Petunia exserta - Unknown
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Internal ID UUID6440416105a2c831267328
Scientific name Petunia exserta
Authority Stehmann
First published in Napaea 2: 19 (-20), fig. 1987

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Estonian punatäht-petuunia

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Varieties (abbr. var.) Top

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Germination/Propagation Top

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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001024427
Tropicos 29608770
KEW urn:lsid:ipni.org:names:932457-1
The Plant List tro-29608770
Open Tree Of Life 446939
NCBI Taxonomy 323115
IPNI 282563-2
GBIF 3803157
Freebase /m/0p3mr82
EOL 5703134
USDA GRIN 431969
Wikipedia Petunia_exserta

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
Elucidating the callus-to-shoot-forming mechanism in Capsicum annuum ‘Dempsey’ through comparative transcriptome analyses Han SY, Park SY, Won KH, Park SI, Park JH, Shim D, Hwang I, Jeong DH, Kim H BMC Plant Biol 07-May-2024
PMCID:PMC11075324
doi:10.1186/s12870-024-05033-4
PMID:38711041
Shades of white: The Petunia long corolla tube clade evolutionary history Backes A, Turchetto C, Mäder G, Segatto AL, Bonatto SL, Freitas LB Genet Mol Biol 12-Feb-2024
PMCID:PMC10882218
doi:10.1590/1415-4757-GMB-2023-0279
PMID:38385448
How the switch to hummingbird pollination has greatly contributed to our understanding of evolutionary processes Wessinger CA New Phytol 18-Oct-2023
PMCID:PMC10843001
doi:10.1111/nph.19335
PMID:37853523
Cell layer–specific expression of the homeotic MADS-box transcription factor PhDEF contributes to modular petal morphogenesis in petunia Chopy M, Cavallini-Speisser Q, Chambrier P, Morel P, Just J, Hugouvieux V, Rodrigues Bento S, Zubieta C, Vandenbussche M, Monniaux M Plant Cell 06-Oct-2023
PMCID:PMC10827313
doi:10.1093/plcell/koad258
PMID:37804091
Sterol composition in plants is specific to pollen, leaf, pollination and pollinator Furse S, Martel C, Yusuf A, Shearman GC, Koch H, Stevenson PC Phytochemistry 01-Oct-2023
PMCID:PMC10493607
doi:10.1016/j.phytochem.2023.113800
PMID:37532086
Evolutionary walks through flower colour space driven by gene expression in Petunia and allies (Petunieae) Wheeler LC, Dunbar-Wallis A, Schutz K, Smith SD Proc Biol Sci 05-Jul-2023
PMCID:PMC10320354
doi:10.1098/rspb.2023.0275
PMID:37403504
The Amsterdam petunia germplasm collection: A tool in plant science Strazzer P, Verbree B, Bliek M, Koes R, Quattrocchio FM Front Plant Sci 21-Mar-2023
PMCID:PMC10070740
doi:10.3389/fpls.2023.1129724
PMID:37025133
Tight genetic linkage of genes causing hybrid necrosis and pollinator isolation between young species Li C, Binaghi M, Pichon V, Cannarozzi G, Brandão de Freitas L, Hanemian M, Kuhlemeier C Nat Plants 20-Feb-2023
PMCID:PMC10027609
doi:10.1038/s41477-023-01354-8
PMID:36805038
Analyses of Cullin1 homologs reveal functional redundancy in S-RNase-based self-incompatibility and evolutionary relationships in eudicots Sun L, Cao S, Zheng N, Kao TH Plant Cell 08-Dec-2022
PMCID:PMC9940881
doi:10.1093/plcell/koac357
PMID:36478090
Phylogenetic Analyses of Some Key Genes Provide Information on Pollinator Attraction in Solanaceae Pereira AG, Guzmán-Rodriguez S, Freitas LB Genes (Basel) 03-Dec-2022
PMCID:PMC9778481
doi:10.3390/genes13122278
PMID:36553545
The mungbean VrP locus encoding MYB90, an R2R3-type MYB protein, regulates anthocyanin biosynthesis Lin Y, Laosatit K, Liu J, Chen J, Yuan X, Somta P, Chen X Front Plant Sci 22-Jul-2022
PMCID:PMC9355716
doi:10.3389/fpls.2022.895634
PMID:35937322
The Isolation and Characterization of a Broad Host Range Bcep22-like Podovirus JC1 Davis CM, Ruest MK, Cole JH, Dennis JJ Viruses 29-Apr-2022
PMCID:PMC9144972
doi:10.3390/v14050938
PMID:35632679
A peroxisomal heterodimeric enzyme is involved in benzaldehyde synthesis in plants Huang XQ, Li R, Fu J, Dudareva N Nat Commun 15-Mar-2022
PMCID:PMC8924275
doi:10.1038/s41467-022-28978-2
PMID:35292635
One Step Away From Extinction: A Population Genomic Analysis of A Narrow Endemic, Tropical Plant Species Teixeira TM, Nazareno AG Front Plant Sci 23-Sep-2021
PMCID:PMC8496504
doi:10.3389/fpls.2021.730258
PMID:34630476
Complete chloroplast genome of the medicinal plant Evolvulus alsinoides: comparative analysis, identification of mutational hotspots and evolutionary dynamics with species of Solanales Shidhi PR, Nadiya F, Biju VC, Vijayan S, Sasi A, Vipin CL, Janardhanan A, Aswathy S, Rajan VS, Nair AS Physiol Mol Biol Plants 25-Aug-2021
PMCID:PMC8405790
doi:10.1007/s12298-021-01051-w
PMID:34539121

