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Internal ID UUID64404192cd0ed982142021
Scientific name Solanum cernuum
Authority Vell.
First published in Fl. Flumin. 84. 1829 [1825]; Fl. Flumin. Icon. 2: t. 103. 1831 [1827].

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Synonyms Top

Scientific name Authority First published in
Solanum jubatum Dunal Prodr. [A. P. de Candolle] 13(1): 132. 1852.
Solanum paleatum Sendtn. Fl. Bras. (Martius) 10: 42. 1846.
Solanum sisleyanum Lambertye REv. Hort. [Paris] 1868: 470. 1868.

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil Southeast
      • Brazil West-central

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001026936
Tropicos 29600099
KEW urn:lsid:ipni.org:names:818648-1
The Plant List tro-29600099
Open Tree Of Life 915428
NCBI Taxonomy 397274
IUCN Red List 146118223
IPNI 818648-1
iNaturalist 559746
GBIF 2931263
USDA GRIN 310700

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
Why Are There So Few Basidiomycota and Basal Fungi as Endophytes? A Review Rungjindamai N, Jones EB J Fungi (Basel) 15-Jan-2024
PMCID:PMC10820240
doi:10.3390/jof10010067
PMID:38248976
Flavonoids-Rich Plant Extracts Against Helicobacter pylori Infection as Prevention to Gastric Cancer Ivyna de Araújo Rêgo R, Guedes Silvestre GF, Ferreira de Melo D, Albino SL, Pimentel MM, Silva Costa Cruz SB, Silva Wurzba SD, Rodrigues WF, Goulart de Lima Damasceno BP, Cançado Castellano LR Front Pharmacol 31-Aug-2022
PMCID:PMC9470917
doi:10.3389/fphar.2022.951125
PMID:36120379
Matrix Metalloproteinases in Chemoresistance: Regulatory Roles, Molecular Interactions, and Potential Inhibitors Tune BX, Sim MS, Poh CL, Guad RM, Woon CK, Hazarika I, Das A, Gopinath SC, Rajan M, Sekar M, Subramaniyan V, Fuloria NK, Fuloria S, Batumalaie K, Wu YS J Oncol 09-May-2022
PMCID:PMC9110224
doi:10.1155/2022/3249766
PMID:35586209
Hidden in Plants—A Review of the Anticancer Potential of the Solanaceae Family in In Vitro and In Vivo Studies Kowalczyk T, Merecz-Sadowska A, Rijo P, Mori M, Hatziantoniou S, Górski K, Szemraj J, Piekarski J, Śliwiński T, Bijak M, Sitarek P Cancers (Basel) 11-Mar-2022
PMCID:PMC8946528
doi:10.3390/cancers14061455
PMID:35326606
Cabbage Production in West Africa and IPM with a Focus on Plant-Based Extracts and a Complementary Worldwide Vision Mondédji AD, Silvie P, Nyamador WS, Martin P, Agboyi LK, Amévoin K, Ketoh GK, Glitho IA Plants (Basel) 11-Mar-2021
PMCID:PMC7998567
doi:10.3390/plants10030529
PMID:33799877
Natural Products Targeting the Mitochondria in Cancers Yang Y, He PY, Zhang Y, Li N Molecules 28-Dec-2020
PMCID:PMC7795732
doi:10.3390/molecules26010092
PMID:33379233
Screening of plants from the Brazilian Atlantic Forest led to the identification of Athenaea velutina (Solanaceae) as a novel source of antimetastatic agents Almeida AA, Lima GD, Simão MV, Moreira GA, Siqueira RP, Zanatta AC, Vilegas W, Machado‐Neves M, Bressan GC, Leite JP Int J Exp Pathol 26-May-2020
PMCID:PMC7370850
doi:10.1111/iep.12351
PMID:32452573
Antifungal activity of 8-methoxynaphthalen-1-ol isolated from the endophytic fungus Diatrype palmicola MFLUCC 17-0313 against the plant pathogenic fungus Athelia rolfsii on tomatoes Tanapichatsakul C, Pansanit A, Monggoot S, Brooks S, Prachya S, Kittakoop P, Panuwet P, Pripdeevech P PeerJ 04-May-2020
PMCID:PMC7204883
doi:10.7717/peerj.9103
PMID:32411538
Synthetic Approaches to a Challenging and Unusual Structure—An Amino-Pyrrolidine Guanine Core Rippel R, Pinheiro L, Lopes M, Lourenço A, Ferreira LM, Branco PS Molecules 12-Feb-2020
PMCID:PMC7070370
doi:10.3390/molecules25040797
PMID:32059504
Acetic Acid-Induced Ulcerative Colitis in Sprague Dawley Rats Is Suppressed by Hydroethanolic Extract of Cordia vignei Leaves through Reduced Serum Levels of TNF-α and IL-6 Owusu G, Obiri DD, Ainooson GK, Osafo N, Antwi AO, Duduyemi BM, Ansah C Int J Chronic Dis 06-Feb-2020
PMCID:PMC7026722
doi:10.1155/2020/8785497
PMID:32090060
Prenylated flavonoid-enriched fraction from Maclura tinctoria shows biological activity against Staphylococcus aureus and protects Galleria mellonella larvae from bacterial infection das Chagas Almeida A, Azevedo Rodrigues L, dos Santos Paulino G, Pereira Aguilar A, Andrade Almeida A, Olavo Ferreira S, Brandão GC, Viana Leite JP, de Oliveira Barros Ribon A BMC Complement Altern Med 29-Jul-2019
PMCID:PMC6664575
doi:10.1186/s12906-019-2600-y
PMID:31357964
The Confrontation between Ethnopharmacology and Pharmacological Tests of Medicinal Plants Associated with Mental and Neurological Disorders Cavalcante e Costa GF, Nishijo H, Caixeta LF, Aversi-Ferreira TA Evid Based Complement Alternat Med 02-Jul-2018
PMCID:PMC6051267
doi:10.1155/2018/7686913
PMID:30057646
Local ecological knowledge and its relationship with biodiversity conservation among two Quilombola groups living in the Atlantic Rainforest, Brazil Conde BE, Ticktin T, Fonseca AS, Macedo AL, Orsi TO, Chedier LM, Rodrigues E, Pimenta DS PLoS One 28-Nov-2017
PMCID:PMC5705149
doi:10.1371/journal.pone.0187599
PMID:29182637
Endophytes from medicinal plants and their potential for producing indole acetic acid, improving seed germination and mitigating oxidative stress Khan AL, Gilani SA, Waqas M, Al-Hosni K, Al-Khiziri S, Kim YH, Ali L, Kang SM, Asaf S, Shahzad R, Hussain J, Lee IJ, Al-Harrasi A J Zhejiang Univ Sci B 01-Feb-2017
PMCID:PMC5296229
doi:10.1631/jzus.B1500271
PMID:28124841
Plants Consumption and Liver Health Guan YS, He Q Evid Based Complement Alternat Med 28-Jun-2015
PMCID:PMC4499388
doi:10.1155/2015/824185
PMID:26221179

