Actinidia polygama

Details

Ethnobotanical Use

General Uses

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Gallery

Contributors

Collections

Details Top

Internal ID	UUID6440073e45db4497841221
Scientific name	Actinidia polygama
Authority	(Siebold & Zucc.) Planch. ex Maxim.
First published in	Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 64 (1859)

Ethnobotanical Use Top

Suggest a correction!

Important notice

Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

I should begin by noting that there are no verified ethnobotanical records for *Actinidia polygama* involving teas, tinctures, decoctions, macerations, or poultices across any cultures or regions. Despite some chemotaxonomic interest in its iridoid content, reputable sources like historical pharmacopoeias, ethnobotanical surveys of East Asia (its native region), or peer-reviewed ethnomedicinal studies do not document traditional medicinal or culinary preparation methods for this species. While related *Actinidia* species (like *A. deliciosa* or *A. chinensis*) have culinary uses, *A. polygama* itself lacks documented traditional applications meeting your specified criteria.

General Uses Top

Suggest a correction!

Common products:
- Fresh fruit: eaten raw as a sweet‑tart snack.
- Fruit juice: extracted and bottled or used as a base for beverages.
- Jam and preserves: fruit pulp cooked with sugar to produce spreads.
- Dried fruit: fruit sliced and dried for a shelf‑stable snack.
- Fruit wine: fermented pulp used to produce a low‑alcohol beverage.
- Fruit puree: used as a base for sauces, desserts and frozen desserts.

Industrial and craft applications:
- Ornamental horticulture: cultivated for silvery foliage, autumn colour and climbing habit; used in landscaping, trellises and erosion control.
- Scientific model organism: employed in fruit development and ethylene regulation studies; draft genome and transcriptome data are publicly available (e.g., NCBI BioProject), supporting comparative genomics.

Food and beverages (non-medicinal):
- The fruit is consumed fresh or processed into juice, jam, dried slices and wine.
- It serves as a flavoring ingredient in desserts, sauces, cocktails and smoothies.
- No traditional medicinal preparations are considered.

Properties relevant to use:
- Soluble‑solid content (≈15‑20 °Brix) confers high sweetness.
- Vitamin C content of ~200‑250 mg 100 g⁻¹ fresh weight adds acidity and contributes to preservation.
- Pectin levels in the pulp provide the gel‑forming capacity required for jam production.
- Organic acids (citric and malic) and a balanced sugar–acid ratio support stable fermentation for wine.
- The fruit has a thin, tender skin and moderate pH (~3.5), facilitating straightforward processing and juicing.

Standards and regulation:
- Products such as juice, jam and wine must meet Codex Alimentarius standards for fruit juice (Codex Stan 247‑2005) and jams (Codex Stan 79‑1981).
- In the US, foods are regulated under FDA 21 CFR (e.g., Part 114 for juice, Part 150 for jams) and in the EU under Regulation (EC) No 852/2004 (hygiene) and No 1333/2008 (food additives).

Sustainability and sourcing:
- Natural range includes Japan, Korea and China; fruit is harvested from wild stands and small‑scale cultivated plots, with collection limited to ≤30 % of the crop per plant.
- The species is not listed in CITES and trade follows national plant‑trade regulations; its tolerance of temperate climates and marginal soils enables production on land unsuitable for major food crops.

