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Internal ID UUID64402a8d0d9c9233737692
Scientific name Jasminum sambac
Authority (L.) Aiton
First published in Hort. Kew. 1: 8 (1789)

Ethnobotanical Use Top

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Important notice
  • 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.

Jasminum sambac (L.) Aiton is used in several Asian traditions as a mild, aromatic infusion prepared from the flowers. In the Philippines, the flowers are steeped in hot water and taken for cough and colds, and the same infusion is employed as an eyewash for sore eyes (Hernandez & Javier, 2012). In Vietnam, folk practice adds a few flowers to hot water to make a calming evening tea considered helpful for sore throat and catarrh (Nguyen & Do, 2000). In parts of Bangladesh, a flower infusion is taken for stomach discomfort and as a febrifuge (Das & Ara, 2013). Alongside teas, poultices of fresh flowers are applied to boils and burns for soothing relief in Vietnam (Nguyen & Do, 2000) and to inflamed wounds in Bangladesh (Das & Ara, 2013). Compresses made from fresh leaves are used for headache and eye irritation in the same regions (Nguyen & Do, 2000; Das & Ara, 2013).

A practical way to prepare a mild flower tea is to float approximately 6–8 fresh flowers in 250 mL of nearly boiling water, cover, and steep for 5–8 minutes. This amount is typical for one serving of a comforting tea used traditionally for cough or sore throat. Because flowers are often consumed as aromatics and flavoring in foods, use only pesticide‑free plant material. Do not exceed 1–2 cups per day unless advised by a qualified practitioner. While the plant is generally recognized as mild, safety data in pregnancy and lactation are insufficient; avoid use during these periods.

The traditional activities are plausibly related to well‑established constituents in J. sambac. The flowers contain benzyl alcohol, linalool, α‑farnesene, indole, and jasmone, terpenoids and aromatic compounds that are known to have antimicrobial, anti‑inflammatory, and spasmolytic properties (Gewali, 2008). These phytochemicals align with reported uses in poultices for skin inflammations and as a tea to calm coughs and mild digestive discomfort.

While authoritative monographs emphasize J. officinale as a medicinal species, recent Asian ethnobotanical surveys confirm that J. sambac continues to be employed in traditional practice, and extracts are under investigation for antimicrobial and anti‑inflammatory activity (Hernandez & Javier, 2012; Nguyen & Do, 2000; Das & Ara, 2013).

General Uses Top

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Common products:
- Jasmine absolute and essential oil (solvent extraction of flowers).
- Jasmine aromachemicals (e.g., linalool, linalyl acetate, benzyl acetate, jasmone derivatives).

Fragrance and cosmetics:
- Jasmine sambac absolute is used in fine fragrances, personal-care bases, and some household products as a high-intensity floral accord.
- Traditional standardization relies on gas-chromatographic profiles that reflect major odorants derived from the flower extract, such as linalool, linalyl acetate, benzyl acetate, and jasmone.

Industrial and craft applications:
- Perfume and flavor houses process large quantities of fresh flowers by solvent extraction to obtain concrete and absolute; the residual concrete wax can be repurposed for perfumery rather than discarded.
- Absolute is employed as a fragrance ingredient in cosmetics and toiletries; use levels in leave-on products are guided by IFRA Standards on fragrance materials.

Food and beverages (non-medicinal):
- Jasmine-scented green tea is produced by scenting cured green tea (Camellia sinensis) with J. sambac flowers; the scenting is a traditional post-manufacturing step to impart aroma, not a medicinal claim.
- The absolute can be used as a natural flavoring in specialty beverages and confectionery at trace levels; these applications depend on the GC profile rather than traditional or medicinal use.

Properties relevant to use:
- The aroma profile of J. sambac is characterized by abundant monoterpenes (linalool, linalyl acetate) and benzyl acetate, with jasmone derivatives contributing characteristic top notes, enabling applications in fragrance formulation where a sweet-jasmine bouquet is required.
- Solvent extraction yields a concrete that is further processed to absolute, a viscous, intensely scented product suitable for compounding and flavoring.

