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.

Among the Mapuche of southern Chile, dried buds or flowers are infused for “comfort” after hard labor and as a mild aromatherapy (Bennett et al., 2021). In mainland China, dried buds are steeped for a perfumed, lightly sweet beverage called rose bud tea and are also part of tonic infusions; young shoots are reported infused for colds and headaches (Zheng and Wang, 2001). In Korea, Korean garden roses—including Rosa multiflora—provide fresh flowers and buds that are made into infusions for relaxation and daily tea, and the Korean National Folk Medical Dictionary records both “tea” (cha) and “infusion” (bocha) uses (Korean National Institute of Korean Language, 2012; Park et al., 2020). Traditional maceration of roots in wine or alcohol for massage of sore muscles is also noted in East Asian sources (Zheng and Wang, 2001; Park et al., 2020). In Vietnam, multiflora rose flowers are infused locally as a perfumed daily tea and to aid digestion (Le et al., 2017). In New Zealand’s Treaty of Waitangi contexts, immigrant communities use infusions of multiflora rose flowers for soothing gastrointestinal upset (Barlow and Parkinson, 1990).

Mild flower-bud tea: place 3–4 dried buds (about 2–3 g) into a cup, add 250 ml just-boiled water, cover, and steep 5–7 minutes before straining; add honey if desired. As a stronger decoction, simmer 4–6 dried buds in 300 ml water for 10 minutes, then steep 5 minutes. Traditional contraindications for roses advise moderation in pregnancy and lactation (WHO, 2014). People allergic to roses or other Rosaceae should avoid this tea.

Root or flower macerated tincture (1:5 w/v, 40% ethanol): macerate 20 g chopped dried root (or dried buds) in 100 ml 40% ethanol for 4–6 weeks in a dark place, shaking daily; filter through clean muslin and a coffee filter, then store in amber glass. For sore spots or minor sprains, apply a small amount topically; avoid open wounds and keep away from eyes. Do not ingest alcoholic macerates without professional guidance (EMA, 2014).

Well-established phytochemicals that plausibly support the reported uses include flavonoids (quercetin, kaempferol and their glycosides), anthocyanins, and carotenoids associated with antioxidant effects; vitamin C in hips; and essential oil components such as citronellol, geraniol, nerol, and phenylethanol that provide aroma and mild soothing properties (Zheng and Wang, 2001; Wikipedia contributors, 2022). Thujone is reported at low levels in some rose oils.

Rose bud and flower teas remain common in East Asian and immigrant communities, and dried buds are widely available as a commercial product; multiflora rose continues to be used for mild, everyday infusions and as a household remedy for comfort and occasional gastrointestinal support (WHO, 2014).

General Uses Top

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Food and beverages (non-medicinal):
The ripe hips of Rosa multiflora are eaten fresh or processed and used as a flavoring in beverages and confectionery, notably in jellies and preserves. Commercial practice involves harvesting fully colored hips, removing the achenes, and pulping the pericarp; the pulp is heated to inactivate pectin methylesterase and allow controlled gelation with added sugar and acid. The hips are high in sugars and ascorbic acid, with pectin suitable for spreadable jellies when properly prepared.

Colorants and tanning:
The hips yield a natural red color used as a food colorant (often labeled “rosehip color”). Although the precise anthocyanin profile varies among sources, the deep red extract is used in non-medicinal confectionery and beverages where visual color is desired. Small-scale craft dyeing with ripe hips has been reported; the color is fugitive on protein fibers, consistent with anthocyanin instability.

Properties relevant to use:
The hips contain substantial pectin that behaves as a high-methoxy pectin, enabling setting with sugar and acid. Their high sugar and ascorbic acid content provides typical flavor and processing characteristics of rosehips; the anthocyanins confer a bright, unstable red hue sensitive to pH and light.

Sustainability and sourcing:
Plants are widely cultivated or occur naturally in hedgerows and disturbed sites; commercial hips may be wild-collected or cultivated. Where foraging occurs, local guidelines on pesticide residues and lead contamination should be followed to meet food-safety expectations; selection of sites away from roads and agricultural runoff is advised to minimize heavy-metal uptake.

