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Internal ID UUID643fe048aa413611917739
Scientific name Lagopsis supina
Authority (Steph.) Ikonn.-Gal.
First published in Bot. Mater. Gerb. Bot. Inst. Komarova Akad. Nauk S.S.S.R. 7: 45 (1937)

Description Top

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Synonyms Top

Scientific name Authority First published in
Leonurus supinus Stephan ex Willd. Sp. Pl., ed. 4 , 3: 116 (1800)
Marrubium incisum Benth. Labiat. Gen. Spec. : 586 (1834)
Marrubium supinum (Steph. ex Willd.) Hu ex P'ei Contr. Biol. Lab. Sci. Soc. China, Bot. Ser. 10: 53 1935

Common names Top

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Language Common/alternative name
Chinese 夏枯草
Chinese 光刺兔唇花
Chinese 夏至草
Chinese 灯笼棵
Chinese 白花夏枯
Chinese 白花益母

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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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
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Xinjiang
    • Eastern Asia
      • Korea
    • Mongolia
      • Mongolia
    • Siberia
      • Buryatiya
      • Irkutsk

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000222381
KEW urn:lsid:ipni.org:names:448771-1
The Plant List kew-107319
Open Tree Of Life 365897
Observations.org 146668
NCBI Taxonomy 516545
IPNI 448771-1
iNaturalist 544443
GBIF 5609121
EPPO LGPSU
EPPO MAQIN
EOL 2893892
Elurikkus 556298

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
Antimicrobial and Cytotoxic Activity of Endophytic Fungi from Lagopsis supina Zhang D, Sun W, Xu W, Ji C, Zhou Y, Sun J, Tian Y, Li Y, Zhao F, Tian Y J Microbiol Biotechnol 30-Dec-2022
PMCID:PMC10164720
doi:10.4014/jmb.2211.11055
PMID:36781157
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
The therapeutic effects of Lagopsis supina (Steph. ex Willd.) Ikonn.-Gal. fractions in trauma-induced blood stasis model rats Xia X, Wang H, Duan Y, Yang L, He J Heliyon 22-Oct-2022
PMCID:PMC9634278
doi:10.1016/j.heliyon.2022.e11176
PMID:36339767
The Diuretic Effects of Coconut Water by Suppressing Aquaporin and Renin–Angiotensin–Aldosterone System in Saline-Loaded Rats Wei J, Zhao M, Meng K, Xia G, Pan Y, Li C, Zhang W Front Nutr 23-Jun-2022
PMCID:PMC9262403
doi:10.3389/fnut.2022.930506
PMID:35811978
Flowers and Leaves Extracts of Stachys palustris L. Exhibit Stronger Anti-Proliferative, Antioxidant, Anti-Diabetic, and Anti-Obesity Potencies than Stems and Roots Due to More Phenolic Compounds as Revealed by UPLC-PDA-ESI-TQD-MS/MS Lachowicz-Wiśniewska S, Pratap-Singh A, Kapusta I, Kruszyńska A, Rapak A, Ochmian I, Cebulak T, Żukiewicz-Sobczak W, Rubiński P Pharmaceuticals (Basel) 23-Jun-2022
PMCID:PMC9317270
doi:10.3390/ph15070785
PMID:35890084
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
Walls offer potential to improve urban biodiversity Chen C, Mao L, Qiu Y, Cui J, Wang Y Sci Rep 18-Jun-2020
PMCID:PMC7303168
doi:10.1038/s41598-020-66527-3
PMID:32555243
Diuretic and Antidiuretic Activities of Ethanol Extract and Fractions of Lagopsis supina in Normal Rats Liu Z, Yang L, Li L, Wei R, Luo X, Xu T, Huang Y, Mu Z, He J Biomed Res Int 04-Dec-2019
PMCID:PMC6914927
doi:10.1155/2019/6927374
PMID:31886241
Responses of weed community, soil nutrients, and microbes to different weed management practices in a fallow field in Northern China Gu X, Cen Y, Guo L, Li C, Yuan H, Xu Z, Jiang G PeerJ 06-Sep-2019
PMCID:PMC6733240
doi:10.7717/peerj.7650
PMID:31534864
Managing Floral Resources in Apple Orchards for Pest Control: Ideas, Experiences and Future Directions Herz A, Cahenzli F, Penvern S, Pfiffner L, Tasin M, Sigsgaard L Insects 11-Aug-2019
PMCID:PMC6723448
doi:10.3390/insects10080247
PMID:31405257

