Solanum pubescens - Unknown
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Internal ID UUID644041da035f0514293221
Scientific name Solanum pubescens
Authority Willd.
First published in Phytographia 1: 5, tab. 3. 1794.

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Scientific name Authority First published in
Solanum blattaroioides Koen. ex Dunal Prodr. [A. P. de Candolle] 13(1): 127. 1852.
Solanum calycinum Nees Trans. Linn. Soc. London 17(1): 60 1834.
Solanum conanthum Dunal Prodr. [A. P. de Candolle] 13(1): 127. 1852.
Solanum esenbeckii Steud. Nomencl. Bot. ed. 2, 2: 602. 1841.

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

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Database ID/link to page
World Flora Online wfo-0001030658
KEW urn:lsid:ipni.org:names:820632-1
Open Tree Of Life 47884
NCBI Taxonomy 1097646
IPNI 820632-1
GBIF 2929764
Freebase /m/010pdd9_
Elurikkus 336729
Wikipedia Solanum_pubescens

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed CentralĀ®) and other sources (DOI number only)!
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Title Authors Publication Released IDs
Antidiabetic activity of Solanum torvum fruit extract in streptozotocin-induced diabetic rats Satyanarayana N, Chinni SV, Gobinath R, Sunitha P, Uma Sankar A, Muthuvenkatachalam BS Front Nutr 28-Oct-2022
PMCID:PMC9650639
doi:10.3389/fnut.2022.987552
PMID:36386935
High-performance thin layer chromatography based assay and stress study of a rare steroidal alkaloid solanopubamine in six species of Solanum grown in Saudi Arabia Siddiqui NA, Parvez MK, Al-Rehaily AJ, Al Dosari MS, Alam P, Shakeel F, Al Harbi HA Saudi Pharm J 26-May-2016
PMCID:PMC5355553
doi:10.1016/j.jsps.2016.05.003
PMID:28344468
Flavonol 3-O-Methyl Ethers from Solanum pubescens G. N. Krishna Kumari, L. Jagan Mohan Rao, N. S. Prakasa Rao American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50037A036
Myricetin methyl ethers from Solanum pubescens G.N.Krishna Kumari, L.Jagan Mohan Rao, N.S.Prakasa Rao Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84140-0
Solanopubamides a and b, two further steroidal alkaloids from solanum pu bescens G.N.Krishna Kumari, L.Jagan Mohan Rao, K.V.Raja Rao, N.S.Prakasa Rao, Ko Kaneko, Hiroshi Mitsuhashi Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81199-1

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 / Diterpenoids
(12Z)-8-Hydroxylabda-12,14-diene-19-al 101412319 Click to see CC(=CCC1C2(CCCC(C2CCC1(C)O)(C)C=O)C)C=C 304.50 unknown https://doi.org/10.1016/S0031-9422(00)81199-1
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
(1S,2R,5S,7S,10S,11S,14S,15R,16S,17S,18S,20S,23S)-7-amino-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracosan-18-ol 21573769 Click to see CC1CC(C2C(C3C(N2C1)CC4C3(CCC5C4CCC6C5(CCC(C6)N)C)C)C)O 414.70 unknown https://doi.org/10.1016/S0031-9422(00)81199-1
7-Amino-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracosan-18-ol 14191826 Click to see CC1CC(C2C(C3C(N2C1)CC4C3(CCC5C4CCC6C5(CCC(C6)N)C)C)C)O 414.70 unknown https://doi.org/10.1016/S0031-9422(00)81199-1
N-(18-hydroxy-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracosan-7-yl)acetamide 163090649 Click to see CC1CC(C2C(C3C(N2C1)CC4C3(CCC5C4CCC6C5(CCC(C6)NC(=O)C)C)C)C)O 456.70 unknown https://doi.org/10.1016/S0031-9422(00)81199-1
N-(18-hydroxy-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracosan-7-yl)formamide 163060578 Click to see CC1CC(C2C(C3C(N2C1)CC4C3(CCC5C4CCC6C5(CCC(C6)NC=O)C)C)C)O 442.70 unknown https://doi.org/10.1016/S0031-9422(00)81199-1
N-[(1S,2R,5S,7S,10S,11S,14S,15R,16S,17R,18S,20S,23S)-18-hydroxy-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracosan-7-yl]formamide 163060580 Click to see CC1CC(C2C(C3C(N2C1)CC4C3(CCC5C4CCC6C5(CCC(C6)NC=O)C)C)C)O 442.70 unknown https://doi.org/10.1016/S0031-9422(00)81199-1
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1021/NP50037A036
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1021/NP50037A036
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1021/NP50037A036
Kaempferol-3-O-rutinoside 5318767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O 594.50 unknown https://doi.org/10.1021/NP50037A036
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ayanin 5280682 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)O 344.30 unknown https://doi.org/10.1021/NP50037A036
Jaranol 5318869 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 314.29 unknown https://doi.org/10.1021/NP50037A036
Myricetin 3,7,3'-trimethyl ether 21676154 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)OC)O)O)O 360.30 unknown https://doi.org/10.1016/S0031-9422(00)84140-0
Myricetin 3,7,3',5'-tetramethyl ether 44259713 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)OC)O)OC)O 374.30 unknown https://doi.org/10.1016/S0031-9422(00)84140-0
Retusin 5352005 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)OC 358.30 unknown https://doi.org/10.1021/NP50037A036

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