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Lotus creticus

Lotus creticus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Lotus creticus - 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 UUID643fdeb13c919541001357
Scientific name Lotus creticus
Authority L.
First published in Sp. Pl.: 775 (1753)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lotus carthaginiensis Andr. Bot. Közlem.36: 73 (1939)
Lotus salzmannii Boiss. & Reut. Pugill. Pl. Afr. Bor. Hispan.: 37 (1852)
Lotus commutatus Guss. Fl. Sicul. Prodr.2: 545 (1828)
Lotus obtusatus Ser. A.P.de Candolle, Prodr.2: 212 (1825)
Lotus varians Desv. J. Bot. Agric.3: 77 (1814)
Lotus pseudo-creticus Maire, Weiller & Wilczek Bull. Soc. Hist. Nat. Afrique N. 26: 120 (1935)
Lotus creticus subsp. commutatus (Guss.) Ball J. Linn. Soc., Bot.16: 423 (1878)
Lotus creticus subsp. commutatus Arcang. Comp. Fl. Ital.: 180 (1882)
Lotus creticus subsp. commutatus (Guss.) Batt. J.A.Battandier & L.C.Trabut, Fl. Algérie, Dicot.: 246 (1888)
Lotus creticus subsp. salzmannii (Boiss. & Reut.) H.Lindb. Acta Soc. Sci. Fenn., Ser. B, Opera Biol.1(2): 83 (1932)
Lotus creticus var. micranthus Maire Bull. Soc. Sci. Nat. Maroc8: 131 (1928)
Lotus creticus f. grandiflorus Heyn & Herrnst. Kew Bull.21: 308 (1967)
Lotus sericeus Moench Suppl. Meth.: 53 (1802)

Common names Top

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Language Common/alternative name
English creta trefoil
Catalan trèvol femella
Catalan lot de creta
German kreta-hornklee
Hebrew לוטוס מכסיף

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
    • Macaronesia
      • Azores
      • Canary Islands
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
  • Asia-temperate
    • Western Asia
      • East Aegean Islands
      • Lebanon-Syria
      • Palestine
      • Sinai
  • Europe
    • Southeastern Europe
      • Greece
      • Sicilia
      • Yugoslavia
    • Southwestern Europe
      • Portugal
      • Spain

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000212182
USDA Plants LOCR3
INPN 106656
Flora of Italy 2714
KEW urn:lsid:ipni.org:names:503576-1
The Plant List ild-7262
Open Tree Of Life 472038
NCBI Taxonomy 181267
NBN Atlas NBNSYS0200002568
IPNI 503576-1
iNaturalist 337708
GBIF 5356939
EPPO LOTCR
EOL 702890
USDA GRIN 22705
Wikipedia Lotus_creticus

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
The Lotus angustissumus Group (Fabaceae): Can Phylogenetic Patterns Be Accommodated by a Taxonomic Concept? Kramina TE, Hadziev TR, Samigullin TH Plants (Basel) 28-Dec-2023
PMCID:PMC10780816
doi:10.3390/plants13010101
PMID:38202409
Helichrysum stoechas (L.) Moench Inflorescence Extract for Tomato Disease Management Sánchez-Hernández E, Álvarez-Martínez J, González-García V, Casanova-Gascón J, Martín-Gil J, Martín-Ramos P Molecules 03-Aug-2023
PMCID:PMC10421166
doi:10.3390/molecules28155861
PMID:37570830
Salt-Tolerant Plants, Halophytes, as Renewable Natural Resources for Cancer Prevention and Treatment: Roles of Phenolics and Flavonoids in Immunomodulation and Suppression of Oxidative Stress towards Cancer Management Mohammed HA, Emwas AH, Khan RA Int J Mol Sci 08-Mar-2023
PMCID:PMC10048981
doi:10.3390/ijms24065171
PMID:36982245
Brevibacillus DesertYSK and Rhizobium MAP7 stimulate the growth and pigmentation of Lactuca sativa L. Mowafy AM, Khalifa S, Elsayed A J Genet Eng Biotechnol 13-Feb-2023
PMCID:PMC9925635
doi:10.1186/s43141-023-00465-1
PMID:36780046
Sustainable Applications of Endophytic Bacteria and Their Physiological/Biochemical Roles on Medicinal and Herbal Plants: Review Tshikhudo PP, Ntushelo K, Mudau FN Microorganisms 10-Feb-2023
PMCID:PMC9967847
doi:10.3390/microorganisms11020453
PMID:36838418
Rice DST transcription factor negatively regulates heat tolerance through ROS-mediated stomatal movement and heat-responsive gene expression Ding Y, Zhou M, Wang K, Qu A, Hu S, Jiang Q, Yi K, Wang F, Cai C, Zhu C, Chen Z Front Plant Sci 31-Jan-2023
PMCID:PMC9927019
doi:10.3389/fpls.2023.1068296
PMID:36798712
From Biodiversity to Musketry: Detection of Plant Diversity in Pre-Industrial Peloponnese during the Flora Graeca Expedition Chimona C, Papadopoulou S, Kolyva F, Mina M, Rhizopoulou S Life (Basel) 23-Nov-2022
PMCID:PMC9785030
doi:10.3390/life12121957
PMID:36556322
Effects of Water Availability on Leaf Trichome Density and Plant Growth and Development of Shepherdia ×utahensis Chen JJ, Sun Y, Kopp K, Oki L, Jones SB, Hipps L Front Plant Sci 18-May-2022
PMCID:PMC9158747
doi:10.3389/fpls.2022.855858
PMID:35665162
Tomato Defense against Whiteflies under Drought Stress: Non-Additive Effects and Cultivar-Specific Responses González-Klenner FJ, Albornoz MV, Ávila-Sákar G, Verdugo JA Plants (Basel) 12-Apr-2022
PMCID:PMC9030952
doi:10.3390/plants11081049
PMID:35448777
When Morphology and Biogeography Approximate Nuclear ITS but Conflict with Plastid Phylogeny: Phylogeography of the Lotus dorycnium Species Complex (Leguminosae) Kramina TE, Lysova MV, Samigullin TH, Özbek MU, Sokoloff DD Plants (Basel) 02-Feb-2022
PMCID:PMC8840542
doi:10.3390/plants11030410
PMID:35161391
No escape: The influence of substrate sodium on plant growth and tissue sodium responses Santiago‐Rosario LY, Harms KE, Elderd BD, Hart PB, Dassanayake M Ecol Evol 23-Sep-2021
PMCID:PMC8525147
doi:10.1002/ece3.8138
PMID:34707851
Ionomic Approaches for Discovery of Novel Stress-Resilient Genes in Plants Ali S, Tyagi A, Bae H Int J Mol Sci 02-Jul-2021
PMCID:PMC8267685
doi:10.3390/ijms22137182
PMID:34281232
Floristic and Vegetation Changes on a Small Mediterranean Island over the Last Century Sciandrello S, Cambria S, Giusso del Galdo G, Guarino R, Minissale P, Pasta S, Tavilla G, Cristaudo A Plants (Basel) 01-Apr-2021
PMCID:PMC8065674
doi:10.3390/plants10040680
PMID:33916121
The suitability of native flowers as pollen sources for Chrysoperla lucasina (Neuroptera: Chrysopidae) Alcalá Herrera R, Fernández Sierra ML, Ruano F PLoS One 23-Oct-2020
PMCID:PMC7584243
doi:10.1371/journal.pone.0239847
PMID:33095792
Root response in Pisum sativum under naproxen stress: Morpho-anatomical, cytological, and biochemical traits Svobodníková L, Kummerová M, Zezulka Š, Babula P, Sendecká K Chemosphere 16-Jun-2020
PMCID:PMC7308076
doi:10.1016/j.chemosphere.2020.127411
PMID:32947668

