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Internal ID UUID64403236c1114690196297
Scientific name Clinopodium polycephalum
Authority (Vaniot) C.Y.Wu & S.J.Hsuan
First published in Observ. Fl. Hwangshan : 168 (1965)

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Synonyms Top

Scientific name Authority First published in
Satureja polycephala (Vaniot) Steward J. Arnold Arbor. 35: 86 (1954)
Calamintha polycephala Vaniot Bull. Acad. Int. Géogr. Bot. 14: 183 (1904)
Calamintha tsacapanensis H.Lév. Repert. Spec. Nov. Regni Veg. 8: 423 (1910)
Calamintha clinopodium var. polycephala (Vaniot) Dunn Notes Roy. Bot. Gard. Edinburgh 6: 160. 1915
Calamintha clinopodium var. pratensis Dunn Notes Roy. Bot. Gard. Edinburgh 6: 159. 1915

Common names Top

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Language Common/alternative name
Chinese 小益母草
Chinese 荫风轮
Chinese 风轮草
Chinese 野鱼腥草
Chinese 走马灯笼草
Chinese 节节草
Chinese 脚癣草
Chinese 第第菜
Chinese 漫胆草
Chinese 楼台草
Chinese 山蕾香
Chinese 灯笼草
Chinese 大叶香薷
Chinese 灯笼草(荫风轮)
Chinese 断血流
Chinese 土防风
Chinese 山藿香
Chinese 绣球草
Chinese 夏枯草
Chinese 土荆芥
Chinese 蜂窝草

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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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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000892923
Tropicos 17606793
KEW urn:lsid:ipni.org:names:445851-1
The Plant List kew-43647
Open Tree Of Life 453498
Observations.org 450741
NCBI Taxonomy 751808
IPNI 445851-1
iNaturalist 565877
GBIF 3885983
EOL 2893719
Elurikkus 433587

