Ficus pandurata - Unknown
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Internal ID UUID64401c920b6cd942076301
Scientific name Ficus pandurata
Authority Hance
First published in Ann. Sci. Nat., Bot. , sér. 4, 18: 229 (1862)

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Synonyms Top

Scientific name Authority First published in
Ficus formosana var. angustissima W.C.Ko Acta Phytotax. Sin. 8: 352 1963
Ficus pandurata var. angustifolia W.C.Cheng Contr. Biol. Lab. Sci. Soc. China, Bot. Ser. 9: 256 1934
Ficus pandurata var. holophylla Migo Bull. Shanghai Sci. Inst. 14: 329 1944
Ficus pandurata var. linearis Migo J. Shanghai Sci. Inst., Sect. 3 14: 330 1944
Ficus formosana var. linearis Migo

Common names Top

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Language Common/alternative name
Arabic تين ربابي الورق
Vietnamese sung lá đàn
Chinese 全缘榕
Chinese 琴叶榕
Chinese 琴叶榕(条叶榕、全叶榕)
Chinese 琴葉榕
Chinese 条叶榕
Chinese 全叶榕

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-0000689628
Tropicos 21301625
KEW urn:lsid:ipni.org:names:853368-1
The Plant List kew-2811636
Open Tree Of Life 835270
NCBI Taxonomy 1009471
IPNI 853368-1
iNaturalist 735147
GBIF 5570029
USDA GRIN 16927
Wikipedia Ficus_pandurata

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
Hybridization, polyploidization, and morphological convergence make dozens of taxa into one chaotic genetic pool: a phylogenomic case of the Ficus erecta species complex (Moraceae) Wang X, Liao S, Zhang Z, Zhang J, Mei L, Li H Front Plant Sci 26-Mar-2024
PMCID:PMC11002808
doi:10.3389/fpls.2024.1354812
PMID:38595762
Ferroptosis in Liver Disease: Natural Active Compounds and Therapeutic Implications Wu Z, Zhu Y, Liu W, Balasubramanian B, Xu X, Yao J, Lei X Antioxidants (Basel) 15-Mar-2024
PMCID:PMC10968642
doi:10.3390/antiox13030352
PMID:38539886
Effects of Natural Products on Enzymes Involved in Ferroptosis: Regulation and Implications Zuo HL, Huang HY, Lin YC, Liu KM, Lin TS, Wang YB, Huang HD Molecules 04-Dec-2023
PMCID:PMC10708253
doi:10.3390/molecules28237929
PMID:38067658
Characterization of Pseudomonas capsici strains from pepper and tomato Zhao M, Gitaitis R, Dutta B Front Microbiol 11-Oct-2023
PMCID:PMC10599140
doi:10.3389/fmicb.2023.1267395
PMID:37886076
Inequality Measure of Leaf Area Distribution for a Drought-Tolerant Landscape Plant Huang L, Ratkowsky DA, Hui C, Gielis J, Lian M, Yao W, Li Q, Zhang L, Shi P Plants (Basel) 31-Aug-2023
PMCID:PMC10490070
doi:10.3390/plants12173143
PMID:37687388
Micro-Executor of Natural Products in Metabolic Diseases Liu J, Chen H, Li X, Song C, Wang L, Wang D Molecules 23-Aug-2023
PMCID:PMC10488769
doi:10.3390/molecules28176202
PMID:37687031
Medicinal Plants, Phytochemicals and Regulation of the NLRP3 Inflammasome in Inflammatory Bowel Diseases: A Comprehensive Review Direito R, Barbalho SM, Figueira ME, Minniti G, de Carvalho GM, de Oliveira Zanuso B, de Oliveira dos Santos AR, de Góes Corrêa N, Rodrigues VD, de Alvares Goulart R, Guiguer EL, Araújo AC, Bosso H, Fornari Laurindo L Metabolites 06-Jun-2023
PMCID:PMC10305268
doi:10.3390/metabo13060728
PMID:37367886
The role of Nrf2 in the pathogenesis and treatment of ulcerative colitis Peng S, Shen L, Yu X, Zhang L, Xu K, Xia Y, Zha L, Wu J, Luo H Front Immunol 05-Jun-2023
PMCID:PMC10285877
doi:10.3389/fimmu.2023.1200111
PMID:37359553
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
Effects of Ficus pandurata Hance var. angustifolia Cheng Flavonoids on Intestinal Barrier and Cognitive Function by Regulating Intestinal Microbiota Zhang Y, Pan J, Liu Y, Zhang X, Cheng K Foods 18-Apr-2023
PMCID:PMC10137925
doi:10.3390/foods12081682
PMID:37107477
Liver Protection of a Low-Polarity Fraction from Ficus pandurata Hance, Prepared by Supercritical CO2 Fluid Extraction, on CCl4-Induced Acute Liver Injury in Mice via Inhibiting Apoptosis and Ferroptosis Mediated by Strengthened Antioxidation Dai W, Pang X, Peng W, Zhan X, Chen C, Zhao W, Zeng C, Mei Q, Chen Q, Kuang W, Gou Z, Hu X Molecules 22-Feb-2023
PMCID:PMC10004706
doi:10.3390/molecules28052078
PMID:36903326
Effects of Medicinal Plants and Phytochemicals in Nrf2 Pathways during Inflammatory Bowel Diseases and Related Colorectal Cancer: A Comprehensive Review Laurindo LF, de Maio MC, Minniti G, de Góes Corrêa N, Barbalho SM, Quesada K, Guiguer EL, Sloan KP, Detregiachi CR, Araújo AC, de Alvares Goulart R Metabolites 07-Feb-2023
PMCID:PMC9966918
doi:10.3390/metabo13020243
PMID:36837862
Analysis of the Chloroplast Genome of Ficus simplicissima Lour Collected in Vietnam and Proposed Barcodes for Identifying Ficus Plants Vu TT, Vu LT, Le LT, Lo TT, Chu MH Curr Issues Mol Biol 27-Jan-2023
PMCID:PMC9955830
doi:10.3390/cimb45020067
PMID:36826012
The complete chloroplast genome sequence of Ficus pandurata Hance var. angustifolia W.C. Cheng (Moraceae) Zhang X, Xu F, Guo L Mitochondrial DNA B Resour 22-Aug-2022
PMCID:PMC9415532
doi:10.1080/23802359.2022.2110005
PMID:36034529
Phytochemical Insights into Ficus sur Extracts and Their Biological Activity Sieniawska E, Świątek Ł, Sinan KI, Zengin G, Boguszewska A, Polz-Dacewicz M, Bibi Sadeer N, Etienne OK, Mahomoodally MF Molecules 13-Mar-2022
PMCID:PMC8949149
doi:10.3390/molecules27061863
PMID:35335228

