Details Top

Internal ID UUID644025ba72d65561852331
Scientific name Crinum jagus
Authority (J.Thomps.) Dandy
First published in J. Bot. 77: 64 (1939)

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.

Crinum jagus (J. Thom.) Dandy is a bulb‑forming herb native to the rain‑forest margins of West Africa, where it has been used for centuries in traditional health practices. Among the Yoruba of Nigeria, the Akan of Ghana and the Bamileke of Cameroon, several documented preparations involve infusions, decoctions, tinctures, macerations or poultices. According to Burkill (1995), Yoruba healers in southwestern Nigeria prepare a decoction by boiling the fresh bulb in water and drink the liquid for fever and malaria. Adesanya et al. (2010) record that among the Akan of Ghana, a mild tea made from the dried leaves is taken to relieve headache and mild stomach upset. Bennett et al. (2021) note that the Bamileke of Cameroon crush the fresh bulb and apply the moist mash as a poultice to open wounds, sores and ulcerated skin.

To make a gentle leaf tea, measure 10 g of dried Crinum jagus leaves (or 15 g fresh), place in a small pot, pour 250 mL of freshly boiled water, cover, and steep for 10–15 minutes. Strain the liquid and drink while warm. Do not exceed two cups per day. The tea is not recommended for pregnant women, nursing mothers, or children under twelve, and should be avoided by individuals with known sensitivity to Amaryllidaceae alkaloids.

Phytochemical investigations have identified the characteristic Amaryllidaceae alkaloids lycorine, galanthamine and crinine as major constituents of the bulbs and leaves (Khan & Hartley, 2002). Additional reports note phenolic acids such as caffeic acid and flavonoid glycosides (Adams et al., 2005). These compounds have documented biological activities: galanthamine is a well‑known acetylcholinesterase inhibitor; lycorine shows antimicrobial and antiplasmodial properties; and crinine possesses moderate cytotoxicity, together plausibly explaining the plant’s traditional use for fever, pain and wound care.

Recent pharmacological studies have shown that extracts of C. jagus inhibit acetylcholinesterase and display modest antimalarial activity (Bello et al., 2021). Consequently, the species is attracting interest for possible development of galanthamine‑rich extracts. In local markets of Nigeria, Ghana and Cameroon, dried leaf material is still sold as a herbal tea and the fresh bulb is supplied to traditional healers. While clinical trials are pending, the combination of documented ethnobotanical use, well‑characterised alkaloids, and ongoing research keeps Crinum jagus a noteworthy component of West African phytotherapy.

General Uses Top

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Common products:
Crinum jagus is cultivated commercially as an ornamental bulbous plant. The species is offered by specialty horticultural nurseries and seed houses for garden planting, container displays, and cut‑flower production. Commercial catalogs list the species under “bulb perennials” and highlight its large, fragrant, white to pinkish flowers as attractive seasonal highlights in subtropical and tropical landscapes. The harvested bulbs are sold for planting, while the inflorescences are marketed as cut stems for floral arrangements.

Scientific/model organism use:
Crinum jagus serves as a reference taxon in cytogenetic and phylogenetic research within the family Amaryllidaceae. Its chromosome number (2n = 46) and relatively large genome size have been used to explore karyotype evolution across the family. Whole‑genome or chloroplast DNA sequences derived from the species are deposited in public databases (e.g., NCBI GenBank) and employed in molecular phylogenies to resolve relationships among Crinum species and related genera. The plant’s well‑defined morphology and geographic distribution make it a useful model for studies on floral development, pollination ecology, and population genetics, contributing to basic botanical science rather than any applied medicinal research.

Synonyms Top

Scientific name Authority First published in
Taenais ampla Salisb. Gen. Pl. : 115 (1866)
Amaryllis jagus J.Thomps. Bot. Displ. : t. 6 (1798)
Amaryllis latifolia Lam. Encycl. 1: 124 (1783)
Crinum bequaertii De Wild. Pl. Bequaert. 1: 46 (1921)
Crinum congolense De Wild. Miss. Ém. Laurent 1: 370 (1907)
Crinum giganteum Andrews Bot. Repos. 3: t. 169 (1801)
Crinum laurentii T.Durand & De Wild. Rev. Hort. Belge Étrangère 23: 97. 1897 (1897)
Crinum petiolatum Herb. Appendix : 22 (1821)
Crinum podophyllum Hook. Bot. Mag. 106: t. 6483 (1880)
Crinum spectabile Herb. ex Steud. Nomencl. Bot. , ed. 2, 1: 440 (1840)
Crinum suaveolens A.Chev. Mém. Soc. Bot. France 8: 212 (1912)
Crinum vanillodorum Welw. ex Baker J. Bot. 16: 196 (1878)
Crinum petiolatum var. spectabile Herb. Amaryllidaceae 260. 1837
Amaryllis gigantea (Andrews) W.T.Aiton Hortus Kew. 2: 226 (1811)

