Decaisnea insignis in Genus Decaisnea

Details Top

Internal ID	UUID644015ec8c212409049653
Scientific name	Decaisnea insignis
Authority	Hook.f. & Thomson
First published in	Proc. Linn. Soc. London 2: 350 (1854)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Slackia insignis	Griff.	J. Trav. 2: 187. 1847 (1847)

Common names Top

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Filter by language:

Language	Common/alternative name
Japanese	デカイスネア・インシグニス
Dutch	augurkenstruik
Chinese	猫儿屎
Chinese	猫屎瓜
Chinese	猫儿子
Chinese	矮杞树
Chinese	貓兒屎

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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Start at 4°C for 3 months, then warm to 20°C for another 3 months.

Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.

Requires Soaking: These seeds need to be soaked in warm water until they swell, which can take 24-48 hours. Seeds that float are usually not viable and should be discarded, along with the soaking water.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya
- Indo-China
  - Myanmar

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000638939
Tropicos	17700004
KEW	urn:lsid:ipni.org:names:107240-1
The Plant List	kew-2758557
PFAF	Decaisnea insignis
Open Tree Of Life	512541
NCBI Taxonomy	161261
IPNI	107240-1
GBIF	5686494
EPPO	DEAIN
EOL	2899997
USDA GRIN	13373

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

Endophytic Aspergillii and Penicillii from medicinal plants: a focus on antimicrobial and multidrug resistant pathogens inhibitory activity

Mamangkey J, Mendes LW, Mustopa AZ, Hartanto A

BioTechnologia (Pozn)

29-Mar-2024

PMCID:	PMC11020150
doi:	10.5114/bta.2024.135644
PMID:	38633888

Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China

Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C

J Ethnobiol Ethnomed

15-Jan-2024

PMCID:	PMC10790445
doi:	10.1186/s13002-023-00638-9
PMID:	38225656

Complete chloroplast genome of Tricyrtis xianjuensis Li, Chen & Ma 2014 (Liliaceae): a species endemic to Zhejiang province, China

Huang L, Lu Z, Wang J, Bao H, Zhang H, Jiang M

Mitochondrial DNA B Resour

08-Jan-2024

PMCID:	PMC10776049
doi:	10.1080/23802359.2023.2301021
PMID:	38197054

Novel Mechanisms Underlying Rubber Accumulation and Programmed Cell Death in Laticiferous Canals of Decaisnea insignis Fruits: Cytological and Transcriptomic Analyses

Zhou Y, Li G, Han G, Mao S, Yang L, Wang Y

Plants (Basel)

07-Oct-2023

PMCID:	PMC10575083
doi:	10.3390/plants12193497
PMID:	37836237

Industrial and Ruminant Trans-Fatty Acids-Enriched Diets Differentially Modulate the Microbiome and Fecal Metabolites in C57BL/6 Mice

Mohammadi F, Green M, Tolsdorf E, Greffard K, Leclercq M, Bilodeau JF, Droit A, Foster J, Bertrand N, Rudkowska I

Nutrients

16-Mar-2023

PMCID:	PMC10052023
doi:	10.3390/nu15061433
PMID:	36986163

Characterization of the complete chloroplast genome of Clematoclethra scandens subsp. actinidioides (Actinidiaceae)

Zhang L, Zhang Y, Jia Y, Ding F, Wang F, Yu G, Wu Y

Mitochondrial DNA B Resour

29-Aug-2022

PMCID:	PMC9448431
doi:	10.1080/23802359.2022.2110532
PMID:	36081829

The Beneficial Effects of Natural Extracts and Bioactive Compounds on the Gut-Liver Axis: A Promising Intervention for Alcoholic Liver Disease

Zhao L, Wang S, Zhang N, Zhou J, Mehmood A, Raka RN, Zhou F, Zhao L

Antioxidants (Basel)

20-Jun-2022

PMCID:	PMC9219895
doi:	10.3390/antiox11061211
PMID:	35740108

Original karst tiankeng with underground virgin forest as an inaccessible refugia originated from a degraded surface flora in Yunnan, China

