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Prionosciadium thapsoides

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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 UUID6440470dada84065573927
Scientific name Prionosciadium thapsoides
Authority (DC.) Mathias
First published in Brittonia 2: 245 (1936)

Description Top

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Synonyms Top

Scientific name Authority First published in
Prionosciadium moschatum Rose Contr. U.S. Natl. Herb. 8: 335 (1905)
Elaeoselinum thapsoides DC. Prodr. 4: 215 (1830)
Prionosciadium seleri Rose Contr. U.S. Natl. Herb. 8: 335 (1905)
Prionosciadium mexicanum S.Watson Proc. Amer. Acad. Arts 23: 275 (1888)
Prionosciadium pringlei S.Watson Proc. Amer. Acad. Arts 23: 276 (1888)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Prionosciadium thapsoides var. pringlei (S.Watson) Mathias & Constance Bull. Torrey Bot. Club 69: 247. 1942

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
  • Northern America
    • Mexico
      • Mexico Central
      • Mexico Gulf
      • Mexico Northeast
      • Mexico Southwest

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001068410
Tropicos 1702143
KEW urn:lsid:ipni.org:names:210299-2
The Plant List tro-1702143
Open Tree Of Life 685819
NCBI Taxonomy 884312
IPNI 210299-2
iNaturalist 279179
GBIF 6026363
Freebase /m/0ztf6gx
Wikipedia Prionosciadium_thapsoides

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
Dihydrofurochromones from Prionosciadium thapsoides. Torres-Valencia JM, Chávez-Ríos OE, Cerda-García-Rojas CM, Burgueño-Tapia E, Joseph-Nathan P J Nat Prod 01-Nov-2008
doi:10.1021/NP800387W
PMID:18954117
Phytotoxic compounds from Prionosciadium watsoni. Valencia-Islas N, Abbas H, Bye R, Toscano R, Mata R J Nat Prod 01-Jun-2002
doi:10.1021/NP010448T
PMID:12088423

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
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones / Furanochromones
2-(4-Methoxy-7-methyl-5-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl)propan-2-yl 3-methylbut-2-enoate 162941306 Click to see CC1=CC(=O)C2=C(C3=C(C=C2O1)OC(C3)C(C)(C)OC(=O)C=C(C)C)OC 372.40 unknown https://doi.org/10.1021/NP800387W
2-[(2S)-4-methoxy-7-methyl-5-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]propan-2-yl (Z)-2-methylbut-2-enoate 25158176 Click to see CC=C(C)C(=O)OC(C)(C)C1CC2=C(O1)C=C3C(=C2OC)C(=O)C=C(O3)C 372.40 unknown https://doi.org/10.1021/NP800387W
2-[(2S)-4-methoxy-7-methyl-5-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]propan-2-yl 2-methylbut-2-enoate 162875100 Click to see CC=C(C)C(=O)OC(C)(C)C1CC2=C(O1)C=C3C(=C2OC)C(=O)C=C(O3)C 372.40 unknown https://doi.org/10.1021/NP800387W
2-[(2S)-4-methoxy-7-methyl-5-oxo-2,3-dihydrofuro[3,2-g]chromen-2-yl]propan-2-yl 3-methylbut-2-enoate 25158175 Click to see CC1=CC(=O)C2=C(C3=C(C=C2O1)OC(C3)C(C)(C)OC(=O)C=C(C)C)OC 372.40 unknown https://doi.org/10.1021/NP800387W
5-O-Methylvisamminol 441970 Click to see CC1=CC(=O)C2=C(C3=C(C=C2O1)OC(C3)C(C)(C)O)OC 290.31 unknown https://doi.org/10.1021/NP800387W
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown https://doi.org/10.1021/NP800387W
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1021/NP800387W
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
(-)-Praeruptorin A 9821539 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C 386.40 unknown https://doi.org/10.1021/NP800387W
(+)-Praeruptorin A 73189387 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C 386.40 unknown https://doi.org/10.1021/NP800387W
(9-Acetyloxy-8,8-dimethyl-2-oxo-3,4,9,10-tetrahydropyrano[2,3-f]chromen-10-yl) 3-methylbut-2-enoate 163094399 Click to see CC(=CC(=O)OC1C(C(OC2=C1C3=C(CCC(=O)O3)C=C2)(C)C)OC(=O)C)C 388.40 unknown https://doi.org/10.1021/NP800387W
[(9R,10R)-9-acetyloxy-8,8-dimethyl-2-oxo-3,4,9,10-tetrahydropyrano[2,3-f]chromen-10-yl] 3-methylbut-2-enoate 163094400 Click to see CC(=CC(=O)OC1C(C(OC2=C1C3=C(CCC(=O)O3)C=C2)(C)C)OC(=O)C)C 388.40 unknown https://doi.org/10.1021/NP800387W
[(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/10.1021/NP010448T
https://doi.org/10.1021/NP800387W
Jatamansin 668081 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/10.1021/NP800387W
Praeruptorin A 38347607 Click to see CC=C(C)C(=O)OC1C(C2=C(C=CC3=C2OC(=O)C=C3)OC1(C)C)OC(=O)C 386.40 unknown https://doi.org/10.1021/NP800387W
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/10.1021/NP010448T
https://doi.org/10.1021/NP800387W

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