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Details Top

Internal ID UUID643fcf9b3c54a534673541
Scientific name Sigesbeckia glabrescens
Authority (Makino) Makino
First published in J. Jap. Bot. 1: 25 (1917)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sigesbeckia orientalis f. glabrescens Makino Bot. Mag. (Tokyo) 18: 100 (1904)
Sigesbeckia formosana Kitam. Acta Phytotax. Geobot. 6: 87 (1937)
Sigesbeckia orientalis subsp. glabrescens (Makino) Kitam. Mem. Coll. Sci. Kyoto Imp. Univ., Ser. B, Biol. 16: 263 (1942)
Sigesbeckia glabrescens var. leucoclada Nakai Bot. Mag. (Tokyo) 45: 137 (1937)
Sigesbeckia orientalis var. glabrescens (Makino) Makino Somoku-Dzusetsu , ed. 3, 4: 1092 (1912)
Sigesbeckia pubescens var. glabrescens (Makino) Vorosch. Fl. Sovetsk. Dal'n. Vost. : 404 (1966)

Common names Top

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Language Common/alternative name
Chinese 豨莶
Chinese 拔毒散
Chinese 毛梗 豨莶
Chinese 毛梗豨莶
Chinese 毛梗豨莶(少毛豨莶)
Chinese 烯莶草
Chinese 豨莶草
Chinese 光豨莶

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
      • Hainan
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
    • Russian Far East
      • Primorye

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000091809
Tropicos 50056109
KEW urn:lsid:ipni.org:names:249096-1
The Plant List gcc-48075
Open Tree Of Life 407247
Observations.org 126387
NCBI Taxonomy 371450
IPNI 249096-1
iNaturalist 565415
GBIF 3125899
EPPO SIKGL
EOL 6245893
USDA GRIN 33923
CMAUP NPO28940

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
IκB kinase β (IKKβ): Structure, transduction mechanism, biological function, and discovery of its inhibitors Zhang J, Zhang R, Li W, Ma XC, Qiu F, Sun CP Int J Biol Sci 06-Aug-2023
PMCID:PMC10496512
doi:10.7150/ijbs.85158
PMID:37705738
Evaluation of the Weeds around Capsicum annuum (CA) Cultivation Fields as Potential Habitats of CA-Infecting Viruses Choi MK Plant Pathol J 01-Aug-2023
PMCID:PMC10412962
doi:10.5423/PPJ.OA.04.2023.0066
PMID:37550983
Antiperiodontitis Effects of Siegesbeckia glabrescens In Vitro Bellere AD, Yu D, Oh S, Kim M, Jung J, Fang M, Zheng S, Yi TH Antioxidants (Basel) 13-Feb-2023
PMCID:PMC9952020
doi:10.3390/antiox12020471
PMID:36830029
Comparative analysis of intestinal microbiota composition and transcriptome in diploid and triploid Carassius auratus Cai Y, Wei K BMC Microbiol 02-Jan-2023
PMCID:PMC9806896
doi:10.1186/s12866-022-02709-5
PMID:36593453
Kirenol alleviates diabetic nephropathy via regulating TGF-β/Smads and the NF-κB signal pathway Li J, Zhang J, Yang M, Huang X, Zhang M, Fang X, Wu S Pharm Biol 08-Sep-2022
PMCID:PMC9467559
doi:10.1080/13880209.2022.2112239
PMID:36073930
Ruan Jian Qing Mai Recipe Inhibits the Inflammatory Response in Acute Lower Limb Ischemic Mice through the JAK2/STAT3 Pathway Zhu D, Jia C, Cai T, Li J, Feng X, Chen N, Zhao C, Wang Y, Cao Y, Cao Y Evid Based Complement Alternat Med 18-Aug-2022
PMCID:PMC9410777
doi:10.1155/2022/2481022
PMID:36034959
Sesquiterpene Lactones as Promising Candidates for Cancer Therapy: Focus on Pancreatic Cancer Laurella LC, Mirakian NT, Garcia MN, Grasso DH, Sülsen VP, Papademetrio DL Molecules 29-May-2022
PMCID:PMC9182036
doi:10.3390/molecules27113492
PMID:35684434
Lotus root extract inhibits skin damage through suppression of collagenase production in vitro Iwamoto A, Yamauchi R, Oogai S, Tsuruta Y, Keisuke T, Nagata Y, Yanagita T Cytotechnology 29-Jan-2022
PMCID:PMC8975922
doi:10.1007/s10616-022-00521-7
PMID:35464168
Kirenol: A Potential Natural Lead Molecule for a New Drug Design, Development, and Therapy for Inflammation Nasir NN, Sekar M, Fuloria S, Gan SH, Rani NN, Ravi S, Begum MY, Chidambaram K, Sathasivam KV, Jeyabalan S, Dhiravidamani A, Thangavelu L, Lum PT, Subramaniyan V, Wu YS, Azad AK, Fuloria NK Molecules 23-Jan-2022
PMCID:PMC8839644
doi:10.3390/molecules27030734
PMID:35163999
Siegesbeckiae Herba Extract and Chlorogenic Acid Ameliorate the Death of HaCaT Keratinocytes Exposed to Airborne Particulate Matter by Mitigating Oxidative Stress Ha JW, Boo YC Antioxidants (Basel) 04-Nov-2021
PMCID:PMC8615115
doi:10.3390/antiox10111762
PMID:34829633
A Review on Obesity Management through Natural Compounds and a Green Nanomedicine-Based Approach Bhardwaj M, Yadav P, Vashishth D, Sharma K, Kumar A, Chahal J, Dalal S, Kataria SK Molecules 28-May-2021
PMCID:PMC8198321
doi:10.3390/molecules26113278
PMID:34071722
Antioxidant Compounds, Kirenol and Methyl ent-16α, 17-dihydroxy-kauran-19-oate Bioactivity-Guided Isolated from Siegesbeckia glabrescens Attenuates MITF-Mediated Melanogenesis via Inhibition of Intracellular ROS Production Shim SY, Lee YE, Lee M Molecules 30-Mar-2021
PMCID:PMC8036764
doi:10.3390/molecules26071940
PMID:33808322
Ethnobotany and the Role of Plant Natural Products in Antibiotic Drug Discovery Porras G, Chassagne F, Lyles JT, Marquez L, Dettweiler M, Salam AM, Samarakoon T, Shabih S, Farrokhi DR, Quave CL Chem Rev 09-Nov-2020
PMCID:PMC8183567
doi:10.1021/acs.chemrev.0c00922
PMID:33164487
Sigesbeckia glabrescens Makino extract attenuated the collagen-induced arthritis through inhibiting the synovial hyperplasia and inflammation Ma QS, Linghu KG, Zhang T, Zhao GD, Xiong W, Xiong SH, Zhao M, Xu W, Yu J, Yu H Chin Med 27-Aug-2020
PMCID:PMC7457260
doi:10.1186/s13020-020-00372-4
PMID:32874196
Rediscovery of Seven Long-Forgotten Species of Peronospora and Plasmopara (Oomycota) Lee JS, Shin HD, Choi YJ Mycobiology 12-Aug-2020
PMCID:PMC7580582
doi:10.1080/12298093.2020.1798863
PMID:33177913

