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Taxillus kaempferi

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644047c600f53947519956
Scientific name Taxillus kaempferi
Authority (DC.) Danser
First published in Verh. Kon. Akad. Wetensch., Afd. Natuurk., Sect. 2 , 29(6): 124 (1933)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Phyllodesmis kaempferi Tiegh. Bull. Soc. Bot. France 43: 188 (1896)
Viscum kaempferi DC. Prodr. 4: 285 (1830)
Loranthus kaempferi (DC.) Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 22: 230 (1876)

Common names Top

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Language Common/alternative name
Japanese マツグミ
Chinese 小叶钝果寄生
Chinese 华东松寄生
Chinese 松胡颓子
Chinese 茑萝松

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Taxillus kaempferi var. grandiflora H.S.Kiu Acta Phytotax. Sin. 21: 177 (1983)
Taxillus kaempferi var. obovata Hatus. J. Phytogeogr. Taxon. 35: 63 (1987)

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 South-central
      • China Southeast
    • Eastern Asia
      • Japan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001075797
Tropicos 19102837
KEW urn:lsid:ipni.org:names:552147-1
The Plant List tro-19102837
Open Tree Of Life 5746842
NCBI Taxonomy 2918413
IPNI 552147-1
iNaturalist 510236
GBIF 7287913
Freebase /m/0_qfn70
EPPO TXLKA
EOL 2872700
Wikipedia Taxillus_kaempferi

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
The α-glucosidase inhibitory activity of avicularin and 4-O-methyl gallic acid isolated from Syzygium myrtifolium leaves Nor I, Wirasutisna KR, Hartati R, Insanu M Saudi Pharm J 19-Jun-2023
PMCID:PMC10336581
doi:10.1016/j.jsps.2023.06.010
PMID:37448844
Inhibition of the main protease of SARS-CoV-2 (Mpro) by repurposing/designing drug-like substances and utilizing nature’s toolbox of bioactive compounds Antonopoulou I, Sapountzaki E, Rova U, Christakopoulos P Comput Struct Biotechnol J 14-Mar-2022
PMCID:PMC8920478
doi:10.1016/j.csbj.2022.03.009
PMID:35308802
Natural derivatives with dual binding potential against SARS-CoV-2 main protease and human ACE2 possess low oral bioavailability: a brief computational analysis Sharma P, Shanavas A J Biomol Struct Dyn 21-Jul-2020
PMCID:PMC7441762
doi:10.1080/07391102.2020.1794970
PMID:32691697
cis–trans Isomerization of silybins A and B Novotná M, Gažák R, Biedermann D, Di Meo F, Marhol P, Kuzma M, Bednárová L, Fuksová K, Trouillas P, Křen V Beilstein J Org Chem 08-May-2014
PMCID:PMC4077359
doi:10.3762/bjoc.10.105
PMID:24991256
African Mistletoes (Loranthaceae); Ethnopharmacology, Chemistry and Medicinal Values: An Update Adesina SK, Illoh HC, Johnny II, Jacobs IE Afr J Tradit Complement Altern Med 16-May-2013
PMCID:PMC3794408
doi:10.4314/ajtcam.v10i4.26
PMID:24146518
Chemical Studies on the Mistletoe. V. The Structure of Taxillusin, a New Flavonoid Glycoside Isolated from <i>Taxillus kaempferi</i> Atsushi Sakurai, Yasuaki Okumura Oxford University Press (OUP) 26-Jul-2006
doi:10.1246/BCSJ.56.542
Chemical Studies on the Mistletoe. IV. The Structure of Isoglucodistylin, a New Flavonoid Glycoside Isolated from <i>Taxillus kaempferi</i> Atsushi Sakurai, Kyoji Okada, Yasuaki Okumura Oxford University Press (OUP) 26-Jul-2006
doi:10.1246/BCSJ.55.3051
Oncopharmacological Perspectives of a Plant Lectin (Viscum album Agglutinin-I): Overview of Recent Results from In vitro Experiments and In vivo Animal Models, and Their Possible Relevance for Clinical Applications Hajtó T, Hostanska K, Berki T, Pálinkás L, Boldizsár F, Németh P Evid Based Complement Alternat Med 28-Jan-2005
PMCID:PMC1062151
doi:10.1093/ecam/neh058
PMID:15841279
[The constituents of Taxillus kaempferi and the host, Pinus thunbergii. I. Catechins and flavones of Taxillus kaempferi]. Konishi T, Nishio T, Kiyosawa S, Fujiwara Y, Konoshima T Yakugaku Zasshi 01-Feb-1996
doi:10.1248/YAKUSHI1947.116.2_148
PMID:8717281

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 / Cinnamic acids and derivatives / Cinnamic acid esters
Cinnamyl cinnamate 1550890 Click to see C1=CC=C(C=C1)C=CCOC(=O)C=CC2=CC=CC=C2 264.30 unknown https://doi.org/10.1248/YAKUSHI1947.116.2_148
https://doi.org/10.1246/BCSJ.56.542
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
Procyanidin B3 146798 Click to see 578.50 unknown https://doi.org/10.1248/YAKUSHI1947.116.2_148
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1248/YAKUSHI1947.116.2_148
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3S)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 21721950 Click to see 466.40 unknown https://doi.org/10.1246/BCSJ.55.3051
[6-[[2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-4-oxo-2,3-dihydrochromen-3-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3,4,5-trihydroxybenzoate 14406831 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O 618.50 unknown https://doi.org/10.1246/BCSJ.56.542
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown https://doi.org/10.1248/YAKUSHI1947.116.2_148
Glucodistylin 14187088 Click to see 466.40 unknown https://doi.org/10.1246/BCSJ.55.3051
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1248/YAKUSHI1947.116.2_148
Quercitrin 5280459 Click to see 448.40 unknown https://doi.org/10.1248/YAKUSHI1947.116.2_148

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