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 / Phenols / Methoxyphenols
(E)-N-[(2S)-1-carbamimidoylpyrrolidin-2-yl]-3-(3-hydroxy-4-methoxyphenyl)prop-2-enamide 163055215 Click to see COC1=C(C=C(C=C1)C=CC(=O)NC2CCCN2C(=N)N)O 304.34 unknown https://doi.org/10.1016/J.TETLET.2011.09.060
(Z)-N-[(2R)-1-carbamimidoylpyrrolidin-2-yl]-3-(3-hydroxy-4-methoxyphenyl)prop-2-enamide 163055217 Click to see COC1=C(C=C(C=C1)C=CC(=O)NC2CCCN2C(=N)N)O 304.34 unknown https://doi.org/10.1016/J.TETLET.2011.09.060
N-[(2S)-1-carbamimidoylpyrrolidin-2-yl]-3-(3-hydroxy-4-methoxyphenyl)prop-2-enamide 163055218 Click to see COC1=C(C=C(C=C1)C=CC(=O)NC2CCCN2C(=N)N)O 304.34 unknown https://doi.org/10.1016/J.TETLET.2011.09.060
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-[(2R)-1-carbamimidoylpyrrolidin-2-yl]-3-(3-hydroxy-4-methoxyphenyl)prop-2-enamide 163055216 Click to see COC1=C(C=C(C=C1)C=CC(=O)NC2CCCN2C(=N)N)O 304.34 unknown https://doi.org/10.1016/J.TETLET.2011.09.060
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/J.TETLET.2011.09.060
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/J.TETLET.2011.09.060
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 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 https://doi.org/10.1016/J.TETLET.2011.09.060
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.TETLET.2011.09.060
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/J.TETLET.2011.09.060
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 https://doi.org/10.1016/J.TETLET.2011.09.060

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