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 / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4,5-Trimethoxybenzoic acid 8357 Click to see COC1=CC(=CC(=C1OC)OC)C(=O)O 212.20 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Heptacosanol 74822 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCO 396.70 unknown https://doi.org/10.1111/J.1744-7909.2006.00279.X
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
2,3-Dihydroxypropyl hexadecanoate 14900 Click to see CCCCCCCCCCCCCCCC(=O)OCC(CO)O 330.50 unknown https://doi.org/10.1111/J.1744-7909.2006.00279.X
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Darutigenol 3037565 Click to see CC1(C2CCC3=CC(CCC3C2(CCC1O)C)(C)C(CO)O)C 322.50 unknown via CMAUP database
ent-2-Oxo-15,16,19-trihydroxypimar-8(14)-ene 11302132 Click to see CC1(CCC2C(=C1)CCC3C2(CC(=O)CC3(C)CO)C)C(CO)O 336.50 unknown via CMAUP database
Kirenol 15736732 Click to see CC1(CCC2C(=C1)CCC3C2(CC(CC3(C)CO)O)C)C(CO)O 338.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1R,4S,5R,9S,10S,15S)-15-hydroxy-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 139031795 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4O)(C)C(=O)O 318.40 unknown https://doi.org/10.1111/J.1744-7909.2006.00279.X
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
16-O-Acetyldarutoside 102080494 Click to see CC(=O)OCC(C1(CCC2C(=C1)CCC3C2(CCC(C3(C)C)OC4C(C(C(C(O4)CO)O)O)O)C)C)O 526.70 unknown via CMAUP database
Hythiemoside B 11203296 Click to see CC(=O)OC(CO)C1(CCC2C(=C1)CCC3C2(CCC(C3(C)C)OC4C(C(C(C(O4)CO)O)O)O)C)C 526.70 unknown via CMAUP database
Neodarutoside 130539 Click to see CC1(C2CCC3=CC(CCC3C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)(C)C(CO)OC5C(C(C(C(O5)CO)O)O)O)C 646.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45358157 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid 45483617 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> 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
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives / Phenylalanine and derivatives
Asperglaucide 10026486 Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3 444.50 unknown via CMAUP database
Aurantiamide acetate 124319 Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3 444.50 unknown via CMAUP database
Tifentai 9832120 Click to see CC(=O)OCC(CC1=CC=CC=C1)NC(=O)C(CC2=CC=CC=C2)NC(=O)C3=CC=CC=C3 444.50 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
Ethyl hydrogen malonate 70615 Click to see CCOC(=O)CC(=O)O 132.11 unknown via CMAUP database
Propanedioic acid, monoethyl ester 3595298 Click to see CCOC(=O)CC(=O)[O-] 131.11 unknown via CMAUP database
Succinic Acid 1110 Click to see C(CC(=O)O)C(=O)O 118.09 unknown https://doi.org/10.1111/J.1744-7909.2006.00279.X
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1111/J.1744-7909.2006.00279.X
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 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
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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Dillenetin 5487855 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)OC 330.29 unknown via CMAUP database
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown via CMAUP database
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
Rhamnetin 5281691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 44257674 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown via CMAUP database
Vicenin 2 442664 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O 594.50 unknown via CMAUP database
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Baicalin 64982 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Isoliquiritin 5318591 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 418.40 unknown via CMAUP database
Liquiritin 503737 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O 418.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxy-phenyl)-5,7-dihydroxy-3-(3,4,5-trihydroxy-6-methyl-tetrahydro-pyran-2-yloxy)-chromen-4-one 5353915 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O 448.40 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
4H-1-Benzopyran-4-one, 7-[[6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-2,3-dihydro-5-hydroxy-2-(3-hydroxy-4-methoxyphenyl)-, (S)- 3594 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown via CMAUP database
Hesperetin-rutinoside 53477767 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 unknown via CMAUP database
Hesperidin 10621 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC(=C4C(=O)CC(OC4=C3)C5=CC(=C(C=C5)OC)O)O)O)O)O)O)O)O 610.60 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Quercetin 3,3'-dimethyl ether 5316900 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC)O 330.29 unknown via CMAUP database

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