Sphagneticola calendulacea - Unknown
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Internal ID UUID643fcd75206db803713608
Scientific name Sphagneticola calendulacea
Authority (L.) Pruski
First published in Novon 6(4): 411 (1996)

Description Top

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Sphagneticola calendulacea is a perennial herb found in China, India, Indonesia, Japan, Myanmar, Philippines, Sri Lanka, Thailand, Taiwan and Vietnam. It is tolerant to drought, humidity and barren environment and is used as an ingredient in herbal tea in China and Taiwan. In traditional Chinese medicine, it is classified as a "Heat-clearing herb" and is used to relieve fever and detoxification, cooling blood and dissipating blood stasis. Modern scientific research has found that polyphenols in the plant can inhibit the growth of prostate cancer, breast cancer and nasopharyngeal carcinoma, and its essential oil can prevent the development of lung cancer.

Synonyms Top

Scientific name Authority First published in
Complaya chinensis (Osbeck) Strother Syst. Bot. Monogr. 33: 14 (1991)
Solidago chinensis Osbeck Dagb. Ostind. Resa 241 (1757); Merrill, Intepr. (1757)
Jaegeria calendulacea Spreng. Syst. Veg. 3: 500 (1826)
Seruneum calendulaceum Kuntze Revis. Gen. Pl. 1: 365 (1891)
Verbesina calendulacea L. Sp. Pl. 2: 902. 1753 [1 May 1753]
Wedelia calendulacea Less. Syn. Gen. Compos. : 222 (1832)
Polymnia benghalensis Poir. ex Steud. Nomencl. Bot. 2: 377 (1841)
Thelechitonia chinensis (Osbeck) H.Rob. & Cuatrec. Phytologia 72(2): 142 (1992): (1992)
Wedelia zollingeriana Sch.Bip. ex C.B.Clarke Compos. Ind. : 136 (1876)
Polymnia calendulacea Poir. Encycl. , Suppl. 4: 482 (1816)
Wedelia chinensis Merr. Philipp. J. Sci., C 12: 111 (1917)
Wedelia bengalensis Rich. Syn. Pl. ii. 490

Common names Top

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Language Common/alternative name
English morning flower
Azerbaijani Çin vedeliyası
Chinese 蟛蜞菊
Chinese 黃花蜜菜
Chinese 黄花蜜菜

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

Area

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Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China Southeast
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Nansei-shoto
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • India
      • Laccadive Islands
      • Pakistan
      • Sri Lanka
    • Indo-China
      • Andaman Islands
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Borneo
      • Jawa
      • Malaya
      • Philippines

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000072506
Tropicos 50084451
INPN 920251
Flora of Italy 8622
KEW urn:lsid:ipni.org:names:993278-1
The Plant List gcc-29252
Open Tree Of Life 599499
NCBI Taxonomy 1117039
IPNI 993278-1
iNaturalist 335655
GBIF 3116861
Freebase /m/0czc6l8
Wikipedia Sphagneticola_calendulacea
CMAUP NPO15769

