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Lagotis brevituba

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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 UUID643ffdb27a0f3044373563
Scientific name Lagotis brevituba
Authority Maxim.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 27: 524 (1882)

Description Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Chinese 兔耳草
Chinese 短穗兔耳草
Chinese 洪连
Chinese 短筒兔耳草
Chinese 短筒兔耳草（短管兔耳草）

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000446182
Tropicos 29208162
KEW urn:lsid:ipni.org:names:813199-1
The Plant List kew-2498534
Open Tree Of Life 698563
NCBI Taxonomy 495256
IPNI 813199-1
iNaturalist 907889
GBIF 7707612
EOL 2894534
CMAUP NPO6029

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 to fight against COVID-19: Basic theory and therapeutic drugs Zhang K, Wang L, Peng J, Sangji K, Luo Y, Zeng Y, Zeweng Y, Fan G Front Pharmacol 16-Feb-2023
PMCID:PMC9978713
doi:10.3389/fphar.2023.1098253
PMID:36874035
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
Leucosceptosides A and B: Two Phenyl-Ethanoid Glycosides with Important Occurrence and Biological Activities Frezza C, De Vita D, Toniolo C, Sciubba F, Tomassini L, Venditti A, Bianco A, Serafini M, Foddai S Biomolecules 02-Dec-2022
PMCID:PMC9775335
doi:10.3390/biom12121807
PMID:36551235
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
Antitumor Potential and Structure Characterization of Polysaccharides From Lagotis brevituba Maxim in the Tibetan Plateau Gong R, Cao W, Huang H, Yu B, Chen H, Tao W, Luorong Q, Luo J, Zhang D Front Nutr 12-Jul-2022
PMCID:PMC9320327
doi:10.3389/fnut.2022.921892
PMID:35903443
Comparison of Herbal Medicines Used for Women’s Menstruation Diseases in Different Areas of the World Jiao M, Liu X, Ren Y, Wang Y, Cheng L, Liang Y, Li Y, Zhang T, Wang W, Mei Z Front Pharmacol 04-Feb-2022
PMCID:PMC8854496
doi:10.3389/fphar.2021.751207
PMID:35185533
Oxidative Stress, Kinase Activation, and Inflammatory Pathways Involved in Effects on Smooth Muscle Cells During Pulmonary Artery Hypertension Under Hypobaric Hypoxia Exposure Siques P, Pena E, Brito J, El Alam S Front Physiol 09-Aug-2021
PMCID:PMC8381601
doi:10.3389/fphys.2021.690341
PMID:34434114
Complete chloroplast genome sequences of Lagotis brevituba (Plantaginaceae): a famous Tibetan medicine plant Fan CX, Zhang YM, Pu SB, Li GD Mitochondrial DNA B Resour 17-May-2021
PMCID:PMC8143624
doi:10.1080/23802359.2021.1927216
PMID:34104723
The Efficacy and Mechanism of Chinese Herbal Medicines in Lowering Serum Uric Acid Levels: A Systematic Review Chen L, Luo Z, Wang M, Cheng J, Li F, Lu H, He Q, You Y, Zhou X, Kwan HY, Zhao X, Zhou L Front Pharmacol 25-Jan-2021
PMCID:PMC7868570
doi:10.3389/fphar.2020.578318
PMID:33568990
In Vitro and In Vivo Antioxidative Activity against Radiation-Induced Damage and the Systematic Chemical Components of Different Extracts of Lagotis brevituba Maxim Zhang D, Tan L, Yao L, Tao W, Gong R, LuoRong Q, Cao W Evid Based Complement Alternat Med 16-Dec-2020
PMCID:PMC7758126
doi:10.1155/2020/9726431
PMID:33381219
Traditional Tibetan Medicine in Cancer Therapy by Targeting Apoptosis Pathways Tang C, Zhao CC, Yi H, Geng ZJ, Wu XY, Zhang Y, Liu Y, Fan G Front Pharmacol 07-Jul-2020
PMCID:PMC7381342
doi:10.3389/fphar.2020.00976
PMID:32774302
Protective role of phenylethanoid glycosides, Torenoside B and Savatiside A, in Alzheimer's disease Ji S, Li S, Zhao X, Kang N, Cao K, Zhu Y, Peng P, Fan J, Xu Q, Yang S, Liu Y Exp Ther Med 07-Mar-2019
PMCID:PMC6447766
doi:10.3892/etm.2019.7355
PMID:30988761
Natural Medicines Used in the Traditional Tibetan Medical System for the Treatment of Liver Diseases Li Q, Li HJ, Xu T, Du H, Huan Gang CL, Fan G, Zhang Y Front Pharmacol 30-Jan-2018
PMCID:PMC5797630
doi:10.3389/fphar.2018.00029
PMID:29441019
Natural Products Improving Hyperuricemia with Hepatorenal Dual Effects Hao S, Zhang C, Song H Evid Based Complement Alternat Med 25-Oct-2016
PMCID:PMC5099468
doi:10.1155/2016/7390504
PMID:27847526
Phenylethanoid Glycosides: Research Advances in Their Phytochemistry, Pharmacological Activity and Pharmacokinetics Xue Z, Yang B Molecules 29-Jul-2016
PMCID:PMC6273160
doi:10.3390/molecules21080991
PMID:27483229

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
2-Dodecyl-3-methylbutanedioic acid 99891 Click to see CCCCCCCCCCCCC(C(C)C(=O)O)C(=O)O 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
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/10.1055/S-2006-959389
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 6432744 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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 via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Butanedioate;hydron 21952380 Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-] 118.09 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R)-2-[[(1R,2S,6S)-5-hydroxy-2-(hydroxymethyl)-3,9-dioxatricyclo[4.4.0.02,4]dec-7-en-10-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 138107792 Click to see C1=COC(C2C1C(C3C2(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O 362.33 unknown https://doi.org/10.1055/S-2006-959389
Catalpol 91520 Click to see C1=COC(C2C1C(C3C2(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O 362.33 unknown https://doi.org/10.1055/S-2006-959389
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
beta-D-glucose 64689 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1055/S-2006-959389
Grape sugar 79025 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1055/S-2006-959389
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol 11850 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1055/S-2006-959389
Hexitol 453 Click to see C(C(C(C(C(CO)O)O)O)O)O 182.17 unknown https://doi.org/10.1055/S-2006-959389
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see C1=CNC(=O)NC1=O 112.09 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Apigenin 7-O-glucoside 5385553 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown https://doi.org/10.1055/S-2006-959389
> 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 via CMAUP database

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