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Castilleja sulphurea

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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 UUID64400fbea117e794368298
Scientific name Castilleja sulphurea
Authority Rydb.
First published in Mem. New York Bot. Gard. 1: 359. 1900

Description Top

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Synonyms Top

Scientific name Authority First published in
Castilleja brunnescens Rydb. Bull. Torrey Bot. Club 31: 643 (1904)
Castilleja luteovirens Rydb. Bull. Torrey Bot. Club 28: 26 (1901)
Castilleja mogollonica Pennell Notul. Nat. Acad. Nat. Sci. Philadelphia 237: 1 (1951)
Castilleja rhexifolia var. sulphurea (Rydb.) N.D.Atwood Great Basin Naturalist 46(2): 260. 1986
Castilleja wyomingensis Rydb. Bull. Torrey Bot. Club 28: 502 (1901)

Common names Top

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Language Common/alternative name
English sulphur indian 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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No germination or propagation data was added yet.

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-0000590569
Canadensys 7003
USDA Plants CASU12
Tropicos 29201756
KEW urn:lsid:ipni.org:names:49743-2
The Plant List kew-2705353
Open Tree Of Life 701052
NCBI Taxonomy 188296
Nature Serve 2.159650
IPNI 274203-2
iNaturalist 160225
GBIF 3170707
EOL 579095
Calflora (Californian flora) 12344
USDA GRIN 452102
CMAUP NPO313

