Scientific name	Authority	First published in
Vitis dunniana	H.Lév.	Repert. Spec. Nov. Regni Veg. 11: 297 (1912)
Paullinia japonica	Thunb.	Fl. Jap. (Thunberg) 170. 1784 [Aug 1784]
Ampelopsis dissecta	hort. ex Koehne	Deut. Dendrol. : 400 (1893)
Ampelopsis lucida	Carrière	Rev. Hort. (Paris) 40: 39 (1868)
Ampelopsis mirabilis	Diels & Gilg	Bot. Jahrb. Syst. 29: 465 (1900)
Ampelopsis napiformis	Carrière	Rev. Hort. (Paris) 42: 16 (1870)
Ampelopsis rubricaulis	Carrière ex Planch.	Monogr. Phan. 5: 459 (1887)
Ampelopsis serianaefolia	Bunge	Enum. Pl. China Bor. : 12 (1833)
Ampelopsis triloba	Carrière	Rev. Hort. (Paris) 40: 39 (1868)
Ampelopsis tripartita	Carrière	Rev. Hort. (Paris) 40: 39 (1868)
Ampelopsis tuberosa	Carrière	Rev. Hort. (Paris) 42: 16 (1870)
Cissus aconitifolia	Walp.	Repert. Bot. Syst. 1: 441 (1842)
Cissus serjaniaefolia	Walp.	Repert. Bot. Syst. 1: 441 (1842)
Cissus viticifolia	Siebold & Zucc.	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(2): 196 (1845)
Vitis serianiifolia var. aconitifolia	(Bunge) Franch.	Pl. David. 1: 74 1884
Vitis serianiifolia	(Bunge) Maxim.	Mélanges Biol. Bull. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 9: 149

Common names Top

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Filter by language:

Language	Common/alternative name
English	east asian peppervine
Bulgarian	японска лоза
Armenian	Ամպելոպսիս ճապոնական
Japanese	ビャクレン
Japanese	カガミグサ
Korean	가회톱
Russian	Виноградовник японский
Chinese	五爪藤
Chinese	白敛
Chinese	白蔹
Chinese	白蔹子
Chinese	猫儿卵
Chinese	箭猪腰
Chinese	鹅抱蛋
Chinese	白蘞

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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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
  - Manchuria
- Eastern Asia
  - Japan
- Russian Far East
  - Khabarovsk
  - Primorye

Asia-tropical click to expand
- Indo-China
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000531708
UNII	RB28B5Y3UN
Tropicos	34000260
KEW	urn:lsid:ipni.org:names:869647-1
The Plant List	kew-2634539
Open Tree Of Life	704202
Observations.org	129646
NCBI Taxonomy	714442
IPNI	869647-1
iNaturalist	868939
GBIF	4052552
EPPO	AMCJA
USDA GRIN	101073
CMAUP	NPO12328
PFAF	Ampelopsis japonica
Plantarium	2684

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

Efficacy and safety of adjuvant topical application of botanicals in the treatment of melasma: A systematic review and meta-analysis

Guo L, Zhang Y, Wu S, Bai M, Tian S, Miao M

Heliyon

15-Mar-2024

PMCID:	PMC10966692
doi:	10.1016/j.heliyon.2024.e28096
PMID:	38545140

Plastid genome data provide new insights into the dynamic evolution of the tribe Ampelopsideae (Vitaceae)

Zhang L, Meng Y, Wang D, He GH, Zhang JM, Wen J, Nie ZL

BMC Genomics

05-Mar-2024

PMCID:	PMC10916268
doi:	10.1186/s12864-024-10149-w
PMID:	38443830

Use of Medicinal Plants in the Process of Wound Healing: A Literature Review

Cedillo-Cortezano M, Martinez-Cuevas LR, López JA, Barrera López IL, Escutia-Perez S, Petricevich VL

Pharmaceuticals (Basel)

27-Feb-2024

PMCID:	PMC10975678
doi:	10.3390/ph17030303
PMID:	38543089

Role of Hemigraphis alternata in wound healing: metabolomic profiling and molecular insights into mechanisms

