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Solanum chrysotrichum

Solanum chrysotrichum - 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 UUID64404195595f6050912183
Scientific name Solanum chrysotrichum
Authority Schltdl.
First published in Linnaea 19: 304. 1847.

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Solanum antiguense J.M. Coult. Enum. Pl. Guatem. 4: 187. 1895.
Solanum pynaertii De Wild. Miss. Em. Laurent 1: 437, tab. 119. 1907.
Solanum torvum var. pleiotomum C.Y.Wu & S.C.Huang Acta Phytotax. Sin. 16(2) : 73. 1978.
Solanum warscewiczii hort. ex Lambertye REv. Hort. [Paris] 1865: 429. 1865.
Solanum warszewiczioides Huber Cat. Graines 1870: 3. 1870.

Common names Top

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Language Common/alternative name
Chinese 多裂水茄

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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
    • Macaronesia
      • Azores
      • Canary Islands
    • South Tropical Africa
      • Malawi
      • Zambia
      • Zimbabwe
    • West-central Tropical Africa
      • Rwanda
      • Zaïre
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southeast
      • Mexico Southwest
  • Southern America
    • Central America
      • Costa Rica
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá
    • Western South America
      • Peru

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001027050
Tropicos 29603039
KEW urn:lsid:ipni.org:names:818704-1
The Plant List tro-29603039
Open Tree Of Life 939579
NCBI Taxonomy 744061
IUCN Red List 136783671
IPNI 818704-1
iNaturalist 280917
GBIF 2929617
EPPO SOLKR
USDA GRIN 409880

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
Bioreactor Systems for Plant Cell Cultivation at the Institute of Plant Physiology of the Russian Academy of Sciences: 50 Years of Technology Evolution from Laboratory to Industrial Implications Titova M, Popova E, Nosov A Plants (Basel) 01-Feb-2024
PMCID:PMC10857215
doi:10.3390/plants13030430
PMID:38337964
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
Back to Nature: Medicinal Plants as Promising Sources for Antibacterial Drugs in the Post-Antibiotic Era Abdallah EM, Alhatlani BY, de Paula Menezes R, Martins CH Plants (Basel) 28-Aug-2023
PMCID:PMC10490416
doi:10.3390/plants12173077
PMID:37687324
Production of secondary metabolites using tissue culture-based biotechnological applications Ozyigit II, Dogan I, Hocaoglu-Ozyigit A, Yalcin B, Erdogan A, Yalcin IE, Cabi E, Kaya Y Front Plant Sci 29-Jun-2023
PMCID:PMC10339834
doi:10.3389/fpls.2023.1132555
PMID:37457343
Obtaining 2,3-Dihydrobenzofuran and 3-Epilupeol from Ageratina pichinchensis (Kunth) R.King & Ho.Rob. Cell Cultures Grown in Shake Flasks under Photoperiod and Darkness, and Its Scale-Up to an Airlift Bioreactor for Enhanced Production Sánchez-Ramos M, Marquina-Bahena S, Alvarez L, Bernabé-Antonio A, Cabañas-García E, Román-Guerrero A, Cruz-Sosa F Molecules 06-Jan-2023
