Ainsliaea fragrans - Unknown
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Internal ID UUID643fcccf130c8433149188
Scientific name Ainsliaea fragrans
Authority Champ. ex Benth.
First published in Hooker's J. Bot. Kew Gard. Misc. 4: 236 (1852)

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Synonyms Top

Scientific name Authority First published in
Ainsliaea rubrifolia Franch. J. Bot. (Morot) viii. (1894) 296.
Ainsliaea integrifolia Makino Bot. Mag. (Tokyo) 22: 167 (1908)
Ainsliaea mollis Diels Repert. Spec. Nov. Regni Veg. Beih. 12: 514 (1922)
Ainsliaea asarifolia Hayata Icon. Pl. Formosan. 8: 71 (1919)
Ainsliaea ningpoensis Matsuda Bot. Mag. (Tokyo) 27: 236 (1913)

Common names Top

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Language Common/alternative name
Chinese 兔耳风
Chinese 杏香兔儿风
Chinese 杏香兔耳风
Chinese 红背兔儿风
Chinese 红走马胎
Chinese 金边兔耳
Chinese 香鬼督郵

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Varieties (abbr. var.) Top

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Name Authority First published in
Ainsliaea fragrans var. integrifolia (Maxim.) Kitam. Acta Phytotax. Geobot. 8: 67 (1939)

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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
      • Taiwan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000066400
UNII 5FG998PBC2
Tropicos 2745687
KEW urn:lsid:ipni.org:names:175724-1
The Plant List gcc-23285
Open Tree Of Life 119456
NCBI Taxonomy 418257
IPNI 175724-1
iNaturalist 709025
GBIF 3133817

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
Endophytic Microbes from Medicinal Plants in Fenghuang Mountain as a Source of Antibiotics Yang A, Hong Y, Zhou F, Zhang L, Zhu Y, Wang C, Hu Y, Yu L, Chen L, Wang X Molecules 28-Aug-2023
PMCID:PMC10488465
doi:10.3390/molecules28176301
PMID:37687129
Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C J Ethnobiol Ethnomed 30-May-2023
PMCID:PMC10230803
doi:10.1186/s13002-023-00594-4
PMID:37254191
Natural Blockers of PD-1/PD-L1 Interaction for the Immunotherapy of Triple-Negative Breast Cancer-Brain Metastasis Nakhjavani M, Shigdar S Cancers (Basel) 19-Dec-2022
PMCID:PMC9777321
doi:10.3390/cancers14246258
PMID:36551742
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
Tree Size Influences Leaf Shape but Does Not Affect the Proportional Relationship Between Leaf Area and the Product of Length and Width Ma J, Niklas KJ, Liu L, Fang Z, Li Y, Shi P Front Plant Sci 09-Jun-2022
PMCID:PMC9221507
doi:10.3389/fpls.2022.850203
PMID:35755713
Research progress of Chinese herbal medicine compounds and their bioactivities: Fruitful 2020 Gu X, Hao D, Xiao P Chin Herb Med 17-Mar-2022
PMCID:PMC9476823
doi:10.1016/j.chmed.2022.03.004
PMID:36117669
Structures, Occurrences and Biosynthesis of 11,12,13-Tri-nor-Sesquiterpenes, an Intriguing Class of Bioactive Metabolites Coca-Ruíz V, Suárez I, Aleu J, Collado IG Plants (Basel) 14-Mar-2022
PMCID:PMC8949605
doi:10.3390/plants11060769
PMID:35336651
Commodity risk assessment of bonsai plants from China consisting of Pinus parviflora grafted on Pinus thunbergii Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Iacopetti G, Mikulová A, Mosbach‐Schulz O, Stergulc F, Gonthier P EFSA J 08-Feb-2022
PMCID:PMC8822388
doi:10.2903/j.efsa.2022.7077
PMID:35154441
An Overview of Coumarin as a Versatile and Readily Accessible Scaffold with Broad-Ranging Biological Activities Annunziata F, Pinna C, Dallavalle S, Tamborini L, Pinto A Int J Mol Sci 29-Jun-2020
PMCID:PMC7370201
doi:10.3390/ijms21134618
PMID:32610556
Antagonists of Vitamin K—Popular Coumarin Drugs and New Synthetic and Natural Coumarin Derivatives Kasperkiewicz K, Ponczek MB, Owczarek J, Guga P, Budzisz E Molecules 24-Mar-2020
PMCID:PMC7146486
doi:10.3390/molecules25061465
PMID:32213944
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
Natural Products Research in China From 2015 to 2016 Liu H, Zhu G, Fan Y, Du Y, Lan M, Xu Y, Zhu W Front Chem 20-Mar-2018
PMCID:PMC5869933
doi:10.3389/fchem.2018.00045
PMID:29616210
Centella asiatica – Phytochemistry and mechanisms of neuroprotection and cognitive enhancement Gray NE, Alcazar Magana A, Lak P, Wright KM, Quinn J, Stevens JF, Maier CS, Soumyanath A Phytochem Rev 20-Sep-2017
PMCID:PMC6857646
doi:10.1007/s11101-017-9528-y
PMID:31736679
Triterpenoids from Ainsliaea yunnanensis Franch. and Their Biological Activities Li J, Zhang B, Liu H, Zhang X, Shang X, Zhao C Molecules 07-Nov-2016
PMCID:PMC6273999
doi:10.3390/molecules21111481
PMID:27827998
Role of Antioxidants and Natural Products in Inflammation Arulselvan P, Fard MT, Tan WS, Gothai S, Fakurazi S, Norhaizan ME, Kumar SS Oxid Med Cell Longev 10-Oct-2016
PMCID:PMC5075620
doi:10.1155/2016/5276130
PMID:27803762

