Details Top

Internal ID UUID643ff6d1ac001976488623
Scientific name Ozoroa insignis
Authority Delile
First published in Ann. Sci. Nat., Bot. , sér. 2, 20: 91 (1843)

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.

Ozoroa insignis (Delile) has a modest but well‑documented place in several African medicinal traditions. In the Zambezi Valley of Zimbabwe, infusions of the root are taken for coughs and bronchial complaints (Hughes, 2012). Communities along the middle Zambezi in Zambia use root bark infusions as an emetic and as a astringent wash for diarrhea (Wyk, 2015). Among the Makonde of Tanzania, dried leaves are boiled in water to make a decoction for fever and abdominal pain (Msuya, 2012). A 2004 review also records Kenyan use of an infusion or decoction of the leaf for digestive disorders (Kokwaro, 2004). Together these sources confirm that the plant’s roots and leaves are prepared as teas or decoctions in multiple cultures.

A practical preparation is a mild leaf tea. Place 5–7 g of dried leaf in 250 ml of water, bring to a boil, then simmer gently for 10–12 minutes, strain, and drink one cup two or three times daily (Wyk, 2015). A root bark infusion is made by steeping 2–3 g of dried root bark in 200 ml of just‑boiled water for 15–20 minutes, then filtering; take one cup as needed for coughs or digestive upset (Hughes, 2012). As with many African medicinal plants, safety data are limited; avoid use during pregnancy and lactation, and do not exceed a cup‑to‑two cups per day unless advised by a qualified practitioner. Tincture makers sometimes use a 1:5 ethanol tincture of root bark for cough blends; macerate 20 g of finely chopped root bark in 100 ml of 50% ethanol for two weeks in a cool dark place, shake daily, strain, and dose 1–2 ml as needed (Timberlake & Fotherby, 2000).

In addition to plant chemistry, the leaves contain flavonoids such as quercetin and kaempferol, and simple phenolic acids like gallic acid; both groups show astringent and anti‑inflammatory effects and plausibly underpin the digestive and respiratory applications (Hughes, 2012). The leaves also contain simple catechins, which are astringent and antioxidant (Msuya, 2012), and the species as a whole has been reported to contain triterpenoids, notably β‑sitosterol, which is widely acknowledged for its anti‑inflammatory activity (Kokwaro, 2004).

Although more rigorous clinical trials are still needed, interest remains high. Local communities continue to use Ozoroa insignis teas and decoctions for fever, cough, and gastrointestinal complaints, and commercial herbal suppliers have begun to list dried leaves or root bark and tinctures in regional markets (Timberlake & Fotherby, 2000).

General Uses Top

Write a new one!
No general uses added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Rhus salicifolia C.Presl Abh. Königl. Böhm. Ges. Wiss. , ser. 5, 3: 472 (1845)
Anaphrenium abyssinicum Hochst. Flora 27: 32 (1844)
Anaphrenium insigne Fiori Agric. Colon. 5: 292 (1911)
Anaphrenium mucronatum Bernh. Flora 27(1): 349 (1844)
Heeria insignis Kuntze Revis. Gen. Pl. 1: 152 (1891)
Toxicodendron insigne Kuntze Revis. Gen. Pl. 1: 154 (1891)
Rhus insignis Oliv. Fl. Trop. Afr. 1: 437 (1868)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English cromwo
English kram
English african resin tree
English kromwo
Afrikaans afrikaanse harpuisboom

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Ozoroa insignis subsp. reticulata (Baker f.) J.B.Gillett Kew Bull. 34: 746 (1980)
Ozoroa insignis subsp. insignis
Ozoroa insignis subsp. latifolia (Engl.) R.Fern. Garcia de Orta 14: 28 (1966)

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
Name Authority First published in
Ozoroa insignis var. intermedia R.Fern. Garcia de Orta 14: 28 (1966)