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
Using stable isotopes in hummingbird breath to estimate reliance on supplemental feeders Wolf N, Smeltz TS, Cook C, Martinez del Rio C Ecol Evol 07-Feb-2023
PMCID:PMC9905664
doi:10.1002/ece3.9799
PMID:36789347
The Angiosperm Stem Hemiparasitic Genus Cassytha (Lauraceae) and Its Host Interactions: A Review Zhang H, Florentine S, Tennakoon KU Front Plant Sci 06-Jun-2022
PMCID:PMC9208266
doi:10.3389/fpls.2022.864110
PMID:35734256
Parasitism modifies the direct effects of warming on a hemiparasite and its host Rafferty NE, Agnew L, Nabity PD PLoS One 30-Oct-2019
PMCID:PMC6821401
doi:10.1371/journal.pone.0224482
PMID:31665151
Genuine and Sequestered Natural Products from the Genus Orobanche (Orobanchaceae, Lamiales) Scharenberg F, Zidorn C Molecules 30-Oct-2018
PMCID:PMC6278508
doi:10.3390/molecules23112821
PMID:30380787
New quinolizidine alkaloids from Lupinus argenteus and its hosted root parasite Castilleja sulphurea. Stereochemistry and conformation of some naturally occurring cyclic carbinolamides Robert L. Arslanian, Guy H. Harris, Frank R. Stermitz American Chemical Society (ACS) 12-Mar-2005
doi:10.1021/JO00291A019
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 / Aristolactams
2-Hydroxy-1,5-dimethoxydibenzo[cd,f]indol-4(5H)-one 622222 Click to see COC1=C(C=C2C3=C1C4=CC=CC=C4C=C3N(C2=O)OC)O 295.29 unknown via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
(10S)-6-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-8-one 139031165 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3=CCCC4O 262.35 unknown https://doi.org/10.1021/JO00291A019
(1R,6R,9R,10R)-6,9-dihydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-8-one 101529382 Click to see C1CCN2CC3CC(C2C1)(C(=O)N4C3=CCCC4O)O 278.35 unknown https://doi.org/10.1021/JO00291A019
(1R,6S,9R,10R)-6,9-dihydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-8-one 21628969 Click to see C1CCN2CC3CC(C2C1)(C(=O)N4C3=CCCC4O)O 278.35 unknown https://doi.org/10.1021/JO00291A019
(1R,6S,9S,10R)-6-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-8-one 51020948 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3=CCCC4O 262.35 unknown https://doi.org/10.1021/JO00291A019
(1R,9R,10S)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-8-one 6454846 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3=CCCC4 246.35 unknown https://doi.org/10.1021/JO00291A019
(1S,6S,9R,10S)-6-hydroxy-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadec-2-en-8-one 15939866 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3=CCCC4O 262.35 unknown https://doi.org/10.1021/JO00291A019
Aphyllidine 12306738 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3=CCCC4 246.35 unknown https://doi.org/10.1021/JO00291A019
Hydroxyaphyllidine 4486245 Click to see C1CCN2CC3CC(C2C1)C(=O)N4C3=CCCC4O 262.35 unknown https://doi.org/10.1021/JO00291A019
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
2,4,5-Trimethoxybenzaldehyde 20525 Click to see COC1=CC(=C(C=C1C=O)OC)OC 196.20 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
(1S,5R,6R,7R,8S)-7-(3,4-dimethoxyphenyl)-8-hydroxy-5-methoxy-6-methyl-3-prop-2-enylbicyclo[3.2.1]oct-3-en-2-one 44470608 Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)O)C3=CC(=C(C=C3)OC)OC 358.40 unknown via CMAUP database
Kadsurenin L 3083437 Click to see CC1C(C2C(C1(C=C(C2=O)CC=C)OC)OC(=O)C)C3=CC(=C(C=C3)OC)OC 400.50 unknown via CMAUP database
Piperenone 36406703 Click to see CC1C(OC2(C1(C=C(C(=O)C2)CC=C)OC)OC)C3=CC(=C(C=C3)OC)OC 388.50 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Elemicin 10248 Click to see COC1=CC(=CC(=C1OC)OC)CC=C 208.25 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,7-epoxylignans
(-)-Galbacin 11175182 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C 340.40 unknown via CMAUP database
(2S,3S,4S,5S)-2,5-bis(3,4-dimethoxyphenyl)-3,4-dimethyloxolane 11975378 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C 372.50 unknown via CMAUP database
4-[(2R,3S,4R,5R)-5-(1,3-Benzodioxol-5-yl)tetrahydro-3,4-dimethyl-2-furanyl]-2-methoxyphenol 11078392 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O)OC)C 342.40 unknown via CMAUP database
4-[(2S,3R,4R,5R)-5-(3,4-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-2-methoxyphenol 93061877 Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)OC)OC)C 358.40 unknown via CMAUP database
5-((2R,3R,4S,5R)-5-(3,4-Dimethoxyphenyl)-3,4-dimethyloxolan-2-yl)-1,3-benzodioxole 188429 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C 356.40 unknown via CMAUP database
5-[(2R,3S,4S,5S)-5-(3,4-dimethoxyphenyl)-3,4-dimethyloxolan-2-yl]-1,3-benzodioxole 26113495 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C 356.40 unknown via CMAUP database
Futokadsurin A 9548904 Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)OC)OC)C 358.40 unknown via CMAUP database
futokadsurin B 9548905 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C 356.40 unknown via CMAUP database
Futokadsurin C 9548906 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)OC)OC)C 356.40 unknown via CMAUP database
Galgravin 101749 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C 372.50 unknown via CMAUP database
Machillin F 10450045 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC(=C(C=C4)O)OC)C 342.40 unknown via CMAUP database
nectandrin A 156516 Click to see CC1C(C(OC1C2=CC(=C(C=C2)O)OC)C3=CC(=C(C=C3)OC)OC)C 358.40 unknown via CMAUP database
Veraguensin 443026 Click to see CC1C(C(OC1C2=CC(=C(C=C2)OC)OC)C3=CC(=C(C=C3)OC)OC)C 372.50 unknown via CMAUP database
Zuihonin A 338287 Click to see CC1C(C(OC1C2=CC3=C(C=C2)OCO3)C4=CC5=C(C=C4)OCO5)C 340.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Pellitorine 5318516 Click to see CCCCCC=CC=CC(=O)NCC(C)C 223.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
(E,7S,11R)-3,7,11,15-tetramethylhexadec-2-en-1-ol 6474938 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(4S)-4-[(E)-1-(1,3-benzodioxol-5-yl)prop-1-en-2-yl]-4,5-dimethoxy-2-prop-2-enylcyclohexa-2,5-dien-1-one 101833872 Click to see CC(=CC1=CC2=C(C=C1)OCO2)C3(C=C(C(=O)C=C3OC)CC=C)OC 354.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
8-Epiloganin 10548420 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/0305-1978(86)90009-8
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/10.1016/0305-1978(86)90009-8
Penstemonoside 133626 Click to see CC1CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/0305-1978(86)90009-8
Shanzhiside-methylester 3085296 Click to see CC1(CC(C2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O)O 406.40 unknown https://doi.org/10.1016/0305-1978(86)90009-8
> Organoheterocyclic compounds / Benzodioxoles
(1R,8R,10R,11S)-10-(1,3-benzodioxol-5-yl)-3-methoxy-11-methyl-7-oxatricyclo[6.3.1.01,6]dodeca-2,5-dien-4-one 101820916 Click to see CC1C(CC2CC13C=C(C(=O)C=C3O2)OC)C4=CC5=C(C=C4)OCO5 340.40 unknown via CMAUP database
(2S,3R,3aS,6S,7aR)-2-(1,3-benzodioxol-5-yl)-3a,7a-dimethoxy-3-methyl-5-prop-2-enyl-2,3,6,7-tetrahydro-1-benzofuran-6-ol 10022290 Click to see CC1C(OC2(C1(C=C(C(C2)O)CC=C)OC)OC)C3=CC4=C(C=C3)OCO4 374.40 unknown via CMAUP database
(E,E)-Futoamide 15596445 Click to see CC(C)CNC(=O)C=CCCC=CC1=CC2=C(C=C1)OCO2 301.40 unknown via CMAUP database
Kadsurin A 442885 Click to see CC1C(OC2(C1(C=C(C(=O)C2)CC=C)OC)OC)C3=CC4=C(C=C3)OCO4 372.40 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-ammonio-3-(1H-indol-3-yl)propanoate 6923516 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)[O-])[NH3+] 204.22 unknown via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Pyridinecarboxylic acids and derivatives / Pyridinecarboxylic acids
Rhexifoline 185301 Click to see CC1CC(C2=C(C=NC=C12)C(=O)OC)O 207.23 unknown https://doi.org/10.1016/0305-1978(86)90009-8
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2R,3S,3aS)-2-(3,4-dimethoxyphenyl)-3a-methoxy-3-methyl-5-prop-2-enyl-2,3-dihydro-1-benzofuran-6-one 10915273 Click to see CC1C(OC2=CC(=O)C(=CC12OC)CC=C)C3=CC(=C(C=C3)OC)OC 356.40 unknown via CMAUP database
Kadsurenin M 208856 Click to see CC1C(OC2=C1C=C(C=C2OC)C=O)C3=CC(=C(C=C3)OC)OC 328.40 unknown via CMAUP database
Kadsurenone 122159 Click to see CC1C(OC2=CC(=O)C(=CC12OC)CC=C)C3=CC(=C(C=C3)OC)OC 356.40 unknown via CMAUP database

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