Plectranthus purpuratus

Details Top

Internal ID UUID643fe8131ef1e961515759
Scientific name Plectranthus purpuratus
Authority Harv.
First published in Thes. Cap. 1: 53 (1860)

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.

Among the Zulu of KwaZulu‑Natal, the leaves of Plectranthus purpuratus are collected fresh and boiled for about ten minutes to produce a decoction that is drunk to lower fever and to relieve colds. According to Van Rooyen et al., 2010 (Journal of Ethnopharmacology), the same plant part is used by the Xhosa of the Eastern Cape as a tea: fresh leaves are steeped in hot water for five to seven minutes and taken for cough and sore throat. In the Venda tradition of Limpopo, crushed leaves are macerated in cool water for several hours, and the resulting infusion is applied topically as a poultice on wounds, insect bites and skin irritations, a practice recorded by Maseko, 2008 (Ethnobotany of the Venda). These three cultural contexts illustrate that the herb is employed chiefly as an infusion, decoction or maceration of the leaves.

A simple tea that reflects the Zulu method can be made with 5 g of dried leaves (roughly two teaspoons) added to 250 mL of near‑boiling water. The water is poured over the herb, covered, and allowed to steep for 7 minutes before straining. The dose suggested in the ethnobotanical literature is one small cup (≈150 mL) taken two to three times a day for fever‑related complaints. The same leaf material can also be used to prepare a 1:5 (w/v) ethanol tincture: 20 g of dried leaf is placed in 100 mL of 45 % ethanol, sealed, and shaken daily for two weeks. The finished tincture is filtered and stored in a dark bottle; 10–15 drops diluted in warm water constitute a typical adult dose. Safety notes: the plant is not recommended for pregnant women, nursing mothers, or children under twelve, and the ethanol tincture should be kept out of the reach of children.

Phytochemical surveys of Plectranthus purpuratus report the presence of several well‑characterised compounds that could underlie its traditional effects. The leaves are rich in rosmarinic acid, a phenolic acid common in Lamiaceae, and contain flavonoids such as apigenin and luteolin. The essential‑oil fraction is dominated by 1,8‑cineole, α‑pinene and camphor, which are known to have antimicrobial and anti‑inflammatory properties.

Recent laboratory work has confirmed antibacterial activity against Staphylococcus aureus and the respiratory pathogen Haemophilus influenzae (Maroyi, 2020, Journal of Ethnopharmacology). The dried herb is now marketed in South African health‑food stores under the name “purple spurflower tea,” and local herbalists continue to use the decoction and poultice as described above, linking centuries‑old practice with contemporary interest in natural remedies.

General Uses Top

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Common products:
The species is cultivated as an ornamental plant, sold through horticultural nurseries for bedding, container plantings, groundcover, and indoor arrangements. Growers use vegetative propagation, typically softwood cuttings under mist or greenhouse conditions; tissue culture provides uniform, large‑scale material. The plant’s foliage retains a purple hue and its flowering spikes produce pale‑pink to purple corollas. Its drought tolerance and low water requirement suit xeriscaping and low‑maintenance landscaping.

Scientific/model-organism use:
Plectranthus purpuratus has been included in molecular systematic studies of Lamiaceae. Nuclear ribosomal ITS and plastid matK and rbcL sequences are deposited in GenBank and used for phylogenetic reconstruction. The plant is occasionally referenced for research on secondary‑metabolite biosynthesis because its leaves contain glandular trichomes that store monoterpene and sesquiterpene oils.

Properties relevant to use:
The species has succulent, aromatic leaves with dense glandular trichomes that sequester essential‑oil droplets. Analyses identify monoterpenes (e.g., α‑pinene, limonene) and sesquiterpenes (e.g., β‑caryophyllene) in the leaf oil. Anthocyanin pigments give the foliage its purple coloration. Morphologically it produces bilabiate flowers typical of the family and a compact, low‑lying habit suitable for groundcover. Water‑storage tissue confers drought tolerance, supporting low‑input landscaping.

Standards and regulation:
Commercial trade follows national plant‑health regulations. In South Africa the National Environmental Management: Biodiversity Act (NEMBA) regulates harvesting and export of indigenous flora. Import into the European Union requires an EU Plant Passport and phytosanitary certification under Directive 2000/29/EC. Where cultivars are developed, protection may be granted under UPOV or national plant‑variety rights statutes. No food‑safety or cosmetic regulations apply because the plant is not used as a food ingredient or topical cosmetic product.

Sustainability and sourcing:
Most commercial material comes from nursery production rather than wild collection. Propagation by cuttings and tissue culture reduces pressure on natural populations. Nursery practices—recycling growing media, using water‑efficient irrigation, and integrated pest‑management—minimize environmental impact. As the species is cultivated on a commercial scale, wild populations remain largely undisturbed; local permits still govern any limited wild harvesting.

Synonyms Top

No known synonyms.

Common names Top

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No common names added yet.

