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Zilla spinosa

Zilla spinosa - 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 UUID643ffbe81561d536760870
Scientific name Zilla spinosa
Authority Prantl
First published in Nat. Pflanzenfam. 3(2): 175 (1891)

Description Top

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Synonyms Top

Scientific name Authority First published in
Myagrum spinosum Lam. Encycl. 1: 571 (1785)
Zilla macrocarpa D.Dietr. Syn. Pl. 3: 678 (1842)
Zilla myagrum Forssk. Fl. Aegypt.-Arab. : lxix (1775)
Zilla microcarpa Vis. Comment. Med. 2: 209 (1836)
Bunias spinosa L. Mant. Pl. 1: 96 (1767)
Zilla myagroides Forssk. Fl. Aegypt.-Arab. : 121 (1775)
Zilla spinosa var. microcarpa T.Durand & Schinz Consp. Fl. Afr. 1(2): 149 1898
Zilla spinosa var. spinosa (L.) Prantl
Zilla spinosa subsp. myagroides (Forssk.) Maire & Weiller Bull. Soc. Bot. France 30: 260 1939

Common names Top

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Language Common/alternative name
English spiny zilla
Arabic شبرم ، سلة شائكة
Arabic الشبرق، زلة

Subspecies (abbr. subsp./ssp.) Top

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Name Authority First published in
Zilla spinosa subsp. biparmata (O.E.Schulz) Maire & Weiller Bull. Soc. Hist. Nat. Afrique N. 30: 260. 1939 (1939)

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
      • Chad
      • Sudan
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
      • Western Sahara
    • West Tropical Africa
      • Mauritania
  • Asia-temperate
    • Arabian Peninsula
      • Kuwait
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000430153
Tropicos 4100296
KEW urn:lsid:ipni.org:names:291161-1
The Plant List kew-2470433
Open Tree Of Life 779709
NCBI Taxonomy 127626
IPNI 291161-1
iNaturalist 202552
GBIF 5376128
USDA GRIN 460994
CMAUP NPO21775

