Sauromatum venosum - Unknown
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Internal ID UUID643fec35b18be734389958
Scientific name Sauromatum venosum
Authority (Aiton) Kunth
First published in Enum. Pl. 3: 28 (1841)

Description Top

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Synonyms Top

Scientific name Authority First published in
Jaimenostia fernandopoana Guinea & Gomez Mor. Ensayo Geobot. Guin. Continent. Espan. : 248 (1946)
Arum clavatum Desf. Tabl. École Bot. , ed. 3: 385 (1829)
Arum fugax Salisb. Prodr. Stirp. Chap. Allerton : 260 (1796)
Arum pedatum Link & Otto Icon. Pl. Select. : 19 (1821)
Arum sessiliflorum Roxb. Fl. Ind. ed. 1832 , 3: 507 (1832)
Arum simlense hort. ex Engl. Monogr. Phan. 2: 571 (1879)
Arum venosum Aiton Hort. Kew. 3: 315 (1789)
Sauromatum abyssinicum Schott Syn. Aroid. : 25 (1856)
Sauromatum angolense N.E.Br. Fl. Trop. Afr. 8: 142 (1901)
Sauromatum guttatum Schott Melet. Bot. : 17 (1832)
Sauromatum nubicum Schott Syn. Aroid. : 25 (1856)
Sauromatum pedatum (Link & Otto) Schott Melet. Bot. : 17 (1832)
Sauromatum pulchrum Miq. Ann. Mus. Bot. Lugduno-Batavi 1: 221 (1864)
Sauromatum punctatum K.Koch Wochenschr. Gärtnerei Pflanzenk. 1: 263 (1858)
Sauromatum sessiliflorum (Roxb.) Kunth Enum. Pl. 3: 28 (1841)
Sauromatum simlense Schott Oesterr. Bot. Z. 8: 349 (1858)
Typhonium venosum (Aiton) Hett. & P.C.Boyce Aroideana 23: 51 (2000)
Arisaema venosum (Aiton) Blume Rumphia 1: 109 (1836)
Sauromatum guttatum var. punctatum (K.Koch) Engl. Pflanzenr. , IV, 23F: 125 (1920)
Sauromatum guttatum var. pulchrum (Miq.) Engl. Pflanzenr. , IV, 23F: 125 (1920)
Sauromatum guttatum var. sessiliflorum (Roxb.) Engl. Pflanzenr. , IV, 23F: 125 (1920)
Sauromatum guttatum var. pedatum (Link & Otto) Engl. Pflanzenr. , IV, 23F: 125 (1920)
Sauromatum guttatum var. simlense (Schott) Engl. Pflanzenr. , IV, 23F: 125 (1920)
Sauromatum guttatum var. venosum (Aiton) Engl. Pflanzenr. , IV, 23F: 125 (1920)
Desmesia venosa (Aiton) Raf. Fl. Tellur. 3: 63 (1837)
Alocasia pedata Raf. Fl. Tellur. 3: 64 (1837)
Sauromatum nubicum var. angolense (N.E.Br.) Engl.
Arum pedatum Willd. Enum. Pl. Suppl. [Willdenow] 64. 1814 [dt. 1813; issued Jul-Dec 1814]

Common names Top

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Language Common/alternative name
English voodoo lily
Chinese 斑龙芋
Chinese 斑龍芋

Subspecies (abbr. subsp./ssp.) Top

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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
    • East Tropical Africa
      • Kenya
      • Tanzania
      • Uganda
    • Northeast Tropical Africa
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
    • West-central Tropical Africa
      • Cameroon
      • Central African Republic
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre
  • Asia-temperate
    • Arabian Peninsula
      • Saudi Arabia
      • Yemen
    • China
      • China South-central
      • Tibet
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000304979
Tropicos 2104092
KEW urn:lsid:ipni.org:names:88690-1
The Plant List kew-186383
Missouri Botanical Garden 255908
Open Tree Of Life 1008198
Observations.org 195606
NCBI Taxonomy 4463
IUCN Red List 44393221
IPNI 88690-1
iNaturalist 606200
GBIF 2869597
Freebase /m/025z172
EPPO ZMAVE
Elurikkus 321007
USDA GRIN 457599
Wikipedia Sauromatum_venosum