Standards and regulation:
- Jasmine absolute composition and quality are typically assessed by GC analyses aligned with perfumery norms and company specifications.
- Fragrance use is subject to IFRA Standards and, in many jurisdictions, to regulatory frameworks for flavor and fragrance ingredients.

Sustainability and sourcing:
- Production depends on labor-intensive hand-harvesting of freshly opened flowers during morning hours, affecting supply and cost; cultivating J. sambac under controlled agronomic practices helps maintain yield and quality consistency for perfumery and flavor markets.

Synonyms Top

Scientific name Authority First published in
Jasminum odoratum Noronha Verh. Batav. Genootsch. Kunsten 5(4): 10 (1790)
Jasminum pubescens Buch.-Ham. ex Wall. Numer. List : n.º 2880 (1831)
Jasminum quadrifolium Buch.-Ham. ex Wall. Numer. List : n.º 2868 (1831)
Jasminum quinqueflorum var. pubescens G.Don Gen. Hist. 4: 59. 1837
Jasminum quinqueflorum B.Heyne ex Wall. & G.Don Gen. Hist. 4: 59 (1837)
Jasminum sanjurium Buch.-Ham. ex DC. Prodr. 8: 302 (1844)
Jasminum bicorollatum Noronha Verh. Batav. Genootsch. Kunsten 5(4): 10 (1790)
Jasminum blancoi Hassk. Flora 47: 49 (1864)
Jasminum fragrans Salisb. Prodr. Stirp. Chap. Allerton : 12 (1796)
Jasminum heyneanum Wall. Numer. List [Wallich] n. 2871. 1831; G. Don, Gen. Syst. iv. 62.
Mogorium undulatum Lam. Tabl. Encycl. 1: 23 (1791)
Mogorium sambac Lam. Tabl. Encycl. 1: 23 (1791)
Mogorium goaense Zuccagni Cent. Observ. Pl. 1: 2 (1806)
Mogorium gimea Zuccagni Cent. Observ. Pl. 1: 2 (1806)
Nyctanthes goa hort. ex Steud. Nomencl. Bot. , ed. 2, 2: 199 (1841)
Nyctanthes sambac L. Sp. Pl. : 6 (1753)
Nyctanthes undulata L. Sp. Pl. : 6 (1753)
Jasminum sambac var. trifoliatum Vahl Enum. Pl. Obs. 1: 26. 1804
Jasminum sambac var. plenum Stokes Bot. Comm. 16. 1830
Jasminum sambac var. duplex Voigt Hort. Suburb. Calcutt. 550. 1845
Jasminum sambac var. verum DC. Prodr. [A. P. de Candolle] 8: 302. 1844
Jasminum sambac var. gimea (Zuccagni) DC. Prodr. [A. P. de Candolle] 8: 302. 1844
Jasminum sambac var. goaense (Zuccagni) DC. Prodr. [A. P. de Candolle] 8: 302. 1844
Jasminum sambac var. kerianum Kuntze Revis. Gen. Pl. 2: 411. 1891
Jasminum sambac var. nemocalyx Kuntze Revis. Gen. Pl. 2: 411. 1891
Jasminum sambac var. syringifolium Wall. ex Kuntze Revis. Gen. Pl. 2: 411. 1891
Jasminum sambac var. undulatum (L.) Kuntze Revis. Gen. Pl. 2: 411. 1891
Jasminum sambac var. heyneanum C.B.Clarke Fl. Brit. India 3: 592 (1882)
Jasminum undulatum Willd. Sp. Pl., ed. 4 , 1: 36 (1797)
Jasminum zambac Roxb. Hort. Bengal. : 3 (1814)
Jasminum sambac var. trifoliatum (L.) Sims Bot. Mag. 43: t. 1785 1816
Jasminum sambac var. normale Kuntze Revis. Gen. Pl. 2: 411 (1891)
Jasminum trifoliatum Telfair ex G.Don Gen. Hist. 4: 62 (1837)
Jasminum heyneanum Wall. ex G.Don Gen. Hist. 4: 62 (1837)

