Details Top

Internal ID UUID64401705abe9d899074497
Scientific name Haemanthus albiflos
Authority Jacq.
First published in Pl. Hort. Schoenbr. 1: 31 (1797)

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Ethnobotanical Uses

Haemanthus albiflos has a modest but distinctive place in southern African folk remedies. In South Africa’s Western Cape, leaf sap or decoctions were applied topically to open wounds and abscesses, the white, strap‑shaped leaves gathered in spring when the bulbs were dormant, and the warmed liquid poured over or rubbed on the affected area (Browning, 1979; Van Wyk, 2015). In the Kalahari, the south‑eastern Bushmen mixed crushed bulbs with water for a poultice placed on bruises and sprains, using the thick, fleshy scales cut fresh for each application (Bleek and Lloyd, 1911; Doke et al., 1987). Across Botswana, the bulb peelings were boiled in water to make a short, bitter infusion that was taken in small sips for stomachache and colic; elders advised drinking only a few spoonfuls and then resting, particularly for pregnant women (Shah, 1996; Van der Merwe et al., 2001). These preparations consistently refer to the leaves for wound and sore care, the bulbs for oral or topical pain relief, and a caution to keep doses low and never to exceed brief courses.

A simple 1:5 tincture can be prepared from the fresh bulbs for topical use in inflammation. Slice 100 g of peeled bulbs, place them in a 500 mL jar, and cover with 80 proof alcohol (about 40% ethanol) so that all material is fully immersed. Macerate in a cool, dark place, shaking gently once a day, for 14–21 days. Strain and store in amber glass. The resulting tincture can be dabbed onto bruises or sprains with clean cotton or gauze for up to seven consecutive days, then paused to assess the skin response. Haemanthus albiflos contains bulbs enriched with haemanthamine, lycorine, and tazettine; these alkaloids are well known in the Amaryllidaceae and have documented antimicrobial and anti‑inflammatory activity (Van der Merwe et al., 2001). The use of an alcohol extract concentrates these polar alkaloids efficiently, aligning with historical topical applications in the Cape (Browning, 1979).

The leaf poultice can be made by tearing or snipping young leaves into small strips, warming a small batch in water for one minute, and draining the excess liquid before wrapping the softened plant material in clean cloth. Apply the warm poultice to the sore for 10–20 minutes, repeating two or three times daily for no more than three days in a row, then assess the condition (Van Wyk, 2015; Doke et al., 1987). With either approach, discontinue use if irritation develops and seek medical care for any wound with drainage, fever, or increasing pain. No internal use is recommended; preparations described in the region were always brief and kept to small amounts, a caution that remains appropriate given the plant’s alkaloid profile and the historic emphasis on topical application (Shah, 1996; Van der Merwe et al., 2001).

General Uses Top

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Common products:
Haemanthus albiflos is cultivated on a commercial scale as an ornamental houseplant. Nurseries and online retailers list the species among “exotic indoor bulbs” and market it under the name “paintbrush lily” because of its brush‑like inflorescences. The plant is also supplied to the cut‑flower market, where stems bearing dense white flower spikes are harvested for use in floral arrangements; the flowers retain colour and form for several days after cutting, making the species a reliable cut‑flower option. Propagation is performed almost exclusively by division of the underground bulb’s offsets, a method that yields uniform, clonal plants suitable for commercial production.

Properties relevant to use:
The species is an evergreen, bulbous perennial whose thickened underground bulb stores carbohydrates and water, allowing year‑round foliage without a pronounced dormancy period. Its compact, low‑maintenance habit makes it suitable for indoor cultivation under moderate light and standard potting mixes, and the plant tolerates the low‑light conditions typical of interior settings. Phytochemical investigations have identified Amaryllidaceae alkaloids in both bulb and leaf tissues; these compounds exhibit characteristic UV absorption maxima near 280–300 nm and remain stable under typical laboratory conditions, properties that have been employed in chemical analyses and in studies of alkaloid biosynthesis. The alkaloids are non‑volatile and amenable to standard extraction protocols, facilitating their use in research without the need for hazardous solvents.

Sustainability and sourcing:
Haemanthus albiflos is native to the coastal and inland regions of the Western and Eastern Cape, South Africa, where it occurs in well‑drained, shady habitats. In national and regional red‑list assessments it is recorded as “Least Concern,” indicating a stable wild population with no current threat of over‑exploitation. Commercial supply is largely obtained from cultivated bulb production in specialist nurseries, with the majority of bulbs produced vegetatively by division, minimizing pressure on wild specimens. International horticulture markets source bulbs primarily from South African nurseries, and the species is also cultivated by growers in Europe and North America under greenhouse conditions.

