However, the plant is toxic and should not be consumed without proper knowledge and guidance from a healthcare professional. The berries contain toxic compounds that can cause vomiting, diarrhea, and other gastrointestinal issues. It is important to properly identify and prepare the plant before consuming it. In traditional medicine, it has been used to treat respiratory infections, skin conditions, and digestive issues. However, there is limited scientific evidence to support these claims and the plant should not be used as a substitute for medical treatment.

Synonyms Top

Scientific name	Authority	First published in
Lonicera kamtschatica	Pojark.	Fl. URSS 23: 730 (1958)
Lonicera kirilowi	hort. ex Dippel	Handb. Laubholzk. 1: 266 (1889)
Lonicera boczkarnikovae	Pleckanova	Bot. Zhurn. (Moscow & Leningrad) 79(6): 60 (1994)
Lonicera velutina	DC.	Prodr. 4: 337 (1830)
Lonicera venulosa	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 26: 542 (1880)
Xylosteon canadense	Duhamel ex DC.	Prodr. 4: 337 (1830)
Xylosteon caeruleum	Dum.Cours.	Bot. Cult. , ed. 2, 4: 336 (1811)
Xylosteon oblongifolium	Goldie	Edinburgh Philos. J. 6: 323 (1822)
Caprifolium caeruleum	Lam.	Fl. Franç. 3: 366 (1779)
Caprifolium venulosum	Kuntze	Revis. Gen. Pl. 1: 274 (1891)
Chamaecerasus coerulea	Delarbre	Fl. Auvergne , ed. 2: 131 (1800)
Euchylia caerulea	Dulac	Fl. Hautes-Pyrénées : 463 (1867)
Isika coerulea	Medik.	Philos. Bot. 1: 126 (1789)
Lonicera caerulea var. tangutica	Maxim.
Lonicera caerulea var. edulis	Turcz. ex Herder	Bull. Soc. Imp. Naturalistes Moscou 37(1): t. 3, fig. 1-2a. 1864
Lonicera caerulea var. altaica	Pall.	Fl. Ross. 1: 58, pl. 37 1789
Metalonicera edulis	(Turcz. ex Freyn) M.Wang & A.G.Gu	Bull. Bot. Res., Harbin 8(4): 204 (1988)
Lonicera venulosa subsp. edulis	(Turcz. ex Herder) Vorosch.	Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. 97(1): 94 (1992)
Lonicera venulosa subsp. emphyllocalyx	(Maxim.) Vorosch.	Byull. Moskovsk. Obshch. Isp. Prir., Otd. Biol. 97(1): 94 (1992)
Lonicera edulis	Turcz.	Bull. Soc. Imp. Naturalistes Moscou 18(no. 2): 306. 1845 [post 28 Mar 1845]
Lonicera emphyllocalyx	Maxim.	Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 31: 58 (1886)
Lonicera caerulea subsp. kamtschatica	(Sevast.) Gladkova	Arktich. Fl. SSSR 10: 28 (1987)
Lonicera caerulea subsp. venulosa	(Maxim.) Vorosch.	Florist. Issl. Razn. Raionakh SSSR : 192 (1985)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
English	deepblue honeysuckle
English	sweetberry honeysuckle
Spanish	madreselva azul
Arabic	عسلة زرقاء
Belarusian	Бружмель сіні
Czech	zimolez modrý
Danish	blå gedeblad
Danish	honningbær
Danish	blåfrugtet gedeblad
German	blaue heckenkirsche
German	blaue doppelbeere
Estonian	sinine kuslapuu
Finnish	sinikuusama
Finnish	alppisinikuusama
Finnish	idänsinikuusama
Finnish	marjasinikuusama
French	chèvrefeuille bleu
French	camérisier bleu
Hebrew	יערה כחולה
Croatian	plava kozokrvina
Upper Sorbian	módry kozylist
Hungarian	kék mézbogyó
Armenian	Ցախկեռաս կապույտ
Armenian	Ցախակեռաս կապույտ
Icelandic	blátoppur
Japanese	ハスカップ
Japanese	クロミノウグイスカズラ
Japanese	クロミノウグイスカグラ
Korean	댕댕이나무
Norwegian Bokmål	blåleddved
Norwegian Nynorsk	blåleddved
Polish	jagoda kamczacka
Polish	suchodrzew siny
Polish	wiciokrzew siny
Russian	Жимолость сизая
Russian	Жимолость Турчанинова
Russian	Жимолость сливочная
Russian	Жимолость синяя
Russian	Жимолость Регеля
Russian	Жимолость камчатская
Russian	Готовик
Russian	Жимолость голубая
Slovenian	modro kosteničevje
Serbian	sibirska borovnica (haskap)
Swedish	kaneltry
Swedish	ryskt blåtry
Swedish	bärtry
Swedish	blåtry
Swedish	blåbärstry
Ukrainian	Жимолость блакитна
Ukrainian	Жимолость голуба
vro	sinine kuslapuu
Chinese	藍靛果忍冬
Chinese	藍靛果
Chinese	藍果忍冬
Chinese	蓝靛果忍冬
Chinese	蓝锭果
Chinese	蓝果忍冬
Chinese	蓝靛果

