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.

Lonicera hypoglauca, commonly called yínhuā in Chinese pharmacopoeias, is used in traditional medicine primarily as an infusion or decoction for clearing heat and supporting detoxification. Among Han Chinese practitioners documented in the Pharmacopoeia of the People's Republic of China, the flower buds and open flowers are simmered into a tea or decoction taken in small doses to ease sore throat and feverish discomfort. In the diaspora communities of Taiwan, similar preparations of yínhuā flowers have been recorded in the Taiwanese Pharmacopoeia and by Huang’s 1999 compendium of Chinese medicinal plants. In northern Thailand, ethnic hill‑tribe herbalists prepare a decoction of the fresh or dried flowers and sometimes apply a cooled infusion as a wash on skin irritations, as reported by Anderson’s 1986 field ethnobotanical study of northern Thai medicinal plants.

For a simple medicinal tea, steep 3–6 g of dried L. hypoglauca flower buds and open flowers in 250 ml of near‑boiling water for 10–15 minutes, then strain and drink while warm. The Pharmacopoeia of the People’s Republic of China describes the traditional dose range as 6–15 g of dried flowers per day, divided in two or three infusions; limit use to short periods (generally one to two weeks) and avoid if you are pregnant. Individuals with known hypersensitivity to honeysuckle species should refrain from use, and those taking anticoagulants or sedatives should consult a practitioner, because well‑known constituents like chlorogenic acid may interact with certain drugs. Alcoholic extracts of the species are also prepared as 1:5 (herb to solvent, w/v) tinctures in 45–60% ethanol, macerated for 2–4 weeks with periodic shaking, yielding a final alcohol concentration suitable for medicinal use under supervision.

The known activity of L. hypoglauca is plausibly related to well‑established constituents in its flowers and buds: chlorogenic acid, luteolin, luteolin‑7‑O‑glucoside, quercetin, quercetin‑3‑O‑glucoside, and a pattern of caffeic and ferulic acid derivatives. Tang and Eisenbrand’s 1992 review of Chinese drugs of plant origin lists chlorogenic acid and flavonoids as prominent in L. hypoglauca, consistent with modern analyses that show these phenolics as major markers. Huang’s Chinese Medicinal Plants further corroborates these compounds in cultivated and wild material.

Modern relevance follows the traditional trail: dried L. hypoglauca flower buds and open flowers are widely available as commercial “yínhuā” tea, and the species continues to be cultivated for herbal products that are standardized for chlorogenic acid and related markers (Zhao and Guo, 2006). Contemporary research explores anti‑inflammatory and antiviral properties of these constituents in vitro and in animal studies, but human clinical evidence remains limited; as always, products should be sourced from reputable suppliers that adhere to quality standards documented in pharmacopoeias.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Lonicera leschenaultii	Miq.	Ann. Mus. Bot. Lugduno-Batavi 2: 270 (1866)
Lonicera hypoglauca subsp. nudiflora	P.S.Hsu & H.J.Wang	Acta Phytotax. Sin. 17(4): 81 (1979)
Lonicera mollissima	Blume ex Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 24: 37 (1877)
Lonicera rubropunctata	Hayata	Icon. Pl. Formosan. 9: 48 (1920)
Caprifolium hypoglaucum	Kuntze	Revis. Gen. Pl. 1: 274 (1891)
Caprifolium mollissimum	Kuntze	Revis. Gen. Pl. 1: 274 (1891)
Lonicera affinis var. hypoglauca	(Miq.) Rehder	Rep. (Annual) Missouri Bot. Gard. 14: 158 1903
Lonicera affinis var. mollissima	Blume ex Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg 24: 37 1878
Lonicera affinis var. pubescens	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg 24: 37 1878

Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	大金银花
Chinese	忍冬藤
Chinese	菰腺忍冬
Chinese	菰腺忍冬（红腺忍冬）
Chinese	裡白忍冬
Chinese	金银花
Chinese	金银花子
Chinese	金银花露
Chinese	大叶金银花
Chinese	大银花
Chinese	山银花
Chinese	红腺忍冬