Devasahayam Arokia Balaya R, Palollathil A, Kumar ST, Chandrasekaran J, Upadhyay SS, Parate SS, Sajida M, Karthikkeyan G, Prasad TS

Sci Rep

16-Feb-2024

PMCID:	PMC10873326
doi:	10.1038/s41598-024-54352-x
PMID:	38365839

The complete chloroplast genome of Nekemias hypoglauca (Hance) J. Wen & Z. L. Nie 2014 (Family: Vitaceae) and its phylogenetic analysis

He GH, Zhang L, Meng Y, Wen J, Nie ZL

Mitochondrial DNA B Resour

12-Feb-2024

PMCID:	PMC10863506
doi:	10.1080/23802359.2024.2316071
PMID:	38352189

Qilian Formula Inhibits Tumor Cell Growth in a Bone Metastasis Model of Lung Cancer

Wang Q, Zhao B, Li J, Zhao J, Wang C, Li Q, Yang W, Xu L, Gong Y

Integr Cancer Ther

22-Dec-2023

PMCID:	PMC10748605
doi:	10.1177/15347354231217274
PMID:	38130184

Biological Activity of Fermented Plant Extracts for Potential Dermal Applications

Herman A, Herman AP

Pharmaceutics

14-Dec-2023

PMCID:	PMC10748213
doi:	10.3390/pharmaceutics15122775
PMID:	38140115

Advances in research and utilization of botanical pesticides for agricultural pest management in Inner Mongolia, China

Guo C, Wang L, Chen N, Zhang M, Jia J, Lv L, Li M

Chin Herb Med

28-Aug-2023

PMCID:	PMC11064588
doi:	10.1016/j.chmed.2023.04.002
PMID:	38706822

Efficacy and Safety of Woohwangchungsimwon Combined with Donepezil in Behavioral and Psychological Symptoms of Dementia in Patients with Probable Alzheimer’s Disease: Study Protocol for a Randomized Controlled Trial

Kim MG, Hyun MS, Park SG, Cho E, Kim J, Choi HK, Son KL, Lim CY, Kim KK, Koo BS

Healthcare (Basel)

16-Jul-2023

PMCID:	PMC10378906
doi:	10.3390/healthcare11142036
PMID:	37510478

Review of molecular biological studies on acute lymphoblastic leukemia treated by modified shengmaiyin

Guo D, Gu M, Du F, Zhao Y, Gao M, Hao J

Medicine (Baltimore)

09-Jun-2023

PMCID:	PMC10256333
doi:	10.1097/MD.0000000000034013
PMID:	37335634

Efficacy analysis and research progress of complementary and alternative medicines in the adjuvant treatment of COVID-19

Lin JG, Huang GJ, Su YC

J Biomed Sci

03-May-2023

PMCID:	PMC10155165
doi:	10.1186/s12929-023-00923-5
PMID:	37138292

Preclinical evidence of polyherbal formulations on wound healing: A systematic review on research trends and perspectives

Dubey S, Dixit AK

J Ayurveda Integr Med

24-Feb-2023

PMCID:	PMC9988554
doi:	10.1016/j.jaim.2023.100688
PMID:	36841194

Local Drug Delivery Strategies towards Wound Healing

Tiwari R, Pathak K

Pharmaceutics

13-Feb-2023

PMCID:	PMC9964694
doi:	10.3390/pharmaceutics15020634
PMID:	36839956

Inflammatory response: The target for treating hyperpigmentation during the repair of a burn wound

Zhong C, Liang G, Li P, Shi K, Li F, Zhou J, Xu D

Front Immunol

01-Feb-2023

PMCID:	PMC9929571
doi:	10.3389/fimmu.2023.1009137
PMID:	36817442

Biotechnological Approaches to Producing Natural Antioxidants: Anti-Ageing and Skin Longevity Prospects

