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Searsia leptodictya

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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 UUID643ffc8f9b1b7724267505
Scientific name Searsia leptodictya
Authority (Diels) T.S.Yi, A.J.Mill. & J.Wen
First published in Molec. Phylogen. Evol. 33: 864 (2004)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rhus rhombocarpa R.Fern. & A.Fern. Bol. Soc. Brot. , sér. 2, 39: 253 (1965)
Rhus leptodictya Diels Bot. Jahrb. Syst. 40: 86 (1907)
Rhus amerina Meikle Mem. New York Bot. Gard. 8: 243 (1953)

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Africa
    • South Tropical Africa
      • Angola
      • Malawi
      • Mozambique
      • Zimbabwe
    • Southern Africa
      • Botswana
      • Free State
      • Namibia
      • Northern Provinces
      • Swaziland

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000434886
KEW urn:lsid:ipni.org:names:77063303-1
The Plant List kew-2479771
Open Tree Of Life 77306
NCBI Taxonomy 298679
IUCN Red List 149511786
IPNI 77063303-1
iNaturalist 593890
GBIF 7321777
USDA GRIN 457926
CMAUP NPO1828

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
Anti-Biofilm, Antibacterial, and Anti-Quorum Sensing Activities of Selected South African Plants Traditionally Used to Treat Diarrhoea Adeyemo RO, Famuyide IM, Dzoyem JP, Lyndy Joy M Evid Based Complement Alternat Med 28-Sep-2022
PMCID:PMC9534605
doi:10.1155/2022/1307801
PMID:36212949
The Xanthophyll Carotenoid Lutein Reduces the Invasive Potential of Pseudomonas aeruginosa and Increases Its Susceptibility to Tobramycin Mahavy CE, Mol A, Andrianarisoa B, Duez P, Jaziri ME, Baucher M, Rasamiravaka T Int J Mol Sci 28-Jun-2022
PMCID:PMC9266958
doi:10.3390/ijms23137199
PMID:35806201
Effect of Soil Type: Qualitative and Quantitative Analysis of Phytochemicals in Some Browse Species Leaves Found in Savannah Biome of South Africa Mudau HS, Mokoboki HK, Ravhuhali KE, Mkhize Z Molecules 22-Feb-2022
PMCID:PMC8911906
doi:10.3390/molecules27051462
PMID:35268563
Nutrients Profile of 52 Browse Species Found in Semi-Arid Areas of South Africa for Livestock Production: Effect of Harvesting Site Mudau HS, Mokoboki HK, Ravhuhali KE, Mkhize Z Plants (Basel) 07-Oct-2021
PMCID:PMC8538619
doi:10.3390/plants10102127
PMID:34685937
Effects of rainfall, temperature and photoperiod on the phenology of ephemeral resources for selected bushveld woody plant species in southern Africa Barrett A, Brown L PLoS One 11-May-2021
PMCID:PMC8112890
doi:10.1371/journal.pone.0251421
PMID:33975332
In vitro antibacterial activity of Loxostylis alata extracts and isolated compounds against Salmonella species Gado DA, Abdalla MA, Ahmed AS, Madikizela B, Nkadimeng SM, Ehlers MM, McGaw LJ BMC Complement Med Ther 13-Apr-2021
PMCID:PMC8042679
doi:10.1186/s12906-021-03292-4
PMID:33849505
Different Inhibitory Potencies of Oseltamivir Carboxylate, Zanamivir, and Several Tannins on Bacterial and Viral Neuraminidases as Assessed in a Cell-Free Fluorescence-Based Enzyme Inhibition Assay Quosdorf S, Schuetz A, Kolodziej H Molecules 17-Nov-2017
PMCID:PMC6150325
doi:10.3390/molecules22111989
PMID:29149072
The utilization and management of plant resources in rural areas of the Limpopo Province, South Africa Rasethe MT, Semenya SS, Potgieter MJ, Maroyi A J Ethnobiol Ethnomed 16-Apr-2013
PMCID:PMC3643856
doi:10.1186/1746-4269-9-27
PMID:23590903
Ethnopharmacological Survey of Plants Used in the Traditional Treatment of Gastrointestinal Pain, Inflammation and Diarrhea in Africa: Future Perspectives for Integration into Modern Medicine Stark TD, Mtui DJ, Balemba OB Animals (Basel) 04-Mar-2013
PMCID:PMC4495512
doi:10.3390/ani3010158
PMID:26487315

