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Solanum mammosum

Solanum mammosum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID644041c214d5e873864414
Scientific name Solanum mammosum
Authority L.
First published in Sp. Pl. 1: 187. 1753.

Description Top

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Synonyms Top

Scientific name Authority First published in
Solanum corniculatum Huber Cat. Print. 1865: 9. 1865.
Solanum corniculatum André Rev. Hort. [Paris]. 1868: 33.
Solanum cornigerum André REv. Hort. [Paris] 1868: 33. 1868.
Solanum globiferum Dunal Prodr. [A. P. de Candolle] 13(1): 251. 1852.
Solanum mammiforme C.C.Robin Voy. Int. Louisiane, 3: 398. 1807.
Solanum mammosum var. corniculum Ridl. J. Linn. Soc., Bot. 27: 50. 1891.
Solanum mamosissimum Ram.Goyena Fl. Nicarag. 627. 1911.
Solanum platanifolium Sendtn. Fl. Bras. (Martius) 10: 58. 1846.
Solanum villosissimum Zuccagni Cent. Observ. Bot., no. 48: [20]. 1806

Common names Top

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Language Common/alternative name
English nipplefruit
English fox head
English cow's udder
English nipplefruit nightshade
English pig's ears
English lady nipples
English nipple fruit
English apple of sodom
Spanish pichichio
Spanish ubre de vaca
Arabic حدق حلمي
Bengali বুনিফল
German nippelpflanze
German zitzenförmiger nachtschatten
German kuheuterpflanze
Indonesian terung susu
Japanese 角茄子
Japanese カナリアナス
Japanese キツネナス
Japanese ツノナス
Japanese フォックスフェース
Malayalam അഞ്ചുമുലച്ചി
Malayalam അഞ്ചുമുലച്ചി വഴുതന
Portuguese teta-de-vaca
Russian Паслён сосочковый
Swedish käringtomat
Chinese 牛角茄
Chinese 五代同堂
Chinese 五指茄
Chinese 乳茄

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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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Uganda
    • South Tropical Africa
      • Malawi
      • Mozambique
      • Zimbabwe
    • West Tropical Africa
      • Ghana
    • West-central Tropical Africa
      • Burundi
      • Zaïre
    • Western Indian Ocean
      • Mauritius
      • Réunion
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indo-China
      • Laos
      • Myanmar
      • Vietnam
    • Malesia
      • Jawa
      • Malaya
      • Philippines
  • Southern America
    • Brazil
      • Brazil North
      • Brazil Northeast
    • Caribbean
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • Belize
      • Costa Rica
      • Nicaragua
      • Panamá
    • Northern South America
      • French Guiana
      • Guyana
      • Suriname
      • Venezuela
    • Western South America
      • Bolivia
      • Colombia
      • Ecuador
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001029340
UNII Q8GPG0AB6A
USDA Plants SOMA2
Tropicos 29600119
INPN 446813
KEW urn:lsid:ipni.org:names:285235-2
The Plant List tro-29600119
Missouri Botanical Garden 287157
Open Tree Of Life 399736
Observations.org 133310
NCBI Taxonomy 115667
Nature Serve 2.131534
IPNI 285235-2
iNaturalist 169074
GBIF 2930569
Freebase /m/0830lv
EPPO SOLMM
EOL 580443
USDA GRIN 101356
Wikipedia Solanum_mammosum

