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Solanum donianum

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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 UUID644041a1d51d5290132365
Scientific name Solanum donianum
Authority Walp.
First published in Repert. Bot. Syst. (Walpers) 3: 54. 1844.

Description Top

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Synonyms Top

Scientific name Authority First published in
Solanum bahamense Mill. Gard. Dict. ed. 8, no. 24. 1768.
Solanum bahamense var. inerme Dunal Prodr. [A. P. de Candolle] 13(1): 186. 1852.
Solanum blodgettii Chapm. Fl. South. U.S. 349. 1860.
Solanum decurtatum Standl. & Steyerm. Publ. Field Mus. Nat. Hist., Bot. Ser. 23: 20. 1943.
Solanum stenorchis Dunal Prodr. [A. P. de Candolle] 13(1): 270. 1852.

Common names Top

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Language Common/alternative name
English mullein nightshade
Chinese 茄树
Chinese 假烟叶树

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Northwest
      • Mexico Southeast
      • Mexico Southwest
    • Southeastern U.S.A.
      • Florida

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001027636
Florida Plant Atlas 3622
USDA Plants SODO3
Tropicos 29602591
KEW urn:lsid:ipni.org:names:819050-1
The Plant List tro-29602591
Open Tree Of Life 294747
NCBI Taxonomy 744071
Nature Serve 2.131537
IPNI 819050-1
iNaturalist 169061
GBIF 2929566
EPPO SOLVE
EOL 581173
USDA GRIN 457032

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
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
Plant Resource Use and Pattern of Usage by the Naturalized Orchid Bee (Euglossa dilemma: Hymenoptera: Apidae) in Florida Pemberton RW Insects 27-Nov-2023
PMCID:PMC10743517
doi:10.3390/insects14120909
PMID:38132583
Bioactive Natural Products against Systemic Arterial Hypertension: A Past 20-Year Systematic and Prospective Review da Silva MG, Barbosa SL, Silva DS, Bezerra IB, Alves Bezerra É, Coelho AG, Pinheiro da Silva Morais IC, Rezende-Júnior LM, do Carmo IS, Lima-Neto JD, Comerma-Steffensen SG, Citó AM, Arcanjo DD Evid Based Complement Alternat Med 20-Jun-2022
PMCID:PMC9236778
doi:10.1155/2022/8499625
PMID:35769156
Pest categorisation of Maconellicoccus hirsutus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Sven Magnusson C, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Gregoire J, Malumphy C, Antonatos S, Kertesz V, Maiorano A, Papachristos D, MacLeod A EFSA J 11-Jan-2022
PMCID:PMC8749475
doi:10.2903/j.efsa.2022.7024
PMID:35035580
Ethnomedicine study on traditional medicinal plants in the Wuliang Mountains of Jingdong, Yunnan, China Gao L, Wei N, Yang G, Zhang Z, Liu G, Cai C J Ethnobiol Ethnomed 19-Aug-2019
PMCID:PMC6699132
doi:10.1186/s13002-019-0316-1
PMID:31426826
Antioxidant, antihypertensive, anti-hyperglycemic, and antimicrobial activity of aqueous extracts from twelve native plants of the Yucatan coast Rodríguez-García CM, Ruiz-Ruiz JC, Peraza-Echeverría L, Peraza-Sánchez SR, Torres-Tapia LW, Pérez-Brito D, Tapia-Tussell R, Herrera-Chalé FG, Segura-Campos MR, Quijano-Ramayo A, Ramón-Sierra JM, Ortiz-Vázquez E PLoS One 27-Mar-2019
PMCID:PMC6436768
doi:10.1371/journal.pone.0213493
PMID:30917135
Structures of three new steroidal alkaloid glycosides, solaverines I, II and III from Solanum toxicarium and S. verbascifolium. Tomoyuki YAMASHITA, Nobuyo FUJIMURA, Shoji YAHARA, Toshihiro NOHARA, Syuji KAWANOBU, Kunimitsu FUJIEDA Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.38.827
Solaverbascine—a new 22,26-epiminocholestane alkaloid from Solanum verbascifolium G. Adam, H.Th. Huong, N.H. Khoi Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)85168-5