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
Ethnobotanical, Phytochemical, and Pharmacological Properties of the Subfamily Nepetoideae (Lamiaceae) in Inflammatory Diseases Ortiz-Mendoza N, Martínez-Gordillo MJ, Martínez-Ambriz E, Basurto-Peña FA, González-Trujano ME, Aguirre-Hernández E Plants (Basel) 02-Nov-2023
PMCID:PMC10648697
doi:10.3390/plants12213752
PMID:37960108
Hypericum sampsonii Hance: a review of its botany, traditional uses, phytochemistry, biological activity, and safety Sun Z, Li Y, Zhong R, Li R Front Pharmacol 19-Sep-2023
PMCID:PMC10546196
doi:10.3389/fphar.2023.1247675
PMID:37795026
Functional divergence of CYP76AKs shapes the chemodiversity of abietane-type diterpenoids in genus Salvia Hu J, Qiu S, Wang F, Li Q, Xiang CL, Di P, Wu Z, Jiang R, Li J, Zeng Z, Wang J, Wang X, Zhang Y, Fang S, Qiao Y, Ding J, Jiang Y, Xu Z, Chen J, Chen W Nat Commun 04-Aug-2023
PMCID:PMC10403556
doi:10.1038/s41467-023-40401-y
PMID:37542034
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
A Rapid and Efficient Strategy for Quality Control of Clinopodii herba Encompassing Optimized Ultrasound-Assisted Extraction Coupled with Sensitive Variable Wavelength Detection Liu Y, Song X, Shen X, Xiong Y, Liu L, Yang Y, Nian S, Liu L Molecules 10-Jul-2022
PMCID:PMC9316769
doi:10.3390/molecules27144418
PMID:35889291
Transcriptome Analysis of Clinopodium chinense (Benth.) O. Kuntze and Identification of Genes Involved in Triterpenoid Saponin Biosynthesis Shi Y, Zhang S, Peng D, Wang C, Zhao D, Ma K, Wu J, Huang L Int J Mol Sci 29-May-2019
PMCID:PMC6600151
doi:10.3390/ijms20112643
PMID:31146369
Intraspecific Trait Variation and Phenotypic Plasticity Mediate Alpine Plant Species Response to Climate Change Henn JJ, Buzzard V, Enquist BJ, Halbritter AH, Klanderud K, Maitner BS, Michaletz ST, Pötsch C, Seltzer L, Telford RJ, Yang Y, Zhang L, Vandvik V Front Plant Sci 13-Nov-2018
PMCID:PMC6243391
doi:10.3389/fpls.2018.01548
PMID:30483276
Transplants, Open Top Chambers (OTCs) and Gradient Studies Ask Different Questions in Climate Change Effects Studies Yang Y, Halbritter AH, Klanderud K, Telford RJ, Wang G, Vandvik V Front Plant Sci 02-Nov-2018
PMCID:PMC6224372
doi:10.3389/fpls.2018.01574
PMID:30450107
Plastic Population Effects and Conservative Leaf Traits in a Reciprocal Transplant Experiment Simulating Climate Warming in the Himalayas Cui H, Töpper JP, Yang Y, Vandvik V, Wang G Front Plant Sci 30-Jul-2018
PMCID:PMC6077237
doi:10.3389/fpls.2018.01069
PMID:30105040
Soil seed banks along elevational gradients in tropical, subtropical and subalpine forests in Yunnan Province, southwest China Luo X, Cao M, Zhang M, Song X, Li J, Nakamura A, Kitching R Plant Divers 18-Oct-2017
PMCID:PMC6112287
doi:10.1016/j.pld.2017.10.001
PMID:30159520
Stemphylium revisited Woudenberg JH, Hanse B, van Leeuwen GC, Groenewald JZ, Crous PW Stud Mycol 06-Jun-2017
PMCID:PMC5480992
doi:10.1016/j.simyco.2017.06.001
PMID:28663603
Traditional Livelihoods, Conservation and Meadow Ecology in Jiuzhaigou National Park, Sichuan, China Urgenson L, Schmidt AH, Combs J, Harrell S, Hinckley T, Yang Q, Ma Z, Yongxian L, Hongliang L, MacIver A Hum Ecol Interdiscip J 21-Feb-2014
PMCID:PMC4474163
doi:10.1007/s10745-014-9650-z
PMID:26097267
Triterpenoid saponins from Clinopodium polycephalum X Shen-Ru Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(92)80218-4
Triterpenoid saponins from Clinopodium polycephalum. Xue SR, Liu JQ, Wang G Phytochemistry 01-Mar-1992
doi:10.1016/0031-9422(92)80072-M
PMID:1368035

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 glycosides / Triterpene glycosides / Triterpene saponins
(2R,3R,4S,5S,6R)-2-[[(2R,3S,4R,5R,6R)-6-[[(3S,4R,4aR,6aR,6bS,8S,8aS,14aR,14bS)-8-hydroxy-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,14a-dodecahydropicen-3-yl]oxy]-4,5-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 90470000 Click to see CC1(CCC2(C(CC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)C)O)CO)C 959.10 unknown https://doi.org/10.1016/0031-9422(92)80072-M
(2S,3S,4R,5R,6S)-2-[[(2S,3R,4S,5S,6S)-6-[[(3R,4S,4aS,6aS,6bR,8R,8aR,14aS,14bR)-8-hydroxy-4,8a-bis(hydroxymethyl)-4,6a,6b,11,11,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,12,14a-dodecahydropicen-3-yl]oxy]-4,5-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 133562452 Click to see CC1(CCC2(C(CC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)C)O)CO)C 959.10 unknown https://doi.org/10.1016/0031-9422(92)80218-4
Clinopodiside A 197477 Click to see CC1(CCC2(C(CC3(C(=C2C1)C=CC4C3(CCC5C4(CCC(C5(C)CO)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)C)C)C)O)CO)C 959.10 unknown https://doi.org/10.1016/0031-9422(92)80218-4
https://doi.org/10.1016/0031-9422(92)80072-M

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