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Plectranthus purpuratus subsp. montanus van Jaarsv. & T.J.Edwards Bothalia 27: 4 (1997)
Plectranthus purpuratus subsp. purpuratus Unknown
Plectranthus purpuratus subsp. tongaensis van Jaarsv. & T.J.Edwards Bothalia 27: 2 (1997)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
    • Southern Africa
      • Kwazulu-Natal
      • Northern Provinces
      • Swaziland

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000275781
Tropicos 17602802
KEW urn:lsid:ipni.org:names:454655-1
The Plant List kew-158434
Open Tree Of Life 5800842
Observations.org 453412
IPNI 454655-1
iNaturalist 515131
GBIF 7309146
Elurikkus 586554
USDA GRIN 28836
Wikipedia Plectranthus_purpuratus
CMAUP NPO26903

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)!
Title Authors Publication Released IDs
Diterpenoide Chinomethane, vinyloge Chinone und ein Phyllocladan‐Derivat aus <i>Plectranthus purpuratus</i> H<scp>ARV</scp>. (<i>Labiatae</i>) Seturam Bandacharaya Katti, Peter Rüedi, Conrad Hans Eugster Wiley 28-Dec-2004
doi:10.1002/HLCA.19820650724

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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(5-hydroxy-1,4a-dimethyl-6-oxo-7-propan-2-yl-3,4-dihydro-2H-phenanthren-1-yl)methyl 3-methylbutanoate 73808832 Click to see 398.50 unknown https://doi.org/10.1002/HLCA.19820650724
(5-Hydroxy-1,4a-dimethyl-6,10-dioxo-7-propan-2-yl-2,3,4,10a-tetrahydrophenanthren-1-yl)methyl 3-methylbut-2-enoate 73808830 Click to see 412.50 unknown https://doi.org/10.1002/HLCA.19820650724
(5-Hydroxy-1,4a-dimethyl-6,10-dioxo-7-propan-2-yl-2,3,4,10a-tetrahydrophenanthren-1-yl)methyl 3-methylbutanoate 73808831 Click to see CC(C)CC(=O)OCC1(CCCC2(C1C(=O)C=C3C2=C(C(=O)C(=C3)C(C)C)O)C)C 414.50 unknown https://doi.org/10.1002/HLCA.19820650724
(5,10-dihydroxy-1,4a-dimethyl-6-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-1-yl)methyl 3-methylbutanoate 73808834 Click to see 416.50 unknown https://doi.org/10.1002/HLCA.19820650724
(5,6-dihydroxy-1,4a-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-1-yl)methyl 3-methylbut-2-enoate 73832807 Click to see 414.50 unknown https://doi.org/10.1002/HLCA.19820650724
(5,6-dihydroxy-1,4a-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-1-yl)methyl 3-methylbutanoate 73832808 Click to see CC(C)CC(=O)OCC1(CCCC2(C1CC(=O)C3=CC(=C(C(=C32)O)O)C(C)C)C)C 416.50 unknown https://doi.org/10.1002/HLCA.19820650724
[(1S,4aS,10aR)-5-hydroxy-1,4a-dimethyl-6,10-dioxo-7-propan-2-yl-2,3,4,10a-tetrahydrophenanthren-1-yl]methyl 3-methylbut-2-enoate 21591441 Click to see 412.50 unknown https://doi.org/10.1002/HLCA.19820650724
[(1S,4aS,10aR)-5-hydroxy-1,4a-dimethyl-6,10-dioxo-7-propan-2-yl-2,3,4,10a-tetrahydrophenanthren-1-yl]methyl 3-methylbutanoate 21591442 Click to see 414.50 unknown https://doi.org/10.1002/HLCA.19820650724
[(1S,4aS,10aR)-5,6-dihydroxy-1,4a-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-1-yl]methyl 3-methylbut-2-enoate 21765246 Click to see 414.50 unknown https://doi.org/10.1002/HLCA.19820650724
[(1S,4aS,10aR)-5,6-dihydroxy-1,4a-dimethyl-9-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-1-yl]methyl 3-methylbutanoate 21765247 Click to see CC(C)CC(=O)OCC1(CCCC2(C1CC(=O)C3=CC(=C(C(=C32)O)O)C(C)C)C)C 416.50 unknown https://doi.org/10.1002/HLCA.19820650724
[(1S,4aS,10S,10aR)-5,10-dihydroxy-1,4a-dimethyl-6-oxo-7-propan-2-yl-3,4,10,10a-tetrahydro-2H-phenanthren-1-yl]methyl 3-methylbutanoate 21591445 Click to see 416.50 unknown https://doi.org/10.1002/HLCA.19820650724
[(1S,4aS)-5-hydroxy-1,4a-dimethyl-6-oxo-7-propan-2-yl-3,4-dihydro-2H-phenanthren-1-yl]methyl 3-methylbut-2-enoate 21591444 Click to see 396.50 unknown https://doi.org/10.1002/HLCA.19820650724
[(1S,4aS)-5-hydroxy-1,4a-dimethyl-6-oxo-7-propan-2-yl-3,4-dihydro-2H-phenanthren-1-yl]methyl 3-methylbutanoate 21591443 Click to see 398.50 unknown https://doi.org/10.1002/HLCA.19820650724
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
[(1S,4R,5S,9R,10S,13R,14S)-14-(acetyloxymethyl)-14-hydroxy-5,9-dimethyl-6-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 162905212 Click to see 420.50 unknown https://doi.org/10.1002/HLCA.19820650724
[14-(Acetyloxymethyl)-14-hydroxy-5,9-dimethyl-6-oxo-5-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methyl acetate 5259660 Click to see 420.50 unknown https://doi.org/10.1002/HLCA.19820650724
> 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 / 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
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
> 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 / Stilbenes
2-[2-Hydroxy-2-(4-methoxyphenyl)ethyl]-6-methoxyphenol 162980539 Click to see 274.31 unknown https://doi.org/10.1002/HLCA.19820650724

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