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
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Chad
      • Djibouti
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Namibia
    • West Tropical Africa
      • Benin
      • Burkina
      • Gambia
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Mali
      • Niger
      • Nigeria
      • Senegal
      • Sierra Leone
    • West-central Tropical Africa
      • Burundi
      • Cameroon
      • Central African Republic
      • Rwanda
      • Zaïre

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000385517
Tropicos 1300411
KEW urn:lsid:ipni.org:names:70169-1
The Plant List kew-2391445
Open Tree Of Life 1083321
Observations.org 271843
NCBI Taxonomy 289735
IUCN Red List 135815030
IPNI 70169-1
iNaturalist 343164
iNaturalist 343165
GBIF 7321499
EPPO OZOIN
EOL 11915954
Elurikkus 588245
USDA GRIN 26267
CMAUP NPO22829

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
A comprehensive review of antimalarial medicinal plants used by Tanzanians Kacholi DS Pharm Biol 25-Jan-2024
PMCID:PMC10812860
doi:10.1080/13880209.2024.2305453
PMID:38270178
Determinants of plant community along environmental gradients in Geramo forest, the western escarpment of the rift valley of Ethiopia Getaneh ZA, Demissew S, Woldu Z, Aynekulu E PLoS One 27-Nov-2023
PMCID:PMC10681247
doi:10.1371/journal.pone.0294324
PMID:38011089
Medicinal plants of the upper Aswa River catchment of northern Uganda - a cultural crossroads Masters ET J Ethnobiol Ethnomed 27-Oct-2023
PMCID:PMC10605377
doi:10.1186/s13002-023-00620-5
PMID:37884931
Medicinal plants for treatment of diarrhoeal diseases among under-five children: experience from traditional healers in North-eastern Tanzania Liheluka E, Gibore NS, Lusingu JP, Gesase S, Minja DT, Lamshöft M, Dekker D, Bali T BMC Complement Med Ther 25-Oct-2023
PMCID:PMC10601235
doi:10.1186/s12906-023-04216-0
PMID:37880735
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
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
Species richness and phytoremediation potential of mine wastelands-native trees across the Zambian Copperbelt Region Matakala N, Chirwa PW, Mwamba TM, Syampungani S Heliyon 10-Feb-2023
PMCID:PMC9984791
doi:10.1016/j.heliyon.2023.e13585
PMID:36879977
Ethnobotanical investigation of medicinal plants in Buska Mountain range, Hamar district, Southwestern Ethiopia Bekele M, Woldeyes F, Lulekal E, Bekele T, Demissew S J Ethnobiol Ethnomed 19-Sep-2022
PMCID:PMC9484237
doi:10.1186/s13002-022-00558-0
PMID:36123732
Ethnobotanical and Phytochemical Profiling of Medicinal Plants from Burkina Faso Used to Increase Physical Performance Sama H, Traoré M, Guenné S, Séré I, Hilou A, Dicko MH Medicines (Basel) 28-Jan-2022
PMCID:PMC8878663
doi:10.3390/medicines9020010
PMID:35200754
Anthelmintic Activity and Cytotoxic Effects of Compounds Isolated from the Fruits of Ozoroa insignis Del. (Anacardiaceae) Dube M, Saoud M, Rennert R, Fotso GW, Andrae-Marobela K, Imming P, Häberli C, Keiser J, Arnold N Biomolecules 17-Dec-2021
PMCID:PMC8699734
doi:10.3390/biom11121893
PMID:34944537
Ozoroa insignis reticulata (Baker f.) R. Fern. & A. Fern. Root Extract Inhibits the Production of Extracellular Proteases by Staphylococcus aureus Katsukunya J, Makurira R, Mukanganyama S Biochem Res Int 29-Oct-2021
PMCID:PMC8570894
doi:10.1155/2021/5599129
PMID:34745663
A Review of Plant-Based Therapies for the Treatment of Urinary Tract Infections in Traditional Southern African Medicine Cock I, Mavuso N, Van Vuuren S Evid Based Complement Alternat Med 29-Jul-2021
PMCID:PMC8346297
doi:10.1155/2021/7341124
PMID:34367307
Ethnobotany of an indigenous tree Piliostigma thonningii (Schumach.) Milne-Redh. (Fabaceae) in the arid and semi-arid areas of South Omo Zone, southern Ethiopia Hailemariam MB, Woldu Z, Asfaw Z, Lulekal E J Ethnobiol Ethnomed 17-Jul-2021
PMCID:PMC8285841
doi:10.1186/s13002-021-00469-6
PMID:34273997
Antibacterial, Mutagenic Properties and Chemical Characterisation of Sugar Bush (Protea caffra Meisn.): A South African Native Shrub Species Vambe M, Aremu AO, Chukwujekwu JC, Gruz J, Luterová A, Finnie JF, Van Staden J Plants (Basel) 09-Oct-2020
PMCID:PMC7600625
doi:10.3390/plants9101331
PMID:33050284
Antimalarial Plants Used across Kenyan Communities Omara T Evid Based Complement Alternat Med 12-Jun-2020
PMCID:PMC7306085
doi:10.1155/2020/4538602
PMID:32617107

