Nerine bowdenii
Details Top
| Internal ID | UUID64401da80fc2e655227928 |
| Scientific name | Nerine bowdenii |
| Authority | W.Watson |
| First published in | Gard. Chron. , ser. 3, 36: 365 (1904) |
General Uses Top
Suggest a correction!Common products:
Flowers used in cut‑flower trade; harvested and sold for seasonal floral arrangements and bouquets (Nerine bowdenii is a commonly cultivated ornamental grown for its autumn-flowering spikes).
Industrial and craft applications:
No documented uses beyond ornamental horticulture.
Food and beverages (non-medicinal):
No culinary uses reported.
Colorants and tanning:
No dye, ink, or tannin uses reported.
Wood and fiber:
No wood, timber, or fiber uses reported.
Fragrance and cosmetics:
No fragrance or cosmetic uses reported.
Properties relevant to use:
Late-season flowering and long vase life enable commercial production as a cut flower.
Standards and regulation:
Subject to general horticultural trade regulations for ornamental plants and cut flowers (national phytosanitary and plant variety regulations); no species‑specific standards documented.
Sustainability and sourcing:
Commercially propagated vegetatively; main source countries for Nerine cut flowers include the Netherlands and South Africa.
Synonyms Top
| Scientific name | Authority | First published in |
|---|---|---|
| Nerine veitchii | auct. | Gard. Chron. III, 1: 244 1911 |
Common names Top
Add a new one! Suggest a correction!| Language | Common/alternative name |
|---|---|
| English | large pink nerine |
| Finnish | ruusuneidikki |
| Chinese | 白纳丽花 |
Subspecies (abbr. subsp./ssp.) Top
Add a new one! Suggest a correction!| Name | Authority | First published in |
|---|---|---|
| Nerine bowdenii subsp. bowdenii | ||
| Nerine bowdenii subsp. wellsii | C.A.Norris ex G.D.Duncan | Bot. Mag. 31: 235 (2014) |
Germination/Propagation Top
Suggest a correction or add new data!| 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
-
Africa click to expand
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Southern Africa
- Cape Provinces
- Free State
- Kwazulu-Natal
-
Southern Africa
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Europe click to expand
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Northern Europe
- Great Britain
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Northern Europe
Links to other databases Top
Suggest others/fix!| Database | ID/link to page |
|---|---|
| World Flora Online | wfo-0000697973 |
| USDA Plants | NEBO |
| KEW | urn:lsid:ipni.org:names:66292-1 |
| The Plant List | kew-282092 |
| Open Tree Of Life | 695840 |
| Observations.org | 271131 |
| NCBI Taxonomy | 59042 |
| NBN Atlas | NHMSYS0000460979 |
| IPNI | 66292-1 |
| iNaturalist | 461606 |
| GBIF | 5326845 |
| Freebase | /m/0b6mv_m |
| EPPO | NRIBO |
| EOL | 1009928 |
| Elurikkus | 516581 |
| USDA GRIN | 411359 |
| Wikipedia | Nerine_bowdenii |
| CMAUP | NPO1346 |
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.
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 |
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| Design of semisynthetic derivatives of the Amaryllidaceae alkaloid ambelline and exploration of their in vitro cytotoxic activities | Ritomská A, Koutova D, Křoustková J, Královec K, Muthná D, Kuneš J, Nováková L, Havelek R, Cahlíková L | Saudi Pharm J | 24-Jun-2023 |
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| Chemical Characterization and Cytotoxic and Antioxidant Activity Evaluation of the Ethanol Extract from the Bulbs of Pancratium maritimun Collected in Sicily | Cicio A, Sut S, Dall’Acqua S, Bruno M, Luparello C, Serio R, Zizzo MG | Molecules | 09-May-2023 |
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| 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 |
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| Chemical Profiling and Molecular Docking Study of Agathophora alopecuroides | Amin E, Abdel-Bakky MS, Mohammed HA, Hassan MH | Life (Basel) | 11-Nov-2022 |