Common names Top

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Language Common/alternative name
English mogra
English sampaguita
English jasminium sambac (flower)
English arabian jasmine
Arabic فل
Arabic الراسقي
Assamese মল্লিকা ফুল
Azerbaijani sambak jasmini
Azerbaijani Ərəb jasmini
ban melati
Bengali বেলি ফুল
Bengali বেল ফুল
Catalan xamelera
Catalan diamela
cdo mĕ̤k-lê
Czech jasmín sambakový
Czech jasmín arabský
Czech jasmín pravý
German arabischer jasmin
Esperanto araba jasmeno
Persian یاس رازقی
Finnish arabianjasmiini
Gujarati મોગરો
Hindi मोगरा
Hindi वनमल्लिका
Indonesian sampaguita
Indonesian melati putih
Japanese マツリカ
Japanese ピカケ
Japanese 茉莉花
Japanese ムラティ
Kannada ದುಂಡು ಮಲ್ಲಿಗೆ
Kannada ಸೂಜಿಮಲ್ಲಿಗೆ
ks زنٛبَکھ
lzh 茉莉
mad malaṭè
mai बेली फुल
Malayalam ജാസ്മിൻ സംബക്
mnc ᠮᠣᠯᡳ ᡳᠯᡥᠠ
mnw မၠဵု
Marathi मोगरा
Malay melati putih
Malay melur putih
Burmese ကြက်ရုံးပင်
nan ba̍k-nī
Nepali मालती फूल
Dutch melati
Dutch arabische jasmijn
Punjabi ਅਰਬੀਅਨ ਜੈਸਮੀਨ
pam kampuput
Polish jaśmin wielkolistny
Polish jaśminek wielkolistny
Polish dzielżamin wielkolistny
Punjab موتیا
Russian Жасмин самбак
Russian Жасмин арабский
Russian Жасмин индийский
sat ᱢᱟ.ᱞᱤ ᱵᱟᱦᱟ
sd موگرو
Slovenian arabski jasmin
Swedish nyctanthes grandiflora
Swedish mogori undulata
Swedish arabisk jasmin
Tamil கொகுடி
Tamil இருள்நாறி
Thai มะลิลา
Thai มะลิซ้อน
ty pītate
Ukrainian Жасмин самбак
Urdu موتیا
Urdu عربی یاسمین یا سمباک یاسمین
Vietnamese nhài
war sampaguita
war marol
war sampagita
Chinese 茉莉
Chinese 茉莉花露
Chinese 茉莉根
Chinese 茉莉叶
Chinese 茉莉花

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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
      • Bangladesh
      • East Himalaya
      • India
      • Maldives
    • Indo-China
      • Cambodia
    • Malesia
      • Christmas Island
      • Jawa
  • Pacific
    • Northwestern Pacific
      • Caroline Islands
      • Marianas
      • Marshall Islands
    • South-central Pacific
      • Tubuai Islands
    • Southwestern Pacific
      • Gilbert Islands
      • Vanuatu
  • Southern America
    • Caribbean
      • Bahamas
      • Cuba
      • Dominican Republic
      • Haiti
      • Jamaica
      • Leeward Islands
      • Puerto Rico
      • Trinidad-Tobago
      • Windward Islands
    • Central America
      • El Salvador
      • Guatemala
      • Honduras
      • Nicaragua
      • Panamá

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000813548
UNII 1Z81V275I0
Florida Plant Atlas 1441
USDA Plants JASA
Tropicos 23000205
INPN 445866
KEW urn:lsid:ipni.org:names:609755-1
The Plant List kew-351647
Missouri Botanical Garden 282952
PFAF Jasminum sambac
Open Tree Of Life 295476
NCBI Taxonomy 660624
Nature Serve 2.144623
IPNI 609755-1
iNaturalist 135425
GBIF 3172265
Freebase /m/0bmxd8
EPPO IASSA
EOL 579168
USDA GRIN 20676
Wikipedia Jasminum_sambac
CMAUP NPO19860

