Cordyline rubra - Unknown
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Internal ID UUID644025b073717002589207
Scientific name Cordyline rubra
Authority Otto & A.Dietr.
First published in Allg. Gartenzeitung 16: 121 (1848)

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Synonyms Top

Scientific name Authority First published in
Charlwoodia rubra (Otto & A.Dietr.) Planch. Fl. des Serres vi. (1850-51) 138.
Terminalis rubra (Otto & A.Dietr.) Kuntze Revis. Gen. Pl. 2: 716 (1891)
Cordyline rubra f. violascens (Regel) Voss Vilm. Blumengärtn. ed. 3 1: 1062 1895
Cordyline violascens Regel Index Seminum (LE, Petropolitanus) 1858: 25 (1859)
Dracaena rubra (Otto & A.Dietr.) Parm. Cat. Pl. Rar. : 11 (1853)
Dracaena zeelandica Baker J. Linn. Soc., Bot. 14: 544 (1875)

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Language Common/alternative name
Spanish dracena roja
Spanish drácena roja
Spanish palma de carey
Arabic كورديل حمراء
Chinese 红花朱蕉

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000764301
KEW urn:lsid:ipni.org:names:97540-3
The Plant List kew-303225
Open Tree Of Life 3995176
NCBI Taxonomy 1619826
IUCN Red List 192204741
IPNI 533638-1
iNaturalist 425878
GBIF 2766245
Freebase /m/0cc933s
EPPO CDLRU
EOL 1087107
USDA GRIN 11512
Wikipedia Cordyline_rubra

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
Ethnobotany, Phytochemistry, and Biological Activities of the Genus Cordyline Tematio Fouedjou R, Tsakem B, Siwe-Noundou X, Dongmo Fogang HP, Tiombou Donkia A, Kemvoufo Ponou B, Poka M, Demana PH, Teponno RB, Azefack Tapondjou L Biomolecules 12-Dec-2023
PMCID:PMC10741932
doi:10.3390/biom13121783
PMID:38136652
Vegetation structure and ground cover attributes describe the occurrence of a newly discovered carnivorous marsupial on the Tweed Shield Volcano caldera, the endangered black‐tailed dusky antechinus (Antechinus arktos) Riordan CE, Pearce C, McDonald BJ, Gynther I, Baker AM Ecol Evol 12-Feb-2020
PMCID:PMC7042678
doi:10.1002/ece3.6045
PMID:32128142
Fungal Planet description sheets: 868–950 Crous PW, Carnegie AJ, Wingfield MJ, Sharma R, Mughini G, Noordeloos ME, Santini A, Shouche YS, Bezerra JD, Dima B, Guarnaccia V, Imrefi I, Jurjević Ž, Knapp DG, Kovács GM, Magistà D, Perrone G, Rämä T, Rebriev YA, Shivas RG, Singh SM, Souza-Motta CM, Thangavel R, Adhapure NN, Alexandrova AV, Alfenas AC, Alfenas RF, Alvarado P, Alves AL, Andrade DA, Andrade JP, Barbosa RN, Barili A, Barnes CW, Baseia IG, Bellanger JM, Berlanas C, Bessette AE, Bessette AR, Biketova AY, Bomfim FS, Brandrud TE, Bransgrove K, Brito AC, Cano-Lira JF, Cantillo T, Cavalcanti AD, Cheewangkoon R, Chikowski RS, Conforto C, Cordeiro TR, Craine JD, Cruz R, Damm U, de Oliveira RJ, de Souza JT, de Souza HG, Dearnaley JD, Dimitrov RA, Dovana F, Erhard A, Esteve-Raventós F, Félix CR, Ferisin G, Fernandes RA, Ferreira RJ, Ferro LO, Figueiredo CN, Frank JL, Freire KT, García D, Gené J, Gêsiorska A, Gibertoni TB, Gondra RA, Gouliamova DE, Gramaje D, Guard F, Gusmão LF, Haitook S, Hirooka Y, Houbraken J, Hubka V, Inamdar A, Iturriaga T, Iturrieta-González I, Jadan M, Jiang N, Justo A, Kachalkin AV, Kapitonov VI, Karadelev M, Karakehian J, Kasuya T, Kautmanová I, Kruse J, Kušan I, Kuznetsova TA, Landell MF, Larsson KH, Lee HB, Lima DX, Lira CR, Machado AR, Madrid H, Magalhães OM, Majerova H, Malysheva EF, Mapperson RR, Marbach PA, Martín MP, Martín-Sanz A, Matočec N, McTaggart AR, Mello JF, Melo RF, Mešić A, Michereff SJ, Miller AN, Minoshima A, Molinero-Ruiz L, Morozova OV, Mosoh D, Nabe M, Naik R, Nara K, Nascimento SS, Neves RP, Olariaga I, Oliveira RL, Oliveira TG, Ono T, Ordoñez ME, Ottoni AD, Paiva LM, Pancorbo F, Pant B, Pawłowska J, Peterson SW, Raudabaugh DB, Rodríguez-Andrade E, Rubio E, Rusevska K, Santiago AL, Santos AC, Santos C, Sazanova NA, Shah S, Sharma J, Silva BD, Siquier JL, Sonawane MS, Stchigel AM, Svetasheva T, Tamakeaw N, Telleria MT, Tiago PV, Tian CM, Tkalčec Z, Tomashevskaya MA, Truong HH, Vecherskii MV, Visagie CM, Vizzini A, Yilmaz N, Zmitrovich IV, Zvyagina EA, Boekhout T, Kehlet T, Læssøe T, Groenewald JZ Persoonia 19-Jul-2019
PMCID:PMC6712538
doi:10.3767/persoonia.2019.42.11
PMID:31551622
Steroidal Sapogenins From Leaves of Cordyline Species Gerald Blunden, Jaffer A. Jaffer, Kenneth Jewers, William J. Griffin American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50016A007
Rubragenin, chenogenin and wallogenin, steroidal sapogenins from Cordyline rubra Ming-He Yang, Gerald Blunden, Asmita Patel, Trevor A. Crabb, William J. Griffin Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80300-0
Two furostane sapogenins from Cordyline rubra Ming-He Yang, Gerald Blunden, Asmita Patel, Trevor A. Crabb, Keith Brain, William J. Griffin Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(90)85458-R