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
High potential extracts from cocoa byproducts through sonotrode optimal extraction and a comprehensive characterization Ramos-Escudero F, Rojas-García A, Cádiz-Gurrea MD, Segura-Carretero A Ultrason Sonochem 26-Apr-2024
PMCID:PMC11070619
doi:10.1016/j.ultsonch.2024.106887
PMID:38696912
The complete plastome sequences of invasive weed Parthenium hysterophorus: genome organization, evolutionary significance, structural features, and comparative analysis Lubna, Asaf S, Jan R, Asif S, Bilal S, Khan AL, Al-Rawahi AN, Kim KM, AL-Harrasi A Sci Rep 18-Feb-2024
PMCID:PMC10874969
doi:10.1038/s41598-024-54503-0
PMID:38369569
An ethnobotanical survey on phytomedicines based on traditional knowledge in the Barpeta district, Assam, India Bhattacharjya DK, Akhtar J, Deka P, Bharadwaj A J Ayurveda Integr Med 19-Jul-2023
PMCID:PMC10371788
doi:10.1016/j.jaim.2023.100763
PMID:37478633
Invasive clonal plants possess greater capacity for division of labor than natives in high patch contrast environments Zhang J, You WH, Li NN, Du DL Front Plant Sci 10-Jul-2023
PMCID:PMC10363633
doi:10.3389/fpls.2023.1210070
PMID:37492774
Production of secondary metabolites using tissue culture-based biotechnological applications Ozyigit II, Dogan I, Hocaoglu-Ozyigit A, Yalcin B, Erdogan A, Yalcin IE, Cabi E, Kaya Y Front Plant Sci 29-Jun-2023
PMCID:PMC10339834
doi:10.3389/fpls.2023.1132555
PMID:37457343
Searching for Novel Candidate Small Molecules for Ameliorating Idiopathic Pulmonary Fibrosis: a Narrative Review Kim KI, Hossain R, Li X, Lee HJ, Lee CJ Biomol Ther (Seoul) 31-May-2023
PMCID:PMC10468426
doi:10.4062/biomolther.2023.056
PMID:37254717
Impact of Light and Dark Treatment on Phenylpropanoid Pathway Genes, Primary and Secondary Metabolites in Agastache rugosa Transgenic Hairy Root Cultures by Overexpressing Arabidopsis Transcription Factor AtMYB12 Do TM, Choi M, Kim JK, Kim YJ, Park C, Park CH, Park NI, Kim C, Sathasivam R, Park SU Life (Basel) 19-Apr-2023
PMCID:PMC10142052
doi:10.3390/life13041042
PMID:37109572
Hairy Root Cultures as a Source of Phenolic Antioxidants: Simple Phenolics, Phenolic Acids, Phenylethanoids, and Hydroxycinnamates Malarz J, Yudina YV, Stojakowska A Int J Mol Sci 07-Apr-2023
PMCID:PMC10138958
doi:10.3390/ijms24086920
PMID:37108084
Pest categorisation of Paracoccus marginatus Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 31-Mar-2023
PMCID:PMC10064853
doi:10.2903/j.efsa.2023.7899
PMID:37009439
Signaling and Detoxification Strategies in Plant-Microbes Symbiosis under Heavy Metal Stress: A Mechanistic Understanding Liu Y, He G, He T, Saleem M Microorganisms 26-Dec-2022
PMCID:PMC9865731
doi:10.3390/microorganisms11010069
PMID:36677361
In-vitro anti-bacterial activity of medicinal plants against Urinary Tract Infection (UTI) causing bacteria along with their synergistic effects with commercially available antibiotics Acharjee M, Zerin N, Ishma T, Mahmud MR New Microbes New Infect 24-Dec-2022
PMCID:PMC9823205
doi:10.1016/j.nmni.2022.101076
PMID:36624873
Chemical characterization and the intrusion through elicitation and Agrobacterium rhizogenes mediated hairy root transformation in Saussurea costus C.B. Clarke Kour S, Singh S, Wani TA, Kaloo ZA Physiol Mol Biol Plants 23-Dec-2022
PMCID:PMC9886768
doi:10.1007/s12298-022-01270-9
PMID:36733833
Differences in Phenotypic Plasticity between Invasive and Native Plants Responding to Three Environmental Factors Zhang L, Chen A, Li Y, Li D, Cheng S, Cheng L, Liu Y Life (Basel) 25-Nov-2022
PMCID:PMC9781723
doi:10.3390/life12121970
PMID:36556335
Adaptation of the Invasive Plant (Sphagneticola trilobata L. Pruski) to a High Cadmium Environment by Hybridizing With Native Relatives Gao L, Cai M, Zeng L, Zhang Q, Zhu H, Gu X, Peng C Front Plant Sci 28-Jun-2022
PMCID:PMC9277564
doi:10.3389/fpls.2022.905577
PMID:35845659
Expression Level Dominance and Homeolog Expression Bias Upon Cold Stress in the F1 Hybrid Between the Invasive Sphagneticola trilobata and the Native S. calendulacea in South China, and Implications for Its Invasiveness Wu W, Guo W, Ni G, Wang L, Zhang H, Ng WL Front Genet 19-May-2022
PMCID:PMC9160872
doi:10.3389/fgene.2022.833406
PMID:35664338

