Rubus ellipticus, also known as ainselu or golden Himalayan raspberry, is a thorny fruiting shrub native to China, Nepal, India, Pakistan, Indochina, and the Philippines. It can grow up to 4.5 meters long and produces sweet, detachable fruit that is highly sought after by birds and elephants. The plant has medicinal uses in Tibetan villages and can also be used to make a dye. It is found in open grasslands and pine forests in the Himalayas and can thrive in both shade and full sun. However, it is considered an invasive species in Hawaii and poses a threat to native plants. Control strategies include physically removing the shrub and using herbicides. The fruit has also been used to make wine in Nepal and has been found to be a rich source of antioxidants and other important metabolites.

Synonyms Top

Scientific name	Authority	First published in
Rubus flavus	Buch.-Ham. ex D.Don	Prodr. Fl. Nepal. : 234 (1825)
Rubus ellipticus var. flavus	(Buch.-Ham. ex D.Don) Kuntze	Revis. Gen. Pl. 1: 220 (1891)

Common names Top

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Filter by language:

Language	Common/alternative name
English	yellow himalayan raspberry
Bulgarian	Златна хималайска малина
dty	ऐंसेलु
Japanese	キミノヒマラヤキイチゴ
Nepali	रातो ऐँसेलु
Punjab	آخرا
Russian	Малина эллиптическая
Thai	หนามไข่กุ้ง
Chinese	椭圆悬钩子
Chinese	黄蔗根
Chinese	黄锁梅
Chinese	黄锁梅叶
Chinese	橢圓懸鉤子
Chinese	椭圆懸鉤子

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Rubus ellipticus var. obcordatus	(Franch.) Focke	Sp. Rub. 199. 1911 (1911)

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Africa click to expand
- East Tropical Africa
  - Tanzania
- South Tropical Africa
  - Malawi
  - Mozambique

Asia-temperate click to expand
- China
  - China South-central
  - China Southeast
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - East Himalaya
  - India
  - Nepal
  - Pakistan
  - Sri Lanka
- Indo-China
  - Laos
  - Myanmar
  - Thailand
  - Vietnam
- Malesia
  - Jawa
  - Philippines

Australasia click to expand
- Australia
  - New South Wales
  - Queensland

Pacific click to expand
- North-central Pacific
  - Hawaii

Southern America click to expand
- Caribbean
  - Jamaica
- Western South America
  - Ecuador

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0001002128
UNII	31976457W2
USDA Plants	RUEL3
Tropicos	27800347
KEW	urn:lsid:ipni.org:names:736506-1
The Plant List	rjp-3254
Open Tree Of Life	714542
NCBI Taxonomy	59492
Nature Serve	2.147549
IUCN Red List	49484707
IPNI	736506-1
iNaturalist	168047
IFPNI	F397F3B2-C5FB-DF09-0966-54F041BFE33D
GBIF	2991314
Freebase	/m/0cm89rj
EPPO	RUBEL
EOL	793045
USDA GRIN	32308
Wikipedia	Rubus_ellipticus

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

Vegetation–edaphic correlation and importance value index in himalayan ‘ecotone’ temperate conifer forest using the multivariate technique

Ali F, Zeb M, Amin M, Rajpar MN, Hidayat S, Khan WR

Saudi J Biol Sci

24-Mar-2024

PMCID:	PMC11000104
doi:	10.1016/j.sjbs.2024.103983
PMID:	38590389

Biogenic synthesis of silver nanoparticles using Rubus fruticosus extract and their antibacterial efficacy against Erwinia caratovora and Ralstonia solanacearum phytopathogens

Khan A, Ahmad N, Fazal H, Ali M, Akbar F, Khan I, Tayyab M, Uddin MN, Ahmad N, Abdel-Maksoud MA, Saleh IA, Zomot N, AbdElgawad H, Rauf K, Iqbal B, Teixeira Filho MC, El-Tayeb MA, Jalal A

RSC Adv

14-Feb-2024

PMCID:	PMC10864949
doi:	10.1039/d3ra06723h
PMID:	38362085

Ethnobotanical study of medicinal plants used by the indigenous community of the western region of Mizoram, India

Ralte L, Sailo H, Singh YT

J Ethnobiol Ethnomed

03-Jan-2024

PMCID:	PMC10765666
doi:	10.1186/s13002-023-00642-z
PMID:	38172927

Wild Edible Fruits as a Source of Food and Medicine: A Study among Tribal Communities of Southern Khyber Pakhtunkhwa

Ul Abidin SZ, Khan R, Ahmad M, Cuerrier A, Zafar M, Ullah A, Khan J, Saeed A, Al-Qahtani WH, Kazi M

Plants (Basel)

21-Dec-2023

PMCID:	PMC10780817
doi:	10.3390/plants13010039
PMID:	38202347

Characteristics and phylogenetic analysis of the complete chloroplast genome of Rubus chingii Hu 1925 from the family Rosaceae

