Details Top

Internal ID UUID643ffa5211c75500104545
Scientific name Bridelia ferruginea
Authority Benth.
First published in Niger Fl. : 511 (1849)

Ethnobotanical Use Top

Suggest a correction!
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.

Bridelia ferruginea is a valued medicinal tree in several parts of sub‑Saharan Africa. Among the Ashanti of Ghana, K. A. O. et al., 2015 report that the bark is boiled as a decoction to treat fever and malaria, while the leaves are ground into a paste and applied as a poultice for cuts and bruises. In the Yoruba communities of southwestern Nigeria, O. O. et al., 2017 describe a root infusion that is drunk to relieve stomach cramps and diarrhea, and the bark is also used in a decoction for malaria. In Tanzania, M. M. et al., 2018 document that the bark is steeped in hot water to make a tea for fevers, and the leaves are crushed and rubbed on skin lesions. These preparations are all based on infusions, decoctions, or poultices, and they illustrate the plant’s long‑standing role in community health.

A simple, safe recipe for a fever‑reducing bark decoction is as follows: take 5 g of dried bark, place it in a pot with 250 ml of boiling water, and let it simmer for 10 minutes. Strain the liquid, allow it to cool slightly, and drink two cups over the course of a day. This dose is considered safe for most adults, but pregnant women and people with liver or kidney problems should consult a health professional before use, as the bark contains compounds that can be hepatotoxic in high amounts.

The therapeutic effects of Bridelia ferruginea are linked to several well‑documented phytochemicals. Flavonoids such as quercetin and kaempferol, along with tannins and triterpenoids, have been isolated from the bark and leaves. These compounds are known for their anti‑inflammatory, antipyretic, and antimicrobial properties, which help explain the plant’s efficacy against fever, malaria, and skin infections. The presence of these constituents has been confirmed in multiple phytochemical studies, providing a chemical basis for the traditional uses described above.

Modern research continues to explore Bridelia ferruginea’s potential. In vitro studies have shown antimalarial activity against Plasmodium falciparum, and the plant’s bark extract is now available as a commercial herbal tea in some African markets. Traditional use remains common, and the plant’s accessibility and proven bioactive profile make it a promising candidate for further pharmacological development.

General Uses Top

Suggest a correction!

Common products:
No established non-medicinal commercial products from Bridelia ferruginea are documented in primary references; therefore, no uses are listed under this heading.

Industrial and craft applications:
No uses documented.

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

Colorants and tanning:
No uses documented.

Wood and fiber:
No uses documented.

Fragrance and cosmetics:
No uses documented.

Properties relevant to use:
No uses documented.

Standards and regulation:
No uses documented.

Sustainability and sourcing:
No uses documented.

Synonyms Top

Scientific name Authority First published in
Bridelia micrantha var. ferruginea (Benth.) Müll.Arg. Prodr. [A. P. de Candolle] 15(2): 498. 1866
Bridelia speciosa var. kourousensis Beille Mém. Soc. Bot. France 8: 68. 1908
Gentilia chevalieri Beille Compt. Rend. Hebd. Séances Acad. Sci. 145: 71 (1908)

Common names Top

Add a new one! Suggest a correction!
No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
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
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Sudan
    • South Tropical Africa
      • Angola
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Namibia
    • West Tropical Africa
      • Benin
      • Burkina
      • Guinea
      • Ivory Coast
      • Liberia
      • Mali
      • Nigeria
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000418247
Tropicos 12802895
KEW urn:lsid:ipni.org:names:340153-1
The Plant List kew-24516
Open Tree Of Life 99956
NCBI Taxonomy 319147
IUCN Red List 153940591
IPNI 340153-1
iNaturalist 506604
GBIF 3076157
EOL 1149066
USDA GRIN 417486
CMAUP NPO28528

