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Balsamorhiza macrophylla

Balsamorhiza macrophylla - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID643fd294f0859591419659
Scientific name Balsamorhiza macrophylla
Authority Nutt.
First published in Trans. Amer. Philos. Soc. , ser. 2, 7: 350 (1840)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English cutleaf balsamroot

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

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000124885
USDA Plants BAMA4
Tropicos 2709551
KEW urn:lsid:ipni.org:names:184066-1
The Plant List gcc-85975
Open Tree Of Life 3899802
Nature Serve 2.1088452
IPNI 184066-1
iNaturalist 159140
GBIF 3137236
Freebase /m/0139z_8q
EOL 467893
USDA GRIN 448089
Wikipedia Balsamorhiza_macrophylla

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
Highly oxygenated guaianolides and eudesman-12-oic acids from Balsamorhiza sagittata and Balsamorhiza macrophylla. El-Hamd H Mohamed A, Ahmed AA, Wollenweber E, Bohm B, Asakawa Y Chem Pharm Bull (Tokyo) 01-Feb-2006
doi:10.1248/CPB.54.152
PMID:16462056
Flavonoids of Balsamorhiza and Wyethia Bruce A. Bohm, Jonathan B. Choy, Angela Y.-M. Lee Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(89)80041-X
Methylated flavonols from Wyethia bolanderi and Balsamorhiza macrophylla Susan McCormick, Kathleen Robson, Bruce Bohm Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83143-X

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 / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
2-(4a-hydroxy-8,8a-dimethyl-7-oxo-2,3,4,8-tetrahydro-1H-naphthalen-2-yl)prop-2-enoic acid 163019769 Click to see CC1C(=O)C=CC2(C1(CC(CC2)C(=C)C(=O)O)C)O 264.32 unknown https://doi.org/10.1248/CPB.54.152
2-(8,8a-Dimethyl-7-oxo-1,2,3,5,6,8-hexahydronaphthalen-2-yl)prop-2-enoic acid 162877333 Click to see CC1C(=O)CCC2=CCC(CC12C)C(=C)C(=O)O 248.32 unknown https://doi.org/10.1248/CPB.54.152
2-[(2R,4aS,8R,8aR)-4a-hydroxy-8,8a-dimethyl-7-oxo-2,3,4,8-tetrahydro-1H-naphthalen-2-yl]prop-2-enoic acid 15699284 Click to see CC1C(=O)C=CC2(C1(CC(CC2)C(=C)C(=O)O)C)O 264.32 unknown https://doi.org/10.1248/CPB.54.152
2-[(2R,8R,8aR)-8,8a-dimethyl-7-oxo-1,2,3,5,6,8-hexahydronaphthalen-2-yl]prop-2-enoic acid 15699267 Click to see CC1C(=O)CCC2=CCC(CC12C)C(=C)C(=O)O 248.32 unknown https://doi.org/10.1248/CPB.54.152
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
2-(4a,8-Dimethyl-7-oxo-1,2,3,4,5,6-hexahydronaphthalen-2-yl)prop-2-enoic acid 13819151 Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C(=O)O 248.32 unknown https://doi.org/10.1248/CPB.54.152
Pterodonoic acid 11054003 Click to see CC1=C2CC(CCC2(CCC1=O)C)C(=C)C(=O)O 248.32 unknown https://doi.org/10.1248/CPB.54.152
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,7,8-Trihydroxy-2-(4-hydroxy-3-methoxyphenyl)-6-methoxychromen-4-one 162943201 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=CC(=C(C(=C3O2)O)O)OC)O)O 346.30 unknown https://doi.org/10.1016/0031-9422(89)80041-X
Spinacetin 5321435 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)O)O 346.30 unknown https://doi.org/10.1016/S0031-9422(00)83143-X
Tamarixetin 5281699 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1016/S0031-9422(00)83143-X
> 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/10.1016/0031-9422(89)80041-X
https://doi.org/10.1016/S0031-9422(00)83143-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Quercetin 3,4'-dimethyl ether 5380905 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O 330.29 unknown https://doi.org/10.1016/S0031-9422(00)83143-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
2-(3,4-Dihydroxyphenyl)-7,8-dihydroxy-3,6-dimethoxychromen-4-one 162978157 Click to see COC1=C(C(=C2C(=C1)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O)O 346.30 unknown https://doi.org/10.1016/0031-9422(89)80041-X
7,8-Dihydroxy-2-(3-hydroxy-4-methoxyphenyl)-3,6-dimethoxychromen-4-one 162915306 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=CC(=C(C(=C3O2)O)O)OC)OC)O 360.30 unknown https://doi.org/10.1016/0031-9422(89)80041-X
Axillarin 5281603 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O 346.30 unknown https://doi.org/10.1016/S0031-9422(00)83143-X
Centaureidin 5315773 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown https://doi.org/10.1016/S0031-9422(00)83143-X

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