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Eriodictyon californicum

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644046cb43e60809001292
Scientific name Eriodictyon californicum
Authority (Hook. & Arn.) Torr.
First published in Rep. U.S. Mex. Bound. 2(1): 148 1859

Ethnobotanical Use Top

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General Uses Top

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Common products: No widely commercialized products are documented for Eriodictyon californicum.

Industrial and craft applications: No established industrial or craft uses with verified technical properties are recorded for this species.

Food and beverages (non-medicinal): No documented culinary use.

Colorants and tanning: No documented use as a dye, ink, or tannin source.

Wood and fiber: No timber or bast-fiber uses reported; the plant is a shrub without documented lignocellulosic utilization.

Fragrance and cosmetics: No documented use in perfumery or cosmetics.

Properties relevant to use: No documented properties that underpin industrial utilization.

Standards and regulation: Not applicable.

Sustainability and sourcing: No recorded commercial sourcing framework; it occurs as a native shrub in California and Oregon shrublands.

Synonyms Top

Scientific name Authority First published in
Eriodictyon californicum subsp. australe Brand Pflanzenr. , IV, 251: 141 (1913)
Eriodictyon californicum subsp. glutinosum (Benth.) Brand Pflanzenr. , IV, 251: 141 (1913)
Eriodictyon californicum f. latifolia Brand Pflanzenr. (Engler) 4, fam. 251: 141. 1913
Eriodictyon californicum f. linearis Brand Univ. Calif. Publ. Bot. 4: 224. 1912
Eriodictyon californicum var. pubens Brand Pflanzenr. , IV, 251: 142 (1913)
Eriodictyon glutinosum Benth. Bot. Voy. Sulphur [Bentham] 36. 1844 [2 Apr 1844]
Eriodictyon glutinosum var. serratum Choisy Prodr. 10: 183 (1846)
Wigandia californica Hook. & Arn. Bot. Beechey Voy. : 364 (1839)
Eriodictyon californicum subvar. coarctatum Brand Pflanzenr. (Engler) 4, fam. 251: 142. 1913
Eriodictyon californicum (Hook. & Arn.) Decne. Voy. Venus, Bot. [Atl.] 5(2): 22 (1864)
Eriodictyon californicum (Hook. & Arn.) Greene Pittonia 2(7): 23 (1889)

Common names Top

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Language Common/alternative name
English california yerba santa
French yerba santa
Chinese 北美聖草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Northwestern U.S.A.
      • Oregon
    • Southwestern U.S.A.
      • California

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001066643
UNII 5B3RVA127P
USDA Plants ERCA6
KEW urn:lsid:ipni.org:names:432090-1
The Plant List kew-2795509
Open Tree Of Life 544709
NCBI Taxonomy 4132
Nature Serve 2.136633
IPNI 432090-1
iNaturalist 57095
GBIF 2928346
Freebase /m/02rvbhx
FEIS plants/shrub/erical
EPPO ERTCA
EOL 595684
Calflora (Californian flora) 3182
USDA GRIN 402585
Wikipedia Eriodictyon_californicum
CMAUP NPO11318

