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Pedicularis grayi

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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 UUID64404e40910b0859258852
Scientific name Pedicularis grayi
Authority A.Nelson
First published in Proc. Biol. Soc. Washington 17: 100. 1904 [9 Apr 1904]

Description Top

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Synonyms Top

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Common names Top

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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

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001136929
KEW urn:lsid:ipni.org:names:186415-2
The Plant List tro-29201215
Open Tree Of Life 5232496
GBIF 3171710

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
Iridoid glycosides of Pedicularis Marilyn J. Schneider, James D. Lynch, Limor Deutsch, Cheryl M. Duda, Julie C. Green, Diane McPeak Elsevier BV 16-Feb-2012
doi:10.1016/S0305-1978(96)00061-0
Proceroside, an iridoid glucoside from Pedicularis procera Marilyn J. Schneider, Julie C. Green, Diane McPeak Elsevier BV 01-May-2003
doi:10.1016/S0031-9422(96)00712-1

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 / Terpene glycosides / Iridoid O-glycosides
(1S,4aR,7S,7aS)-7-(hydroxymethyl)-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-one 162909417 Click to see C1C2C=COC(C2C(C1=O)CO)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1016/S0031-9422(96)00712-1
7-(hydroxymethyl)-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,7,7a-tetrahydro-1H-cyclopenta[c]pyran-6-one 162909416 Click to see C1C2C=COC(C2C(C1=O)CO)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1016/S0031-9422(96)00712-1
8-Epiloganic acid 158144 Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 376.36 unknown https://doi.org/10.1016/S0305-1978(96)00061-0
Shanzhiside methyl ester 13892722 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/S0305-1978(96)00061-0
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/S0305-1978(96)00061-0
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
6-Deoxycatalpol 129011855 Click to see C1C2C=COC(C2C3(C1O3)CO)OC4C(C(C(C(O4)CO)O)O)O 346.33 unknown https://doi.org/10.1016/S0305-1978(96)00061-0
Gardoside 46173850 Click to see C=C1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O 374.34 unknown https://doi.org/10.1016/S0305-1978(96)00061-0

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