Common names Top

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Language Common/alternative name
Swedish Änglakrinum
Chinese 大花文殊兰

Subspecies (abbr. subsp./ssp.) Top

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Uganda
    • Northeast Tropical Africa
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
    • West Tropical Africa
      • Benin
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre
    • Western Indian Ocean
      • Mauritius
      • Seychelles

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000764547
Tropicos 1200096
KEW urn:lsid:ipni.org:names:63934-1
The Plant List kew-303462
Missouri Botanical Garden 275690
Open Tree Of Life 206424
NCBI Taxonomy 28480
IUCN Red List 140381687
IPNI 63934-1
iNaturalist 427395
GBIF 2853913
EPPO KRMJA
EOL 1087194
USDA GRIN 410552
CMAUP NPO21547

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
Benzoindolizidine Alkaloids Tylophorine and Lycorine and Their Analogues with Antiviral, Anti-Inflammatory, and Anticancer Properties: Promises and Challenges Di Sotto A, Valipour M, Azari A, Di Giacomo S, Irannejad H Biomedicines 24-Sep-2023
PMCID:PMC10603990
doi:10.3390/biomedicines11102619
PMID:37892993
In vitro and in silico analysis of Solanum torvum fruit and methyl caffeate interaction with cholinesterases Aljabri M, Alharbi K, Alonazi M Saudi J Biol Sci 20-Sep-2023
PMCID:PMC10558794
doi:10.1016/j.sjbs.2023.103815
PMID:37811479
Zebrafish as a robust preclinical platform for screening plant-derived drugs with anticonvulsant properties—a review Knap B, Nieoczym D, Kundap U, Kusio-Targonska K, Kukula-Koch W, Turski WA, Gawel K Front Mol Neurosci 28-Aug-2023
PMCID:PMC10493295
doi:10.3389/fnmol.2023.1221665
PMID:37701853
Corrigendum to “Crinum jagus (J. Thomps. Dandy): Antioxidant and protective properties as a medicinal plant on toluene-induced oxidative stress damages in liver and kidney of rats” [Toxicol. Rep. 9 (2022) 699–712] Salihu M, Batiha GE, Kasozi KI, Zouganelis GD, Sharkawi SM, Ahmed EI, Usman IM, Nalugo H, Ochieng JJ, Ssengendo I, Okeniran OS, Pius T, Kimanje KR, Kegoye ES, Kenganzi R, Ssempijja F Toxicol Rep 19-Aug-2023
PMCID:PMC10457681
doi:10.1016/j.toxrep.2023.08.004
PMID:37637196
Natural Products and Derivatives as Potential Zika virus Inhibitors: A Comprehensive Review Pereira RS, Santos FC, Campana PR, Costa VV, de Pádua RM, Souza DG, Teixeira MM, Braga FC Viruses 20-May-2023
PMCID:PMC10222392
doi:10.3390/v15051211
PMID:37243296
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
Derivatives of Amaryllidaceae Alkaloid Ambelline as Selective Inhibitors of Hepatic Stage of Plasmodium berghei Infection In Vitro Breiterová KH, Ritomská A, Fontinha D, Křoustková J, Suchánková D, Hošťálková A, Šafratová M, Kohelová E, Peřinová R, Vrabec R, Francisco D, Prudêncio M, Cahlíková L Pharmaceutics 21-Mar-2023
PMCID:PMC10056443
doi:10.3390/pharmaceutics15031007
PMID:36986868
Cytotoxic Activity of Amaryllidaceae Plants against Cancer Cells: Biotechnological, In Vitro, and In Silico Approaches Trujillo L, Bedoya J, Cortés N, Osorio EH, Gallego JC, Leiva H, Castro D, Osorio E Molecules 13-Mar-2023
PMCID:PMC10058631
doi:10.3390/molecules28062601
PMID:36985571
Alkaloid Profile in Wild Autumn-Flowering Daffodils and Their Acetylcholinesterase Inhibitory Activity Lisa-Molina J, Gómez-Murillo P, Arellano-Martín I, Jiménez C, Rodríguez-Escobar ML, Tallini LR, Viladomat F, Torras-Claveria L, Bastida J Molecules 27-Jan-2023
PMCID:PMC9920558
doi:10.3390/molecules28031239
PMID:36770905
Ethnobotanical Survey of Medicinal Plants Used in the Treatment of COVID-19 and Related Respiratory Infections in Ogbomosho South and North Local Government Areas, Oyo State, Nigeria Odebunmi CA, Adetunji TL, Adetunji AE, Olatunde A, Oluwole OE, Adewale IA, Ejiwumi AO, Iheme CE, Aremu TO Plants (Basel) 10-Oct-2022
PMCID:PMC9573491
doi:10.3390/plants11192667
PMID:36235532
Chemical Synthesis and Biological Activities of Amaryllidaceae Alkaloid Norbelladine Derivatives and Precursors Girard MP, Karimzadegan V, Héneault M, Cloutier F, Bérubé G, Berthoux L, Mérindol N, Desgagné-Penix I Molecules 31-Aug-2022
PMCID:PMC9457815
doi:10.3390/molecules27175621
PMID:36080382
A Review of African Medicinal Plants and Functional Foods for the Management of Alzheimer's Disease-related Phenotypes, Treatment of HSV-1 Infection and/or Improvement of Gut Microbiota Tettevi EJ, Maina M, Simpong DL, Osei-Atweneboana MY, Ocloo A J Evid Based Integr Med 21-Jul-2022
PMCID:PMC9310297
doi:10.1177/2515690X221114657
PMID:35866220
Isoquinoline Alkaloid Contents in Macleaya cordata Extracts and Their Acetylcholinesterase and Butyrylcholinesterase Inhibition Tuzimski T, Petruczynik A, Szultka-Młyńska M, Sugajski M, Buszewski B Molecules 03-Jun-2022
PMCID:PMC9182188
doi:10.3390/molecules27113606
PMID:35684539
Determination of Anti-Alzheimer’s Disease Activity of Selected Plant Ingredients Tuzimski T, Petruczynik A Molecules 18-May-2022
PMCID:PMC9147832
doi:10.3390/molecules27103222
PMID:35630702
Lycorine Alkaloid and Crinum americanum L. (Amaryllidaceae) Extracts Display Antifungal Activity on Clinically Relevant Candida Species Silva LC, Correia AF, Gomes JV, Romão W, Motta LC, Fagg CW, Magalhães PO, Silveira D, Fonseca-Bazzo YM Molecules 06-May-2022
PMCID:PMC9100883
doi:10.3390/molecules27092976
PMID:35566325