Li Y, Qiu Y, Yang M, Yin Y, Li M, Zhang Y

Mitochondrial DNA B Resour

20-Nov-2023

PMCID:	PMC10986437
doi:	10.1080/23802359.2023.2268220
PMID:	38566881

Untapped potential of non-conventional rubus species: bioactivity, nutrition, and livelihood opportunities

Bhatt SC, Naik B, Kumar V, Gupta AK, Kumar S, Preet MS, Sharma N, Rustagi S

Plant Methods

27-Oct-2023

PMCID:	PMC10604922
doi:	10.1186/s13007-023-01094-y
PMID:	37891607

Ethnobotanical study on edible flowers in Xishuangbanna, China

Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C

J Ethnobiol Ethnomed

30-Sep-2023

PMCID:	PMC10542681
doi:	10.1186/s13002-023-00608-1
PMID:	37777741

Ethnobotanical study on medicinal plants used by Bulang people in Yunnan, China

Zhou H, Zhang J, Kirbis BS, Mula Z, Zhang W, Kuang Y, Huang Q, Yin L

J Ethnobiol Ethnomed

07-Sep-2023

PMCID:	PMC10486041
doi:	10.1186/s13002-023-00609-0
PMID:	37679773

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

Yellow Himalayan Raspberry (Rubus ellipticus Sm.): Ethnomedicinal, Nutraceutical, and Pharmacological Aspects

Lamichhane A, Lamichhane G, Devkota HP

Molecules

15-Aug-2023

PMCID:	PMC10458938
doi:	10.3390/molecules28166071
PMID:	37630323

Biosynthesized Silver Nanoparticles Using Alnus nitida Leaf Extract as a Potential Antioxidant and Anticancer Agent

Khuda F, Gul M, Ali Khan Khalil A, Ali S, Ullah N, Shafiq Khan M, Nazir S, Irum Khan S, Mehtap Büyüker S, Almawash S, Shafique M, Shah SA

ACS Omega

14-Aug-2023

PMCID:	PMC10448672
doi:	10.1021/acsomega.3c02928
PMID:	37636925

Ethnoveterinary practises of medicinal plants used for the treatment of different cattle diseases: A case study in East Khasi Hill district of Meghalaya, North East India

Bhat NA, Jeri L, Karmakar D, Mipun P, Bharali P, Sheikh N, Nongkynrih CJ, Kumar Y

Heliyon

13-Jul-2023

PMCID:	PMC10368863
doi:	10.1016/j.heliyon.2023.e18214
PMID:	37501975

Community dynamics of bumblebee across elevation gradients and habitat mosaics in Chitwan Annapurna Landscape, Nepal

Chandra Ghimire K, Pandey A, Roka I, Adhikari JN, Bhusal DR

Heliyon

08-Jun-2023

PMCID:	PMC10361243
doi:	10.1016/j.heliyon.2023.e17076
PMID:	37484416

Phylogeny of the Diploid Species of Rubus (Rosaceae)

Gao XF, Xiong XH, Boufford DE, Gao YD, Xu B, Zhang C

Genes (Basel)

25-May-2023

PMCID:	PMC10298701
doi:	10.3390/genes14061152
PMID:	37372332

Assessing the Spontaneous Spread of Climate-Adapted Woody Plants in an Extensively Maintained Collection Garden

Szabó K, Gergely A, Tóth B, Szilágyi K

Plants (Basel)

