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Kadsura oblongifolia

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643ff3bee0ddf978902335
Scientific name Kadsura oblongifolia
Authority Merr.
First published in Philipp. J. Sci. 23: 241 (1923)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Arabic كدسورة بيضاوية الأوراق
Vietnamese nắm cơm lá thuôn
Chinese 吹风散
Chinese 冷饭藤
Chinese 饭团藤

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 Southeast
      • Hainan
    • Eastern Asia
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000357339
Tropicos 19300578
KEW urn:lsid:ipni.org:names:554588-1
The Plant List kew-2335508
PFAF Kadsura oblongifolia
Open Tree Of Life 533191
NCBI Taxonomy 124783
IPNI 554588-1
GBIF 3745240
EOL 5348459

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
Daniellia oliveri (Rolfe) Hutch and Dalziel: Antimicrobial Activities, Cytotoxicity Evaluation, and Phytochemical Identification by GC-MS Tittikpina NK, Kirsch G, Duval RE, Chaimbault P, Jacob C Antibiotics (Basel) 25-Nov-2022
PMCID:PMC9774647
doi:10.3390/antibiotics11121699
PMID:36551356
Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China Lu Z, Chen H, Lin C, Ou G, Li J, Xu W J Ethnobiol Ethnomed 21-Jun-2022
PMCID:PMC9210605
doi:10.1186/s13002-022-00544-6
PMID:35729593
Chemical Composition and Biological Activities of Essential Oils from the Leaves, Stems, and Roots of Kadsura coccinea Zhao T, Ma C, Zhu G Molecules 16-Oct-2021
PMCID:PMC8537082
doi:10.3390/molecules26206259
PMID:34684838
Phenolic Profiles, Antioxidant, and Inhibitory Activities of Kadsura heteroclita (Roxb.) Craib and Kadsura coccinea (Lem.) A.C. Sm. Sritalahareuthai V, Temviriyanukul P, On-nom N, Charoenkiatkul S, Suttisansanee U Foods 02-Sep-2020
PMCID:PMC7555767
doi:10.3390/foods9091222
PMID:32887386
Carry forward advantages of traditional medicines in prevention and control of outbreak of COVID-19 pandemic Deng JG, Hou XT, Zhang TJ, Bai G, Hao EW, Chu JJ, Wattanathorn J, Sirisa-ard P, Soo Ee C, Low J, Liu CX Chin Herb Med 02-Jun-2020
PMCID:PMC7266592
doi:10.1016/j.chmed.2020.05.003
PMID:32834811
Coevolution with pollinating resin midges led to resin-filled nurseries in the androecia, gynoecia and tepals of Kadsura (Schisandraceae) Luo SX, Liu TT, Cui F, Yang ZY, Hu XY, Renner SS Ann Bot 21-Apr-2017
PMCID:PMC5714246
doi:10.1093/aob/mcx024
PMID:28444386
Kadsufolins A – D and Related Cytotoxic Lignans from <i>Kadsura oblongifolia</i> Zehao Huang, Yan Lu, Yinan Liu, Kenneth F. Bastow, Kuohsiung Lee, Daofeng Chen Wiley 14-Mar-2011
doi:10.1002/HLCA.201000259
Complete assignments of 1H and 13C NMR data for new dibenzocyclooctadiene lignans from Kadsura oblongifolia. Liu HT, Xu LJ, Peng Y, Yang JS, Yang XW, Xiao PG Magn Reson Chem 01-Jul-2009
doi:10.1002/MRC.2430
PMID:19347905