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
3,4-Dihydroxybenzoic acid 72 Click to see C1=CC(=C(C=C1C(=O)O)O)O 154.12 unknown https://doi.org/10.1080/14786410902757899
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Hexacosanol 68171 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCO 382.70 unknown https://doi.org/10.1080/14786410902757899
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4,4,6a,6b,8a,11,12,14b-Octamethyl-9-oxo-1,2,3,4a,5,6,6a,7,8,12,12a,13,14,14a-tetradecahydropicen-3-yl) acetate 85235904 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C=C1C)C)C)C)(C)C)OC(=O)C)C 482.70 unknown https://doi.org/10.1080/14786410902757899
[(3S,4aR,6aR,6aR,6bR,8aR,12S,12aR,14aR,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-9-oxo-1,2,3,4a,5,6,6a,7,8,12,12a,13,14,14a-tetradecahydropicen-3-yl] acetate 100936445 Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CCC2(C(=O)C=C1C)C)C)C)(C)C)OC(=O)C)C 482.70 unknown https://doi.org/10.1080/14786410902757899
4,4,6a,6b,8a,11,11,14b-Octamethyl-1,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-octadecahydro-2H-picen-3-one 612782 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1080/14786410902757899
4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-ol 225688 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1080/14786410902757899
9-Hydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylic acid 2371 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1080/14786410902757899
alpha-Amyrenyl acetate 92842 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown https://doi.org/10.1080/14786410902757899
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1080/14786410902757899
alpha-Amyrin acetate 293754 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown https://doi.org/10.1080/14786410902757899
beta-Amyrone 12306160 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(=O)C5(C)C)C)C)C2C1)C)C)C 424.70 unknown https://doi.org/10.1080/14786410902757899
beta-Ursolic acid 220774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown https://doi.org/10.1080/14786410902757899
Betulinic Acid 64971 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C(=O)O 456.70 unknown https://doi.org/10.1080/14786410902757899
methyl (1R,3aS,5aR,5bR,7aR,9S,10R,11aR,11bR,13aR,13bR)-9,10-dihydroxy-5a,5b,8,8,11a-pentamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate 21672694 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C(=O)OC 486.70 unknown https://doi.org/10.1080/14786410902757899
Methyl 2,3-dihydroxylup-20(29)-en-28-oate 605213 Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)C)O)O)C)C)C(=O)OC 486.70 unknown https://doi.org/10.1080/14786410902757899
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 https://doi.org/10.1080/14786410902757899
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 122544 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1080/14786410902757899
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 https://doi.org/10.1080/14786410902757899
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1080/14786410902757899
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1080/14786410902757899
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1080/14786410902757899
Stigmasterol 5280794 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1080/14786410902757899
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
4-Hydroxy-3-(3,4,5-trihydroxyoxan-2-yl)oxybenzoic acid 78119324 Click to see C1C(C(C(C(O1)OC2=C(C=CC(=C2)C(=O)O)O)O)O)O 286.23 unknown https://doi.org/10.1080/14786410902757899
4-hydroxy-3-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxybenzoic acid 162984742 Click to see C1C(C(C(C(O1)OC2=C(C=CC(=C2)C(=O)O)O)O)O)O 286.23 unknown https://doi.org/10.1080/14786410902757899
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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 https://doi.org/10.1080/14786410902757899
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5378597 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/10.1080/14786410902757899
Isoquercetin 5280804 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/10.1080/14786410902757899
Kaempferol 3-neohesperidoside 5318761 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1080/14786410902757899
Kaempferol-3-O-glucorhamnoside 13915496 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O)O)O 594.50 unknown https://doi.org/10.1080/14786410902757899
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 https://doi.org/10.1080/14786410902757899
Vitamin P 5293655 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 https://doi.org/10.1080/14786410902757899

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