Buddleja albiflora - Unknown
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Internal ID UUID64400e0493abf303216545
Scientific name Buddleja albiflora
Authority Hemsl.
First published in J. Linn. Soc., Bot. 26: 118 (1889)

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Synonyms Top

Scientific name Authority First published in
Buddleja albiflora var. geraldii (Diels) Rehder & E.H.Wilson Pl. Wilson. 1: 569 1913
Buddleja giraldii Diels Bot. Jahrb. Syst. 29: 535 (1900)
Buddleja hemsleyana Koehne Gartenflora 52: 169 (1903)
Buddleja albiflora var. hemsleyana (Koehne) C.K.Schneid.

Common names Top

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Language Common/alternative name
Chinese 巴东醉鱼草
Chinese 醉鱼草
Chinese 白花醉鱼草

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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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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000573902
Tropicos 19001185
INPN 86866
KEW urn:lsid:ipni.org:names:545674-1
The Plant List kew-2685297
Open Tree Of Life 5522108
Observations.org 115639
NCBI Taxonomy 1503305
IPNI 545674-1
iNaturalist 446883
iNaturalist 446881
iNaturalist 446882
GBIF 4055853
Freebase /m/0gkxch8
EPPO BUDAB
EOL 2892383
Elurikkus 458376
USDA GRIN 8071
Wikipedia Buddleja_albiflora

Genomes (via NCBI) Top

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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
Interactions of naturally occurring compounds with antimicrobials Malczak I, Gajda A J Pharm Anal 23-Sep-2023
PMCID:PMC10785267
doi:10.1016/j.jpha.2023.09.014
PMID:38223447
Wood and bark structure in Buddleja: anatomical background of stem morphology Frankiewicz KE, Chau JH, Baczyński J, Wdowiak A, Oskolski A AoB Plants 24-Jan-2023
PMCID:PMC10060081
doi:10.1093/aobpla/plad003
PMID:37007612
Insecticidal and Enzyme Inhibition Activities of Leaf/Bark Extracts, Fractions, Seed Oil and Isolated Compounds from Triadica sebifera (L.) Small against Aphis craccivora Koch Dolma SK, Singh PP, Reddy SG Molecules 18-Mar-2022
PMCID:PMC8954943
doi:10.3390/molecules27061967
PMID:35335330
Impacts of growth form and phylogenetic relatedness on seed germination: A large‐scale analysis of a subtropical regional flora Wang J, Xu G, Chen W, Ma Y, Qi W, Zhang C, Cui X Ecol Evol 07-Jan-2021
PMCID:PMC7863672
doi:10.1002/ece3.7132
PMID:33598130
Comparison of taxon‐specific versus general locus sets for targeted sequence capture in plant phylogenomics Chau JH, Rahfeldt WA, Olmstead RG Appl Plant Sci 31-Mar-2018
PMCID:PMC5895190
doi:10.1002/aps3.1032
PMID:29732262
Responses to shading of naturalized and non-naturalized exotic woody species Feng Y, van Kleunen M Ann Bot 13-Aug-2014
PMCID:PMC4171072
doi:10.1093/aob/mcu163
PMID:25122655
Quantitative determination of total and individual flavonoids in stems and leaves of Buddleja davidii and Buddleja albiflora Ying C, Wan D Pharmacogn Mag 01-Oct-2012
PMCID:PMC3785164
doi:10.4103/0973-1296.103651
PMID:24082630
Buddlejone, a diterpene from Buddleja albiflora Peter J. Houghton, Tibebe Z. Woldemariam, Maria Candau, Anthony Barnardo, Omodele Khen-Alafun, Li Shangxiao Elsevier BV 23-Apr-2003
doi:10.1016/0031-9422(96)00001-5
Early stages in the biosynthesis of aucubin and harpagide. Deuterium labelling studies Søren Damtoft, Søren Rosendal Jensen, Inge Weiergang Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)90574-0

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
[1-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,7a-tetrahydrocyclopenta[c]pyran-7-yl]methyl 4-hydroxybenzoate 163038698 Click to see C1C=C(C2C1C=COC2OC3C(C(C(C(O3)CO)O)O)O)COC(=O)C4=CC=C(C=C4)O 450.40 unknown https://doi.org/10.1016/0031-9422(96)00001-5
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown https://doi.org/10.1016/S0031-9422(00)90574-0
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(1S,2R,3R,9S,10S,17S)-2-[(2R,3R)-3-(3,5-dihydroxyphenyl)-6-hydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-1-benzofuran-4-yl]-3,9,17-tris(4-hydroxyphenyl)-8-oxapentacyclo[8.7.2.04,18.07,19.011,16]nonadeca-4(18),5,7(19),11(16),12,14-hexaene-5,13,15-triol 21606288 Click to see C1=CC(=CC=C1C2C(C3C(C4=C(C=C(C=C4O)O)C5C(OC6=C5C3=C2C(=C6)O)C7=CC=C(C=C7)O)C8=CC=C(C=C8)O)C9=C1C(C(OC1=CC(=C9)O)C1=CC=C(C=C1)O)C1=CC(=CC(=C1)O)O)O 906.90 unknown https://doi.org/10.1016/0031-9422(96)00001-5

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