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Musineon divaricatum

Musineon divaricatum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Musineon divaricatum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Musineon divaricatum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Musineon divaricatum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Musineon divaricatum - 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 UUID644046ed8a356212893486
Scientific name Musineon divaricatum
Authority (Pursh) Nutt.
First published in Fl. N. Amer. (Torr. & A. Gray) 1(4): 642. 1840 [Jun 1840] (as Musenium)

Description Top

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Synonyms Top

Scientific name Authority First published in
Musenium pedunculatum A.Nelson Bull. Torrey Bot. Club 28: 225 (1901)
Musenium angustifolium Nutt. Fl. N. Amer. 1: 642 (1840)
Marathrum divaricatum Raf. J. Phys. Chim. Hist. Nat. Arts 89: 101. 1819
Adorium crassifolium Raf. Neogenyton : 3 (1825)
Adorium divaricatum Rydb. Bot. Surv. Nebraska 3: 37 (1894)
Adorium hookeri Rydb. Contr. U.S. Natl. Herb. 3: 501 (1895)
Adorium lucidum Kuntze Revis. Gen. Pl. 1: 264 (1891)
Seseli divaricatum Pursh Fl. Amer. Sept. 2: 732 (1813)
Musineon angustifolium Nutt. Fl. N. Amer. 1: 642 (1840)
Seseli lucidum Nutt. Gen. N. Amer. Pl. 1: 195 (1818)

Common names Top

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Language Common/alternative name
English leafy wildparsley

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Musineon divaricatum var. hookeri Torr. & A.Gray Fl. N. Amer. 1: 642 (1840)

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

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Database ID/link to page
World Flora Online wfo-0001067682
Canadensys 2616
USDA Plants MUDI
Tropicos 1700159
KEW urn:lsid:ipni.org:names:845056-1
The Plant List tro-1700159
Open Tree Of Life 629885
NCBI Taxonomy 178688
Nature Serve 2.157291
IPNI 30108727-2
iNaturalist 165591
GBIF 3034880
EOL 579549
USDA GRIN 414430

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
Coumarins from Musineon divaricatum Tim M. Swager, John H. Cardellina Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)84899-2
Native American food and medicinal plants, 5. Isolation of the lipid altering visnagin from Musineon divaricatum. Cardellina JH 2nd, Swager TM J Nat Prod 01-Nov-1984
doi:10.1021/NP50036A040
PMID:6533266

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
Laserpitin 5281524 Click to see CC=C(C)C(=O)OC1CC(C(=O)C(C2(C1C(CC2)(C(C)C)O)C)OC(=O)C(=CC)C)(C)O 450.60 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones / Furanochromones
Visnagin 6716 Click to see CC1=CC(=O)C2=C(O1)C=C3C(=C2OC)C=CO3 230.22 unknown https://doi.org/10.1021/NP50036A040
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(-)-Praeruptorin B 10251869 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C(=CC)C 426.50 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
(+)-Pteryxin 511787 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C 386.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
(10-Hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl) 2-methylbut-2-enoate 511783 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)O 344.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
(10-Hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl) 2-methylpropanoate 163087320 Click to see CC(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)O 332.30 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
(10-Hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl) 3-methylbut-2-enoate 511784 Click to see CC(=CC(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)O)C 344.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
(8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-h]chromen-9-yl) (E)-2-methylbut-2-enoate 5367834 Click to see CC=C(C)C(=O)OC1CC2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C 328.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
(9-Acetyloxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl) 3-methylbut-2-enoate 5089290 Click to see CC(=CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C)C 386.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
(9-Hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl) 2-methylbut-2-enoate 511782 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O 344.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
(9-Hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl) 2-methylbutanoate 455900 Click to see CCC(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
(9-Hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl) 3-methylbut-2-enoate 13964643 Click to see CC(=CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O)C 344.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
(9-Hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl) 3-methylbutanoate 455908 Click to see CC(C)CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[(9R,10R)-10-hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] (E)-2-methylbut-2-enoate 102373118 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)O 344.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[(9R,10R)-10-hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] (Z)-2-methylbut-2-enoate 11244847 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)O 344.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[(9R,10R)-10-hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] 2-methylpropanoate 163087321 Click to see CC(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)O 332.30 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[(9R,10R)-10-hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] 3-methylbut-2-enoate 162927133 Click to see CC(=CC(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)O)C 344.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[(9R,10R)-8,8-dimethyl-9-(3-methylbut-2-enoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (Z)-2-methylbut-2-enoate 163195351 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C=C(C)C 426.50 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[(9R,10R)-9-hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (2R)-2-methylbutanoate 51422443 Click to see CCC(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[(9R,10R)-9-hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] (Z)-2-methylbut-2-enoate 5320810 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O 344.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[(9R,10R)-9-hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] 3-methylbut-2-enoate 51669194 Click to see CC(=CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O)C 344.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[(9R,10R)-9-hydroxy-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] 3-methylbutanoate 163027223 Click to see CC(C)CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)O 346.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[(9S)-8,8-dimethyl-2-oxo-9,10-dihydropyrano[2,3-h]chromen-9-yl] (Z)-2-methylbut-2-enoate 668079 Click to see CC=C(C)C(=O)OC1CC2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C 328.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[8,8-Dimethyl-10-(2-methylpropanoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] 2-methylbut-2-enoate 74990346 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C(C)C 414.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[8,8-Dimethyl-10-(3-methylbut-2-enoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] 2-methylbut-2-enoate 73202226 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C=C(C)C 426.50 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[8,8-Dimethyl-10-(3-methylbutanoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-9-yl] 2-methylbut-2-enoate 75596126 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)CC(C)C 428.50 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[8,8-Dimethyl-9-(2-methylbut-2-enoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] 2-methylbut-2-enoate 163334 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C(=CC)C 426.50 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
[8,8-Dimethyl-9-(3-methylbut-2-enoyloxy)-2-oxo-9,10-dihydropyrano[2,3-f]chromen-10-yl] 2-methylbut-2-enoate 163013195 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C=C(C)C 426.50 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
9-(acetyloxy)-8,8-dimethyl-2-oxo-9,10-dihydro-2H,8H-pyrano[2,3-f]chromen-10-yl 3-methylbutanoate 455909 Click to see CC(C)CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C 388.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
Calipteryxin 15945070 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C=C(C)C 426.50 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
CID 13592767 13592767 Click to see CC(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C 374.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
Hyuganin B 10319604 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C(C)C 414.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
Hyuganin D 10317265 Click to see CC(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C 374.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
Isosamidin 442133 Click to see CC(=CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C)C 386.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
Khellactone 253856 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)O)C 262.26 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
Khellactone, cis-(+)- 455821 Click to see CC1(C(C(C2=C(O1)C=CC3=C2OC(=O)C=C3)O)O)C 262.26 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
Praeruptorin B 5319259 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C(=CC)C 426.50 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
Praeruptorin C 5320692 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)CC(C)C 428.50 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
Praeruptorin E 6440581 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)CC(C)C 428.50 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
Pteryxin 5281425 Click to see CC=C(C)C(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C 386.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
Selinidin 511786 Click to see CC=C(C)C(=O)OC1CC2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C 328.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2
Suksdorfin 72414 Click to see CC(C)CC(=O)OC1C(C(OC2=C1C3=C(C=C2)C=CC(=O)O3)(C)C)OC(=O)C 388.40 unknown https://doi.org/10.1016/S0031-9422(00)84899-2

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