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| Standardization of the ethanolic extract of Crinum latifolium leaves by two bioactive markers with antiproliferative activity against TGF-β-promoted prostate stromal cells (WPMY-1) | Thongphichai W, Uttarawichien T, Chanvorachote P, Pitiporn S, Charoen-ame T, Kwankhao P, Towiwat P, Sukrong S | BMC Complement Med Ther | 18-May-2022 |
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| Prophyll in Monocots: The Starting Point of Lateral Shoot Phyllotaxis | Choob V | Front Plant Sci | 13-Apr-2022 |
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| Recent Progress on Biological Activity of Amaryllidaceae and Further Isoquinoline Alkaloids in Connection with Alzheimer’s Disease | Cahlíková L, Vrabec R, Pidaný F, Peřinová R, Maafi N, Mamun AA, Ritomská A, Wijaya V, Blunden G | Molecules | 29-Aug-2021 |
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| Fusarium: more than a node or a foot-shaped basal cell | Crous PW, Lombard L, Sandoval-Denis M, Seifert KA, Schroers HJ, Chaverri P, Gené J, Guarro J, Hirooka Y, Bensch K, Kema GH, Lamprecht SC, Cai L, Rossman AY, Stadler M, Summerbell RC, Taylor JW, Ploch S, Visagie CM, Yilmaz N, Frisvad JC, Abdel-Azeem AM, Abdollahzadeh J, Abdolrasouli A, Akulov A, Alberts JF, Araújo JP, Ariyawansa HA, Bakhshi M, Bendiksby M, Ben Hadj Amor A, Bezerra JD, Boekhout T, Câmara MP, Carbia M, Cardinali G, Castañeda-Ruiz RF, Celis A, Chaturvedi V, Collemare J, Croll D, Damm U, Decock CA, de Vries RP, Ezekiel CN, Fan XL, Fernández NB, Gaya E, González CD, Gramaje D, Groenewald JZ, Grube M, Guevara-Suarez M, Gupta VK, Guarnaccia V, Haddaji A, Hagen F, Haelewaters D, Hansen K, Hashimoto A, Hernández-Restrepo M, Houbraken J, Hubka V, Hyde KD, Iturriaga T, Jeewon R, Johnston PR, Jurjević Ž, Karalti İ, Korsten L, Kuramae EE, Kušan I, Labuda R, Lawrence DP, Lee HB, Lechat C, Li HY, Litovka YA, Maharachchikumbura SS, Marin-Felix Y, Matio Kemkuignou B, Matočec N, McTaggart AR, Mlčoch P, Mugnai L, Nakashima C, Nilsson RH, Noumeur SR, Pavlov IN, Peralta MP, Phillips AJ, Pitt JI, Polizzi G, Quaedvlieg W, Rajeshkumar KC, Restrepo S, Rhaiem A, Robert J, Robert V, Rodrigues AM, Salgado-Salazar C, Samson RA, Santos AC, Shivas RG, Souza-Motta CM, Sun GY, Swart WJ, Szoke S, Tan YP, Taylor JE, Taylor PW, Tiago PV, Váczy KZ, van de Wiele N, van der Merwe NA, Verkley GJ, Vieira WA, Vizzini A, Weir BS, Wijayawardene NN, Xia JW, Yáñez-Morales MJ, Yurkov A, Zamora JC, Zare R, Zhang CL, Thines M | Stud Mycol | 17-Aug-2021 |
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| Redefining species limits in the Fusarium fujikuroi species complex | Yilmaz N, Sandoval-Denis M, Lombard L, Visagie CM, Wingfield BD, Crous PW | Persoonia | 30-Mar-2021 |
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| Fusarium Consortium Populations Associated with Asparagus Crop in Spain and Their Role on Field Decline Syndrome | Brizuela AM, De la Lastra E, Marín-Guirao JI, Gálvez L, de Cara-García M, Capote N, Palmero D | J Fungi (Basel) | 04-Dec-2020 |
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| Biosynthesis and Biological Activities of Newly Discovered Amaryllidaceae Alkaloids | Ka S, Koirala M, Mérindol N, Desgagné-Penix I | Molecules | 23-Oct-2020 |
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| Studies on the cholinesterases inhibiting compounds from the Cassiopea andromeda venom | Darabi AH, Nabipour I, Mohebbi G, Vazirizadeh A, Vatanpour H, Maryamabadi A | Bioinformation | 30-Sep-2020 |
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| Biologically Active Isoquinoline Alkaloids covering 2014-2018 | Shang XF, Yang CJ, Morris-Natschke SL, Li JC, Yin XD, Liu YQ, Guo X, Peng JW, Goto M, Zhang JY, Lee KH | Med Res Rev | 29-Jul-2020 |
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| Amaryllidaceae Alkaloids of Belladine-Type from Narcissus pseudonarcissus cv. Carlton as New Selective Inhibitors of Butyrylcholinesterase | Al Mamun A, Maříková J, Hulcová D, Janoušek J, Šafratová M, Nováková L, Kučera T, Hrabinová M, Kuneš J, Korábečný J, Cahlíková L | Biomolecules | 22-May-2020 |
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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.
You can also contribute to this by clicking here.
