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Crotalaria aegyptiaca

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 UUID643fde4aad336545716669
Scientific name Crotalaria aegyptiaca
Authority Benth.
First published in London J. Bot.2: 473 (1843)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Crotalaria wissmannii O.Schwartz Mitt. Inst. Allg. Bot. Hamburg10: 93 (1939)
Crotalaria wissmannii O.Schwartz

Common names Top

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Language Common/alternative name
Arabic نطش مصري
Arabic نطش

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
  • Africa
    • Northeast Tropical Africa
      • Somalia
      • Sudan
    • Northern Africa
      • Egypt
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Palestine
      • Sinai

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000210586
Tropicos 13028979
KEW urn:lsid:ipni.org:names:487765-1
The Plant List ild-5706
Open Tree Of Life 3927941
NCBI Taxonomy 1977568
IPNI 487765-1
iNaturalist 464019
GBIF 2941794
EPPO CVTAE
EOL 691107
CMAUP NPO5541

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
Impacts of Anthropogenic Disturbance on Vegetation Dynamics: A Case Study of Wadi Hagul, Eastern Desert, Egypt Bedair R, Ibrahim AA, Alyamani AA, Aloufi S, Ramadan S Plants (Basel) 14-Sep-2021
PMCID:PMC8466335
doi:10.3390/plants10091906
PMID:34579436
Pest categorisation of the non‐EU phytoplasmas of tuber‐forming Solanum spp. Bragard C, Dehnen‐Schmutz K, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Bosco D, Chiumenti M, Di Serio F, Galetto L, Marzachì C, Pautasso M, Jacques M EFSA J 23-Dec-2020
PMCID:PMC7757785
doi:10.2903/j.efsa.2020.6356
PMID:33376553
Pest categorisation of the non‐EU phytoplasmas of Cydonia Mill., Fragaria L., Malus Mill., Prunus L., Pyrus L., Ribes L., Rubus L. and Vitis L. Bragard C, Dehnen‐Schmutz K, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Bosco D, Chiumenti M, Di Serio F, Galetto L, Marzachì C, Pautasso M, Jacques M EFSA J 13-Jan-2020
PMCID:PMC7008834
doi:10.2903/j.efsa.2020.5929
PMID:32626484
Classification of a new phytoplasmas subgroup 16SrII-W associated with Crotalaria witches’ broom diseases in Oman based on multigene sequence analysis Al-Subhi A, Hogenhout SA, Al-Yahyai RA, Al-Sadi AM BMC Microbiol 25-Nov-2017
PMCID:PMC5702145
doi:10.1186/s12866-017-1130-3
PMID:29178845
Vanishing Knowledge of Plant Species in the Wadi Allaqi Desert Area of Egypt Kandal HA, Yacoub HA, Gerkema MP, Swart JA Hum Ecol Interdiscip J 19-May-2016
PMCID:PMC5011154
doi:10.1007/s10745-016-9826-9
PMID:27642218
Floral diversity in desert ecosystems: Comparing field sampling to image analyses in assessing species cover Ksiksi TS, El-Keblawy AA BMC Ecol 10-Jun-2013
PMCID:PMC3702427
doi:10.1186/1472-6785-13-22
PMID:23758667
Pyrrolizidine Alkaloids From Middle Eastern Plants L. H. Zalkow, S. Bonetii, L. Gelbaum, M. M. Gordon, B. B. Patil, A. Shani, D. Van Derveer American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50006A005
Pyrrolizidine alkaloids from Crotalaria aegyptiaca E. Roeder, T. Sarg, S. El-Dahmy, A.Abdel Ghani Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(91)80041-X

