Actinidia kolomikta

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID6440073c7b918585901462
Scientific name	Actinidia kolomikta
Authority	Maxim.
First published in	Mém. Acad. Imp. Sci. St.-Pétersbourg Divers Savans 9: 63 (1859)

Description Top

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Synonyms Top

Scientific name	Authority	First published in
Actinidia gagnepainii	Nakai	Bot. Mag. (Tokyo) 47: 258 (1933)
Actinidia kolomikta var. gagnepainii	(Nakai) H.L.Li	J. Arnold Arbor. 33: 19 1952
Actinidia leptophylla	C.Y.Wu	Fl. Yunnanica 1: 63 (1977)
Actinidia maloides	H.L.Li	J. Arnold Arbor. 33: 25 (1952)
Actinidia maloides f. cordata	C.F.Liang	Fl. Reipubl. Popularis Sin. 49(2): 311, 215 (1984).
Actinidia tetramera var. maloides	(H.L.Li) C.Y.Wu	Fl. Yunnanica 1: 69 (1977)
Prunus kolomikta	Maxim.	Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 15: 129 (1856)
Prunus kolomikta	Maxim. & Rupr.	Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 15: 129 1857
Kalomikta mandshurica	Regel	Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 15: 219. 1857
Trochostigma kolomikta	Rupr.	Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 15: 261 (1857)

Common names Top

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Filter by language:

Language	Common/alternative name
English	kolomikta
English	arctic beauty
English	variegated-leaf hardy kiwi
English	miyamatatabi
Arabic	اكتينيديا كولوميتا
Azerbaijani	kolomikt aktinidiyası
azb	کولومیکت آکتینیدیاسی
Belarusian	актынідыя каламікта
Czech	aktinidie kolomikta
Danish	kamæleonbusk
Estonian	südajas aktiniidia
Finnish	kiinanlaikkuköynnös
French	kiwi arctique
Icelandic	kattaflétta
Japanese	ミヤママタタビ
Korean	쥐다래
Dutch	ananas actinidie
Norwegian Nynorsk	raudkattebusk
os	Лывзгæрдæг
Polish	aktinidia pstrolistna
Russian	актинидия коломикта
Russian	ползун
Russian	Амурский крыжовник
Russian	Актинидия Сугавары
Russian	Актинидия амурская
Swedish	kameleontbuske
Chinese	狗棗獼猴桃
Chinese	深山木天蓼
Chinese	深山木天寥
Chinese	狗枣猕猴桃
Chinese	狗枣子

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

subject to damping off

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
  - Manchuria
- Eastern Asia
  - Japan
  - Korea
- Middle Asia
  - Uzbekistan
- Russian Far East
  - Khabarovsk
  - Kuril Islands
  - Primorye
  - Sakhalin

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000519272
Cornell Woody Plants	16
UConn	34
Tropicos	500172
KEW	urn:lsid:ipni.org:names:828402-1
The Plant List	kew-2620720
Plantarium	696
Missouri Botanical Garden	275436
PFAF	Actinidia kolomikta
Open Tree Of Life	279941
Observations.org	130460
NCBI Taxonomy	165710
IPNI	828402-1
iNaturalist	710266
GBIF	7270682
Freebase	/m/0463wfc
EPPO	ATIKO
EOL	231266
Elurikkus	581072
USDA GRIN	1409
Wikipedia	Actinidia_kolomikta
CMAUP	NPO16109

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

Phenolic Compounds in Berries of Winter-Resistant Actinidia arguta Miq. and Actinidia kolomikta Maxim.: Evidence of Antioxidative Activity

Česonienė L, Januškevičė V, Saunoriūtė S, Liaudanskas M, Žvikas V, Krikštolaitis R, Viškelis P, Urbonavičienė D, Martusevičė P, Zych M, Daubaras R, Balčiūnaitienė A, Viškelis J

Antioxidants (Basel)