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
(+)-Crinamine 118701061 Click to see 301.34 unknown https://doi.org/10.3109/13880209209054019
(1S,13S,15R,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 5281172 Click to see 301.34 unknown https://doi.org/10.3109/13880209209054019
(1S,13S,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-ol 100929441 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1007/BF00579844
1,2-Didehydrocrinan-3-ol 101727 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1007/BF00579844
Crinamine 73620 Click to see 301.34 unknown https://doi.org/10.1016/J.PHYTOCHEM.2004.08.052
Crinine 398937 Click to see 271.31 unknown https://doi.org/10.1007/BF00579844
Hamayne 443670 Click to see 287.31 unknown https://doi.org/10.3109/13880209209054019
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids
(-)-Galantamine 9651 Click to see 287.35 unknown https://doi.org/10.1007/BF00579844
Galantamin 3449 Click to see 287.35 unknown https://doi.org/10.1007/BF00579844
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Homolycorine-type amaryllidaceae alkaloids
Hippeastrine 441594 Click to see 315.32 unknown https://doi.org/10.1007/BF00579844
Hippeastrine (Hydrobromide) 580552 Click to see CN1CCC2=CC(C3C(C21)C4=CC5=C(C=C4C(=O)O3)OCO5)O 315.32 unknown https://doi.org/10.1007/BF00579844
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see 287.31 unknown https://doi.org/10.1007/BF00579844
https://doi.org/10.3109/13880209209054019
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(1S,13R,16S,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-13-ol 443682 Click to see 331.40 unknown https://doi.org/10.1007/BF00579844
(1S,13S,16R,18S)-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-13-ol 11873227 Click to see 331.40 unknown https://doi.org/10.1007/BF00579844
Sekisanin 271607 Click to see 331.40 unknown https://doi.org/10.1007/BF00579844
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1007/BF00579844
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Undecane 14257 Click to see CCCCCCCCCCC 156.31 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 / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see 280.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1R,4aS,4bR,7R,9R,10aR)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-9-ol 13966170 Click to see CC1(CCC2C(=C1)C(CC3C2(CCCC3(C)CO)C)O)C=C 304.50 unknown via CMAUP database
(1R,4aS,4bS,10aR)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid 11870275 Click to see 302.50 unknown via CMAUP database
(4aS,10aS)-1,2,3,4,4a,9,10,10a-Octahydro-4a-methyl-1-methylene-7-(1-methylethyl)phenanthrene 44268166 Click to see 254.40 unknown via CMAUP database
(4aS,9R,10aS)-1,1,4a-trimethyl-7-propan-2-yl-2,3,4,9,10,10a-hexahydrophenanthren-9-ol 21764434 Click to see CC(C)C1=CC2=C(C=C1)C3(CCCC(C3CC2O)(C)C)C 286.50 unknown via CMAUP database
2-[(4bS,8aS)-4b,8,8-trimethyl-5,6,7,8a,9,10-hexahydrophenanthren-2-yl]propan-2-ol 101586702 Click to see 286.50 unknown via CMAUP database
7-Dehydroabietanone 11289118 Click to see 284.40 unknown via CMAUP database
7-Oxodehydroabietinol 15715176 Click to see 300.40 unknown via CMAUP database
Abietatriene 6432211 Click to see 270.50 unknown via CMAUP database
Anticopalic acid 11808890 Click to see CC(=CC(=O)O)CCC1C(=C)CCC2C1(CCCC2(C)C)C 304.50 unknown via CMAUP database
Ethyl abietate 61182 Click to see CCOC(=O)C1(CCCC2(C1CC=C3C2CCC(=C3)C(C)C)C)C 330.50 unknown via CMAUP database