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.
Title Authors Publication Released IDs
Alternative Oxidase: From Molecule and Function to Future Inhibitors Li J, Yang S, Wu Y, Wang R, Liu Y, Liu J, Ye Z, Tang R, Whiteway M, Lv Q, Yan L ACS Omega 04-Mar-2024
PMCID:PMC10955580
doi:10.1021/acsomega.3c09339
PMID:38524433
Labellum Features and Chemical Composition of Floral Scent in Bulbophyllum carunculatum Garay, Hamer & Siegrist (Section Lepidorhiza Schltr., Bulbophyllinae Schltr., Orchidaceae Juss.) Wiśniewska N, Gołębiowski M, Kowalkowska AK Plants (Basel) 06-Apr-2023
PMCID:PMC10097095
doi:10.3390/plants12071568
PMID:37050195
Terpenoid Transport in Plants: How Far from the Final Picture? Demurtas OC, Nicolia A, Diretto G Plants (Basel) 01-Feb-2023
PMCID:PMC9919377
doi:10.3390/plants12030634
PMID:36771716
Sordaria macrospora Sterile Mutant pro34 Is Impaired in Respiratory Complex I Assembly Hamann A, Osiewacz HD, Teichert I J Fungi (Basel) 27-Sep-2022
PMCID:PMC9605262
doi:10.3390/jof8101015
PMID:36294581
Lectins from plants and algae act as anti-viral against HIV, influenza and coronaviruses Naik S, Kumar S Mol Biol Rep 22-Sep-2022
PMCID:PMC9510388
doi:10.1007/s11033-022-07854-8
PMID:36138301
Medicinal plants used for management of hemorrhoids in Ethiopia: A systematic review Getachew M, Belayneh A, Kebede B, Alimaw Y, Biyazin Y, Abebaw A, Abebe D Heliyon 13-Aug-2022
PMCID:PMC9403375
doi:10.1016/j.heliyon.2022.e10211
PMID:36033288
Errata N/A Arq Bras Cardiol 04-May-2022
PMCID:PMC9368880
doi:10.36660/abc.20220302
PMID:35613206
O Ano de 2021 na Pesquisa Básica: a Procura por Modelos Translacionais Gatto M, Mota GA, Okoshi MP Arq Bras Cardiol 07-Apr-2022
PMCID:PMC9007007
doi:10.36660/abc.20220186
PMID:35508043
Environmental variables drive plant species composition and distribution in the moist temperate forests of Northwestern Himalaya, Pakistan Rahman IU, Hart RE, Ijaz F, Afzal A, Iqbal Z, Calixto ES, Abd_Allah EF, Alqarawi AA, Hashem A, Al-Arjani AB, Kausar R, Haq SM PLoS One 24-Feb-2022
PMCID:PMC8870539
doi:10.1371/journal.pone.0260687
PMID:35202409
Legume Alternative Oxidase Isoforms Show Differential Sensitivity to Pyruvate Activation Sweetman C, Selinski J, Miller TK, Whelan J, Day DA Front Plant Sci 17-Jan-2022
PMCID:PMC8801435
doi:10.3389/fpls.2021.813691
PMID:35111186
Pesquisando Compostos de Ocorrência Natural para Tratar Hipertensão Souza DS, Roman-Campos D Arq Bras Cardiol 22-Nov-2021
PMCID:PMC8757164
doi:10.36660/abc.20210869
PMID:35613167
O Efeito Anti-Hipertensivo de Sauromatum Guttatum Mediado por Efeitos Vasorrelaxante e Depressivos Miocárdicos Bibi R, Salma U, Bashir K, Khan T, Shah AJ Arq Bras Cardiol 22-Nov-2021
PMCID:PMC8757165
doi:10.36660/abc.20200055
PMID:35613166
Comparison of the Kinetic Parameters of Alternative Oxidases From Trypanosoma brucei and Arabidopsis thaliana—A Tale of Two Cavities Xu F, Copsey AC, Young L, Barsottini MR, Albury MS, Moore AL Front Plant Sci 22-Oct-2021
PMCID:PMC8569227
doi:10.3389/fpls.2021.744218
PMID:34745175
Floral Scents of a Deceptive Plant Are Hyperdiverse and Under Population-Specific Phenotypic Selection Gfrerer E, Laina D, Gibernau M, Fuchs R, Happ M, Tolasch T, Trutschnig W, Hörger AC, Comes HP, Dötterl S Front Plant Sci 24-Sep-2021
PMCID:PMC8500232
doi:10.3389/fpls.2021.719092
PMID:34630465
DIA-Based Quantitative Proteomics Reveals the Protein Regulatory Networks of Floral Thermogenesis in Nelumbo nucifera Sun Y, Zou Y, Jin J, Chen H, Liu Z, Zi Q, Xiong Z, Wang Y, Li Q, Peng J, Ding Y Int J Mol Sci 31-Jul-2021
PMCID:PMC8347412
doi:10.3390/ijms22158251
PMID:34361015