Synonyms Top

Scientific name	Authority	First published in
Trochostigma volubile	Siebold & Zucc.	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 3(2): 728 (1843)
Actinidia inflammans	Nakai	Bull. Natl. Sci. Mus. Tokyo 33: 17 (1953)
Actinidia lecomtei	Nakai	Bot. Mag. (Tokyo) 47: 253 (1933)
Actinidia polygama var. latifolia	Miq.	Ann. Mus. Bot. Lugduno-Batavi 3: 15 1867
Actinidia repanda	Honda	Siebold Kentyu : 564 (1938)
Actinidia volubilis	Franch. & Sav.	Enum. Pl. Jap. 1: 59. 1873 [4 Nov 1873]
Trochostigma polygamum	Siebold & Zucc.	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 3(2): 728 (1843)
Actinidia polygama var. lecomtei	(Nakai) H.L.Li	J. Arnold Arbor. 33: 22 (1952)
Actinidia volubilis	(Siebold & Zucc.) Planch. ex Miq.	Ann. Mus. Bot. Lugduno-Batavi 3: 15 (1867)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	silver vine
Arabic	اكتينيديا بوليغاما
Arabic	اكتينيديه
Arabic	ماتاتابي
Azerbaijani	poliqam aktinidiya
Czech	aktinidie stříbrná
German	japanischer strahlengriffel
German	silberwein
German	matatabi
Estonian	mõru aktiniidia
Persian	اکتینیدیا پلیگاما
Finnish	mantsurianlaikkuköynnös
Finnish	mantšurianlaikkuköynnös
Icelandic	silfurflétta
Japanese	木天蓼
Japanese	マタタビ
Japanese	またたび
Japanese	モクテンリョウ
Japanese	夏梅
Korean	개다래
lzh	木天蓼
Dutch	matatabi
Russian	Актинидия полигамная
Swedish	klätteraktinidia
Turkish	matatabi
Ukrainian	Актинідія полігамна
Chinese	木天蓼
Chinese	葛枣
Chinese	木天蓼子
Chinese	木天蓼根
Chinese	葛棗獼猴桃
Chinese	葛枣子
Chinese	木天寥
Chinese	葛枣猕猴桃

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Inner Mongolia
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
- Russian Far East
  - Kuril Islands
  - Primorye

Northern America click to expand
- Northeastern U.S.A.
  - New York

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000519316
UNII	1H09UQ1KQM
USDA Plants	ACPO9
Tropicos	500157
KEW	urn:lsid:ipni.org:names:60472666-2
The Plant List	kew-2620762
Open Tree Of Life	9477
Observations.org	139109
NCBI Taxonomy	64480
IPNI	60472666-2
iNaturalist	447065
GBIF	3189692
Freebase	/m/04y8y_9
EPPO	ATIPO
EOL	392752
Elurikkus	374157
USDA GRIN	1411
Wikipedia	Actinidia_polygama
CMAUP	NPO20123
Plantarium	698
PFAF	Actinidia polygama

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_030159135.1	APO_r1.1	Scaffold	Kazusa DNA Research Institute	2023-03-16	20	591.64 Mb

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

In vitro immune-enhancing effects of Platycodon grandiflorum combined with Salvia plebeian via MAPK and NF-κB signaling in RAW264.7 cells

Jang AY, Kim M, Rod-in W, Nam YS, Yoo TY, Park WJ

PLoS One

02-Feb-2024

PMCID:	PMC10836713
doi:	10.1371/journal.pone.0297512
PMID:	38306362

Actinidia polygama Water Extract (APWE) Protects Against UVB-Induced Photoaging via MAPK/AP-1 and TGFβ-Smad Pathway

Lee JM, Park SJ, Kim YJ, Kim SY, Jang YN, Park AY, Ho SH, Kim D, Lee JO, Yoo KH, Kim BJ

Ann Dermatol

20-Dec-2023

PMCID:	PMC10861301
doi:	10.5021/ad.23.010
PMID:	38325430

Adipose tissue inflammation linked to obesity: A review of current understanding, therapies and relevance of phyto-therapeutics

Aruwa CE, Sabiu S

Heliyon

02-Dec-2023

PMCID:	PMC10755291
doi:	10.1016/j.heliyon.2023.e23114
PMID:	38163110

Assessing the safety and suitability of using silver vine as an olfactory enrichment for cats

Uenoyama R, Ooka S, Miyazaki T, Mizumoto H, Nishikawa T, Hurst JL, Miyazaki M

iScience

07-Sep-2023

PMCID:	PMC10558724
doi:	10.1016/j.isci.2023.107848
PMID:	37810229

Comparative transcriptomic and plastid development analysis sheds light on the differential carotenoid accumulation in kiwifruit flesh

Bhargava N, Ampomah-Dwamena C, Voogd C, Allan AC

Front Plant Sci

30-Aug-2023

PMCID:	PMC10499360
doi:	10.3389/fpls.2023.1213086
PMID:	37711308

Investigation of Small-Molecule Constituents in Voacanga africana Seeds and Mapping of Their Spatial Distributions Using Laser Ablation Direct Analysis in Real-Time Imaging–Mass Spectrometry (LADI-MS)