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 lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3aS,6aR,8S,9S,9aR,9bR)-8-hydroxy-9-methyl-3,6-dimethylidene-4,5,6a,7,8,9,9a,9b-octahydro-3aH-azuleno[4,5-b]furan-2-one 163069975 Click to see CC1C(CC2C1C3C(CCC2=C)C(=C)C(=O)O3)O 248.32 unknown https://doi.org/10.1016/0031-9422(82)83061-6
(3aS)-3a,4,5,6,6abeta,7,8,9,9abeta,9balpha-Decahydro-8alpha-(beta-D-glucopyranosyloxy)-3,6,9-tris(methylene)azuleno[4,5-b]furan-2(3H)-one 321680 Click to see C=C1CCC2C(C3C1CC(C3=C)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C2=C 408.40 unknown https://doi.org/10.1002/MRC.2294
(3R,3aR,4S,6aR,8S,9aR,9bR)-4-hydroxy-3-methyl-6,9-dimethylidene-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 25103437 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)OC4C(C(C(C(O4)CO)O)O)O)O 426.50 unknown https://doi.org/10.1002/MRC.2294
(3R,3aS,6aR,8S,9aR,9bS)-3-methyl-6,9-dimethylidene-8-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 162926002 Click to see CC1C2CCC(=C)C3CC(C(=C)C3C2OC1=O)OC4C(C(C(C(O4)CO)O)O)O 410.50 unknown https://doi.org/10.1002/MRC.2294
(3R,3aS,6aR,8S,9aR,9bS)-Decahydro-8-hydroxy-3-methyl-6,9-bis(methylene)azuleno[4,5-b]furan-2(3H)-one 14314701 Click to see CC1C2CCC(=C)C3CC(C(=C)C3C2OC1=O)O 248.32 unknown https://doi.org/10.1016/0031-9422(82)83061-6
(3R,3aS,6aR,8S,9S,9aR,9bS)-8-hydroxy-3,9-dimethyl-6-methylidene-3,3a,4,5,6a,7,8,9,9a,9b-decahydroazuleno[4,5-b]furan-2-one 162886956 Click to see CC1C(CC2C1C3C(CCC2=C)C(C(=O)O3)C)O 250.33 unknown https://doi.org/10.1016/0031-9422(82)83061-6
(3R,3aS,8S,9aR,9bS)-8-hydroxy-3-methyl-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 163193679 Click to see CC1C2CCC(=C)C3CC(C(=C)C3C2OC1=O)O 248.32 unknown https://doi.org/10.1016/0031-9422(82)83061-6
11beta,13-Dihydrodesacylcynaropicrin 25103558 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)O 264.32 unknown https://doi.org/10.1002/MRC.2294
https://doi.org/10.1016/0031-9422(82)83061-6
3-methyl-6,9-dimethylidene-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 73817502 Click to see CC1C2CCC(=C)C3CC(C(=C)C3C2OC1=O)OC4C(C(C(C(O4)CO)O)O)O 410.50 unknown https://doi.org/10.1002/MRC.2294
4-hydroxy-3-methyl-6,9-dimethylidene-8-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 73818322 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)OC4C(C(C(C(O4)CO)O)O)O)O 426.50 unknown https://doi.org/10.1002/MRC.2294
4,8-dihydroxy-3-methyl-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 15628151 Click to see CC1C2C(CC(=C)C3CC(C(=C)C3C2OC1=O)O)O 264.32 unknown https://doi.org/10.1002/MRC.2294
https://doi.org/10.1016/0031-9422(82)83061-6
8-hydroxy-3-methyl-6,9-dimethylidene-3a,4,5,6a,7,8,9a,9b-octahydro-3H-azuleno[4,5-b]furan-2-one 14314698 Click to see CC1C2CCC(=C)C3CC(C(=C)C3C2OC1=O)O 248.32 unknown https://doi.org/10.1016/0031-9422(82)83061-6
Vernoflexuoside 442320 Click to see C=C1CCC2C(C3C1CC(C3=C)OC4C(C(C(C(O4)CO)O)O)O)OC(=O)C2=C 408.40 unknown https://doi.org/10.1002/MRC.2294
Zaluzanin C 72646 Click to see C=C1CCC2C(C3C1CC(C3=C)O)OC(=O)C2=C 246.30 unknown https://doi.org/10.1016/0031-9422(82)83061-6

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