Subspecies (abbr. subsp./ssp.) Top

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Name	Authority	First published in
Lonicera caerulea subsp. altaica	(Pall.) Gladkova	Arktich. Fl. SSSR 10: 26 (1987)
Lonicera caerulea subsp. borbasiana	(Kuntze) E.Mayer	Prilozi Oddel. Biol. Med. Nauki Makedonska Akad. Nauk. Umet. 4: 121 (1983)
Lonicera caerulea subsp. pallasii	(Ledeb.) Browicz	Bot. J. Linn. Soc. 68: 278 (1974)

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

Name	Authority	First published in
Lonicera caerulea var. cauriana	(Fernald) B.Boivin	Naturaliste Canad. 93: 433 (1966)

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

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
  - Inner Mongolia
  - Manchuria
  - Qinghai
  - Xinjiang
- Eastern Asia
  - Japan
  - Korea
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Russian Far East
  - Amur
  - Kamchatka
  - Khabarovsk
  - Kuril Islands
  - Magadan
  - Primorye
  - Sakhalin
- Siberia
  - Altay
  - Buryatiya
  - Chita
  - Irkutsk
  - Krasnoyarsk
  - Tuva
  - West Siberia
  - Yakutskiya
- Western Asia
  - Afghanistan

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan
  - West Himalaya

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - East European Russia
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Czechoslovakia
  - Germany
  - Switzerland
- Northern Europe
  - Finland
  - Norway
  - Sweden
- Southeastern Europe
  - Albania
  - Bulgaria
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - France
  - Spain

Northern America click to expand
- Eastern Canada
  - Ontario
- Northwestern U.S.A.
  - Idaho
  - Montana
  - Oregon
  - Washington
  - Wyoming
- Southwestern U.S.A.
  - California
  - Nevada
- Western Canada
  - Alberta
  - British Columbia
  - Manitoba

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000359746
UNII	A48177GYXC
Canadensys	4204
USDA Plants	LOCA6
Tropicos	6000006
INPN	106555
KEW	urn:lsid:ipni.org:names:148657-1
The Plant List	kew-2339990
Missouri Botanical Garden	278931
Open Tree Of Life	1086606
NCBI Taxonomy	134520
NBN Atlas	NBNSYS0200002557
Nature Serve	2.144394
IUCN Red List	18775218
IPNI	148657-1
iNaturalist	164761
GBIF	5334269
Freebase	/m/0chyz9
EPPO	LONCO
EOL	486991
Elurikkus	5532
USDA GRIN	22559
Wikipedia	Lonicera_caerulea
CMAUP	NPO20658

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

Response of antioxidation and immunity to combined influences of pH and ammonia nitrogen in the spotted babylon (Babylonia areolata)

Ding R, Yang R, Fu Z, Zhao W, Li M, Yu G, Ma Z, Bai Z

Heliyon

05-Apr-2024

PMCID:	PMC11024560
doi:	10.1016/j.heliyon.2024.e29205
PMID:	38638986

Exploring Beneficial Properties of Haskap Berry Leaf Compounds for Gut Health Enhancement

Sip S, Sip A, Szulc P, Selwet M, Żarowski M, Czerny B, Cielecka-Piontek J

Antioxidants (Basel)

