Nerine bowdenii
Table of Contents
Details Top
Internal ID | UUID64401da80fc2e655227928 |
Scientific name | Nerine bowdenii |
Authority | W.Watson |
First published in | Gard. Chron. , ser. 3, 36: 365 (1904) |
Description Top
Suggest a correction or write a new one!
No description added yet. Help us by writing one.
Common names Top
Add a new one! Suggest a correction!Language | Common/alternative name |
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English | large pink nerine |
Czech | nerine bowdenova |
Chinese | 白纳丽花 |
Subspecies (abbr. subsp./ssp.) Top
Add a new one! Suggest a correction!Name | Authority | First published in |
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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
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Africa click to expand
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Southern Africa
- Cape Provinces
- Free State
- Kwazulu-Natal
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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 | ||||||
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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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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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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 |
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Phytochemical Profile Top
Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
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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 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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In private collections | 0 |
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