PMCID:PMC9865622
doi:10.3390/molecules28020578
PMID:36677637
Improving the production of podophyllotoxin in hairy roots of Hyptis suaveolens induced from regenerated plantlets Bazaldúa C, Cardoso-Taketa A, Trejo-Tapia G, Camacho-Diaz B, Arellano J, Ventura-Zapata E, Villarreal ML PLoS One 12-Sep-2019
PMCID:PMC6874312
doi:10.1371/journal.pone.0222464
PMID:31513694
Antifungal Activity of Crude Extract from the Rhizome and Root of Smilacina japonica A. Gray Liu W, Sun B, Yang M, Zhang Z, Zhang X, Pang T, Wang S Evid Based Complement Alternat Med 15-Jul-2019
PMCID:PMC6662278
doi:10.1155/2019/5320203
PMID:31379963
Biotechnology, In Vitro Production of Natural Bioactive Compounds, Herbal Preparation, and Disease Management (Treatment and Prevention) Alamgir AN Therapeutic Use of Medicinal Plants and their Extracts: Volume 2 24-Jun-2018
PMCID:PMC7123938
doi:10.1007/978-3-319-92387-1_7
Plants’ Natural Products as Alternative Promising Anti-Candida Drugs Soliman S, Alnajdy D, El-Keblawy AA, Mosa KA, Khoder G, Noreddin AM Pharmacogn Rev 01-Jul-2017
PMCID:PMC5628516
doi:10.4103/phrev.phrev_8_17
PMID:28989245
Cellular Structural Changes in Candida albicans Caused by the Hydroalcoholic Extract from Sapindus saponaria L. Shinobu-Mesquita CS, Bonfim-Mendonça PS, Moreira AL, Ferreira IC, Donatti L, Fiorini A, Svidzinski TI Molecules 22-May-2015
PMCID:PMC6272372
doi:10.3390/molecules20059405
PMID:26007191
Topical antifungals for seborrhoeic dermatitis Okokon EO, Verbeek JH, Ruotsalainen JH, Ojo OA, Bakhoya VN Cochrane Database Syst Rev 02-May-2015
PMCID:PMC7177303
doi:10.1002/14651858.CD008138.pub3
Topical antifungals for seborrhoeic dermatitis Okokon EO, Verbeek JH, Ruotsalainen JH, Ojo OA, Bakhoya VN Cochrane Database Syst Rev 29-Apr-2015
PMCID:PMC4448221
doi:10.1002/14651858.CD008138.pub2
PMID:25933684
Deagrarianisation and Forest Revegetation in a Biodiversity Hotspot on the Wild Coast, South Africa Shackleton R, Shackleton C, Shackleton S, Gambiza J PLoS One 14-Oct-2013
PMCID:PMC3796566
doi:10.1371/journal.pone.0076939
PMID:24155911
Production of asiaticoside from centella (Centella asiatica L. Urban) cells in bioreactor Loc NH, Nhat NT Asian Pac J Trop Biomed 01-Oct-2013
PMCID:PMC3761140
doi:10.1016/S2221-1691(13)60159-8
PMID:24075346
Use of Antifungal Saponin SC-2 of Solanum Chrysotrichum for the Treatment of Vulvovaginal Candidiasis: In Vitro Studies and Clinical Experiences Herrera-Arellano A, López-Villegas EO, Rodríguez-Tovar AV, Zamilpa A, Jiménez-Ferrer E, Tortoriello J, Martínez-Rivera MA Afr J Tradit Complement Altern Med 12-Apr-2013
PMCID:PMC3777579
PMID:24146467