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
Name Level Submitter Released Coverage Size
GCA_018223645.1 ASM1822364v1 Complete Genome China Agricultural University 2021-05-02 100 482.08 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
Twelve newly assembled jasmine chloroplast genomes: unveiling genomic diversity, phylogenetic relationships and evolutionary patterns among Oleaceae and Jasminum species Xu X, Huang H, Lin S, Zhou L, Yi Y, Lin E, Feng L, Zheng Y, Lin A, Yu L, Shen Y, Henry RJ, Fang J BMC Plant Biol 25-Apr-2024
PMCID:PMC11044428
doi:10.1186/s12870-024-04995-9
PMID:38664619
离子色谱在中草药成分分析中的应用 ZHANG B, TIAN J, CHAI G, HE W, LAN X, HAN X Se Pu 08-Apr-2024
PMCID:PMC10988573
doi:10.3724/SP.J.1123.2023.10009
PMID:38566420
Corythauma ayyari (Insecta, Heteroptera, Tingidae) depends on its host plant to spread in Europe Durand M, Guilbert E PLoS One 26-Mar-2024
PMCID:PMC10965059
doi:10.1371/journal.pone.0295102
PMID:38530816
A Study on the Antibacterial, Antispasmodic, Antipyretic, and Anti-Inflammatory Activity of ZnO Nanoparticles Using Leaf Extract from Jasminum sambac (L. Aiton) Sugitha SK, Venkatesan R, Latha RG, Vetcher AA, Al-Asbahi BA, Kim SC Molecules 25-Mar-2024
PMCID:PMC11012760
doi:10.3390/molecules29071464
PMID:38611744
Variation in the Floral Scent Chemistry of Nymphaea ‘Eldorado’, a Valuable Water Lily, with Different Flowering Stages and Flower Parts Zhou Q, Zhao F, Shi M, Zhang H, Zhu Z Plants (Basel) 24-Mar-2024
PMCID:PMC11013332
doi:10.3390/plants13070939
PMID:38611469
Synthesis of eco-friendly layered double hydroxide and nanoemulsion for jasmine and peppermint oils and their larvicidal activities against Culex pipiens Linnaeus Radwan IT, Khater HF, Mohammed SH, Khalil A, Farghali MA, Mahmoud MG, Selim A, Manaa EA, Bagato N, Baz MM Sci Rep 22-Mar-2024
PMCID:PMC10959945
doi:10.1038/s41598-024-56802-y
PMID:38519561
Evolution of the WRKY Family in Angiosperms and Functional Diversity under Environmental Stress Wu W, Yang J, Yu N, Li R, Yuan Z, Shi J, Chen J Int J Mol Sci 21-Mar-2024
PMCID:PMC10971295
doi:10.3390/ijms25063551
PMID:38542523
Pest categorisation of Pyrrhoderma noxium Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Golic D, Gobbi A, Maiorano A, Pautasso M, Reignault PL EFSA J 19-Mar-2024
PMCID:PMC10949325
doi:10.2903/j.efsa.2024.8667
PMID:38505477
Plant Essential Oils: Dual Action of Toxicity and Egg-Laying Inhibition on Tetranychus urticae (Acari: Tetranychidae), Unveiling Their Potential as Botanical Pesticides Zhu Y, Wu T, Hu Q, He W, Zheng Y, Xie Y, Rao Q, Liu X Plants (Basel) 08-Mar-2024
PMCID:PMC10975855
doi:10.3390/plants13060763
PMID:38592755
Molecular cloning and characterization of farnesyl diphosphate synthase from Rosa rugosa Thunb associated with salinity stress Wei G, Chen Y, Wang J, Feng L PeerJ 29-Feb-2024
PMCID:PMC10909355
doi:10.7717/peerj.16929
PMID:38435988
Physiological and Biochemical Analysis Revealing the Key Factors Influencing 2-Phenylethanol and Benzyl Alcohol Production in Crabapple Flowers Peng Q, Tao W, Yu F, Xiong Q, Nong C, Zhang W, Fan J Plants (Basel) 25-Feb-2024
PMCID:PMC10935373
doi:10.3390/plants13050631
PMID:38475477
The Greater Celandine: Identification and Characterization of an Antimicrobial Peptide from Chelidonium majus Sadecki PW, Laws GD, Morgan JJ, Wommack AJ, Nawrot R, Hicks LM J Nat Prod 17-Feb-2024
PMCID:PMC10959680
doi:10.1021/acs.jnatprod.3c00939
PMID:38366995
Genome-Wide Bioinformatics Analysis of SWEET Gene Family and Expression Verification of Candidate PaSWEET Genes in Potentilla anserina Iqbal J, Zhang W, Fan Y, Dong J, Xie Y, Li R, Yang T, Zhang J, Che D Plants (Basel) 30-Jan-2024
PMCID:PMC10856985
doi:10.3390/plants13030406
PMID:38337939
PMAT: an efficient plant mitogenome assembly toolkit using low-coverage HiFi sequencing data Bi C, Shen F, Han F, Qu Y, Hou J, Xu K, Xu LA, He W, Wu Z, Yin T Hortic Res 26-Jan-2024
PMCID:PMC10925850
doi:10.1093/hr/uhae023
PMID:38469379
Toxicological effects of dimethlybenzeneanthracene in Balb C mice and pharmacological intervention by silk sericin–conjugated silver nanoparticles Mumtaz S, Ali S, Pervaiz A, Awan UA, Nauroze T, Kanwal L, Summer M, Mumtaz S, Mughal TA, Tahir HM Sci Prog 17-Jan-2024
PMCID:PMC10798092
doi:10.1177/00368504231221670
PMID:38232951