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 / Diterpenoids
CID 90670462 90670462 Click to see CC1C(C(C2C(CCCC2(C13CCC4(O3)CC(OC4)O)C)(C)C)OC(=O)C)O 396.50 unknown https://doi.org/10.1021/NP5001329
CID 90670463 90670463 Click to see CC1C(C(C2C(CCCC2(C13CCC4(O3)CC(OC4)O)C)(C)C)OC(=O)C)O 396.50 unknown https://doi.org/10.1021/NP5001329
CID 90670464 90670464 Click to see CC1C(C(C2C(CCCC2(C13CCC4(O3)CC(OC4)O)C)(C)C)OC(=O)C)O 396.50 unknown https://doi.org/10.1021/NP5001329
CID 90670465 90670465 Click to see CC1C(C(C2C(CCCC2(C13CCC4(O3)CC(OC4)O)C)(C)C)OC(=O)C)O 396.50 unknown https://doi.org/10.1021/NP5001329
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
(1S,2R,3R,4R,4aS,8aS)-4-[2-(furan-3-yl)ethyl]-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydro-1H-naphthalene-1,2,4-triol 25137130 Click to see CC1C(C(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)O)O 336.50 unknown https://doi.org/10.1021/NP5001329
(3R,4S,4aS)-4-[2-(furan-3-yl)ethyl]-3,4-dihydroxy-3,4a,8,8-tetramethyl-6,7-dihydro-5H-naphthalen-2-one 90670467 Click to see CC1(CCCC2(C1=CC(=O)C(C2(CCC3=COC=C3)O)(C)O)C)C 332.40 unknown https://doi.org/10.1021/NP5001329
(3S,4R,4aS)-4-[2-(furan-3-yl)ethyl]-4-hydroxy-3,4a,8,8-tetramethyl-3,5,6,7-tetrahydronaphthalen-2-one 86302558 Click to see CC1C(=O)C=C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C 316.40 unknown https://doi.org/10.1021/NP5001329
(4aR)-4-[2-(furan-3-yl)ethyl]-3,4a,8,8-tetramethyl-6,7-dihydro-5H-naphthalen-2-one 86302559 Click to see CC1=C(C2(CCCC(C2=CC1=O)(C)C)C)CCC3=COC=C3 298.40 unknown https://doi.org/10.1021/NP5001329
[(1S,2R,3R,4R,4aS,8aS)-1-acetyloxy-4-[2-(furan-3-yl)ethyl]-4-hydroxy-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydro-1H-naphthalen-2-yl] acetate 90670461 Click to see CC1C(C(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C)OC(=O)C 420.50 unknown https://doi.org/10.1021/NP5001329
[(1S,2R,3R,4R,4aS,8aS)-4-[2-(furan-3-yl)ethyl]-1,4-dihydroxy-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydro-1H-naphthalen-2-yl] acetate 90670468 Click to see CC1C(C(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)O)OC(=O)C 378.50 unknown https://doi.org/10.1021/NP5001329
[(1S,2R,3R,4R,4aS,8aS)-4-[2-(furan-3-yl)ethyl]-2,4-dihydroxy-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 90670460 Click to see CC1C(C(C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)OC(=O)C)O 378.50 unknown https://doi.org/10.1021/NP5001329
Leoheterin 15726751 Click to see CC1C(C(=O)C2C(CCCC2(C1(CCC3=COC=C3)O)C)(C)C)O 334.40 unknown https://doi.org/10.1021/NP5001329
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
[1-[(1S,2S)-2-[3-(furan-3-yl)propanoyl]-2,6,6-trimethylcyclohexyl]-2-oxobutyl] acetate 90670466 Click to see CCC(=O)C(C1C(CCCC1(C)C(=O)CCC2=COC=C2)(C)C)OC(=O)C 376.50 unknown https://doi.org/10.1021/NP5001329
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
[2-oxo-1-[(1S,6S)-2,2,6-trimethyl-6-[3-(5-oxo-2H-furan-4-yl)propanoyl]cyclohexyl]butyl] acetate 86302557 Click to see CCC(=O)C(C1C(CCCC1(C)C(=O)CCC2=CCOC2=O)(C)C)OC(=O)C 392.50 unknown https://doi.org/10.1021/NP5001329
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
[(1S,2R,3R,4R,4aS,8aS)-2,4-dihydroxy-4-[2-(2-methoxy-5-oxo-2H-furan-4-yl)ethyl]-3,4a,8,8-tetramethyl-2,3,5,6,7,8a-hexahydro-1H-naphthalen-1-yl] acetate 86302556 Click to see CC1C(C(C2C(CCCC2(C1(CCC3=CC(OC3=O)OC)O)C)(C)C)OC(=O)C)O 424.50 unknown https://doi.org/10.1021/NP5001329

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