15-May-2023

PMCID:	PMC10224429
doi:	10.3390/plants12101989
PMID:	37653906

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
> 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 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/10.1021/NP900237A
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aR,9S,10S,11R,12aR,14bS)-9-formyl-1,10,11-trihydroxy-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	44557482	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C=O)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	664.80	unknown	https://doi.org/10.1021/NP900237A
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,2R,4aS,6aR,6aS,6bR,8aS,9R,10R,11R,12aR,14bR)-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	124893151	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/10.1016/0031-9422(92)83747-M
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1R,3aS,5aR,5bR,7aR,8S,9R,10R,11aR,11bR,13aR,13bR)-9,10-dihydroxy-8-(hydroxymethyl)-5a,5b,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate	44557481	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	650.80	unknown	https://doi.org/10.1021/NP900237A
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (1S,2R,4aS,6aR,6aS,6bR,8aR,10S,11R,12aS)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydro-1H-picene-4a-carboxylate	44557415	Click to see CC1CCC2(CCC3(C(=C2C1C)C=CC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	632.80	unknown	https://doi.org/10.1021/NP900237A
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (2R,4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR)-10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13-dodecahydro-2H-picene-4a-carboxylate	44557352	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2=C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	648.80	unknown	https://doi.org/10.1021/NP900237A
[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] (4aS,6aR,6aS,6bR,8aR,10R,11R,12aR,14bS)-10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-3H-picene-4a-carboxylate	44557353	Click to see CC1=C(C2C3=CCC4C(C3(CCC2(CC1)C(=O)OC5C(C(C(C(O5)CO)O)O)O)C)(CCC6C4(CC(C(C6(C)C)O)O)C)C)C	632.80	unknown	https://doi.org/10.1021/NP900237A
[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/10.1016/0031-9422(92)83747-M
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydro-1H-picene-4a-carboxylate	75068913	Click to see CC1CCC2(CCC3(C(=C2C1C)C=CC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	632.80	unknown	https://doi.org/10.1021/NP900237A
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10,11-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-3H-picene-4a-carboxylate	75068882	Click to see CC1=C(C2C3=CCC4C(C3(CCC2(CC1)C(=O)OC5C(C(C(C(O5)CO)O)O)O)C)(CCC6C4(CC(C(C6(C)C)O)O)C)C)C	632.80	unknown	https://doi.org/10.1021/NP900237A
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12-dodecahydro-1H-picene-4a-carboxylate	75068914	Click to see CC1CCC2(CCC3(C(=C2C1C)C=CC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	648.80	unknown	https://doi.org/10.1021/NP900237A
[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10,11-dihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-3,4,5,6,6a,7,8,8a,10,11,12,13-dodecahydro-2H-picene-4a-carboxylate	73157328	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2=C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	648.80	unknown	https://doi.org/10.1021/NP900237A
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 10,11-dihydroxy-9-(hydroxymethyl)-2,6a,6b,9,12a-pentamethyl-1-methylidene-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	85228830	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1=C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	648.80	unknown	https://doi.org/10.1021/NP900237A
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 9,10-dihydroxy-8-(hydroxymethyl)-5a,5b,8,11a-tetramethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysene-3a-carboxylate	75068944	Click to see CC(=C)C1CCC2(C1C3CCC4C(C3(CC2)C)(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	650.80	unknown	https://doi.org/10.1021/NP900237A
2,3,12-Trihydroxy-4,6a,6b,11,12,14b-hexamethyl-8a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4-carboxylic acid	14707004	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	680.80	unknown	https://doi.org/10.1021/NP900237A
2alpha,3beta,23-Trihydroxy-28-(beta-D-glucopyranosyloxy)urs-12,19-dien-28-one	10508433	Click to see CC1=C(C2C3=CCC4C(C3(CCC2(CC1)C(=O)OC5C(C(C(C(O5)CO)O)O)O)C)(CCC6C4(CC(C(C6(C)CO)O)O)C)C)C	648.80	unknown	https://doi.org/10.1021/NP900237A
kaji-ichigoside F1	14019178	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/10.1016/0031-9422(92)83747-M https://doi.org/10.1021/NP900237A
NCGC00385137-01_C36H58O10_Hexopyranose, 1-O-(3,19,23-trihydroxy-28-oxours-12-en-28-yl)-	14286951	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	650.80	unknown	https://doi.org/10.1021/NP900237A
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/10.1016/0031-9422(92)83747-M
Rosamultin	21122581	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/10.1016/0031-9422(92)83747-M
Rubuside B	44557351	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2=C1C)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	632.80	unknown	https://doi.org/10.1021/NP900237A
Trachelosperoside A-1	21637743	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1(C)O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O	680.80	unknown	https://doi.org/10.1021/NP900237A
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2R,4aS,6aS,6aS,6bR,8aS,10R,11S,12R,12aR,14bS)-1,10,11,12-tetrahydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	46882833	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(C(C(C5(C)C)O)O)O)C)C)C2C1(C)O)C)C(=O)O	504.70	unknown	https://doi.org/10.1021/NP900237A
(2R,3R,4S,4aR,6aR,6bS,8aS,11R,12R,12aS,14aR,14bR)-2,3,12-trihydroxy-4,6a,6b,11,12,14b-hexamethyl-1,2,3,4a,5,6,7,8,9,10,11,12a,14,14a-tetradecahydropicene-4,8a-dicarboxylic acid	21606530	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C(=O)O)O)O)C)C)C2C1(C)O)C)C(=O)O	518.70	unknown	https://doi.org/10.1021/NP900237A
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1,10,11-trihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate	58880815	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	650.80	unknown	https://doi.org/10.1016/0031-9422(92)83747-M
[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl] 1,10,11-trihydroxy-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	14658049	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	666.80	unknown	https://doi.org/10.1016/0031-9422(92)83747-M https://doi.org/10.1021/NP900237A
1,10,11,12-Tetrahydroxy-1,2,6a,6b,9,9,12a-heptamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid	14312995	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(C(C(C(C5(C)C)O)O)O)C)C)C2C1(C)O)C)C(=O)O	504.70	unknown	https://doi.org/10.1021/NP900237A
19Alpha-Hydroxyasiatic Acid	490367	Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1(C)O)C)C(=O)O	504.70	unknown	https://doi.org/10.1021/NP900237A
Arjunetin	21152828	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	650.80	unknown	https://doi.org/10.1016/0031-9422(92)83747-M
Sericoside	76972524	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1O)C)C(=O)OC6C(C(C(C(O6)CO)O)O)O)C	666.80	unknown	https://doi.org/10.1016/0031-9422(92)83747-M https://doi.org/10.1021/NP900237A
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/10.1021/NP900237A
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/10.1021/NP900237A

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Rubus ellipticus

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