19-Mar-2024

PMCID:	PMC10968433
doi:	10.3390/antiox13030372
PMID:	38539905

Targeted multi-platform metabolome analysis and enzyme activity analysis of kiwifruit during postharvest ripening

Mao J, Gao Z, Lin M, Zhang X, Ning X, Gong X, Lu Y, Chen L, Wang X

Front Plant Sci

07-Mar-2023

PMCID:	PMC10028114
doi:	10.3389/fpls.2023.1120166
PMID:	36959943

Advances in genomics for diversity studies and trait improvement in temperate fruit and nut crops under changing climatic scenarios

Manzoor I, Samantara K, Bhat MS, Farooq I, Bhat KM, Mir MA, Wani SH

Front Plant Sci

19-Jan-2023

PMCID:	PMC9893892
doi:	10.3389/fpls.2022.1048217
PMID:	36743560

Telomere-to-telomere and gap-free reference genome assembly of the kiwifruit Actinidia chinensis

Yue J, Chen Q, Wang Y, Zhang L, Ye C, Wang X, Cao S, Lin Y, Huang W, Xian H, Qin H, Wang Y, Zhang S, Wu Y, Wang S, Yue Y, Liu Y

Hortic Res

02-Dec-2022

PMCID:	PMC9909506
doi:	10.1093/hr/uhac264
PMID:	36778189

Size- and environment-driven seedling survival and growth are mediated by leaf functional traits

Jiang F, Cadotte MW, Jin G

Proc Biol Sci

28-Sep-2022

PMCID:	PMC9515624
doi:	10.1098/rspb.2022.1400
PMID:	36168755

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

Enhancement of Photosynthetic Capacity in Spongy Mesophyll Cells in White Leaves of Actinidia kolomikta

Yu M, Chen L, Liu DH, Sun D, Shi GL, Yin Y, Wen DQ, Wang ZX, Ai J

Front Plant Sci

11-May-2022

PMCID:	PMC9131848
doi:	10.3389/fpls.2022.856732
PMID:	35646000

Comparative Analysis of the Metabolome and Transcriptome between the Green and Yellow-Green Regions of Variegated Leaves in a Mutant Variety of the Tree Species Pteroceltis tatarinowii

Qiao Q, Wu C, Cheng TT, Yan Y, Zhang L, Wan YL, Wang JW, Liu QZ, Feng Z, Liu Y

Int J Mol Sci

29-Apr-2022

PMCID:	PMC9101679
doi:	10.3390/ijms23094950
PMID:	35563341

Windborne migration amplifies insect-mediated pollination services

Jia H, Liu Y, Li X, Li H, Pan Y, Hu C, Zhou X, Wyckhuys KA, Wu K

eLife

13-Apr-2022

PMCID:	PMC9042232
doi:	10.7554/eLife.76230
PMID:	35416148

Berries and Leaves of Actinidia kolomikta (Rupr. & Maxim.) Maxim.: A Source of Phenolic Compounds

Česonienė L, Štreimikytė P, Liaudanskas M, Žvikas V, Viškelis P, Viškelis J, Daubaras R

Plants (Basel)

06-Jan-2022

PMCID:	PMC8781454
doi:	10.3390/plants11020147
PMID:	35050034

Transcriptomic and Proteomic Profiling Reveal the Key Role of AcMYB16 in the Response of Pseudomonas syringae pv. actinidiae in Kiwifruit

Wang X, Li Y, Liu Y, Zhang D, Ni M, Jia B, Heng W, Fang Z, Zhu LW, Liu P

Front Plant Sci

11-Nov-2021

PMCID:	PMC8632638
doi:	10.3389/fpls.2021.756330
PMID:	34868148

Pulsed Power Applications for Protein Conformational Change and the Permeabilization of Agricultural Products