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
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown https://doi.org/10.1271/BBB.57.1101
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Methyl Anthranilate 8635 Click to see COC(=O)C1=CC=CC=C1N 151.16 unknown https://doi.org/10.1271/BBB.57.1101
> Benzenoids / Naphthalenes / Naphthoquinones
7-Methyljuglone 26905 Click to see CC1=CC2=C(C(=O)C=CC2=O)C(=C1)O 188.18 unknown via CMAUP database
> Benzenoids / Phenol esters
Eugenyl Acetate 7136 Click to see 206.24 unknown via CMAUP database
> Lignans, neolignans and related compounds / Lignan glycosides
CID 133562314 133562314 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OC45COC(C4COC5C6=CC(=C(C=C6)O)OC)C7=CC(=C(C=C7)O)OC)O)O)O 922.90 unknown https://doi.org/10.1248/CPB.35.5032
methyl (4S,5E,6S)-4-[2-[[(2R,3S,4S,5R,6S)-6-[[(3R,3aS,6S,6aR)-3,6-bis(4-hydroxy-3-methoxyphenyl)-3,4,6,6a-tetrahydro-1H-furo[3,4-c]furan-3a-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 75412002 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(C(C(O3)OC45COC(C4COC5C6=CC(=C(C=C6)O)OC)C7=CC(=C(C=C7)O)OC)O)O)O 922.90 unknown https://doi.org/10.1248/CPB.35.5032
methyl 4-[2-[[6-[[3,6-bis(4-hydroxy-3-methoxyphenyl)-3,4,6,6a-tetrahydro-1H-furo[3,4-c]furan-3a-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methoxy]-2-oxoethyl]-5-ethylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 75111059 Click to see 922.90 unknown https://doi.org/10.1248/CPB.35.5032
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
2-(3,7-Dimethylocta-1,6-dien-3-yloxy)-6-(hydroxymethyl)oxane-3,4,5-triol 14190656 Click to see 316.39 unknown https://doi.org/10.1016/S0031-9422(00)89737-X
D-Linalool 3-glucoside 10087123 Click to see CC(=CCCC(C)(C=C)OC1C(C(C(C(O1)CO)O)O)O)C 316.39 unknown https://doi.org/10.1016/S0031-9422(00)89737-X
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives / Jasmonic acids
(-)-Methyl jasmonate 5281929 Click to see 224.30 unknown via CMAUP database
2-[(1R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl]acetate 25245750 Click to see 209.26 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
5-(4-carboxy-3-methylbut-3-enyl)-1,4a-dimethyl-6-methylidene-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylic acid 541901 Click to see 334.40 unknown https://doi.org/10.1016/S0040-4039(00)82045-6
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
2-(3,7-Dimethylocta-1,6-dien-3-yl)benzoate 22447367 Click to see CC(=CCCC(C)(C=C)C1=CC=CC=C1C(=O)[O-])C 257.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Agarofurans
Celastrine B 5315764 Click to see CC1CC(C(C2(C13CC(CC2OC(=O)C=CC4=CC=CC=C4)C(O3)(C)C)C)OC(=O)C)OC(=O)C=CC5=CC=CC=C5 572.70 unknown https://doi.org/10.21608/BFSA.1984.89861
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(-)-Oleoside 11-methyl ester 131753164 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)O 404.40 unknown https://doi.org/10.1248/CPB.35.5032
2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetic acid 74256813 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)O 404.40 unknown https://doi.org/10.1248/CPB.35.5032
methyl (4S,5E,6S)-4-[2-[[(1S,2R,3R,5R)-5-(1,3-dihydroxypropan-2-yl)-3-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162951245 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(CC3C(CO)CO)OC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)C 977.00 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
methyl (4S,5E,6S)-5-ethylidene-4-(2-methoxy-2-oxoethyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 10788149 Click to see 418.40 unknown https://doi.org/10.1248/CPB.35.5032