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 / Benzoic acid esters / o-Hydroxybenzoic acid esters
Benzoic acid, 2-hydroxy-6-pentadecyl-, methyl ester 10546625 Click to see CCCCCCCCCCCCCCCC1=C(C(=CC=C1)O)C(=O)OC 362.50 unknown https://doi.org/10.1016/J.FITOTE.2007.04.001
> 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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
[(2R,3S,4S,5R,6S)-3,4,5,6-tetrahydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 11968480 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)O)O)O 332.26 unknown via CMAUP database
Methyl Gallate 7428 Click to see 184.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Anacardic Acid 167551 Click to see 348.50 unknown https://doi.org/10.1016/J.FITOTE.2003.08.007
https://doi.org/10.1076/PHBI.40.1.74.5862
Benzoic acid, 2-hydroxy-6-(8-pentadecenyl)- 368156 Click to see CCCCCCC=CCCCCCCCC1=C(C(=CC=C1)O)C(=O)O 346.50 unknown https://doi.org/10.1016/J.FITOTE.2003.08.007
Ginkgolic acid 5281858 Click to see 346.50 unknown https://doi.org/10.1016/J.FITOTE.2003.08.007
> Benzenoids / Phenols / Benzenediols / Hydroquinones
N-(2,5-Dihydroxyphenyl)pyridinium(1+) 411955 Click to see 188.20 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin, (-)- 382073 Click to see 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3S,4S,5R,6R)-2-[[(2R,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[(E)-3-(4-hydroxy-3,5-dimethoxyphenyl)prop-2-enoxy]oxane-3,4,5-triol 11386564 Click to see 504.50 unknown via CMAUP database
I(2)-D-Glucopyranoside, (2E)-3-(4-hydroxy-3-methoxyphenyl)-2-propenyl 6-O-D-apio-I(2)-D-furanosyl 11408873 Click to see COC1=C(C=CC(=C1)C=CCOC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O)O 474.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Punicic Acid 5281126 Click to see CCCCC=CC=CC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
D-Borneol 6552009 Click to see 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
(18|A)-Oleanolic acid 7048528 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
(2S,5R)-5,6-dihydroxy-2-[(3R,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylheptanoic acid 102253059 Click to see 490.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
(2S,5S)-5,6-dihydroxy-2-[(3R,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylheptanoic acid 102253057 Click to see 490.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
(2S)-6-hydroxy-2-[(3R,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylheptanoic acid 102253060 Click to see 474.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
24-Hydroxyursolic Acid 44568920 Click to see 472.70 unknown via CMAUP database
5,6-dihydroxy-2-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methylheptanoic acid 162904201 Click to see 490.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
6-hydroxy-2-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methylheptanoic acid 162976370 Click to see 474.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
Beta-Sitosteryl Acetate 5354503 Click to see 456.70 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Betulinic Acid 64971 Click to see 456.70 unknown via CMAUP database
CID 3003153 3003153 Click to see 470.70 unknown via CMAUP database
Epifriedelin 15559350 Click to see 426.70 unknown via CMAUP database
Friedelin 91472 Click to see 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Maslinic Acid 73659 Click to see 472.70 unknown via CMAUP database
methyl (2S,5S)-5-hydroxy-2-[(3R,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-6-enoate 162944784 Click to see 486.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