Bouzroud S, El Maaiden E, Sobeh M, Merghoub N, Boukcim H, Kouisni L, El Kharrassi Y

Int J Mol Sci

11-Jan-2023

PMCID:	PMC9867058
doi:	10.3390/ijms24021397
PMID:	36674916

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
> Benzenoids / Anthracenes / Anthraquinones
Chrysophanic acid	10208	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O	254.24	unknown	via CMAUP database
Physcione	10639	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC	284.26	unknown	via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin	3220	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O	270.24	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
2,5-Dihydroxybenzoic acid	3469	Click to see C1=CC(=C(C=C1O)C(=O)O)O	154.12	unknown	via CMAUP database
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	154.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
3,4,5-Trihydroxybenzoate	54675821	Click to see C1=C(C=C(C(=C1O)[O-])O)C(=O)O	169.11	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid	370	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)O	170.12	unknown	https://doi.org/10.1007/S10600-017-2124-Y
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Pentacosane	12406	Click to see CCCCCCCCCCCCCCCCCCCCCCCCC	352.70	unknown	https://doi.org/10.1007/S10600-017-2124-Y
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
Isolariciresinol, (+)-	160521	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)CO)C3=CC(=C(C=C3)O)OC)O	360.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
Schizandriside	14521043	Click to see COC1=C(C=C2C(C(C(CC2=C1)CO)COC3C(C(C(CO3)O)O)O)C4=CC(=C(C=C4)O)OC)O	492.50	unknown	https://doi.org/10.1007/S11418-006-0119-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	256.42	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Straight chain fatty acids
2-Butenoic acid	19499	Click to see CC=CC(=O)O	86.09	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Octacosanoic acid	10470	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	424.70	unknown	https://doi.org/10.1007/S10600-017-2124-Y
Triacontanoic acid	10471	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	452.80	unknown	https://doi.org/10.1007/S10600-017-2124-Y
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol	259846	Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C	426.70	unknown	via CMAUP database
Oleanolic Acid	10494	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C	456.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Azasteroids and derivatives
(E)-N-[(3S,5S,8R,9S,10S,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]-N,3,4-trimethylpent-2-enamide	11113449	Click to see CC(C)C(=CC(=O)N(C)C1CCC2(C(C1)CCC3C2CCC4(C3CCC4C(C)N(C)C)C)C)C	470.80	unknown	via CMAUP database
(E)-N-[(3S,5S,8R,9S,10S,13S,14S,17S)-17-[(1S)-1-[formyl(methyl)amino]ethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]-N,3,4-trimethylpent-2-enamide	11213879	Click to see CC(C)C(=CC(=O)N(C)C1CCC2(C(C1)CCC3C2CCC4(C3CCC4C(C)N(C)C=O)C)C)C	484.80	unknown	via CMAUP database
[(2S,3R,5S,8R,9S,10S,13R,17S)-17-[(1S)-1-(dimethylamino)ethyl]-10,13-dimethyl-3-(3-methylbut-2-enoylamino)-2,3,4,5,6,7,8,9,11,12,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-2-yl] acetate	11431683	Click to see CC(C1CC=C2C1(CCC3C2CCC4C3(CC(C(C4)NC(=O)C=C(C)C)OC(=O)C)C)C)N(C)C	484.70	unknown	via CMAUP database
Dictyophlebine	11417103	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4)NC)C)C)N(C)C	360.60	unknown	via CMAUP database
Epipachysamine B	70688998	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4)NC(=O)C5=CN=CC=C5)C)C)N(C)C	451.70	unknown	via CMAUP database
Hookerianamide I	44587245	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4)N(C)C(=O)C5=CC=CC=C5)C)C)NC	450.70	unknown	via CMAUP database
Hookerianamide K	25016412	Click to see CC(C1CC=C2C1(CCC3C2CCC4=CC(CCC34C)N(C)C)C)N(C)C	370.60	unknown	via CMAUP database
Hookerianamine A	12095947	Click to see CC(C1CC=C2C1(CCC3C2CCC4C3(CCC(C4)NC)C)C)N(C)C	358.60	unknown	via CMAUP database