methyl (4S,5E,6S)-5-ethylidene-4-[2-[(2S)-2-[(1R,2S,3R,4R)-4-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-2-(hydroxymethyl)-3-methylcyclopentyl]-3-hydroxypropoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162927104 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC(CO)C3CC(C(C3CO)C)OC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC 977.00 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
methyl (4S,5E,6S)-5-ethylidene-4-[2-[[(1R,2R,3R,5R)-5-[(1R)-1-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-2-hydroxyethyl]-3-hydroxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162844251 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(CC3C(CO)OC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)O)C 962.90 unknown https://doi.org/10.1002/JCCS.200000049
methyl (4S,5E,6S)-5-ethylidene-4-[2-[[(1S,2R,3R,5R)-5-[(2R)-1-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-hydroxypropan-2-yl]-3-hydroxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163187710 Click to see 977.00 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
methyl (4S,5E,6S)-5-ethylidene-4-[2-[[(1S,2R,3R,5R)-5-[(2S)-1-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-hydroxypropan-2-yl]-3-hydroxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162978407 Click to see 977.00 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
methyl (4S,5Z,6S)-4-[2-[[(1S,2R,3R,5R)-5-(1,3-dihydroxypropan-2-yl)-3-[2-[(2S,3Z,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 101920415 Click to see 977.00 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
methyl (4S,5Z,6S)-5-ethylidene-4-[2-[(2S)-2-[(1R,2S,3R,4R)-4-[2-[(2S,3Z,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-2-(hydroxymethyl)-3-methylcyclopentyl]-3-hydroxypropoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 101920647 Click to see 977.00 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
methyl (4S,5Z,6S)-5-ethylidene-4-[2-[[(1S,2R,3R,5R)-5-[(2R)-1-[2-[(2S,3Z,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-hydroxypropan-2-yl]-3-hydroxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 101920649 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(CC3C(CO)COC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)O)C 977.00 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
methyl (4S,5Z,6S)-5-ethylidene-4-[2-[[(1S,2R,3R,5R)-5-[(2S)-1-[2-[(2S,3Z,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-hydroxypropan-2-yl]-3-hydroxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 101920648 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(CC3C(CO)COC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)O)C 977.00 unknown https://doi.org/10.1002/JCCS.200000049
https://doi.org/10.1016/0031-9422(94)E0200-C
methyl 4-[2-[[5-(1,3-dihydroxypropan-2-yl)-3-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-5-ethylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 156602789 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(CC3C(CO)CO)OC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)C 977.00 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
methyl 5-ethylidene-4-(2-methoxy-2-oxoethyl)-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 72726525 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OC 418.40 unknown https://doi.org/10.1248/CPB.35.5032
methyl 5-ethylidene-4-[2-[[5-[1-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-2-hydroxyethyl]-3-hydroxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162844250 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(CC3C(CO)OC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)O)C 962.90 unknown https://doi.org/10.1002/JCCS.200000049
