Nassauvia revoluta - Unknown
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Internal ID UUID643fd4379b096707429678
Scientific name Nassauvia revoluta
Authority D.Don
First published in Philos. Mag. Ann. Chem. xi. (1832) 390; Gill. ex Hook (1832)

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Synonyms Top

Scientific name Authority First published in
Nassauvia nivalis Poepp. ex Less.
Nassauvia nivalis Poepp. & Endl. Nov. Gen. Sp. Pl. (Poeppig & Endlicher) i. 13. t. 22. 1832
Nassauvia brevifolia Phil. Anales Univ. Chile 87: 85 (1894)
Nassauvia sericea Phil. Anales Univ. Chile 87: 86 (1894)
Nassauvia nivalis var. sericea Phil. Linnaea 33: 115 (1864)
Nassauvia revoluta var. nivalis Hosseus
Nassauvia nivalis var. brevifolia Reiche Anales Univ. Chile 115: 570 (1905)

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Southern America
    • Southern South America
      • Argentina Northwest
      • Argentina South
      • Chile Central
      • Chile South

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Database ID/link to page
World Flora Online wfo-0000138651
Tropicos 2723280
KEW urn:lsid:ipni.org:names:234219-1
The Plant List gcc-99283
Open Tree Of Life 892475
NCBI Taxonomy 460340
IPNI 234219-1
iNaturalist 451789
GBIF 3099068

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
Relieving your stress: PGPB associated with Andean xerophytic plants are most abundant and active on the most extreme slopes Aguilera-Torres C, Riveros G, Morales LV, Sierra-Almeida A, Schoebitz M, Hasbún R Front Microbiol 18-Jan-2023
PMCID:PMC9889642
doi:10.3389/fmicb.2022.1062414
PMID:36741893
5-methylcoumarins from Nassauvia species M. Bittner, J. Jakupovic, F. Bohlmann, M. Silva Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83029-2

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown https://doi.org/10.1016/0031-9422(88)83029-2
> Benzenoids / Phenols / Methoxyphenols
Vanillyl alcohol 62348 Click to see COC1=C(C=CC(=C1)CO)O 154.16 unknown https://doi.org/10.1016/0031-9422(88)83029-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(E)-3-[3-methoxy-4-[(2E,6E)-3,7,11-trimethyldodeca-2,6,10-trienoxy]phenyl]prop-2-en-1-ol 14186846 Click to see CC(=CCCC(=CCCC(=CCOC1=C(C=C(C=C1)C=CCO)OC)C)C)C 384.60 unknown https://doi.org/10.1016/0031-9422(88)83029-2
3-[3-Methoxy-4-(3,7,11-trimethyldodeca-2,6,10-trienoxy)phenyl]prop-2-en-1-ol 162881097 Click to see CC(=CCCC(=CCCC(=CCOC1=C(C=C(C=C1)C=CCO)OC)C)C)C 384.60 unknown https://doi.org/10.1016/0031-9422(88)83029-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
4-[(E)-5-[(1R,3S)-3-hydroxy-2,2-dimethyl-6-methylidenecyclohexyl]-3-methylpent-2-enoxy]-5-methylchromen-2-one 162904591 Click to see CC1=C2C(=CC=C1)OC(=O)C=C2OCC=C(C)CCC3C(=C)CCC(C3(C)C)O 396.50 unknown https://doi.org/10.1016/0031-9422(88)83029-2
4-[(E)-5-[(1R)-2,2-dimethyl-6-methylidene-3-oxocyclohexyl]-3-methylpent-2-enoxy]-5-methylchromen-2-one 14186840 Click to see CC1=C2C(=CC=C1)OC(=O)C=C2OCC=C(C)CCC3C(=C)CCC(=O)C3(C)C 394.50 unknown https://doi.org/10.1016/0031-9422(88)83029-2
4-[5-(2,2-Dimethyl-6-methylidene-3-oxocyclohexyl)-3-methylpent-2-enoxy]-5-methylchromen-2-one 162891518 Click to see CC1=C2C(=CC=C1)OC(=O)C=C2OCC=C(C)CCC3C(=C)CCC(=O)C3(C)C 394.50 unknown https://doi.org/10.1016/0031-9422(88)83029-2
4-[5-(3-Hydroxy-2,2-dimethyl-6-methylidenecyclohexyl)-3-methylpent-2-enoxy]-5-methylchromen-2-one 162904589 Click to see CC1=C2C(=CC=C1)OC(=O)C=C2OCC=C(C)CCC3C(=C)CCC(C3(C)C)O 396.50 unknown https://doi.org/10.1016/0031-9422(88)83029-2
> Organoheterocyclic compounds / Bi- and oligothiophenes
(2R)-4-(5-thiophen-2-ylthiophen-2-yl)but-3-yne-1,2-diol 163077222 Click to see C1=CSC(=C1)C2=CC=C(S2)C#CC(CO)O 250.30 unknown https://doi.org/10.1016/0031-9422(88)83029-2
(2S)-4-[5-(5-methylthiophen-2-yl)thiophen-2-yl]but-3-yne-1,2-diol 162985809 Click to see CC1=CC=C(S1)C2=CC=C(S2)C#CC(CO)O 264.40 unknown https://doi.org/10.1016/0031-9422(88)83029-2
4-([2,2'-Bithiophen]-5-yl)but-3-yne-1,2-diol 14186845 Click to see C1=CSC(=C1)C2=CC=C(S2)C#CC(CO)O 250.30 unknown https://doi.org/10.1016/0031-9422(88)83029-2
4-[5-(5-Methylthiophen-2-yl)thiophen-2-yl]but-3-yne-1,2-diol 14186844 Click to see CC1=CC=C(S1)C2=CC=C(S2)C#CC(CO)O 264.40 unknown https://doi.org/10.1016/0031-9422(88)83029-2
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Suffruticosol B 10652146 Click to see C1=CC(=CC=C1C2C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C(C2C7=CC(=CC(=C7)O)O)C(=C6)O)C8=CC=C(C=C8)O)C9=CC=C(C=C9)O)O 680.70 unknown https://doi.org/10.1016/0031-9422(88)83029-2
> Phenylpropanoids and polyketides / Coumarins and derivatives
4-[(6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)methoxy]-5-methylchromen-2-one 14186841 Click to see CC1=C2C(=CC=C1)OC(=O)C=C2OCC3C(=C)CCC4C3(CCC(C4(C)C)O)C 396.50 unknown https://doi.org/10.1016/0031-9422(88)83029-2
4-[[(1S,4aR,6S,8aS)-6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]methoxy]-5-methylchromen-2-one 162952167 Click to see CC1=C2C(=CC=C1)OC(=O)C=C2OCC3C(=C)CCC4C3(CCC(C4(C)C)O)C 396.50 unknown https://doi.org/10.1016/0031-9422(88)83029-2

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