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Rhus punjabensis

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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 UUID6440443aafdef003337570
Scientific name Rhus punjabensis
Authority J.L.Stewart
First published in Forest Fl. N.W. India : 120 (1874)

Description Top

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Synonyms Top

Scientific name Authority First published in
Toxicodendron punjabense Kuntze Revis. Gen. Pl. 1: 154 (1891)

Common names Top

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Language Common/alternative name
Chinese 旁遮普麸杨

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Rhus punjabensis var. sinica (Diels) Rehder & E.H.Wilson Pl. Wilson. 2: 176. 1914 (1914)

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Tibet
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001049377
USDA Plants RHPU11
Tropicos 1300008
KEW urn:lsid:ipni.org:names:70803-1
The Plant List tro-1300008
Open Tree Of Life 598798
NCBI Taxonomy 298665
IUCN Red List 147027313
IPNI 70803-1
GBIF 3661835
EPPO RHUPN
EOL 2888763
USDA GRIN 31703
CMAUP NPO4075

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
Chemical Fingerprint Analysis and Content Determination of Horned Gallnut and Bellied Gallnut in Galla Chinensis Long X, Guo S, Gu J, Zhang L, Liu H, Fan Y, Wen W Int J Anal Chem 31-Dec-2023
PMCID:PMC10771921
doi:10.1155/2023/8849341
PMID:38188368
Differences of oribatid mite community and trophic structure between karst caves and surface different moss habitats Gong T, Yin X, Liu W, Chen H, Shi Z PLoS One 17-Aug-2023
PMCID:PMC10434907
doi:10.1371/journal.pone.0290144
PMID:37590253
Woody plant functional traits and phylogenetic signals correlate with urbanization in remnant forest patches Yang J, Wang Z, Pan Y, Zheng Y Ecol Evol 31-Jul-2023
PMCID:PMC10388403
doi:10.1002/ece3.10366
PMID:37529580
Pentagalloyl Glucose: A Review of Anticancer Properties, Molecular Targets, Mechanisms of Action, Pharmacokinetics, and Safety Profile Wen C, Dechsupa N, Yu Z, Zhang X, Liang S, Lei X, Xu T, Gao X, Hu Q, Innuan P, Kantapan J, Lü M Molecules 19-Jun-2023
PMCID:PMC10300743
doi:10.3390/molecules28124856
PMID:37375411
Biogenic Synthesis of Copper Nanoparticles: A Systematic Review of Their Features and Main Applications Luque-Jacobo CM, Cespedes-Loayza AL, Echegaray-Ugarte TS, Cruz-Loayza JL, Cruz I, de Carvalho JC, Goyzueta-Mamani LD Molecules 18-Jun-2023
PMCID:PMC10301071
doi:10.3390/molecules28124838
PMID:37375393
Updates on Biogenic Metallic and Metal Oxide Nanoparticles: Therapy, Drug Delivery and Cytotoxicity Nikolova MP, Joshi PB, Chavali MS Pharmaceutics 03-Jun-2023
PMCID:PMC10301310
doi:10.3390/pharmaceutics15061650
PMID:37376098
Molecular evolution and phylogenomic analysis of complete chloroplast genomes of Cotinus (Anacardiaceae) Liu Q, Yang N, Dong W, Zhao L Ecol Evol 29-May-2023
PMCID:PMC10227175
doi:10.1002/ece3.10134
PMID:37261318
Reports of Plant-Derived Nanoparticles for Prostate Cancer Therapy Elbagory AM, Hull R, Meyer M, Dlamini Z Plants (Basel) 03-May-2023
PMCID:PMC10181082
doi:10.3390/plants12091870
PMID:37176928
Advanced Phytochemical-Based Nanocarrier Systems for the Treatment of Breast Cancer Chavda VP, Nalla LV, Balar P, Bezbaruah R, Apostolopoulos V, Singla RK, Khadela A, Vora L, Uversky VN Cancers (Basel) 06-Feb-2023
PMCID:PMC9954440
doi:10.3390/cancers15041023
PMID:36831369
Targeting Apoptotic Pathway of Cancer Cells with Phytochemicals and Plant-Based Nanomaterials Wani AK, Akhtar N, Mir TU, Singh R, Jha PK, Mallik SK, Sinha S, Tripathi SK, Jain A, Jha A, Devkota HP, Prakash A Biomolecules 18-Jan-2023
PMCID:PMC9953589
doi:10.3390/biom13020194
PMID:36830564
Synthesis, biomedical applications, and toxicity of CuO nanoparticles Naz S, Gul A, Zia M, Javed R Appl Microbiol Biotechnol 13-Jan-2023
PMCID:PMC9838533
doi:10.1007/s00253-023-12364-z
PMID:36635395
Antimicrobial Activity of Silver Nanoparticles Synthesized by the Green Method Using Rhus coriaria L. Extract Against Oral Pathogenic Microorganisms Nazemi Salman B, Mohammadi Gheidari M, Yazdi nejad A, Zeighami H, Mohammadi A, Basir Shabestari S Med J Islam Repub Iran 15-Dec-2022
PMCID:PMC9832934
doi:10.47176/mjiri.36.154
PMID:36654848
Significance of Capping Agents of Colloidal Nanoparticles from the Perspective of Drug and Gene Delivery, Bioimaging, and Biosensing: An Insight Javed R, Sajjad A, Naz S, Sajjad H, Ao Q Int J Mol Sci 10-Sep-2022
PMCID:PMC9505579
doi:10.3390/ijms231810521
PMID:36142435
Mycosynthesis of Hematite (α-Fe2O3) Nanoparticles Using Aspergillus niger and Their Antimicrobial and Photocatalytic Activities Saied E, Salem SS, Al-Askar AA, Elkady FM, Arishi AA, Hashem AH Bioengineering (Basel) 17-Aug-2022
PMCID:PMC9404788
doi:10.3390/bioengineering9080397
PMID:36004922
Biosynthesis of Iron Oxide Nanoparticles: Physico-Chemical Characterization and Their In Vitro Cytotoxicity on Healthy and Tumorigenic Cell Lines Moacă EA, Watz CG, (Ionescu) DF, Păcurariu C, Tudoran LB, Ianoș R, Socoliuc V, Drăghici GA, Iftode A, Liga S, Dragoș D, Dehelean CA Nanomaterials (Basel) 10-Jun-2022
PMCID:PMC9230869
doi:10.3390/nano12122012
PMID:35745350

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
3,4,5-Trihydroxybenzoate 54675821 Click to see C1=C(C=C(C(=C1O)[O-])O)C(=O)O 169.11 unknown via CMAUP database
> 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 via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Betulonic acid 122844 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C(=O)O 454.70 unknown via CMAUP database
Moronic acid 489941 Click to see CC1(CCC2(CCC3(C(C2=C1)CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C)C(=O)O)C 454.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Depsides and depsidones
Digallic acid 341 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)O 322.22 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Agathisflavone 5281599 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4=C(C=C(C5=C4OC(=CC5=O)C6=CC=C(C=C6)O)O)O)O)O 538.50 unknown https://doi.org/10.1007/S10600-015-1336-2
Amentoflavone 5281600 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://doi.org/10.1007/S10600-015-1336-2
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Hinokiflavone 5281627 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)OC4=CC=C(C=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O 538.50 unknown https://doi.org/10.1007/S10600-015-1336-2

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