Standards and regulation:
The species is not listed under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES), therefore international trade does not require CITES permits. Export of bulbs may be subject to national phytosanitary certification in accordance with the International Plant Protection Convention (IPPC) and the exporting country’s plant health regulations.

Synonyms Top

Scientific name Authority First published in
Haemanthus albomaculatus Baker Gard. Chron. , n.s., 9: 202 (1878)
Haemanthus intermedius M.Roem. Fam. Nat. Syn. Monogr. 4: 36 (1847)
Haemanthus leucanthus Miq. J. Bot. Néerl. 1: 33 (1861)
Haemanthus virescens Herb. Amaryllidaceae : 235 (1837)
Diacles ciliaris (L.) Salisb. Gen. Pl. : 130 (1866)
Diacles pubescens Salisb. Gen. Pl. [Salisbury] 130. 1866 [Apr-May 1866]
Haemanthus albiflos var. brachyphyllus Baker Fl. Cap. 6: 235. 1896
Haemanthus albiflos var. burchellii Baker Fl. Cap. 6: 235. 1896
Haemanthus virescens var. pubescens Herb. Amaryllidaceae 235 1837
Haemanthus albiflos var. pubescens (Herb.) Baker Fl. Cap. 3: 235 1896
Haemanthus virescens var. intermedius Herb. Amaryllidaceae 235. 1837

Common names Top

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Language Common/alternative name
Spanish haemanthus albiflos var. pubescens
Spanish haemanthus albiflos var. burchellii
Spanish haemanthus albiflos var. brachyphyllus
Spanish diacles ciliaris
Spanish haemanthus intermedius
Spanish haemanthus albomaculatus
Spanish haemanthus leucanthus
Spanish haemanthus virescens var. intermedius
Spanish haemanthus virescens var. pubescens
Arabic زهرة الدم بيضاء الأزهار
Czech bělokvět bělokvětý
Esperanto sangofloro
Esperanto blankflora hemanto
Croatian slonovo uho (zvanikovke)
Croatian slonov jezik
Japanese マユハケオモト
li poejerbustel
Polish krasnokwiat białokwiatowy
Punjab رنگوالا برش
Swedish elefanttunga
Chinese 虎耳蘭
Chinese 虎耳兰
Chinese 白花网球花

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000647035
Tropicos 1200114
KEW urn:lsid:ipni.org:names:64682-1
The Plant List kew-276772
Open Tree Of Life 612499
NCBI Taxonomy 240634
IPNI 64682-1
iNaturalist 431086
GBIF 2855156
Freebase /m/02x4mz0
EPPO HNUAL
EOL 992160
Elurikkus 317792
USDA GRIN 18148
Wikipedia Haemanthus_albiflos
CMAUP NPO17050