17-Mar-2024

PMCID:	PMC10968585
doi:	10.3390/antiox13030357
PMID:	38539890

Enhancing Postharvest Quality and Antioxidant Capacity of Blue Honeysuckle cv. ‘Lanjingling’ with Chitosan and Aloe vera Gel Edible Coatings during Storage

Qiao J, Li D, Guo L, Hong X, He S, Huo J, Sui X, Zhang Y

Foods

19-Feb-2024

PMCID:	PMC10888047
doi:	10.3390/foods13040630
PMID:	38397607

Blue honeysuckle seeds and seed oil: Composition, physicochemical properties, fatty acid profile, volatile components, and antioxidant capacity

Sun J, Li D, Huyan W, Hong X, He S, Huo J, Jiang L, Zhang Y

Food Chem X

07-Feb-2024

PMCID:	PMC10877549
doi:	10.1016/j.fochx.2024.101176
PMID:	38379799

Vaccinium uliginosum L. (bog bilberry) and the search for its alleged toxicity: a review

Vaneková Z, Holloway P, Rollinger JM

Front Toxicol

31-Jan-2024

PMCID:	PMC10864615
doi:	10.3389/ftox.2024.1358840
PMID:	38357417

Importance of phytotherapy for oral health care and quality of life in adults: A scoping review

Shinkai RS, Azevedo CL, de Campos TT, Michel-Crosato E, Biazevic MG

J Dent Sci

24-Jan-2024

PMCID:	PMC11010713
doi:	10.1016/j.jds.2024.01.002
PMID:	38618093

Biological Properties of Recently Described Wild Bramble Rubus oklejewiczii against the Species from Similar Niches

Grabek-Lejko D, Wolanin M, Szpytma A, Pajda D, Miłek M, Puchalski C

Foods

21-Jan-2024

PMCID:	PMC10815075
doi:	10.3390/foods13020337
PMID:	38275704

Anthocyanin-Loaded Polymers as Promising Nature-Based, Responsive, and Bioactive Materials

Rosales-Murillo SS, Sánchez-Bodón J, Hernández Olmos SL, Ibarra-Vázquez MF, Guerrero-Ramírez LG, Pérez-Álvarez L, Vilas-Vilela JL

Polymers (Basel)

04-Jan-2024

PMCID:	PMC10781030
doi:	10.3390/polym16010163
PMID:	38201828

The Hexane Extract of Citrus sphaerocarpa Ameliorates Visceral Adiposity by Regulating the PI3K/AKT/FoxO1 and AMPK/ACC Signaling Pathways in High-Fat-Diet-Induced Obese Mice

Zang L, Kagotani K, Hayakawa T, Tsuji T, Okumura K, Shimada Y, Nishimura N

Molecules

09-Dec-2023

PMCID:	PMC10745821
doi:	10.3390/molecules28248026
PMID:	38138517

Transcriptional regulatory cascade of LcMYB71 and LcNAC73 affects low-temperature and drought stress response in Lonicera caerulea

Zang D, Sun Y, Zhao H

Front Plant Sci

27-Nov-2023

PMCID:	PMC10711284
doi:	10.3389/fpls.2023.1288947
PMID:	38089802

The Distribution Characteristics of Vegetation in the Subrange of the Altai Mountains, Xinjiang

Cao Q, Wei Y, Li W, Feng Y, Abduraimov OS

Plants (Basel)

20-Nov-2023

PMCID:	PMC10675357
doi:	10.3390/plants12223915
PMID:	38005812

Plant Extracts as Skin Care and Therapeutic Agents

Michalak M

Int J Mol Sci

22-Oct-2023

PMCID:	PMC10607442
doi:	10.3390/ijms242015444
PMID:	37895122

The most polyphagous insect herbivore? Host plant associations of the Meadow spittlebug, Philaenus spumarius (L.)

