Chamaebatia foliolosa

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Internal ID UUID64403f9407889027683378
Scientific name Chamaebatia foliolosa
Authority Benth.
First published in Pl. Hartw. [Bentham] 308. 1849 [undated prob. 25 Jan 1849]

Ethnobotanical Use Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
English mountain misery

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Germination/Propagation Top

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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-0001003392
USDA Plants CHFO
Tropicos 27801486
KEW urn:lsid:ipni.org:names:30342115-2
The Plant List rjp-3444
Open Tree Of Life 653073
NCBI Taxonomy 140996
Nature Serve 2.147976
IPNI 722137-1
iNaturalist 56573
GBIF 3000918
Freebase /m/03g_zc3
FEIS plants/shrub/chafol
EPPO CHMFO
EOL 229998
Calflora (Californian flora) 1914
USDA GRIN 404419
Wikipedia Chamaebatia_foliolosa

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
Ecological and genomic responses of soil microbiomes to high-severity wildfire: linking community assembly to functional potential Dove NC, Taş N, Hart SC ISME J 16-Apr-2022
PMCID:PMC9213548
doi:10.1038/s41396-022-01232-9
PMID:35430593
Landscape of stress: Tree mortality influences physiological stress and survival in a native mesocarnivore Kordosky JR, Gese EM, Thompson CM, Terletzky PA, Neuman-Lee LA, Schneiderman JD, Purcell KL, French SS PLoS One 01-Jul-2021
PMCID:PMC8248622
doi:10.1371/journal.pone.0253604
PMID:34197517
Pyric tree spatial patterning interactions in historical and contemporary mixed conifer forests, California, USA Ziegler JP, Hoffman CM, Collins BM, Knapp EE, Mell W( Ecol Evol 25-Dec-2020
PMCID:PMC7820164
doi:10.1002/ece3.7084
PMID:33520169
Exchange of medicinal plant information in California missions McBride JR, Cavero RY, Cheshire AL, Calvo MI, McBride DL J Ethnobiol Ethnomed 15-Jun-2020
PMCID:PMC7296748
doi:10.1186/s13002-020-00388-y
PMID:32539795
Quantifying beryllium concentrations in plant shoots from forest ecosystems using cation‐exchange chromatography and quadrupole ICP‐MS Uhlig D, Goldberg T, Frick DA, von Blanckenburg F Anal Sci Adv 08-Jun-2020
PMCID:PMC10989106
doi:10.1002/ansa.202000036
PMID:38715846
Ecological stoichiometry of the honeybee: Pollen diversity and adequate species composition are needed to mitigate limitations imposed on the growth and development of bees by pollen quality Filipiak M, Kuszewska K, Asselman M, Denisow B, Stawiarz E, Woyciechowski M, Weiner J PLoS One 22-Aug-2017
PMCID:PMC5568746
doi:10.1371/journal.pone.0183236
PMID:28829793
Functional Characterization of Proanthocyanidin Pathway Enzymes from Tea and Their Application for Metabolic Engineering Pang Y, Abeysinghe IS, He J, He X, Huhman D, Mewan KM, Sumner LW, Yun J, Dixon RA Plant Physiol 03-Jan-2013
PMCID:PMC3585583
doi:10.1104/pp.112.212050
PMID:23288883
Past Climate Change and Plant Evolution in Western North America: A Case Study in Rosaceae Töpel M, Antonelli A, Yesson C, Eriksen B PLoS One 07-Dec-2012
PMCID:PMC3517582
doi:10.1371/journal.pone.0050358
PMID:23236369
Enantiomeric Natural Products: Occurrence and Biogenesis Finefield JM, Sherman DH, Kreitman M, Williams RM Angew Chem Int Ed Engl 03-May-2012
PMCID:PMC3498912
doi:10.1002/anie.201107204
PMID:22555867
Diversity and Distribution of Frankia Strains Symbiotic with Ceanothus in California Oakley B, North M, Franklin JF, Hedlund BP, Staley JT Appl Environ Microbiol 01-Nov-2004
PMCID:PMC525117
doi:10.1128/AEM.70.11.6444-6452.2004
PMID:15528504
Dhurrin, (−)-catechin, flavonol glycosides and flavones from Chamaebatia foliolosa Adolf Nahrstedt, Peter Proksch, Eric E. Conn Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)81860-9

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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(2R)-Taxiphyllin 4475719 Click to see C1=CC(=CC=C1C(C#N)OC2C(C(C(C(O2)CO)O)O)O)O 311.29 unknown https://doi.org/10.1016/S0031-9422(00)81860-9
Dhurrin 161355 Click to see C1=CC(=CC=C1C(C#N)OC2C(C(C(C(O2)CO)O)O)O)O 311.29 unknown https://doi.org/10.1016/S0031-9422(00)81860-9
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(-)-Catechol 73160 Click to see 290.27 unknown https://doi.org/10.1016/S0031-9422(00)81860-9
2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,5,7-triol 1203 Click to see 290.27 unknown https://doi.org/10.1016/S0031-9422(00)81860-9
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one 51402807 Click to see 464.40 unknown https://doi.org/10.1016/S0031-9422(00)81860-9
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-2,3-dihydrochromen-4-one 5317364 Click to see 436.40 unknown https://doi.org/10.1016/S0031-9422(00)81860-9
Hyperoside 5281643 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 https://doi.org/10.1016/S0031-9422(00)81860-9
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1016/S0031-9422(00)81860-9

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