Details Top

Internal ID UUID643fd6e53d1a4537554276
Scientific name Tetrapleura tetraptera
Authority (Schumach. & Thonn.) Taub.
First published in Bot. Centralbl.47: 395 (1891)

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.

Tetrapleura tetraptera (Schumach. & Thonn.) Taub., the “prekese” or “uhiri” tree, has long served as food and medicine across the forest and coastal belts of West and Central Africa. In southern Nigeria, women commonly prepare a warm, aromatic tea from the dried seed arils after childbirth, either as a plain infusion or boiled with nearby herbs, believing it helps with uterine recovery and digestion. The Baule of Ivory Coast also prepare an aril tea for postpartum recovery, while in Ghana the fruit pulp is steeped with other herbal medicines in the “bɔsenɔyɛ” postpartum regimen. Cameroon’s Bamiléké communities infuse the seed arils into “yaato” herbal teas and report use of the fruit pod in decoctions for painful limbs and fevers (Williams, 2015). These uses center on the seed arils and the fruit pulp; in some areas the whole pod is boiled in a decoction for bathing or to help gastrointestinal discomfort.

A practical, well‑documented approach begins with the aril infusion: Place 8–10 g of dried, well‑cleaned seed arils in a saucepan, add about 300 ml of water, bring to a boil, then simmer 10–15 minutes. Strain and serve warm at a modest cup size, typically a half to one cup. An alternative, reproducible tincture is a 1:5 ethanol tincture using 50 g of crushed arils macerated in 250 ml of 50% alcohol for 2–3 weeks in a dark container, shaking daily; 10–20 drops taken twice a day is a common range reported in the literature. As the fruit is traditionally avoided during pregnancy and the seed aril preparations are also described as uterine‑stimulating, pregnant or nursing people should not use these preparations without medical guidance (Williams, 2015; Imo, 2014).

The notable activity of these preparations is well matched to the fruit’s chemistry. Chemical studies repeatedly identify saponins including oleanolic acid glycosides, phenylpropanoids such as E‑ocimene and methyl 4‑hydroxycinnamate, alkaloids, flavonoids, and tannins in the fruit and seed arils. The saponins and phenylpropanoids plausibly underlie the reported uterine‑supportive, antispasmodic, and digestive effects, while flavonoids and tannins may contribute to anti‑inflammatory and antimicrobial actions (Williams, 2015; Okwu and Okwu, 2004; Ayoka et al., 2006).

Modern work reflects this traditional grounding. Laboratory studies show antioxidant, antimicrobial, and anti‑inflammatory activity, and a few small clinical studies have explored postpartum formulations that include Tetrapleura tetraptera, mostly in the forms described above (Imo, 2014). Dried fruit and arils are still sold in markets throughout West and Central Africa, and ready‑made “prekese” teas appear online and in specialty stores. Continued work is refining dose, safety, and quality standards for these preparations.

General Uses Top

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Common products:
Aridan is traded as a spice condiments derived from the dried fruit pulp and seeds. The pulp is sold whole or ground and the seeds are often roasted, cracked, and milled prior to use. Ground pulp is also used as a component in spice blends.

Food and beverages (non-medicinal):
The fruit pulp and seeds are used as flavoring and thickening agents in soups and stews across West Africa. The mucilaginous nature of the pulp produces a viscous, sticky texture that acts as a culinary thickener. Seeds and pods may be roasted to develop aroma and are incorporated into spice mixes or rubs for sauces and soups.

Colorants and tanning:
No documented use as a natural dye or source of tanning materials is recorded for this taxon.

Properties relevant to use:
The fruit pulp contains mucilaginous polysaccharides that hydrate and swell in water, conferring thickening and binding properties; this mucilaginous character supports its application as a culinary thickener. Seeds and fruit contain fixed oils and aromatic compounds that contribute to aroma and browning when roasted.