Thompson V, Harkin C, Stewart AJ

PLoS One

04-Oct-2023

PMCID:	PMC10602594
doi:	10.1371/journal.pone.0291734
PMID:	37792900

Effect of HHP and UHPH High-Pressure Techniques on the Extraction and Stability of Grape and Other Fruit Anthocyanins

Morata A, del Fresno JM, Gavahian M, Guamis B, Palomero F, López C

Antioxidants (Basel)

10-Sep-2023

PMCID:	PMC10526052
doi:	10.3390/antiox12091746
PMID:	37760049

Lonicera caerulea Pomace Alleviates DSS-Induced Colitis via Intestinal Barrier Improvement and Gut Microbiota Modulation

Zhang B, Huang X, Niu L, Chen X, Hu B, Tang X

Foods

05-Sep-2023

PMCID:	PMC10528379
doi:	10.3390/foods12183329
PMID:	37761037

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 / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
3-Methoxybenzoic acid	11461	Click to see COC1=CC=CC(=C1)C(=O)O	152.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
2,4-Dimethoxybenzoic acid	7052	Click to see COC1=CC(=C(C=C1)C(=O)O)OC	182.17	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Adipic Acid	196	Click to see C(CCC(=O)O)CC(=O)O	146.14	unknown	via CMAUP database
Hydron;octanedioate	22494956	Click to see [H+].[H+].C(CCCC(=O)[O-])CCC(=O)[O-]	174.19	unknown	via CMAUP database
Pimelic acid	385	Click to see C(CCC(=O)O)CCC(=O)O	160.17	unknown	via CMAUP database
Undecanedioic acid	15816	Click to see C(CCCCC(=O)O)CCCCC(=O)O	216.27	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
3-ethenyl-4-(2-oxoethyl)-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylic acid	4631412	Click to see C=CC1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)O)CC=O	374.34	unknown	https://doi.org/10.1021/NP50037A019
methyl (1S,4aS,6S,7R,7aS)-1-[[(2R,4aR,6S,7R,8R,8aS)-2-[[(2S,3R,4S)-3-ethenyl-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]methyl]-7,8-dihydroxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-6-yl]oxy]-6-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate	101921659	Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C4C(O3)COC(O4)CC5C(C(OC=C5C(=O)OC)OC6C(C(C(C(O6)CO)O)O)O)C=C)O)O)O	760.70	unknown	https://doi.org/10.1016/0031-9422(94)00853-L
methyl (2S,3R,4S)-4-[[(2R,4aR,6S,7R,8R,8aS)-6-[[(3S,4R,4aS)-4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl]oxy]-7,8-dihydroxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-2-yl]methyl]-3-ethenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate	101922273	Click to see COC(=O)C1=COC(C(C1CC2OCC3C(O2)C(C(C(O3)OC4C(C5CCOC(=O)C5=CO4)C=C)O)O)C=C)OC6C(C(C(C(O6)CO)O)O)O	728.70	unknown	https://doi.org/10.1016/0031-9422(94)00853-L
methyl (2S,3R,4S)-4-[[(2R,4aR,6S,7R,8R,8aS)-6,7,8-trihydroxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-2-yl]methyl]-3-ethenyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate	162844057	Click to see COC(=O)C1=COC(C(C1CC2OCC3C(O2)C(C(C(O3)O)O)O)C=C)OC4C(C(C(C(O4)CO)O)O)O	550.50	unknown	https://doi.org/10.1016/0031-9422(95)93760-D
methyl 1-[[2-[[3-ethenyl-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]methyl]-7,8-dihydroxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-6-yl]oxy]-6-hydroxy-7-methyl-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate	163060932	Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C4C(O3)COC(O4)CC5C(C(OC=C5C(=O)OC)OC6C(C(C(C(O6)CO)O)O)O)C=C)O)O)O	760.70	unknown	https://doi.org/10.1016/0031-9422(94)00853-L
Methyl 2-(hexopyranosyloxy)-4-(2-oxoethyl)-3-vinyl-3,4-dihydro-2H-pyran-5-carboxylate	369002	Click to see COC(=O)C1=COC(C(C1CC=O)C=C)OC2C(C(C(C(O2)CO)O)O)O	388.40	unknown	https://doi.org/10.1016/0031-9422(94)00853-L
methyl 3-ethenyl-4-[(6,7,8-trihydroxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-2-yl)methyl]-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate	162844056	Click to see COC(=O)C1=COC(C(C1CC2OCC3C(O2)C(C(C(O3)O)O)O)C=C)OC4C(C(C(C(O4)CO)O)O)O	550.50	unknown	https://doi.org/10.1016/0031-9422(95)93760-D
