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Sapindus rarak

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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID64404df6de292494796147
Scientific name Sapindus rarak
Authority DC.
First published in Prodr. 1: 608 (1824)

Description Top

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Synonyms Top

Scientific name Authority First published in
Sapindus pinnatus Mill. Gard. Dict. ed. 8 : n.º 3 (1768)
Cupania oblongifolia Turcz. Bull. Soc. Imp. Naturalistes Moscou 36(1): 587. 1863
Dittelasma rarak (DC.) Hiern Fl. Brit. India 1: 672 (1875)
Dittelasma rarak Hook.f. Gen. Pl. [Bentham & Hooker f.] 1(1): 396. 1862 [7 Aug 1862]
Sapindus rarak var. velutina C.Y.Wu & T.L.Ming Fl. Yunnanica 1: 261 (1977)

Common names Top

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Language Common/alternative name
Arabic صابونية راراك
ban rerek
Persian فندوق صابونی هندی
Indonesian lerak
Malay lerak
su rerek
Thai มะคำดีควาย
Thai มะซัก
Thai ประคำดีควาย
Chinese 无患子中仁
Chinese 毛瓣无患子
Chinese 毛瓣無患子
Chinese 买马萨

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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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
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • Sri Lanka
    • Indo-China
      • Cambodia
      • Laos
      • Myanmar
      • Thailand
      • Vietnam
    • Malesia
      • Jawa
      • Lesser Sunda Islands
      • Malaya
      • Sumatera

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001135253
UNII TB28UXH983
Tropicos 28601622
KEW urn:lsid:ipni.org:names:784673-1
The Plant List tro-28601622
Open Tree Of Life 5747876
NCBI Taxonomy 1679327
IUCN Red List 150296444
IPNI 784673-1
iNaturalist 1168022
GBIF 7264721
Freebase /m/0gtw7dw
EOL 2889091
USDA GRIN 33089
Wikipedia Sapindus_rarak

