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Paralychnophora bicolor

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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 UUID643fc9b32a3b0173906036
Scientific name Paralychnophora bicolor
Authority (DC.) MacLeish
First published in Taxon 33: 106 (1984)

Description Top

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Synonyms Top

Scientific name Authority First published in
Paralychnophora schwackei (Glaz.) MacLeish Taxon 33: 106 (1984)
Sphaerophora bicolor Sch.Bip. Jahresber. Pollichia 20-21: 403 (1863)
Vanillosmopsis bicolor Sch.Bip. Jahresber. Pollichia 18-19: 168 (1861)
Eremanthus schwackei Glaz. Bull. Soc. Bot. France 56(Mém. 3d): 380 (1909)
Albertinia bicolor DC. Prodr. 5: 81 (1836)
Eremanthus bicolor Baker Fl. Bras. 6(2): 165 (1873)
Paralychnophora santosii (H.Rob.) D.J.N.Hind Kew Bull. 55(2): 370 (2000)
Lychnocephalus bicolor Mart. ex DC. Prodr. 5: 83 (1836)

Common names Top

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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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Distribution (via POWO/KEW) Top

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000032704
Tropicos 50227970
KEW urn:lsid:ipni.org:names:182982-2
The Plant List gcc-131624
Open Tree Of Life 5794895
NCBI Taxonomy 1569432
IPNI 182982-2
iNaturalist 1007290
GBIF 3137730

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)!
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Title Authors Publication Released IDs
Sesquiterpene lactones from Eremanthus species Ferdinand Bohlmann, Christa Zdero, Robert M. King, Harold Robinson Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83940-0

