Palisota barteri - Unknown
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Internal ID UUID6440031765a53836367389
Scientific name Palisota barteri
Authority Hook.f.
First published in Bot. Mag. 88: t. 5318 1862

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Synonyms Top

Scientific name Authority First published in
Palisota bicolor Mast. Gard. Chron. , n.s., 9: 527 (1878)
Palisota ombrophila K.Schum. ex C.B.Clarke Fl. Trop. Afr. 8: 29 (1901)
Palisota staudtii K.Schum. Bot. Jahrb. Syst. 24: 346 (1897)

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Language Common/alternative name
Chinese 浆果鸭跖草

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Varieties (abbr. var.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • West Tropical Africa
      • Ghana
      • Guinea
      • Ivory Coast
      • Liberia
      • Nigeria
      • Sierra Leone
      • Togo
    • West-central Tropical Africa
      • Cameroon
      • Congo
      • Equatorial Guinea
      • Gabon
      • Gulf Of Guinea Islands
      • Zaïre

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000488645
KEW urn:lsid:ipni.org:names:172909-1
The Plant List kew-257294
Open Tree Of Life 3945617
NCBI Taxonomy 1415684
IPNI 172909-1
GBIF 2763803
Freebase /m/04f5tv4
EOL 245775
Wikipedia Palisota_barteri

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
Insights into phylogenetic relationships and genome evolution of subfamily Commelinoideae (Commelinaceae Mirb.) inferred from complete chloroplast genomes Jung J, Kim C, Kim JH BMC Genomics 02-Apr-2021
PMCID:PMC8017861
doi:10.1186/s12864-021-07541-1
PMID:33794772
An Appraisal of Antidotes’ Effectiveness: Evidence of the Use of Phyto-Antidotes and Biotechnological Advancements Aruwa CE, Mukaila YO, Ajao AA, Sabiu S Molecules 26-Mar-2020
PMCID:PMC7181008
doi:10.3390/molecules25071516
PMID:32225103
Unique chromoplast organisation and carotenoid gene expression in carotenoid-rich carrot callus Oleszkiewicz T, Klimek-Chodacka M, Milewska-Hendel A, Zubko M, Stróż D, Kurczyńska E, Boba A, Szopa J, Baranski R Planta 21-Aug-2018
PMCID:PMC6244651
doi:10.1007/s00425-018-2988-5
PMID:30132151
Genome-Wide Identification and Expression Analyses of the Fibrillin Family Genes Suggest Their Involvement in Photoprotection in Cucumber Kim I, Lee SC, Kim EH, Song K, Yang TJ, Kim HU Plants (Basel) 27-Jun-2018
PMCID:PMC6161074
doi:10.3390/plants7030050
PMID:29954122
Carotinoide der Commelinacee Palisota barteri — ein neues β-Citraurin-Vorkommen Kurt Egger, Hella Kleinig-Voigt Walter de Gruyter GmbH 26-Feb-2015
doi:10.1515/ZNB-1968-0817
A new look at sporoderm ontogeny in Persea americana and the hidden side of development Gabarayeva NI, Grigorjeva VV, Rowley JR Ann Bot 17-Apr-2010
PMCID:PMC2876015
doi:10.1093/aob/mcq075
PMID:20400758
Co-Association of Cytochrome f Catabolites and Plastid-Lipid-Associated Protein with Chloroplast Lipid Particles Smith MD, Licatalosi DD, Thompson JE Plant Physiol 01-Sep-2000
PMCID:PMC59136
doi:10.1104/pp.124.1.211
PMID:10982436
Inflorescence and Leaf Galls on Palisota barteri Caused by Meloidogyne javanica Lehman PS, MacGowan JB J Nematol 01-Oct-1986
PMCID:PMC2618570
PMID:19294231

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 / Tetraterpenoids / Carotenoids / Carotenes
1,3,3-trimethyl-2-[(1E,3E,5E,7E,9E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene 152743364 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown https://doi.org/10.1515/ZNB-1968-0817
2,6,10,14,19,23,27,31-Octamethyl 2,6,8,10,12,14,16,18,20,22,24,26,30-dotriacontatridecaene 3977 Click to see CC(=CCCC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)C)C 536.90 unknown https://doi.org/10.1515/ZNB-1968-0817
Beta-Carotene 5280489 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CCCC2(C)C)C)C)C 536.90 unknown https://doi.org/10.1515/ZNB-1968-0817
Lycopene 446925 Click to see CC(=CCCC(=CC=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C)C)C 536.90 unknown https://doi.org/10.1515/ZNB-1968-0817
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Apocarotenal 5478003 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=O)C)C 416.60 unknown https://doi.org/10.1515/ZNB-1968-0817
beta-Citraurin 9845703 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=O)C)C 432.60 unknown https://doi.org/10.1515/ZNB-1968-0817
> Organic Polymers / Polypeptides
Baciguent 65281 Click to see CCC(C)C1C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NC(C(=O)NCCCCC(C(=O)NC(C(=O)N1)CCCN)NC(=O)C(C(C)CC)NC(=O)C(CCC(=O)O)NC(=O)C(CC(C)C)NC(=O)C2CSC(=N2)C(C(C)CC)N)CC(=O)N)CC(=O)O)CC3=CN=CN3)CC4=CC=CC=C4 1422.70 unknown https://doi.org/10.1515/ZNB-1968-0817
> Organoheterocyclic compounds / Naphthopyrans
(1S,8R,9S,12R,13R,14R,15R,16S)-15-chloro-8-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-13,14-dihydroxy-1,12-dimethyl-6-propan-2-yl-5,10-dioxatetracyclo[7.6.1.02,7.012,16]hexadeca-2,6-diene-4,11-dione 11387018 Click to see CC(C)C1=C2C(C3C4C(C(C(C(C4(C2=CC(=O)O1)C)Cl)O)O)(C(=O)O3)C)OC5C(C(CO5)(CO)O)O 530.90 unknown https://doi.org/10.1515/ZNB-1968-0817

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