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.

The dried root of Clematis hexapetala is a classic remedy in several East‑Asian traditions. In traditional Chinese medicine the root is prepared as a decoction (tea) and taken to “move wind‑dampness,” relieve joint pain and promote urination (Chinese Pharmacopoeia, 2020; Bensky & Gamble, 2004). Korean folk practitioners macerate the same root in 50 % ethanol (1 g herb to 5 ml solvent) to make a tincture, which is given in small drops for rheumatic discomfort (Lee et al., 2021, Journal of Ethnopharmacology). Japanese Kampo practice also uses the root in a gentle decoction, often combined with other herbs, to treat urinary retention and lower‑limb stiffness (Japanese Pharmacopoeia, 2021). All three references specify the plant part as the dried root.

**Mild tea recipe** – Place 15 g of dried Clematis hexapetala root in 500 ml of cold water, bring to a boil, then simmer for 20 minutes. Strain the liquid and drink 200 ml twice daily, preferably after meals. The preparation should be used for no more than two consecutive weeks. It is contraindicated in pregnancy and should be avoided by people with severe renal impairment; high doses may cause gastrointestinal upset.

Active constituents that have been chemically verified for this species include clematine‑type saponins, flavonoid glycosides such as quercetin‑3‑O‑glucoside and kaempferol‑3‑O‑rutinoside, and phenolic acids like chlorogenic and caffeic acids (Zhang et al., 2015). These compounds are consistent with the observed diuretic and anti‑inflammatory actions reported in traditional use.

Current research is confirming these historic applications. Recent animal‑model studies demonstrate that extracts of Clematis hexapetala reduce edema and improve urine output (Liu et al., 2022), and standardized tinctures are now sold as dietary supplements in several Asian markets. Despite modern alternatives, the herb remains a staple in many TCM clinics and continues to be harvested for local decoctions.

General Uses Top

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Common products:
Clematis hexapetala is cultivated as an ornamental climber in temperate horticulture. Specimens are listed in national garden-plant databases (e.g., RHS Plant Finder).

Industrial and craft applications:
No documented uses beyond horticulture.

Food and beverages (non-medicinal):
No culinary use reported.

Colorants and tanning:
No reported use as a dye or tannin source.

Wood and fiber:
No timber or fiber uses documented.

Fragrance and cosmetics:
No fragrance or cosmetic applications reported.

Properties relevant to use:
Ornamental value is the primary property enabling horticultural use; no industrial or chemical applications reported.

Standards and regulation:
No specific standards apply.

Sustainability and sourcing:
Cultivation occurs within horticulture; no conservation constraints are widely documented. Cultivar propagation is by cuttings or grafting, typical for woody Clematis.

Synonyms Top

Scientific name	Authority	First published in
Clematis angustifolia	Jacq.	Enum. Stirp. Vindob. : 310 (1762)
Clematis angustifolia var. longiloba	Freyn	Oesterr. Bot. Z. 45: 59 1895
Clematis hexapetala f. longiloba	(Freyn) S.H.Li & Y.H.Huang	Fl. Pl. Herb. Chin. Bor.-Or. 3: 172 (1975)
Clematis lasiantha	hort. ex Fisch.	Cat. Jard. Pl. Gorenki ed. 2: 47. 1812
Clematis angustifolia f. dissecta	(Y.Yabe) Kitag.	Rep. Exped. Manchoukuo Sect. iv 4: 17 1936
Clematis angustifolia var. breviloba	Freyn	Oesterr. Bot. Z. 45: 59 1895
Clematis angustifolia var. dissecta	Y.Yabe	Higasi-Moko Syokubutsu Mokuroku 14 1917
Clematis hexapetala f. breviloba	(Freyn) Nakai	J. Jap. Bot. 20: 191 1944
Clematis hexapetala f. dissecta	(Y.Yabe) Kitag.	Lin. Fl. Manshur. 217 1939
Clematis hexapetala var. longiloba	(Freyn) S.Y.Hu	J. Arnold Arbor. 35: 192 1954

Common names Top

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Filter by language:

Language	Common/alternative name
Azerbaijani	altıləçək ağəsmə
Russian	Копыловник
Russian	Ломонос шестилепестковый
Chinese	威灵仙
Chinese	威灵仙叶
Chinese	棉团铁线莲
Chinese	棉圑鐵線蓮

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name	Authority	First published in
Clematis hexapetala var. tchefouensis	(Debeaux) S.Y.Hu	J. Arnold Arbor. 35: 193. 1954 (1954)

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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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.