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
Enhanced photocatalytic efficiency of porous ZnO coral-like nanoplates for organic dye degradation Hanh NH, Thi Minh Nguyet Q, Van Chinh T, Duong LD, Xuan Tien T, Van Duy L, Hoa ND RSC Adv 03-May-2024
PMCID:PMC11067434
doi:10.1039/d4ra01345j
PMID:38708121
Saponin Extracts Utilization as Dietary Additive in Ruminant Nutrition: A Meta-Analysis of In Vivo Studies Yanza YR, Irawan A, Jayanegara A, Ramadhani F, Respati AN, Fitri A, Hidayat C, Niderkorn V, Cieslak A, Szumacher-Strabel M, Hidayat R, Tanuwiria UH Animals (Basel) 19-Apr-2024
PMCID:PMC11047613
doi:10.3390/ani14081231
PMID:38672383
Synthesis of mesoporous zeolite Y using Sapindus rarak extract as natural organic surfactant for deoxygenation of Reutealis trisperma oil to biofuel Aziz A, Andini Putri BG, Prasetyoko D, Nugraha RE, Holilah H, Bahruji H, Jalil AA, Suprapto S, Hartati H, Asikin-Mijan N RSC Adv 06-Nov-2023
PMCID:PMC10626525
doi:10.1039/d3ra05390c
PMID:37936636
A Review of Effect of Saponins on Ruminal Fermentation, Health and Performance of Ruminants Kholif AE Vet Sci 10-Jul-2023
PMCID:PMC10385484
doi:10.3390/vetsci10070450
PMID:37505855
Comparative efficacy of chemical and botanical pediculicides in Thailand and 4% dimeticone against head louse, Pediculus humanus capitis Yingklang M, Gordon CN, Jaidee PH, Thongpon P, Pinlaor S PLoS One 23-Jun-2023
PMCID:PMC10289457
doi:10.1371/journal.pone.0287616
PMID:37352268
Peumus boldus Used in the Synthesis of ZnO Semiconductor Nanoparticles and Their Evaluation in Organic Contaminants Maro CA, Gálvez HE, Olivas OD, Morales ML, Hernández DV, Flores HG, Carmona VM, Chinchillas MD Materials (Basel) 13-Jun-2023
PMCID:PMC10305226
doi:10.3390/ma16124344
PMID:37374529
Controlled Drug Release from Nanoengineered Polysaccharides Bayer IS Pharmaceutics 28-Apr-2023
PMCID:PMC10221078
doi:10.3390/pharmaceutics15051364
PMID:37242606
Galyean appreciation club review: a holistic perspective of the societal relevance of beef production and its impacts on climate change Tedeschi LO, Beauchemin KA J Anim Sci 16-Jan-2023
PMCID:PMC10022392
doi:10.1093/jas/skad024
PMID:36645233
Taxonomic Novelties of Woody Litter Fungi (Didymosphaeriaceae, Pleosporales) from the Greater Mekong Subregion Ren G, Wanasinghe DN, de Farias AR, Hyde KD, Yasanthika E, Xu J, Balasuriya A, Chethana KW, Gui H Biology (Basel) 13-Nov-2022
PMCID:PMC9687740
doi:10.3390/biology11111660
PMID:36421373
Garlic and Its Bioactive Compounds: Implications for Methane Emissions and Ruminant Nutrition Sari NF, Ray P, Rymer C, Kliem KE, Stergiadis S Animals (Basel) 31-Oct-2022
PMCID:PMC9654579
doi:10.3390/ani12212998
PMID:36359121
A Gedunin-Type Limonoid, 7-Deacetoxy-7-Oxogedunin, from Andiroba (Carapa guianensis Aublet) Reduced Intracellular Triglyceride Content and Enhanced Autophagy in HepG2 Cells Nagatomo A, Ninomiya K, Marumoto S, Sakai C, Watanabe S, Ishikawa W, Manse Y, Kikuchi T, Yamada T, Tanaka R, Muraoka O, Morikawa T Int J Mol Sci 28-Oct-2022
PMCID:PMC9655357
doi:10.3390/ijms232113141
PMID:36361930
Effects of Polymeric Media-Coated Gynosaponin on Microbial Abundance, Rumen Fermentation Properties and Methanogenesis in Xinjiang Goats Li P, Mehmood IM, Chen W Animals (Basel) 10-Aug-2022
PMCID:PMC9404421
doi:10.3390/ani12162035
PMID:36009625
Potential of Hibiscus sabdariffa L. Calyx (Rosella) extract as antibacterial agent in dental disease: Phytochemical and chemical components profiling Suniarti DF, Suwandi T, Putri SA, Kurnia D J Adv Pharm Technol Res 05-Jul-2022
PMCID:PMC9355063
doi:10.4103/japtr.japtr_64_22
PMID:35935698
Development of a DNA barcode library of plants in the Thai Herbal Pharmacopoeia and Monographs for authentication of herbal products Urumarudappa SK, Tungphatthong C, Jaipaew J, Pornputtapong N, Pakdeesattayapong D, Vimolmangkang S, Sukrong S Sci Rep 10-Jun-2022
PMCID:PMC9187672
doi:10.1038/s41598-022-13287-x
PMID:35688884
Local Wisdom and Diversity of Medicinal Plants in Cha Miang Forest in Mae Kampong Village, Chiang Mai, Thailand, and Their Potential for Use as Osteoprotective Products Sukkho T, Khanongnuch C, Lumyong S, Ruangsuriya J, Pattananandecha T, Apichai S, Ogata F, Kawasaki N, Saenjum C Plants (Basel) 01-Jun-2022
PMCID:PMC9182823
doi:10.3390/plants11111492
PMID:35684265