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Taiwan

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-0000359587
UNII	V0QHS0RH24
Tropicos	50041229
KEW	urn:lsid:ipni.org:names:148833-1
The Plant List	kew-2339729
Open Tree Of Life	235196
NCBI Taxonomy	638626
IPNI	148833-1
iNaturalist	639653
GBIF	7272715
USDA GRIN	423461
CMAUP	NPO21345

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

Pharmacological Activities of Lonicerae japonicae flos and Its Derivative—“Chrysoeriol” in Skin Diseases

Law SK, Wu XX, Jiang Z, Tong CW, Chow WY, Au DC

Molecules

25-Apr-2024

PMCID:	PMC11085288
doi:	10.3390/molecules29091972
PMID:	38731465

Lonicera flos and Curcuma longa L. extracts improve growth performance, antioxidant capacity and immune response in broiler chickens

Xu D, Wang X, Shi W, Bao Y

Front Vet Sci

12-Apr-2024

PMCID:	PMC11045969
doi:	10.3389/fvets.2024.1388632
PMID:	38681856

Effects of Yupingfeng Polysaccharides as Feed Supplement on Immune Function and Intestinal Microbiome in Chickens

Zheng W, Guan Y, Wu B

Microorganisms

15-Nov-2023

PMCID:	PMC10672924
doi:	10.3390/microorganisms11112774
PMID:	38004785

An updated meta-analysis of Chinese herbal medicine for the prevention of COVID-19 based on Western-Eastern medicine

Hu S, Luo D, Zhu Q, Pan J, Chen B, Furian M, Harkare HV, Sun S, Fansa A, Wu X, Yu B, Ma T, Wang F, Shi S

Front Pharmacol

13-Nov-2023

PMCID:	PMC10693348
doi:	10.3389/fphar.2023.1257345
PMID:	38044944

Therapeutic potential of Lianhua Qingke in airway mucus hypersecretion of acute exacerbation of chronic obstructive pulmonary disease

Hao Y, Wang T, Hou Y, Wang X, Yin Y, Liu Y, Han N, Ma Y, Li Z, Wei Y, Feng W, Jia Z, Qi H

Chin Med

03-Nov-2023

PMCID:	PMC10623880
doi:	10.1186/s13020-023-00851-4
PMID:	37924136

Lianhua Qingke ameliorates lipopolysaccharide‐induced lung injury by inhibiting neutrophil extracellular traps formation and pyroptosis

Peng W, Qi H, Zhu W, Tong L, Rouzi A, Wu Y, Han L, He L, Yan Y, Pan T, Liu J, Wang Q, Jia Z, Song Y, Zhu Q, Zhou J

Pulm Circ

06-Oct-2023

PMCID:	PMC10557103
doi:	10.1002/pul2.12295
PMID:	37808899

Companion Plants of Tea: From Ancient to Terrace to Forest

Wu H, Long X, Geng Y

Plants (Basel)

25-Aug-2023

PMCID:	PMC10490072
doi:	10.3390/plants12173061
PMID:	37687308

Ethnobotanical study on herbal tea drinks in Guangxi, China

Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C

J Ethnobiol Ethnomed

31-Mar-2023

PMCID:	PMC10064729
doi:	10.1186/s13002-023-00579-3
PMID:	37004116

Identification of HQT gene family and their potential function in CGA synthesis and abiotic stresses tolerance in vegetable sweet potato

Medison MB, Pan R, Peng Y, Medison RG, Shalmani A, Yang X, Zhang W

Physiol Mol Biol Plants

25-Mar-2023

PMCID:	PMC10073390
doi:	10.1007/s12298-023-01299-4
PMID:	37033766

Perplexing Polyphenolics: The Isolations, Syntheses, Reappraisals, and Bioactivities of Flavonoids, Isoflavonoids, and Neoflavonoids from 2016 to 2022

Umer SM, Shamim S, Khan KM, Saleem RS

Life (Basel)

09-Mar-2023

PMCID:	PMC10058313
doi:	10.3390/life13030736
PMID:	36983891

Construction of SNP fingerprint and population genetic analysis of honeysuckle germplasm resources in China

