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Penstemon acuminatus

Penstemon acuminatus - 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 UUID64404e4250fd7591602262
Scientific name Penstemon acuminatus
Authority Douglas ex Lindl.
First published in Edwards's Bot. Reg. 15: t. 1285 (1829)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
English sharpleaf penstemon

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Penstemon acuminatus var. latibracteatus N.H.Holmgren Brittonia 31: 232 (1979)

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

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-0001136944
Canadensys 7265
USDA Plants PEAC
Tropicos 29201235
KEW urn:lsid:ipni.org:names:30076629-2
The Plant List tro-29201235
Open Tree Of Life 34996
NCBI Taxonomy 388112
Nature Serve 2.136068
IPNI 807978-1
iNaturalist 166316
GBIF 3171447
Freebase /m/0j_5zbd
EOL 578325
USDA GRIN 448220
Wikipedia Penstemon_acuminatus

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
Multiplexed shotgun genotyping resolves species relationships within the North American genus Penstemon Wessinger CA, Freeman CC, Mort ME, Rausher MD, Hileman LC Am J Bot 10-May-2016
PMCID:PMC10874106
doi:10.3732/ajb.1500519
PMID:27208359
Iridoids and other glucosides from Penstemon acuminatus Thorsten Vesper, Karlheinz Seifert Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)89534-5

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,5S,7aS)-5-hydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 101675241 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2=CC(C3C2C(OC=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 522.50 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
[(1S,4aR,5S,7aS)-5-hydroxy-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl (E)-3-phenylprop-2-enoate 44715743 Click to see C1=CC=C(C=C1)C=CC(=O)OCC2=CC(C3C2C(OC=C3)OC4C(C(C(C(O4)CO)O)O)O)O 476.50 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
[4a,5-dihydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7a-dihydro-1H-cyclopenta[c]pyran-7-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 162916671 Click to see C1=CC(=CC=C1C=CC(=O)OCC2=CC(C3(C2C(OC=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 508.50 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
[5-Hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 162864583 Click to see COC1=C(C=CC(=C1)C=CC(=O)OCC2=CC(C3C2C(OC=C3)OC4C(C(C(C(O4)CO)O)O)O)O)O 522.50 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
[5-Hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 73717558 Click to see C1=COC(C2C1C(C=C2COC(=O)C=CC3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 492.50 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
[5-Hydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 3-phenylprop-2-enoate 4303692 Click to see C1=CC=C(C=C1)C=CC(=O)OCC2=CC(C3C2C(OC=C3)OC4C(C(C(C(O4)CO)O)O)O)O 476.50 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
10-(Z)-p-Coumaroylaucubin 101675242 Click to see C1=COC(C2C1C(C=C2COC(=O)C=CC3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 492.50 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
5-chloro-2-(4-(2-(2-hydroxyethoxy)ethyl)piperazin-1-yl)-N-(6-(3-methoxybenzamido)pyridin-3-yl)isonicotinamide 13848072 Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
8-Epiloganin 10548420 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
Eurostoside 20839507 Click to see C1=COC(C2C1C(C=C2COC(=O)C=CC3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O 492.50 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
Methyl 6-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate 601562 Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
Mussaenoside 182423 Click to see CC1(CCC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O 390.40 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-(Hydroxymethyl)-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol 4961358 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
Gardoside methyl ester 51692952 Click to see COC(=O)C1=COC(C2C1CC(C2=C)O)OC3C(C(C(C(O3)CO)O)O)O 388.40 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
methyl 6-hydroxy-7-methylidene-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate 14313744 Click to see COC(=O)C1=COC(C2C1CC(C2=C)O)OC3C(C(C(C(O3)CO)O)O)O 388.40 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
Salidroside 159278 Click to see C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O 300.30 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-Acetylphenyl hexopyranoside 539591 Click to see CC(=O)C1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 298.29 unknown https://doi.org/10.1016/S0031-9422(00)89534-5
Picein 92123 Click to see CC(=O)C1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O 298.29 unknown https://doi.org/10.1016/S0031-9422(00)89534-5

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