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Astragalus oxyphysus

Astragalus oxyphysus - 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 UUID643fd6a2e4dde569234461
Scientific name Astragalus oxyphysus
Authority A.Gray
First published in Proc. Calif. Acad. Sci.3: 103 (1864)

Description Top

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Synonyms Top

Scientific name Authority First published in
Tragacantha oxyphysa (A.Gray) Kuntze Revis. Gen. Pl.2: 947 (1891)
Phaca oxyphysa (A.Gray) A.Heller Muhlenbergia2: 86 (1905)

Common names Top

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Language Common/alternative name
English mt. diablo milkvetch

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

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-0000170037
USDA Plants ASOX
Tropicos 13017061
KEW urn:lsid:ipni.org:names:479043-1
The Plant List ild-16331
Open Tree Of Life 803268
NCBI Taxonomy 90201
Nature Serve 2.158743
IPNI 25382-2
iNaturalist 58150
GBIF 5345708
Freebase /m/04_13kg
EOL 639328
Calflora (Californian flora) 905
USDA GRIN 411734
Wikipedia Astragalus_oxyphysus
CMAUP NPO15688

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
Swainsonine Biosynthesis Genes in Diverse Symbiotic and Pathogenic Fungi Cook D, Donzelli BG, Creamer R, Baucom DL, Gardner DR, Pan J, Moore N, Krasnoff SB, Jaromczyk JW, Schardl CL G3 (Bethesda) 03-Apr-2017
PMCID:PMC5473758
doi:10.1534/g3.117.041384
PMID:28381497
Blackpatch of Clover, Cause of Slobbers Syndrome: A Review of the Disease and the Pathogen, Rhizoctonia leguminicola Kagan IA Front Vet Sci 27-Jan-2016
PMCID:PMC4728212
doi:10.3389/fvets.2016.00003
PMID:26858953
Unambiguous nuclear magnetic resonance assignments for swainsonine, an indolizidine alkaloid with α‐mannosidase inhibitory activity Leonardus B. S. Kardono, A. Douglas Kinghorn, Russell J. Molyneux Wiley 07-Mar-2007
doi:10.1002/PCA.2800020306
Biosynthesis of swainsonine in the diablo locoweed (Astragalus oxyphyrus) Constance M. Harris, Bruce C. Campbell, Russell J. Molyneux, Thomas M. Harris Elsevier BV 25-Jul-2002
doi:10.1016/S0040-4039(00)80616-4
Alkaloid Glycosidase Inhibitors Elbein AD, Molyneux RJ Comprehensive Natural Products Chemistry 01-Jan-1999
PMCID:PMC7271188
doi:10.1016/B978-0-08-091283-7.00098-9