methyl 5-ethylidene-4-[2-[[5-[1-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-hydroxypropan-2-yl]-3-hydroxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162978406 Click to see 977.00 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
methyl 5-ethylidene-4-[2-[2-[4-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-2-(hydroxymethyl)-3-methylcyclopentyl]-3-hydroxypropoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162927102 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC(CO)C3CC(C(C3CO)C)OC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC 977.00 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
Oleoside 11-Methyl Ester 10692563 Click to see 404.40 unknown https://doi.org/10.1248/CPB.35.5032
> Organic acids and derivatives / Carboxylic acids and derivatives / Hexacarboxylic acids and derivatives
methyl (4S,5E,6S)-4-[2-[(2S)-2-[(1R,2S,3R,4R)-2-[[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]acetyl]oxymethyl]-4-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-methylcyclopentyl]-3-hydroxypropoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163010672 Click to see 1363.30 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
methyl (4S,5E,6S)-4-[2-[[(1S,2R,3R,5R)-5-[1,3-bis[[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy]propan-2-yl]-3-hydroxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162953336 Click to see 1363.30 unknown https://doi.org/10.1016/S0040-4039(00)82045-6
methyl (4S,5E,6S)-5-ethylidene-4-[2-[[(1R,2R,3R,5R)-3-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-5-[(1R)-1-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-2-hydroxyethyl]-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163036834 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(CC3C(CO)OC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)OC(=O)CC6C(=COC(C6=CC)OC7C(C(C(C(O7)CO)O)O)O)C(=O)OC)C 1349.30 unknown https://doi.org/10.1002/JCCS.200000049
methyl (4S,5E,6S)-5-ethylidene-4-[2-[[(1S,2R,3R,5R)-3-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-5-[(2R)-1-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-hydroxypropan-2-yl]-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162848085 Click to see 1363.30 unknown https://doi.org/10.1016/S0040-4039(00)82045-6
methyl (4S,5E,6S)-5-ethylidene-4-[2-[[(1S,2R,3R,5R)-3-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-5-[(2S)-1-[2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-hydroxypropan-2-yl]-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162848087 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(CC3C(CO)COC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)OC(=O)CC6C(=COC(C6=CC)OC7C(C(C(C(O7)CO)O)O)O)C(=O)OC)C 1363.30 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
https://doi.org/10.1016/S0040-4039(00)82045-6
methyl (4S,5Z,6S)-4-[2-[(2S)-2-[(1R,2S,3R,4R)-2-[[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]acetyl]oxymethyl]-4-[2-[(2S,3Z,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-methylcyclopentyl]-3-hydroxypropoxy]-2-oxoethyl]-5-ethylidene-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 101920646 Click to see 1363.30 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
methyl (4S,5Z,6S)-5-ethylidene-4-[2-[[(1S,2R,3R,5R)-3-[2-[(2S,3Z,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-5-[(2S)-1-[2-[(2S,3Z,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-hydroxypropan-2-yl]-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 101920645 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(CC3C(CO)COC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)OC(=O)CC6C(=COC(C6=CC)OC7C(C(C(C(O7)CO)O)O)O)C(=O)OC)C 1363.30 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
https://doi.org/10.1002/JCCS.200000049
https://doi.org/10.1016/S0040-4039(00)82045-6
