Gynura divaricata - Unknown
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Internal ID UUID643fd2a4c4d44215290899
Scientific name Gynura divaricata
Authority DC.
First published in Prodr. 6: 301 (1838)

Description Top

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Synonyms Top

Scientific name Authority First published in
Gynura ovalis DC. Prodr. 6: 300 (1838)
Gynura glabrata Hook.f. Fl. Brit. India 3(8): 335 (1881)
Kleinia hieracioides Less. Linnaea 6: 133 (1831)
Gynura hemsleyana H.Lév. Bull. Géogr. Bot. 24: 284 (1914)
Cacalia incana L. Sp. Pl. ed. 2 2: 1169 (1763)
Senecio divaricatus L. Sp. Pl. : 866 (1753)
Gynura pseudo-china Benth. Fl. Hongk. : 189 (1861)
Senecio boryanus Sch.Bip. Beitr. Fl. Aethiop. : 159 (1867)
Cacalia hieracioides Willd. Sp. Pl., ed. 4 , 3: 1781 (1803)
Gynura ovalis var. pinnatifida Hemsl. J. Linn. Soc., Bot. 23: 448 (1888)
Cacalia ovalis Ker Gawl. Bot. Reg. 2: t. 101 (1816)
Gynura auriculata Cass. Opusc. Phyt. 3: 100. 1834
Porophyllum hieracioides DC. Prodr. 5: 650 (1836)

Common names Top

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Language Common/alternative name
Indonesian daun dewa
jv godhong déwa
Malay pokok daun dewa
Chinese 大肥牛
Chinese 白子菜
Chinese 鸡草
Chinese 鸡菜
Chinese 箐跌打
Chinese 白子菜(三百棒、叉花土三七、白子草)
Chinese 白背三七
Chinese 叉花土三七

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 South-central
      • China Southeast
      • Hainan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000125459
Tropicos 50157444
INPN 706343
KEW urn:lsid:ipni.org:names:211249-1
The Plant List gcc-86536
Open Tree Of Life 7051810
NCBI Taxonomy 904593
IPNI 211249-1
iNaturalist 347638
GBIF 3139895
USDA GRIN 462353