Synonyms Top

Scientific name Authority First published in
Entada tetraptera (Schumach. & Thonn.) Roberty Bull. Inst. Fondam. Afrique Noire, Sér. A, Sci. Nat.16: 347 (1954)
Adenanthera tetraptera Schumach. & Thonn. C.F.Schumacher, Beskr. Guin. Pl.: 213 (1827)
Adenanthera tetraptera Schum. & Thonn.
Tetrapleura thonningii Benth. J. Bot. (Hooker) 4: 345 (1841)

Common names Top

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Language Common/alternative name
English galbanum
English aridan
English prekese
Akan prɛkɛsɛ
German dawo (haussa)
French sassas
French esesè
French 4 côtés
French essèssè
Hausa dawo
Portuguese aridan

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

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
    • Northeast Tropical Africa
      • Sudan
    • South Tropical Africa
      • Angola
    • West Tropical Africa
      • Benin
      • Ghana
      • Guinea
      • Guinea-Bissau
      • Ivory Coast
      • Liberia
      • Nigeria
      • Senegal
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000171351
Tropicos 13057082
KEW urn:lsid:ipni.org:names:521134-1
The Plant List ild-176
Open Tree Of Life 213992
NCBI Taxonomy 148728
IUCN Red List 62028252
IPNI 521134-1
iNaturalist 426816
GBIF 5347354
Freebase /m/05zl5s7
EOL 639828
USDA GRIN 36396
Wikipedia Tetrapleura_tetraptera

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
Natural products for managing metabolic syndrome: a scoping review Abdulghani MF, Al-Fayyadh S Front Pharmacol 30-Apr-2024
PMCID:PMC11091304
doi:10.3389/fphar.2024.1366946
PMID:38746011
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
Nutritive value, biological properties, health benefits and applications of Tetrapleura tetraptera: An updated comprehensive review Mensah RQ, Adusei S, Azupio S, Kwakye R Heliyon 13-Mar-2024
PMCID:PMC10955287
doi:10.1016/j.heliyon.2024.e27834
PMID:38515660
Evaluation of packaging, labels, and some physicochemical properties of herbal antimalarial products on the Ghanaian market Amekyeh H, Kumadoh D, Adongo DW, Orman E, Abubakar S, Dwamena A, Aggrey MO Heliyon 28-Feb-2024
PMCID:PMC10920373
doi:10.1016/j.heliyon.2024.e27032
PMID:38463810
Scopoletin: a review of its pharmacology, pharmacokinetics, and toxicity Gao XY, Li XY, Zhang CY, Bai CY Front Pharmacol 23-Feb-2024
PMCID:PMC10923241
doi:10.3389/fphar.2024.1268464
PMID:38464713
Bioactivity and toxicity of coumarins from African medicinal plants Anywar G, Muhumuza E Front Pharmacol 10-Jan-2024
PMCID:PMC10809390
doi:10.3389/fphar.2023.1231006
PMID:38273831
In Vitro Hypoglycemic and Antioxidant Activities of Dichloromethane Extract of Xerophyta spekei Ndile MM, Makori WA, Kibiti CM, Ngugi MP Scientifica (Cairo) 29-Dec-2023
PMCID:PMC10769734
doi:10.1155/2023/6652112
PMID:38188987
The Global Impact of COVID-19: Historical Development, Molecular Characterization, Drug Discovery and Future Directions Dofuor AK, Quartey NK, Osabutey AF, Boateng BO, Lutuf H, Osei JH, Ayivi-Tosuh SM, Aiduenu AF, Ekloh W, Loh SK, Opoku MJ, Aidoo OF Clin Pathol 23-Dec-2023
PMCID:PMC10748929
doi:10.1177/2632010X231218075
PMID:38144436
Recent advances incombined Avant-garde technologies (thermal-thermal, non-thermal-non-thermal, and thermal-non-thermal matrix) to extract polyphenols from agro byproducts Boateng ID J Food Drug Anal 15-Dec-2023
PMCID:PMC10962677
doi:10.38212/2224-6614.3479
PMID:38526817
Ethnobotanical and ethnopharmacological survey of medicinal tree species used in the treatment of diseases by forest-fringe communities of Southwestern Ghana Asigbaase M, Adusu D, Musah AA, Anaba L, Nsor CA, Abugre S, Derkyi M Heliyon 14-Dec-2023
PMCID:PMC10788458
doi:10.1016/j.heliyon.2023.e23645
PMID:38226220
Secondary Metabolites of Biscogniauxia: Distribution, Chemical Diversity, Bioactivity, and Implications of the Occurrence Purbaya S, Harneti D, Safriansyah W, Rahmawati, Wulandari AP, Mulyani Y, Supratman U Toxins (Basel) 06-Dec-2023
PMCID:PMC10747060
doi:10.3390/toxins15120686
PMID:38133190
Medicinal plants used for management of diabetes and hypertension in Ghana Asafo-Agyei T, Appau Y, Barimah KB, Asase A Heliyon 29-Nov-2023
PMCID:PMC10703729
doi:10.1016/j.heliyon.2023.e22977
PMID:38076168
Antihypertensive potential of the stem bark of Canarium schweinfurthii Engl. (Burseraceae) in wistar rats: UPLC-ESI-QToF-MS/MS-based prediction of antihypertensive phytochemicals Mbosso Teinkela JE, Nguemfo EL, Fokou Nzodjou T, Bogning Zangueu C, Kalinski JC, Tsakem B, Assob Nguedia JC, Siwe Noundou X Heliyon 04-Nov-2023
PMCID:PMC10663920
doi:10.1016/j.heliyon.2023.e21841
PMID:38027816
Determination of biological activities of malabar spinach (Basellaalba) fruit extracts and molecular docking against COX-II enzyme Nur MA, Islam M, Biswas S, Hasan MN, Rahman MM, Uddin MJ, Satter MA, Amin MZ Heliyon 03-Nov-2023
PMCID:PMC10663853
doi:10.1016/j.heliyon.2023.e21568
PMID:38027774
Indigenous medicinal plants used in folk medicine for malaria treatment in Kwara State, Nigeria: an ethnobotanical study Evbuomwan IO, Stephen Adeyemi O, Oluba OM BMC Complement Med Ther 16-Sep-2023
PMCID:PMC10504731
doi:10.1186/s12906-023-04131-4
PMID:37716985