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 / Terpene lactones
(3aR,6R,7S,7aR)-7-[2-[(2R)-2-hydroxy-5-oxo-2H-furan-3-yl]ethyl]-3,3a,6,7-tetramethyl-4,5,6,7a-tetrahydro-1H-indene-2-carbaldehyde 14487080 Click to see CC1CCC2(C(C1(C)CCC3=CC(=O)OC3O)CC(=C2C)C=O)C 332.40 unknown https://doi.org/10.1016/S0031-9422(99)00026-6
2-(4,8-dimethylnona-1,3,7-trienyl)-2,3,9-trimethyl-3H-furo[3,2-c]chromen-4-one 163009330 Click to see CC1C2=C(C3=C(C=CC=C3OC2=O)C)OC1(C)C=CC=C(C)CCC=C(C)C 378.50 unknown https://doi.org/10.1016/S0031-9422(99)00026-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Isoarborinol 12305182 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(99)00026-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(3R,5S,8S,9S,10S,11R,13R,14S,17R)-17-ethenyl-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate 25180961 Click to see CC(=O)OC1CC2(C(CCC2C3C1C4(CCC(CC4CC3)O)C)C=C)C 360.50 unknown https://doi.org/10.1016/S0031-9422(99)00026-6
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
(12R,14S,15R)-14-[(12R,14S,15S)-2,15-dihydroxy-12-methoxy-6-methyl-4,11-dioxo-5,13-dioxatetracyclo[8.5.0.03,8.012,14]pentadeca-1(10),2,6,8-tetraen-14-yl]-2,15-dihydroxy-12-methoxy-6-methyl-5,13-dioxatetracyclo[8.5.0.03,8.012,14]pentadeca-1(10),2,6,8-tetraene-4,11-dione 163060622 Click to see CC1=CC2=CC3=C(C(C4(C(C3=O)(O4)OC)C56C(C7=C(C=C8C=C(OC(=O)C8=C7O)C)C(=O)C5(O6)OC)O)O)C(=C2C(=O)O1)O 606.50 unknown https://doi.org/10.1016/S0031-9422(99)00026-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2R,3R,4S,5R,6R)-2-[[(2R,3S,4R,5R,6S)-6-[2-(3,4-dihydroxy-5-methoxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 154497197 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)OC)O)O)O)O)O)O)O)O)O)O 625.60 unknown https://doi.org/10.1016/S0031-9422(00)00113-8
(2R,3R,4S,5R,6S)-2-[[(2R,3S,4R,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 154496406 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 595.50 unknown https://doi.org/10.1016/S0031-9422(99)00026-6
(2R,3R,4S,5R,6S)-2-[[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)chromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 154497170 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC=C(C=C5)O)O)O)O)O)O)O)O)O 579.50 unknown https://doi.org/10.1016/S0031-9422(99)00026-6
(2R,3S,4S,5R,6S)-2-[[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 154497631 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O)O)O)O 611.50 unknown https://doi.org/10.1016/S0031-9422(00)00113-8
(2S,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256715 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1016/S0031-9422(99)00026-6
Keracyanin cation 441674 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 595.50 unknown https://doi.org/10.1016/S0031-9422(99)00026-6
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1016/S0031-9422(99)00026-6
Pelargonidin 3-glucoside ion 443648 Click to see C1=CC(=CC=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O 433.40 unknown https://doi.org/10.1016/S0031-9422(99)00026-6
Pelargonidin 3-rutinoside 44256626 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC=C(C=C5)O)O)O)O)O)O)O)O)O 579.50 unknown https://doi.org/10.1016/S0031-9422(99)00026-6
> Phenylpropanoids and polyketides / Flavonoids / Hydroxyflavonoids / 7-hydroxyflavonoids
Cyanidin 128861 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O)O 287.24 unknown https://doi.org/10.1016/S0031-9422(99)00026-6
Pelargonidin 440832 Click to see C1=CC(=CC=C1C2=[O+]C3=CC(=CC(=C3C=C2O)O)O)O 271.24 unknown https://doi.org/10.1016/S0031-9422(99)00026-6

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