Bidens parviflora - Unknown
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Internal ID UUID643fc7e235ccf599281585
Scientific name Bidens parviflora
Authority Willd.
First published in Enum. Pl. 2: 840 (1809)

Description Top

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Synonyms Top

Scientific name Authority First published in
Bidens macrosperma Fisch. Cat. Jard. Gorenki 59; ed. 2, 37 (1812) (1808)
Bidens messerschmidii Turcz. ex Ledeb. Fl. Ross. 2(2,6): 518 (1845)
Bidens pauciflora Poir. Encycl. , Suppl. 1: 630 (1811)

Common names Top

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Language Common/alternative name
Azerbaijani xırdaçiçək yatıqqanqal
Korean 까치발
Chinese 细叶刺针草
Chinese 小刺叉
Chinese 小花鬼针草
Chinese 小鬼叉
Chinese 锅叉草
Chinese 一包针
Chinese 小鬼钗
Chinese 小花鬼針草

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
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Qinghai
    • Eastern Asia
      • Japan
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
      • Sakhalin
    • Siberia
      • Altay
      • Buryatiya
      • Chita
      • Tuva

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000018174
Tropicos 2717220
KEW urn:lsid:ipni.org:names:185131-1
The Plant List gcc-117576
PaleoBotany 59208
Open Tree Of Life 5794538
Observations.org 137706
NCBI Taxonomy 1527830
IPNI 185131-1
iNaturalist 867960
GBIF 5391777
EPPO BIDPV
EOL 6234072
CMAUP NPO11532

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
The complete mitochondrial genome of Cuminum cyminum (Apiales: Apiaceae) and phylogenetic analysis Chen G, Kang R, Wang Z, Jiang Y, Zhou H, Abuduaini A, Suo F, Huang L Mitochondrial DNA B Resour 27-Jul-2023
PMCID:PMC10375935
doi:10.1080/23802359.2023.2238357
PMID:37521907
In Vitro and In Silico Investigation of Polyacetylenes from Launaea capitata (Spreng.) Dandy as Potential COX-2, 5-LOX, and BchE Inhibitors Abdel Bar FM, Mira A, Foudah AI, Alossaimi MA, Alkanhal SF, Aldaej AM, ElNaggar MH Molecules 17-Apr-2023
PMCID:PMC10145610
doi:10.3390/molecules28083526
PMID:37110760
Characterizing conflict and congruence of molecular evolution across organellar genome sequences for phylogenetics in land plants Tyszka AS, Bretz EC, Robertson HM, Woodcock-Girard MD, Ramanauskas K, Larson DA, Stull GW, Walker JF Front Plant Sci 30-Mar-2023
PMCID:PMC10098128
doi:10.3389/fpls.2023.1125107
PMID:37063179
Effects of Arbuscular Mycorrhizal Fungi on Alleviating Cadmium Stress in Medicago truncatula Gaertn Li W, Chen K, Li Q, Tang Y, Jiang Y, Su Y Plants (Basel) 25-Jan-2023
PMCID:PMC9920379
doi:10.3390/plants12030547
PMID:36771633
Comparative analysis of the plastid and mitochondrial genomes of Artemisia giraldii Pamp. Yue J, Lu Q, Ni Y, Chen P, Liu C Sci Rep 17-Aug-2022
PMCID:PMC9385723
doi:10.1038/s41598-022-18387-2
PMID:35978085
Arbuscular Mycorrhizal Fungi and Glomalin Play a Crucial Role in Soil Aggregate Stability in Pb-Contaminated Soil Li Y, Xu J, Hu J, Zhang T, Wu X, Yang Y Int J Environ Res Public Health 21-Apr-2022
PMCID:PMC9099716
doi:10.3390/ijerph19095029
PMID:35564424
Isolation, Characterization and In Silico Studies of Secondary Metabolites from the Whole Plant of Polygala inexpectata Peşmen & Erik Ünlü A, Teralı K, Uğurlu Aydın Z, Dönmez AA, Yusufoğlu HS, Çalış İ Molecules 21-Jan-2022
PMCID:PMC8838668
doi:10.3390/molecules27030684
PMID:35163950
Thermal treatment of luteolin-7-O-β-glucoside improves its immunomodulatory and antioxidant potencies Maatouk M, Mustapha N, Mokdad-Bzeouich I, Chaaban H, Abed B, Iaonnou I, Ghedira K, Ghoul M, Ghedira LC Cell Stress Chaperones 04-Jun-2017
PMCID:PMC5655366
doi:10.1007/s12192-017-0808-7
PMID:28578499
Indigenous Uses and Pharmacological Activity of Traditional Medicinal Plants in Mount Taibai, China Chang N, Luo Z, Li D, Song H Evid Based Complement Alternat Med 20-Feb-2017
PMCID:PMC5338068
doi:10.1155/2017/8329817
PMID:28303162
An Update on Oligosaccharides and Their Esters from Traditional Chinese Medicines: Chemical Structures and Biological Activities Chen XY, Wang RF, Liu B Evid Based Complement Alternat Med 15-Mar-2015
PMCID:PMC4377491
doi:10.1155/2015/512675
PMID:25861364
Diversity of wetland plants used traditionally in China: a literature review Zhang Y, Xu H, Chen H, Wang F, Huai H J Ethnobiol Ethnomed 15-Oct-2014
PMCID:PMC4210556
doi:10.1186/1746-4269-10-72
PMID:25318542
A review on herbal antiasthmatics Mali RG, Dhake AS Orient Pharm Exp Med 05-Jul-2011
PMCID:PMC3245822
doi:10.1007/s13596-011-0019-1
PMID:22207824
Flavonoids and a New Polyacetylene from Bidens parviflora Willd Li YL, Li J, Wang NL, Yao XS Molecules 28-Aug-2008
PMCID:PMC6244959
doi:10.3390/molecules13081931
PMID:18794794
Comparison of plants used for skin and stomach problems in Trinidad and Tobago with Asian ethnomedicine Lans C J Ethnobiol Ethnomed 05-Jan-2007
PMCID:PMC1781930
doi:10.1186/1746-4269-3-3
PMID:17207273
Two neolignan glucosides and antihistamine release activities from Bidens parviflora WILLD. Wang NL, Wang J, Yao XS, Kitanaka S Chem Pharm Bull (Tokyo) 01-Aug-2006
doi:10.1248/CPB.54.1190
PMID:16880667