Coon AM, Musah RA

ACS Omega

18-Jul-2023

PMCID:	PMC10399170
doi:	10.1021/acsomega.3c02464
PMID:	37546641

The Role of Comparative Psychology in the Training of Veterinarians

Boughton BA, Abramson CI

Animals (Basel)

14-Jul-2023

PMCID:	PMC10376381
doi:	10.3390/ani13142315
PMID:	37508092

Evaluation of Lipid Extracts from the Marine Fungi Emericellopsis cladophorae and Zalerion maritima as a Source of Anti-Inflammatory, Antioxidant and Antibacterial Compounds

Abraúl M, Alves A, Hilário S, Melo T, Conde T, Domingues MR, Rey F

Mar Drugs

23-Mar-2023

PMCID:	PMC10142463
doi:	10.3390/md21040199
PMID:	37103339

Comparing information derived on food habits of a terrestrial carnivore between animal-borne video systems and fecal analyses methods

Tezuka S, Tanaka M, Naganuma T, Tochigi K, Inagaki A, Myojo H, Yamazaki K, Allen ML, Koike S

J Mammal

25-Nov-2022

PMCID:	PMC9976756
doi:	10.1093/jmammal/gyac101
PMID:	36876239

Sources, Transformations, Syntheses, and Bioactivities of Monoterpene Pyridine Alkaloids and Cyclopenta[c]pyridine Derivatives

Zhang X, Tao F, Cui T, Luo C, Zhou Z, Huang Y, Tan L, Peng W, Wu C

Molecules

24-Oct-2022

PMCID:	PMC9656638
doi:	10.3390/molecules27217187
PMID:	36364013

Enhancement of linalool production in Saccharomyces cerevisiae by utilizing isopentenol utilization pathway

Zhang Y, Cao X, Wang J, Tang F

Microb Cell Fact

15-Oct-2022

PMCID:	PMC9571491
doi:	10.1186/s12934-022-01934-x
PMID:	36243714

Biogeography and Ecological Differentiation of Pseudasphondylia gall midges (Diptera: Cecidomyiidae) Distributed in Taiwan and Japan, with Description of a New Species P. kiwiphila sp. nov. and the Southernmost Record of P. elaeocarpi

Lin SF, Tokuda M, Tung GS, Pan LY, Kim W, Yukawa J, Yang MM

Zool Stud

11-Oct-2022

PMCID:	PMC9745572
doi:	10.6620/ZS.2022.61-39
PMID:	36568810

Lotus germ extract rejuvenates aging fibroblasts via restoration of disrupted proteostasis by the induction of autophagy

Machihara K, Kageyama S, Oki S, Makino H, Sasaki M, Iwahashi H, Namba T

Aging (Albany NY)

26-Sep-2022

PMCID:	PMC9596218
doi:	10.18632/aging.204303
PMID:	36170016

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

Dwarf Kiwi (Actinidia arguta Miq.), a Source of Antioxidants for a Healthy and Sustainable Diet

Garcia-Herrera P, Maieves HA, Vega EN, Perez-Rodriguez ML, Fernandez-Ruiz V, Iriondo-DeHond A, del Castillo MD, Sanchez-Mata MC

Molecules

26-Aug-2022

PMCID:	PMC9457597
doi:	10.3390/molecules27175495
PMID:	36080263

Phytochemical Profile Top

Add a new one!