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)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Olive Flounder By-Product Prozyme2000P Hydrolysate Ameliorates Age-Related Kidney Decline by Inhibiting Ferroptosis Son M, Jeon YJ, Ryu B, Kim DY Int J Mol Sci 25-Apr-2024
PMCID:PMC11083375
doi:10.3390/ijms25094668
PMID:38731887
The Neuroprotective Flavonoids Sterubin and Fisetin Maintain Mitochondrial Health under Oxytotic/Ferroptotic Stress and Improve Bioenergetic Efficiency in HT22 Neuronal Cells Goujon M, Liang Z, Soriano-Castell D, Currais A, Maher P Antioxidants (Basel) 13-Apr-2024
PMCID:PMC11047672
doi:10.3390/antiox13040460
PMID:38671908
Protective effect of sterubin against neurochemical and behavioral impairments in rotenone-induced Parkinson's disease Alqurashi MM, Al-Abbasi FA, Afzal M, Alghamdi AM, Zeyadi M, Sheikh RA, Alshehri S, Imam SS, Sayyed N, Kazmi I Braz J Med Biol Res 09-Feb-2024
PMCID:PMC10868181
doi:10.1590/1414-431X2023e12829
PMID:38359270
A journey from molecule to physiology and in silico tools for drug discovery targeting the transient receptor potential vanilloid type 1 (TRPV1) channel Amaya-Rodriguez CA, Carvajal-Zamorano K, Bustos D, Alegría-Arcos M, Castillo K Front Pharmacol 24-Jan-2024
PMCID:PMC10847257
doi:10.3389/fphar.2023.1251061
PMID:38328578
Alternative Crops for the European Tobacco Industry: A Systematic Review Mavroeidis A, Stavropoulos P, Papadopoulos G, Tsela A, Roussis I, Kakabouki I Plants (Basel) 15-Jan-2024
PMCID:PMC10818552
doi:10.3390/plants13020236
PMID:38256796
Conservation Genetics of the Endangered Lompoc Yerba Santa (Eriodictyon capitatum Eastw., Namaceae), including Phylogenomic Insights into the Evolution of Eriodictyon Guilliams CM, Hasenstab-Lehman KE Plants (Basel) 27-Dec-2023
PMCID:PMC10780715
doi:10.3390/plants13010090
PMID:38202398
Phytochemicals as Antimicrobials: Prospecting Himalayan Medicinal Plants as Source of Alternate Medicine to Combat Antimicrobial Resistance Ashraf MV, Pant S, Khan MA, Shah AA, Siddiqui S, Jeridi M, Alhamdi HW, Ahmad S Pharmaceuticals (Basel) 15-Jun-2023
PMCID:PMC10302623
doi:10.3390/ph16060881
PMID:37375828
The Impact of Commercially Available Dry Mouth Products on the Corrosion Resistance of Common Dental Alloys Turkina AY, Makeeva IM, Dubinin ON, Bondareva JV, Chernodoubov DA, Shibalova AA, Arzukanyan AV, Antoshin AA, Timashev PS, Evlashin SA Materials (Basel) 05-Jun-2023
PMCID:PMC10254468
doi:10.3390/ma16114195
PMID:37297329
Optimized De Novo Eriodictyol Biosynthesis in Streptomyces albidoflavus Using an Expansion of the Golden Standard Toolkit for Its Use in Actinomycetes Magadán-Corpas P, Ye S, Pérez-Valero Á, McAlpine PL, Valdés-Chiara P, Torres-Bacete J, Nogales J, Villar CJ, Lombó F Int J Mol Sci 17-May-2023
PMCID:PMC10219347
doi:10.3390/ijms24108879
PMID:37240225
Three Major Causes of Metabolic Retinal Degenerations and Three Ways to Avoid Them Kovács-Valasek A, Rák T, Pöstyéni E, Csutak A, Gábriel R Int J Mol Sci 13-May-2023
PMCID:PMC10218427
doi:10.3390/ijms24108728
PMID:37240082
Tanshinone-I for the treatment of uterine fibroids: Molecular docking, simulation, and density functional theory investigations Tiwari A, Tiwari V, Sharma A, Singh D, Singh Rawat M, Virmani T, Virmani R, Kumar G, Kumar M, Alhalmi A, Noman OM, Mothana RA, Alali M Saudi Pharm J 08-May-2023
PMCID:PMC10209546
doi:10.1016/j.jsps.2023.05.002
PMID:37250358
Drug target of natural products and COVID-19: how far has science progressed? Raman K, Rajagopal K, Ramesh B, Nallasivan PK, Raja MK, Jupudi S, Byran G, Khan SL, Bin Emran T Ann Med Surg (Lond) 19-Apr-2023
PMCID:PMC10289732
doi:10.1097/MS9.0000000000000703
PMID:37363478
Phytobioactive compounds as therapeutic agents for human diseases: A review Riaz M, Khalid R, Afzal M, Anjum F, Fatima H, Zia S, Rasool G, Egbuna C, Mtewa AG, Uche CZ, Aslam MA Food Sci Nutr 17-Apr-2023
PMCID:PMC10261751
doi:10.1002/fsn3.3308
PMID:37324906
Phenolic Phytochemicals for Prevention and Treatment of Colorectal Cancer: A Critical Evaluation of In Vivo Studies De S, Paul S, Manna A, Majumder C, Pal K, Casarcia N, Mondal A, Banerjee S, Nelson VK, Ghosh S, Hazra J, Bhattacharjee A, Mandal SC, Pal M, Bishayee A Cancers (Basel) 03-Feb-2023
PMCID:PMC9913554
doi:10.3390/cancers15030993
PMID:36765950
Sterubin protects against chemically-induced Alzheimer’s disease by reducing biomarkers of inflammation- IL-6/ IL-β/ TNF-α and oxidative stress- SOD/MDA in rats Kazmi I, Al-Abbasi FA, Afzal M, Shahid Nadeem M, Altayb HN Saudi J Biol Sci 13-Jan-2023
PMCID:PMC9876951
doi:10.1016/j.sjbs.2023.103560
PMID:36712184

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid 10467 Click to see 312.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1021/NP50081A012
Pinocembrin 68071 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=CC=C3 256.25 unknown https://doi.org/10.1021/NP50081A012
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Chrysin 5281607 Click to see 254.24 unknown https://doi.org/10.1021/NP50081A012
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/0305-1978(83)90056-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
[4-[(2S)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-2-yl]-2-methoxyphenyl] 2-methylpropanoate 44576022 Click to see 372.40 unknown https://doi.org/10.1021/NP50081A012
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1039/CT9079100887
https://doi.org/10.1039/CT9099500081
https://doi.org/10.1021/NP50081A012
Homoeriodictyol 73635 Click to see 302.28 unknown https://doi.org/10.1016/0305-1978(85)90004-3
https://doi.org/10.1021/NP50081A012
https://doi.org/10.1007/BF02262470
> 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/10.1016/0305-1978(83)90056-X
Hesperetin 72281 Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/0305-1978(85)90004-3
Isosakuranetin 160481 Click to see COC1=CC=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O 286.28 unknown https://doi.org/10.1021/NP50081A012
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
5,7,4'-Trihydroxy-6,3'-dimethoxyflavanon 14034286 Click to see 332.30 unknown https://doi.org/10.1021/NP50081A012
Hispidulin 5281628 Click to see 300.26 unknown https://doi.org/10.1021/NP50081A012
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',5-Dihydroxy-4',7-dimethoxyflavone 5320496 Click to see 314.29 unknown https://doi.org/10.1016/0305-1978(83)90056-X
5,4'-Dihydroxy-6,7-Dimethoxyflavanone 14078484 Click to see 316.30 unknown https://doi.org/10.1021/NP50081A012
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown https://doi.org/10.1021/NP50081A012
Persicogenin 320054 Click to see COC1=C(C=C(C=C1)C2CC(=O)C3=C(C=C(C=C3O2)OC)O)O 316.30 unknown https://doi.org/10.1016/0305-1978(83)90056-X
Sakuranetin 73571 Click to see 286.28 unknown https://doi.org/10.1021/NP50081A012
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/10.1016/0305-1978(83)90056-X

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