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 / Phenols / Benzenediols / Catechols
Dimethyl 2,4-bis(3,4-dihydroxyphenyl)cyclobutane-1,3-dicarboxylate 639638 Click to see COC(=O)C1C(C(C1C2=CC(=C(C=C2)O)O)C(=O)OC)C3=CC(=C(C=C3)O)O 388.40 unknown https://doi.org/10.1016/S0031-9422(02)00454-5
> Lignans, neolignans and related compounds / Cyclobutane lignans
(1R,3S,4S,5S,6R,10S,11S,12S,13R,17R,18S,19S,20R)-4,5,18,19,20-pentahydroxy-3-(hydroxymethyl)-11,12-bis(4-hydroxyphenyl)-2,8,15,21,22-pentaoxatetracyclo[15.3.1.13,6.010,13]docosane-9,14-dione 162898780 Click to see C1C2C(C(C(C(O2)OC3(C(C(C(O3)COC(=O)C4C(C(C4C(=O)O1)C5=CC=C(C=C5)O)C6=CC=C(C=C6)O)O)O)CO)O)O)O 634.60 unknown https://doi.org/10.1016/S0031-9422(02)00454-5
4,5,18,19,20-Pentahydroxy-3-(hydroxymethyl)-11,12-bis(4-hydroxyphenyl)-2,8,15,21,22-pentaoxatetracyclo[15.3.1.13,6.010,13]docosane-9,14-dione 162898778 Click to see C1C2C(C(C(C(O2)OC3(C(C(C(O3)COC(=O)C4C(C(C4C(=O)O1)C5=CC=C(C=C5)O)C6=CC=C(C=C6)O)O)O)CO)O)O)O 634.60 unknown https://doi.org/10.1016/S0031-9422(02)00454-5
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
(Z,9R)-9-hydroxyoctadec-12-enoic acid 5312848 Click to see CCCCCC=CCCC(CCCCCCCC(=O)O)O 298.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(2R,3R,4S,5S,6R)-2-[(E)-10-hydroxydec-8-en-4,6-diynoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 9923364 Click to see C(CC#CC#CC=CCO)COC1C(C(C(C(O1)CO)O)O)O 326.34 unknown https://doi.org/10.1248/CPB.49.938
(2R,3R,4S,5S,6R)-2-[(Z,3R)-3-hydroxydec-8-en-4,6-diynoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 10980311 Click to see CC=CC#CC#CC(CCOC1C(C(C(C(O1)CO)O)O)O)O 326.34 unknown https://doi.org/10.1248/CPB.49.938
2-(10-Hydroxydec-8-en-4,6-diynoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 85068794 Click to see C(CC#CC#CC=CCO)COC1C(C(C(C(O1)CO)O)O)O 326.34 unknown https://doi.org/10.1248/CPB.49.938
2-(3-Hydroxydec-8-en-4,6-diynoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 85059308 Click to see CC=CC#CC#CC(CCOC1C(C(C(C(O1)CO)O)O)O)O 326.34 unknown https://doi.org/10.1248/CPB.49.938
2-(3-Hydroxydeca-4,6,8-triynoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 85069342 Click to see CC#CC#CC#CC(CCOC1C(C(C(C(O1)CO)O)O)O)O 324.32 unknown https://doi.org/10.1248/CPB.49.938
2-(3,10-Dihydroxydec-8-en-4,6-diynoxy)-6-(hydroxymethyl)oxane-3,4,5-triol 73802886 Click to see C(COC1C(C(C(C(O1)CO)O)O)O)C(C#CC#CC=CCO)O 342.34 unknown https://doi.org/10.1248/CPB.49.938
Bidensyneoside A1 10903496 Click to see CC=CC#CC#CC(CCOC1C(C(C(C(O1)CO)O)O)O)O 326.34 unknown https://doi.org/10.1248/CPB.49.938
Bidensyneoside B 10892676 Click to see CC#CC#CC#CC(CCOC1C(C(C(C(O1)CO)O)O)O)O 324.32 unknown https://doi.org/10.1248/CPB.49.938
Bidensyneoside C 10936789 Click to see C(COC1C(C(C(C(O1)CO)O)O)O)C(C#CC#CC=CCO)O 342.34 unknown https://doi.org/10.1248/CPB.49.938
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Eudesmanolides, secoeudesmanolides, and derivatives
7-hydroxy-5,8a-dimethyl-3-methylidene-4,6,7,8,9,9a-hexahydro-3aH-benzo[f][1]benzofuran-2-one 14864225 Click to see CC1=C2CC3C(CC2(CC(C1)O)C)OC(=O)C3=C 248.32 unknown https://doi.org/10.1016/S0031-9422(02)00454-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
11alpha-Hydroxyandrosta-1,4-diene-3,17-dione 111337 Click to see CC12CC(C3C(C1CCC2=O)CCC4=CC(=O)C=CC34C)O 300.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Azasteroids and derivatives
