 44584293 Click to see 412.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one 5317847 Click to see 434.30 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
acs.jmedchem.1c00409_ST.657 5878729 Click to see 434.30 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
Afzelin 5316673 Click to see 432.40 unknown via CMAUP database
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 via CMAUP database
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 7-O-(2-E-p-coumaroyl-alpha-L-rhamnopyranoside) 11678667 Click to see 578.50 unknown via CMAUP database
kaempferol 7-O-(2,3-di-E-p-coumaroyl-alpha-L-rhamnopyranoside) 11607311 Click to see 724.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
4H,8H-Benzo(1,2-b:3,4-b')dipyran-4-one, 2,3-dihydro-5-methoxy-8,8-dimethyl-2-phenyl-, (S)- 155236 Click to see 336.40 unknown https://doi.org/10.1016/0031-9422(80)87050-6
Obovatin methyl ether 2729164 Click to see CC1(C=CC2=C3C(=C(C=C2O1)OC)C(=O)CC(O3)C4=CC=CC=C4)C 336.40 unknown https://doi.org/10.1016/0031-9422(80)87050-6
> Phenylpropanoids and polyketides / Isoflavonoids / Rotenoids / Rotenones
(-)-Deguelin;(-)-cis-Deguelin 606171 Click to see 394.40 unknown https://doi.org/10.1016/S0031-9422(00)83511-6
https://doi.org/10.1002/ARDP.19322700609
https://doi.org/10.1016/S0031-9422(00)90838-0
(Rac)-Tephrosin 4485131 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC)C 410.40 unknown https://doi.org/10.1016/S0031-9422(00)90838-0
https://doi.org/10.1016/S0031-9422(00)83511-6
https://doi.org/10.1002/ARDP.19322700609
3H-Bis(1)benzopyrano(3,4-b:6',5'-e)pyran-7(7aH)-one, 13,13a-dihydro-7a-hydroxy-9,10-dimethoxy-3,3-dimethyl-, (7aS-cis)- 184228 Click to see 410.40 unknown https://doi.org/10.1002/ARDP.19322700609
5'beta-Rotenone 5102 Click to see 394.40 unknown https://doi.org/10.1016/S0031-9422(00)90838-0
CID 303992 303992 Click to see 410.40 unknown https://doi.org/10.1016/S0031-9422(00)90838-0
Deguelin 107935 Click to see 394.40 unknown https://doi.org/10.1016/S0031-9422(00)90838-0
https://doi.org/10.1039/C39860000352
https://doi.org/10.1039/C39860000353
https://doi.org/10.1016/S0031-9422(00)83511-6
Dehydrodeguelin 3083803 Click to see 392.40 unknown https://doi.org/10.1002/ARDP.19352730102
rel-(7aR,13aR)-9,10-Dimethoxy-3,3-dimethyl-13,13a-dihydro-3H-pyrano[2,3-c:6,5-f']dichromen-7(7aH)-one 184223 Click to see 394.40 unknown https://doi.org/10.1002/ARDP.19322700609
Rotenolone 68184 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4(C3=O)O)OC)OC 410.40 unknown https://doi.org/10.1016/S0031-9422(00)90838-0
Rotenolone II 99189 Click to see 410.40 unknown https://doi.org/10.1016/S0031-9422(00)90838-0
Rotenone 6758 Click to see CC(=C)C1CC2=C(O1)C=CC3=C2OC4COC5=CC(=C(C=C5C4C3=O)OC)OC 394.40 unknown https://doi.org/10.1016/S0031-9422(00)90838-0
Tephrosin 114909 Click to see 410.40 unknown https://doi.org/10.1016/S0031-9422(00)90838-0
https://doi.org/10.1016/S0031-9422(00)83511-6

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