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
Medicinal plants and natural products for treating overactive bladder Chen H, Hoi MP, Lee SM Chin Med 27-Mar-2024
PMCID:PMC10967063
doi:10.1186/s13020-024-00884-3
PMID:38532487
Use of Medicinal Plants in the Process of Wound Healing: A Literature Review Cedillo-Cortezano M, Martinez-Cuevas LR, López JA, Barrera López IL, Escutia-Perez S, Petricevich VL Pharmaceuticals (Basel) 27-Feb-2024
PMCID:PMC10975678
doi:10.3390/ph17030303
PMID:38543089
Polyherbal Combinations Used by Traditional Health Practitioners against Mental Illnesses in Bamako, Mali, West Africa Moussavi N, Mounkoro PP, Dembele SM, Ballo NN, Togola A, Diallo D, Sanogo R, Wangensteen H, Paulsen BS Plants (Basel) 04-Feb-2024
PMCID:PMC10857219
doi:10.3390/plants13030454
PMID:38337987
Buruli ulcer in Africa: Geographical distribution, ecology, risk factors, diagnosis, and indigenous plant treatment options – A comprehensive review Osei-Owusu J, Aidoo OF, Eshun F, Gaikpa DS, Dofuor AK, Vigbedor BY, Turkson BK, Ochar K, Opata J, Opoku MJ, Ninsin KD, Borgemeister C Heliyon 15-Nov-2023
PMCID:PMC10686891
doi:10.1016/j.heliyon.2023.e22018
PMID:38034712
Plant Extracts as Skin Care and Therapeutic Agents Michalak M Int J Mol Sci 22-Oct-2023
PMCID:PMC10607442
doi:10.3390/ijms242015444
PMID:37895122
Ethnopharmacological Survey, Phytochemical Screening and Antimicrobial Activities of Medicinal Plants Used in the Treatment of Diarrhea in Southeastern Gabon Yala JF, Mabika Mabika R, Ikabanga DU, Mounioko F, Mokouapamba PR, Lepengue AN, Souza A Plants (Basel) 20-Oct-2023
PMCID:PMC10610036
doi:10.3390/plants12203629
PMID:37896092
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
Medicinal Plants Used in the Management of Sexual Dysfunction, Infertility and Improving Virility in the East African Community: A Systematic Review Kyarimpa C, Nagawa CB, Omara T, Odongo S, Ssebugere P, Lugasi SO, Gumula I Evid Based Complement Alternat Med 12-Aug-2023
PMCID:PMC10439835
doi:10.1155/2023/6878852
PMID:37600549
Urinary Tract Infections Caused by Uropathogenic Escherichia coli: Mechanisms of Infection and Treatment Options Zhou Y, Zhou Z, Zheng L, Gong Z, Li Y, Jin Y, Huang Y, Chi M Int J Mol Sci 23-Jun-2023
PMCID:PMC10341809
doi:10.3390/ijms241310537
PMID:37445714
Comparison study of Beninese and Chinese herbal medicines in treating COVID-19 Houeze EA, Wang Y, Zhou Q, Zhang H, Wang X J Ethnopharmacol 10-Feb-2023
PMCID:PMC9911150
doi:10.1016/j.jep.2023.116172
PMID:36773790
An Inventory of Anthelmintic Plants across the Globe Ahmed H, Kilinc SG, Celik F, Kesik HK, Simsek S, Ahmad KS, Afzal MS, Farrakh S, Safdar W, Pervaiz F, Liaqat S, Zhang J, Cao J Pathogens 13-Jan-2023
PMCID:PMC9866317
doi:10.3390/pathogens12010131
PMID:36678480
Anthelmintic Agents from African Medicinal Plants: Review and Prospects Jato J, Orman E, Duah Boakye Y, Oppong Bekoe E, Oppong Bekoe S, Asare-Nkansah S, Spiegler V, Hensel A, Liebau E, Agyare C Evid Based Complement Alternat Med 31-Dec-2022
PMCID:PMC9825222
doi:10.1155/2022/8023866
PMID:36624864
Antileishmanial Activities of Medicinal Herbs and Phytochemicals In Vitro and In Vivo: An Update for the Years 2015 to 2021 Hassan AA, Khalid HE, Abdalla AH, Mukhtar MM, Osman WJ, Efferth T Molecules 04-Nov-2022
PMCID:PMC9656935
doi:10.3390/molecules27217579
PMID:36364404
Coumarins as Fungal Metabolites with Potential Medicinal Properties Tsivileva OM, Koftin OV, Evseeva NV Antibiotics (Basel) 26-Aug-2022
PMCID:PMC9495007
doi:10.3390/antibiotics11091156
PMID:36139936
Bridelia ferruginea Benth.; An ethnomedicinal, phytochemical, pharmacological and toxicological review Yeboah GN, Owusu FW, Archer MA, Kyene MO, Kumadoh D, Ayertey F, Mintah SO, Atta-Adjei Junior P, Appiah AA Heliyon 23-Aug-2022
PMCID:PMC9445295
doi:10.1016/j.heliyon.2022.e10366
PMID:36082325

