Crinum stuhlmannii - Unknown
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Internal ID UUID644025bf19ca3907157048
Scientific name Crinum stuhlmannii
Authority Baker
First published in Fl. Trop. Afr. 7: 578 (1898)

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Name Authority First published in
Crinum stuhlmannii subsp. delagoense (I.Verd.) Kwembeya & Nordal Kirkia 18: 162 (2007)
Crinum stuhlmannii subsp. stuhlmannii Unknown

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Northeast Tropical Africa
      • Somalia
    • South Tropical Africa
      • Mozambique
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Kwazulu-Natal
      • Northern Provinces

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000764697
Tropicos 1201799
KEW urn:lsid:ipni.org:names:64076-1
The Plant List kew-303600
Open Tree Of Life 965404
NCBI Taxonomy 414790
IPNI 64076-1
iNaturalist 583009
GBIF 2853683
EOL 1087183
CMAUP NPO20070

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)!
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Title Authors Publication Released IDs
Antileishmanial Activity of Clinanthus milagroanthus S. Leiva & Meerow (Amaryllidaceae) Collected in Peru Soto-Vásquez MR, Alvarado-García PA, Osorio EH, Tallini LR, Bastida J Plants (Basel) 10-Jan-2023
PMCID:PMC9866881
doi:10.3390/plants12020322
PMID:36679035
The anti‐Trypanosoma activities of medicinal plants: A systematic review of the literature Nekoei S, Khamesipour F, Habtemariam S, de Souza W, Mohammadi Pour P, Hosseini SR Vet Med Sci 29-Aug-2022
PMCID:PMC9677405
doi:10.1002/vms3.912
PMID:36037401
Amaryllidaceae alkaloids with anti-Trypanosoma cruzi activity Martinez-Peinado N, Cortes-Serra N, Torras-Claveria L, Pinazo MJ, Gascon J, Bastida J, Alonso-Padilla J Parasit Vectors 10-Jun-2020
PMCID:PMC7288428
doi:10.1186/s13071-020-04171-6
PMID:32522289
Ethnobotanical survey in Canhane village, district of Massingir, Mozambique: medicinal plants and traditional knowledge Ribeiro A, Romeiras MM, Tavares J, Faria MT J Ethnobiol Ethnomed 03-Dec-2010
PMCID:PMC3016261
doi:10.1186/1746-4269-6-33
PMID:21129187
Alkaloids from Crinum stuhlmannii. Machocho A, Chhabra SC, Viladomat F, Codina C, Bastida J Planta Med 01-Oct-1998
doi:10.1055/S-2006-957554
PMID:9810280

