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Kadsura induta

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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 UUID643ff3bddc418708105066
Scientific name Kadsura induta
Authority A.C.Sm.
First published in Sargentia 7: 173 (1947)

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 متشابكة
Chinese 毛南五味子

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000357310
Tropicos 50099273
KEW urn:lsid:ipni.org:names:554577-1
The Plant List kew-2335473
Open Tree Of Life 152956
NCBI Taxonomy 238547
IPNI 554577-1
GBIF 3745227

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
New dibenzocyclooctadiene lignans from Kadsura induta with their anti-inflammatory activity Tai BH, Yen PH, Hoang NH, Thanh Huong PT, Dung NV, Van Thanh B, Cuong NT, Bang NA, Nhiem NX, Van Kiem P RSC Adv 07-Sep-2022
PMCID:PMC9451003
doi:10.1039/d2ra05052h
PMID:36199356
Anti-hepatitis B activities of Myanmar medicinal plants: a narrative review of current evidence Linn YH, Ei WW, Myint LM, Lwin KM Virusdisease 14-Jul-2021
PMCID:PMC8473485
doi:10.1007/s13337-021-00714-2
PMID:34631974
Plant-derived lignans as potential antiviral agents: a systematic review Xu XY, Wang DY, Li YP, Deyrup ST, Zhang HJ Phytochem Rev 31-May-2021
PMCID:PMC8165688
doi:10.1007/s11101-021-09758-0
PMID:34093097
Antiviral activities of Radix isatidis polysaccharide against pseudorabies virus in swine testicle cells Tong C, Chen Z, Liu F, Qiao Y, Chen T, Wang X BMC Complement Med Ther 11-Feb-2020
PMCID:PMC7076820
doi:10.1186/s12906-020-2838-4
PMID:32046705
Lignans and Triterpenoids from the Stems of <i>Kadsura induta</i> Wenhui Ma, Xiaolin Ma, Yan Lu, Daofeng Chen Wiley 07-Apr-2009
doi:10.1002/HLCA.200800363

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
> Lignans, neolignans and related compounds / Aryltetralin lignans
(5S,6S,7R)-4-methoxy-5-(7-methoxy-1,3-benzodioxol-5-yl)-6,7-dimethyl-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole 102480442 Click to see CC1CC2=CC3=C(C(=C2C(C1C)C4=CC5=C(C(=C4)OC)OCO5)OC)OCO3 384.40 unknown https://doi.org/10.1002/HLCA.200800363
4-Methoxy-5-(7-methoxy-1,3-benzodioxol-5-yl)-6,7-dimethyl-5,6,7,8-tetrahydrobenzo[f][1,3]benzodioxole 163027990 Click to see CC1CC2=CC3=C(C(=C2C(C1C)C4=CC5=C(C(=C4)OC)OCO5)OC)OCO3 384.40 unknown https://doi.org/10.1002/HLCA.200800363
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
butyl (3S)-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanoate 163102293 Click to see CCCCOC(=O)CC(C)OC1C(C(C(C(O1)CO)O)O)O 322.35 unknown https://doi.org/10.1002/HLCA.200800363
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(Z,6R)-2-methyl-6-[(5R,10S,12R,14S)-4,4,10,12,14-pentamethyl-3-oxo-2,5,6,7,11,12,15,16-octahydro-1H-cyclopenta[a]phenanthren-17-yl]hept-2-enoic acid 162852990 Click to see CC1CC2=C(CCC3C2(CCC(=O)C3(C)C)C)C4(C1=C(CC4)C(C)CCC=C(C)C(=O)O)C 452.70 unknown https://doi.org/10.1002/HLCA.200800363
(Z,6R)-6-[(3S,5R,10S,13R,14R,17R)-3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid 14104880 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1002/HLCA.200800363
(Z,6R)-6-[(5R,10S,12S,13R,14S,17R)-12-hydroxy-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]-2-methylhept-2-enoic acid 162910715 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(C(CC3=C2CCC4C3(CCC(=O)C4(C)C)C)O)C)C 470.70 unknown https://doi.org/10.1002/HLCA.200800363
2-methyl-6-(4,4,10,12,14-pentamethyl-3-oxo-2,5,6,7,11,12,15,16-octahydro-1H-cyclopenta[a]phenanthren-17-yl)hept-2-enoic acid 162852989 Click to see CC1CC2=C(CCC3C2(CCC(=O)C3(C)C)C)C4(C1=C(CC4)C(C)CCC=C(C)C(=O)O)C 452.70 unknown https://doi.org/10.1002/HLCA.200800363
2-Methyl-6-(4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)hept-2-enoic acid 53427596 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1002/HLCA.200800363
6-(12-Hydroxy-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,7,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl)-2-methylhept-2-enoic acid 162910713 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(C(CC3=C2CCC4C3(CCC(=O)C4(C)C)C)O)C)C 470.70 unknown https://doi.org/10.1002/HLCA.200800363
6-(3-hydroxy-4,4,10,13,14-pentamethyl-2,3,5,6,7,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-methylhept-2-enoic acid 435761 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2CCC4C3(CCC(C4(C)C)O)C)C)C 456.70 unknown https://doi.org/10.1002/HLCA.200800363
Anwuweizonic acid 6451093 Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3=C2CCC4C3(CCC(=O)C4(C)C)C)C)C 454.70 unknown https://doi.org/10.1002/HLCA.200800363
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
3,22-Dimethoxy-12,13-dimethyl-5,7,18,20-tetraoxapentacyclo[13.7.0.02,10.04,8.017,21]docosa-1(22),2,4(8),9,15,17(21)-hexaen-11-ol 56660178 Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4C(C1C)O)OCO5)OC)OC)OCO3 400.40 unknown https://doi.org/10.1002/HLCA.200800363
Gomisin R 11516888 Click to see CC1CC2=CC3=C(C(=C2C4=C(C5=C(C=C4C(C1C)O)OCO5)OC)OC)OCO3 400.40 unknown https://doi.org/10.1002/HLCA.200800363
Kadsurindutin H 10364453 Click to see CC1C(C(=O)C2=CC3=C(C(=C2C4=C(C5=C(C=C4C1O)OCO5)OC)OC)OCO3)C 414.40 unknown https://doi.org/10.1002/HLCA.200800363

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