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
Environmental impacts of industrial activities on floral coverage with special emphasis on detoxification enzyme activities in Cataglyphis savignyi as pollution biomarker Hamza YI, Bream AS, Mahmoud MA, El-Tabakh MA Environ Sci Pollut Res Int 18-Oct-2023
PMCID:PMC10663209
doi:10.1007/s11356-023-30367-1
PMID:37851257
Distinguishing features of Lycium L. species (family Solanaceae) distributed in Egypt based on their anatomical, metabolic, molecular, and ecological characteristics Ragab OG, Mamdouh D, Bedair R, Smetanska I, Gruda NS, Yousif SK, Omer RM, Althobaiti AT, Abd El-Raouf HS, El-Taher AM, El-Sayed AS, Eldemerdash MM Front Plant Sci 12-May-2023
PMCID:PMC10213676
doi:10.3389/fpls.2023.1162695
PMID:37251766
The Life Cycle of the Xylophagous Beetle, Steraspis speciosa (Coleoptera, Buprestidae), Feeding on Acacia Trees in Saudi Arabia Alanazi NA, Ghorbel M, Brini F, Mseddi K Life (Basel) 02-Dec-2022
PMCID:PMC9782656
doi:10.3390/life12122015
PMID:36556380
Morphological, Molecular and Metabolic Characterization of the Pigmented Fungus Subramaniula asteroids El-Sayed H, Osman ME, Abdelsalam A, Boroujerdi A, Sonbol H, Elsaba YM J Fungi (Basel) 29-Oct-2022
PMCID:PMC9699277
doi:10.3390/jof8111149
PMID:36354915
Phytochemical Composition and Bioactivities of Aqueous Extract of Rambutan (Nephelium lappaceum L. cv. Rong Rian) Peel Jantapaso H, Mittraparp-arthorn P Antioxidants (Basel) 12-May-2022
PMCID:PMC9137458
doi:10.3390/antiox11050956
PMID:35624820
Climate change and hydrological regime in arid lands: Impacts of dams on the plant diversity, vegetation structure and soil in Saudi Arabia Al-Munqedhi BM, El-Sheikh MA, Alfarhan AH, Alkahtani AM, Arif IA, Rajagopal R, Alharthi ST Saudi J Biol Sci 25-Jan-2022
PMCID:PMC9280318
doi:10.1016/j.sjbs.2022.01.043
PMID:35844430
Comparative Phytochemical Profile and Biological Activity of Four Major Medicinal Halophytes from Qassim Flora Mohammed HA, Ali HM, Qureshi KA, Alsharidah M, Kandil YI, Said R, Mohammed SA, Al-Omar MS, Rugaie OA, Abdellatif AA, Abd-Elmoniem E, Abbas MM, Mohany KM, Khan RA Plants (Basel) 18-Oct-2021
PMCID:PMC8538075
doi:10.3390/plants10102208
PMID:34686017
Midden site selection in Dorcas gazelle: Larger is not always better Soultan A, Nagy A, Attum O Ecol Evol 22-Sep-2021
PMCID:PMC8525146
doi:10.1002/ece3.8141
PMID:34707807
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
Climatic Zone and Soil Properties Determine the Biodiversity of the Soil Bacterial Communities Associated to Native Plants from Desert Areas of North-Central Algeria Bona E, Massa N, Toumatia O, Novello G, Cesaro P, Todeschini V, Boatti L, Mignone F, Titouah H, Zitouni A, Lingua G, Vuolo F, Gamalero E Microorganisms 23-Jun-2021
PMCID:PMC8303931
doi:10.3390/microorganisms9071359
PMID:34201731
Ecology of inland sand dunes “nafuds” as a hyper-arid habitat, Saudi Arabia: Floristic and plant associations diversity El-Sheikh MA, Thomas J, Arif IA, El-Sheikh HM Saudi J Biol Sci 08-Dec-2020
PMCID:PMC7938194
doi:10.1016/j.sjbs.2020.12.002
PMID:33732034
Antimicrobial and Antioxidant Activities of Different Extracts from Different Parts of Zilla spinosa (L.) Prantl Suleiman MH, Ateeg AA Evid Based Complement Alternat Med 03-Dec-2020
PMCID:PMC7728470
doi:10.1155/2020/6690433
PMID:33343678
Influence of Maternal Habitat on Salinity Tolerance of Zygophyllum coccineum with Regard to Seed Germination and Growth Parameters Mohamed E, Kasem AM, Gobouri AA, Elkelish A, Azab E Plants (Basel) 06-Nov-2020
PMCID:PMC7694771
doi:10.3390/plants9111504
PMID:33172127
Botanical Products in the Treatment and Control of Schistosomiasis: Recent Studies and Distribution of Active Plant Resources According to Affected Regions Duarte Galhardo de Albuquerque RD, Mahomoodally MF, Lobine D, Suroowan S, Rengasamy KR Biology (Basel) 13-Aug-2020
PMCID:PMC7464741
doi:10.3390/biology9080223
PMID:32823660
Changes in chemical composition of Zilla spinosa Forssk. medicinal plants grown in Saudi Arabia in response to spatial and seasonal variations Al-Qahtani H, Alfarhan AH, Al-Othman ZM Saudi J Biol Sci 26-Jun-2020
PMCID:PMC7499393
doi:10.1016/j.sjbs.2020.06.035
PMID:32994735