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
> Alkaloids and derivatives / Gelsemium alkaloids
(2S,7S)-7-ethyl-7-hydroxy-1'-methoxyspiro[11-oxa-5-azatricyclo[6.3.1.04,9]dodecane-2,3'-indole]-2'-one	10991969	Click to see	358.40	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Cytisine and derivatives
(1S,9R)-7-aza-11-azoniatricyclo[7.3.1.02,7]trideca-2,4-dien-6-one	11859180	Click to see	191.25	unknown	via CMAUP database
> Alkaloids and derivatives / Lupin alkaloids / Matrine alkaloids
(+)-Sophoranol	12442899	Click to see	264.36	unknown	via CMAUP database
> Alkaloids and derivatives / Strychnos alkaloids
Nortoxiferine, dihydro-	6440874	Click to see	552.70	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives
Phenylethyl Alcohol	6054	Click to see C1=CC=C(C=C1)CCO	122.16	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid	135	Click to see C1=CC(=CC=C1C(=O)O)O	138.12	unknown	via CMAUP database
Protocatechuic Acid	72	Click to see	154.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzonitriles
3,4-Dimethylbenzonitrile	89884	Click to see	131.17	unknown	via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Isodiospyrin	99298	Click to see	374.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
methyl (Z)-8-hydroxydec-2-en-4,6-diynoate	6475135	Click to see	192.21	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
CID 14239432	14239432	Click to see	310.50	unknown	via CMAUP database
methyl (3R)-5-[(1S,2S,4aR,8aR)-2-hydroxy-2,5,5,8a-tetramethyl-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl]-3-methylpentanoate	102118407	Click to see	338.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
(+)-Neomatatabiol	442429	Click to see CC1CCC2C1C(OCC2C)O	170.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
(2S)-2-[(1R)-2-(hydroxymethyl)-3-methylcyclopent-2-en-1-yl]propan-1-ol	10877559	Click to see	170.25	unknown	https://doi.org/10.1016/0040-4020(80)88041-0
(5R)-2-methyl-5-[(2S)-1-oxopropan-2-yl]cyclopentene-1-carbaldehyde	11019224	Click to see	166.22	unknown	https://doi.org/10.1246/CL.1978.433
(5S)-2-methyl-5-[(2R)-1-oxopropan-2-yl]cyclopentene-1-carbaldehyde	124350940	Click to see CC1=C(C(CC1)C(C)C=O)C=O	166.22	unknown	https://doi.org/10.1246/CL.1978.433
2-Cyclopentene-1-acetaldehyde, 2-formyl-alpha,3-dimethyl-	557095	Click to see CC1=C(C(CC1)C(C)C=O)C=O	166.22	unknown	https://doi.org/10.1246/CL.1978.433
> Lipids and lipid-like molecules / Prenol lipids / Sesterterpenoids
Uyshrhkohclbce-phrmgerwsa-	11969877	Click to see CC(=CCCC(=CC=CC(=CC1CC2(C(C(=C(C)C=O)CCC2(C)O)CCCO)C(O1)O)C)C)C	486.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4R,4aR,7S,7aS)-4,7-dimethyl-4,4a,5,6,7,7a-hexahydro-3H-cyclopenta[c]pyran-1-one	11816081	Click to see	168.23	unknown	https://doi.org/10.1246/BCSJ.53.3683
(4R,4aS,7S,7aS)-4,7-dimethyl-4,4a,5,6,7,7a-hexahydro-1H-cyclopenta[c]pyran-3-one	101911406	Click to see	168.23	unknown	https://doi.org/10.1246/BCSJ.53.3683
(4S,4aR,7S,7aS)-4,7-dimethyl-4,4a,5,6,7,7a-hexahydro-3H-cyclopenta[c]pyran-1-one	12310929	Click to see	168.23	unknown	https://doi.org/10.1246/BCSJ.53.3683
4abeta,7alpha,7abeta-Nepetalactone	6431022	Click to see	166.22	unknown	via CMAUP database
Cyclopenta[c]pyran-3(1H)-one, hexahydro-4,7-dimethyl-, [4S-(4alpha,4abeta,7beta,7abeta)]-	6432464	Click to see	168.23	unknown	via CMAUP database
Dihydronepetalactone	519465	Click to see	168.23	unknown	https://doi.org/10.1246/BCSJ.53.3683
Iridomirmecina	95453	Click to see	168.23	unknown	https://doi.org/10.1246/BCSJ.53.3683
