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Internal ID UUID64404ed8a5485551904072
Scientific name Lagotis yunnanensis
Authority W.W.Sm.
First published in Notes Roy. Bot. Gard. Edinburgh 11: 219 (1919)

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Language Common/alternative name
Chinese 云南兔耳草

Subspecies (abbr. subsp./ssp.) Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001140018
Tropicos 29208169
KEW urn:lsid:ipni.org:names:804154-1
The Plant List tro-29208169
Open Tree Of Life 5145175
NCBI Taxonomy 1310066
IPNI 804154-1
iNaturalist 907911
GBIF 8213969
EOL 2894547

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
Characterization of the complete chloroplast genome sequence of Limnophila sessiliflora Blume 1826 (Plantaginaceae) Dong H, Huang R, Wang S, Yu J Mitochondrial DNA B Resour 18-May-2023
PMCID:PMC10197986
doi:10.1080/23802359.2023.2209390
PMID:37213788
Plastid Phylogenomic Insights into the Inter-Tribal Relationships of Plantaginaceae Xie P, Tang L, Luo Y, Liu C, Yan H Biology (Basel) 07-Feb-2023
PMCID:PMC9953724
doi:10.3390/biology12020263
PMID:36829541
In Vivo Hepatoprotective and Nephroprotective Activity of Acylated Iridoid Glycosides from Scrophularia hepericifolia Abdel-Kader MS, Alqasoumi SI Biology (Basel) 12-Feb-2021
PMCID:PMC7918105
doi:10.3390/biology10020145
PMID:33673028
Complete chloroplast genome sequences of Lagotis yunnanensis (Scrophulariaceae): an Endangered species endemic to the Hengduan Mountains region Cheng JP, Zhang YM, Qian ZG, Li GD Mitochondrial DNA B Resour 27-Jan-2020
PMCID:PMC7748441
doi:10.1080/23802359.2020.1717394
PMID:33366802
Study on Chemical Constituents of <i>Lagotis yunnanensis</i> Jin Yang, Hai Yan Wu, Qing Hua Li, Ping Yi, Yong Min, Wei Liu, Xiao Dong Yang, Liang Li Trans Tech Publications, Ltd. 26-Jul-2012
doi:10.4028/WWW.SCIENTIFIC.NET/AMR.554-556.1845
Constituents of Lagotis yunnanensis. Yang XD, Zhao JF, Mei SX, Zhang HB, Li L Fitoterapia 01-Jul-2003
doi:10.1016/S0367-326X(03)00056-X
PMID:12837373

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 / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
p-Anisic acid 7478 Click to see COC1=CC=C(C=C1)C(=O)O 152.15 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
https://doi.org/10.4028/WWW.SCIENTIFIC.NET/AMR.554-556.1845
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.4028/WWW.SCIENTIFIC.NET/AMR.554-556.1845
https://doi.org/10.1016/S0367-326X(03)00056-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
https://doi.org/10.4028/WWW.SCIENTIFIC.NET/AMR.554-556.1845
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Xyl(b1-3)Glc(b)-O-EtPh 100930979 Click to see C1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC=CC=C3)CO)O)O)O)O 416.40 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
2-Propenoic acid, 3-phenyl- 8784 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
https://doi.org/10.4028/WWW.SCIENTIFIC.NET/AMR.554-556.1845
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/S0367-326X(03)00056-X
https://doi.org/10.4028/WWW.SCIENTIFIC.NET/AMR.554-556.1845

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