Takaki K, Takahashi K, Guionet A, Ohshima T

Molecules

18-Oct-2021

PMCID:	PMC8537387
doi:	10.3390/molecules26206288
PMID:	34684869

Full-length transcriptome profiling reveals insight into the cold response of two kiwifruit genotypes (A. arguta) with contrasting freezing tolerances

Sun S, Lin M, Qi X, Chen J, Gu H, Zhong Y, Sun L, Muhammad A, Bai D, Hu C, Fang J

BMC Plant Biol

11-Aug-2021

PMCID:	PMC8356467
doi:	10.1186/s12870-021-03152-w
PMID:	34380415

Plant Byproducts as Part of Edible Coatings: A Case Study with Parsley, Grape and Blueberry Pomace

Tauferova A, Pospiech M, Javurkova Z, Tremlova B, Dordevic D, Jancikova S, Tesikova K, Zdarsky M, Vitez T, Vitezova M

Polymers (Basel)

03-Aug-2021

PMCID:	PMC8348254
doi:	10.3390/polym13152578
PMID:	34372181

Potential antidiabetic phytochemicals in plant roots: a review of in vivo studies

Ardalani H, Hejazi Amiri F, Hadipanah A, Kongstad KT

J Diabetes Metab Disord

12-Jul-2021

PMCID:	PMC8630315
doi:	10.1007/s40200-021-00853-9
PMID:	34900828

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
(S)-Mandelonitrile	439767	Click to see C1=CC=C(C=C1)C(C#N)O	133.15	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid	6950479	Click to see CCC(C)C(=O)O	102.13	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid	10467	Click to see CCCCCCCCCCCCCCCCCCCC(=O)O	312.50	unknown	via CMAUP database
Myristic Acid	11005	Click to see CCCCCCCCCCCCCC(=O)O	228.37	unknown	via CMAUP database
Palmitoleic Acid	445638	Click to see CCCCCCC=CCCCCCCCC(=O)O	254.41	unknown	via CMAUP database
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Hexen-1-OL	5318042	Click to see CCCC=CCO	100.16	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
Linolenic Acid	5280934	Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O	278.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral	638011	Click to see CC(=CCCC(=CC=O)C)C	152.23	unknown	via CMAUP database
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE	7463	Click to see CC1=CC=C(C=C1)C(C)C	134.22	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol	442501	Click to see CC1=CCC(CC1)C(C)(C)O	154.25	unknown	via CMAUP database
Terpinolene	11463	Click to see CC1=CCC(=C(C)C)CC1	136.23	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Ionone	638014	Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C	192.30	unknown	via CMAUP database
Vomifoliol	5280462	Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C	224.30	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Flavoxanthin	5281238	Click to see CC1=CC(CC(C1C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C2C=C3C(CC(CC3(O2)C)O)(C)C)C)C)(C)C)O	584.90	unknown	via CMAUP database
Rubixanthin	5281252	Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C	552.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
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	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(8S,9S,13S,14R)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one	670995	Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O	270.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Poriferasterol	5281330	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
Stigmasteryl-beta-d-glucopyranoside	12895774	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	574.80	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron	88113319	Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O	192.12	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
beta-D-GlcpA-(1->6)-beta-D-Galp	70680285	Click to see C(C1C(C(C(C(O1)O)O)O)O)OC2C(C(C(C(O2)C(=O)O)O)O)O	356.28	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Amygdalin	656516	Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O	457.40	unknown	via CMAUP database
Neoamygdalin	441462	Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O	457.40	unknown	via CMAUP database
Prunasin	119033	Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O	295.29	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Hexenal	5281168	Click to see CCCC=CC=O	98.14	unknown	via CMAUP database
2-Nonenal	5283335	Click to see CCCCCCC=CC=O	140.22	unknown	via CMAUP database
2,4-Decadienal	5283349	Click to see CCCCCC=CC=CC=O	152.23	unknown	via CMAUP database
Hexanal	6184	Click to see CCCCCC=O	100.16	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(R)-gamma-Decalactone	183870	Click to see CCCCCCC1CCC(=O)O1	170.25	unknown	via CMAUP database