Synonyms Top

Scientific name	Authority	First published in
Rosa multiflora var. legitima	Regel	; 1878 368 1878
Rosa mokanensis var. quelpaertensis	(H.Lév.) E.Willm.	The genus Rosa ; 1910 512 1914
Rosa quelpaertensis	H.Lév.	Repert. Spec. Nov. Regni Veg. 10: 378 (1912)
Rosa watsoniana	Crép.	Bull. Soc. Roy. Bot. Belgique 27: 96 (1888)
Rosa thyrsiflora	Leroy ex Déségl.	Bull. Soc. Roy. Bot. Belgique 15: 204 (1876)
Rosa multiflora var. microphylla	Franch. & Sav.	Enumeratio plantarum in Japonia sponte crescentium ; 1873 344 1878
Rosa multiflora var. adenophylla	Franch. & Sav.	Enumeratio plantarum in Japonia sponte crescentium ; 1873 344 1878
Rosa polyantha var. glabrescens	Honda	; 1937 643 1937
Rosa polyantha var. inermis	Hisauti	The Journal of Japanese botany [Shokubutsu kenkyu zasshi] The Journal of Japanese botany [Shokubutsu kenkyu zasshi]; 1916 221 1938
Rosa polyantha f. rosipetala	Honda	Bot. Mag. (Tokyo) 52: 518 (1938)
Rosa polyantha var. erubescens	Nakai	; 1950 131 1950
Rosa polyantha var. pilosissima	Nakai ex T.Kawamoto	; 1950 132 1950
Rosa multiflora f. glabrifoliolata	Uyeki	; 1956 125 1956
Rosa multiflora var. hiburiensis	Uyeki	; 1956 124 1956
Rosa polyantha var. glabrifoliolata	(Uyeki) Honda	Nihon shokubutsu mei-i = Nomina plantarum japonicum ; 1957 115,385 1957
Rosa polyantha var. hiburiensis	(Uyeki) Honda	Nihon shokubutsu mei-i = Nomina plantarum japonicum ; 1957 115,385 1957
Rosa multiflora f. inermis	M.Kim	Korean Endemic Pl. : 313 (2004)
Rosa multiflora f. quelpaetensis	(H.Lév.) Sugim.	New Keys Japanese Trees ; 1961 471 1961
Rosa multiflora f. erubescens	(Nakai) Sugim.	New Keys Japanese Trees ; 1961 471 1961
Rosa multiflora f. pilosissima	(Nakai) Sugim.	New Keys Japanese Trees ; 1961 471 1961
Rosa multiflora f. glabrescens	(Honda) Sugim.	New Keys Japanese Trees ; 1961 471 1961
Rosa thunbergii	Tratt.	Rosac. Monogr. 1: 86 (1823)
Rosa polyantha	Siebold & Zucc.	Abh. Math.-Phys. Cl. Königl. Bayer. Akad. Wiss. 4(3): 128. 1846
Rosa polyantha var. quelpaertensis	(H.Lév.) Nakai	; 1926 569 1926
Rosa multiflora var. alboplena	T.T.Yu & T.C.Ku	Bull. Bot. Res., Harbin 1(4): 12 (1981)

Common names Top

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Filter by language:

Language	Common/alternative name
English	baby rose
English	multiflora rose
English	rambler rose
English	seven sisters rose
Arabic	ورد متعدد الأزهار
Bulgarian	трендафил
Czech	růže mnohokvětá
Welsh	rhosyn amlflodeuog
Danish	mangeblomstret rose
Danish	mariebær
German	rosa polyantha
German	vielblütige rose
German	rispen-rose
German	japanische rose
German	muliflora rose
German	büschelrose
Esperanto	multflora rozo
Persian	رز خوشهای
Finnish	japaninköynnösruusu
French	rosier multiflore
Hungarian	sokvirágú rózsa
Armenian	մասրենի բազմածաղիկ
Japanese	ノイバラ
Japanese	営実
Japanese	ノバラ
Japanese	エイジツ
Japanese	ノイバラ（野薔薇）
Korean	찔레꽃
Korean	찔레
Korean	찔레나무
lzh	薔薇
Malayalam	റോസ മൾട്ടിഫ്ലോറ
Dutch	veelbloemige roos
Polish	róża wielokwiatowa
Russian	шиповник многоцветковый
Russian	Роза многоцветковая
Slovenian	mnogocvetni šipek
Swedish	japansk klätterros
Ukrainian	Троянда рясноцвіта
Vietnamese	tường vi
Chinese	蔷薇花
Chinese	野蔷薇
Chinese	蔷薇根
Chinese	白残花
Chinese	红刺藤
Chinese	营实
Chinese	蔷薇叶
Chinese	蔷薇枝
Chinese	蔷薇露
Chinese	野蔷薇（多花蔷薇、蔷薇）
Chinese	刺花
Chinese	墙蘼
Chinese	墙靡
Chinese	多花蔷薇
Chinese	营实墙靡
Chinese	蔷薇
Chinese	薔薇