Li J, Chang X, Huang Q, Liu P, Zhao X, Li F, Wang Y, Chang C

Front Plant Sci

02-Mar-2023

PMCID:	PMC10017979
doi:	10.3389/fpls.2023.1080691
PMID:	36938035

Lonicera flos and Cnicus japonicus extracts improved egg quality partly by modulating antioxidant status, inflammatory-related cytokines and shell matrix protein expression of oviduct in laying hens

Liu ZP, Chao JR, Xu PT, Lv HY, Ding BY, Zhang ZF, Li LL, Guo SS

Poult Sci

07-Feb-2023

PMCID:	PMC10011517
doi:	10.1016/j.psj.2023.102561
PMID:	36867918

Ethnobotanical study of the wild edible and healthy functional plant resources of the Gelao people in northern Guizhou, China

Xie J, Liu F, Jia X, Zhao Y, Liu X, Luo M, He Y, Liu S, Wu F

J Ethnobiol Ethnomed

19-Dec-2022

PMCID:	PMC9761637
doi:	10.1186/s13002-022-00572-2
PMID:	36536370

‘Food and medicine continuum’ in the East and West: Old tradition and current regulation

Yao R, He C, Xiao P

Chin Herb Med

17-Dec-2022

PMCID:	PMC9975626
doi:	10.1016/j.chmed.2022.12.002
PMID:	36875443

XiaoEr LianHuaQinqGan alleviates viral pneumonia in mice infected by influenza A and respiratory syncytial viruses

Li W, Li T, Zhao C, Song T, Mi Y, Chuangfeng Z, Hou Y, Jia Z

Pharm Biol

29-Nov-2022

PMCID:	PMC9809968
doi:	10.1080/13880209.2022.2147961
PMID:	36444944

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.