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 / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(Z)-hex-3-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 5318045 Click to see CCC=CCCOC1C(C(C(C(O1)CO)O)O)O 262.30 unknown via CMAUP database
methyl 4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanoate 10564679 Click to see COC(=O)CCCOC1C(C(C(C(O1)CO)O)O)O 280.27 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Menthiafolic acid, (S)- 10845194 Click to see CC(=CCCC(C)(C=C)O)C(=O)O 184.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
Carvacrol 10364 Click to see CC1=C(C=C(C=C1)C(C)C)O 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-trans-Carveol 94221 Click to see CC1=CCC(CC1O)C(=C)C 152.23 unknown via CMAUP database
(+)-alpha-Phellandrene 443160 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown via CMAUP database
(+)-Dihydrocarvone 22227 Click to see CC1CCC(CC1=O)C(=C)C 152.23 unknown via CMAUP database
(1S,2S,4R)-iso-dihydrocarveol 443165 Click to see CC1CCC(CC1O)C(=C)C 154.25 unknown via CMAUP database
(1S,4S)-Dihydrocarvone 443183 Click to see CC1CCC(CC1=O)C(=C)C 152.23 unknown via CMAUP database
(2S,5S)-5-[(2S)-1,2-dihydroxypropan-2-yl]-2-methylcyclohexan-1-one 10867057 Click to see CC1CCC(CC1=O)C(C)(CO)O 186.25 unknown via CMAUP database
(4s,8r)-8,9-Dihydroxy-p-menth-1(6)-en-2-one 11830092 Click to see CC1=CCC(CC1=O)C(C)(CO)O 184.23 unknown via CMAUP database
(5S)-5-[(2S)-1,2-dihydroxypropan-2-yl]-2-methylcyclohex-2-en-1-one 10877793 Click to see CC1=CCC(CC1=O)C(C)(CO)O 184.23 unknown via CMAUP database
alpha-Terpinene 7462 Click to see CC1=CC=C(CC1)C(C)C 136.23 unknown via CMAUP database
Carvone, (-)- 439570 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown via CMAUP database
Carvone, (+)- 16724 Click to see CC1=CCC(CC1=O)C(=C)C 150.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,4R)-4-[(E,3R)-3-hydroxybut-1-enyl]-3,5,5-trimethylcyclohex-2-en-1-ol 101338767 Click to see CC1=CC(CC(C1C=CC(C)O)(C)C)O 210.31 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(1S,2R,4R,8R)-2-(beta-D-Glucopyranosyloxy)-p-menthane-8,9-diol 102021736 Click to see CC1CCC(CC1OC2C(C(C(C(O2)CO)O)O)O)C(C)(CO)O 350.40 unknown via CMAUP database
(1S,2R,4R,8S)-2-(beta-D-Glucopyranosyloxy)-p-menthane-8,9-diol 11727818 Click to see CC1CCC(CC1OC2C(C(C(C(O2)CO)O)O)O)C(C)(CO)O 350.40 unknown via CMAUP database
(1S,2S,4R)-2-(6-O-D-Apio-beta-D-furanosyl-beta-D-glucopyranosyloxy)-p-mentha-8-ene-1-ol 10885097 Click to see CC(=C)C1CCC(C(C1)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O)(C)O 464.50 unknown via CMAUP database
(2R,3R,4S,5S,6R)-2-[(2E,6E)-8-hydroxy-3,7-dimethylocta-2,6-dienoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 14729929 Click to see CC(=CCOC1C(C(C(C(O1)CO)O)O)O)CCC=C(C)CO 332.39 unknown via CMAUP database
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(1S,2S,5R)-2-hydroxy-2-methyl-5-prop-1-en-2-ylcyclohexyl]oxyoxane-3,4,5-triol 11823766 Click to see CC(=C)C1CCC(C(C1)OC2C(C(C(C(O2)CO)O)O)O)(C)O 332.39 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[(1S,2S,5R)-2-hydroxy-5-(2-hydroxypropan-2-yl)-2-methylcyclohexyl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 11810246 Click to see CC1(CCC(CC1OC2C(C(C(C(O2)CO)O)O)O)C(C)(C)O)O 350.40 unknown via CMAUP database
(2S,5S)-5-[(2S)-2-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2-methylcyclohexan-1-one 11089348 Click to see CC1CCC(CC1=O)C(C)(COC2C(C(C(C(O2)CO)O)O)O)O 348.39 unknown via CMAUP database
(5S)-5-[(2S)-2-hydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-2-methylcyclohex-2-en-1-one 11024434 Click to see CC1=CCC(CC1=O)C(C)(COC2C(C(C(C(O2)CO)O)O)O)O 346.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
Umbelliprenin 1781413 Click to see CC(=CCCC(=CCCC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)C)C)C 366.50 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
