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Pseudognaphalium gaudichaudianum

Pseudognaphalium gaudichaudianum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fc5ec5d6f6559569400
Scientific name Pseudognaphalium gaudichaudianum
Authority (DC.) Anderb.
First published in Opera Bot. 104: 147 (1991):.

Description Top

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Synonyms Top

Scientific name Authority First published in
Pseudognaphalium austrobrasilicum Deble & Marchiori Balduinia 6: 4 (-6; fig. 1) (2006)
Gnaphalium mendocinum Phil. Anales Univ. Chile (1870) 184
Pseudognaphalium mendocinum (Phil.) Deble & Marchiori Balduinia 9: 15 (2006)
Gnaphalium gaudichaudianum DC. Prodr. [A. P. de Candolle] 6: 226. 1838 [1837 publ. early Jan 1838]
Gnaphalium mandonii Sch.Bip. Linnaea 34: 532, nomen (1866)

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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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000001164
Tropicos 50271001
KEW urn:lsid:ipni.org:names:283850-2
The Plant List gcc-101106
Open Tree Of Life 3898938
NCBI Taxonomy 1754171
IPNI 963017-1
iNaturalist 523870
GBIF 3101011
EPPO GNAGA
Wikipedia Pseudognaphalium_gaudichaudianum

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
Ent-pimarane type diterpenes from Gnaphalium gaudichaudianum. Meragelman TL, Silva GL, Mongelli E, Gil RR Phytochemistry 01-Feb-2003
doi:10.1016/S0031-9422(02)00611-8
PMID:12560027
5,8-Dihydroxy-3,6,7-trimethoxyflavone from Gnaphalium gaudichaudianum Eduardo Guerreiro, Juan Kavka, Oscar S. Giordano Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(82)85269-2

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 / Diterpenoids
((1R,4aR,4bS,7R,10aR)-1,4a,7-Trimethyl-7-vinyl-1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydrophenanthren-1-yl)methanol 12314283 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
(1R,2R,4aS,4bR,7R,10aS)-7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-2-ol 12313648 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)C=C 304.50 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
(1S,4aS,4bR,7R,10aS)-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthrene-1-carboxylic acid 24721193 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
(2R,4aS,4bR,7R,10aS)-7-ethenyl-1,1,4a,7-tetramethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-2-ol 53475568 Click to see CC1(C2CCC3=CC(CCC3C2(CCC1O)C)(C)C=C)C 288.50 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
(5beta,8alpha,9beta,10alpha,13S)-Pimara-15-ene-3alpha,8-diol 637235 Click to see CC1(C2CCC3(CC(CCC3C2(CCC1O)C)(C)C=C)O)C 306.50 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
[(1R,4aS,4bR,7R,10aS)-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-1-yl]methanol 12314284 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)CO)C)C=C 288.50 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
15-Isopimarene-8,18-diol 543955 Click to see CC1(CCC2C3(CCCC(C3CCC2(C1)O)(C)CO)C)C=C 306.50 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
7-ethenyl-1-(hydroxymethyl)-1,4a,7-trimethyl-3,4,4b,5,6,9,10,10a-octahydro-2H-phenanthren-2-ol 578235 Click to see CC1(CCC2C(=C1)CCC3C2(CCC(C3(C)CO)O)C)C=C 304.50 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
7-Ethenyl-1,1,4a,7-tetramethyl-2,3,4,4b,5,6,8,9,10,10a-decahydrophenanthrene-2,8a-diol 73803352 Click to see CC1(C2CCC3(CC(CCC3C2(CCC1O)C)(C)C=C)O)C 306.50 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
Continentalic acid 10086296 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
delta8(14)-Pimaric acid 10116 Click to see CC1(CCC2C(=C1)CCC3C2(CCCC3(C)C(=O)O)C)C=C 302.50 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
ent-Isopimara-8(14),15-diene-3beta-ol 584511 Click to see CC1(C2CCC3=CC(CCC3C2(CCC1O)C)(C)C=C)C 288.50 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
Thermarol 21593604 Click to see CC1(CCC2C3(CCCC(C3CCC2(C1)O)(C)CO)C)C=C 306.50 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Squalene 638072 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
Super Squalene; trans-Squalene;AddaVax 1105 Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C)C 410.70 unknown https://doi.org/10.1016/S0031-9422(02)00611-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 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(02)00611-8
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(02)00611-8
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,8-Dihydroxy-3,6,7-trimethoxyflavone 15290567 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=CC=C3)OC)O)OC 344.30 unknown https://doi.org/10.1016/0031-9422(82)85269-2
5,8-Dihydroxy-6,7-dimethoxyflavone 153441 Click to see COC1=C(C(=C2C(=C1O)C(=O)C=C(O2)C3=CC=CC=C3)O)OC 314.29 unknown https://doi.org/10.1016/0031-9422(82)85269-2
Velutin 5464381 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)OC)O 314.29 unknown https://doi.org/10.1016/S0031-9422(02)00611-8

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