Isoiridomyrmecin	120743	Click to see	168.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	https://doi.org/10.1016/S0031-9422(00)94767-8 https://doi.org/10.1016/0031-9422(92)83634-B
(1S,2R,4aS,6aR,6aS,6bR,8aR,10S,11R,12aR,14bS)-10,11-dihydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	101630850	Click to see	504.70	unknown	https://doi.org/10.1016/0031-9422(92)83634-B
(1S,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bS)-11-hydroxy-9-(hydroxymethyl)-10-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	163185830	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)O	634.80	unknown	https://doi.org/10.1016/0031-9422(92)83634-B
(1S,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bS)-9-formyl-10,11-dihydroxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	101630851	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C=O)O)O)C)C)C2C1C)C)C(=O)O	486.70	unknown	https://doi.org/10.1016/0031-9422(92)83634-B
(1S,2R,4aS,6aR,6aS,6bR,8aR,9S,10R,11R,12aR,14bS)-11-hydroxy-9-(hydroxymethyl)-10-[(E)-3-(4-hydroxyphenyl)prop-2-enoyl]oxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	163186861	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)O	634.80	unknown	https://doi.org/10.1016/S0031-9422(00)94767-8
(1S,4S,5R,8R,9S,10S,11R,13S,14R,17S,18R,19S,20R)-10,11-dihydroxy-9-(hydroxymethyl)-4,5,9,13,19,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-23-one	162980581	Click to see	486.70	unknown	https://doi.org/10.1016/S0031-9422(00)94767-8
(2R,3S,4R,4aR,6aR,6bS,8aS,11R,12S,12aS,14aR,14bR)-2,3-dihydroxy-4-(hydroxymethyl)-6a,6b,11,12,14b-pentamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-4,8a-dicarboxylic acid	101630394	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(CO)C(=O)O)O)O)C)C)C2C1C)C)C(=O)O	518.70	unknown	https://doi.org/10.1016/0031-9422(92)83634-B
10-hydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	14136880	Click to see	472.70	unknown	https://doi.org/10.1016/S0031-9422(00)94767-8
10,11-Dihydroxy-9-(hydroxymethyl)-1,6a,6b,9,12a-pentamethyl-2-methylidene-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	23132228	Click to see	486.70	unknown	https://doi.org/10.1016/0031-9422(92)83634-B
10,11-dihydroxy-9,9-bis(hydroxymethyl)-1,2,6a,6b,12a-pentamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	14105934	Click to see	504.70	unknown	https://doi.org/10.1016/0031-9422(92)83634-B
11-hydroxy-9-(hydroxymethyl)-10-[3-(4-hydroxyphenyl)prop-2-enoyloxy]-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	85052452	Click to see	634.80	unknown	https://doi.org/10.1016/S0031-9422(00)94767-8 https://doi.org/10.1016/0031-9422(92)83634-B
2,24-Dihydroxyursolic acid	69570833	Click to see	488.70	unknown	https://doi.org/10.1016/0031-9422(92)83634-B https://doi.org/10.1016/S0031-9422(00)94767-8
2,3-dihydroxy-4-(hydroxymethyl)-6a,6b,11,12,14b-pentamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picene-4,8a-dicarboxylic acid	162980159	Click to see	518.70	unknown	https://doi.org/10.1016/0031-9422(92)83634-B
2,3,24-Trihydroxy-12-ursen-28-oic acid	296191	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O	488.70	unknown	https://doi.org/10.1016/S0031-9422(00)94767-8 https://doi.org/10.1016/0031-9422(92)83634-B
2,3,24-Trihydroxy-12-ursen-28-oic acid	12308659	Click to see	488.70	unknown	https://doi.org/10.1016/0031-9422(92)83634-B https://doi.org/10.1016/S0031-9422(00)94767-8
24-Hydroxyursolic Acid	44568920	Click to see	472.70	unknown	https://doi.org/10.1016/S0031-9422(00)94767-8