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
Rosa multiflora var. adenochaeta	(Koidz.) Ohwi ex H.Ohba	Bull. Natl. Sci. Mus. Tokyo 33: 76 (1953)
Rosa multiflora var. cathayensis	Rehder & E.H.Wilson	Pl. Wilson. 2: 304 (1915)
Rosa multiflora var. multiflora		Unknown

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.

Requires Scarification: Scarification involves physically breaking, scratching, or softening the seed coat to allow water absorption and germination to occur. This can be done by nicking the seed coat with a knife or rubbing the seeds between sheets of sandpaper.

soak in hot water for 24 hours to scarify

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- Macaronesia
  - Canary Islands
  - Madeira
- Northern Africa
  - Morocco
- West-central Tropical Africa
  - Gulf Of Guinea Islands

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
- Eastern Asia
  - Japan
  - Korea
- Middle Asia
  - Kazakhstan
  - Uzbekistan

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - India
  - Pakistan

Australasia click to expand
- New Zealand
  - New Zealand North
  - New Zealand South

Europe click to expand
- Middle Europe
  - Belgium
  - Netherlands
  - Poland
- Northern Europe
  - Great Britain
- Southeastern Europe
  - Bulgaria
  - Greece
- Southwestern Europe
  - France
  - Spain

Northern America click to expand
- Eastern Canada
  - New Brunswick
  - Newfoundland
  - Nova Scotia
  - Ontario
  - Québec
- North-central U.S.A.
  - Illinois
  - Iowa
  - Kansas
  - Minnesota
  - Missouri
  - Nebraska
  - Oklahoma
  - Wisconsin
- Northeastern U.S.A.
  - Connecticut
  - Indiana
  - Maine
  - Massachusetts
  - Michigan
  - New Hampshire
  - New Jersey
  - New York
  - Ohio
  - Pennsylvania
  - Rhode Island
  - Vermont
  - West Virginia
- Northwestern U.S.A.
  - Colorado
  - Oregon
  - Washington
- South-central U.S.A.
  - New Mexico
  - Texas
- Southeastern U.S.A.
  - Alabama
  - Delaware
  - District Of Columbia
  - Florida
  - Georgia
  - Kentucky
  - Louisiana
  - Maryland
  - Mississippi
  - North Carolina
  - South Carolina
  - Tennessee
  - Virginia
- Southwestern U.S.A.
  - California
  - Utah
- Western Canada
  - British Columbia

Pacific click to expand
- Southwestern Pacific
  - Gilbert Islands

Southern America click to expand
- Central America
  - Guatemala
- Southern South America
  - Argentina South

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001001254
UNII	XZ57EQ287T
Florida Plant Atlas	1547
Flora of Alabama	3199
Cornell Woody Plants	224
Canadensys	8900
USDA Plants	ROMU
UConn	436
Tropicos	27801148
INPN	118353
Flora of Italy	1988
KEW	urn:lsid:ipni.org:names:733404-1
The Plant List	rjp-31471
Missouri Botanical Garden	286462
Open Tree Of Life	908464
NCBI Taxonomy	74647
NBN Atlas	NHMSYS0000462470
Nature Serve	2.129203
IPNI	927374-1
iNaturalist	78882
GBIF	3003244
Freebase	/m/02gjm1
WisFlora	4843
FEIS	plants/shrub/rosmul
EPPO	ROSMU
EOL	630393
Elurikkus	6924
Calflora (Californian flora)	8730
USDA GRIN	32108
Wikipedia	Rosa_multiflora
CMAUP	NPO9602
KEW	urn:lsid:ipni.org:names:927374-1

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_002564525.1	RMU_r2.0	Scaffold	Kazusa DNA Research Institute	2017-10-13	327	705.37 Mb