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
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
Glycocyamine 763 Click to see C(C(=O)O)N=C(N)N 117.11 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Alpha amino acids / L-alpha-amino acids
(2S)-6-amino-2-azaniumylhexanoate 122198194 Click to see C(CCN)CC(C(=O)[O-])[NH3+] 146.19 unknown via CMAUP database
Arginine 6322 Click to see C(CC(C(=O)O)N)CN=C(N)N 174.20 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Histidine and derivatives
(2S)-2-azaniumyl-3-(1H-imidazol-5-yl)propanoate 6971009 Click to see C1=C(NC=N1)CC(C(=O)[O-])[NH3+] 155.15 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / 2-arylethylamines
Histamine 774 Click to see C1=C(NC=N1)CCN 111.15 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / Monoalkylamines
1,4-Diaminobutane 1045 Click to see C(CCN)CN 88.15 unknown via CMAUP database
Ethylamine 6341 Click to see CCN 45.08 unknown via CMAUP database
Isoamylamine 7894 Click to see CC(C)CCN 87.16 unknown via CMAUP database
Propylamine 7852 Click to see CCCN 59.11 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Secondary amines / Dialkylamines
Dimethylamine 674 Click to see CNC 45.08 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Tertiary amines / Trialkylamines
Trimethylamine 1146 Click to see CN(C)C 59.11 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Guanidines
Agmatine 199 Click to see C(CCN=C(N)N)CN 130.19 unknown via CMAUP database
Guanidine 3520 Click to see C(=N)(N)N 59.07 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see C[N+](C)(C)CCO 104.17 unknown via CMAUP database
> Organoheterocyclic compounds / Azoles / Imidazoles / Substituted imidazoles / Imidazolyl carboxylic acids and derivatives
(S)-2-hydroxy-3-(1H-imidazol-4-yl)propanoic acid 440129 Click to see C1=C(NC=N1)CC(C(=O)O)O 156.14 unknown via CMAUP database
2-(1H-imidazol-3-ium-5-yl)acetate 28305488 Click to see C1=C(NC=[NH+]1)CC(=O)[O-] 126.11 unknown via CMAUP database
Urocanic acid 736715 Click to see C1=C(NC=N1)C=CC(=O)O 138.12 unknown via CMAUP database
> Organoheterocyclic compounds / Indolizidines
(1-Acetyloxy-1,2,3,5,6,7,8,8a-octahydroindolizin-2-yl) acetate 13308888 Click to see CC(=O)OC1CN2CCCCC2C1OC(=O)C 241.28 unknown https://doi.org/10.1016/S0040-4039(00)80616-4
(1,2-Diacetyloxy-1,2,3,5,6,7,8,8a-octahydroindolizin-8-yl) acetate 13870671 Click to see CC(=O)OC1CCCN2C1C(C(C2)OC(=O)C)OC(=O)C 299.32 unknown https://doi.org/10.1016/S0040-4039(00)80616-4
(1R,8aS)-1,2,3,5,6,7,8,8a-octahydroindolizin-1-ol 11182655 Click to see C1CCN2CCC(C2C1)O 141.21 unknown https://doi.org/10.1016/S0040-4039(00)80616-4
[(1R,8aS)-1,2,3,5,6,7,8,8a-octahydroindolizin-1-yl] acetate 163010677 Click to see CC(=O)OC1CCN2C1CCCC2 183.25 unknown https://doi.org/10.1016/S0040-4039(00)80616-4
[(1S,2R,8aS)-1-acetyloxy-1,2,3,5,6,7,8,8a-octahydroindolizin-2-yl] acetate 13308893 Click to see CC(=O)OC1CN2CCCCC2C1OC(=O)C 241.28 unknown https://doi.org/10.1016/S0040-4039(00)80616-4
[(1S,2R,8R,8aR)-1,2-diacetyloxy-1,2,3,5,6,7,8,8a-octahydroindolizin-8-yl] acetate 11822669 Click to see CC(=O)OC1CCCN2C1C(C(C2)OC(=O)C)OC(=O)C 299.32 unknown https://doi.org/10.1016/S0040-4039(00)80616-4
1-Hydroxyindolizidine 13818696 Click to see C1CCN2CCC(C2C1)O 141.21 unknown https://doi.org/10.1016/S0040-4039(00)80616-4
1,2,3,5,6,7,8,8a-Octahydroindolizin-1-yl acetate 14110557 Click to see CC(=O)OC1CCN2C1CCCC2 183.25 unknown https://doi.org/10.1016/S0040-4039(00)80616-4
2-Epilentiginosine 11084135 Click to see C1CCN2CC(C(C2C1)O)O 157.21 unknown https://doi.org/10.1016/S0040-4039(00)80616-4
Octahydroindolizine-1,2-diol 4361605 Click to see C1CCN2CC(C(C2C1)O)O 157.21 unknown https://doi.org/10.1016/S0040-4039(00)80616-4
Octahydroindolizine-1,2,8-triol 5363 Click to see C1CC(C2C(C(CN2C1)O)O)O 173.21 unknown https://doi.org/10.1016/S0040-4039(00)80616-4
Swainsonine 51683 Click to see C1CC(C2C(C(CN2C1)O)O)O 173.21 unknown https://doi.org/10.1002/PCA.2800020306
https://doi.org/10.1016/S0040-4039(00)80616-4

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