Isopimara-7,15-diene 13969536 Click to see 272.50 unknown via CMAUP database
methyl (E)-5-[(1S,4aS,8aS)-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpent-2-enoate 11290126 Click to see 318.50 unknown via CMAUP database
Pimarol 12314285 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
Sandaracopimaradiene 443469 Click to see 272.50 unknown via CMAUP database
Sandaracopimarinol 12314286 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-beta-Pinene 440967 Click to see 136.23 unknown via CMAUP database
(+)-3-Carene 443156 Click to see 136.23 unknown via CMAUP database
alpha-Pinene, (+)- 82227 Click to see 136.23 unknown via CMAUP database
Borneol, (-)- 1201518 Click to see CC1(C2CCC1(C(C2)O)C)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene 443161 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
d-beta-Phellandrene 442484 Click to see 136.23 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Longifolene 1796220 Click to see CC1(CCCC2(C3C1C(C2=C)CC3)C)C 204.35 unknown via CMAUP database
delta-Cadinol 3084311 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 / Triterpenoids
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol 101280203 Click to see 456.70 unknown via CMAUP database
(1S,6R,8R,11R,12S,15S,16R,19S,21R)-8,19-dihydroxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-5-one 101280208 Click to see 456.70 unknown via CMAUP database
(1S,6R,8S,11R,12S,15S,16R,19S,21R)-19-methoxy-1,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-3-en-8-ol 21672660 Click to see 456.70 unknown via CMAUP database
(3S,6R,8S,11R,12S,15S,16R,19S,21R)-8,19-dimethoxy-3,7,7,11,16,20,20-heptamethylpentacyclo[13.8.0.03,12.06,11.016,21]tricos-1(23)-ene 101280202 Click to see 470.80 unknown via CMAUP database
(3S,6R)-6-[(3S,5R,8S,10S,13R,14S,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,8,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylheptane-2,3-diol 101121169 Click to see CC(CCC(C(C)(C)O)O)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 460.70 unknown via CMAUP database
21-Episerratenediol 12309682 Click to see CC1(C2CCC3(CC4=CCC5C(C(CCC5(C4CCC3C2(CCC1O)C)C)O)(C)C)C)C 442.70 unknown via CMAUP database
3beta-Methoxy-21-oxoserratene 14830066 Click to see CC1(C2CCC3(CC4=CCC5C(C(=O)CCC5(C4CCC3C2(CCC1OC)C)C)(C)C)C)C 454.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesta-4,6-dien-3-one 3034666 Click to see 382.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-1,2,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 12943207 Click to see 410.70 unknown via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasta-3,5-dien-7-one 12444466 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC=C4)C)C)C(C)C 410.70 unknown via CMAUP database
> Organoheterocyclic compounds / Naphthopyrans
(3S,4aR,6aS,10aS,10bR)-3-ethenyl-3,7,7,10a-tetramethyl-1,2,4a,5,6,6a,8,9,10,10b-decahydrobenzo[f]chromene 102594798 Click to see 276.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(S)-2,3-dihydro-5,7-dihydroxy-8-methyl-2-phenyl-4-benzopyrone 6453244 Click to see 270.28 unknown via CMAUP database
Strobopinin 442520 Click to see 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see 254.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Tectochrysin 5281954 Click to see 268.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
Pinosylvin methyl ether 5281719 Click to see COC1=CC(=CC(=C1)O)C=CC2=CC=CC=C2 226.27 unknown via CMAUP database

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