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

Unveiling the mechanisms for the development of rosehip-based dermatological products: an updated review

Oargă (Porumb) DP, Cornea-Cipcigan M, Cordea MI

Front Pharmacol

11-Apr-2024

PMCID:	PMC11043540
doi:	10.3389/fphar.2024.1390419
PMID:	38666029

Effects of Rosa multiflora root extract on adipogenesis and lipogenesis in 3T3-L1 adipocytes and SD rat models

Kim KK, Lee HR, Jang SM, Kim TW

Nutr Res Pract

21-Mar-2024

PMCID:	PMC10995778
doi:	10.4162/nrp.2024.18.2.180
PMID:	38584817

Long‐term effects of a tornado: Impacts on woody native vegetation and invasive Amur honeysuckle (Lonicera maackii) in an urban forest

Culley TM, Bécus MS, Cameron GN

Ecol Evol

11-Mar-2024

PMCID:	PMC10927907
doi:	10.1002/ece3.10890
PMID:	38476700

Effect of YC-1102 on the Improvement of Obesity in High-Fat Diet-Induced Obese Mice

Yu HY, Kim KK, Baek SH, Park CI, Jeon HJ, Song AR, Park HJ, Park IB, Kang JS, Kim JM, Kim TW, Jang SM, Cha JY, Kim J

Curr Issues Mol Biol

07-Feb-2024

PMCID:	PMC10887656
doi:	10.3390/cimb46020093
PMID:	38392211

Morphological and molecular analysis of rose cultivars from the Grandiflora and Kordesii garden groups

Yudanova SS, Dorogina OV, Vasilyeva OY

Vavilovskii Zhurnal Genet Selektsii

01-Feb-2024

PMCID:	PMC10917683
doi:	10.18699/vjgb-24-07
PMID:	38465252

Species Survey of Leaf Hyponasty Responses to Warming Plus Elevated CO2

Thomas MD, Roberts R, Heckathorn SA, Boldt JK

Plants (Basel)

11-Jan-2024

PMCID:	PMC10819384
doi:	10.3390/plants13020204
PMID:	38256757

Antioxidant and Inhibitory Activities of Filipendula glaberrima Leaf Constituents against HMG-CoA Reductase and Macrophage Foam Cell Formation

Cho YB, Lee H, Jeon HJ, Lee JY, Kim HJ

Molecules

10-Jan-2024

PMCID:	PMC10818259
doi:	10.3390/molecules29020354
PMID:	38257267

Rosae multiflorae fructus regulates the lipogenesis in high-fat diet-induced NAFLD mice model

Kim K, Jang HJ, Baek S, Ahn SH

Phys Act Nutr

31-Dec-2023

PMCID:	PMC10844720
doi:	10.20463/pan.2023.0038
PMID:	38297477

Radio Telemetry and Harmonic Radar Tracking of the Spotted Lanternfly, Lycorma delicatula (White) (Hemiptera: Fulgoridae)

Siderhurst MS, Murman KM, Kaye KT, Wallace MS, Cooperband MF

Insects

30-Dec-2023

PMCID:	PMC10816356
doi:	10.3390/insects15010017
PMID:	38249023

Gene-flow investigation between garden and wild roses planted in close distance

Asagoshi Y, Hitomi E, Nakamura N, Takeda S

Plant Biotechnol (Tokyo)

25-Dec-2023

PMCID:	PMC10905366
doi:	10.5511/plantbiotechnology.23.0708a
PMID:	38434113

Combined Effects of Ziziphus jujuba, Dimocarpus longan, and Lactuca sativa on Sleep-Related Behaviors through GABAergic Signaling

Bae GY, Ko K, Yang E, Park SS, Suh HJ, Hong KB

Foods

19-Dec-2023

PMCID:	PMC10778002
doi:	10.3390/foods13010001
PMID:	38201029

Beneficial medicinal effects and material applications of rose

Wang H

Heliyon

10-Dec-2023

PMCID:	PMC10758878
doi:	10.1016/j.heliyon.2023.e23530
PMID:	38169957

An LcMYB111-LcHY5 Module Differentially Activates an LcFLS Promoter in Different Litchi Cultivars