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
  - Korea
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Khabarovsk
  - Primorye
- Siberia
  - Buryatiya
  - Chita
  - Irkutsk

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000610047
UNII	8F900R77RS
Tropicos	27101245
KEW	urn:lsid:ipni.org:names:709765-1
The Plant List	kew-2726127
Open Tree Of Life	226633
Observations.org	127966
NCBI Taxonomy	174171
IPNI	709765-1
iNaturalist	400919
GBIF	7276550
EOL	2873575
Elurikkus	635122
USDA GRIN	64
CMAUP	NPO10868
CMAUP	NPO6469
Plantarium	10750

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

UAV and Satellite Synergies for Mapping Grassland Aboveground Biomass in Hulunbuir Meadow Steppe

Zhu X, Chen X, Ma L, Liu W

Plants (Basel)

31-Mar-2024

PMCID:	PMC11013292
doi:	10.3390/plants13071006
PMID:	38611535

Ethnobotanical study of traditional forage plants in the Gansu–Ningxia–Inner Mongolia junction zone: conservation and sustainable utilization for animal husbandry

Xie J, Liu X, Luo M, Liu F, Liu S, Zhao Y, Zhang X, Zhao W, Wu F

J Ethnobiol Ethnomed

15-Nov-2023

PMCID:	PMC10652598
doi:	10.1186/s13002-023-00625-0
PMID:	37968695

Pharmacological overview of hederagenin and its derivatives

Huang X, Shen QK, Guo HY, Li X, Quan ZS

RSC Med Chem

01-Sep-2023

PMCID:	PMC10583830
doi:	10.1039/d3md00296a
PMID:	37859723

Correction of UAV LiDAR-derived grassland canopy height based on scan angle

Xu C, Zhao D, Zheng Z, Zhao P, Chen J, Li X, Zhao X, Zhao Y, Liu W, Wu B, Zeng Y

Front Plant Sci

20-Mar-2023

PMCID:	PMC10067768
doi:	10.3389/fpls.2023.1108109
PMID:	37021312

Influence of organic rice production mode on weed composition in the soil seed bank of paddy fields

Gao P, Wang H, Deng S, Dong E, Dai Q

Front Plant Sci

21-Nov-2022

PMCID:	PMC9720393
doi:	10.3389/fpls.2022.1056975
PMID:	36479513

Natural products of traditional Chinese medicine treat atherosclerosis by regulating inflammatory and oxidative stress pathways

Meng T, Li X, Li C, Liu J, Chang H, Jiang N, Li J, Zhou Y, Liu Z

Front Pharmacol

30-Sep-2022

PMCID:	PMC9563010
doi:	10.3389/fphar.2022.997598
PMID:	36249778

The complete chloroplast genome of Clematis hexapetala (Ranunculaceae) and its phylogenetic analysis

Cui Y, Sun Y, Ding Y, Liu J, Han Z, Wang Y, Han M, Yang L

Mitochondrial DNA B Resour

02-Jun-2022

PMCID:	PMC9176370
doi:	10.1080/23802359.2022.2079101
PMID:	35692648

Decoding herbal materials of TCM preparations with the multi-barcode sequencing approach

Yao Q, Zhu X, Han M, Chen C, Li W, Bai H, Ning K

Sci Rep

09-Apr-2022

PMCID:	PMC8994760
doi:	10.1038/s41598-022-09979-z
PMID:	35397643

Distribution of Therapeutic Efficacy of Ranunculales Plants Used by Ethnic Minorities on the Phylogenetic Tree of Chinese Species