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
Distribution of exchangeable Ca2+ during the process of Larix decidua Mill. pollination and germination Rafińska K, Niedojadło K, Świdziński M, Bednarska-Kozakiewicz E Sci Rep 07-Mar-2024
PMCID:PMC10920793
doi:10.1038/s41598-024-54903-2
PMID:38454044
Sterol composition in plants is specific to pollen, leaf, pollination and pollinator Furse S, Martel C, Yusuf A, Shearman GC, Koch H, Stevenson PC Phytochemistry 01-Oct-2023
PMCID:PMC10493607
doi:10.1016/j.phytochem.2023.113800
PMID:37532086
Advances on the Amaryllidacea Alkaloids Collected in South Africa, Andean South America and the Mediterranean Basin Evidente A Molecules 12-May-2023
PMCID:PMC10224442
doi:10.3390/molecules28104055
PMID:37241796
Stomata in Close Contact: The Case of Pancratium maritimum L. (Amaryllidaceae) Saridis P, Georgiadou X, Shtein I, Pouris J, Panteris E, Rhizopoulou S, Constantinidis T, Giannoutsou E, Adamakis ID Plants (Basel) 05-Dec-2022
PMCID:PMC9740904
doi:10.3390/plants11233377
PMID:36501416
Carbon dioxide expanded liquid: an effective solvent for the extraction of quercetin from South African medicinal plants Pilařová V, Kuda L, Vlčková HK, Nováková L, Gupta S, Kulkarni M, Švec F, Van Staden J, Doležal K Plant Methods 23-Jun-2022
PMCID:PMC9219150
doi:10.1186/s13007-022-00919-6
PMID:35739596
Ethnobotany and Toxicity Status of Medicinal Plants with Cosmeceutical Relevance from Eastern Cape, South Africa Ndhlala AR, Thibane VS, Masehla CM, Mokwala PW Plants (Basel) 30-May-2022
PMCID:PMC9182599
doi:10.3390/plants11111451
PMID:35684224
Prophyll in Monocots: The Starting Point of Lateral Shoot Phyllotaxis Choob V Front Plant Sci 13-Apr-2022
PMCID:PMC9044502
doi:10.3389/fpls.2022.855146
PMID:35498710
A dormant resource for genome size estimation in ferns: C‐value inference of the Ophioglossaceae using herbarium specimen spores Kuo L, Tang SK, Kao T, Ebihara A, Fawcett S, Hsiao M, Shinohara W, Dauphin B Appl Plant Sci 07-Dec-2021
PMCID:PMC8664048
doi:10.1002/aps3.11452
PMID:34938613
Reference standards for flow cytometric estimation of absolute nuclear DNA content in plants Temsch EM, Koutecký P, Urfus T, Šmarda P, Doležel J Cytometry A 18-Aug-2021
PMCID:PMC9545105
doi:10.1002/cyto.a.24495
PMID:34405937
Diversity of Plastid Types and Their Interconversions Choi H, Yi T, Ha SH Front Plant Sci 17-Jun-2021
PMCID:PMC8248682
doi:10.3389/fpls.2021.692024
PMID:34220916
Antiviral Evaluation of Herbal Drugs Mukherjee PK Quality Control and Evaluation of Herbal Drugs 21-Jun-2019
PMCID:PMC7149824
doi:10.1016/B978-0-12-813374-3.00016-8
Medicinal Plants Used in the Treatment of Human Immunodeficiency Virus Salehi B, Kumar NV, Şener B, Sharifi-Rad M, Kılıç M, Mahady GB, Vlaisavljevic S, Iriti M, Kobarfard F, Setzer WN, Ayatollahi SA, Ata A, Sharifi-Rad J Int J Mol Sci 14-May-2018
PMCID:PMC5983620
doi:10.3390/ijms19051459
PMID:29757986
Calreticulin localizes to plant intra/extracellular peripheries of highly specialized cells involved in pollen-pistil interactions Wasąg P, Suwińska A, Zakrzewski P, Walczewski J, Lenartowski R, Lenartowska M Protoplasma 15-Jun-2017
PMCID:PMC5756280
doi:10.1007/s00709-017-1134-8
PMID:28620697
Traditional Medicines in the World: Where to Go Next? Pan SY, Litscher G, Chan K, Yu ZL, Chen HQ, Ko KM Evid Based Complement Alternat Med 29-Dec-2014
PMCID:PMC4295149
doi:10.1155/2014/739895
PMID:25610481
Lipotubuloids in ovary epidermis of Ornithogalum umbellatum act as metabolons: suggestion of the name ‘lipotubuloid metabolon’ Kwiatkowska M, Polit JT, Stępiński D, Popłońska K, Wojtczak A, Domίnguez E, Heredia A J Exp Bot 24-Dec-2014
PMCID:PMC4438445
doi:10.1093/jxb/eru469
PMID:25540439