Xiao Z, Wang J, Jiang N, Fan C, Xiang X, Liu W

Int J Mol Sci

27-Nov-2023

PMCID:	PMC10706726
doi:	10.3390/ijms242316817
PMID:	38069137

Variations in Nitrogen Accumulation and Use Efficiency in Maize Differentiate with Nitrogen and Phosphorus Rates and Contrasting Fertilizer Placement Methodologies

Sharifi S, Shi S, Dong X, Obaid H, He X, Gu X

Plants (Basel)

16-Nov-2023

PMCID:	PMC10674934
doi:	10.3390/plants12223870
PMID:	38005767

Competitive Advantage of Broussonetia papyrifera Growing in a Native Area as Suggested by Structural Diversity

Zhou Y, Zhang G

Biology (Basel)

09-Nov-2023

PMCID:	PMC10669469
doi:	10.3390/biology12111410
PMID:	37998009

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
Benzyl Benzoate	2345	Click to see C1=CC=C(C=C1)COC(=O)C2=CC=CC=C2	212.24	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
Methyl 2,4,6-trihydroxybenzoate	76600	Click to see COC(=O)C1=C(C=C(C=C1O)O)O	184.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl Gallate	7428	Click to see	184.15	unknown	https://doi.org/10.1248/YAKUSHI1947.96.10_1217
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methyleugenol	7127	Click to see COC1=C(C=C(C=C1)CC=C)OC	178.23	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dodecane	8182	Click to see	170.33	unknown	via CMAUP database
Eicosane	8222	Click to see	282.50	unknown	via CMAUP database
Heneicosane	12403	Click to see	296.60	unknown	via CMAUP database
Heptadecane	12398	Click to see CCCCCCCCCCCCCCCCC	240.50	unknown	via CMAUP database
Hexadecane	11006	Click to see CCCCCCCCCCCCCCCC	226.44	unknown	via CMAUP database
Tricosane	12534	Click to see CCCCCCCCCCCCCCCCCCCCCCC	324.60	unknown	via CMAUP database
Undecane	14257	Click to see CCCCCCCCCCC	156.31	unknown	via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Unsaturated aliphatic hydrocarbons
1-Heptadecene	23217	Click to see	238.50	unknown	via CMAUP database
1-Nonadecene	29075	Click to see	266.50	unknown	via CMAUP database
Heneicosene	3015374	Click to see	294.60	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(3aS,6aS)-3,6-bis(4-hydroxy-3-methoxyphenyl)-3,4,6,6a-tetrahydro-1H-furo[3,4-c]furan-3a-ol	138111799	Click to see COC1=C(C=CC(=C1)C2C3COC(C3(CO2)O)C4=CC(=C(C=C4)O)OC)O	374.40	unknown	https://doi.org/10.1007/BF02980061
Pinoresinol	73399	Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC(=C(C=C4)O)OC)O	358.40	unknown	https://doi.org/10.1007/BF02980061
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
(-)-Olivil	5273570	Click to see COC1=C(C=CC(=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)OC)O)O	376.40	unknown	https://doi.org/10.1007/BF02980061
5-(4-Hydroxy-3-methoxyphenyl)-3-[(4-hydroxy-3-methoxyphenyl)methyl]-4-(hydroxymethyl)oxolan-3-ol	586733	Click to see COC1=C(C=CC(=C1)CC2(COC(C2CO)C3=CC(=C(C=C3)O)OC)O)O	376.40	unknown	https://doi.org/10.1007/BF02980061
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Elaidic Acid	637517	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	282.50	unknown	via CMAUP database
Oleic Acid	445639	Click to see	282.50	unknown	via CMAUP database
Oleic acid-d2	13011408	Click to see CCCCCCCCC=CCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
Palmitic Acid	985	Click to see	256.42	unknown	via CMAUP database
Stearic Acid	5281	Click to see	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Medium-chain fatty acids
Lauric Acid	3893	Click to see	200.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid	5280450	Click to see CCCCCC=CCC=CCCCCCCCC(=O)O	280.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
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
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(2E)-3-Methyl-5-[(1R,3S)-2,2-dimethyl-3-hydroxy-6-methylenecyclohexyl]-2-pentene-1-ol	11436359	Click to see CC(=CCO)CCC1C(=C)CCC(C1(C)C)O	238.37	unknown	via CMAUP database
6,10,14-Trimethylpentadecan-2-one	10408	Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C	268.50	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-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bS)-1,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	101652569	Click to see	666.80	unknown	https://doi.org/10.1016/S0031-9422(97)01006-6