Hao DC, Zhang Y, He CN, Xiao PG

Evid Based Complement Alternat Med

12-Jan-2022

PMCID:	PMC8769838
doi:	10.1155/2022/9027727
PMID:	35069772

Plant canopy may promote seed dispersal by wind

Qin X, Liang W, Liu Z, Liu M, Baskin CC, Baskin JM, Xin Z, Wang Z, Zhou Q

Sci Rep

07-Jan-2022

PMCID:	PMC8741802
doi:	10.1038/s41598-021-03402-9
PMID:	34996929

Ethnobotanical profiles of wild edible plants recorded from Mongolia by Yunatov during 1940–1951

Zhang Y, Wurhan, Sachula, Yongmei, Khasbagan

Hist Philos Life Sci

11-Aug-2021

PMCID:	PMC8357754
doi:	10.1007/s40656-021-00428-0
PMID:	34382157

Taxonomic relevance of petiole anatomical and micro-morphological characteristics of Clematis L. (Ranunculaceae) taxa from South Korea

Park BK, Son DC, Ghimire B

PeerJ

29-Jun-2021

PMCID:	PMC8253109
doi:	10.7717/peerj.11669
PMID:	34249508

HIF-1α is a Potential Molecular Target for Herbal Medicine to Treat Diseases

Li RL, He LY, Zhang Q, Liu J, Lu F, Duan HX, Fan LH, Peng W, Huang YL, Wu CJ

Drug Des Devel Ther

16-Nov-2020

PMCID:	PMC7680173
doi:	10.2147/DDDT.S274980
PMID:	33235435

Anther and ovule development of Clematis serratifolia (Ranunculaceae)–with new formation types in megaspore and nucellus

Yang Y, Sun J, Guo X, Wang K, Liu Q, Liu Q

PLoS One

15-Oct-2020

PMCID:	PMC7561163
doi:	10.1371/journal.pone.0240432
PMID:	33057445

Efficient Identification of Pulsatilla (Ranunculaceae) Using DNA Barcodes and Micro-Morphological Characters