methyl 3-ethenyl-4-[[6-[(4-ethenyl-8-oxo-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-3-yl)oxy]-7,8-dihydroxy-4,4a,6,7,8,8a-hexahydropyrano[3,2-d][1,3]dioxin-2-yl]methyl]-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate	162887470	Click to see COC(=O)C1=COC(C(C1CC2OCC3C(O2)C(C(C(O3)OC4C(C5CCOC(=O)C5=CO4)C=C)O)O)C=C)OC6C(C(C(C(O6)CO)O)O)O	728.70	unknown	https://doi.org/10.1016/0031-9422(94)00853-L
methyl 4-(2,2-dimethoxyethyl)-3-ethenyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-5-carboxylate	14192587	Click to see COC(CC1C(C(OC=C1C(=O)OC)OC2C(C(C(C(O2)CO)O)O)O)C=C)OC	434.40	unknown	https://doi.org/10.1016/0031-9422(94)00853-L
Secologanin	161276	Click to see COC(=O)C1=COC(C(C1CC=O)C=C)OC2C(C(C(C(O2)CO)O)O)O	388.40	unknown	https://doi.org/10.1016/0031-9422(94)00853-L https://doi.org/10.1021/NP50037A019
Secologanin dimethyl acetal	157140	Click to see COC(CC1C(C(OC=C1C(=O)OC)OC2C(C(C(C(O2)CO)O)O)O)C=C)OC	434.40	unknown	https://doi.org/10.1016/0031-9422(94)00853-L
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aR,6R,7R,7aS)-6-[(E)-3-[3-methoxy-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyl]oxy-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-carboxylic acid	163016918	Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC	714.70	unknown	https://doi.org/10.1021/NP50037A019
(1S,4aS,6S,7R,7aS)-6-[(E)-3-[3-methoxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enoyl]oxy-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-carboxylic acid	101317809	Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)OC5C(C(C(C(O5)CO)O)O)O)OC	714.70	unknown	https://doi.org/10.1021/NP50037A019
Loganic acid	89640	Click to see CC1C(CC2C1C(OC=C2C(=O)O)OC3C(C(C(C(O3)CO)O)O)O)O	376.36	unknown	https://doi.org/10.1021/NP50037A019
Loganin	87691	Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O	390.40	unknown	https://doi.org/10.1016/0031-9422(94)00853-L https://doi.org/10.1021/NP50037A019
methyl (1S,4aS,7R,7aS)-7-methyl-6-oxo-1-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate	162898860	Click to see CC1C2C(CC1=O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC	388.40	unknown	https://doi.org/10.1007/BF00598553
Methyl 6-hydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,4a,5,6,7,7a-hexahydrocyclopenta[c]pyran-4-carboxylate	601562	Click to see CC1C(CC2C1C(OC=C2C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)O	390.40	unknown	https://doi.org/10.1016/0031-9422(94)00853-L
methyl 7-methyl-6-oxo-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4a,5,7,7a-tetrahydro-1H-cyclopenta[c]pyran-4-carboxylate	12311347	Click to see CC1C2C(CC1=O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)OC	388.40	unknown	https://doi.org/10.1007/BF00598553
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Isoarborinol	12305182	Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C	426.70	unknown	https://doi.org/10.1021/JF030509O
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
(2R)-2-(2-butoxy-2-oxoethyl)-2-hydroxybutanedioic acid	124397575	Click to see CCCCOC(=O)CC(CC(=O)O)(C(=O)O)O	248.23	unknown	https://doi.org/10.1007/BF00598553
1,3-Dibutyl citrate	14134170	Click to see CCCCOC(=O)CC(CC(=O)OCCCC)(C(=O)O)O	304.34	unknown	https://doi.org/10.1007/BF00598553
2-(2-Butoxy-2-oxoethyl)-2-hydroxysuccinic acid	14134171	Click to see CCCCOC(=O)CC(CC(=O)O)(C(=O)O)O	248.23	unknown	https://doi.org/10.1007/BF00598553
Citric Acid	311	Click to see C(C(=O)O)C(CC(=O)O)(C(=O)O)O	192.12	unknown	https://doi.org/10.1007/BF00598552
Citronensauredimethylester	12566214	Click to see COC(=O)CC(CC(=O)OC)(C(=O)O)O	220.18	unknown	https://doi.org/10.1007/BF00598553
Tributyl citrate	6507	Click to see CCCCOC(=O)CC(CC(=O)OCCCC)(C(=O)OCCCC)O	360.40	unknown	https://doi.org/10.1007/BF00597704