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2R,3R,4S,5R,6R)-2-[(2R,3S,4R,5R,6R)-2-[(2E,6E,11R)-12-[(2R,3R,4R,5R,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,7,11-trimethyldodeca-2,6-dienoxy]-5-hydroxy-6-(hydroxymethyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol 163039566 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(C(O3)C)O)O)O)OCC=C(C)CCC=C(C)CCCC(C)COC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)C)O)O)O)CO)O)O)O)O 1003.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.015
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-2-[(2E,6E,10E)-12-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,7,11-trimethyldodeca-2,6,10-trienoxy]-5-hydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol 101614954 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(C(O3)C)O)O)O)OCC=C(C)CCC=C(C)CCC=C(C)COC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)C)O)O)O)CO)O)O)O)O 1001.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.015
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-5-hydroxy-2-[(2E,6E,10E)-12-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy]oxan-2-yl]oxy-3,7,11-trimethyldodeca-2,6,10-trienoxy]-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol 16749736 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(C(O3)C)O)O)O)OCC=C(C)CCC=C(C)CCC=C(C)COC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)C)O)O)O)OC6C(C(C(C(O6)C)O)O)O)CO)O)O)O)O 1147.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.015
(2S,3R,4S,5S,6R)-2-[(2R,3R,4R,5S,6R)-5-hydroxy-2-[(2E,6E,11R)-12-[(2S,3S,4R,5S,6S)-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3S,4S,5S,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3,7,11-trimethyldodeca-2,6-dienoxy]-6-(hydroxymethyl)-3-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-4-yl]oxy-6-methyloxane-3,4,5-triol 162876396 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC3C(C(C(C(O3)C)O)O)O)OCC=C(C)CCC=C(C)CCCC(C)COC4C(C(C(C(O4)CO)O)OC5C(C(C(C(O5)C)O)O)O)OC6C(C(C(C(O6)C)O)O)O)CO)O)O)O)O 1149.20 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.015
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R,5S)-4,5-diacetyloxy-3-hydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 102316698 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)OC(=O)C)O)O 967.10 unknown https://doi.org/10.1248/CPB.57.198
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4R,5S)-5-acetyloxy-3,4-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 24866792 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)O)O 925.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.015
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4S,5S)-3-acetyloxy-4,5-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 44250225 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)OC(=O)C)O 925.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.015
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4S,5S)-3,5-diacetyloxy-4-hydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 101749122 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)OC(=O)C)O 967.10 unknown https://doi.org/10.1248/CPB.57.198
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aR,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4S,5S)-4-acetyloxy-3,5-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 24866957 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)OC(=O)C)O)O 925.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.015
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aS,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(2S,3R,4S,5S)-3-acetyloxy-4,5-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 162895995 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)OC(=O)C)O 925.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.015
(4aS,6aR,6aS,6bR,8aR,9R,10S,12aS,14bS)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-4-[(3R,4S,5S)-3-acetyloxy-4,5-dihydroxyoxan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 163190089 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)OC(=O)C)O 925.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.015
(4aS,6bR,9S,10S,12aR)-10-[(2S,3R,4S,5S)-3-[(2S,3R,4R,5S,6S)-3,5-dihydroxy-6-methyl-4-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 6325965 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O 883.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.015
https://doi.org/10.1002/PCA.2800030507
10-[3-[4-(3,5-Diacetyloxy-4-hydroxyoxan-2-yl)oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 74338812 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)OC(=O)C)O 967.10 unknown https://doi.org/10.1248/CPB.57.198
10-[3-[4-(4,5-Diacetyloxy-3-hydroxyoxan-2-yl)oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 16196966 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)OC(=O)C)O)O 967.10 unknown https://doi.org/10.1248/CPB.57.198
10-[3-[4-[4-Acetyloxy-3-hydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 74429249 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(O8)CO)OC(=O)C)O)O 925.10 unknown https://doi.org/10.1248/CPB.57.198
10-[5-Acetyloxy-3-[4-(4,5-diacetyloxy-3-hydroxyoxan-2-yl)oxy-3,5-dihydroxy-6-methyloxan-2-yl]oxy-4-hydroxyoxan-2-yl]oxy-9-(hydroxymethyl)-2,2,6a,6b,9,12a-hexamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 74429248 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)OC(=O)C)O)O)OC8C(C(C(CO8)OC(=O)C)OC(=O)C)O)O 1009.20 unknown https://doi.org/10.1248/CPB.57.198
Rarasaponin IV 25208200 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)OC(=O)C)O)O)OC8C(C(C(CO8)OC(=O)C)OC(=O)C)O)O 1009.20 unknown https://doi.org/10.1248/CPB.57.198
Rarasaponin V 25208201 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(O8)CO)OC(=O)C)O)O 925.10 unknown https://doi.org/10.1248/CPB.57.198
Rarasaponin VI 24866959 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)OC(=O)C)O)OC(=O)C)O 967.10 unknown https://doi.org/10.1248/CPB.57.198
Sapindoside B 161686 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C(C3(C)CO)CCC5(C4CC=C6C5(CCC7(C6CC(CC7)(C)C)C(=O)O)C)C)C)O)O)O)OC8C(C(C(CO8)O)O)O)O 883.10 unknown https://doi.org/10.1016/J.PHYTOCHEM.2009.06.015

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