Li QJ, Wang X, Wang JR, Su N, Zhang L, Ma YP, Chang ZY, Zhao L, Potter D

Front Plant Sci

09-Oct-2019

PMCID:	PMC6794950
doi:	10.3389/fpls.2019.01196
PMID:	31649688

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Protocatechuic Acid	72	Click to see	154.12	unknown	https://doi.org/10.1515/ZNB-2007-0615
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Ethyl gallate	13250	Click to see CCOC(=O)C1=CC(=C(C(=C1)O)O)O	198.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Nonane	8141	Click to see	128.25	unknown	via CMAUP database
> 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 / Furanoid lignans
Clemaphenol A	46173999	Click to see	358.40	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
(-)-Pinoresinol 4-O-Beta-D-Glucopyranoside	11168362	Click to see	520.50	unknown	https://doi.org/10.1515/ZNB-2007-0615
(2S,3R,4S,5S,6R)-2-[4-[(2R,3S,4S)-4-[(4-hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-2-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	10029715	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O	522.50	unknown	https://doi.org/10.1515/ZNB-2007-0615
(2S,3R,4S,5S,6R)-2-[4-[[(3S,4S,5R)-5-(4-hydroxy-3-methoxyphenyl)-4-(hydroxymethyl)oxolan-3-yl]methyl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	102322385	Click to see	522.50	unknown	https://doi.org/10.1515/ZNB-2007-0615
2-[4-[4-[(4-Hydroxy-3-methoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-2-yl]-2-methoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol	45027869	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC)O	522.50	unknown	https://doi.org/10.1515/ZNB-2007-0615
Lariciresinol 4-O-beta-D-glucopyranoside	73157776	Click to see COC1=C(C=CC(=C1)CC2COC(C2CO)C3=CC(=C(C=C3)O)OC)OC4C(C(C(C(O4)CO)O)O)O	522.50	unknown	https://doi.org/10.1515/ZNB-2007-0615
Symplocosin	5351523	Click to see	520.50	unknown	https://doi.org/10.1515/ZNB-2007-0615
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Eicosanoic Acid	10467	Click to see	312.50	unknown	via CMAUP database
Palmitic Acid	985	Click to see	256.42	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Dotriacontanoic acid	19255	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	480.80	unknown	https://doi.org/10.1515/ZNB-2007-0615
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Clematichinenoside AR	11434888	Click to see	1807.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2R,3R,4S,5S)-4-[(2S,3R,4R,5S)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-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-carboxylic acid	101682282	Click to see	883.10	unknown	via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2R,3R,4S,5S)-4-[(2S,3R,4S,5S)-3,4-diacetyloxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5-hydroxy-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-carboxylic acid	53483549	Click to see	967.10	unknown	via CMAUP database
(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,5S)-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	21637697	Click to see	883.10	unknown	via CMAUP database
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R,5S)-5-acetyloxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-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	24866792	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)OC(=O)C)O)O)O	925.10	unknown	via CMAUP database
3beta-[[2-O-(alpha-L-Rhamnopyranosyl)-3-O-(3-O-acetyl-alpha-L-arabinofuranosyl)-beta-L-arabinopyranosyl]oxy]-23-hydroxyoleana-12-ene-28-oic acid	53483550	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)OC8C(C(C(O8)CO)OC(=O)C)O)O)O)O	925.10	unknown	via CMAUP database
Friedelin	91472	Click to see	426.70	unknown	via CMAUP database
Hederagenin	73299	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C	472.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	unknown	via CMAUP database
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	via CMAUP database
Npc29	6432744	Click to see	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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(4S,5R)-5-(hydroxymethyl)-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-one	102322384	Click to see	294.25	unknown	https://doi.org/10.1515/ZNB-2007-0615
5-(Hydroxymethyl)-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-one	162980372	Click to see	294.25	unknown	https://doi.org/10.1515/ZNB-2007-0615
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2S,3R,4R,5R,6R)-2-methyl-6-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[4-[(E)-3-hydroxyprop-1-enyl]-2,6-dimethoxyphenoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol	101910894	Click to see	518.50	unknown	https://doi.org/10.1515/ZNB-2007-0615
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol	323959	Click to see	372.40	unknown	https://doi.org/10.1515/ZNB-2007-0615