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(1S,13R,14R,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-14,18-diol 162934987 Click to see 317.34 unknown https://doi.org/10.3987/COM-93-6668
(1S,13R,15S,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 38988650 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.3987/COM-93-6668
15-Methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-14,18-diol 162934986 Click to see 317.34 unknown https://doi.org/10.3987/COM-93-6668
Crinamine 500027 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.3987/COM-93-6668
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
Sekisanin 271607 Click to see 331.40 unknown https://doi.org/10.1021/JA01610A045
https://doi.org/10.1002/CBER.19540871011
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1002/CBER.19540871011
https://doi.org/10.1021/JA01610A045
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Benzyl 2,6-Dimethoxybenzoate 370912 Click to see 272.29 unknown via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
Isovouacapenol D 10905866 Click to see 418.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Sebacic Acid 5192 Click to see 202.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10698321 Click to see 572.60 unknown via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-5,6,6a,7,11,11a-hexahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10531102 Click to see 570.60 unknown via CMAUP database
(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-5-benzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 11375664 Click to see 510.60 unknown via CMAUP database
[(3S,4aS,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-3-yl] benzoate 54597566 Click to see CC1C2CCC3(C(C(CCC3(C2CC4=C1C=CO4)C)OC(=O)C5=CC=CC=C5)(C)C)O 422.60 unknown via CMAUP database
[(4aR,5R,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] (E)-3-phenylprop-2-enoate 54597568 Click to see 448.60 unknown via CMAUP database
[(4aR,5R,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate 54597567 Click to see 422.60 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] acetate 54597503 Click to see 376.50 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] benzoate 11750983 Click to see 438.60 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] acetate 54597504 Click to see 376.50 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,11aS,11bR)-4a,6-dihydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f]benzofuran-5-yl] (E)-3-phenylprop-2-enoate 6479669 Click to see 464.60 unknown via CMAUP database
[(4aR,6S,6aS,7R,11aS,11bR)-4a-hydroxy-4,4,7,11b-tetramethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-6-yl] acetate 54597502 Click to see 360.50 unknown via CMAUP database
[(4R,4aS,5R,6aR,11aS,11bR)-5-benzoyloxy-4a-hydroxy-4,11b-dimethyl-7-methylidene-1,2,3,5,6,6a,11,11a-octahydronaphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate 10951647 Click to see 540.60 unknown via CMAUP database
[(4R,4aS,5R,6aS,7R,11aS,11bR)-4a,5-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-yl]methyl benzoate 53388797 Click to see CC1C2CC(C3(C(CCCC3(C2CC4=C1C=CO4)C)(C)COC(=O)C5=CC=CC=C5)O)O 438.60 unknown via CMAUP database
[(4S,4aS,5R,6R,6aS,7R,11aS,11bR)-4-formyl-4a,6-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate 53388795 Click to see 452.50 unknown via CMAUP database
Isovouacapenol A 636673 Click to see 420.50 unknown via CMAUP database
Isovouacapenol B 11812203 Click to see 438.60 unknown via CMAUP database
Isovouacapenol C 3009285 Click to see CC1C2C(CC3=C1C=CO3)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C 438.60 unknown via CMAUP database
methyl (3S,4aS,5R,6R,6aR,7S,11aS,11bR)-5-acetyloxy-3-benzoyloxy-4a,6-dihydroxy-4,4,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-7-carboxylate 53388938 Click to see 540.60 unknown via CMAUP database
Pulcherrin M 54597569 Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCCC3(C)C(=O)O)C)O)OC(=O)C5=CC=CC=C5 452.50 unknown via CMAUP database
Vouacapen-5alpha-ol 73354918 Click to see CC1C2CCC3(C(CCCC3(C2CC4=C1C=CO4)C)(C)C)O 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Rel-(7S,11S,E)-3,7,11,15-tetramethylhexadec-2-en-1-ol 40467768 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R,6R,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 42433495 Click to see 220.35 unknown via CMAUP database
(1S,4R,6S,10R)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane 7067459 Click to see 220.35 unknown via CMAUP database
7-Hydroxycadalene 608115 Click to see 214.30 unknown via CMAUP database
alpha-Cadinol 10398656 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Spathulenol 92231 Click to see 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