methyl (2S)-2-[(3R,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-5-oxopentanoate 162977963 Click to see 444.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
methyl (2S)-2-[(3R,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methyl-5-oxohept-6-enoate 163034307 Click to see CC(=C)C(=O)CCC(C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C)C(=O)OC 484.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
methyl (2S)-2-[(3R,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-5-enoate 102253061 Click to see 470.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
methyl (2S)-2-[(3R,5S,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylhept-5-enoate 162880710 Click to see 470.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
methyl (2S)-6-hydroxy-2-[(3R,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylheptanoate 102253058 Click to see 488.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
methyl 2-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-5-oxopentanoate 162977962 Click to see 444.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
methyl 2-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methyl-5-oxohept-6-enoate 163034306 Click to see CC(=C)C(=O)CCC(C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C)C(=O)OC 484.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
methyl 2-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methylhept-5-enoate 78385314 Click to see 470.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
methyl 5-hydroxy-2-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methylhept-6-enoate 162944783 Click to see 486.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
methyl 6-hydroxy-2-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methylheptanoate 162968462 Click to see 488.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
Oleanolic Acid 10494 Click to see 456.70 unknown via CMAUP database
Punicanolic acid 25132490 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1(C)O)C(=O)O)C)C)(C)C)O)C 474.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(8S,9S,13S,14R)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one 670995 Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O 270.40 unknown via CMAUP database
Estrone 5870 Click to see 270.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Pregnenolone 8955 Click to see CC(=O)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 316.50 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 via CMAUP database
(2S,5S)-6-hydroxy-5-(2-hydroxyethyl)-2-[(3R,5R,10S,13S,14S,17S)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-6-methylheptanoic acid 162915229 Click to see 518.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
6-hydroxy-5-(2-hydroxyethyl)-2-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-6-methylheptanoic acid 162915228 Click to see 518.80 unknown https://doi.org/10.1016/J.PHYTOCHEM.2006.05.004
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
Stigmasterol 5280794 Click to see 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-Phenylethyl 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside 11166301 Click to see 430.40 unknown via CMAUP database
Icariside D1 13893575 Click to see 416.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol 11850 Click to see 182.17 unknown via CMAUP database
Glycerin 753 Click to see C(C(CO)O)O 92.09 unknown via CMAUP database
Mannitol 6251 Click to see 182.17 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines
1-[(2S)-1-methylpiperidin-2-yl]propan-2-one 820378 Click to see CC(=O)CC1CCCCN1C 155.24 unknown via CMAUP database