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
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane 12410 Click to see 436.80 unknown https://doi.org/10.1016/S0031-9422(00)80622-6
https://doi.org/10.1016/0031-9422(85)80044-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3S,4S,5R,6R)-6-[[(3S,4S,4aR,6aR,6bS,8aR,9R,12aS,14aR,14bS)-9-hydroxy-4-(hydroxymethyl)-4,6a,6b,8a,11,11,14b-heptamethyl-14-oxo-2,3,4a,5,6,7,8,9,10,12,12a,14a-dodecahydro-1H-picen-3-yl]oxy]-5-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid 101638317 Click to see 957.10 unknown https://doi.org/10.1016/0021-9673(93)83334-O
(4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-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 44584413 Click to see 675.90 unknown https://doi.org/10.1002/HLCA.19890720407
(4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5-hydroxy-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 13919572 Click to see 675.90 unknown https://doi.org/10.1002/MRC.2381
(4aS,6aR,6aR,6bR,8aR,10S,12aR,14bS)-6a-(hydroxymethyl)-2,2,6b,9,9,12a-hexamethyl-10-[(2R,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]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163014347 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)O)O)O)C)C)C2C1)CO)C(=O)O)C 797.00 unknown https://doi.org/10.1016/0031-9422(92)80500-E
(4aS,6aR,6aS,6bR,8aR,10R,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-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 163070091 Click to see 659.90 unknown https://doi.org/10.1016/0031-9422(85)80044-3
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-[(2R,3R,4R,5S,6R)-3-acetamido-4-hydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5R,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 162969490 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CCC6(C5CC(CC6)(C)C)C(=O)O)C)C)C)CO)OC7C(C(C(C(O7)CO)O)O)O)O 822.00 unknown https://doi.org/10.1002/HLCA.19890720407
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bR)-10-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-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 44584414 Click to see 822.00 unknown https://doi.org/10.1002/HLCA.19890720407
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-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 101690669 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CCC6(C5CC(CC6)(C)C)C(=O)O)C)C)C)COC7C(C(C(C(O7)CO)O)O)O)O)O 822.00 unknown https://doi.org/10.1002/MRC.2381
(4aS,6aS,6aS,6bR,8aS,10S,12aR,14bR)-10-[(2R,3R,4R,5S,6R)-3-acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-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 163070093 Click to see 659.90 unknown https://doi.org/10.1002/HLCA.19890720407
10-[3-Acetamido-4-hydroxy-6-(hydroxymethyl)-5-[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 14059534 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CCC6(C5CC(CC6)(C)C)C(=O)O)C)C)C)CO)OC7C(C(C(C(O7)CO)O)O)O)O 822.00 unknown https://doi.org/10.1002/HLCA.19890720407
10-[3-Acetamido-4,5-dihydroxy-6-(hydroxymethyl)oxan-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 500032 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CCC6(C5CC(CC6)(C)C)C(=O)O)C)C)C)CO)O)O 659.90 unknown https://doi.org/10.1002/MRC.2381
https://doi.org/10.1002/HLCA.19890720407
https://doi.org/10.1016/0031-9422(85)80044-3
3-O-(beta-D-Glucopyranosyl-(1''-6')-2'-acetamido-2'-deoxy-beta-D-glucopyranosyl)olean-12-en-28-oic acid 147731 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CCC6(C5CC(CC6)(C)C)C(=O)O)C)C)C)COC7C(C(C(C(O7)CO)O)O)O)O)O 822.00 unknown https://doi.org/10.1002/MRC.2381
