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Castilleja rhexifolia

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 UUID64400fbb9f632320966253
Scientific name Castilleja rhexifolia
Authority Rydb.
First published in Mem. New York Bot. Gard. 1: 356 (1900)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Castilleja humilis Rydb. Bull. Torrey Bot. Club 34: 37 (1907)
Castilleja lanceifolia Rydb. Mem. New York Bot. Gard. 1: 357 (1900)
Castilleja lauta A.Nelson Bull. Torrey Bot. Club 27: 269 (1900)
Castilleja leonardii Rydb. Bull. Torrey Bot. Club 34: 36 (1907)
Castilleja magna Rydb. Bull. Torrey Bot. Club 34: 36 (1907)
Castilleja obtusiloba Rydb. Bull. Torrey Bot. Club 31: 644 (1904)
Castilleja oregonensis Gand. Bull. Soc. Bot. France 66: 217 (1919)
Castilleja purpurascens Rydb. Bull. Torrey Bot. Club 34: 38. 1907
Castilleja subpurpurascens Rydb. Fl. Rocky Mts. : 791 (1917)

Common names Top

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Language Common/alternative name
English alpine indian paintbrush
English alpine paintbrush

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000590507
The Plant List kew-2705298
Observations.org 493036
iNaturalist 363343
EPPO CSLRX
Elurikkus 638190

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)!
Title Authors Publication Released IDs
Penstemonoside and Other Iridoids from Castilleja rhexifolia. Conversion of Penstemonoside to the Pyridine Monoterpene Alkaloid Rhexifoline Mark R. Roby, Frank R. Stermitz American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50035A017
Pyrrolizidine and Pyridine Monoterpene Alkaloids from Two Castilleja Plant Hosts of the Plume Moth, Platyptilia pica Mark R. Roby, Frank R. Stermitz American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50035A016
Iridoids and alkaloids from Castilleja host plants for platyptilia pica. Rhexifoline content of P. pica Frank R. Stermitz, Guy H. Harris, Wang Jing Elsevier BV 10-Feb-2003
doi:10.1016/0305-1978(86)90009-8

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
> Alkaloids and derivatives
Senecionine N-oxide 5380876 Click to see CC=C1CC(C(C(=O)OCC2=CC[N+]3(C2C(CC3)OC1=O)[O-])(C)O)C 351.40 unknown https://doi.org/10.1021/NP50035A016
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1021/NP50035A017
methyl (1S,4aR,5R,7R,7aR)-4a,5-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,6,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 101637370 Click to see 406.40 unknown https://doi.org/10.1021/NP50035A017
methyl (1S,4aS,5R,7R,7aR)-5-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 101643005 Click to see 390.40 unknown https://doi.org/10.1016/0305-1978(86)90009-8
https://doi.org/10.1021/NP50035A017
Penstemonoside 133626 Click to see 390.40 unknown https://doi.org/10.1021/NP50035A017
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R)-2-[[(1R,2S,6S)-5-hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 138107792 Click to see 362.33 unknown https://doi.org/10.1021/NP50035A017
Catalpol 91520 Click to see 362.33 unknown https://doi.org/10.1021/NP50035A017
Catapol 24721256 Click to see 362.33 unknown https://doi.org/10.1021/NP50035A017
Gardoside methyl ester 51692952 Click to see COC(=O)C1=COC(C2C1CC(C2=C)O)OC3C(C(C(C(O3)CO)O)O)O 388.40 unknown https://doi.org/10.1016/0305-1978(86)90009-8
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
methyl 7-methyl-6,7-dihydro-5H-cyclopenta[c]pyridine-4-carboxylate 14378639 Click to see 191.23 unknown https://doi.org/10.1021/NP50035A016
Rhexifoline 185301 Click to see 207.23 unknown https://doi.org/10.1021/NP50035A017
https://doi.org/10.1021/NP50035A016
> Organoheterocyclic compounds / Pyrrolizidines
(7-hydroxy-2,3,5,6,7,8-hexahydro-1H-pyrrolizin-1-yl)methyl 2-methylbut-2-enoate 526537 Click to see 239.31 unknown https://doi.org/10.1021/NP50035A016
7-Angeloylplatynecine 12314977 Click to see CC=C(C)C(=O)OC1CCN2C1C(CC2)CO 239.31 unknown https://doi.org/10.1021/NP50035A016
Sarracine 5281746 Click to see 337.40 unknown https://doi.org/10.1021/NP50035A016
> Phenylpropanoids and polyketides / Macrolides and analogues
Senecionine 5280906 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1021/NP50035A016

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