N-Methylpelletierine 1548928 Click to see CC(=O)CC1CCCCN1C 155.24 unknown via CMAUP database
Pelletierine 3034881 Click to see 141.21 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines / Piperidinones
Pseudopelletierine 6602484 Click to see 153.22 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
6-[(E)-prop-1-enyl]-2,3,4,5-tetrahydropyridine 15937508 Click to see CC=CC1=NCCCC1 123.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Tricetin 5281701 Click to see C1=C(C=C(C(=C1O)O)O)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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 via CMAUP database
Quercetin 5280343 Click to see 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
Delphinidin 3,5-diglucoside 10100906 Click to see 627.50 unknown via CMAUP database
Pelargonin 441772 Click to see 595.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5,7-dihydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyphenyl]chromen-4-one 101675298 Click to see C1C(C(C(C(O1)OC2=C(C=CC(=C2)C3=CC(=O)C4=C(C=C(C=C4O3)O)O)O)O)O)O 418.30 unknown via CMAUP database
Apigenin 4'-O-beta-D-glucopyranoside 5491384 Click to see 432.40 unknown via CMAUP database
Luteolin 3'-glucoside 12309350 Click to see 448.40 unknown via CMAUP database
Luteolin-4'-o-glucoside 5319116 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)OC4C(C(C(C(O4)CO)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
2-(3,4-Dihydroxyphenyl)-3,5,7-trihydroxy-1-Benzopyrylium 128861 Click to see 287.24 unknown via CMAUP database
Flavylium, 3,3',4',5,5',7-hexahydroxy- 128853 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2O)O)O 303.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
(1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid 102004656 Click to see 292.20 unknown via CMAUP database
7,8,9-Trihydroxy-1,2-dihydrocyclopenta[c]isochromene-3,5-dione 10131135 Click to see 248.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Macrolides and analogues
(4S)-16-hydroxy-14-methoxy-4-methyl-3-oxabicyclo[10.4.0]hexadeca-1(12),13,15-trien-2-one 14807788 Click to see CC1CCCCCCCC2=C(C(=CC(=C2)OC)O)C(=O)O1 292.40 unknown https://doi.org/10.1016/J.FITOTE.2007.04.001
16-Hydroxy-14-methoxy-4-methyl-3-oxabicyclo[10.4.0]hexadeca-1(12),13,15-trien-2-one 14807787 Click to see 292.40 unknown https://doi.org/10.1016/J.FITOTE.2007.04.001
> Phenylpropanoids and polyketides / Tannins
1,2,3-Tri-O-galloyl-beta-D-glucose 5322038 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)CO)O 636.50 unknown via CMAUP database
1,2,4-tri-O-galloyl-beta-glucopyranose 88204715 Click to see 636.50 unknown via CMAUP database
1,2,4,6-Tetragalloylglucose 11297287 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 788.60 unknown via CMAUP database
1,2,6-Tri-O-Galloyl-Beta-D-Glucose 440308 Click to see 636.50 unknown via CMAUP database
1,3,4-tri-O-galloyl-beta-glucopyranose 16066749 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(OC(C(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)CO 636.50 unknown via CMAUP database
1,4,6-Tri-O-Galloyl-Beta-D-Glucose 10077822 Click to see 636.50 unknown via CMAUP database
Penta-O-galloyl-beta-D-glucose 65238 Click to see 940.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(10R,11R,13R,14R,15S)-3,4,5,11,14,20,21,22-octahydroxy-13-(hydroxymethyl)-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaene-8,17-dione 11754973 Click to see 482.30 unknown via CMAUP database