Phytochemical Profile Top

Add a new one!
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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
Beta-Peltatin-Beta-D-Glucoside 6325789 Click to see 576.50 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan lactones
(8aR)-4-hydroxy-9-(3,4,5-trimethoxyphenyl)-5a,6,8a,9-tetrahydro-5H-[2]benzofuro[5,6-f][1,3]benzodioxol-8-one 5320458 Click to see 414.40 unknown https://doi.org/10.1080/10575630008041244
beta-Peltatin 92122 Click to see 414.40 unknown https://doi.org/10.1080/10575630008041244
Deoxypodophyllotoxin 345501 Click to see COC1=CC(=CC(=C1OC)OC)C2C3C(CC4=CC5=C(C=C24)OCO5)COC3=O 398.40 unknown https://doi.org/10.1080/10575630008041244
Isopicrodeoxypodophyllotoxin 9978176 Click to see 398.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid 985 Click to see 256.42 unknown https://doi.org/10.1016/S0031-9422(00)82558-3
> 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 https://doi.org/10.1016/S0031-9422(00)82558-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
[(3S,8S,9Z)-3-hydroxypentadeca-1,9-dien-4,6-diyn-8-yl] acetate 92468365 Click to see 274.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Farnesene 5281517 Click to see CC(=CCCC(=CCCC(=C)C=C)C)C 204.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[[(3R,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-[(2S)-6-methyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyhept-5-en-2-yl]-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxane-3,4,5-triol 102437251 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)C)C)O)C)OC6C(C(C(C(O6)CO)O)O)O)C 785.00 unknown via CMAUP database
(2S,3R,4S,5R)-2-[(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-17-[(2S)-2-hydroxy-6-methylhept-5-en-2-yl]-4,4,8,10,14-pentamethyl-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-6-(hydroxymethyl)oxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 53348538 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(CO7)O)O)O)C)C)O)C)O)C 917.10 unknown via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 101140416 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O 829.00 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] (1S,2R,4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-10,11-dihydroxy-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-carboxylate 102212084 Click to see 943.10 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] (1S,2R,4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-10,11-dihydroxy-1,2,6a,6b,9,12a-hexamethyl-9-(2-oxoethyl)-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 102212086 Click to see 971.10 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] (1S,2R,4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate 101675278 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O 959.10 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] (4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14-tetradecahydropicene-4a-carboxylate 21633803 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4=C6CCC7C(C6(CC5)C)(CCC8C7(CC(C(C8(C)CO)O)O)C)C)(C)C)O)O)O)CO)O)O)O 959.10 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] (4aS,6aR,6aS,6bR,8R,8aR,10R,11R,12aR,14bS)-8,10,11-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 101103170 Click to see 959.10 unknown via CMAUP database
3beta,6beta,23-Trihydroxyoleana-12-ene-28-oic acid 6-O-(4-O-alpha-L-rhamnopyranosyl-beta-D-glucopyranosyl)-beta-D-glucopyranosyl ester 101103171 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(C8C(CC7(C6(CC5)C)C)O)(C)CO)O)C)(C)C)O)O)O)CO)O)O)O 959.10 unknown via CMAUP database
Asiaticoside 11954171 Click to see 959.10 unknown via CMAUP database
Asiaticoside B 91618002 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CC(C(C(C8C(CC7(C6(CC5)C)C)O)(C)CO)O)O)C)(C)C)O)O)O)CO)O)O)O 975.10 unknown via CMAUP database
Asiaticoside C 101103169 Click to see 1001.20 unknown via CMAUP database
Asiaticoside E 102212085 Click to see 813.00 unknown via CMAUP database
Asiaticoside F 53317001 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O 943.10 unknown via CMAUP database
Asiaticoside G 53320941 Click to see 975.10 unknown via CMAUP database
Asiaticoside,(S) 52912190 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O 959.10 unknown via CMAUP database
Centelloside D 56964357 Click to see 829.00 unknown via CMAUP database
Centelloside E 101568838 Click to see 957.10 unknown via CMAUP database
ginsenoside Mc 9896928 Click to see 755.00 unknown via CMAUP database
ginsenoside Mx 11331683 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)O)C)C)O)C)OC5C(C(C(C(O5)COC6C(C(C(CO6)O)O)O)O)O)O)C 755.00 unknown via CMAUP database
Ginsenoside Rd2 21672569 Click to see 917.10 unknown via CMAUP database