Irehdiamine C 102090481 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)C)NC 330.50 unknown via CMAUP database
Kurchessine 442979 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N(C)C)C)C)N(C)C 372.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methylenecholesterol 92113 Click to see CC(C)C(=C)CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 18-hydroxysteroids
Holadysenterine 16742955 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)CO)N(C(=O)C)O 390.60 unknown via CMAUP database
Regholarrhenine F 14543701 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N(C)C)C)CO)N(C)C 388.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 21-hydroxysteroids
Hydrocortisone 5754 Click to see CC12CCC(=O)C=C1CCC3C2C(CC4(C3CCC4(C(=O)CO)O)C)O 362.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(1S,2S,5S,6S,9R,11R,12S,13R)-11-hydroxy-6,13-dimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosa-14,17-dien-16-one 21573748 Click to see CC1C2CCC3C2(CC(C4C3CCC5=CC(=O)C=CC45C)O)CN1 327.50 unknown via CMAUP database
Holanamine 76308534 Click to see CC1C2CCC3C2(CC(C4C3CCC5=CC(=O)C=CC45C)O)C=N1 325.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids
Holadysine 102093813 Click to see CCC1C(=O)CC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)C 329.50 unknown via CMAUP database
Holarrhimine 15559632 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)CO)N 332.50 unknown via CMAUP database
Irehdiamine B 15560372 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)C)N 330.50 unknown via CMAUP database
Pregn-5-en-18-ol, 20-amino-3-(methylamino)-, (3beta,20S)- 22214001 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)CO)N 346.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Conanine-type alkaloids
(1S,2S,5S,6S,9R,11R,12S,13R)-11-hydroxy-6,7,13-trimethyl-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icosa-14,17-dien-16-one 21573749 Click to see CC1C2CCC3C2(CC(C4C3CCC5=CC(=O)C=CC45C)O)CN1C 341.50 unknown via CMAUP database
7-Hydroxyconessine 102093825 Click to see CC1C2CCC3C2(CCC4C3C(C=C5C4(CCC(C5)N(C)C)C)O)CN1C 372.60 unknown via CMAUP database
Con-5-enin-12-ol, 3-(dimethylamino)-, 4-methyl-3-pentenoate (ester), (3beta,12beta)- 11225162 Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)N(C)C)C)OC(=O)CC=C(C)C 468.70 unknown via CMAUP database
Conessine 441082 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1C 356.60 unknown via CMAUP database
Conkuressine 12303833 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1C 356.60 unknown via CMAUP database
Holadienine 12310532 Click to see CC1C2CCC3C2(CCC4C3CCC5=CC(=O)C=CC45C)CN1C 325.50 unknown via CMAUP database
Holarrhenine 12310556 Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)N(C)C)C)O 372.60 unknown via CMAUP database
Isoconessimine 11772257 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)CN1C 342.60 unknown via CMAUP database
Kurcholessine 20054951 Click to see CC1C(CCC2(C1(CC(C3C2CCC45C3CCC4C(N(C5)C)C)O)O)C)N(C)C 404.60 unknown via CMAUP database
Regholarrhenine E 101529338 Click to see CC1C(CCC2(C1(CC(C3C2CCC45C3CCC4C(N(C5)C)C)O)O)C)N(C)C 404.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
24-ethylcholesta-5,23E-dien-3beta-ol 5283668 Click to see CCC(=CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
> Organoheterocyclic compounds / Azaspirodecane derivatives