methyl 4-[2-[[5-[1,3-bis[[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy]propan-2-yl]-3-hydroxy-2-methylcyclopentyl]methoxy]-2-oxoethyl]-5-ethylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 162953334 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC3C(C(CC3C(COC(=O)CC4C(=COC(C4=CC)OC5C(C(C(C(O5)CO)O)O)O)C(=O)OC)COC(=O)CC6C(=COC(C6=CC)OC7C(C(C(C(O7)CO)O)O)O)C(=O)OC)O)C 1363.30 unknown https://doi.org/10.1016/S0040-4039(00)82045-6
methyl 4-[2-[2-[2-[[2-[3-ethenyl-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3,4-dihydro-2H-pyran-4-yl]acetyl]oxymethyl]-4-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-methylcyclopentyl]-3-hydroxypropoxy]-2-oxoethyl]-5-ethylidene-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163010671 Click to see CC=C1C(C(=COC1OC2C(C(C(C(O2)CO)O)O)O)C(=O)OC)CC(=O)OCC(CO)C3CC(C(C3COC(=O)CC4C(C(OC=C4C(=O)OC)OC5C(C(C(C(O5)CO)O)O)O)C=C)C)OC(=O)CC6C(=COC(C6=CC)OC7C(C(C(C(O7)CO)O)O)O)C(=O)OC 1363.30 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
methyl 5-ethylidene-4-[2-[[3-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-5-[1-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-2-hydroxyethyl]-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 163036833 Click to see 1349.30 unknown https://doi.org/10.1002/JCCS.200000049
methyl 5-ethylidene-4-[2-[[3-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-5-[1-[2-[3-ethylidene-5-methoxycarbonyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetyl]oxy-3-hydroxypropan-2-yl]-2-methylcyclopentyl]methoxy]-2-oxoethyl]-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-3-carboxylate 74191801 Click to see 1363.30 unknown https://doi.org/10.1016/0031-9422(94)E0200-C
https://doi.org/10.1016/S0040-4039(00)82045-6
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1R,7S,8E,9S,14S,15S,17R)-8-ethylidene-15-[(2R)-1-hydroxypropan-2-yl]-17-methyl-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,6,12-trioxatricyclo[12.2.1.04,9]heptadec-4-ene-3,11-dione 137706262 Click to see CC=C1C2CC(=O)OCC3C(C(CC3C(C)CO)OC(=O)C2=COC1OC4C(C(C(C(O4)CO)O)O)O)C 542.60 unknown https://doi.org/10.21608/BFSA.1984.89861
2-Phenylethyl 6-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranoside 11166301 Click to see 430.40 unknown https://doi.org/10.1271/BBB.59.738
2-Phenylethyl beta-primeveroside 131129 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=CC=C3)O)O)O)O)O)O 416.40 unknown https://doi.org/10.1271/BBB.59.738
Benzyl b-primeveroside 14730864 Click to see 402.40 unknown https://doi.org/10.1271/BBB.59.738
Benzyl beta-primeveroside 131248 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC3=CC=CC=C3)O)O)O)O)O)O 402.40 unknown https://doi.org/10.1271/BBB.59.738
Phenethyl rutinoside 14312558 Click to see 430.40 unknown https://doi.org/10.1271/BBB.59.738
Phenylethyl primeveroside 14704521 Click to see 416.40 unknown https://doi.org/10.1271/BBB.59.738
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
trans-Jasmone 1549019 Click to see 164.24 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones / Beta-hydroxy ketones
Diacetone Alcohol 31256 Click to see 116.16 unknown https://doi.org/10.1271/BBB.57.1101
> Phenylpropanoids and polyketides / Aurone flavonoids
Sulfuretin 5281295 Click to see 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
Liquiritigenin 114829 Click to see 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
7-Hydroxyflavone 5281894 Click to see 238.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 4-O-methylated isoflavonoids / 3-hydroxy,4-methoxyisoflavonoids
Calycosin 5280448 Click to see 284.26 unknown via CMAUP database

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