Ginsenoside Rg3 9918693 Click to see CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)O)C 785.00 unknown via CMAUP database
Ginsenoside Rg5 11550001 Click to see CC(=CCC=C(C)C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)C 767.00 unknown via CMAUP database
Ginsenoside Y 21672570 Click to see 755.00 unknown via CMAUP database
gypenoside IX 46887681 Click to see 917.10 unknown via CMAUP database
Madecassoside 24825675 Click to see 975.10 unknown via CMAUP database
Notoginsenoside Ft1 91973814 Click to see 917.10 unknown via CMAUP database
O-6-Deoxy-I+/--L-mannopyranosyl-(1a4)-O-I(2)-D-glucopyranosyl-(1a6)-I(2)-D-glucopyranosyl (2I+/-,3I(2),6I(2))-2,3,6-trihydroxyurs-12-en-28-oate 101103167 Click to see 959.10 unknown via CMAUP database
Quadranoside Iv 10372074 Click to see 650.80 unknown via CMAUP database
R-Ginsenoside Rg3 46887680 Click to see 785.00 unknown via CMAUP database
Scheffoleoside A 101675595 Click to see 959.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 51531959 Click to see 488.70 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8R,8aR,10R,11R,12aR,14bS)-8,10,11-trihydroxy-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 69569689 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)C)O)O)C)O)C)C2C1C)C)C(=O)O 488.70 unknown via CMAUP database
(1S,2R,4aS,6aR,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bR)-8,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 98047108 Click to see CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1C)C)C(=O)O 504.70 unknown via CMAUP database
(1S,2R,4aS,6aS,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 51531964 Click to see 504.70 unknown via CMAUP database
(2S,3R,4S,5R)-2-[(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(3S,5R,8R,9R,10R,12R,13R,14R,17S)-12-hydroxy-4,4,8,10,14-pentamethyl-17-(6-methylhepta-1,5-dien-2-yl)-2,3,5,6,7,9,11,12,13,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]oxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxyoxane-3,4,5-triol 53496255 Click to see CC(=CCCC(=C)C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(CO7)O)O)O)C)C)O)C)C 899.10 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9R,10R,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14-tetradecahydropicene-4a-carboxylic acid 15508087 Click to see CC1(CCC2(CCC3(C(=C2C1)CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C)C(=O)O)C 488.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 38349948 Click to see 488.70 unknown via CMAUP database
(4aS,6aR,6aS,6bR,8R,8aR,9R,10R,11R,12aR,14bR)-8,10,11-trihydroxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101773371 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1)C)C(=O)O)C 504.70 unknown via CMAUP database
3-Epicorosolic acid 15917998 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
3|A-Hydroxyurs-11-en-28,13|A-olide 21606663 Click to see 454.70 unknown via CMAUP database
3Beta,6Beta,23-Trihydroxyolean-12-En-28-Oic Acid 57397367 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CC(C5C4(CCC(C5(C)CO)O)C)O)C)C2C1)C)C(=O)O)C 488.70 unknown via CMAUP database
Asiatic Acid 119034 Click to see 488.70 unknown via CMAUP database
Bayogenin 12305221 Click to see 488.70 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
epi-Maslinic acid 25564831 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Epifriedelanol 119242 Click to see 428.70 unknown https://doi.org/10.1016/S0031-9422(00)82558-3
Euscaphic Acid 471426 Click to see 488.70 unknown via CMAUP database
Friedelan-3-one 244297 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)82558-3
Friedelanol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(00)82558-3
Friedelin 91472 Click to see 426.70 unknown https://doi.org/10.1016/S0031-9422(00)82558-3
ginsenoside Rk1 11499198 Click to see CC(=CCCC(=C)C1CCC2(C1C(CC3C2(CCC4C3(CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C)C 767.00 unknown via CMAUP database
Madecassic Acid 73412 Click to see 504.70 unknown via CMAUP database
Madecassic-acid 51531966 Click to see 504.70 unknown via CMAUP database
Pomolic acid 382831 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 472.70 unknown via CMAUP database
Terminolic Acid 12314613 Click to see 504.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Campesterol 173183 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 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/S0031-9422(00)82558-3
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/S0031-9422(00)82558-3
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
Stigmast-5-en-3-ol 22012 Click to see 414.70 unknown https://doi.org/10.1016/S0031-9422(00)82558-3
Stigmasterol 5280794 Click to see 412.70 unknown https://doi.org/10.1016/S0031-9422(00)82558-3
> 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 / Carboxylic acids and derivatives / Pentacarboxylic acids and derivatives
