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Reaumuria vermiculata

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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 UUID6440000a9c319986498121
Scientific name Reaumuria vermiculata
Authority L.
First published in Syst. Nat., ed. 10. 2: 1081. 1759 [7 Jun 1759]

Description Top

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Synonyms Top

Scientific name Authority First published in
Reaumuria mucronata Jaub. & Spach Ill. Pl. Orient. 3: 54 (1848)

Common names Top

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Language Common/alternative name
Arabic ملاح دودي

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

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000464014
Tropicos 50106097
Flora of Italy 3285
KEW urn:lsid:ipni.org:names:828022-1
The Plant List kew-2527785
Open Tree Of Life 5729050
NCBI Taxonomy 1518163
IPNI 828022-1
iNaturalist 928556
GBIF 5535223
CMAUP NPO14896

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
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
Diversity of desert rangelands of Tunisia Gamoun M, Belgacem AO, Louhaichi M Plant Divers 20-Aug-2018
PMCID:PMC6224667
doi:10.1016/j.pld.2018.06.004
PMID:30740567
Sulphated Flavonoids: Biosynthesis, Structures, and Biological Activities Teles YC, Souza MS, de Souza MD Molecules 23-Feb-2018
PMCID:PMC6017314
doi:10.3390/molecules23020480
PMID:29473839
Antioxidant, anti-inflammatory and anticancer activities of the medicinal halophyte Reaumuria vermiculata Karker M, Falleh H, Msaada K, Smaoui A, Abdelly C, Legault J, Ksouri R EXCLI J 25-Apr-2016
PMCID:PMC4897625
doi:10.17179/excli2016-187
PMID:27298615
The Chemistry and Biological Activities of Natural Products from Northern African Plant Families: From Taccaceae to Zygophyllaceae Ntie-Kang F, Njume LE, Malange YI, Günther S, Sippl W, Yong JN Nat Prod Bioprospect 01-Mar-2016
PMCID:PMC4805656
doi:10.1007/s13659-016-0091-9
PMID:26931529
Cytotoxic ellagitannins from Reaumuria vermiculata. Nawwar MA, Ayoub NA, El-Rai MA, Bassyouny F, Mostafa ES, Al-Abd AM, Harms M, Wende K, Lindequist U, Linscheid MW Fitoterapia 01-Oct-2012
doi:10.1016/J.FITOTE.2012.06.007
PMID:22742959

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O 170.12 unknown https://doi.org/10.1016/J.FITOTE.2012.06.007
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
2, 6-di-O-galloyl-D-glucose 44584093 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O 484.40 unknown https://doi.org/10.1016/J.FITOTE.2012.06.007
2,3-Bis-O-(3,4,5-trihydroxybenzoyl)hexopyranose 14213991 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3)O)O)O)O)CO)O 484.40 unknown https://doi.org/10.1016/J.FITOTE.2012.06.007
> Benzenoids / Benzene and substituted derivatives / Diphenylethers
3,4-Dihydroxy-5-(2,3,4-trihydroxyphenoxy)benzoic acid 15714543 Click to see C1=CC(=C(C(=C1O)O)O)OC2=CC(=CC(=C2O)O)C(=O)O 294.21 unknown https://doi.org/10.1016/J.FITOTE.2012.06.007
Dehydrodigallic acid 14057208 Click to see C1=C(C=C(C(=C1O)O)OC2=C(C(=C(C=C2C(=O)O)O)O)O)C(=O)O 338.22 unknown https://doi.org/10.1016/J.FITOTE.2012.06.007
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin 69894 Click to see COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol 3,7-di-O-sulfate 12988285 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OS(=O)(=O)O)O)OS(=O)(=O)O)O 446.40 unknown via CMAUP database
Quercetin 3,7-di-O-sulfate 12988287 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)OS(=O)(=O)O)O)OS(=O)(=O)O)O)O 462.40 unknown https://doi.org/10.1016/J.FITOTE.2012.06.007
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
Tamarixetin 5281699 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
[5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxo-3-sulfonatooxychromen-7-yl] sulfate 21676171 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OS(=O)(=O)[O-])O)OS(=O)(=O)[O-])O 474.40 unknown via CMAUP database
[5-Hydroxy-2-(3-hydroxy-4-methoxyphenyl)-4-oxo-3-sulfooxychromen-7-yl] hydrogen sulfate 14016796 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OS(=O)(=O)O)O)OS(=O)(=O)O)O 476.40 unknown https://doi.org/10.1016/J.FITOTE.2012.06.007
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(13,14-Dihydroxy-7-methoxy-3,10-dioxo-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl) hydrogen sulfate 163049964 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O)OS(=O)(=O)O 396.30 unknown https://doi.org/10.1016/J.FITOTE.2012.06.007
(7-Hydroxy-14-methoxy-3,10-dioxo-13-sulfooxy-2,9-dioxatetracyclo[6.6.2.04,16.011,15]hexadeca-1(15),4,6,8(16),11,13-hexaen-6-yl) hydrogen sulfate 162817056 Click to see COC1=C(C=C2C3=C1OC(=O)C4=CC(=C(C(=C43)OC2=O)O)OS(=O)(=O)O)OS(=O)(=O)O 476.30 unknown https://doi.org/10.1016/J.FITOTE.2012.06.007
[4,5,6,13,21,22,26,27,28,34,35-Undecahydroxy-14,36-bis(hydroxymethyl)-9,18,31,40-tetraoxo-2,10,15,17,24,32,37,39-octaoxaheptacyclo[39.3.1.119,23.03,8.011,16.025,30.033,38]hexatetraconta-1(44),3,5,7,19,21,23(46),25,27,29,41(45),42-dodecaen-12-yl] 3,4,5-trihydroxybenzoate 162909388 Click to see C1=CC2=CC(=C1)OC3=C(C(=C(C=C3C(=O)OC4C(C(C(OC4OC(=O)C5=CC(=C(C(=C5)OC6=C(C(=C(C=C6C(=O)OC7C(C(C(OC7OC2=O)CO)O)O)O)O)O)O)O)CO)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)O)O)O 1084.80 unknown https://doi.org/10.1016/J.FITOTE.2012.06.007
2-[5-[(2R,4S,5R)-2,5-dihydroxy-6-(hydroxymethyl)-4-(3,4,5-trihydroxybenzoyl)oxyoxan-3-yl]oxycarbonyl-2,3-dihydroxyphenoxy]-3,4,5-trihydroxybenzoic acid 162857704 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2C(C(OC(C2OC(=O)C3=CC(=C(C(=C3)OC4=C(C(=C(C=C4C(=O)O)O)O)O)O)O)O)CO)O 652.50 unknown https://doi.org/10.1016/J.FITOTE.2012.06.007
2-[5-[[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl]oxycarbonyl]-2,3-dihydroxyphenoxy]-3,4,5-trihydroxybenzoic acid 163102813 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)OC5=C(C(=C(C=C5C(=O)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O 954.70 unknown https://doi.org/10.1016/J.FITOTE.2012.06.007
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown https://doi.org/10.1016/J.FITOTE.2012.06.007

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