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 4-ethyl-3-hydroxy-2,3,4-trimethyl-5-oxooxolane-2-carboxylate 162885709 Click to see CCC1(C(=O)OC(C1(C)O)(C)C(=O)OCC2=CCN3C2C(CC3)O)C 353.40 unknown https://doi.org/10.1016/0031-9422(91)80041-X
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
3-Galloylshikimic acid 10449030 Click to see 326.25 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3R,4S,5R)-1,3-dihydroxy-4,5-bis[(3,4,5-trihydroxybenzoyl)oxy]cyclohexane-1-carboxylic acid 13270012 Click to see 496.40 unknown via CMAUP database
3,4-di-O-galloylquinic acid 460895 Click to see 496.40 unknown via CMAUP database
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
Neochlorogenic acid 5280633 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Alpha-acyloxy carbonyl compounds / Alpha-acyloxy ketones
Croaegyptine 91753267 Click to see 339.40 unknown https://doi.org/10.1016/0031-9422(91)80041-X
> Organoheterocyclic compounds / Pyrrolizines
(12xi,13xi)-14,19-Dihydro-12,13-dihydroxy-14-methylcrotalanan-11,15-dione 73745631 Click to see 353.40 unknown https://doi.org/10.1016/0031-9422(91)80041-X
(1R,4R,5S,6R,16S)-6,16-dihydroxy-5,6,13-trimethyl-4-propan-2-yl-2,8-dioxa-13-azoniatricyclo[8.5.1.013,16]hexadec-10-ene-3,7-dione 101306807 Click to see CC1C(C(=O)OC2CC[N+]3(C2(C(=CC3)COC(=O)C1(C)O)O)C)C(C)C 368.40 unknown https://doi.org/10.1016/0031-9422(91)80041-X
https://doi.org/10.1021/NP50006A005
(1R,4S,5S,6R,16R)-5,6-dihydroxy-5,6-dimethyl-4-propan-2-yl-2,8-dioxa-13-azatricyclo[8.5.1.013,16]hexadec-10-ene-3,7-dione 101922689 Click to see CC(C)C1C(=O)OC2CCN3C2C(=CC3)COC(=O)C(C1(C)O)(C)O 353.40 unknown https://doi.org/10.1016/0031-9422(91)80041-X
5,6-Dihydroxy-5,6-dimethyl-4-methylidene-7-propan-2-yl-3-oxa-13-azatricyclo[8.5.1.013,16]hexadec-1(15)-en-8-one 5322016 Click to see 349.50 unknown https://doi.org/10.1016/0031-9422(91)80041-X
Crosemperine 169196 Click to see 368.40 unknown https://doi.org/10.1016/0031-9422(91)80041-X
https://doi.org/10.1021/NP50006A005
Monocrotaline 9415 Click to see 325.36 unknown https://doi.org/10.1016/0031-9422(91)80041-X
https://doi.org/10.1021/NP50006A005
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S,4R)-2-(3,4-dihydroxyphenyl)-4-[(2R,3S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-8-yl]-8-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 101228664 Click to see C1C(C(OC2=C1C(=CC(=C2C3C(C(OC4=C3C(=CC(=C4C5C(C(OC6=C(C(=CC(=C56)O)O)C7C(C(OC8=CC(=CC(=C78)O)O)C9=CC(=C(C=C9)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O)O)O)C1=CC(=C(C=C1)O)O)O 1155.00 unknown via CMAUP database
Procyanidin B3 146798 Click to see 578.50 unknown via CMAUP database
Procyanidin C2 11182062 Click to see 866.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(2R,3S,4S)-2-(3,4-Dihydroxyphenyl)-3,4-dihydro-2H-1-benzopyran-3,4,5,7-tetrol 440833 Click to see 306.27 unknown via CMAUP database
Catechin 9064 Click to see 290.27 unknown via CMAUP database
Epicatechin 72276 Click to see 290.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Gallocatechin 9882981 Click to see 306.27 unknown via CMAUP database
Epigallocatechin 72277 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O 306.27 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
Delphinidin 3-O-glucoside cation 443650 Click to see C1=C(C=C(C(=C1O)O)O)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O 465.40 unknown via CMAUP database
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
3',5'-Dimethoxy-4',7-dihydroxy-5-(beta-D-glucopyranosyloxy)-3-[(6-O-acetyl-beta-D-glucopyranosyl)oxy]flavylium 101918997 Click to see CC(=O)OCC1C(C(C(C(O1)OC2=C([O+]=C3C=C(C=C(C3=C2)OC4C(C(C(C(O4)CO)O)O)O)O)C5=CC(=C(C(=C5)OC)O)OC)O)O)O 697.60 unknown via CMAUP database
Cyanin 441688 Click to see 611.50 unknown via CMAUP database
Malvin 441765 Click to see 655.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-((2S,3R,4S,5R,6R)-3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-yl)Oxy-Chromen-4-one 12304323 Click to see 464.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
kaempferol 3-O-beta-L-glucopyranoside 9911508 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
Quercetin 3-(6''-galloylgalactoside) 5491814 Click to see 616.50 unknown via CMAUP database
Quercetin 3-(6''-galloylglucoside) 9830456 Click to see 616.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
(1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid 102004656 Click to see 292.20 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
(2R,3R,4S,5R,6R)-6-(((3,4,5-Trihydroxybenzoyl)oxy)methyl)tetrahydro-2H-pyran-2,3,4,5-tetrayl tetrakis(3,4,5-trihydroxybenzoate) 9876301 Click to see 940.70 unknown via CMAUP database
1,2,3,6-Tetra-O-Galloyl-Beta-D-Glucose 73178 Click to see 788.60 unknown via CMAUP database
beta-Glucogallin 124021 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(C(C(O2)CO)O)O)O 332.26 unknown via CMAUP database
Penta-O-galloyl-beta-D-glucose 65238 Click to see 940.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
1,2-Di-O-galloyl-4,6-O-(S)-hexahydroxydiphenoyl-beta-D-glucopyranose 101259865 Click to see 786.60 unknown via CMAUP database
3-O-digalloyl-1,2,4,6-tetra-O-beta-D-galloylglucose 16164119 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)OC(=O)C6=CC(=C(C(=C6)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7)O)O)O 1092.80 unknown via CMAUP database
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database
Geraniin 3001497 Click to see 952.60 unknown via CMAUP database
Xcxwmhrrisfuff-xngpzlstsa- 21636130 Click to see 1110.80 unknown via CMAUP database

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