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Internal ID UUID643ffb808670c390782662
Scientific name Valeriana laxiflora
Authority DC.
First published in Prodr. 4: 638 (1830)

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Synonyms Top

Scientific name Authority First published in
Valeriana astrephioides Höck Bot. Jahrb. Syst. 3: 53 (1882)
Valerianella laxa (Hook. & Arn.) C.Presl Repert. Bot. Syst. : 11 (1833)
Valeriana pearcei Phil. Linnaea 33: 101 (1864)
Astrephia laxa (Hook. & Arn.) Hook. & Arn. Bot. Misc. 3: 364 (1833)
Fedia laxa Hook. & Arn. Bot. Beechey Voy. : 28 (1830)
Valeriana laxa Phil. Linnaea 28: 701 (1858)
Valeriana laxiflora var. cardaminifolia Poepp. Nov. Gen. Sp. Pl. Bras. 3: 17 (1841)
Valeriana rupicola Poepp. & Endl. Nov. Gen. Sp. Pl. (Poeppig & Endlicher) iii. 16. t. 217.
Valeriana foliosa Phil. Linnaea 28: 698 (1858)
Valeriana oxyrioides Graebn. Bot. Jahrb. Syst. 37: 444 (1906)
Valeriana sparsiflora Clos Fl. Chil. 3: 218 (1848)
Valeriana remota Ball J. Linn. Soc., Bot. 22: 42. 1885 [1887 publ. 24 Dec 1885]

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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
  • Southern America
    • Southern South America
      • Argentina South
      • Chile Central
      • Chile South

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000426713
Tropicos 33500102
KEW urn:lsid:ipni.org:names:859920-1
The Plant List kew-2464149
Open Tree Of Life 844983
NCBI Taxonomy 947117
IPNI 859920-1
iNaturalist 777988
GBIF 7298947
EOL 5236840

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
Phenolic Compounds as Promising Drug Candidates in Tuberculosis Therapy Mazlun MH, Sabran SF, Mohamed M, Abu Bakar MF, Abdullah Z Molecules 04-Jul-2019
PMCID:PMC6651284
doi:10.3390/molecules24132449
PMID:31277371
(4R,4aR,6S,7S,7aS)-6-Hydroxy-7-hydroxymethyl-4-methylperhydrocyclopenta[c]pyran-1-one chloroform solvate from Valeriana laxiflora. Khera S, Carducci MD, Gu JQ, Timmermann BN Acta Crystallogr C 01-Nov-2004
doi:10.1107/S0108270104021511
PMID:15528817
Antitubercular constituents of Valeriana laxiflora. Gu JQ, Wang Y, Franzblau SG, Montenegro G, Yang D, Timmermann BN Planta Med 01-Jun-2004
doi:10.1055/S-2004-827149
PMID:15229801

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
> Lignans, neolignans and related compounds / Furanoid lignans
1H,3H-Furo[3,4-c]furan-3a(4H)-ol, dihydro-1,4-bis(4-hydroxy-3-methoxyphenyl)-, (1R,3aS,4S,6aR)- 3010925 Click to see COC1=C(C=CC(=C1)C2C3COC(C3(CO2)O)C4=CC(=C(C=C4)O)OC)O 374.40 unknown https://doi.org/10.1055/S-2004-827149
3,6-Bis(4-hydroxy-3-methoxyphenyl)-1,3,4,6-tetrahydrofuro[3,4-c]furan-3a,6a-diol 14890536 Click to see COC1=C(C=CC(=C1)C2C3(COC(C3(CO2)O)C4=CC(=C(C=C4)O)OC)O)O 390.40 unknown https://doi.org/10.1055/S-2004-827149
3,6-Bis(4-hydroxy-3-methoxyphenyl)-3,4,6,6a-tetrahydro-1H-furo[3,4-c]furan-3a-ol 13824420 Click to see COC1=C(C=CC(=C1)C2C3COC(C3(CO2)O)C4=CC(=C(C=C4)O)OC)O 374.40 unknown https://doi.org/10.1055/S-2004-827149
8-Hydroxypinoresinol 3010930 Click to see COC1=C(C=CC(=C1)C2C3COC(C3(CO2)O)C4=CC(=C(C=C4)O)OC)O 374.40 unknown https://doi.org/10.1055/S-2004-827149
Prinsepiol 3010931 Click to see COC1=C(C=CC(=C1)C2C3(COC(C3(CO2)O)C4=CC(=C(C=C4)O)OC)O)O 390.40 unknown https://doi.org/10.1055/S-2004-827149
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4R,4aR,6S,7S,7aS)-6-hydroxy-7-(hydroxymethyl)-4-methyl-4,4a,5,6,7,7a-hexahydro-3H-cyclopenta[c]pyran-1-one 45096715 Click to see CC1COC(=O)C2C1CC(C2CO)O 200.23 unknown https://doi.org/10.1055/S-2004-827149
https://doi.org/10.1107/S0108270104021511
6-hydroxy-7-(hydroxymethyl)-4-methyl-4,4a,5,6,7,7a-hexahydro-3H-cyclopenta[c]pyran-1-one 71440392 Click to see CC1COC(=O)C2C1CC(C2CO)O 200.23 unknown https://doi.org/10.1055/S-2004-827149
https://doi.org/10.1107/S0108270104021511
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
10-hydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 14136880 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1055/S-2004-827149
23-Hydroxyursolic Acid 14136881 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O 472.70 unknown https://doi.org/10.1055/S-2004-827149
3-Hydroxyolean-12-en-28-oic acid 619166 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-2004-827149
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1055/S-2004-827149
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1055/S-2004-827149
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1055/S-2004-827149
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1055/S-2004-827149
Lup-20(29)-ene-3beta,28-diol 221023 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown https://doi.org/10.1055/S-2004-827149
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1055/S-2004-827149
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 https://doi.org/10.1055/S-2004-827149
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1055/S-2004-827149
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1055/S-2004-827149
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Tricin 5281702 Click to see COC1=CC(=CC(=C1O)OC)C2=CC(=O)C3=C(C=C(C=C3O2)O)O 330.29 unknown https://doi.org/10.1055/S-2004-827149
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Diosmetin 5281612 Click to see COC1=C(C=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1055/S-2004-827149
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Santin 5281695 Click to see COC1=CC=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 344.30 unknown https://doi.org/10.1055/S-2004-827149

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