2a,3a,23-Trihydroxyurs-12,20(30)-dien-28-oic acid	70697438	Click to see CC1C2C3=CCC4C(C3(CCC2(CCC1=C)C(=O)O)C)(CCC5C4(CC(C(C5(C)CO)O)O)C)C	486.70	unknown	https://doi.org/10.1016/0031-9422(92)83634-B
3-O-Coumaroylasiatic acid	9898761	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)OC(=O)C=CC6=CC=C(C=C6)O)O)C)C)C2C1C)C)C(=O)O	634.80	unknown	https://doi.org/10.1016/S0031-9422(00)94767-8
9-formyl-10,11-dihydroxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	162968205	Click to see	486.70	unknown	https://doi.org/10.1016/0031-9422(92)83634-B
Asiatic Acid	119034	Click to see	488.70	unknown	https://doi.org/10.1016/S0031-9422(00)94767-8 https://doi.org/10.1016/0031-9422(92)83634-B
Colosolic acid	15917996	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	https://doi.org/10.1016/0031-9422(92)83634-B https://doi.org/10.1016/S0031-9422(00)94767-8
Corosolic acid	6918774	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O	472.70	unknown	https://doi.org/10.1016/S0031-9422(00)94767-8 https://doi.org/10.1016/0031-9422(92)83634-B
Esculentic acid	9898760	Click to see	488.70	unknown	https://doi.org/10.1016/S0031-9422(00)94767-8 https://doi.org/10.1016/0031-9422(92)83634-B
Npc3247	619164	Click to see	498.70	unknown	https://doi.org/10.1016/S0031-9422(00)94767-8 https://doi.org/10.1016/0031-9422(92)83634-B
Urs-12-en-28-oic acid, 3-hydroxy-, (3beta)-	220774	Click to see	456.70	unknown	https://doi.org/10.1016/0031-9422(92)83634-B https://doi.org/10.1016/S0031-9422(00)94767-8
Ursolic acid acetate	6475119	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C(=O)O	498.70	unknown	https://doi.org/10.1016/0031-9422(92)83634-B https://doi.org/10.1016/S0031-9422(00)94767-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
8-Hydroxy-6-methoxy-9b-methyl-7-propan-2-yl-3,3b,4,5,10,11-hexahydronaphtho[2,1-e][2]benzofuran-1-one	5318610	Click to see	342.40	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1R,5R,9S)-5-hydroxy-10,10-dimethyl-6-methylidenebicyclo[7.2.0]undecan-2-one	7067857	Click to see	222.32	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
4,4,7a-Trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one	27209	Click to see CC1(CCCC2(C1=CC(=O)O2)C)C	180.24	unknown	https://doi.org/10.1055/S-0028-1097333
4,4,7a-trimethyl-5H-1-benzofuran-2-one	15558330	Click to see	178.23	unknown	via CMAUP database
Dihydroactinidiolide	6432173	Click to see	180.24	unknown	https://doi.org/10.1055/S-0028-1097333
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
Methyl 2,2-dimethylchromene-6-carboxylate	5316881	Click to see CC1(C=CC2=C(O1)C=CC(=C2)C(=O)OC)C	218.25	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Delta valerolactones
(4R,4aR)-4,7-dimethyl-4,4a,5,6-tetrahydro-1H-cyclopenta[c]pyran-3-one	11094994	Click to see	166.22	unknown	https://doi.org/10.1246/BCSJ.53.3683
(4S,4aR)-4,7-dimethyl-4,4a,5,6-tetrahydro-1H-cyclopenta[c]pyran-3-one	24881148	Click to see	166.22	unknown	https://doi.org/10.1246/BCSJ.53.3683
(4S,4aR)-4,7-dimethyl-4,4a,5,6-tetrahydro-3H-cyclopenta[c]pyran-1-one	11073784	Click to see CC1COC(=O)C2=C(CCC12)C	166.22	unknown	via CMAUP database
4,7-dimethyl-4,4a,5,6-tetrahydro-1H-cyclopenta[c]pyran-3-one	15768154	Click to see CC1C2CCC(=C2COC1=O)C	166.22	unknown	https://doi.org/10.1246/BCSJ.53.3683
4,7-dimethyl-4,4a,5,6-tetrahydro-3H-cyclopenta[c]pyran-1-one	5320104	Click to see	166.22	unknown	https://doi.org/10.1246/BCSJ.53.3683
Neonepetalactone	12313200	Click to see	166.22	unknown	https://doi.org/10.1246/BCSJ.53.3683