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
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Crinine- and Haemanthamine-type amaryllidaceae alkaloids
(+)-epi-Vittatine 12304132 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
(1R,13R,15S,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 40469675 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
(1S,11S,13S,15R,18R)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraene-11,18-diol 101297739 Click to see COC1CC2C3(C=C1)C(CN2C(C4=CC5=C(C=C34)OCO5)O)O 317.34 unknown via CMAUP database
(1S,13R,15R,18S)-15-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-18-ol 42579248 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
[(1S,13R,15R)-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,16-tetraen-15-yl] acetate 101935954 Click to see CC(=O)OC1CC2C3(CCN2CC4=CC5=C(C=C43)OCO5)C=C1 313.30 unknown via CMAUP database
3-O-Acetylhamayne 443671 Click to see CC(=O)OC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 329.30 unknown via CMAUP database
Crinamidine 399204 Click to see COC1=C2CN3CCC4(C3CC(C5C4O5)O)C2=CC6=C1OCO6 317.34 unknown via CMAUP database
Crinamin 73620 Click to see COC1CC2C3(C=C1)C(CN2CC4=CC5=C(C=C34)OCO5)O 301.34 unknown via CMAUP database
O-Demethylhaemanthamine 44445844 Click to see C1C(C=CC23C1N(CC2O)CC4=CC5=C(C=C34)OCO5)O 287.31 unknown via CMAUP database
Vittatine 443693 Click to see C1CN2CC3=CC4=C(C=C3C15C2CC(C=C5)O)OCO4 271.31 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Lycorine-type amaryllidaceae alkaloids
Lycorine 72378 Click to see C1CN2CC3=CC4=C(C=C3C5C2C1=CC(C5O)O)OCO4 287.31 unknown via CMAUP database
> Alkaloids and derivatives / Amaryllidaceae alkaloids / Tazettine-type amaryllidaceae alkaloids
(1S,11S,13R,16S,18R)-11-ethoxy-18-methoxy-15-methyl-5,7,12-trioxa-15-azapentacyclo[11.7.0.01,16.02,10.04,8]icosa-2,4(8),9,19-tetraene 15483834 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4N(CC5O1)C)OC)OCO3 359.40 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
6-(4-Hydroxyphenyl)-1,3-benzodioxole-5-carbaldehyde 15549895 Click to see C1OC2=C(O1)C=C(C(=C2)C=O)C3=CC=C(C=C3)O 242.23 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
N-Desmethyl-8alpha-ethoxypretazettine 15483835 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown via CMAUP database
N-Desmethyl-8beta-ethoxypretazettine 15483836 Click to see CCOC1C2=CC3=C(C=C2C45C=CC(CC4NCC5O1)OC)OCO3 345.40 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Benzoquinolines / Phenanthridines and derivatives
(1S,13R)-9-methoxy-5,7-dioxa-12-azapentacyclo[10.5.2.01,13.02,10.04,8]nonadeca-2,4(8),9,14,16-pentaene 21723147 Click to see COC1=C2CN3CCC4(C3C=CC=C4)C2=CC5=C1OCO5 283.32 unknown via CMAUP database
1-Epideacetylbowdensine 443673 Click to see COC1=C2CN3CCC4(C3CCC(C4O)O)C2=CC5=C1OCO5 319.40 unknown via CMAUP database
7H-Pyrrolo(3,2,1-de)phenanthridin-7-one, 10-hydroxy-9-methoxy- 5488695 Click to see COC1=C(C=C2C3=CC=CC4=C3N(C=C4)C(=O)C2=C1)O 265.26 unknown via CMAUP database
Hippacine 10015025 Click to see C1=CC2=C3C(=C1)C4=CC(=C(C=C4C(=O)N3C=C2)O)O 251.24 unknown via CMAUP database
Hippadine 100605 Click to see C1OC2=C(O1)C=C3C(=C2)C4=CC=CC5=C4N(C3=O)C=C5 263.25 unknown via CMAUP database
Pratorimine 181937 Click to see COC1=C(C=C2C(=C1)C3=CC=CC4=C3N(C2=O)C=C4)O 265.26 unknown via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines / 4-phenyltetrahydroisoquinolines
Cherylline 90075 Click to see CN1CC(C2=CC(=C(C=C2C1)O)OC)C3=CC=C(C=C3)O 285.34 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Liquiritigenin 114829 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)O 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3',4'-Dihydroxy-7-methoxyflavan 14157886 Click to see COC1=CC2=C(CCC(O2)C3=CC(=C(C=C3)O)O)C=C1 272.29 unknown via CMAUP database
Guibourtinidol-7-methyl ether 15549896 Click to see COC1=CC2=C(CC(C(O2)C3=CC=C(C=C3)O)O)C=C1 272.29 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
(2S)-7-hydroxy-8-methoxy-2-phenyl-2,3-dihydrochromen-4-one 15549894 Click to see COC1=C(C=CC2=C1OC(CC2=O)C3=CC=CC=C3)O 270.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
4-Hydroxy-2',4'-dimethoxydihydrochalcone 15549893 Click to see COC1=CC(=C(C=C1)C(=O)CCC2=CC=C(C=C2)O)OC 286.32 unknown via CMAUP database

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