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Cryptantha leiocarpa

Cryptantha leiocarpa - 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 UUID6440142ca5051909234956
Scientific name Cryptantha leiocarpa
Authority (Fisch. & C.A.Mey.) Greene
First published in Pittonia 1: 117 (1887)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cryptantha leiocarpa var. eremocaryoides Brand Pflanzenr. , IV, 252(97): 53 (1931)
Echinospermum leiocarpum Fisch. & C.A.Mey. Index Seminum (LE, Petropolitanus) 2: 36 (1836)

Common names Top

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Language Common/alternative name
English coastal cryptantha

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Northern America
    • Northwestern U.S.A.
      • Oregon
    • Southwestern U.S.A.
      • California

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000627541
USDA Plants CRLE4
Tropicos 4001772
KEW urn:lsid:ipni.org:names:71452-2
The Plant List kew-2745611
Open Tree Of Life 25432
NCBI Taxonomy 1213317
Nature Serve 2.130194
IPNI 71452-2
iNaturalist 57704
GBIF 2926316
Freebase /m/047rnkq
EOL 579995
Calflora (Californian flora) 2472
Wikipedia Cryptantha_leiocarpa

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
Pyrrolizidine alkaloids from Cryptantha species Frank R. Stermitz, Michael A. Pass, Ronald B. Kelley, J. Richard Liddell Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(93)85524-U

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
> Alkaloids and derivatives
(7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl)methyl 2-(1-acetyloxyethyl)-2-hydroxy-3-methylbutanoate 78384682 Click to see CC(C)C(C(C)OC(=O)C)(C(=O)OCC1=CCN2C1C(CC2)O)O 341.40 unknown https://doi.org/10.1016/0031-9422(93)85524-U
[(1R,8R)-7-[[(2S)-2-hydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoyl]oxymethyl]-2,3,5,8-tetrahydro-1H-pyrrolizin-1-yl] (2S,3S)-2,3-dimethyloxirane-2-carboxylate 163034001 Click to see CC1C(O1)(C)C(=O)OC2CCN3C2C(=CC3)COC(=O)C(C(C)C)(C(C)O)O 397.50 unknown https://doi.org/10.1016/0031-9422(93)85524-U
[(7R,8R)-7-hydroxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-[(1R)-1-acetyloxyethyl]-2-hydroxy-3-methylbutanoate 162973292 Click to see CC(C)C(C(C)OC(=O)C)(C(=O)OCC1=CCN2C1C(CC2)O)O 341.40 unknown https://doi.org/10.1016/0031-9422(93)85524-U
[(7R,8S)-7-[(2R,3R)-3-chloro-2-hydroxy-2-methylbutanoyl]oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-hydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoate 162986068 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C(C)(C(C)Cl)O)O 433.90 unknown https://doi.org/10.1016/0031-9422(93)85524-U
[(7R,8S)-7-[(2S,3S)-2,3-dihydroxy-2-methylbutanoyl]oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl (2S)-2-hydroxy-2-[(1R)-1-hydroxyethyl]-3-methylbutanoate 162981148 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C(C)(C(C)O)O)O 415.50 unknown https://doi.org/10.1016/0031-9422(93)85524-U
[7-(2-methylbut-2-enoyloxy)-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 4581422 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)C)(C(C)O)O 381.50 unknown https://doi.org/10.1016/0031-9422(93)85524-U
[7-(2,3-dihydroxy-2-methylbutanoyl)oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 162981147 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C(C)(C(C)O)O)O 415.50 unknown https://doi.org/10.1016/0031-9422(93)85524-U
[7-(3-chloro-2-hydroxy-2-methylbutanoyl)oxy-5,6,7,8-tetrahydro-3H-pyrrolizin-1-yl]methyl 2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoate 162986067 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)OC(=O)C(C)(C(C)Cl)O)O 433.90 unknown https://doi.org/10.1016/0031-9422(93)85524-U
[7-[[2-hydroxy-2-(1-hydroxyethyl)-3-methylbutanoyl]oxymethyl]-2,3,5,8-tetrahydro-1H-pyrrolizin-1-yl] 2,3-dimethyloxirane-2-carboxylate 163034000 Click to see CC1C(O1)(C)C(=O)OC2CCN3C2C(=CC3)COC(=O)C(C(C)C)(C(C)O)O 397.50 unknown https://doi.org/10.1016/0031-9422(93)85524-U
7-Angelylretronecine 6440943 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)CO 237.29 unknown https://doi.org/10.1016/0031-9422(93)85524-U
9-Angeloylretronecine 638872 Click to see CC=C(C)C(=O)OCC1=CCN2C1C(CC2)O 237.29 unknown https://doi.org/10.1016/0031-9422(93)85524-U
Echinatine 22384 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown https://doi.org/10.1016/0031-9422(93)85524-U
Echiumine 15559084 Click to see CC=C(C)C(=O)OC1CCN2C1C(=CC2)COC(=O)C(C(C)C)(C(C)O)O 381.50 unknown https://doi.org/10.1016/0031-9422(93)85524-U
Intermedine, (+)- 114843 Click to see CC(C)C(C(C)O)(C(=O)OCC1=CCN2C1C(CC2)O)O 299.36 unknown https://doi.org/10.1016/0031-9422(93)85524-U

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