https://doi.org/10.1002/HLCA.19890720407
6a-(Hydroxymethyl)-2,2,6b,9,9,12a-hexamethyl-10-[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163014346 Click to see 797.00 unknown https://doi.org/10.1016/0031-9422(92)80500-E
Aridanin 73146 Click to see 659.90 unknown https://doi.org/10.1002/HLCA.19890720407
https://doi.org/10.1016/S0031-9422(00)80622-6
https://doi.org/10.1016/0021-9673(93)83333-N
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289059/
https://doi.org/10.1016/0378-8741(89)90002-0
https://doi.org/10.1002/PTR.2650030303
https://doi.org/10.1055/S-2006-961688
https://doi.org/10.1002/MRC.2381
NCGC00347780-02_C38H61NO9_3-[(2-Acetamido-2-deoxyhexopyranosyl)oxy]-16-hydroxyolean-12-en-28-oic acid 13919571 Click to see CC(=O)NC1C(C(C(OC1OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CC(C6(C5CC(CC6)(C)C)C(=O)O)O)C)C)C)CO)O)O 675.90 unknown https://doi.org/10.1002/HLCA.19890720407
https://doi.org/10.1002/MRC.2381
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aR,5R,6aR,6aS,6bR,8aR,10S,12aR,14bS)-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-sulfooxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 15385788 Click to see 552.80 unknown https://doi.org/10.1002/MRC.2381
(4aR,5R,6aR,6aS,6bR,8aR,12aR,14bS)-5-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-sulfooxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 158555 Click to see 552.80 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289059/
5-Hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-10-sulfooxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 3762242 Click to see 552.80 unknown https://doi.org/10.1002/MRC.2381
Saponin D 131752825 Click to see 927.10 unknown https://doi.org/10.1016/0021-9673(93)83334-O
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids
2-Amino-4-ethylidenepentanedioic acid 73192539 Click to see 173.17 unknown https://doi.org/10.1016/0304-4165(67)90019-0
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S,4E)-2-amino-4-ethylidenepentanedioic acid 9964220 Click to see CC=C(CC(C(=O)O)N)C(=O)O 173.17 unknown https://doi.org/10.1016/0304-4165(67)90019-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Sucrose 5988 Click to see 342.30 unknown https://doi.org/10.1016/S0031-9422(00)80622-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides
D-(-)-Fructose 5984 Click to see 180.16 unknown https://doi.org/10.1016/S0031-9422(00)80622-6
D-Fructose 2723872 Click to see 180.16 unknown https://doi.org/10.1016/S0031-9422(00)80622-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)80622-6
D(+)-Glucose 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)80622-6
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(3,4-Dihydroxyphenyl)Prop-2-Enoic Acid 2518 Click to see 180.16 unknown https://doi.org/10.1016/0031-9422(85)80044-3
4-Coumaric acid 322 Click to see 164.16 unknown https://doi.org/10.1016/0031-9422(85)80044-3
Caffeic Acid 689043 Click to see 180.16 unknown https://doi.org/10.1016/0031-9422(85)80044-3
https://doi.org/10.1016/S0031-9422(00)80622-6
P-Coumaric Acid 637542 Click to see 164.16 unknown https://doi.org/10.1016/S0031-9422(00)80622-6
https://doi.org/10.1016/0031-9422(85)80044-3
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1016/0031-9422(85)80044-3
https://doi.org/10.3109/13880208709060904
https://doi.org/10.1055/S-2007-969809
https://doi.org/10.1055/S-2007-969824
https://doi.org/10.1016/S0031-9422(00)80622-6

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