Vernonia galamensis subsp. galamensis

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Internal ID UUID6440697c4d103469793277
Scientific name Vernonia galamensis subsp. galamensis
First published in Unknown

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Database ID/link to page
World Flora Online wfo-0001425654
KEW urn:lsid:ipni.org:names:77180134-1
GBIF 9241057

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Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
Title Authors Publication Released IDs
Vernonia galamensis, Potential new crop source of epoxy acid Robert E. Perdue, Kenneth D. Carlson, Michael G. Gilbert Springer Science and Business Media LLC 04-Dec-2010
doi:10.1007/BF02858947
Preliminary observation of the chemical composition of callus derived from immature seeds of<i>Vernonia galamensis</i>, Var. Ethiopica, Gilbert Seifu Belay, John P. Rier, Folahan O. Ayorinde Wiley 16-Jul-2007
doi:10.1007/BF02653678
Sterols of seed oils of <i>Vernonia galamensis</i>, <i>Amaranthus cruentus</i>, <i>Amaranthus caudatus</i>, <i>Amaranthus hybridus</i> and <i>Amaranthus hypochondriacus</i> grown in the humid tropics M O Ologunde, F O Ayorinde, R L Shepard, O A Afolabi, O L Oke Wiley 05-Mar-2007
doi:10.1002/JSFA.2740580210
Flavonol glycosides from Vernonia galamensis ssp. nairobiensis François Miserez, Olivier Potterat, Andrew Marston, Geoffrey M. Mungai, Kurt Hostettmann Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(96)00252-X
Prevernocistifolides from Vernonia galamensis R.E. Perdue, F. Tsichritzis, J. Jakupovic Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90717-9
In vivo studies of the biosynthesis of vernolic acid in the seed of Vernonia galamensis. Liu L, Hammond EG, Nikolau BJ Lipids 01-Dec-1998
doi:10.1007/S11745-998-0326-3
PMID:9930408

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
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
2-Butenoic acid, 3-methyl-, phenylmethyl ester 162264 Click to see CC(=CC(=O)OCC1=CC=CC=C1)C 190.24 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(-)-leukotoxin B 5281128 Click to see CCCCCC1C(O1)CC=CCCCCCCCC(=O)O 296.40 unknown https://doi.org/10.1007/S11745-998-0326-3
https://doi.org/10.1016/S0031-9422(00)90717-9
https://doi.org/10.1007/BF02858947
https://doi.org/10.1007/BF02653678
(9Z)-(12S,13R)-12,13-Epoxyoctadecenoic acid 6449780 Click to see CCCCCC1C(O1)CC=CCCCCCCCC(=O)O 296.40 unknown https://doi.org/10.1007/S11745-998-0326-3
https://doi.org/10.1007/BF02858947
https://doi.org/10.1016/S0031-9422(00)90717-9
https://doi.org/10.1007/BF02653678
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
2,3-bis[[(Z)-11-[(2S,3R)-3-pentyloxiran-2-yl]undec-9-enoyl]oxy]propyl (Z)-11-[(2S,3R)-3-pentyloxiran-2-yl]undec-9-enoate 101623850 Click to see CCCCCC1C(O1)CC=CCCCCCCCC(=O)OCC(COC(=O)CCCCCCCC=CCC2C(O2)CCCCC)OC(=O)CCCCCCCC=CCC3C(O3)CCCCC 927.40 unknown https://doi.org/10.1007/BF02858947
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(-)-Cyperene 12308843 Click to see CC1CCC2CC3=C(CCC13C2(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
Cyperene 99856 Click to see CC1CCC2CC3=C(CCC13C2(C)C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
Humulene 5281520 Click to see CC1=CCC(C=CCC(=CCC1)C)(C)C 204.35 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
[(4aR,6aS,6aR,6bR,8aR,12aS,14aS,14bR)-4,4,6a,6b,8a,12,14b-heptamethyl-11-methylidene-1,2,3,4a,5,6,6a,7,8,9,10,12,12a,13,14,14a-hexadecahydropicen-3-yl] acetate 137704689 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
Beta-Amyrin 73145 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
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)90717-9
Taraxasterol, acetate 344468 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(CCC1=C)C)C)C)(C)C)OC(=O)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
Cholesterol 5997 Click to see CC(C)CCCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 386.70 unknown https://doi.org/10.1002/JSFA.2740580210
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/S0031-9422(00)90717-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1016/0031-9422(96)00252-X

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