Conarrhimine 12303820 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N)C)CN1 314.50 unknown via CMAUP database
Conessimine 12303831 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1 342.60 unknown via CMAUP database
Conimin 101686 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)CN1 328.50 unknown via CMAUP database
Regholarrhenine D 101529337 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1O 358.60 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
Paravallarine 442980 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)C(=O)O1 343.50 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolines
Conckurchine 76330309 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N)C)C=N1 312.50 unknown via CMAUP database
Conessidine 22214027 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)C=N1 326.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Anthracyclines
Aranciamycin J 122177931 Click to see CC1C(C(C(C(O1)OC2CC(C(=O)C3=CC4=C(C(=C23)O)C(=O)C5=C(C4=O)C=CC=C5O)(C)O)OC)O)O 514.50 unknown https://doi.org/10.1016/S0031-9422(02)00454-5
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
[(2R,3S,4S,5R,6R)-6-[(2S,3S,4S,5R)-3,4-dihydroxy-2-(hydroxymethyl)-5-[[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxymethyl]oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-hydroxyphenyl)prop-2-enoate 11093420 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)CO)O)O)O)O 634.60 unknown https://doi.org/10.1016/S0031-9422(02)00454-5
[6-[3,4-Dihydroxy-2-(hydroxymethyl)-5-[3-(4-hydroxyphenyl)prop-2-enoyloxymethyl]oxolan-2-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 162967613 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)O)O)O)CO)O)O)O)O 634.60 unknown https://doi.org/10.1016/S0031-9422(02)00454-5
coumaroyl(-6)Fruf(b2-1a)Glc 11027343 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(O2)(CO)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 488.40 unknown https://doi.org/10.1016/S0031-9422(02)00454-5
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(3S)-3-hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-[5-[(E)-3-hydroxyprop-1-enyl]-3-methoxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 162897595 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)C(CC(=O)C3=CC(=C(C=C3)O)OC)O)C=CCO 536.50 unknown https://doi.org/10.1248/CPB.54.1190
3-Hydroxy-1-(4-hydroxy-3-methoxyphenyl)-3-[5-(3-hydroxyprop-1-enyl)-3-methoxy-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]propan-1-one 73236254 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)C(CC(=O)C3=CC(=C(C=C3)O)OC)O)C=CCO 536.50 unknown https://doi.org/10.1248/CPB.54.1190
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
(2R,3R,4S,5S,6R)-2-[(E)-3-[3-[(1S,3S)-1,3-dihydroxy-3-(4-hydroxy-3-methoxyphenyl)propyl]-4-hydroxy-5-methoxyphenyl]prop-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163031186 Click to see COC1=CC(=CC(=C1O)C(CC(C2=CC(=C(C=C2)O)OC)O)O)C=CCOC3C(C(C(C(O3)CO)O)O)O 538.50 unknown https://doi.org/10.1248/CPB.54.1190
2-[3-[3-[1,3-Dihydroxy-3-(4-hydroxy-3-methoxyphenyl)propyl]-4-hydroxy-5-methoxyphenyl]prop-2-enoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73236255 Click to see COC1=CC(=CC(=C1O)C(CC(C2=CC(=C(C=C2)O)OC)O)O)C=CCOC3C(C(C(C(O3)CO)O)O)O 538.50 unknown https://doi.org/10.1248/CPB.54.1190

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