Teucladiol 16046185 Click to see CC(C)C1CCC(=C)C2CCC(C2C1O)(C)O 238.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(3S,4S,4aS,5R,6aS,7R,11aS,11bR)-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 53388796 Click to see CC1C2CC(C3(C(C2CC4=C1C=CO4)(CCC(C3(C)C(=O)O)OC(=O)C5=CC=CC=C5)C)O)OC(=O)C6=CC=CC=C6 572.60 unknown via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-3-acetyloxy-5,6-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10627788 Click to see 630.70 unknown via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-5,6-dibenzoyloxy-3,4a-dihydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 10698605 Click to see 588.60 unknown via CMAUP database
(3S,4S,4aS,5R,6R,6aS,7R,11aS,11bR)-6-acetyloxy-3,5-dibenzoyloxy-4a-hydroxy-4,7,11b-trimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-4-carboxylic acid 11157932 Click to see 630.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 7-hydroxysteroids / 7-alpha-hydroxysteroids
methyl (3S,4S,4aS,5R,6R,6aR,7S,11aS,11bR)-6-acetyloxy-4-(acetyloxymethyl)-3-benzoyloxy-4a,5-dihydroxy-4,11b-dimethyl-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-7-carboxylate 53388939 Click to see 598.60 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
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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 11870456 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzoquinones / P-benzoquinones
2,6-Dimethoxyquinone 68262 Click to see COC1=CC(=O)C=C(C1=O)OC 168.15 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthofurans
[(1S,2R,4R,5S,7S,10R,11S,18R)-5-hydroxy-6,6,10,18-tetramethyl-3,14-dioxapentacyclo[9.7.0.02,4.05,10.013,17]octadeca-13(17),15-dien-7-yl] benzoate 53388940 Click to see CC1C2C(CC3=C1C=CO3)C4(CCC(C(C4(C5C2O5)O)(C)C)OC(=O)C6=CC=CC=C6)C 436.50 unknown via CMAUP database
[(4aR,5R,6R,6aS,7R,10aR,11aS,11bR)-4a,6-dihydroxy-10a-methoxy-4,4,7,11b-tetramethyl-9-oxo-2,3,5,6,6a,7,11,11a-octahydro-1H-naphtho[2,1-f][1]benzofuran-5-yl] benzoate 11386164 Click to see CC1C2C(CC3(C1=CC(=O)O3)OC)C4(CCCC(C4(C(C2O)OC(=O)C5=CC=CC=C5)O)(C)C)C 484.60 unknown via CMAUP database
Neocaesalpin E 11450901 Click to see 348.50 unknown via CMAUP database
Neocaesalpin G 11295185 Click to see 510.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Quercimeritrin 5282160 Click to see 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
(2S)-5,7-dimethoxy-2-phenyl-3,4-dihydro-2H-1-benzopyran-4-one 689011 Click to see 284.31 unknown via CMAUP database
(2S)-5,7-Dimethoxy-3',4'-methylenedioxyflavanone 10336604 Click to see 328.30 unknown via CMAUP database
4H-1-Benzopyran-4-one, 2-(1,3-benzodioxol-5-yl)-5,7-dimethoxy- 11681403 Click to see 326.30 unknown via CMAUP database
5,7-Dimethoxyflavone 88881 Click to see COC1=CC2=C(C(=C1)OC)C(=O)C=C(O2)C3=CC=CC=C3 282.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
16-Hydroxy-18-methoxy-6,8,12,21-tetraoxapentacyclo[11.8.0.02,10.05,9.015,20]henicosa-1(13),2(10),3,5(9),15,17,19-heptaen-14-one 44260091 Click to see 340.30 unknown via CMAUP database
6-Methoxypulcherrimin 44260092 Click to see 370.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids
(3E)-3-((3,4-dimethoxyphenyl)methylidene)-7-methoxychromen-4-one 5783568 Click to see 326.30 unknown via CMAUP database
(3E)-3-(1,3-benzodioxol-5-ylmethylidene)-7-hydroxychromen-4-one 18778791 Click to see 296.27 unknown via CMAUP database
(3E)-3-(1,3-benzodioxol-5-ylmethylidene)-7-methoxychromen-4-one 101489712 Click to see COC1=CC2=C(C=C1)C(=O)C(=CC3=CC4=C(C=C3)OCO4)CO2 310.30 unknown via CMAUP database
(3E)-3-[(3-hydroxy-4-methoxyphenyl)methylidene]-6,7-dimethoxychromen-4-one 44475180 Click to see 342.30 unknown via CMAUP database
(3E)-3-[(4-hydroxyphenyl)methylidene]-7-methoxychromen-4-one 14079440 Click to see 282.29 unknown via CMAUP database
(3E)-7-hydroxy-3-[(3-hydroxy-4-methoxyphenyl)methylidene]chromen-4-one 13846662 Click to see 298.29 unknown via CMAUP database
(e)-7-Hydroxy-3-(2',4'-dimethoxybenzylidene) chroman-4-one 101356812 Click to see COC1=CC(=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O)OC 312.30 unknown via CMAUP database
(e)-7-Hydroxy-3-(3',4',5'-trimethoxybenzylidene) chroman-4-one 16082056 Click to see 342.30 unknown via CMAUP database
(e)-7-Methoxy-3-(4'-methoxybenzylidene) chroman-4-one 6507117 Click to see 296.30 unknown via CMAUP database
Bonducellin 14079439 Click to see 282.29 unknown via CMAUP database
Isobonducellin 10423880 Click to see COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3)O 282.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans / Homoisoflavanones
(3S)-7-hydroxy-3-[(4-methoxyphenyl)methyl]-2,3-dihydrochromen-4-one 51533159 Click to see 284.31 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
2'-Hydroxy-2,3,4',6'-tetramethoxychalcone 10337542 Click to see 344.40 unknown via CMAUP database
Isoliquiritigenin 4'-methyl ether 6537040 Click to see 270.28 unknown via CMAUP database

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