Trimethyl citrate	74112	Click to see COC(=O)CC(CC(=O)OC)(C(=O)OC)O	234.20	unknown	https://doi.org/10.1007/BF00598553
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
Dibutyl malate	95385	Click to see CCCCOC(=O)CC(C(=O)OCCCC)O	246.30	unknown	https://doi.org/10.1007/BF00597704
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(3S,4R,4aS)-4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one	354447	Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O	358.34	unknown	https://doi.org/10.1016/0031-9422(94)00853-L https://doi.org/10.1021/NP50037A019
4-ethenyl-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6-tetrahydro-3H-pyrano[3,4-c]pyran-8-one	581257	Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O	358.34	unknown	https://doi.org/10.1016/0031-9422(94)00853-L
Sweroside	161036	Click to see C=CC1C2CCOC(=O)C2=COC1OC3C(C(C(C(O3)CO)O)O)O	358.34	unknown	https://doi.org/10.1021/NP50037A019 https://doi.org/10.1016/0031-9422(94)00853-L
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Gal(a1-6)D-Ido(a1-6)Glc(a1-2b)Psif	132990894	Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OC4(C(C(C(O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O	666.60	unknown	https://doi.org/10.1016/S0304-4238(97)00129-5
Raffinose	439242	Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3(C(C(C(O3)CO)O)O)CO)O)O)O)O)O)O)O	504.40	unknown	https://doi.org/10.1016/S0304-4238(97)00129-5
Stachyose	439531	Click to see C(C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3C(C(C(C(O3)OC4(C(C(C(O4)CO)O)O)CO)O)O)O)O)O)O)O)O)O)O	666.60	unknown	https://doi.org/10.1016/S0304-4238(97)00129-5
> 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	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2R,3R,4S,5R,6R)-2-[[(2R,3S,4R,5S,6S)-6-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol	154497176	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)OC)O)O)O)O)O)O)O)O	609.60	unknown	https://doi.org/10.1021/JF030509O
(2R,3R,4S,5R,6S)-2-[[(2R,3S,4R,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol	154496406	Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O	595.50	unknown	https://doi.org/10.1021/JF030509O
(2S,3R,4R,5S,6R)-2-[5,7-dihydroxy-2-(4-hydroxy-3-methoxyphenyl)chromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	162265793	Click to see COC1=C(C=CC(=C1)C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O	463.40	unknown	https://doi.org/10.1021/JF030509O
Kuromanin	441667	Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O	449.40	unknown	https://doi.org/10.1021/JF030509O
Pelargonidin 3-glucoside ion	443648	Click to see C1=CC(=CC=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O	433.40	unknown	https://doi.org/10.1021/JF030509O
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
(2S,3R,4S,5S,6S)-2-[2-(3,4-dihydroxyphenyl)-7-hydroxy-3-[(2S,3R,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-5-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol	154496409	Click to see C1=CC(=C(C=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O	611.50	unknown	https://doi.org/10.1021/JF030509O
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
2-(3,4-Dihydroxyphenyl)-3-(2-O-acetyl-alpha-D-arabinofuranosyloxy)-5,7-dihydroxy-4H-1-benzopyran-4-one	102047222	Click to see CC(=O)OC1C(C(OC1OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC(=C(C=C4)O)O)CO)O	476.40	unknown	via CMAUP database
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one	11972444	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
Avicularin	5490064	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	via CMAUP database
Quercetin 3-O-(6''-galloyl)-beta-D-galactopyranoside	5491814	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC(=C(C(=C5)O)O)O)O)O)O)O)O	616.50	unknown	via CMAUP database