Phytochemical Profile Top

Add a new one!
Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(25R)-5alpha-Spirostan-3beta-ol 219836 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown https://doi.org/10.1016/S0031-9422(00)95233-6
2-[5-[4-[3,5-Dihydroxy-6-(hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4-hydroxy-2-[(2-hydroxy-4,5,9,9,13,20,20-heptamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracosan-10-yl)oxy]oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162822199 Click to see CC1(CCC23COC4(C2C1)CCC5C6(CCC(C(C6CCC5(C4(CC3O)C)C)(C)C)OC7C(C(C(CO7)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)OC1C(C(C(C(O1)CO)O)O)O)O)OC1C(C(C(CO1)O)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)C)C 1371.50 unknown https://doi.org/10.1021/NP50052A010
Chlorogenin 12303065 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)O)C)C)OC1 432.60 unknown https://doi.org/10.1021/NP50052A010
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)95233-6
Hecogenin 91453 Click to see CC1CCC2(C(C3C(O2)CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 430.60 unknown https://doi.org/10.1016/S0031-9422(00)95233-6
Neochlorogenin 12303066 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)O)C)C)OC1 432.60 unknown https://doi.org/10.1021/NP50052A010
Neohecogenin 90473944 Click to see CC1CCC2(C(C3C(O2)(CC4C3(C(=O)CC5C4CCC6C5(CCC(C6)O)C)C)C)C)OC1 444.60 unknown https://doi.org/10.1016/S0031-9422(00)95233-6
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)95233-6
Tigogenin 99516 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown https://doi.org/10.1016/S0031-9422(00)95233-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-beta-hydroxysteroids
(2S,4S,7S,8R,9S,12S,13S,16S,18R,19S)-19-(2,6-dimethylphenyl)-4,4',7,9,12,13-hexamethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,1'-cyclohexane]-16-ol 163190005 Click to see CC1CCC2(CC1)C(C3C4(CCC5(C(C4CC3(O2)C)CC(C6C5(CCC(C6)O)C)C7=C(C=CC=C7C)C)C)C)C 546.90 unknown https://doi.org/10.1021/NP0305019
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3R,4S,5S,6R)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S,19S)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-yl]oxy-6-methyloxane-3,4,5-triol 10940859 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)OC7C(C(C(C(O7)C)O)O)O)C)C)OC1 578.80 unknown https://doi.org/10.1021/NP020261H
https://doi.org/10.1055/S-2004-827145
(2R,3S,4S,5R,6R)-2-methyl-6-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S,19R)-19-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-2-yl]methoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol 101128815 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(C(O8)COC9C(C(C(C(O9)C)O)O)O)O)O)O)O)O)O)C)O)C)C)OC1 903.10 unknown https://doi.org/10.1055/S-2001-14332
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S,19S)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-yl]oxy-6-methyloxan-4-yl]oxy-6-methyloxane-3,4,5-triol 11039877 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)C)O)O)O)O)C)C)OC1 724.90 unknown https://doi.org/10.1021/NP020261H
https://doi.org/10.1055/S-2004-827145
(2S,3R,4S,5R)-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S,19S)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-yl]oxyoxane-3,4,5-triol 10951900 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)OC7C(C(C(CO7)O)O)O)C)C)OC1 564.70 unknown https://doi.org/10.1055/S-2004-827145
https://doi.org/10.1021/NP020261H
(2S,3R,4S,5R)-2-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-2-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S,19S)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-yl]oxy-6-methyloxan-4-yl]oxyoxane-3,4,5-triol 11115214 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)OC7C(C(C(C(O7)C)O)OC8C(C(C(CO8)O)O)O)O)C)C)OC1 710.90 unknown https://doi.org/10.1055/S-2004-827145
https://doi.org/10.1021/NP020261H
https://doi.org/10.1055/S-2007-993744
2-(16-Hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-yl)oxy-6-methyloxane-3,4,5-triol 72808810 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)OC7C(C(C(C(O7)C)O)O)O)C)C)OC1 578.80 unknown https://doi.org/10.1055/S-2004-827145
https://doi.org/10.1021/NP020261H
2-(16-Hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-yl)oxyoxane-3,4,5-triol 85343525 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)OC7C(C(C(CO7)O)O)O)C)C)OC1 564.70 unknown https://doi.org/10.1055/S-2004-827145
https://doi.org/10.1021/NP020261H
2-[3,5-Dihydroxy-2-(16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-yl)oxy-6-methyloxan-4-yl]oxy-6-methyloxane-3,4,5-triol 75069484 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)C)O)O)O)O)C)C)OC1 724.90 unknown https://doi.org/10.1021/NP020261H
https://doi.org/10.1055/S-2004-827145
2-[3,5-Dihydroxy-2-(16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-yl)oxy-6-methyloxan-4-yl]oxyoxane-3,4,5-triol 75069483 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)OC7C(C(C(C(O7)C)O)OC8C(C(C(CO8)O)O)O)O)C)C)OC1 710.90 unknown https://doi.org/10.1055/S-2004-827145
https://doi.org/10.1055/S-2007-993744
https://doi.org/10.1021/NP020261H
2-Methyl-6-[[3,4,5-trihydroxy-6-[[3,4,5-trihydroxy-6-(19-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl)oxyoxan-2-yl]methoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol 85084716 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(C(O8)COC9C(C(C(C(O9)C)O)O)O)O)O)O)O)O)O)C)O)C)C)OC1 903.10 unknown https://doi.org/10.1055/S-2001-14332
Torvoside C 12313943 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)C)O)O)O)O)C)C)OC1)O 740.90 unknown https://doi.org/10.1055/S-2004-827145
https://doi.org/10.1021/NP020261H
Torvoside K 11018078 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)O)C)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)C)O)O)O)O)C)C)OC1)O 740.90 unknown https://doi.org/10.1055/S-2004-827145
https://doi.org/10.1021/NP020261H
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1021/NP020261H
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 https://doi.org/10.1021/NP020261H
Stigmasterol glucoside 6602508 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown https://doi.org/10.1021/NP020261H

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