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Internal ID UUID64401fad2f266206951682
Scientific name Haloxylon scoparium
Authority Pomel
First published in Nouv. Mat. Fl. Atl. 2: 335 (1875)

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Synonyms Top

Scientific name Authority First published in
Arthrophytum scoparium (Pomel) Iljin Mater. Istorii Fl. Rastitel'n. S.S.S.R. 2: 222 (1946)
Arthrophytum scoparium (Pomel) Iljin ex Maire & Weiller Fl. Afrique N. 8: 161 (1962)
Hammada articulata subsp. scoparia (Pomel) O.Bolòs & Vigo Butl. Inst. Catalana Hist. Nat., Secc. Bot. 38(1): 89 (1974)
Hammada scoparia (Pomel) Iljin Bot. Zhurn. (Moscow & Leningrad) 33: 583 (1948)
Haloxylon articulatum var. scoparium (Pomel) Hochr. Annuaire Conserv. Jard. Bot. Genève 7-8: 133 1904
Haloxylon articulatum subsp. scoparium (Pomel) Batt. Fl. Algérie Dicot.: 765 1890

Common names Top

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Language Common/alternative name
English hammada scoparia
German hammada scoparia
French hammada scoparia

Subspecies (abbr. subsp./ssp.) Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • Northern Africa
      • Algeria
      • Egypt
      • Libya
      • Morocco
      • Tunisia
      • Western Sahara
    • West Tropical Africa
      • Mauritania
  • Asia-temperate
    • Western Asia
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000715248
KEW urn:lsid:ipni.org:names:165856-1
The Plant List kew-2838925
IPNI 165856-1
iNaturalist 495955
GBIF 3758941
EPPO HAXSC
Wikipedia Haloxylon_scoparium
Open Tree Of Life 3944081

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)!
Title Authors Publication Released IDs
Hammada scoparia flavonoids and rutin kill adherent and chemoresistant leukemic cells. Bourogaa E, Bertrand J, Despeaux M, Jarraya R, Fabre N, Payrastre L, Demur C, Fournié JJ, Damak M, Feki AE, Racaud-Sultan C Leuk Res 01-Aug-2011
doi:10.1016/J.LEUKRES.2010.12.011
PMID:21216465
HPLC-based activity profiling for GABA(A) receptor modulators: a new dihydroisocoumarin from Haloxylon scoparium. Li Y, Plitzko I, Zaugg J, Hering S, Hamburger M J Nat Prod 23-Apr-2010
doi:10.1021/NP900803W
PMID:20210326
Flavonol triglycosides from the leaves of Hammada scoparia (POMEL) ILJIN. Ben Salah H, Jarraya R, Martin MT, Veitch NC, Grayer RJ, Simmonds MS, Damak M Chem Pharm Bull (Tokyo) 01-Sep-2002
doi:10.1248/CPB.50.1268
PMID:12237550

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
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(S)-4-Methoxy-7-Phenyl-7,8-Dihydro(1,3)Dioxolo(4,5-G)Isochromen-5-One 46210741 Click to see 298.29 unknown https://doi.org/10.1021/NP900803W
4-Methoxy-7-phenyl-7,8-dihydro-[1,3]dioxolo[4,5-g]isochromen-5-one 75149544 Click to see COC1=C2C(=CC3=C1OCO3)CC(OC2=O)C4=CC=CC=C4 298.29 unknown https://doi.org/10.1021/NP900803W
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4S,5R,6R)-3-[(2S,3R,4R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxy-4,5-dihydroxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 11803230 Click to see 756.70 unknown https://doi.org/10.1248/CPB.50.1268
3-[(2S,3R,4S,5R,6R)-4,5-dihydroxy-3-[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-6-[[(2R,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 101925489 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 770.70 unknown https://doi.org/10.1248/CPB.50.1268
3-[(2S,3R,4S,5R,6R)-6-[[(2R,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 101190646 Click to see 756.70 unknown https://doi.org/10.1248/CPB.50.1268
3-[(2S,3R,4S,5R,6S)-6-[[(2R,3S,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)-2,3-dihydrochromen-4-one 162961495 Click to see 758.70 unknown https://doi.org/10.1248/CPB.50.1268
3-[(2S,3S,4S,5S,6R)-6-[[(2R,3S,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 163099535 Click to see 756.70 unknown https://doi.org/10.1248/CPB.50.1268
3-[6-[[3,5-Dihydroxy-6-methyl-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromen-4-one 73093860 Click to see 756.70 unknown https://doi.org/10.1248/CPB.50.1268
CID 14353383 14353383 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)OC)OC6C(C(C(C(O6)C)O)O)O)O)O)O)O)O 770.70 unknown https://doi.org/10.1248/CPB.50.1268
Isorhamnetin 3-(2G-apiosylrutinoside) 44259363 Click to see 756.70 unknown https://doi.org/10.1248/CPB.50.1268
Rutin 5280805 Click to see 610.50 unknown https://doi.org/10.1016/J.LEUKRES.2010.12.011
Vitamin P 5293655 Click to see 610.50 unknown https://doi.org/10.1016/J.LEUKRES.2010.12.011

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