(S)-gamma-Octanolactone	7057972	Click to see CCCCC1CCC(=O)O1	142.20	unknown	via CMAUP database
2(3H)-Furanone, dihydro-5-octyl-, (5R)-	10888889	Click to see CCCCCCCCC1CCC(=O)O1	198.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydrofurans
2-[(2R,5S)-5-ethenyl-5-methyloxolan-2-yl]propan-2-ol	6428573	Click to see CC1(CCC(O1)C(C)(C)O)C=C	170.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
[(1S,5R,6R,13R,21S)-6,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-yl] 4-hydroxybenzoate	10723070	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)OC(=O)C7=CC=C(C=C7)O)O)C8=CC=C(C=C8)O)O	664.60	unknown	via CMAUP database
ent-Epiafzelechin-(2alpha-O-7,4alpha-8)-afzelechin	73353883	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O	544.50	unknown	via CMAUP database
ent-Epiafzelechin-(2alpha-O-7,4alpha-8)-ent-epiafzelechin	5317051	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O	544.50	unknown	via CMAUP database
Geranin A	5317050	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O	544.50	unknown	via CMAUP database
Mahuannin A	5317052	Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O	544.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	via CMAUP database
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	via CMAUP database
> 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/10.1007/S10600-010-9569-6
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	5462193	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1007/S10600-010-9569-6
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/10.1007/S10600-010-9569-6
Isorhamnetin 3-galactoside	13245586	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	https://doi.org/10.1007/S10600-010-9569-6
isorhamnetin 3-O-glucoside	5318645	Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	478.40	unknown	https://doi.org/10.1007/S10600-010-9569-6
Kaempferol 3-O-rhamninoside	14186901	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)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)O	740.70	unknown	https://doi.org/10.1007/S10600-010-9569-6
Kaempferol3-rhamninoside	23815364	Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)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)O	740.70	unknown	https://doi.org/10.1007/S10600-010-9569-6
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	via CMAUP database
Trifolin	5282149	Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O	448.40	unknown	https://doi.org/10.1007/S10600-010-9569-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
[(2S,3R,4S,5R,6S)-6-[3,5-dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate	46845192	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)OC)O)O)O)OC(=O)C	488.40	unknown	https://doi.org/10.1007/S10600-010-9569-6
[6-[3,5-Dihydroxy-2-(4-methoxyphenyl)-4-oxochromen-7-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate	75219348	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)OC)O)O)O)OC(=O)C	488.40	unknown	https://doi.org/10.1007/S10600-010-9569-6
3,5-Dihydroxy-2-(4-hydroxyphenyl)-7-[(3,4,5-trihydroxy-6-methyltetrahydro-2H-pyran-2-yl)oxy]-4H-1-benzopyran-4-one	13940823	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O	432.40	unknown	https://doi.org/10.1007/S10600-010-9569-6
5-hydroxy-2-(4-hydroxyphenyl)-3-[(1S,2R,3S,4R,5R)-1,2,3,4,5-pentahydroxy-6-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyhexoxy]-7-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	162926999	Click to see CC1C(C(C(C(O1)OCC(C(C(C(C(O)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O	758.70	unknown	https://doi.org/10.1007/S10600-010-9569-6
5-Hydroxy-2-(4-hydroxyphenyl)-3-[1,2,3,4,5-pentahydroxy-6-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyhexoxy]-7-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxychromen-4-one	162926998	Click to see CC1C(C(C(C(O1)OCC(C(C(C(C(O)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)C)O)O)O)C5=CC=C(C=C5)O)O)O)O)O)O)O)O	758.70	unknown	https://doi.org/10.1007/S10600-010-9569-6
Kaempferol-7-rhamnoside	25079965	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)O)O)O	432.40	unknown	https://doi.org/10.1007/S10600-010-9569-6

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Actinidia kolomikta

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