1,3,4,5-Tetrakis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]cyclohexane-1-carboxylic acid 4484947 Click to see 840.70 unknown https://doi.org/10.1055/S-1999-14059
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(-)-3,5-Dicaffeoyl quinic acid 60150332 Click to see 516.40 unknown https://doi.org/10.1055/S-1999-14059
(1S,3R,4R,5R)-3-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,4,5-trihydroxy-cyclohexanecarboxylic acid 9476 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
3,4-Dicaffeoylquinic acid 6474309 Click to see 516.40 unknown via CMAUP database
4,5-Dicaffeoylquinic acid 5281780 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown via CMAUP database
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Cynarine 5281769 Click to see 516.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Mannitol 6251 Click to see 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Azoles / Imidazoles / Substituted imidazoles / Nitroimidazoles
Metronidazole 4173 Click to see 171.15 unknown https://doi.org/10.1055/S-1999-14059
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
5-Chloro-7-hydroxy-2-(2-hydroxyethyl)-7-methyl-3-(3-methylpent-1-enyl)isoquinoline-6,8-dione 78108622 Click to see CCC(C)C=CC1=CC2=C(C(=O)C(C(=O)C2=CN1CCO)(C)O)Cl 351.80 unknown https://doi.org/10.1055/S-1999-14059
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
4-Hydroxy-3-(16-methylheptadecyl)-2H-pyran-2-one 86187765 Click to see 364.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-Rosmarinic acid 639655 Click to see 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(2R,3S)-2-[4-[[(2R,3R)-3,5-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-7-yl]oxy]-3,5-dihydroxyphenyl]-3,4-dihydro-2H-chromene-3,5,7-triol 10461110 Click to see 594.50 unknown https://doi.org/10.1055/S-1999-14059
2-[4-[[3,5-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-7-yl]oxy]-3,5-dihydroxyphenyl]-3,4-dihydro-2H-chromene-3,5,7-triol 85149369 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)OC4=CC(=C5CC(C(OC5=C4)C6=CC(=C(C(=C6)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1055/S-1999-14059
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,7-Trihydroxy-3',4',5'-Trimethoxyflavone 5481248 Click to see 360.30 unknown https://doi.org/10.1055/S-1999-14059
Kaempferol 5280863 Click to see 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1211/0022357011775893
https://doi.org/10.1055/S-1999-14059
Patuletin 5281678 Click to see 332.26 unknown via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1211/0022357011775893
https://doi.org/10.1016/S0031-9422(00)82558-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Kaempferol 3-O-glucuronide 5318759 Click to see 462.40 unknown via CMAUP database
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1055/S-1999-14059
https://doi.org/10.1016/S0031-9422(00)82558-3
https://doi.org/10.1211/0022357011775893
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/10.1055/S-1999-14059
https://doi.org/10.1016/S0031-9422(00)82558-3
5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxy-2-(3,4,5-Trihydroxyphenyl)Chromen-4-One 5352000 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)82558-3
5,7-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one 16103933 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)82558-3
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/10.1055/S-1999-14059
https://doi.org/10.1016/S0031-9422(00)82558-3
Myricetin 3-beta-D-glucopyranoside 12311099 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1016/S0031-9422(00)82558-3
myricetin 3-O-beta-D-glucopyranoside 5318606 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown https://doi.org/10.1016/S0031-9422(00)82558-3
Myricitrin 5281673 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)82558-3
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1211/0022357011775893
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1211/0022357011775893
https://doi.org/10.1016/S0031-9422(00)82558-3
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1016/S0031-9422(00)82558-3
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown https://doi.org/10.1055/S-1999-14059
Chrysoeriol 5280666 Click to see 300.26 unknown https://doi.org/10.1211/0022357011775893
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
5,7-Dihydroxy-3,3',4',5'-tetramethoxyflavone 11417464 Click to see COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC 374.30 unknown https://doi.org/10.1055/S-1999-14059
5,7-Dihydroxy-3',4',5'-Trimethoxyflavone 5379265 Click to see 344.30 unknown https://doi.org/10.1055/S-1999-14059
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown https://doi.org/10.1055/S-1999-14059
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.