5-Methyluridine 445408 Click to see CC1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 258.23 unknown via CMAUP database
Uridine 6029 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides / Pyrimidine 2-deoxyribonucleosides
Thymidine 5789 Click to see CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O 242.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
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
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Polyols / 1,2-diols
(2R,3R,4S)-pentane-1,2,3,4-tetrol 10796790 Click to see CC(C(C(CO)O)O)O 136.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
5-Deoxy-D-ribitol 166761 Click to see CC(C(C(CO)O)O)O 136.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucosinolates / Alkylglucosinolates
1-S-[3-hydroxy-N-(sulfooxy)pent-4-enimidoyl]-1-thio-beta-D-glucopyranose 138453913 Click to see C=CC(CC(=NOS(=O)(=O)O)SC1C(C(C(C(O1)CO)O)O)O)O 389.40 unknown https://doi.org/10.1021/NP50010A018
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(1S,2S,4R)-2-hydroxy-1-methyl-4-prop-1-en-2-ylcyclohexyl]oxyoxane-3,4,5-triol 11099619 Click to see CC(=C)C1CCC(C(C1)O)(C)OC2C(C(C(C(O2)CO)O)O)O 332.39 unknown via CMAUP database
4-Hydroxybenzyl beta-d-glucopyranoside 49871127 Click to see C1=CC(=CC=C1COC2C(C(C(C(O2)CO)O)O)O)O 286.28 unknown via CMAUP database
Benzyl beta-d-glucopyranoside 188977 Click to see C1=CC=C(C=C1)COC2C(C(C(C(O2)CO)O)O)O 270.28 unknown via CMAUP database
ethyl beta-D-glucopyranoside 121667 Click to see CCOC1C(C(C(C(O1)CO)O)O)O 208.21 unknown via CMAUP database
glycerol 2-O-alpha-l-fucopyranoside 101159096 Click to see CC1C(C(C(C(O1)OC(CO)CO)O)O)O 238.23 unknown via CMAUP database
Icariside F2 14079045 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)(CO)O 402.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[3-methoxy-5-prop-2-enyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenoxy]oxane-3,4,5-triol 15714546 Click to see COC1=C(C(=CC(=C1)CC=C)OC2C(C(C(C(O2)CO)O)O)O)OC3C(C(C(C(O3)CO)O)O)O 504.50 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[4-[(2S)-2,3-dihydroxypropyl]-3-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 102021738 Click to see COC1=C(C=CC(=C1)OC2C(C(C(C(O2)CO)O)O)O)CC(CO)O 360.36 unknown via CMAUP database
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown via CMAUP database
Gastrodin 115067 Click to see C1=CC(=CC=C1CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
1-Deoxy-D-glucitol 10678630 Click to see CC(C(C(C(CO)O)O)O)O 166.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
2-C-methyl-D-erythritol 11400799 Click to see CC(CO)(C(CO)O)O 136.15 unknown via CMAUP database
D-Threitol 169019 Click to see C(C(C(CO)O)O)O 122.12 unknown via CMAUP database
Erythritol 222285 Click to see C(C(C(CO)O)O)O 122.12 unknown via CMAUP database
Glycerin 753 Click to see C(C(CO)O)O 92.09 unknown via CMAUP database
L-Apiitol 10820745 Click to see C(C(C(CO)(CO)O)O)O 152.15 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Apiole 10659 Click to see COC1=C2C(=C(C(=C1)CC=C)OC)OCO2 222.24 unknown via CMAUP database
Dillapiol 10231 Click to see COC1=C(C2=C(C=C1CC=C)OCO2)OC 222.24 unknown via CMAUP database
Safrole 5144 Click to see C=CCC1=CC2=C(C=C1)OCO2 162.18 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Anethofuran 126537 Click to see CC1COC2C1CCC(=C2)C 152.23 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(4S,5R)-4-hydroxy-5-(hydroxymethyl)dihydrofuran-2(3H)-one 161815 Click to see C1C(C(OC1=O)CO)O 132.11 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Graveolone 177751 Click to see CC1(CC(=O)C2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 244.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
Querciturone 5274585 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 478.40 unknown via CMAUP database

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