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1016/0031-9422(90)89077-M
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(90)89077-M
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/0031-9422(90)89077-M
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/0031-9422(90)89077-M
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/0031-9422(90)89077-M
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
(2RS)-Lotaustralin 23638286 Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 261.27 unknown https://doi.org/10.1016/0031-9422(90)89077-M
Linamarin 11128 Click to see CC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 247.24 unknown https://doi.org/10.1016/0031-9422(90)89077-M
Lotaustralin 441467 Click to see CCC(C)(C#N)OC1C(C(C(C(O1)CO)O)O)O 261.27 unknown https://doi.org/10.1016/0031-9422(90)89077-M
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
5,7-Dihydroxy-2-[4-hydroxy-3-(3-methylbut-2-enyl)phenyl]-6-(3-methylbut-2-enyl)chroman-4-one 480769 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)97837-3
Macarangaflavanone B 14309760 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)97837-3
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
5,7,4'-Trihydroxy-3',8-diprenylflavanone 10319282 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)97837-3
Euchrestaflavanone A 484588 Click to see CC(=CCC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)C 408.50 unknown https://doi.org/10.1016/S0031-9422(00)97837-3
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
3,9-Dihydroxy-1-methoxy-8-prenylcoumestan 14463173 Click to see CC(=CCC1=CC2=C(C=C1O)OC3=C2C(=O)OC4=C3C(=CC(=C4)O)OC)C 366.40 unknown https://doi.org/10.1016/0031-9422(90)89077-M
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflav-2-enes / Isoflavones
Lupinalbin A 5324349 Click to see C1=CC2=C(C=C1O)OC3=C2C(=O)C4=C(C=C(C=C4O3)O)O 284.22 unknown https://doi.org/10.1016/S0031-9422(00)97837-3
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones / 6-prenylated isoflavanones
(17S)-7,20-dihydroxy-17-(2-hydroxypropan-2-yl)-10,12,16-trioxapentacyclo[11.7.0.03,11.04,9.015,19]icosa-1(20),3(11),4(9),5,7,13,15(19)-heptaen-2-one 162893299 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)OC5=C4C=CC(=C5)O)O 368.30 unknown https://doi.org/10.1016/S0031-9422(00)97837-3
Gancaonin A 5317478 Click to see CC(=CCC1=C(C2=C(C=C1O)OC=C(C2=O)C3=CC=C(C=C3)OC)O)C 352.40 unknown https://doi.org/10.1016/S0031-9422(00)97837-3
Lupinalbin B 14309761 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3=C(C2=O)C4=C(O3)C=C(C=C4)O)O)C 352.30 unknown https://doi.org/10.1016/S0031-9422(00)97837-3
Lupinalbin C 14309762 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2O)C(=O)C4=C(O3)OC5=C4C=CC(=C5)O)O 368.30 unknown https://doi.org/10.1016/S0031-9422(00)97837-3

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