Pseudognaphalium oligandrum - Unknown
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Internal ID UUID643fc680d1e83452088955
Scientific name Pseudognaphalium oligandrum
Authority (DC.) Hilliard & B.L.Burtt
First published in Bot. J. Linn. Soc. 82(3): 204 (1981): (1981)

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Synonyms Top

Scientific name Authority First published in
Helichrysum steudelii Sch.Bip. ex A.Rich. Tent. Fl. Abyss. 1: 421 (1848)
Gnaphalium oligandrum (DC.) Hilliard & B.L.Burtt Notes Roy. Bot. Gard. Edinburgh 34(3): 256 (1976)
Gnaphalium steudelii (Sch.Bip. ex A.Rich.) Oliv. & Hiern Fl. Trop. Afr. 2: 343 (1877)
Anaphalis oligandra DC. Prodr. 6: 275 (1838)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
      • Sudan
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zambia
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Cape Provinces
      • Free State
      • Kwazulu-Natal
      • Lesotho
      • Namibia
      • Northern Provinces
      • Swaziland
    • West-central Tropical Africa
      • Rwanda
      • Zaïre
    • Western Indian Ocean
      • Madagascar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000005683
Tropicos 2719020
KEW urn:lsid:ipni.org:names:909627-1
The Plant List gcc-10547
Open Tree Of Life 641758
NCBI Taxonomy 857096
IPNI 909627-1
iNaturalist 592566
GBIF 3101017
EPPO GNAOL
CMAUP NPO13868

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
Phylogeny of Leontopodium (Asteraceae) in China—with a reference to plastid genome and nuclear ribosomal DNA Xu XM, Wei Z, Sun JZ, Zhao QF, Lu Y, Wang ZL, Zhu SX Front Plant Sci 31-Jul-2023
PMCID:PMC10425225
doi:10.3389/fpls.2023.1163065
PMID:37583593
Neue diterpene aus Gnaphalium-arten Ferdinand Bohlmann, Jürgen Ziesche Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(80)85015-1

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Terphenyls / P-terphenyls
3-Hydroxyterphenyllin 191796 Click to see COC1=C(C(=C(C(=C1)C2=CC=C(C=C2)O)OC)O)C3=CC(=C(C=C3)O)O 354.40 unknown via CMAUP database
3,3''-Dihydroxyterphenyllin 10429220 Click to see COC1=C(C(=C(C(=C1)C2=CC(=C(C=C2)O)O)OC)O)C3=CC(=C(C=C3)O)O 370.40 unknown via CMAUP database
4''-Dehydro-3-hydroxyterphenyllin 53262867 Click to see COC1=C(C(=C(C(=C1)C2=CC=CC=C2)OC)O)C3=CC(=C(C=C3)O)O 338.40 unknown via CMAUP database
4''-Deoxyterphenyllin 57345621 Click to see COC1=C(C(=C(C(=C1)C2=CC=CC=C2)OC)O)C3=CC=C(C=C3)O 322.40 unknown via CMAUP database
Prenylterphenyllin 23630784 Click to see CC(=CCC1=C(C=CC(=C1)C2=C(C=C(C(=C2O)OC)C3=CC=C(C=C3)O)OC)O)C 406.50 unknown via CMAUP database
Prenylterphenyllin A 53262866 Click to see CC(=CCC1=C(C=CC(=C1)C2=CC(=C(C(=C2OC)O)C3=CC(=C(C=C3)O)O)OC)O)C 422.50 unknown via CMAUP database
Prenylterphenyllin B 53356515 Click to see CC(=CCC1=C(C=CC(=C1)C2=CC(=C(C(=C2OC)O)C3=CC=C(C=C3)O)OC)O)C 406.50 unknown via CMAUP database
Prenylterphenyllin C 53354805 Click to see CC(=CCC1=C(C(=CC(=C1)C2=C(C=C(C(=C2O)OC)C3=CC=C(C=C3)O)OC)O)O)C 422.50 unknown via CMAUP database
Terphenyllin 100437 Click to see COC1=C(C(=C(C(=C1)C2=CC=C(C=C2)O)OC)O)C3=CC=C(C=C3)O 338.40 unknown via CMAUP database
Terprenin 9932003 Click to see CC(=CCOC1=C(C=C(C=C1)C2=C(C=C(C(=C2O)OC)C3=CC=C(C=C3)O)OC)O)C 422.50 unknown via CMAUP database
> Benzenoids / Indanes / Indanones
(2R,3S)-sulfated pterosin C, (+)- 54672170 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOS(=O)(=O)O)C)O 314.36 unknown via CMAUP database
(2R)-pterosin P 70698132 Click to see CC1CC2=CC(=C(C(=C2C1=O)C)CCO)CO 234.29 unknown via CMAUP database
(2S,3S)-Sulfated pterosin C 54669844 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOS(=O)(=O)O)C)O 314.36 unknown via CMAUP database
Pterosin C 186209 Click to see CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCO)C)O 234.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Tetracosanoic acid 11197 Click to see CCCCCCCCCCCCCCCCCCCCCCCC(=O)O 368.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4R,5R,9S,10R,13R)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 92529179 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/0031-9422(80)85015-1
5,9-Dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 433869 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/0031-9422(80)85015-1
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1R,2E,6E,10R)-7,11,11-trimethylbicyclo[8.1.0]undeca-2,6-diene 163090851 Click to see CC1=CCCC=CC2C(C2(C)C)CC1 190.32 unknown https://doi.org/10.1016/0031-9422(80)85015-1
1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)- 91104 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(80)85015-1
7,11,11-Trimethylbicyclo[8.1.0]undeca-2,6-diene 86060105 Click to see CC1=CCCC=CC2C(C2(C)C)CC1 190.32 unknown https://doi.org/10.1016/0031-9422(80)85015-1
Germacrene D 5317570 Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C 204.35 unknown https://doi.org/10.1016/0031-9422(80)85015-1
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4R,4aS,6aR,6aS,6bR,8aR,12aR,14aS,14bR)-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1H-picen-3-one 7067822 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Pentahydroxy bile acids, alcohols and derivatives
Ponasterone A 115127 Click to see CC(C)CCC(C(C)(C1CCC2(C1(CCC3C2=CC(=O)C4C3(CC(C(C4)O)O)C)C)O)O)O 464.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Phenylbenzofurans
Candidusin A 24011606 Click to see COC1=C2C3=CC(=C(C=C3OC2=C(C(=C1)C4=CC=C(C=C4)O)OC)O)O 352.30 unknown via CMAUP database
Candidusin C 56659541 Click to see COC1=CC=C(C=C1)C2=CC(=C3C4=CC(=C(C=C4OC3=C2OC)O)O)OC 366.40 unknown via CMAUP database
Prenylcandidusin A 53354806 Click to see CC(=CCC1=C(C=CC(=C1)C2=CC(=C3C4=CC(=C(C=C4OC3=C2OC)O)O)OC)O)C 420.50 unknown via CMAUP database
Prenylcandidusin B 53262877 Click to see CC(=CCC1=C(C=CC(=C1)C2=CC(=C3C4=CC(=C(C=C4OC3=C2OC)OC)OC)OC)O)C 448.50 unknown via CMAUP database
Prenylcandidusin C 53354807 Click to see CC(=CCC1=C(C=CC(=C1)C2=CC(=C3C4=CC(=C(C=C4OC3=C2OC)OC)O)OC)O)C 434.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 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 via CMAUP database

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