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
Probiotic Characteristics of Streptococcus thermophilus and Lactobacillus bulgaricus as Influenced by New Food Sources Castro A, Aleman RS, Tabora M, Kazemzadeh S, Pournaki LK, Cedillos R, Marcia J, Aryana K Microorganisms 12-Sep-2023
PMCID:PMC10535690
doi:10.3390/microorganisms11092291
PMID:37764135
Hairy root culture: a potent method for improved secondary metabolite production of Solanaceous plants Biswas D, Chakraborty A, Mukherjee S, Ghosh B Front Plant Sci 04-Sep-2023
PMCID:PMC10507345
doi:10.3389/fpls.2023.1197555
PMID:37731987
Female naturalists and the patterns of suppression of women scientists in history: the example of Maria Sibylla Merian and her contributions about useful plants Mariath F, Baratto LC J Ethnobiol Ethnomed 12-May-2023
PMCID:PMC10182609
doi:10.1186/s13002-023-00589-1
PMID:37173737
Traditional Approaches and Emerging Biotechnologies in Grapevine Virology Tarquini G, Dall’Ara M, Ermacora P, Ratti C Viruses 24-Mar-2023
PMCID:PMC10142720
doi:10.3390/v15040826
PMID:37112807
Botrytis cinerea identifies host plants via the recognition of antifungal capsidiol to induce expression of a specific detoxification gene Kuroyanagi T, Bulasag AS, Fukushima K, Ashida A, Suzuki T, Tanaka A, Camagna M, Sato I, Chiba S, Ojika M, Takemoto D PNAS Nexus 21-Dec-2022
PMCID:PMC9802192
doi:10.1093/pnasnexus/pgac274
PMID:36712336
Biogenic Synthesis of Copper-Based Nanomaterials Using Plant Extracts and Their Applications: Current and Future Directions Vincent J, Lau KS, Evyan YC, Chin SX, Sillanpää M, Chia CH Nanomaterials (Basel) 23-Sep-2022
PMCID:PMC9565561
doi:10.3390/nano12193312
PMID:36234439
Targeting Virulence Factors of Candida albicans with Natural Products Bu QR, Bao MY, Yang Y, Wang TM, Wang CZ Foods 21-Sep-2022
PMCID:PMC9562657
doi:10.3390/foods11192951
PMID:36230026
Medicinal Plants from Latin America with Wound Healing Activity: Ethnomedicine, Phytochemistry, Preclinical and Clinical Studies—A Review Salazar-Gómez A, Alonso-Castro AJ Pharmaceuticals (Basel) 31-Aug-2022
PMCID:PMC9505834
doi:10.3390/ph15091095
PMID:36145316
Light-emitting diode (LED)-directed green synthesis of silver nanoparticles and evaluation of their multifaceted clinical and biological activities Anjum S, Chaudhary R, Khan AK, Hashim M, Anjum I, Hano C, Abbasi BH RSC Adv 10-Aug-2022
PMCID:PMC9364226
doi:10.1039/d2ra03503k
PMID:36043104
Pest categorisation of Leucinodes orbonalis Bragard C, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Gregoire J, Malumphy C, Czwienczek E, Maiorano A, MacLeod A EFSA J 12-Nov-2021
PMCID:PMC8586846
doi:10.2903/j.efsa.2021.6890
PMID:34804235
Determination of Antioxidant Activity by Oxygen Radical Absorbance Capacity (ORAC-FL), Cellular Antioxidant Activity (CAA), Electrochemical and Microbiological Analyses of Silver Nanoparticles Using the Aqueous Leaf Extract of Solanum mammosum L. Pilaquinga F, Morey J, Fernandez L, Espinoza-Montero P, Moncada-Basualto M, Pozo-Martinez J, Olea-Azar C, Bosch R, Meneses L, Debut A, Piña MD Int J Nanomedicine 26-Aug-2021
PMCID:PMC8405165
doi:10.2147/IJN.S302935
PMID:34471354
The Potential of Traditional Knowledge to Develop Effective Medicines for the Treatment of Leishmaniasis Passero LF, Brunelli ED, Sauini T, Amorim Pavani TF, Jesus JA, Rodrigues E Front Pharmacol 08-Jun-2021
PMCID:PMC8248671
doi:10.3389/fphar.2021.690432
PMID:34220515
Modern Trends in the In Vitro Production and Use of Callus, Suspension Cells and Root Cultures of Medicinal Plants Babich O, Sukhikh S, Pungin A, Ivanova S, Asyakina L, Prosekov A Molecules 09-Dec-2020
PMCID:PMC7763305
doi:10.3390/molecules25245805
PMID:33316965
Metal Nanoparticles: a Promising Treatment for Viral and Arboviral Infections Maduray K, Parboosing R Biol Trace Elem Res 07-Oct-2020
PMCID:PMC7540915
doi:10.1007/s12011-020-02414-2
PMID:33029761
Virus Latency and the Impact on Plants Takahashi H, Fukuhara T, Kitazawa H, Kormelink R Front Microbiol 06-Dec-2019
PMCID:PMC6908805
doi:10.3389/fmicb.2019.02764
PMID:31866963

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
Diosgenin 99474 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1016/S0031-9422(00)84970-5
Spirost-5-en-3-ol 234096 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1016/S0031-9422(00)84970-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1055/S-2007-969208
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(3S,8S,9S,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 134766514 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1055/S-2007-969208
5-Cholestene-3-ol, 24-methyl- 312822 Click to see CC(C)C(C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 400.70 unknown https://doi.org/10.1055/S-2007-969208
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 20-oxosteroids
16-Dehydropregnenolone 92871 Click to see CC(=O)C1=CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 314.50 unknown https://doi.org/10.1016/S0031-9422(00)84970-5
Pregna-5,16-dien-20-one, 3beta-hydroxy- 518013 Click to see CC(=O)C1=CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 314.50 unknown https://doi.org/10.1016/S0031-9422(00)84970-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-16,18-diene-6,2'-piperidine] 11876122 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC=C6)C)C)C)NC1 395.60 unknown https://doi.org/10.1016/S0031-9422(00)84970-5
Solancarpidine 5250 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown https://doi.org/10.1016/0031-9422(80)83101-3
https://doi.org/10.1016/S0031-9422(00)84970-5
Solasodiene 495009 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC=C6)C)C)C)NC1 395.60 unknown https://doi.org/10.1016/S0031-9422(00)84970-5
Solasodine 442985 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown https://doi.org/10.1016/S0031-9422(00)84970-5
Tomatidenol 12442871 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)NC1 413.60 unknown https://doi.org/10.1016/0031-9422(80)83101-3
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5R,6S)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl]oxy-5-[(2S,3R,4R,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 163075701 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1 868.10 unknown https://doi.org/10.1016/0031-9422(75)83144-X
(2S,3R,4S,5R,6S)-2-[(2S,3S,4S,5S,6S)-5-hydroxy-6-(hydroxymethyl)-2-[(1S,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl]oxy-4-[(2S,3S,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162980342 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1 884.10 unknown https://doi.org/10.1016/0031-9422(75)83144-X
2-[4,5-dihydroxy-2-(hydroxymethyl)-6-[(1S,2S,4S,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 138114744 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)NC1 721.90 unknown https://doi.org/10.1021/NP50107A004
L-Rhamnopyranosyl-14-D-glucopyranose solasodine 73606 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)C)C)C)NC1 721.90 unknown https://doi.org/10.1021/NP50107A004
Solamargine 73611 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1 868.10 unknown https://doi.org/10.1021/NP50107A004
https://doi.org/10.1016/0031-9422(75)83144-X
Solasonine 119247 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1 884.10 unknown https://doi.org/10.1016/0031-9422(75)83144-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2007-969208
https://doi.org/10.1016/0031-9422(80)83101-3
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1055/S-2007-969208
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(80)83101-3
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1055/S-2007-969208

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