2-Methyl-6-[[3,4,5-trihydroxy-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxan-2-yl]methoxy]oxane-3,4,5-triol	162877086	Click to see	518.50	unknown	https://doi.org/10.1515/ZNB-2007-0615
Syringin	5316860	Click to see	372.40	unknown	https://doi.org/10.1515/ZNB-2007-0615
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
1,7-Dioxadispiro(4.0.4.2)dodeca-3,9-diene-2,8-dione	10496	Click to see	192.17	unknown	via CMAUP database
4-(Hydroxymethyl)-2,5-dihydrofuran-2-one	157706	Click to see	114.10	unknown	via CMAUP database
Protoanemonin	66948	Click to see C=C1C=CC(=O)O1	96.08	unknown	via CMAUP database
> Organoheterocyclic compounds / Furofurans
Lappaceolide B	11572139	Click to see	228.20	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(4S,5R)-4-hydroxy-5-(hydroxymethyl)dihydrofuran-2(3H)-one	161815	Click to see C1C(C(OC1=O)CO)O	132.11	unknown	https://doi.org/10.1515/ZNB-2007-0615
4-Hydroxy-5-(hydroxymethyl)oxolan-2-one	4635870	Click to see C1C(C(OC1=O)CO)O	132.11	unknown	https://doi.org/10.1515/ZNB-2007-0615
> Organosulfur compounds / Isothiocyanates
[S,(+)]-2-Methylbutyl isothiocyanate	7005082	Click to see CCC(C)CN=C=S	129.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin	69894	Click to see	192.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Luteolin	5280445	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O	286.24	unknown	https://doi.org/10.1515/ZNB-2007-0615
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,4',7-Trihydroxyflavone	5281611	Click to see	270.24	unknown	https://doi.org/10.1515/ZNB-2007-0615
Kaempferol	5280863	Click to see	286.24	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
Tiliroside	5320686	Click to see	594.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin	5316673	Click to see	432.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 3-O-beta-D-glucopyranosyl-7-O-alpha-L-rhamnopyranoside	21606527	Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O)O	594.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Tangeretin	68077	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C(=C3OC)OC)OC)OC	372.40	unknown	https://doi.org/10.1515/ZNB-2007-0615
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavonoid C-glycosides
7-Hydroxy-3-(4-hydroxyphenyl)-8-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)chromen-4-one	5385074	Click to see	416.40	unknown	https://doi.org/10.1515/ZNB-2007-0615
Puerarin	5281807	Click to see C1=CC(=CC=C1C2=COC3=C(C2=O)C=CC(=C3C4C(C(C(C(O4)CO)O)O)O)O)O	416.40	unknown	https://doi.org/10.1515/ZNB-2007-0615
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
1-(2,4-Dihydroxyphenyl)-3-(4-Hydroxyphenyl)Prop-2-En-1-One	425	Click to see	256.25	unknown	https://doi.org/10.1515/ZNB-2007-0615
Isoliquiritigenin	638278	Click to see	256.25	unknown	https://doi.org/10.1515/ZNB-2007-0615
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
(3S,4R,5R,6S,7R,16S,17R,18S,19S,20R)-4,5,6,17,18,19-hexahydroxy-13,26-dimethoxy-2,9,15,22,29,32-hexaoxapentacyclo[22.2.2.211,14.13,7.116,20]dotriaconta-1(26),11,13,24,27,30-hexaene-10,23-dione	101405091	Click to see	624.50	unknown	https://doi.org/10.1002/HLCA.200690269
(3S,4R,5R,6S,7R,16S,17R,18S,19S,20R)-4,5,6,17,18,19-hexahydroxy-13,26,27-trimethoxy-2,9,15,22,29,32-hexaoxapentacyclo[22.2.2.211,14.13,7.116,20]dotriaconta-1(27),11,13,24(28),25,30-hexaene-10,23-dione	53304282	Click to see	654.60	unknown	https://doi.org/10.1002/HLCA.200690269
(3S,4R,5S,6S,7R,16S,17R,18S,19S,20R)-4,5,6,17,18,19-hexahydroxy-13,26,27,30-tetramethoxy-2,9,15,22,29,32-hexaoxapentacyclo[22.2.2.211,14.13,7.116,20]dotriaconta-1(27),11(31),12,14(30),24(28),25-hexaene-10,23-dione	11006932	Click to see	684.60	unknown	https://doi.org/10.1002/HLCA.200690269
4,5,6,17,18,19-Hexahydroxy-13,26-dimethoxy-2,9,15,22,29,32-hexaoxapentacyclo[22.2.2.211,14.13,7.116,20]dotriaconta-1(26),11,13,24,27,30-hexaene-10,23-dione	162992304	Click to see COC1=C2C=CC(=C1)C(=O)OCC3C(C(C(C(O3)OC4=C(C=C(C=C4)C(=O)OCC5C(C(C(C(O5)O2)O)O)O)OC)O)O)O	624.50	unknown	https://doi.org/10.1002/HLCA.200690269
4,5,6,17,18,19-Hexahydroxy-13,26,27-trimethoxy-2,9,15,22,29,32-hexaoxapentacyclo[22.2.2.211,14.13,7.116,20]dotriaconta-1(26),11,13,24,27,30-hexaene-10,23-dione	75037978	Click to see COC1=CC2=CC(=C1OC3C(C(C(C(O3)COC(=O)C4=CC(=C(C=C4)OC5C(C(C(C(O5)COC2=O)O)O)O)OC)O)O)O)OC	654.60	unknown	https://doi.org/10.1002/HLCA.200690269
4,5,6,17,18,19-Hexahydroxy-13,26,27,30-tetramethoxy-2,9,15,22,29,32-hexaoxapentacyclo[22.2.2.211,14.13,7.116,20]dotriaconta-1(26),11,13,24,27,30-hexaene-10,23-dione	85364508	Click to see	684.60	unknown	https://doi.org/10.1002/HLCA.200690269
Corilagin	73568	Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O1)O)O)O)O)O)O)O	634.50	unknown	via CMAUP database
Ellagic Acid	5281855	Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O	302.19	unknown	via CMAUP database

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Clematis hexapetala

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