N-[(3S,5S,8R,9S,10S,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yl]-N-methylbenzamide	10004669	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4)N(C)C(=O)C5=CC=CC=C5)C)C)N(C)C	464.70	unknown	via CMAUP database
N-Formylchonemorphine	101938440	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4)NC=O)C)C)N(C)C	374.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
Hookerianamide J	25016666	Click to see CC(C1=CCC2C1(CCC3C2CCC4C3(CCC(C4O)NC(=O)C=C(C)C)C)C)N(C)C	442.70	unknown	via CMAUP database
N-[(2S,3S,4R,5R,8R,9S,10R,13S,14S)-17-[(1S)-1-(dimethylamino)ethyl]-2,4-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]-3-methylbut-2-enamide	102333328	Click to see CC(C1=CCC2C1(CCC3C2CCC4C3(CC(C(C4O)NC(=O)C=C(C)C)O)C)C)N(C)C	458.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids
(E)-N-[(5R,8R,9S,10R,13S,14S)-17-[(1S)-1-(dimethylamino)ethyl]-10,13-dimethyl-4-oxo-1,5,6,7,8,9,11,12,14,15-decahydrocyclopenta[a]phenanthren-3-yl]-2-methylbut-2-enamide	101936590	Click to see CC=C(C)C(=O)NC1=CCC2(C3CCC4(C(C3CCC2C1=O)CC=C4C(C)N(C)C)C)C	438.60	unknown	via CMAUP database
(E)-N-[(5R,8S,9S,10R,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-10,13-dimethyl-4-oxo-1,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-3-yl]-2-methylbut-2-enamide	101726070	Click to see CC=C(C)C(=O)NC1=CCC2(C3CCC4(C(C3CCC2C1=O)CCC4C(C)N(C)C)C)C	440.70	unknown	via CMAUP database
2,3-Dehydrosarsalignone	44587283	Click to see CC=C(C)C(=O)NC1=CCC2(C3CCC4(C(C3CC=C2C1=O)CCC4C(C)NC)C)C	424.60	unknown	via CMAUP database
epipachysamine-E-5-en-4-one	44587247	Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4=O)NC(=O)C=C(C)C)C)C)NC	426.60	unknown	via CMAUP database
Hookerianamide H	44587217	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CC=C(C4=O)NC=O)C)C)N(C)C	386.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxosteroids / 16-oxosteroids
(20S)-3beta-(3-Methyl-2-butenoylamino)-4beta-acetoxy-20-(methylamino)-5alpha-pregnane	44587282	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4OC(=O)C)NC(=O)C=C(C)C)C)C)NC	472.70	unknown	via CMAUP database
(20S)-3beta-[(3-Methyl-2-butenoyl)amino]-20-(dimethylamino)-5alpha-pregnane-2alpha,4beta-diol diacetate	12095949	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CC(C(C4OC(=O)C)NC(=O)C=C(C)C)OC(=O)C)C)C)N(C)C	544.80	unknown	via CMAUP database
[(3S,4R,5R,8S,9S,10R,13S,14S,17S)-17-[(1S)-1-(dimethylamino)ethyl]-10,13-dimethyl-3-[[(E)-2-methylbut-2-enoyl]amino]-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-4-yl] acetate	11225523	Click to see CC=C(C)C(=O)NC1CCC2(C(C1OC(=O)C)CCC3C2CCC4(C3CCC4C(C)N(C)C)C)C	486.70	unknown	via CMAUP database
[(3S,4R,5R,8S,9S,10R,13S,14S,17S)-3-[benzoyl(methyl)amino]-17-[(1S)-1-(dimethylamino)ethyl]-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-4-yl] acetate	11249447	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4OC(=O)C)N(C)C(=O)C5=CC=CC=C5)C)C)N(C)C	522.80	unknown	via CMAUP database
Sarcovagine C	25033601	Click to see CC=C(C)C(=O)NC1CCC2(C(C1OC(=O)C)CCC3C2CCC4(C3CCC4C(C)NC)C)C	472.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
Terminaline	177562	Click to see CC(C1CCC2C1(CCC3C2CCC4C3(CCC(C4O)O)C)C)N(C)C	363.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	86821	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	https://doi.org/10.1007/S10600-017-2124-Y
3-epi-beta-Sitosterol	12303645	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
alpha-Spinasterin	5281331	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	via CMAUP database
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
Stigmasterol	5280794	Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	412.70	unknown	https://doi.org/10.1007/S10600-017-2124-Y
Stigmasterol glucoside	6602508	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	https://doi.org/10.1007/S10600-017-2124-Y
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine	60961	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