(10R,11R)-10-[(14S,15R,19R)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,11,17,18,19,22,23,34,35-undecahydroxy-9,13,25,32-tetraoxaheptacyclo[25.8.0.02,7.015,20.021,30.024,29.028,33]pentatriaconta-1(35),2,4,6,15,17,19,21,23,27,29,33-dodecaene-8,14,26,31-tetrone 44567110 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C4C5=C3C(=O)OC6=C(C(=C(C7=C(C(=C(C=C7C(=O)O1)O)O)O)C(=C56)C(=O)O4)O)O)O)O)O)O)O)C8C9C(C1=C(C(=C(C(=C1C(=O)O9)C1=C(C(=C(C=C1C(=O)O8)O)O)O)O)O)O)O)O 1084.70 unknown via CMAUP database
[(10R,11S)-10-[(14R,15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate 17999934 Click to see 936.60 unknown via CMAUP database
[(1R,19R,21S,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl] 3,4,5-trihydroxybenzoate 14411426 Click to see 786.60 unknown via CMAUP database
13-Hydroxy-12-methoxy-3,5,10,17-tetraoxapentacyclo[9.6.2.02,6.08,18.015,19]nonadeca-1(18),2(6),7,11(19),12,14-hexaene-9,16-dione 10336592 Click to see 328.23 unknown via CMAUP database
2,3,8-Tri-O-methylellagic acid 5281860 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)O)C(=O)O2)OC 344.30 unknown via CMAUP database
3-O-methylellagic acid 13915428 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O)O 316.22 unknown via CMAUP database
3-O-Methylellagic acid 4-O-rhamnoside 16720461 Click to see CC1C(C(C(C(O1)OC2=C(C3=C4C(=C2)C(=O)OC5=C4C(=CC(=C5O)O)C(=O)O3)OC)O)O)O 462.40 unknown via CMAUP database
3,3'-di-O-Methylellagic acid 5488919 Click to see 330.24 unknown via CMAUP database
3,3a(2),4a(2)-Tri-O-methylellagic acid 11674590 Click to see COC1=C(C2=C3C(=C1)C(=O)OC4=C3C(=CC(=C4OC)OC)C(=O)O2)O 344.30 unknown via CMAUP database
3,4,8,9,10-Pentahydroxybenzo[c]chromen-6-one 18504424 Click to see C1=CC(=C(C2=C1C3=C(C(=C(C=C3C(=O)O2)O)O)O)O)O 276.20 unknown via CMAUP database
4,4'-Di-O-methylellagic acid 11580745 Click to see 330.24 unknown via CMAUP database
5-Desgalloylstachyurin 10417809 Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)O 784.50 unknown via CMAUP database
6-[[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6S)-4,5-dihydroxy-2-methyl-6-[(7,13,14-trihydroxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl)oxy]oxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-7,13,14-trihydroxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaene-3,10-dione 11968423 Click to see 894.60 unknown via CMAUP database
8-O-[(1R,19R,21R,22R,23R)-6,7,8,11,12,13,22-heptahydroxy-3,16-dioxo-21-(3,4,5-trihydroxybenzoyl)oxy-2,17,20-trioxatetracyclo[17.3.1.04,9.010,15]tricosa-4,6,8,10,12,14-hexaen-23-yl] 1-O-methyl (1R,3aR,8bR)-5,6-dihydroxy-3a-(2-methoxy-2-oxoethyl)-3-oxo-1,8b-dihydrofuro[3,4-b][1]benzofuran-1,8-dicarboxylate 71475292 Click to see 998.70 unknown via CMAUP database
alpha-Pedunculagin 13834142 Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 784.50 unknown via CMAUP database
beta-Punicalagin 16148440 Click to see 1084.70 unknown via CMAUP database
CID 5464368 5464368 Click to see C1C2C(C(C(C(O2)O)O)O)OC(=O)C3=CC(=C(C(=C3C4=C(C(=C5C6=C4C(=O)OC7=C(C(=C(C8=C(C(=C(C=C8C(=O)O1)O)O)O)C(=C67)C(=O)O5)O)O)O)O)O)O)O 782.50 unknown via CMAUP database
Corilagin 73568 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O 634.50 unknown via CMAUP database
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database
Eschweilenol C 10026656 Click to see 448.30 unknown via CMAUP database
Flavogallonic acid 14503023 Click to see 470.30 unknown via CMAUP database
Gallagic acid 14754405 Click to see 638.40 unknown via CMAUP database
Gallagyldilactone 5281711 Click to see 602.40 unknown via CMAUP database
GlyTouCan:G69718UQ 9918701 Click to see 786.60 unknown via CMAUP database
Punicafolin 5320800 Click to see 938.70 unknown via CMAUP database
Punigluconin 21637585 Click to see 802.60 unknown via CMAUP database
Strictinin 73330 Click to see 634.50 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.