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
(+)-Crinamine 118701061 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1055/S-2006-957554
(1R,13S,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-ol 92211489 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown https://doi.org/10.1055/S-2006-957554
(1S,13R,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 42579248 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1055/S-2006-957554
(1S,13R,15R,18S)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-15,18-diol 162950864 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1055/S-2006-957554
(1S,13S,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-ol 100929441 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1055/S-2006-957554
1,2-Didehydrocrinan-3-ol 101727 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1055/S-2006-957554
Ambelline 25092366 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown https://doi.org/10.1055/S-2006-957554
Amberline 494154 Click to see COC1CC2C3(C=C1)C(CN2CC4=C(C5=C(C=C34)OCO5)OC)O 331.40 unknown https://doi.org/10.1055/S-2006-957554
Crinamine 500027 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown https://doi.org/10.1055/S-2006-957554
Crinine 398937 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown https://doi.org/10.1055/S-2006-957554
Hamayne 443670 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1055/S-2006-957554
Vittatine, 11-hydroxy- 602595 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown https://doi.org/10.1055/S-2006-957554
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown https://doi.org/10.1055/S-2006-957554
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
(3E,5Z)-1,3,5-Tridecatriene-7,9,11-triyne 5322029 Click to see CC#CC#CC#CC=CC=CC=C 166.22 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
[(Z)-5-[[(2E,4E,6E)-7-thiophen-2-ylhepta-2,4,6-trienoyl]amino]pent-2-enyl] 3-methylbutanoate 72696081 Click to see CC(C)CC(=O)OCC=CCCNC(=O)C=CC=CC=CC1=CC=CS1 373.50 unknown via CMAUP database
Docosanoic acid, pentyl ester 22608915 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)OCCCCC 410.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E,6E)-N-Isobutyl-7-(2-Thienyl)-2,4,6-Heptatrienamide 73349612 Click to see CC(C)CNC(=O)C=CC=CC=CC1=CC=CS1 261.40 unknown via CMAUP database
(2E,4E,6E)-N-Isopentyl-7-(2-Thienyl)-2,4,6-Heptatrienamide 72696080 Click to see CC(C)CCNC(=O)C=CC=CC=CC1=CC=CS1 275.40 unknown via CMAUP database
(2E,4E,8Z)-N-(2-methylpropyl)tetradeca-2,4,8-trienamide 73355665 Click to see CCCCCC=CCCC=CC=CC(=O)NCC(C)C 277.40 unknown via CMAUP database
(2E,4E)-N-isobutylundeca-2,4-dien-8,10-diynamide 5373537 Click to see CC(C)CNC(=O)C=CC=CCCC#CC#C 229.32 unknown via CMAUP database
2,4-Dodecadienamide, N-(2-methylpropyl)-, (2E,4E)- 6443006 Click to see CCCCCCCC=CC=CC(=O)NCC(C)C 251.41 unknown via CMAUP database
N-(2-methylpropyl)-7-thiophen-2-ylhepta-2,4,6-trienamide 71365555 Click to see CC(C)CNC(=O)C=CC=CC=CC1=CC=CS1 261.40 unknown via CMAUP database
N-Isobutyl-(2E,4E)-tetradecadienamide 10731388 Click to see CCCCCCCCCC=CC=CC(=O)NCC(C)C 279.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Hexadeca-2,6,10,14-tetraen-1-ol, 3,7,11,16-tetramethyl- 5365865 Click to see CC(=CCCC(=CCCC(=CCCC(=CCO)C)C)C)C 290.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
1-(5-Acetyl-2-methoxy-phenyl)-3-methyl-butan-1-one 3009228 Click to see CC(C)CC(=O)C1=C(C=CC(=C1)C(=O)C)OC 234.29 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines / N-acylpiperidines
(2E,4E,8Z)-1-Piperidino-2,4,8-tetradecatriene-1-one 11173777 Click to see CCCCCC=CCCC=CC=CC(=O)N1CCCCC1 289.50 unknown via CMAUP database
(2E,4E)-1-(Piperidin-1-yl)tetradeca-2,4-dien-1-one 11130083 Click to see CCCCCCCCCC=CC=CC(=O)N1CCCCC1 291.50 unknown via CMAUP database
1-[(2e,4e,6e)-7-(2-Thienyl)-2,4,6-heptatrienoyl]piperidine 11821786 Click to see C1CCN(CC1)C(=O)C=CC=CC=CC2=CC=CS2 273.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Hydropyridines / Tetrahydropyridines
(2E,4E,6E)-1-(3,4-dihydro-2H-pyridin-1-yl)-7-thiophen-2-ylhepta-2,4,6-trien-1-one 73346583 Click to see C1CC=CN(C1)C(=O)C=CC=CC=CC2=CC=CS2 271.40 unknown via CMAUP database
(2E,4E)-1-(3,4-dihydro-2H-pyridin-1-yl)undeca-2,4-dien-8,10-diyn-1-one 14427416 Click to see C#CC#CCCC=CC=CC(=O)N1CCCC=C1 239.31 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1|A,2|A)-crinan-1,2-diol 399199 Click to see C1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C(C1O)O 289.33 unknown https://doi.org/10.1055/S-2006-957554
(1S,13S,16R,17S)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-triene-16,17-diol 163084523 Click to see C1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C(C1O)O 289.33 unknown https://doi.org/10.1055/S-2006-957554
5,7-Dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9-triene-16,17-diol 74952092 Click to see C1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C(C1O)O 289.33 unknown https://doi.org/10.1055/S-2006-957554
Kirkine 399198 Click to see COC1=C(C=C2CN3CCC4=CCC(C(C43)C2=C1)O)O 273.33 unknown https://doi.org/10.1055/S-2006-957554
Norpluviine 12313583 Click to see COC1=C(C=C2CN3CCC4=CCC(C(C43)C2=C1)O)O 273.33 unknown https://doi.org/10.1055/S-2006-957554
Norpluvine 615152 Click to see COC1=C(C=C2CN3CCC4=CCC(C(C43)C2=C1)O)O 273.33 unknown https://doi.org/10.1055/S-2006-957554
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
[(2R,3S)-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-5-[(E)-3-oxoprop-1-enyl]-2,3-dihydro-1-benzofuran-3-yl]methyl 3-methylbutanoate 72696082 Click to see CC(C)CC(=O)OCC1C(OC2=C1C=C(C=C2OC)C=CC=O)C3=CC(=C(C=C3)O)OC 440.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5-Hydroxy-3',4',6,7-tetramethoxyflavone 152430 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC 358.30 unknown via CMAUP database
Umuhengerin 73648 Click to see COC1=CC(=CC(=C1OC)OC)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 388.40 unknown via CMAUP database

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