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 / Steroids and steroid derivatives / Steroidal alkaloids / 22,26-epiminocholestanes
(3S,8S,9S,10R,13S,14S,16S,17R)-10,13-dimethyl-17-[(1S)-1-[(2S,5R)-5-methylpiperidin-2-yl]ethyl]-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthrene-3,16-diol 15559003 Click to see CC1CCC(NC1)C(C)C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)O 415.70 unknown https://doi.org/10.1016/0031-9422(80)85168-5
16-Epi-dihydro-solasodine 312781 Click to see CC1CCC(NC1)C(C)C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)O)C)C)O 415.70 unknown https://doi.org/10.1016/0031-9422(80)85168-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Spirosolanes and derivatives
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)85168-5
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/10.1016/0031-9422(80)85168-5
Spirosolan-3-ol 312827 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)NC1 415.70 unknown https://doi.org/10.1016/0031-9422(80)85168-5
Tomatidine 65576 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)NC1 415.70 unknown https://doi.org/10.1016/0031-9422(80)85168-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-6-hydroxy-2-(hydroxymethyl)-4-[(1S,2R,3'S,4S,5'R,6S,7S,8R,9S,12R,13R,16S)-3'-hydroxy-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,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162935695 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(OC(C7OC8C(C(C(C(O8)C)O)O)O)O)CO)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1)O 884.10 unknown https://doi.org/10.1248/CPB.38.827
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-6-hydroxy-4-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl]oxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162951557 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(OC(C6OC7C(C(C(C(O7)C)O)O)O)O)CO)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CN9)CO)O 900.10 unknown https://doi.org/10.1248/CPB.38.827
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-2-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-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,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21636347 Click to see CC1CC(C2(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)O 900.10 unknown https://doi.org/10.1248/CPB.38.827
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-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,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21636346 Click to see CC1CC(C2(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)O 884.10 unknown https://doi.org/10.1248/CPB.38.827
(2S,3R,4R,5R,6S)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-6-[(1S,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S)-3'-hydroxy-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl]oxy-2-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21636348 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CN9)CO)O 900.10 unknown https://doi.org/10.1248/CPB.38.827
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5S,6R)-5-hydroxy-6-(hydroxymethyl)-4-[(1S,2R,3'S,4S,5'R,6S,7S,8R,9S,12R,13R,16S)-3'-hydroxy-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-2-[(2R,3R,4S,5R,6R)-2,3,5-trihydroxy-6-(hydroxymethyl)oxan-4-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162987409 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(OC(C7OC8C(C(C(C(O8)C)O)O)O)OC9C(C(OC(C9O)O)CO)O)CO)O)C)C)C)NC1)O 900.10 unknown https://doi.org/10.1248/CPB.38.827
(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(80)85168-5
2-[5-Hydroxy-6-(hydroxymethyl)-4-(3'-hydroxy-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-2-[2,3,5-trihydroxy-6-(hydroxymethyl)oxan-4-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162987408 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(OC(C7OC8C(C(C(C(O8)C)O)O)O)OC9C(C(OC(C9O)O)CO)O)CO)O)C)C)C)NC1)O 900.10 unknown https://doi.org/10.1248/CPB.38.827
2-[6-Hydroxy-2-(hydroxymethyl)-4-(3'-hydroxy-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-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162935694 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(OC(C7OC8C(C(C(C(O8)C)O)O)O)O)CO)OC9C(C(C(C(O9)C)O)O)O)C)C)C)NC1)O 884.10 unknown https://doi.org/10.1248/CPB.38.827
2-[6-Hydroxy-4-[3'-hydroxy-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-piperidine]-16-yl]oxy-2-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 162951556 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(OC(C6OC7C(C(C(C(O7)C)O)O)O)O)CO)OC8C(C(C(C(O8)C)O)O)O)C)C)OC19C(CC(CN9)CO)O 900.10 unknown https://doi.org/10.1248/CPB.38.827
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(80)85168-5

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