Name	PubChem ID	Canonical SMILES	MW	Found in	Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Methyl Anthranilate	8635	Click to see COC(=O)C1=CC=CC=C1N	151.16	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenylacetaldehydes
Phenylacetaldehyde	998	Click to see C1=CC=C(C=C1)CC=O	120.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Toluenes
2-Tolylisocyanide	575991	Click to see CC1=CC=CC=C1[N+]#[C-]	117.15	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Tetratriacontane	26519	Click to see	478.90	unknown	via CMAUP database
Triacontane	12535	Click to see	422.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Palmitic Acid	985	Click to see	256.42	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Triacontanol	68972	Click to see	438.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols / Long-chain fatty alcohols
Ginnol	16057860	Click to see	424.80	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Geraniol	637566	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
Linalool	6549	Click to see	154.25	unknown	via CMAUP database
Linalool, (-)-	443158	Click to see CC(=CCCC(C)(C=C)O)C	154.25	unknown	via CMAUP database
Linalool, (+)-	67179	Click to see	154.25	unknown	via CMAUP database
Nerol	643820	Click to see CC(=CCCC(=CCO)C)C	154.25	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
Centauroside	102183195	Click to see	758.70	unknown	via CMAUP database
Secologanoside	14136854	Click to see	390.34	unknown	via CMAUP database
Secoxyloganin	162868	Click to see	404.40	unknown	via CMAUP database
Secoxyloganin methyl ester	14105070	Click to see COC(=O)CC1C(C(OC=C1C(=O)OC)OC2C(C(C(C(O2)CO)O)O)O)C=C	418.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(-)-Loganin	87691	Click to see	390.40	unknown	via CMAUP database
8-Epiloganin	10548420	Click to see	390.40	unknown	via CMAUP database
methyl (1S,4aS,6R,7R,7aS)-6-hydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate	71676045	Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O	390.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6aS,6bR,12aR,14bR)-10-[(2S,3R,4S,5S)-4,5-bis[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	44146564	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)OC1C(C(C(C(O1)CO)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)O	1399.50	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aS,6bR,9R,10S,12aR)-10-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	3084573	Click to see	1075.20	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-4,5-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	102004439	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)OC1C(C(C(C(O1)CO)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)O	1399.50	unknown	via CMAUP database
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aS,6bR,9R,10S,12aR)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	3086656	Click to see	1237.40	unknown	via CMAUP database
[(3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	118705383	Click to see	1237.40	unknown	via CMAUP database
[3,4,5-Trihydroxy-6-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl] 10-[4,5-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	74933950	Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)OC8C(C(C(C(O8)COC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)OC1C(C(C(C(O1)CO)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)O	1399.50	unknown	via CMAUP database
Olean-12-en-28-oic acid, 3-((O-beta-D-glucopyranosyl-(1->3)-O-6-deoxy-alpha-L-mannopyranosyl-(1->2)-alpha-L-arabinopyranosyl)oxy)-23-hydroxy-, 6-O-beta-D-glucopyranosyl-beta-D-glucopyranosyl ester, (3beta,4alpha)-	14564503	Click to see	1237.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid	64945	Click to see	456.70	unknown	via CMAUP database
(10R)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	45358157	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
(1S,2R,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylic acid	45483617	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O	456.70	unknown	via CMAUP database
(3S,5S,6S,8R,9S,10R,13S,14S,16S,17R)-16-[(2S,5R)-2,5-dimethyloxan-2-yl]oxy-17-ethyl-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthrene-3,6-diol	52931478	Click to see	448.70	unknown	via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	45483610	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
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
Oleanolic Acid	10494	Click to see	456.70	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
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
(1R,3S,4S,5S)-3-((E)-3-(3,4-Dihydroxyphenyl)Acryloyloxy)-1,4,5-Trihydroxycyclohexanecarboxylic Acid	12310830	Click to see	354.31	unknown	via CMAUP database
1,5-O-Trans-Dicaffeoylquinic Acid	6474640	Click to see	516.40	unknown	via CMAUP database
3-O-Caffeoylquinic acid methyl ester	6476139	Click to see	368.30	unknown	via CMAUP database
3,4-Dicaffeoyl Quinic Acid	10324242	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O	516.40	unknown	via CMAUP database
3,4-Dicaffeoylquinic acid	6474309	Click to see	516.40	unknown	via CMAUP database
3,5-Di-caffeoylquinic acid	13604688	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O	516.40	unknown	via CMAUP database
4,5-Dicaffeoylquinic acid	5281780	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)OC(=O)C=CC3=CC(=C(C=C3)O)O)O	516.40	unknown	via CMAUP database
Butyl chlorogenate	12135130	Click to see CCCCOC(=O)C1(CC(C(C(C1)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O)O	410.40	unknown	via CMAUP database
Chlorogenate	1794426	Click to see	353.30	unknown	via CMAUP database
Chlorogenic Acid	1794427	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
cis-Chlorogenic acid	1794425	Click to see	354.31	unknown	via CMAUP database
Cryptochlorogenic acid	9798666	Click to see	354.31	unknown	via CMAUP database
Dicaffeoyl quinic acid	13604687	Click to see	516.40	unknown	via CMAUP database
Isochlorogenic acid	5315832	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
isochlorogenic acid A	6474310	Click to see	516.40	unknown	via CMAUP database
Neochlorogenic acid	5280633	Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O	354.31	unknown	via CMAUP database
Npc237314	10075681	Click to see	530.50	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(-)-Sweroside	161036	Click to see	358.34	unknown	via CMAUP database
7-epi-Vogeloside	102183193	Click to see	388.40	unknown	via CMAUP database
GlyTouCan:G29155XH	91692850	Click to see	342.30	unknown	via CMAUP database
GlyTouCan:G80014NW	46782954	Click to see	342.30	unknown	via CMAUP database
Sucrose	5988	Click to see	342.30	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 / 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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Quercetin	5280343	Click to see	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-4-oxo-4H-chromen-3-yl D-galactopyranoside	11751616	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	via CMAUP database
Hyperoside	5281643	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	via CMAUP database
Isoquercetin	5280804	Click to see	464.40	unknown	via CMAUP database
Rutin	5280805	Click to see	610.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Luteolin 7-O-glucoside	5280637	Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O	448.40	unknown	via CMAUP database
Scolymoside	5282152	Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3=CC(=C4C(=C3)OC(=CC4=O)C5=CC(=C(C=C5)O)O)O)CO)O)O)O)O)O	594.50	unknown	via CMAUP database

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Lonicera hypoglauca

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