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(3R,3aR,6aS)-3,6,6a-trimethyl-3a,4-dihydro-3H-cyclopenta[b]furan-2-one	163010359	Click to see	166.22	unknown	https://doi.org/10.1246/BCSJ.53.3683
3,6,6a-trimethyl-3a,4-dihydro-3H-cyclopenta[b]furan-2-one	163010358	Click to see	166.22	unknown	https://doi.org/10.1246/BCSJ.53.3683
Actinidialactone	101410414	Click to see CC1C2CC=C(C2(OC1=O)C)C	166.22	unknown	https://doi.org/10.1246/BCSJ.53.3683
> Organoheterocyclic compounds / Oxanes
4,7-Dimethyl-1,3,4,4a,5,6-hexahydrocyclopenta[c]pyran-6-ol	5317459	Click to see	168.23	unknown	via CMAUP database
Matatabiether	5319300	Click to see	166.26	unknown	https://doi.org/10.1016/S0040-4039(00)75373-1
> Organoheterocyclic compounds / Oxepanes
(1,4-Dimethyl-2-oxabicyclo[3.2.1]octan-8-yl)methanol	5318195	Click to see CC1COC2(CCC1C2CO)C	170.25	unknown	via CMAUP database
1,4-Dimethyl-8-methylidene-2-oxabicyclo[3.2.1]octan-7-ol	5318260	Click to see CC1COC2(C(CC1C2=C)O)C	168.23	unknown	via CMAUP database
1,4-Dimethyl-8-methylidene-2-oxabicyclo[3.2.1]octane	15560143	Click to see	152.23	unknown	https://doi.org/10.1016/S0040-4039(00)75373-1
> Organoheterocyclic compounds / Oxolanes
(3,6-Dimethyl-2,3,3a,4-tetrahydrocyclopenta[b]furan-6a-yl)methanol	5319301	Click to see CC1COC2(C1CC=C2C)CO	168.23	unknown	via CMAUP database
> Organoheterocyclic compounds / Pyridines and derivatives / Methylpyridines
(+)-Actinidine	9812811	Click to see	147.22	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid	689043	Click to see	180.16	unknown	via CMAUP database
cis-Caffeic acid	1549111	Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O	180.16	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
4-(2-Hydroxy-7-phenylheptyl)-2-methoxyphenol	5320105	Click to see COC1=C(C=CC(=C1)CC(CCCCCC2=CC=CC=C2)O)O	314.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S)-2-(3,4-dihydroxyphenyl)-5-hydroxy-8-[(Z)-4-hydroxy-3-methylbut-2-enyl]-7-methoxy-2,3-dihydrochromen-4-one	163193739	Click to see	386.40	unknown	https://doi.org/10.1016/S0031-9422(00)94767-8
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3R,4S,5S,6R)-2-[[(2S,3R,4R,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-hydroxy-6-methyl-5-[(2S,3R,4S,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl] acetate	163044764	Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2OC(=O)C)O)OCC3C(C(C(C(O3)OC4=C(OC5=CC(=CC(=C5C4=O)O)O)C6=CC=C(C=C6)O)O)O)O)C)O)O)O	782.70	unknown	https://doi.org/10.1016/0031-9422(90)89052-B
[(2S,3S,4R,5S,6R)-2-[[(2S,3S,4R,5S,6R)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-hydroxy-6-methyl-5-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl] acetate	163044765	Click to see	782.70	unknown	https://doi.org/10.1016/0031-9422(90)89052-B
[2-[[6-[5,7-Dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-hydroxy-6-methyl-5-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-4-yl] acetate	14463121	Click to see	782.70	unknown	https://doi.org/10.1016/0031-9422(90)89052-B
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Penduletin 4'-methyl ether	5318355	Click to see	358.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid O-glycosides
Iristectorigenin A 7-O-glucoside	44257353	Click to see	492.40	unknown	via CMAUP database
Iristectorigenin B 7-O-glucoside	44257354	Click to see COC1=C(C=CC(=C1)C2=COC3=CC(=C(C(=C3C2=O)O)OC)OC4C(C(C(C(O4)CO)O)O)O)O	492.40	unknown	via CMAUP database

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Actinidia polygama

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