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
> Hydrocarbons / Unsaturated hydrocarbons / Enynes
1-Tridecene-3,5,7,9,11-pentayne 441552 Click to see CC#CC#CC#CC#CC#CC=C 162.19 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(2,11-Dimethyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-1(13)-en-9-yl) 2-methylbut-2-enoate 162971531 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(CC3C1C(=C)C(=O)O3)C)C 360.40 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
[(2S,4S,8R,9S,11R)-2,11-dimethyl-7-methylidene-6,12-dioxo-5,14-dioxatricyclo[9.2.1.04,8]tetradec-1(13)-en-9-yl] (E)-2-methylbut-2-enoate 162971538 Click to see CC=C(C)C(=O)OC1CC2(C(=O)C=C(O2)C(CC3C1C(=C)C(=O)O3)C)C 360.40 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(1,10-Dimethyl-6-methylidene-5,13-dioxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-9,11-dien-8-yl) 2-methylbut-2-enoate 163017310 Click to see CC=C(C)C(=O)OC1C=C(C2=CC(=O)C(O2)(CC3C1C(=C)C(=O)O3)C)C 358.40 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
(1,10-Dimethyl-6-methylidene-5,13-dioxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-9,11-dien-8-yl) 2-methylprop-2-enoate 163045855 Click to see CC1=CC(C2C(CC3(C(=O)C=C1O3)C)OC(=O)C2=C)OC(=O)C(=C)C 344.40 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
[(1R,3S,7R,8S,9Z)-1,10-dimethyl-6-methylidene-5,13-dioxo-4,14-dioxatricyclo[9.2.1.03,7]tetradeca-9,11-dien-8-yl] 2-methylprop-2-enoate 163045856 Click to see CC1=CC(C2C(CC3(C(=O)C=C1O3)C)OC(=O)C2=C)OC(=O)C(=C)C 344.40 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aS,6aR,9S,9aR,9bR)-9-methyl-3,6-dimethylidene-3a,4,5,6a,7,9,9a,9b-octahydroazuleno[4,5-b]furan-2,8-dione 15559183 Click to see CC1C2C(CC1=O)C(=C)CCC3C2OC(=O)C3=C 246.30 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
3,6,9-trimethylidene-4,5,6a,7,9a,9b-hexahydro-3aH-azuleno[4,5-b]furan-2,8-dione 73834415 Click to see C=C1CCC2C(C3C1CC(=O)C3=C)OC(=O)C2=C 244.28 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
9-Methyl-3,6-dimethylidene-3a,4,5,6a,7,9,9a,9b-octahydroazuleno[4,5-b]furan-2,8-dione 15559181 Click to see CC1C2C(CC1=O)C(=C)CCC3C2OC(=O)C3=C 246.30 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
Dehydrocostus lactone, (-)- 73174 Click to see C=C1CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
Dehydrocostuslactone 4426320 Click to see C=C1CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
Dehydrozaluzanin C 10538257 Click to see C=C1CCC2C(C3C1CC(=O)C3=C)OC(=O)C2=C 244.28 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
Eremanthin 100572 Click to see CC1=CCC2C(C3C1CCC3=C)OC(=O)C2=C 230.30 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Epifriedelanol 119242 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
Friedelinol 348029 Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 428.70 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
Lupeol acetate 92157 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)OC(=O)C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthones / 4-prenylated xanthones
1,3,5-Trihydroxy-4-(3-methylbut-2-en-1-yl)-9H-xanthen-9-one 10335672 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3=C(O2)C(=CC=C3)O)C 312.30 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
> Organoheterocyclic compounds / Furofurans
(1S,3R,7S,9S,12S,13R,15R)-13-hydroxy-3,7,12-trimethyl-13-prop-1-en-2-yl-10,14,16-trioxatetracyclo[7.5.1.13,6.012,15]hexadec-5-ene-4,11-dione 162963319 Click to see CC1CC2C3C(CC4(C(=O)C=C1O4)C)OC(C3(C(=O)O2)C)(C(=C)C)O 348.40 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
(1S,3R,7S,9S,12S,13R,15R)-13-hydroxy-3,7,12-trimethyl-13-propan-2-yl-10,14,16-trioxatetracyclo[7.5.1.13,6.012,15]hexadec-5-ene-4,11-dione 163015008 Click to see CC1CC2C3C(CC4(C(=O)C=C1O4)C)OC(C3(C(=O)O2)C)(C(C)C)O 350.40 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
(1S,3R,7Z,9S,12S,13R,15R)-13-hydroxy-3,7,12-trimethyl-13-prop-1-en-2-yl-10,14,16-trioxatetracyclo[7.5.1.13,6.012,15]hexadeca-5,7-diene-4,11-dione 163003287 Click to see CC1=CC2C3C(CC4(C(=O)C=C1O4)C)OC(C3(C(=O)O2)C)(C(=C)C)O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
(1S,3R,7Z,9S,12S,13R,15R)-13-hydroxy-3,7,12-trimethyl-13-propan-2-yl-10,14,16-trioxatetracyclo[7.5.1.13,6.012,15]hexadeca-5,7-diene-4,11-dione 162948862 Click to see CC1=CC2C3C(CC4(C(=O)C=C1O4)C)OC(C3(C(=O)O2)C)(C(C)C)O 348.40 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
13-Hydroxy-3,7,12-trimethyl-13-prop-1-en-2-yl-10,14,16-trioxatetracyclo[7.5.1.13,6.012,15]hexadec-5-ene-4,11-dione 14314496 Click to see CC1CC2C3C(CC4(C(=O)C=C1O4)C)OC(C3(C(=O)O2)C)(C(=C)C)O 348.40 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
13-Hydroxy-3,7,12-trimethyl-13-prop-1-en-2-yl-10,14,16-trioxatetracyclo[7.5.1.13,6.012,15]hexadeca-5,7-diene-4,11-dione 495811 Click to see CC1=CC2C3C(CC4(C(=O)C=C1O4)C)OC(C3(C(=O)O2)C)(C(=C)C)O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)83940-0
13-Hydroxy-3,7,12-trimethyl-13-propan-2-yl-10,14,16-trioxatetracyclo[7.5.1.13,6.012,15]hexadec-5-ene-4,11-dione 163015007 Click to see CC1CC2C3C(CC4(C(=O)C=C1O4)C)OC(C3(C(=O)O2)C)(C(C)C)O 350.40 unknown https://doi.org/10.1016/S0031-9422(00)83940-0

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