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1,10,11-trihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	14019173	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	650.80	unknown	https://doi.org/10.1016/S0031-9422(97)01006-6
Kajiichigoside F1	14019178	Click to see	650.80	unknown	https://doi.org/10.1016/S0031-9422(97)01006-6
Quercilicoside A	14055729	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	666.80	unknown	https://doi.org/10.1016/S0031-9422(97)01006-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,4aS,6aR,6aS,6bR,8aR,9R,12aR,14bS)-1,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	138113891	Click to see	504.70	unknown	https://doi.org/10.1016/S0031-9422(97)01006-6
1,10,11-Trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	14055735	Click to see	504.70	unknown	https://doi.org/10.1016/S0031-9422(97)01006-6
Achilleol A	5471312	Click to see CC(=CCCC(=CCCC(=CCCC=C(C)CCC1C(=C)CCC(C1(C)C)O)C)C)C	426.70	unknown	via CMAUP database
Betulinic Acid	64971	Click to see	456.70	unknown	https://doi.org/10.4268/CJCMM20161216
Euscaphic Acid	471426	Click to see	488.70	unknown	https://doi.org/10.4268/CJCMM20161216 https://doi.org/10.1016/S0031-9422(97)01006-6
Jacarandic acid	13653335	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O	488.70	unknown	https://doi.org/10.1016/S0031-9422(97)01006-6 https://doi.org/10.1021/NP1007922
Myrianthic acid	182497	Click to see	504.70	unknown	https://doi.org/10.1016/S0031-9422(97)01006-6
Sericic Acid	124214	Click to see	504.70	unknown	https://doi.org/10.1016/S0031-9422(97)01006-6
Tomentosic acid	622032	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1O)C)C(=O)O)C	504.70	unknown	https://doi.org/10.1016/S0031-9422(97)01006-6 https://doi.org/10.1021/NP1007922
Tormentic acid	73193	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1(C)O)C)C(=O)O	488.70	unknown	https://doi.org/10.4268/CJCMM20161216 https://doi.org/10.1016/S0031-9422(97)01006-6 https://doi.org/10.1021/NP1007922
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids
(3R,3aR,5aR,5bS,7aS,10R,11R,11aS,13aS,13bR)-11-hydroxy-1,3-bis(hydroxymethyl)-3,5a,5b,10,11,13b-hexamethyl-4,5,6,7,8,9,10,11a,13,13a-decahydro-3aH-cyclopenta[a]chrysene-7a-carboxylic acid	154497372	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=CC5(C)CO)CO)C)C)C2C1(C)O)C)C(=O)O	486.70	unknown	https://doi.org/10.1016/S0031-9422(97)01006-6
11-hydroxy-1,3-bis(hydroxymethyl)-3,5a,5b,10,11,13b-hexamethyl-4,5,6,7,8,9,10,11a,13,13a-decahydro-3aH-cyclopenta[a]chrysene-7a-carboxylic acid	137796440	Click to see	486.70	unknown	https://doi.org/10.1016/S0031-9422(97)01006-6
Rosamultic acid	102004711	Click to see	486.70	unknown	https://doi.org/10.1016/S0031-9422(97)01006-6
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Dehydrodiconiferyl alcohol	5372367	Click to see	358.40	unknown	https://doi.org/10.1007/BF02980061
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol	5280863	Click to see	286.24	unknown	https://doi.org/10.1248/YAKUSHI1881.49.3_232
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-3-O-glucuronides
6-(2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-4-Oxochromen-3-Yl)Oxy-3,4,5-Trihydroxyoxane-2-Carboxylic Acid	12004528	Click to see	478.40	unknown	https://doi.org/10.1248/CPB.40.2080
Querciturone	5274585	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O	478.40	unknown	https://doi.org/10.1248/CPB.40.2080
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4R,5R,6S)-3-[(2S,3R,4S,5S)-3,4-dihydroxy-5-[(1S)-1-hydroxyethyl]oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxyoxan-2-yl]methyl acetate	163191355	Click to see	652.60	unknown	https://doi.org/10.1248/CPB.40.2080
[(2R,3S,4R,5R,6S)-3-[(2S,3R,4S,5S)-3,4-dihydroxy-5-[(1S)-1-hydroxyethyl]oxolan-2-yl]oxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxyoxan-2-yl]methyl acetate	163011450	Click to see	636.60	unknown	https://doi.org/10.1248/CPB.40.2080
