Nerine bowdenii - Unknown
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Internal ID UUID64401da80fc2e655227928
Scientific name Nerine bowdenii
Authority W.Watson
First published in Gard. Chron. , ser. 3, 36: 365 (1904)

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English large pink nerine
Czech nerine bowdenova
Chinese 白纳丽花

Subspecies (abbr. subsp./ssp.) Top

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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)

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
  • Africa
    • Southern Africa
      • Cape Provinces
      • Free State
      • Kwazulu-Natal

Links to other databases Top

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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)!
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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
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
PMCID:PMC10345363
doi:10.1016/j.jsps.2023.06.017
PMID:37457365
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
PMCID:PMC10222022
doi:10.3390/molecules28103986
PMID:37241726
Chemical Profiling and Molecular Docking Study of Agathophora alopecuroides Amin E, Abdel-Bakky MS, Mohammed HA, Hassan MH Life (Basel) 11-Nov-2022
PMCID:PMC9696702
doi:10.3390/life12111852
PMID:36430987
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
PMCID:PMC9118764
doi:10.1186/s12906-022-03617-x
PMID:35585532
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
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
PMCID:PMC8434202
doi:10.3390/molecules26175240
PMID:34500673
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
PMCID:PMC8379525
doi:10.1016/j.simyco.2021.100116
PMID:34466168
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
PMCID:PMC9311392
doi:10.3767/persoonia.2021.46.05
PMID:35935895
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
PMCID:PMC7761792
doi:10.3390/jof6040336
PMID:33291584
Biosynthesis and Biological Activities of Newly Discovered Amaryllidaceae Alkaloids Ka S, Koirala M, Mérindol N, Desgagné-Penix I Molecules 23-Oct-2020
PMCID:PMC7660210
doi:10.3390/molecules25214901
PMID:33113950
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
PMCID:PMC8457019
doi:10.6026/97320630016702
PMID:34621116
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
PMCID:PMC7554109
doi:10.1002/med.21703
PMID:32729169
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
PMCID:PMC7277649
doi:10.3390/biom10050800
PMID:32455879
The Genus Nerine Herb. (Amaryllidaceae): Ethnobotany, Phytochemistry, and Biological Activity Cahlíková L, Vaněčková N, Šafratová M, Breiterová K, Blunden G, Hulcová D, Opletal L Molecules 21-Nov-2019
PMCID:PMC6930486
doi:10.3390/molecules24234238
PMID:31766438

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
(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 CC(=O)OC1CN2CC3=C(C4=C(C=C3C15C2CC(C=C5)OC)OCO4)OC 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 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,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 COC1=C2CN3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6 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
Amberline 494154 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 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
Buphanisin 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 COC1=C2CN3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6 317.34 unknown https://doi.org/10.1002/CBER.19560890910
Crinan-12-ol, 1,2-didehydro-3alpha,7-dimethoxy- 441585 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown https://doi.org/10.1080/14786410802263758
Crinine 398937 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1002/CBER.19560890910
Undulatine 3083985 Click to see COC1CC2C3(CCN2CC4=C(C5=C(C=C43)OCO5)OC)C6C1O6 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 CN1CCC23C=CC(CC2OC4=C(C=CC(=C34)C1)OC)O 287.35 unknown https://doi.org/10.1002/PCA.675
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Norbelladine-type amaryllidaceae alkaloids
Belladine 441586 Click to see CN(CCC1=CC=C(C=C1)OC)CC2=CC(=C(C=C2)OC)OC 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 C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-Caffeoyltyramine 9994897 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC(=C(C=C2)O)O)O 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 COC1=CC(=CC(=C1O)O)C(=O)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C(=C4)O)O)O)O)O 472.40 unknown via CMAUP database
Epigallocatechin 3-O-(3,5-di-O-methylgallate) 9913276 Click to see COC1=CC(=CC(=C1O)OC)C(=O)OC2CC3=C(C=C(C=C3OC2C4=CC(=C(C(=C4)O)O)O)O)O 486.40 unknown via CMAUP database
Epigallocatechin Gallate 65064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O 458.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(2R,3S)-3,4',5,7-Tetrahydroxy-3',5'-dimethoxy-2,3-dihydroflavone 101034223 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 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 C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 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 CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 616.50 unknown via CMAUP database
2''-O-Galloylquercitrin 10031482 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)O)O 600.50 unknown via CMAUP database
3-[2-O-(4-Hydroxybenzoyl)-alpha-L-rhamnopyranosyloxy]-3',4',5,5',7-pentahydroxyflavone 101044324 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)OC(=O)C5=CC=C(C=C5)O)O)O 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-galactoside 5491408 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O 480.40 unknown via CMAUP database
Myricetin 3-O-beta-D-galactoside 6''-O-gallate 5319985 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O 632.50 unknown via CMAUP database
Myricitrin 5281673 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)O)O 464.40 unknown via CMAUP database
Quercitrin 5280459 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)O 448.40 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 COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown via CMAUP database

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