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
Name PubChem ID Canonical SMILES MW Found in Proof
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(11-Acetyloxy-3,9-dihydroxy-4,5,19-trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl) benzoate 162987235 Click to see CC1C(C2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC(=O)C5=CC=CC=C5)OC)OC)O)OC)OCO3)OC(=O)C 580.60 unknown https://doi.org/10.1002/MRC.2430
(11-Acetyloxy-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl) 2-methylbut-2-enoate 75072516 Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C(C1(C)O)C)OC(=O)C)OCO4)OC)OC)OC)OC 572.60 unknown https://doi.org/10.1002/MRC.2430
(11-Acetyloxy-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl) benzoate 162849662 Click to see CC1C(C2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3)OC(=O)C 594.60 unknown https://doi.org/10.1002/MRC.2430
(11-Acetyloxy-9,19-dihydroxy-3,4,5-trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl) 2-methylbut-2-enoate 162919694 Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C(C1(C)O)C)OC(=O)C)OCO4)O)OC)OC)OC 558.60 unknown https://doi.org/10.1002/MRC.2430
(3,4,5,14,15,16-Hexamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl) 2-methylbut-2-enoate 75952090 Click to see CC=C(C)C(=O)OC1C(C(CC2=CC(=C(C(=C2C3=C(C(=C(C=C13)OC)OC)OC)OC)OC)OC)C)C 514.60 unknown https://doi.org/10.1002/HLCA.201000259
(3,4,5,14,15,16-Hexamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl) acetate 75215361 Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1C)OC(=O)C)OC)OC)OC)OC)OC)OC 474.50 unknown https://doi.org/10.1002/HLCA.201000259
(5-Hydroxy-3,4,19-trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl) 3-phenylprop-2-enoate 74941628 Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1C)OC(=O)C=CC5=CC=CC=C5)O)OC)OC)OC)OCO3 532.60 unknown https://doi.org/10.1002/HLCA.201000259
(5-Hydroxy-3,4,19-trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl) benzoate 53353757 Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1C)OC(=O)C5=CC=CC=C5)O)OC)OC)OC)OCO3 506.50 unknown https://doi.org/10.1002/HLCA.201000259
(9,19-Dihydroxy-3,4,5-trimethoxy-9,10-dimethyl-11-propanoyloxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl) 2-methylbut-2-enoate 162846499 Click to see CCC(=O)OC1C(C(C(C2=CC(=C(C(=C2C3=C(C4=C(C=C13)OCO4)O)OC)OC)OC)OC(=O)C(=CC)C)(C)O)C 572.60 unknown https://doi.org/10.1002/MRC.2430
(9S,10S)-10-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-one 163006854 Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(=O)C1(C)O)OCO4)OC)OC)OC)OC 430.40 unknown https://doi.org/10.1002/MRC.2430
[(8R,9R,10R)-3,4,5,14,15,16-hexamethoxy-9,10-dimethyl-8-tricyclo[10.4.0.02,7]hexadeca-1(16),2,4,6,12,14-hexaenyl] (Z)-2-methylbut-2-enoate 52914110 Click to see CC=C(C)C(=O)OC1C(C(CC2=CC(=C(C(=C2C3=C(C(=C(C=C13)OC)OC)OC)OC)OC)OC)C)C 514.60 unknown https://doi.org/10.1002/HLCA.201000259
[(8R,9S,10S)-5-hydroxy-3,4,19-trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] (E)-3-phenylprop-2-enoate 53349180 Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1C)OC(=O)C=CC5=CC=CC=C5)O)OC)OC)OC)OCO3 532.60 unknown https://doi.org/10.1002/HLCA.201000259
[(8S,9S,10S,11R)-11-acetyloxy-9-hydroxy-3,4,5,19-tetramethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] (Z)-2-methylbut-2-enoate 53389593 Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C(C1(C)O)C)OC(=O)C)OCO4)OC)OC)OC)OC 572.60 unknown https://doi.org/10.1002/MRC.2430
[(8S,9S,10S,11R)-9,19-dihydroxy-3,4,5-trimethoxy-9,10-dimethyl-11-propanoyloxy-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-8-yl] (Z)-2-methylbut-2-enoate 163195352 Click to see CCC(=O)OC1C(C(C(C2=CC(=C(C(=C2C3=C(C4=C(C=C13)OCO4)O)OC)OC)OC)OC(=O)C(=CC)C)(C)O)C 572.60 unknown https://doi.org/10.1002/MRC.2430
3,10-Dihydroxy-4,5,19-trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-one 163009418 Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(=O)C1(C)O)OCO4)OC)O)OC)OC 416.40 unknown https://doi.org/10.1002/MRC.2430
5,10-Dihydroxy-3,4,19-trimethoxy-9,10-dimethyl-15,17-dioxatetracyclo[10.7.0.02,7.014,18]nonadeca-1(19),2,4,6,12,14(18)-hexaen-11-one 163017160 Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(=O)C1(C)O)OCO4)OC)OC)OC)O 416.40 unknown https://doi.org/10.1002/MRC.2430
ArisanschininA 52914210 Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1C)OC(=O)C5=CC=CC=C5)O)OC)OC)OC)OCO3 506.50 unknown https://doi.org/10.1002/HLCA.201000259
HeteroclitinQ 16203510 Click to see CC1C(C2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC(=O)C5=CC=CC=C5)OC)OC)O)OC)OCO3)OC(=O)C 580.60 unknown https://doi.org/10.1002/MRC.2430
KadoblongifolinA 145709445 Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(=O)C1(C)O)OCO4)OC)O)OC)OC 416.40 unknown https://doi.org/10.1002/MRC.2430
KadoblongifolinB 145709462 Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(=O)C1(C)O)OCO4)OC)OC)OC)O 416.40 unknown https://doi.org/10.1002/MRC.2430
KadoblongifolinC 138112236 Click to see CC1CC2=CC(=C(C(=C2C3=C(C4=C(C=C3C(=O)C1(C)O)OCO4)OC)OC)OC)OC 430.40 unknown https://doi.org/10.1002/MRC.2430
KadsufolinB 53349075 Click to see CC1CC2=CC(=C(C(=C2C3=C(C(=C(C=C3C(C1C)OC(=O)C)OC)OC)OC)OC)OC)OC 474.50 unknown https://doi.org/10.1002/HLCA.201000259
SchisantherinG 145709288 Click to see CC=C(C)C(=O)OC1C2=CC(=C(C(=C2C3=C(C4=C(C=C3C(C(C1(C)O)C)OC(=O)C)OCO4)O)OC)OC)OC 558.60 unknown https://doi.org/10.1002/MRC.2430
SchizanrinF 10077212 Click to see CC1C(C2=CC3=C(C(=C2C4=C(C(=C(C=C4C(C1(C)O)OC(=O)C5=CC=CC=C5)OC)OC)OC)OC)OCO3)OC(=O)C 594.60 unknown https://doi.org/10.1002/MRC.2430

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