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Internal ID UUID644025ca6e853433318613
Scientific name Cyrtanthus obliquus
Authority (L.f.) L.f.
First published in Hort. Kew. 1: 414 (1789)

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Synonyms Top

Scientific name Authority First published in
Loxanthes pendula Salisb. Gen. Pl. : 117 (1866)
Timmia obliqua J.F.Gmel. Syst. Nat. ed. 13[bis] : 524 (1791)
Amaryllis pendula Salisb. Prodr. Stirp. Chap. Allerton : 231 (1796)
Amaryllis umbella L'Hér. Sert. Angl. : 15 (1789)
Crinum obliquum L.f. Suppl. Pl. : 195 (1782)
Cyrtanthus varius M.Roem. Fam. Nat. Syn. Monogr. 4: 48 (1847)

Common names Top

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Language Common/alternative name
English justafina
English knysna lily
Afrikaans knysnalelie
Arabic حجينة عوجاء
Chinese 偏花曲管花
Chinese 斜叶垂筒花

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000764942
Tropicos 1201084
KEW urn:lsid:ipni.org:names:64237-1
The Plant List kew-303843
Open Tree Of Life 50113
NCBI Taxonomy 527298
IPNI 64237-1
iNaturalist 578660
GBIF 5326072
EOL 1087327
USDA GRIN 312696
Wikipedia Cyrtanthus_obliquus

Genomes (via NCBI) Top

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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
Natural products for the treatment and management of diabetes mellitus in Zimbabwe-a review Usai R, Majoni S, Rwere F Front Pharmacol 24-Aug-2022
PMCID:PMC9449367
doi:10.3389/fphar.2022.980819
PMID:36091798
The Phytochemistry and Pharmacology of Tulbaghia, Allium, Crinum and Cyrtanthus: ‘Talented’ Taxa from the Amaryllidaceae Danquah CA, Minkah PA, Agana TA, Moyo P, Ofori M, Doe P, Rali S, Osei Duah Junior I, Amankwah KB, Somuah SO, Nugbemado IN, Maharaj VJ, Bhakta S, Gibbons S Molecules 13-Jul-2022
PMCID:PMC9316996
doi:10.3390/molecules27144475
PMID:35889346
Carbon dioxide expanded liquid: an effective solvent for the extraction of quercetin from South African medicinal plants Pilařová V, Kuda L, Vlčková HK, Nováková L, Gupta S, Kulkarni M, Švec F, Van Staden J, Doležal K Plant Methods 23-Jun-2022
PMCID:PMC9219150
doi:10.1186/s13007-022-00919-6
PMID:35739596
Cytotoxicity and Antiviral Properties of Alkaloids Isolated from Pancratium maritimum Masi M, Di Lecce R, Mérindol N, Girard MP, Berthoux L, Desgagné-Penix I, Calabrò V, Evidente A Toxins (Basel) 07-Apr-2022
PMCID:PMC9029599
doi:10.3390/toxins14040262
PMID:35448871
Review of Ethnomedicinal Uses, Phytochemistry and Pharmacological Properties of Euclea natalensis A.DC. Maroyi A Molecules 02-Dec-2017
PMCID:PMC6149716
doi:10.3390/molecules22122128
PMID:29207467
Lippia javanica (Burm.f.) Spreng.: Traditional and Commercial Uses and Phytochemical and Pharmacological Significance in the African and Indian Subcontinent Maroyi A Evid Based Complement Alternat Med 01-Jan-2017
PMCID:PMC5237467
doi:10.1155/2017/6746071
PMID:28115974
From Traditional Usage to Pharmacological Evidence: Systematic Review of Gunnera perpensa L. Maroyi A Evid Based Complement Alternat Med 07-Dec-2016
PMCID:PMC5174174
doi:10.1155/2016/1720123
PMID:28053640
Medicinal Plants Used as Home Remedies: A Family Survey by First Year Medical Students Sewani-Rusike CR, Mammen M Afr J Tradit Complement Altern Med 23-Aug-2014
PMCID:PMC4202520
doi:10.4314/ajtcam.v11i5.11
PMID:25395707
A dinitrogenous alkaloid from Cyrtanthus obliquus. Brine ND, Campbell WE, Bastida J, Herrera MR, Viladomat F, Codina C, Smith PJ Phytochemistry 01-Oct-2002
doi:10.1016/S0031-9422(02)00206-6
PMID:12377241

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 / Galanthamine-type amaryllidaceae alkaloids
(1S,3S,12S,14R)-9-methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraene-3,14-diol 20846211 Click to see 303.35 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
11alpha-Hydroxygalanthamine 11969444 Click to see 303.35 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
9-Methoxy-4-methyl-11-oxa-4-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraene-3,14-diol 73720782 Click to see 303.35 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
> 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/10.1016/S0031-9422(02)00206-6
(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/10.1016/S0031-9422(02)00206-6
3-Epimacronine 375117 Click to see 329.30 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
3-Methoxy-5-methyl-3,4,4a,5,6,6a-hexahydro-8H-[1,3]dioxolo[4',5':6,7]isochromeno[3,4-c]indol-8-ol 419046 Click to see 331.40 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
3-Methoxy-5-methyl-3,4,4a,5,6,6a-hexahydro-8H-[1,3]dioxolo[4',5':6,7]isochromeno[3,4-c]indol-8-one 500134 Click to see CN1CC2C3(C1CC(C=C3)OC)C4=CC5=C(C=C4C(=O)O2)OCO5 329.30 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
Pretazettine 73360 Click to see 331.40 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
Sekisanolin 5321780 Click to see CN1CC2(C3(C1CC(C=C3)OC)C4=CC5=C(C=C4CO2)OCO5)O 331.40 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
> Organoheterocyclic compounds / Benzazepines
(1R,2R,12S,14S)-9-methoxy-3-methyl-11-oxa-3-azatetracyclo[8.6.1.01,12.06,17]heptadeca-6(17),7,9,15-tetraene-2,14-diol 163103952 Click to see 303.35 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1R)-1-[(4-hydroxyphenyl)methyl]-7-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-8-ol 101677941 Click to see 314.40 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
2,9,10-Trimethoxy-4,12-didehydrogalanthan-1,3-diol 282781 Click to see 333.40 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
Narcissidine 443686 Click to see 333.40 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
Trisphaeridine 443684 Click to see 223.23 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
> Organoheterocyclic compounds / Tetrahydroisoquinolines
12-[2-(4-Hydroxyphenyl)ethyl]-18-methoxy-15-methyl-5,7-dioxa-12,15-diazapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraen-14-one 72768089 Click to see 448.50 unknown https://doi.org/10.1016/S0031-9422(02)00206-6
Obliquine 443685 Click to see CN1C2CC(C=CC23C(C1=O)N(CC4=CC5=C(C=C34)OCO5)CCC6=CC=C(C=C6)O)OC 448.50 unknown https://doi.org/10.1016/S0031-9422(02)00206-6

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