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Centaurea glomerata

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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 UUID643fcd3f922c2271055467
Scientific name Centaurea glomerata
Authority Vahl
First published in Symb. Bot. ii. 94. (1791)

Description Top

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Synonyms Top

Scientific name Authority First published in
Calcitrapoides glomerata (Vahl) Holub Folia Geobot. Phytotax. 8(2): 170 (1973)
Seridia prolifera Sweet Hort. Brit. : 218 (1826)
Seridia straminea Sweet Hort. Brit. : 218 (1826)
Centaurea straminea Willd. Sp. Pl., ed. 4 , 3: 2312 (1803)
Centaurea coarctata Spreng. Syst. Veg. 3: 407 (1826)
Centaurea glomerata var. glabriceps Asch. & Schweinf.
Centaurea acaulis Forssk. Fl. Aegypt.-Arab. : 52 (1775)
Centaurea acaulis Desf.
Centaurea prolifera Vent. Descr. Pl. Nouv. : 16
Seridia glomerata Cass. Dict. Sci. Nat., ed. 2. 48: 499 (1827)

Common names Top

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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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000070577
Tropicos 2733881
INPN 717127
KEW urn:lsid:ipni.org:names:190579-1
The Plant List gcc-27382
Open Tree Of Life 202719
NCBI Taxonomy 363428
IPNI 190579-1
iNaturalist 521621
GBIF 3128097
EOL 6216310

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
Quercetin: A Functional Food-Flavonoid Incredibly Attenuates Emerging and Re-Emerging Viral Infections through Immunomodulatory Actions Shorobi FM, Nisa FY, Saha S, Chowdhury MA, Srisuphanunt M, Hossain KH, Rahman MA Molecules 17-Jan-2023
PMCID:PMC9920550
doi:10.3390/molecules28030938
PMID:36770606
Plant as an Alternative Source of Antifungals against Aspergillus Infections: A Review Tan LF, Yap VL, Rajagopal M, Wiart C, Selvaraja M, Leong MY, Tan PL Plants (Basel) 08-Nov-2022
PMCID:PMC9697101
doi:10.3390/plants11223009
PMID:36432738
Chemical Composition of Reichardia tingitana Methanolic Extract and Its Potential Antioxidant, Antimicrobial, Cytotoxic and Larvicidal Activity Salama SA, AL-Faifi ZE, El-Amier YA Plants (Basel) 04-Aug-2022
PMCID:PMC9370821
doi:10.3390/plants11152028
PMID:35956506
Habitat variations affect morphological, reproductive and some metabolic traits of Mediterranean Centaurea glomerata Vahl populations Hassan MO, Tammam SA, Galal HK, Saleh SM, Sayed M, Amro A Heliyon 12-Jun-2020
PMCID:PMC7300105
doi:10.1016/j.heliyon.2020.e04173
PMID:32577564
Centaurea Revisited: A Molecular Survey of the Jacea Group GARCIA-JACAS N, UYSAL T, ROMASHCHENKO K, SUÁREZ-SANTIAGO VN, ERTUĞRUL K, SUSANNA A Ann Bot 01-Oct-2006
PMCID:PMC2806161
doi:10.1093/aob/mcl157
PMID:16873424
Sesquiterpene lactones from Centaurea glomerata Sawsan El-Masry, Fikria A. Darwish, Amina Abou-Donia, Mohamed A. Abou-Karam, Michael Grenz Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)83170-2

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 lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aS,4S,6E,10Z,11aR)-10-(hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-2-(hydroxymethyl)but-2-enoate 162951844 Click to see CC=C(CO)C(=O)OC1CC(=CCCC(=CC2C1C(=C)C(=O)O2)CO)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83170-2
[(3aS,4S,6E,10Z,11aR)-10-(hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-4-hydroxy-2-methylbut-2-enoate 162988506 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O2)CO 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83170-2
[(3R,3aS,4S,6E,10Z,11aR)-10-(hydroxymethyl)-3,6-dimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 162899325 Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=C)CO 350.40 unknown https://doi.org/10.1016/S0031-9422(00)83170-2
[(3S,3aS,4S,6E,10Z,11aR)-10-(hydroxymethyl)-3,6-dimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-methylbut-2-enoate 162952219 Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=CCO)C 364.40 unknown https://doi.org/10.1016/S0031-9422(00)83170-2
[(3S,4S,6E,10Z,11aR)-10-(hydroxymethyl)-3,6-dimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] (E)-4-hydroxy-2-methylbut-2-enoate 162952218 Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=CCO)C 364.40 unknown https://doi.org/10.1016/S0031-9422(00)83170-2
[(3S,4S,6E,10Z,11aR)-10-(hydroxymethyl)-3,6-dimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 162899323 Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=C)CO 350.40 unknown https://doi.org/10.1016/S0031-9422(00)83170-2
[(4S,6E,10Z,11aR)-10-(hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (E)-2-(hydroxymethyl)but-2-enoate 162951841 Click to see CC=C(CO)C(=O)OC1CC(=CCCC(=CC2C1C(=C)C(=O)O2)CO)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83170-2
[(4S,6E,10Z,11aR)-10-(hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] (Z)-4-hydroxy-2-methylbut-2-enoate 162988505 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O2)CO 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83170-2
[10-(hydroxymethyl)-3,6-dimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] 2-(hydroxymethyl)prop-2-enoate 162899322 Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=C)CO 350.40 unknown https://doi.org/10.1016/S0031-9422(00)83170-2
[10-(hydroxymethyl)-3,6-dimethyl-2-oxo-3a,4,5,8,9,11a-hexahydro-3H-cyclodeca[b]furan-4-yl] 4-hydroxy-2-methylbut-2-enoate 162952217 Click to see CC1C2C(CC(=CCCC(=CC2OC1=O)CO)C)OC(=O)C(=CCO)C 364.40 unknown https://doi.org/10.1016/S0031-9422(00)83170-2
[10-(Hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 2-(hydroxymethyl)but-2-enoate 75059670 Click to see CC=C(CO)C(=O)OC1CC(=CCCC(=CC2C1C(=C)C(=O)O2)CO)C 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83170-2
[10-(Hydroxymethyl)-6-methyl-3-methylidene-2-oxo-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-4-yl] 4-hydroxy-2-methylbut-2-enoate 156602938 Click to see CC1=CCCC(=CC2C(C(C1)OC(=O)C(=CCO)C)C(=C)C(=O)O2)CO 362.40 unknown https://doi.org/10.1016/S0031-9422(00)83170-2

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