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Harbouria trachypleura

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 UUID644046f409510035856835
Scientific name Harbouria trachypleura
Authority J.M.Coult. & Rose
First published in Rev. N. Amer. Umbell. : 125 (1888)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Cicuta trachypleura S.Watson Bibl. Index N. Amer. Bot. : 417 (1878)
Thaspium trachypleurum A.Gray Proc. Acad. Nat. Sci. Philadelphia 1863: 63 (1864)

Common names Top

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Language Common/alternative name
English whiskbroom parsley
English whisk-broom parsley

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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Northwestern U.S.A.
      • Colorado
      • Wyoming
    • South-central U.S.A.
      • New Mexico

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001067826
USDA Plants HATR
Tropicos 1700818
KEW urn:lsid:ipni.org:names:117877-2
The Plant List tro-1700818
Open Tree Of Life 5167
NCBI Taxonomy 178675
Nature Serve 2.160286
IPNI 117877-2
iNaturalist 157476
GBIF 3034869
EOL 581671
USDA GRIN 453408

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
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
Plant Coumarins with Anti-HIV Activity: Isolation and Mechanisms of Action Sharapov AD, Fatykhov RF, Khalymbadzha IA, Zyryanov GV, Chupakhin ON, Tsurkan MV Int J Mol Sci 02-Feb-2023
PMCID:PMC9917851
doi:10.3390/ijms24032839
PMID:36769163
Oxypeucedanin: Chemotaxonomy, Isolation, and Bioactivities Mottaghipisheh J Plants (Basel) 30-Jul-2021
PMCID:PMC8401860
doi:10.3390/plants10081577
PMID:34451622
New coumarins from Harbouria trachypleura: isolation and synthesis Nathan R Guz, Peter Lorenz, Frank R Stermitz Elsevier BV 25-Mar-2003
doi:10.1016/S0040-4039(01)01355-7

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
> Phenylpropanoids and polyketides / Coumarins and derivatives
(+)-Epoxysuberosin 11184527 Click to see 260.28 unknown https://doi.org/10.1016/S0040-4039(01)01355-7
6-(2-Hydroxy-3-methoxy-3-methylbutyl)-7-methoxychromen-2-one 72952581 Click to see 292.33 unknown https://doi.org/10.1016/S0040-4039(01)01355-7
6-(3-Chloro-2-hydroxy-3-methylbutyl)-7-methoxychromen-2-one 11162279 Click to see 296.74 unknown https://doi.org/10.1016/S0040-4039(01)01355-7
6-[(2R)-2-hydroxy-3-methoxy-3-methylbutyl]-7-methoxychromen-2-one 11415107 Click to see CC(C)(C(CC1=C(C=C2C(=C1)C=CC(=O)O2)OC)O)OC 292.33 unknown https://doi.org/10.1016/S0040-4039(01)01355-7
6-[(2S)-3-chloro-2-hydroxy-3-methylbutyl]-7-methoxychromen-2-one 162954462 Click to see 296.74 unknown https://doi.org/10.1016/S0040-4039(01)01355-7
6-[(2S)-3,3-dimethyloxiran-2-yl]-7-methoxychromen-2-one 101119215 Click to see 246.26 unknown https://doi.org/10.1016/S0040-4039(01)01355-7
Suberosin epoxide 612480 Click to see 260.28 unknown https://doi.org/10.1016/S0040-4039(01)01355-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
(+)-Oxypeucedanin 928465 Click to see CC1(C(O1)COC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 286.28 unknown https://doi.org/10.1016/S0040-4039(01)01355-7
4-(4-Chloro-3-hydroxy-4-methylpentoxy)furo[3,2-g]chromen-7-one 162925352 Click to see CC(C)(C(CCOC1=C2C=CC(=O)OC2=CC3=C1C=CO3)O)Cl 336.80 unknown https://doi.org/10.1016/S0040-4039(01)01355-7
4-[(3R)-4-chloro-3-hydroxy-4-methylpentoxy]furo[3,2-g]chromen-7-one 162925353 Click to see 336.80 unknown https://doi.org/10.1016/S0040-4039(01)01355-7
4-[2-(3,3-Dimethyloxiran-2-yl)ethoxy]furo[3,2-g]chromen-7-one 101733214 Click to see CC1(C(O1)CCOC2=C3C=CC(=O)OC3=CC4=C2C=CO4)C 300.30 unknown https://doi.org/10.1016/S0040-4039(01)01355-7
4-[2-[(2R)-3,3-dimethyloxiran-2-yl]ethoxy]furo[3,2-g]chromen-7-one 162843730 Click to see 300.30 unknown https://doi.org/10.1016/S0040-4039(01)01355-7
Saxalin 182277 Click to see 322.74 unknown https://doi.org/10.1016/S0040-4039(01)01355-7
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1016/S0040-4039(01)01355-7

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