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Internal ID UUID643fe13e8e460112141982
Scientific name Leucas urticifolia
Authority (Vahl) Sm.
First published in Cycl. 20: n.º 4 (1812)

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Synonyms Top

Scientific name Authority First published in
Leucas affinis R.Br. Voy. Abyss. : 64 (1814)
Phlomis urticifolia Vahl Symb. Bot. 3: 76 (1794)
Eneodon urticifolia (Vahl) Raf. Fl. Tellur. 3: 88 (1837)
Hemistoma ovatum Ehrenb. ex Benth. Pl. Asiat. Rar. 1: 60 (1830)
Leucas urticifolia R.Br. Prodr. Fl. Nov. Holland. 504. 1810 [27 Mar 1810]

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Leucas urticifolia var. angustifolia Sebald Stuttgarter Beitr. Naturk., A 341: 137 (1980)
Leucas urticifolia var. annulata Sebald Stuttgarter Beitr. Naturk., A 341: 135 (1980)
Leucas urticifolia var. urticifolia Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Distribution (via Powo/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • East Tropical Africa
      • Kenya
      • Tanzania
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
      • Socotra
      • Somalia
      • Sudan
    • West Tropical Africa
      • Mauritania
  • Asia-temperate
    • Arabian Peninsula
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Afghanistan
      • Iran
  • Asia-tropical
    • Indian Subcontinent
      • India
      • Pakistan
      • West Himalaya

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000227199
KEW urn:lsid:ipni.org:names:60454705-2
The Plant List kew-111912
Open Tree Of Life 582412
NCBI Taxonomy 483843
IPNI 60454705-2
GBIF 7306949
USDA GRIN 401734

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
Potential of Halophytes as Sustainable Fodder Production by Using Saline Resources: A Review of Current Knowledge and Future Directions Hasnain M, Abideen Z, Ali F, Hasanuzzaman M, El-Keblawy A Plants (Basel) 29-May-2023
PMCID:PMC10255648
doi:10.3390/plants12112150
PMID:37299129
Important Medicinal and Food Taxa (Orders and Families) in Kenya, Based on Three Quantitative Approaches Mutie FM, Mbuni YM, Rono PC, Mkala EM, Nzei JM, Phumthum M, Hu GW, Wang QF Plants (Basel) 02-Mar-2023
PMCID:PMC10005506
doi:10.3390/plants12051145
PMID:36904005
Natural Inhibitors of Cholinesterases: Chemistry, Structure–Activity and Methods of Their Analysis Smyrska-Wieleba N, Mroczek T Int J Mol Sci 01-Feb-2023
PMCID:PMC9916849
doi:10.3390/ijms24032722
PMID:36769043
Antioxidant and anticholinesterase investigations of Rumex hastatus D. Don: potential effectiveness in oxidative stress and neurological disorders Ahmad S, Ullah F, Ayaz M, Sadiq A, Imran M Biol Res 26-Mar-2015
PMCID:PMC4381421
doi:10.1186/s40659-015-0010-2
PMID:25857346
A review: Ethnobotanical survey of genus Leucas Das SN, Patro VJ, Dinda SC Pharmacogn Rev 01-Jul-2012
PMCID:PMC3459451
doi:10.4103/0973-7847.99943
PMID:23055635
Leufolins A and B, Potent Butyrylcholinesterase-inhibiting Flavonoid Glucosides from Leucas urticifolia Noor AT, Fatima I, Ahmad I, Malik A, Afza N, Iqbal L, Latif M, Khan SB Molecules 19-Jul-2007
PMCID:PMC6149326
doi:10.3390/12071447
PMID:17909500

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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
[(2R,3S,4S,5R,6S)-6-[4-(6,8-dihydroxy-4-oxochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 163190278 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)C4=CC(=O)C5=C(O4)C(=CC(=C5)O)O)O)O)O)O 578.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149326/
[6-[4-(5,7-Dihydroxy-4-oxo-2,3-dihydrochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 77916003 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O 580.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149326/
[6-[4-(6,8-Dihydroxy-4-oxochromen-2-yl)phenoxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 163027463 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=CC=C(C=C3)C4=CC(=O)C5=C(O4)C(=CC(=C5)O)O)O)O)O)O 578.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149326/
leufolin A 70697844 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)OC4C(C(C(C(O4)COC(=O)C=CC5=CC=C(C=C5)O)O)O)O 580.50 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6149326/

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