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2S,3'R,4S,6R,7S,8R,9S,12S,13S,14R,16S,18S)-3',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,6'-oxane]-3',14,16-triol 12304336 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(C(CC(C5)O)O)C)C)OC16CCC(CO6)(C)O 448.60 unknown https://doi.org/10.1016/0031-9422(89)80300-0
(1S,2S,3'S,4S,6R,7S,8R,9S,12S,13S,14R,16S,18S)-3',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,6'-oxane]-3',14,16-triol 163063034 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(C(CC(C5)O)O)C)C)OC16CCC(CO6)(C)O 448.60 unknown https://doi.org/10.1016/0031-9422(89)80300-0
(25R)-5beta-Spirostane-1beta,3beta,25-triol 12304333 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(C(CC(C5)O)O)C)C)OC16CCC(CO6)(C)O 448.60 unknown https://doi.org/10.1016/0031-9422(89)80300-0
Cannigenin 182281 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(C(CC(C6)O)O)C)C)C)OC1 432.60 unknown https://doi.org/10.1016/0031-9422(89)80300-0
Tigogenin 99516 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown https://doi.org/10.1021/NP50016A007
Yamogenin 441900 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1021/NP50016A007
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Furospirostanes and derivatives
(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13S,14R,16S,18S)-5'-(hydroxymethyl)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxolane]-14,16-diol 14412513 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(C(CC(C5)O)O)C)C)OC16CCC(O6)(C)CO 448.60 unknown https://doi.org/10.1016/0031-9422(89)80300-0
(1S,2S,4S,5'R,6S,7S,8R,9S,12S,13S,14R,16S,18S)-5'-(hydroxymethyl)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxolane]-14,16-diol 14412512 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(C(CC(C5)O)O)C)C)OC16CCC(O6)(C)CO 448.60 unknown https://doi.org/10.1016/0031-9422(89)80300-0
(1S,2S,4S,5'S,6S,7S,8R,9S,12S,13S,14R,16R,18S)-5'-(hydroxymethyl)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxolane]-14,16-diol 101611197 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(C(CC(C5)O)O)C)C)OC16CCC(O6)(C)CO 448.60 unknown https://doi.org/10.1016/0031-9422(89)80300-0
(1S,2S,4S,5'S,6S,7S,8R,9S,12S,13S,14R,16S,18S)-5'-(hydroxymethyl)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxolane]-14,16-diol 14412514 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(C(CC(C5)O)O)C)C)OC16CCC(O6)(C)CO 448.60 unknown https://doi.org/10.1016/0031-9422(89)80300-0
5'-(Hydroxymethyl)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxolane]-14,16-diol 14412511 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(C(CC(C5)O)O)C)C)OC16CCC(O6)(C)CO 448.60 unknown https://doi.org/10.1016/0031-9422(89)80300-0
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Furostanes and derivatives
(1R,2R,4S,6R,7S,8R,9S,12R,13R,14R,16S)-7,9,13-trimethyl-6-(3-methylbutyl)-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-14,16-diol 162866383 Click to see CC1C(OC2C1C3(CCC4C(C3C2)CC=C5C4(C(CC(C5)O)O)C)C)CCC(C)C 416.60 unknown https://doi.org/10.1016/0031-9422(90)85458-R
(1S,2S,4S,6R,7S,8R,9S,12S,13S,14R,16S,18S)-6-[(3S)-4-hydroxy-3-methylbutyl]-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-14,16-diol 163014816 Click to see CC1C(OC2C1C3(CCC4C(C3C2)CCC5C4(C(CC(C5)O)O)C)C)CCC(C)CO 434.70 unknown https://doi.org/10.1016/0031-9422(90)85458-R
6-(4-Hydroxy-3-methylbutyl)-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-14,16-diol 14585496 Click to see CC1C(OC2C1C3(CCC4C(C3C2)CCC5C4(C(CC(C5)O)O)C)C)CCC(C)CO 434.70 unknown https://doi.org/10.1016/0031-9422(90)85458-R
7,9,13-Trimethyl-6-(3-methylbutyl)-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-14,16-diol 14585493 Click to see CC1C(OC2C1C3(CCC4C(C3C2)CC=C5C4(C(CC(C5)O)O)C)C)CCC(C)C 416.60 unknown https://doi.org/10.1016/0031-9422(90)85458-R
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
[(3R,4R,5R,8S,9S,10R,13S,14S,17S)-3-[benzoyl(methyl)amino]-17-[(1S)-1-(dimethylamino)ethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-4-yl] acetate 12313881 Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4OC(=O)C)N(C)C(=O)C5=CC=CC=C5)C)C)N(C)C 522.80 unknown https://doi.org/10.1016/0031-9422(89)80300-0

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