1-[(2R,3R,4S,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]pyrimidine-2,4-dione	7059437	Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O	244.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron	21883788	Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-]	116.07	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Bryonolate	52940232	Click to see CC1(C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)[O-])C)C)C)C	455.70	unknown	via CMAUP database
Bryononic acid	472768	Click to see CC1(C2CCC3=C(C2(CCC1O)C)CCC4(C3(CCC5(C4CC(CC5)(C)C(=O)O)C)C)C)C	456.70	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives
d-Tartaric acid	439655	Click to see C(C(C(=O)O)O)(C(=O)O)O	150.09	unknown	via CMAUP database
L-Tartaric acid	444305	Click to see C(C(C(=O)O)O)(C(=O)O)O	150.09	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Galactitol	11850	Click to see C(C(C(C(C(CO)O)O)O)O)O	182.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Depsides and depsidones
Digallate	54711004	Click to see C1=C(C=C(C(=C1O)[O-])O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)O	321.21	unknown	via CMAUP database
Digallic acid	341	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)O	322.22	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
(+)-Epicatechin	182232	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
2-(3,4-Dihydroxyphenyl)chroman-3,5,7-triol	1203	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	via CMAUP database
Cianidanol	9064	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1007/S11418-006-0119-2
Epicatechin	72276	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O	290.27	unknown	https://doi.org/10.1007/S11418-006-0119-2
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
(-)-Epicatechin gallate	107905	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	442.40	unknown	https://doi.org/10.1007/S11418-006-0119-2
(+)-Catechin gallate	5276454	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	442.40	unknown	via CMAUP database
5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl 3,4,5-trihydroxybenzoate	1287	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	458.40	unknown	via CMAUP database
Epicatechin-3-gallate	65056	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	442.40	unknown	via CMAUP database
Gallocatechin gallate	5276890	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	458.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(-)-Gallocatechin	9882981	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	via CMAUP database
(2R,3R)-3,7-dihydroxy-4-oxo-2-(3,4,5-trihydroxyphenyl)-2,3-dihydrochromen-5-olate	25244375	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)[O-])O	319.24	unknown	via CMAUP database
Dihydromyricetin	161557	Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O	320.25	unknown	via CMAUP database
Gallocatechin	65084	Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O)O	306.27	unknown	https://doi.org/10.1007/S11418-006-0119-2
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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	https://doi.org/10.1007/S10600-017-2124-Y
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Quercitrin	5280459	Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)O)O)O	448.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
1,3-Benzenediol, 5-[(1Z)-2-(4-hydroxyphenyl)ethenyl]-	5056	Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O	228.24	unknown	https://doi.org/10.1007/S11418-006-0119-2
cis-Resveratrol	1548910	Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O	228.24	unknown	via CMAUP database
Resveratrol	445154	Click to see C1=CC(=CC=C1C=CC2=CC(=CC(=C2)O)O)O	228.24	unknown	https://doi.org/10.1007/S11418-006-0119-2
> Phenylpropanoids and polyketides / Tannins
1,4,6-Tri-O-Galloyl-Beta-D-Glucose	10077822	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O	636.50	unknown	via CMAUP database
beta-1,2,3,4,6-Penta-O-galloyl-D-glucopyranose	446509	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O	940.70	unknown	via CMAUP database

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Ampelopsis japonica

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