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
> Benzenoids / Benzene and substituted derivatives
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see C1=CC=C(C(=C1)C(=O)O)O 138.12 unknown https://doi.org/10.1126/SCIENCE.237.4822.1601
> Benzenoids / Benzene and substituted derivatives / Benzophenones
Benzophenone 3102 Click to see C1=CC=C(C=C1)C(=O)C2=CC=CC=C2 182.22 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
2-Ethylbenzaldehyde 123406 Click to see CCC1=CC=CC=C1C=O 134.17 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Benzenoids / Phenol ethers / Anisoles
Anisole 7519 Click to see COC1=CC=CC=C1 108.14 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Decane 15600 Click to see CCCCCCCCCC 142.28 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
Dodecane 8182 Click to see CCCCCCCCCCCC 170.33 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
Hexadecane 11006 Click to see CCCCCCCCCCCCCCCC 226.44 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
Nonadecane 12401 Click to see CCCCCCCCCCCCCCCCCCC 268.50 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
Octadecane 11635 Click to see CCCCCCCCCCCCCCCCCC 254.50 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
Pentadecane 12391 Click to see CCCCCCCCCCCCCCC 212.41 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
Tetradecane 12389 Click to see CCCCCCCCCCCCCC 198.39 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
Tridecane 12388 Click to see CCCCCCCCCCCCC 184.36 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
Undecane 14257 Click to see CCCCCCCCCCC 156.31 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
3-Methylvaleric acid 7755 Click to see CCC(C)CC(=O)O 116.16 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
beta-Ocimene, (3Z)- 5320250 Click to see CC(=CCC=C(C)C=C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
3-Carene 26049 Click to see CC1=CCC2C(C1)C2(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene 134687947 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
Sec-butyl acetate 7758 Click to see CCC(C)OC(=O)C 116.16 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Undecanone 8163 Click to see CCCCCCCCCC(=O)C 170.29 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
4'-Hydroxyacetophenone 7469 Click to see CC(=O)C1=CC=C(C=C1)O 136.15 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
Acetophenone 7410 Click to see CC(=O)C1=CC=CC=C1 120.15 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Indole 798 Click to see C1=CC=C2C(=C1)C=CN2 117.15 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Organoheterocyclic compounds / Indoles and derivatives / Indoles / 3-alkylindoles / 3-methylindoles
3-Methylindole 6736 Click to see CC1=CNC2=CC=CC=C12 131.17 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Organoheterocyclic compounds / Pyridines and derivatives / Methylpyridines
Actinidine 68231 Click to see CC1CCC2=C1C=NC=C2C 147.22 unknown https://doi.org/10.1016/S0031-9422(00)94756-3
> Organosulfur compounds / Sulfenyl compounds
Dimethyl tetrasulfide 79828 Click to see CSSSSC 158.30 unknown https://doi.org/10.1016/S0031-9422(00)94756-3

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