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
Wnt/β-Catenin signaling pathway in hepatocellular carcinoma: pathogenic role and therapeutic target Zhao Z, Cui T, Wei F, Zhou Z, Sun Y, Gao C, Xu X, Zhang H Front Oncol 02-Apr-2024
PMCID:PMC11022604
doi:10.3389/fonc.2024.1367364
PMID:38634048
Wild edible plants and their cultural significance among the Zhuang ethnic group in Fangchenggang, Guangxi, China Liu S, Huang X, Bin Z, Yu B, Lu Z, Hu R, Long C J Ethnobiol Ethnomed 08-Nov-2023
PMCID:PMC10631048
doi:10.1186/s13002-023-00623-2
PMID:37940945
Progress of research on PD-1/PD-L1 in leukemia Cao H, Wu T, Zhou X, Xie S, Sun H, Sun Y, Li Y Front Immunol 26-Sep-2023
PMCID:PMC10562551
doi:10.3389/fimmu.2023.1265299
PMID:37822924
Exploring the mechanism by which aqueous Gynura divaricata inhibits diabetic foot based on network pharmacology, molecular docking and experimental verification Sun Y, Gao C, Liu H, Liu X, Yue T Mol Med 20-Jan-2023
PMCID:PMC9862864
doi:10.1186/s10020-023-00605-w
PMID:36670362
Integrated Chemical Characterization, Network Pharmacology and Transcriptomics to Explore the Mechanism of Sesquiterpenoids Isolated from Gynura divaricata (L.) DC. against Chronic Myelogenous Leukemia Ye X, Wang L, Yang X, Yang J, Zhou J, Lan C, Kantawong F, Kumsaiyai W, Wu J, Zeng J Pharmaceuticals (Basel) 19-Nov-2022
PMCID:PMC9693606
doi:10.3390/ph15111435
PMID:36422564
A Potential Biofertilizer—Siderophilic Bacteria Isolated From the Rhizosphere of Paris polyphylla var. yunnanensis Wang Y, Zhang G, Huang Y, Guo M, Song J, Zhang T, Long Y, Wang B, Liu H Front Microbiol 09-May-2022
PMCID:PMC9125218
doi:10.3389/fmicb.2022.870413
PMID:35615507
The TetR Family Repressor HpaR Negatively Regulates the Catabolism of 5-Hydroxypicolinic Acid in Alcaligenes faecalis JQ135 by Binding to Two Unique DNA Sequences in the Promoter of Hpa Operon Xu S, Jiang Y, Zhang F, Wang X, Zhang K, Zhao L, Hong Q, Qiu J, He J Appl Environ Microbiol 22-Mar-2022
PMCID:PMC8939343
doi:10.1128/aem.02390-21
PMID:35138929
Chondroprotective Effects of 4,5-Dicaffeoylquinic Acid in Osteoarthritis through NF-κB Signaling Inhibition Jang G, Lee SA, Hong JH, Park BR, Kim DK, Kim CS Antioxidants (Basel) 28-Feb-2022
PMCID:PMC8944529
doi:10.3390/antiox11030487
PMID:35326137
Potential Mechanisms Involved in the Protective Effect of Dicaffeoylquinic Acids from Artemisia annua L. Leaves against Diabetes and Its Complications El-Askary H, Salem HH, Abdel Motaal A Molecules 27-Jan-2022
PMCID:PMC8839821
doi:10.3390/molecules27030857
PMID:35164118
The Pharmacological Effects and Pharmacokinetics of Active Compounds of Artemisia capillaris Hsueh TP, Lin WL, Dalley JW, Tsai TH Biomedicines 08-Oct-2021
PMCID:PMC8533588
doi:10.3390/biomedicines9101412
PMID:34680529
Intervention of Gastrodin in Type 2 Diabetes Mellitus and Its Mechanism Bai Y, Mo K, Wang G, Chen W, Zhang W, Guo Y, Sun Z Front Pharmacol 16-Sep-2021
PMCID:PMC8481818
doi:10.3389/fphar.2021.710722
PMID:34603025
Phytochemical screening, antimalarial activities, and genetic relationship of 16 indigenous Thai Asteraceae medicinal plants: A combinatorial approach using phylogeny and ethnobotanical bioprospecting in antimalarial drug discovery Liana D, Rungsihirunrat K J Adv Pharm Technol Res 16-Jul-2021
PMCID:PMC8300331
doi:10.4103/japtr.JAPTR_238_21
PMID:34345604
Phytomedicines Targeting Cancer Stem Cells: Therapeutic Opportunities and Prospects for Pharmaceutical Development Gupta PK, Saraff M, Gahtori R, Negi N, Tripathi SK, Kumar J, Kumar S, Aldhayan SH, Dhanasekaran S, Abomughaid MM, Dua K, Gundamaraju R, Ojha S, Ruokolainen J, Jha NK, Kesari KK Pharmaceuticals (Basel) 15-Jul-2021
PMCID:PMC8308767
doi:10.3390/ph14070676
PMID:34358102
Herbal Medicines Targeting the Improved β-Cell Functions and β-Cell Regeneration for the Management of Diabetes Mellitus Wickramasinghe AS, Kalansuriya P, Attanayake AP Evid Based Complement Alternat Med 14-Jul-2021
PMCID:PMC8298154
doi:10.1155/2021/2920530
PMID:34335803
Quantification of Usaramine and its N-Oxide Metabolite in Rat Plasma Using Liquid Chromatography-Tandem Mass Spectrometry Lin F, Ma Y, Pan A, Ye Y, Liu J J Anal Toxicol 04-Jun-2021
PMCID:PMC9122504
doi:10.1093/jat/bkab060
PMID:34086913

