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Chorizanthe diffusa

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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 UUID644010f891d4a699923574
Scientific name Chorizanthe diffusa
Authority Benth.
First published in Pl. Hartw. : 333 (1857)

Description Top

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Synonyms Top

Scientific name Authority First published in
Chorizanthe andersonii Parry Proc. Davenport Acad. Nat. Sci. 5: 176 (1889)
Chorizanthe diffusa var. nivea (Curran) Hoover Leafl. W. Bot. 10: 342 (1966)
Chorizanthe nivea Jeps. Madroño 1: 62 (1917)
Chorizanthe pungens var. diffusa (Benth.) Parry Proc. Davenport Acad. Nat. Sci. 4: 60 (1884)
Chorizanthe pungens var. nivea Curran Bull. Calif. Acad. Sci. 1: 274 (1885)
Chorizanthe nivea A.Heller Cat. N. Amer. Pl. (ed. 3) 96. 1910

Common names Top

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Language Common/alternative name
English diffuse spineflower

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000603460
USDA Plants CHDI3
Tropicos 26000959
KEW urn:lsid:ipni.org:names:693469-1
The Plant List kew-2719559
Open Tree Of Life 844225
NCBI Taxonomy 549593
Nature Serve 2.160309
IPNI 693469-1
iNaturalist 71084
GBIF 2888935
Freebase /m/05pcqnf
EOL 584497
Calflora (Californian flora) 2027
USDA GRIN 452108
Wikipedia Chorizanthe_diffusa

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
Antifungal Activity of Extracts, Fractions, and Constituents from Coccoloba cowellii Leaves Méndez D, Escalona-Arranz JC, Pérez EM, Foubert K, Matheeussen A, Tuenter E, Cuypers A, Cos P, Pieters L Pharmaceuticals (Basel) 10-Sep-2021
PMCID:PMC8469486
doi:10.3390/ph14090917
PMID:34577616
Flavonoid constituents of Chorizanthe diffusa with potential cancer chemopreventive activity. Chung HS, Chang LC, Lee SK, Shamon LA, van Breemen RB, Mehta RG, Farnsworth NR, Pezzuto JM, Kinghorn AD J Agric Food Chem 01-Jan-1999
doi:10.1021/JF980784O
PMID:10563845

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
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1021/JF980784O
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[2-[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-3,5-dihydroxy-6-methyloxan-4-yl] acetate 74978208 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)OC(=O)C)O 490.40 unknown https://doi.org/10.1021/JF980784O
3''-O-Acetylquercitrin 100956675 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)OC(=O)C)O 490.40 unknown https://doi.org/10.1021/JF980784O
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown https://doi.org/10.1021/JF980784O
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
5,8,3',4',5'-Pentahydroxy-3,7-dimethoxyflavone 10689999 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=C(O2)C3=CC(=C(C(=C3)O)O)O)OC)O 362.30 unknown https://doi.org/10.1021/JF980784O
Gossypetin 3,7-dimethyl ether 13983744 Click to see COC1=C(C2=C(C(=C1)O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O 346.30 unknown https://doi.org/10.1021/JF980784O

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Contributors Top

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Collections Top

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