| Name | PubChem ID | Canonical SMILES | MW | Found in | Proof |
|---|---|---|---|---|---|
| > Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids | |||||
| (9,15-Dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-yl) acetate | 78180690 | Click to see | 373.40 | unknown | https://doi.org/10.1080/14786410802263758 |
| (9,15-Dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-yl) pyridine-3-carboxylate | 72777669 | Click to see | 436.50 | unknown | https://doi.org/10.1080/14786410802263758 |
| [(1R,13R,15R,18R)-9,15-dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-yl] pyridine-3-carboxylate | 162910113 | Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)OC(=O)C6=CN=CC=C6 | 436.50 | unknown | https://doi.org/10.1080/14786410802263758 |
| [(1R,13R,15R,18S)-9,15-dimethoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-yl] acetate | 145967039 | Click to see CC(=O)OC1CN2CC3=C(C4=C(C=C3C15C2CC(C=C5)OC)OCO4)OC | 373.40 | unknown | https://doi.org/10.1080/14786410802263758 |
| 1,2-Didehydrocrinan-3-ol | 101727 | Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 | 271.31 | unknown | https://doi.org/10.1002/CBER.19560890910 |
| 9-Methoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-trien-15-ol | 625708 | Click to see | 317.34 | unknown | https://doi.org/10.1002/CBER.19560890910 |
| 9,15-Dimethoxy-5,7,17-trioxa-12-azahexacyclo[10.6.2.01,13.02,10.04,8.016,18]icosa-2,4(8),9-triene | 271606 | Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 | 331.40 | unknown |
https://doi.org/10.1002/CBER.19560890910 https://doi.org/10.1080/14786410802263758 |
| Ambelline | 441585 | Click to see | 331.40 | unknown | https://doi.org/10.1080/14786410802263758 |
| Buphanisin | 625225 | Click to see COC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 | 285.34 | unknown | https://doi.org/10.1080/14786410802263758 |
| Buphanisine | 12302149 | Click to see COC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 | 285.34 | unknown | https://doi.org/10.1080/14786410802263758 |
| Crinamidine | 399204 | Click to see | 317.34 | unknown | https://doi.org/10.1002/CBER.19560890910 |
| Crinan-12-ol, 1,2-didehydro-3alpha,7-dimethoxy- | 494154 | Click to see | 331.40 | unknown | https://doi.org/10.1080/14786410802263758 |
| Crinine | 398937 | Click to see | 271.31 | unknown | https://doi.org/10.1002/CBER.19560890910 |
| Undulatin | 3083985 | Click to see | 331.40 | unknown |
https://doi.org/10.1080/14786410802263758 https://doi.org/10.1002/CBER.19560890910 |
| > Alkaloids and derivatives / Amaryllidaceae alkaloids / Galanthamine-type amaryllidaceae alkaloids | |||||
| (-)-Galantamine | 9651 | Click to see | 287.35 | unknown | https://doi.org/10.1002/PCA.675 |
| > Alkaloids and derivatives / Amaryllidaceae alkaloids / Norbelladine-type amaryllidaceae alkaloids | |||||
| Belladine | 441586 | Click to see | 315.40 | unknown | via CMAUP database |
| > 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 / Phenols / Methoxyphenols | |||||
| Feruloyltyramine | 5280537 | Click to see | 313.30 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives | |||||
| N-Caffeoyltyramine | 9994897 | Click to see | 299.32 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates | |||||
| Epigallocatechin 3-O-(3-O-methyl)gallate | 9804842 | Click to see | 472.40 | unknown | via CMAUP database |
| Epigallocatechin 3-O-(3,5-di-O-methylgallate) | 9913276 | Click to see | 486.40 | unknown | via CMAUP database |
| Epigallocatechin Gallate | 65064 | Click to see | 458.40 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins | |||||
| (2r,3s)-3,5,7,4'-Tetrahydroxy-3',5'-dimethoxyflavanone | 101034223 | Click to see | 348.30 | unknown | via CMAUP database |
| Epigallocatechin | 72277 | Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O | 306.27 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones | |||||
| (2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one | 667495 | Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O | 272.25 | unknown | via CMAUP database |
| Eriodictyol | 440735 | Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O | 288.25 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / Flavones | |||||
| Apigenin | 5280443 | Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O | 270.24 | unknown | via CMAUP database |
| 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 |
| > 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 / Flavonoid O-glycosides / Flavonoid-3-O-glycosides | |||||
| ((2S,3R,4R,5R,6S)-2-(5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl)oxy-4,5-dihydroxy-6-methyloxan-3-yl) 3,4,5-trihydroxybenzoate | 5316590 | Click to see | 616.50 | unknown | via CMAUP database |
| [(2S,3R,4R,5R,6S)-2-[5,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)chromen-3-yl]oxy-4,5-dihydroxy-6-methyloxan-3-yl] 4-hydroxybenzoate | 101044324 | Click to see | 584.50 | unknown | via CMAUP database |
| 3''-O-Galloylmyricitrin | 101248998 | Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O | 616.50 | unknown | via CMAUP database |
| Myricetin 3-(6''-galloylgalactoside) | 5319985 | Click to see | 632.50 | unknown | via CMAUP database |
| Myricetin 3-O-galactoside | 5491408 | Click to see | 480.40 | unknown | via CMAUP database |
| Myricitrin | 5281673 | Click to see | 464.40 | unknown | via CMAUP database |
| Quercitrin | 5280459 | Click to see | 448.40 | unknown | via CMAUP database |
| Quercitrin 2''-O-Gallate | 10031482 | Click to see | 600.50 | unknown | via CMAUP database |
| > Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids | |||||
| (2R)-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydrochromen-4-one | 12310452 | Click to see | 302.28 | unknown | via CMAUP database |
Collections Top
| In private collections | 0 |
| In public collections | 0 |