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 / Sphingolipids / Glycosphingolipids
(2R)-N-[(E,2S,3S,4R)-3,4-dihydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadec-10-en-2-yl]-2-hydroxytricosanamide 163005028 Click to see CCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C(CCCCCC=CCCCCCCC)O)O)O 830.20 unknown https://doi.org/10.1016/J.FITOTE.2009.06.010
(2R)-N-[(Z,2S,3S,4R)-3,4-dihydroxy-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadec-10-en-2-yl]-2-hydroxytetracosanamide 162983115 Click to see CCCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C(CCCCCC=CCCCCCCC)O)O)O 844.30 unknown https://doi.org/10.1080/14786410902836677
N-[3,4-dihydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadec-10-en-2-yl]-2-hydroxytetracosanamide 162983114 Click to see CCCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C(CCCCCC=CCCCCCCC)O)O)O 844.30 unknown https://doi.org/10.1080/14786410902836677
N-[3,4-dihydroxy-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoctadec-10-en-2-yl]-2-hydroxytricosanamide 163005027 Click to see CCCCCCCCCCCCCCCCCCCCCC(C(=O)NC(COC1C(C(C(C(O1)CO)O)O)O)C(C(CCCCCC=CCCCCCCC)O)O)O 830.20 unknown https://doi.org/10.1016/J.FITOTE.2009.06.010
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
[(2R,3S,4S,5R,6R)-6-[[(3S,8S,9S,10R,13R,14S,17R)-17-[(1R,4R)-4-ethyl-1,5-dimethyl-hexyl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-3,4,5-trihydroxy-tetrahydropyran-2-yl]methyl heptadecanoate 15959352 Click to see CCCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 829.30 unknown https://doi.org/10.1080/14786410902836677
ST 29:1;O;Hex;FA 17:0 73207267 Click to see CCCCCCCCCCCCCCCCC(=O)OCC1C(C(C(C(O1)OC2CCC3(C4CCC5(C(C4CC=C3C2)CCC5C(C)CCC(CC)C(C)C)C)C)O)O)O 829.30 unknown https://doi.org/10.1080/14786410902836677
> Organoheterocyclic compounds / Diazines / Pyrazines
(1R,2S,3R)-1-[6-[(2R,3S)-2,3,4-trihydroxybutyl]pyrazin-2-yl]butane-1,2,3,4-tetrol 162990888 Click to see C1=C(N=C(C=N1)C(C(C(CO)O)O)O)CC(C(CO)O)O 304.30 unknown https://doi.org/10.1080/14786410902836677
1-[6-(2,3,4-Trihydroxybutyl)pyrazin-2-yl]butane-1,2,3,4-tetrol 12285901 Click to see C1=C(N=C(C=N1)C(C(C(CO)O)O)O)CC(C(CO)O)O 304.30 unknown https://doi.org/10.1080/14786410902836677
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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 https://doi.org/10.1080/14786410902836677
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 122173234 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 594.50 unknown https://doi.org/10.1080/14786410902836677
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 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/10.1080/14786410902836677
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxy-6-methyloxan-2-yl)oxymethyl]oxan-2-yl]oxychromen-4-one 12313332 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 594.50 unknown https://doi.org/10.1080/14786410902836677
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/10.1080/14786410902836677
> Phenylpropanoids and polyketides / Macrolides and analogues
(1R,4E,6S,7R,17R)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 5318449 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1055/S-2006-957921
(1S,4Z,7S,17S)-4-ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 133562009 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1055/S-2006-957921
4-Ethylidene-7-hydroxy-6,7-dimethyl-2,9-dioxa-14-azatricyclo[9.5.1.014,17]heptadec-11-ene-3,8-dione 254855 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(C)O)C 335.40 unknown https://doi.org/10.1055/S-2006-957921
Usaramine 5281756 Click to see CC=C1CC(C(C(=O)OCC2=CCN3C2C(CC3)OC1=O)(CO)O)C 351.40 unknown https://doi.org/10.1055/S-2006-957921

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