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 / Phenanthrenes and derivatives
6-Oxopristimerol 11754914 Click to see CC1=C2C(=CC(=C1O)O)C3(CCC4(C5CC(CCC5(CCC4(C3=CC2=O)C)C)(C)C(=O)OC)C)C 480.60 unknown via CMAUP database
Zeylasterone 13945472 Click to see CC12CCC(CC1C3(CCC4(C5=CC(=C(C(=C5C(=O)C=C4C3(CC2)C)C(=O)O)O)O)C)C)(C)C(=O)OC 510.60 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
Anhydrosecoisolariciresinol 9974771 Click to see COC1=C(C=CC(=C1)CC2COCC2CC3=CC(=C(C=C3)O)OC)O 344.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1S,4S,5R,9R)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadec-10-ene-5-carboxylic acid 137705080 Click to see CC12CCCC(C1CCC34C2=CCC(C3)C(=C)C4)(C)C(=O)O 300.40 unknown https://doi.org/10.1016/0031-9422(81)83103-2
(1S,4S,5S,9S,10R,13R,14R)-5-(hydroxymethyl)-5,9,14-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-ol 101297703 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(C)O)C)CO 306.50 unknown via CMAUP database
(5R,9S,13S)-5,9-dimethyl-14-methylidenetetracyclo[11.2.1.01,10.04,9]hexadecane-5-carboxylic acid 49775756 Click to see CC12CCCC(C1CCC34C2CCC(C3)C(=C)C4)(C)C(=O)O 302.50 unknown https://doi.org/10.1016/S0305-1978(02)00181-3
https://doi.org/10.1016/0031-9422(81)83103-2
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aS,4aS,7S,7aR,7bS)-1,1,7-trimethyl-4-methylidene-1a,2,3,4a,5,6,7a,7b-octahydrocyclopropa[h]azulen-7-ol 97032059 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown https://doi.org/10.1016/0031-9422(81)83103-2
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,3aS,4S,5aS,5bR,7aR,9S,11aR,11bR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13b-tetradecahydrocyclopenta[a]chrysene-4,9-diol 44178932 Click to see CC(C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C 442.70 unknown via CMAUP database
(3S,4aR,6aR,6bS,8aS,11R,12aR,14aR,14bR)-11-(hydroxymethyl)-4,4,6a,6b,8a,11,14b-heptamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol 101286253 Click to see CC1(C2CCC3(C(C2(CCC1O)C)CC=C4C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C 442.70 unknown via CMAUP database
(3S,6aS,6aS,6bR,8aS,11R,12aR,14aR,14bS)-11-(hydroxymethyl)-4,4,6a,6b,8a,11,14a-heptamethyl-1,2,3,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydropicen-3-ol 13918509 Click to see CC1(C(CCC2C1=CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)CO)C)C)C)C)O)C 442.70 unknown via CMAUP database
20(29)-Lupene-1beta,3beta-diol 488250 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C 442.70 unknown via CMAUP database
3alpha,16beta-Dihydroxylupa-12-ene 44179020 Click to see CC(C)C1CCC2(C1C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C 442.70 unknown via CMAUP database
3alpha,16beta,28-Trihydroxylupa-20(29)-ene 44178931 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)CO 458.70 unknown via CMAUP database
3beta-Hydroperoxy-7beta,25-epoxy-D:B-friedooleanane-5-ene 101481671 Click to see CC1(CCC2(CCC3(C4C5C=C6C(C4(CCC3(C2C1)C)CO5)CCC(C6(C)C)OO)C)C)C 456.70 unknown via CMAUP database
Calenduladiol 461835 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C 442.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Glochidiol 13969554 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(C(CC(C5(C)C)O)O)C)C)C 442.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Pristimerin 159516 Click to see CC1=C(C(=O)C=C2C1=CC=C3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)OC)C)C)C)C)O 464.60 unknown via CMAUP database
Resinone 101316848 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2O)C)C)(C)C)C)C 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids
16beta-Hydroxy-3,4-secolupane-20(29)-ene-3-oic acid 44179021 Click to see CC(C)C1CCC2(C(C1(C)CCC(=O)O)CCC3C2(CC(C4(C3C(CC4)C(=C)C)C)O)C)C 458.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1S)-3,4-bis[3-(3,4-dihydroxyphenyl)prop-2-enoyloxy]-1,5-dihydroxycyclohexane-1-carboxylic acid 129316855 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1002/PCA.642
3,4-Dicaffeoylquinic acid 6474309 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O 516.40 unknown https://doi.org/10.1002/PCA.642
Isochlorogenic acid A 6474310 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O 516.40 unknown https://doi.org/10.1002/PCA.642
> Organoheterocyclic compounds / Benzofurans
Isololiolide 11019783 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
5,6-Dihydroxy-2-(2',4',6'-trihydroxyphenyl)benzofuran-3-carboxylic acid 44260115 Click to see C1=C(C=C(C(=C1O)C2=C(C3=CC(=C(C=C3O2)O)O)C(=O)O)O)O 318.23 unknown https://doi.org/10.1016/S0031-9422(00)80641-X
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51402807 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1002/PCA.642
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1002/PCA.642
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
Demethylwedelolactone 5489605 Click to see C1=C(C=C2C(=C1O)C3=C(C4=CC(=C(C=C4O3)O)O)C(=O)O2)O 300.22 unknown https://doi.org/10.1016/S0031-9422(00)80641-X
Wedelolactone 5281813 Click to see COC1=CC(=C2C(=C1)OC(=O)C3=C2OC4=CC(=C(C=C43)O)O)O 314.25 unknown https://doi.org/10.1016/S0031-9422(00)80641-X

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