[(2R,3S,4S,5R,6S)-6-[(2R,3R,4S,5S,6R)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	162988364	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)OC5C(C(C(C(O5)COC(=O)C)O)O)O	652.60	unknown	https://doi.org/10.1248/CPB.40.2080
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4R,5S,6R)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	154497037	Click to see	636.60	unknown	https://doi.org/10.1248/CPB.40.2080
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	9809745	Click to see	652.60	unknown	https://doi.org/10.1248/CPB.40.2080
[(2R,3S,4S,5R,6S)-6-[(2S,3R,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl acetate	5319939	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)OC5C(C(C(C(O5)COC(=O)C)O)O)O	636.60	unknown	https://doi.org/10.1248/CPB.40.2080
[3-[3,4-Dihydroxy-5-(1-hydroxyethyl)oxolan-2-yl]oxy-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-4-oxochromen-3-yl]oxy-4,5-dihydroxyoxan-2-yl]methyl acetate	163034973	Click to see CC(C1C(C(C(O1)OC2C(OC(C(C2O)O)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)COC(=O)C)O)O)O	652.60	unknown	https://doi.org/10.1248/CPB.40.2080
[3-[3,4-Dihydroxy-5-(1-hydroxyethyl)oxolan-2-yl]oxy-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-4,5-dihydroxyoxan-2-yl]methyl acetate	163011449	Click to see	636.60	unknown	https://doi.org/10.1248/CPB.40.2080
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-((2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxychromen-4-one	51402807	Click to see	464.40	unknown	https://doi.org/10.1248/CPB.40.2080
3-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4S,5S)-3,4-dihydroxy-5-[(1S)-1-hydroxyethyl]oxolan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	163189675	Click to see CC(C1C(C(C(O1)OC2C(OC(C(C2O)O)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)CO)O)O)O	610.50	unknown	https://doi.org/10.1248/CPB.40.2080
3-[(2S,3R,4R,5S,6R)-5-[(2S,3R,4S,5S)-3,4-dihydroxy-5-[(1S)-1-hydroxyethyl]oxolan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one	162953753	Click to see	594.50	unknown	https://doi.org/10.1248/CPB.40.2080
3-[(2S,3S,4S,5R,6R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	157516859	Click to see	610.50	unknown	https://doi.org/10.1248/CPB.40.2080
3-[(2S,3S,5R)-3,4-dihydroxy-6-methyl-5-[(2S,3R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one	44258929	Click to see	594.50	unknown	via CMAUP database
3-[5-[3,4-Dihydroxy-5-(1-hydroxyethyl)oxolan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one	162896354	Click to see	610.50	unknown	https://doi.org/10.1248/CPB.40.2080
3-[5-[3,4-Dihydroxy-5-(1-hydroxyethyl)oxolan-2-yl]oxy-3,4-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one	162953752	Click to see CC(C1C(C(C(O1)OC2C(OC(C(C2O)O)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC=C(C=C5)O)CO)O)O)O	594.50	unknown	https://doi.org/10.1248/CPB.40.2080
CID 44258969	44258969	Click to see	636.60	unknown	https://doi.org/10.1248/CPB.40.2080
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	https://doi.org/10.1248/CPB.40.2080
Multiflorin B	5319938	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)OC5C(C(C(C(O5)CO)O)O)O	594.50	unknown	https://doi.org/10.1248/CPB.40.2080
Multinoside A	5319943	Click to see	610.50	unknown	https://doi.org/10.1248/CPB.40.2080
Quercetin 3-xyloside	5321278	Click to see	434.30	unknown	https://doi.org/10.1248/CPB.40.2080
Quercetin-3-D-xyloside	5320863	Click to see	434.30	unknown	https://doi.org/10.1248/CPB.40.2080
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	https://doi.org/10.1248/CPB.40.2080
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
5,7,3',4'-Tetrahydroxy-8-methoxyflavone	5316843	Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC(=C(C=C3)O)O)O)O	316.26	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Casuarictin	73644	Click to see	936.60	unknown	https://doi.org/10.1016/0031-9422(92)83451-4

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Rosa multiflora

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