Shui W, Chen Y, Jian X, Jiang C, Wang Q, Zeng Y, Zhu S, Guo P, Li H

Sci Rep

07-Jun-2022

PMCID:	PMC9174222
doi:	10.1038/s41598-022-13678-0
PMID:	35672447

Vegetation Classification and Distribution Patterns in the South Slope of Yarlung Zangbo Grand Canyon National Nature Reserve, Eastern Himalayas

Wu PP, Wang Z, Jia NX, Dong SQ, Qu XY, Qiao XG, Liu CC, Guo K

Plants (Basel)

28-Apr-2022

PMCID:	PMC9105001
doi:	10.3390/plants11091194
PMID:	35567195

Characterization of the complete chloroplast genome of Brassica oleracea var. italica and phylogenetic relationships in Brassicaceae

Zhang Z, Tao M, Shan X, Pan Y, Sun C, Song L, Pei X, Jing Z, Dai Z

PLoS One

24-Feb-2022

PMCID:	PMC8870505
doi:	10.1371/journal.pone.0263310
PMID:	35202392

Endophytic Fungi: An Effective Alternative Source of Plant-Derived Bioactive Compounds for Pharmacological Studies

Wen J, Okyere SK, Wang S, Wang J, Xie L, Ran Y, Hu Y

J Fungi (Basel)

20-Feb-2022

PMCID:	PMC8877053
doi:	10.3390/jof8020205
PMID:	35205959

Fungal Endophytes: A Potential Source of Antibacterial Compounds

Deshmukh SK, Dufossé L, Chhipa H, Saxena S, Mahajan GB, Gupta MK

J Fungi (Basel)

08-Feb-2022

PMCID:	PMC8877021
doi:	10.3390/jof8020164
PMID:	35205918

Ethnobotanical study on wild edible plants used by Dulong people in northwestern Yunnan, China

Cheng Z, Lu X, Lin F, Naeem A, Long C

J Ethnobiol Ethnomed

21-Jan-2022

PMCID:	PMC8781162
doi:	10.1186/s13002-022-00501-3
PMID:	35062974

Development and Evolution of Unisexual Flowers: A Review

Jabbour F, Espinosa F, Dejonghe Q, Le Péchon T

Plants (Basel)

07-Jan-2022

PMCID:	PMC8780417
doi:	10.3390/plants11020155
PMID:	35050043

Herbal plants traded at the Kaili medicinal market, Guizhou, China

Liu S, Zhang B, Zhou J, Lei Q, Fang Q, Kennelly EJ, Long C

J Ethnobiol Ethnomed

29-Nov-2021

PMCID:	PMC8628420
doi:	10.1186/s13002-021-00495-4
PMID:	34844607

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
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	100998350	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)O)O)OC9C(C(C(CO9)O)O)O)O	1045.20	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3S,4R,5R)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162993933	Click to see	1059.20	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3S,4R,5R)-5-hydroxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162940530	Click to see	1221.40	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2R,3S,4R,5R)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	163189662	Click to see	1207.30	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2R,3S,4R,5R)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	162995978	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)CO)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)O)O)C)(C)C)O)O)O)CO)O)O)O	1221.40	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10-[3-[3,5-dihydroxy-6-methyl-4-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	85212470	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C)C)C)O)O)O)OC9C(C(C(CO9)O)O)O)O	1045.20	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
[3,4,5-Trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 10-[4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	14284457	Click to see	1059.20	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
[6-[[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] 10-[4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	14036569	Click to see	1205.40	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
Akebiasaponin PK	3874518	Click to see	1221.40	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
Decaisoside E	100998349	Click to see	1207.30	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
Hederasaponin B	21626480	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)O)O)O)C)(C)C)O)O)O)CO)O)O)O	1205.40	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-[(2R,3S,4R,5R)-5-hydroxy-4-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	162939605	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O	897.10	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2R,3S,4R,5R)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	162932118	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	883.10	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
10-[5-Hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	73813221	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)C)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O	897.10	unknown	https://doi.org/10.1016/0031-9422(93)85533-W
CID 15625347	15625347	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O	883.10	unknown	https://doi.org/10.1016/0031-9422(93)85533-W

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Decaisnea insignis

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top