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Rhododendron anthopogonoides

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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 UUID6440814d943f3345818713
Scientific name Rhododendron anthopogonoides
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 23: 350 (1877)

Description Top

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Synonyms Top

Scientific name Authority First published in
Azalea anthopogonoides (Maxim.) Kuntze Revis. Gen. Pl. 2: 387. 1891 [5 Nov 1891]

Common names Top

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Language Common/alternative name
Chinese 小叶枇杷
Chinese 安徽杜鹃
Chinese 烈香杜鹃

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Qinghai

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001219688
Tropicos 50001544
KEW urn:lsid:ipni.org:names:331935-1
The Plant List tro-50001544
Open Tree Of Life 5759940
NCBI Taxonomy 2575812
IPNI 331935-1
GBIF 7328149
EOL 2891231

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
Traditional Tibetan medicine: therapeutic potential in lung diseases Li C, Li Y, Huang X, Li S, Sangji K, Gu R Front Pharmacol 18-Mar-2024
PMCID:PMC10986185
doi:10.3389/fphar.2024.1365911
PMID:38567353
The complete chloroplast genome sequence of Rhododendron farrerae Tate ex Sweet (Ericaceae) Shen J, Huang L Mitochondrial DNA B Resour 04-Jan-2024
PMCID:PMC10769518
doi:10.1080/23802359.2023.2294897
PMID:38187010
Tibetan medicine Bang Jian: a comprehensive review on botanical characterization, traditional use, phytochemistry, and pharmacology Li Y, Zhang J, Fan JY, Zhong SH, Gu R Front Pharmacol 14-Dec-2023
PMCID:PMC10757618
doi:10.3389/fphar.2023.1295789
PMID:38161696
Antioxidant Capacity and Protective Effects on H2O2-Induced Oxidative Damage in PC12 Cells of the Active Fraction of Brassica rapa L. Wang J, Xiao S, Cai Q, Miao J, Li J Foods 22-May-2023
PMCID:PMC10217163
doi:10.3390/foods12102075
PMID:37238893
Exploring Contact Toxicity of Essential Oils against Sitophilus zeamais through a Meta-Analysis Approach Achimón F, Peschiutta ML, Brito VD, Beato M, Pizzolitto RP, Zygadlo JA, Zunino MP Plants (Basel) 13-Nov-2022
PMCID:PMC9696113
doi:10.3390/plants11223070
PMID:36432799
Current advances on the phytochemical composition, pharmacologic effects, toxicology, and product development of Phyllanthi Fructus Yan X, Li Q, Jing L, Wu S, Duan W, Chen Y, Chen D, Pan X Front Pharmacol 19-Oct-2022
PMCID:PMC9626985
doi:10.3389/fphar.2022.1017268
PMID:36339628
The Application of Pearls in Traditional Medicine of China and Their Chemical Constituents, Pharmacology, Toxicology, and Clinical Research Song Y, Chen W, Fu K, Wang Z Front Pharmacol 23-Aug-2022
PMCID:PMC9445187
doi:10.3389/fphar.2022.893229
PMID:36081944
Chemical constituents, antibacterial, acaricidal and anti-inflammatory activities of the essential oils from four Rhododendron species He J, Shang X, Dai L, Yang X, Li B, Wei Y, Zhang J, Pan H Front Vet Sci 10-Aug-2022
PMCID:PMC9399923
doi:10.3389/fvets.2022.882060
PMID:36032278
Nematicidal Effects of Volatile Organic Compounds from Microorganisms and Plants on Plant-Parasitic Nematodes Deng X, Wang X, Li G Microorganisms 12-Jun-2022
PMCID:PMC9228967
doi:10.3390/microorganisms10061201
PMID:35744719
Mass Spectrometry-Based Metabolomics of Phytocannabinoids from Non-Cannabis Plant Origins Sommano SR, Sunanta P, Leksawasdi N, Jantanasakulwong K, Rachtanapun P, Seesuriyachan P, Phimolsiripol Y, Sringarm K, Ruksiriwanich W, Jantrawut P, Chittasupho C Molecules 20-May-2022
PMCID:PMC9147514
doi:10.3390/molecules27103301
PMID:35630777
Effects of different intensities of long-term grazing on plant diversity, biomass and carbon stock in alpine shrubland on the Qinghai-Tibetan Plateau Wang J, Li W, Cao W, Wang S PeerJ 12-Jan-2022
PMCID:PMC8760858
doi:10.7717/peerj.12771
PMID:35070507
Meroterpenoids: A Comprehensive Update Insight on Structural Diversity and Biology Nazir M, Saleem M, Tousif MI, Anwar MA, Surup F, Ali I, Wang D, Mamadalieva NZ, Alshammari E, Ashour ML, Ashour AM, Ahmed I, E, Green IR, Hussain H Biomolecules 29-Jun-2021
PMCID:PMC8301922
doi:10.3390/biom11070957
PMID:34209734
Individual and Combined Inhalational Sedative Effects in Mice of Low Molecular Weight Aromatic Compounds Found in Agarwood Aroma Castro KP, Ito M Molecules 02-Mar-2021
PMCID:PMC7958121
doi:10.3390/molecules26051320
PMID:33801243
Recent advances in the synthesis of gem-dimethylcyclobutane natural products Hancock EN, Wiest JM, Brown MK Nat Prod Rep 16-Oct-2019
PMCID:PMC6739199
doi:10.1039/c8np00083b
PMID:30855044
Identification of Insecticidal Constituents from the Essential Oil from the Aerial Parts Stachys riederi var. japonica Quan M, Liu QZ, Liu ZL Molecules 17-May-2018
PMCID:PMC6099633
doi:10.3390/molecules23051200
PMID:29772795

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 / Salicylic acid and derivatives
Anthopogochromene A 46872461 Click to see CC1=CC2=C(C=CC(O2)(C)CCC=C(C)CC(=O)CC(C)C)C(=C1C(=O)O)O 386.50 unknown https://doi.org/10.1021/NP900543R
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
2,4-Dihydroxy-6-methyl-3-[(2E,6E)-3,7,11-trimethyl-2,6,10-dodecatrien-1-yl]benzoic acid; Grifolic acid 85080649 Click to see CC1=CC(=C(C(=C1C(=O)O)O)CC=C(C)CCC=C(C)CCC=C(C)C)O 372.50 unknown https://doi.org/10.1021/NP900543R
Grifolic acid 9976563 Click to see CC1=CC(=C(C(=C1C(=O)O)O)CC=C(C)CCC=C(C)CCC=C(C)C)O 372.50 unknown https://doi.org/10.1021/NP900543R
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
Anthopogochromane 46872460 Click to see CC1=CC2=C(C3C(C4(C3C(O2)(CCC4)C)C)C(=O)CC(C)C)C(=C1C(=O)O)O 386.50 unknown https://doi.org/10.1021/NP900543R

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