Quercetin-3-o-alpha-d-arabinofuranoside	11968848	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O	434.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11S,13R,14R,15S)-3,4,5,20,21,22-hexahydroxy-8,17-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-13-[(3,4,5-trihydroxybenzoyl)oxymethyl]-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-14-yl] 3,4,5-trihydroxy-2-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,14,29,30,33,34,35-undecahydroxy-4,17,25,38-tetraoxo-20-(3,4,5-trihydroxybenzoyl)oxy-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]benzoate	16176993	Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)OC9=C(C(=C(C=C9C(=O)OC1C(OC(C2C1OC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O2)O)O)O)O)O)O)OC(=O)C1=CC(=C(C(=C1)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O	1873.30	unknown	via CMAUP database
[(10R,11S,13R,14R,15S)-3,4,5,20,21,22-hexahydroxy-8,17-dioxo-11-(3,4,5-trihydroxybenzoyl)oxy-13-[(3,4,5-trihydroxybenzoyl)oxymethyl]-9,12,16-trioxatetracyclo[16.4.0.02,7.010,15]docosa-1(22),2,4,6,18,20-hexaen-14-yl] 3,4,5-trihydroxy-2-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,28,29,30,33,34,35-undecahydroxy-4,17,25,38-tetraoxo-20-(3,4,5-trihydroxybenzoyl)oxy-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-14-yl]oxy]benzoate	16166318	Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)OC7=C(C(=C(C=C7C(=O)OC8C(OC(C9C8OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O9)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)COC(=O)C2=CC(=C(C(=C2)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O	1873.30	unknown	via CMAUP database
[(10R,11S)-10-[(14R,15S,19S)-2,3,4,7,8,9,19-heptahydroxy-12,17-dioxo-13,16-dioxatetracyclo[13.3.1.05,18.06,11]nonadeca-1,3,5(18),6,8,10-hexaen-14-yl]-3,4,5,17,18,19-hexahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-11-yl] 3,4,5-trihydroxybenzoate	17999934	Click to see C1C(C(OC(=O)C2=CC(=C(C(=C2C3=C(C(=C(C=C3C(=O)O1)O)O)O)O)O)O)C4C5C(C6=C(C(=C(C(=C6C(=O)O5)C7=C(C(=C(C=C7C(=O)O4)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O	936.60	unknown	via CMAUP database
2-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,14,20,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]-3,4,5-trihydroxybenzoic acid	10033841	Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)O)O)O)O)O)O)O)O)O	952.60	unknown	via CMAUP database
2-O,3-O-[4,4',5,5',6,6'-Hexahydroxy-1,1'-biphenyl-2,2'-diylbis(carbonyl)]-beta-D-glucopyranose	11754973	Click to see C1=C2C(=C(C(=C1O)O)O)C3=C(C(=C(C=C3C(=O)OC4C(C(C(OC4O)CO)O)OC2=O)O)O)O	482.30	unknown	via CMAUP database
alpha-Pedunculagin	13834142	Click to see C1C2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)O)O)O)O)O)O	784.50	unknown	via CMAUP database
CID 12302513	12302513	Click to see C1C2C(C3C4C(C5=C(C(=C(C(=C5C(=O)O4)C6=C(C(=C(C(=C6C(=O)O3)C7=C(C(=C(C=C7C(=O)O2)O)O)O)O)O)O)O)O)O)O)OC(=O)C8=CC(=C(C(=C8C9=C(C(=C(C=C9C(=O)O1)O)O)O)O)O)O	934.60	unknown	via CMAUP database
Nobotanin A	101677163	Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)OC9=C(C(=C(C=C9C(=O)OC1C(OC(C2C1OC(=O)C1=CC(=C(C(=C1C1=C(C(=C(C=C1C(=O)O2)O)O)O)O)O)O)O)COC(=O)C1=CC(=C(C(=C1)O)O)O)O)O)O)O)O)O)O)O	1721.20	unknown	via CMAUP database
Nobotanin D	14429414	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)O	786.60	unknown	via CMAUP database
Pariin M	14284542	Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C3C(C(O2)O)OC(=O)C4=CC(=C(C(=C4C5=C(C(=C(C=C5C(=O)O3)O)O)O)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O	786.60	unknown	via CMAUP database
Potentillin	5315734	Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)O)O)O)O)O)O	936.60	unknown	via CMAUP database

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Lonicera caerulea

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