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Rosa rugosa

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID6440408966f21519071191
Scientific name Rosa rugosa
Authority Thunb.
First published in Syst. Veg. , ed. 14: 473 (1784)

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.

Rosa rugosa, the rugged rose, has long been a staple of East Asian folk medicine. In Japan, the dried hips are steeped as a fragrant tea to relieve coughs and colds, a practice documented by Yamada et al., 2015. Korean healers use a decoction of the same fruit to treat sore throats and to boost the immune system, as reported by Kim et al., 2018. In China, the young leaves and stems are macerated in water and applied as a poultice to soothe skin irritations and minor wounds; Li et al., 2017 describe this use in the context of traditional Chinese dermatology. These preparations—infusions, decoctions, macerations, and poultices—highlight the plant’s versatility across three distinct cultural traditions.

A simple, home‑ready recipe is a rosehip tea that captures the essence of the Japanese method. Take 5 g of dried Rosa rugosa hips and add them to 250 ml of freshly boiled water. Let the mixture steep for 10 minutes, then strain. The resulting amber liquid can be enjoyed hot or cold. For safety, limit consumption to no more than 10 g of dried hips per day, as excessive intake may cause mild gastrointestinal upset. Pregnant or nursing individuals should consult a healthcare provider before regular use, although the tea is generally considered safe in moderate amounts.

The therapeutic effects of Rosa rugosa are largely attributed to its rich phytochemical profile. The hips are a powerhouse of vitamin C, providing up to 200 mg per 100 g of dried fruit, which supports immune function and collagen synthesis. Flavonoids such as quercetin and kaempferol, along with phenolic acids and tannins, contribute antioxidant and anti‑inflammatory properties that explain the plant’s traditional use for coughs, colds, and skin healing. These compounds have been isolated and quantified in multiple phytochemical studies, confirming their presence in the species.

Today, Rosa rugosa remains relevant both in traditional settings and in modern markets. Commercial rosehip oil, extracted from the same hips, is widely used in cosmetics for its moisturizing and antioxidant benefits. Ongoing research explores the plant’s potential in nutraceuticals and functional foods, building on the centuries‑old knowledge of its medicinal teas and poultices.

General Uses Top

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Common products:
- Ornamental shrub widely cultivated for landscape horticulture, valued for fragrant flowers, hardiness, and decorative hips.
- Rose hips (fruit) processed into jam, jelly, syrup, and used as flavoring in beverages and liqueurs.
- Essential oil obtained from petals by steam distillation, employed in perfumery.
- Seed oil (rose‑hip oil) extracted by cold‑pressing, used in cosmetic formulations.

Industrial and craft applications:
- Extraction of condensed tannins (proanthocyanidins) from hips and bark; the tannin‑rich material is suitable for vegetable‑tanning of leather.
- Anthocyanin‑rich extracts from hips and petals provide natural brown‑red dyes for wool and silk when applied under alkaline conditions.

Food and beverages (non‑medicinal):
- Ripe hips are harvested and processed into fruit preserves (jam, jelly, syrup) and into flavored beverages and alcoholic liqueurs.

Colorants and tanning:
- The high tannin content (≈15–20 % dry weight) supports use as a natural tanning agent for leather.
- Anthocyanin pigments from the hips yield a brown‑to‑red natural dye on protein fibers.

Fragrance and cosmetics:
- Steam‑distilled petal essential oil (yield 0.2–0.5 % w/w) contains citronellol (≈30 %), geraniol (≈20 %), nerol (≈10 %) and phenylethyl alcohol (≈5 %); it is used in perfume blends and scented cosmetic products.
- Rose‑hip seed oil is rich in linoleic acid (≈55 %) and oleic acid (≈15 %) with a saponification value ≈190–200 mg KOH · g⁻¹ and iodine value ≈100–115 g I₂ · 100 g⁻¹; it functions as an emollient in skin‑care and hair‑care formulations.

Properties relevant to use:
- Fruit: high ascorbic acid (>200 mg · 100 g⁻¹ fresh weight) and condensed tannins (proanthocyanidins) 15–20 % dry weight, both supporting flavor and tannin extraction.
- Petal essential oil: characteristic composition and low yield enabling fragrance applications.
- Seed oil: fatty‑acid profile typical of a non‑drying cosmetic oil, with saponification and iodine values indicating stability.

Standards and regulation:
- Cosmetic use of petal essential oil and seed oil must comply with the EU Cosmetic Regulation (EC No 1223/2009) and the US FDA Cosmetic Ingredient Review (CIR) guidelines.
- Rose hips as a food ingredient are listed as Generally Recognized As Safe (GRAS) in the United States (21 CFR 182.20) and have regulatory status in the European Union as a novel food under Regulation (EU) 2015/2283.

Sustainability and sourcing:
- Rosa rugosa is cultivated in Japan, Korea, China and eastern Russia for ornamental and fruit production; it tolerates saline soils and is employed in coastal dune restoration projects, providing ecological benefits.
- Harvesting of ripe hips for food and industrial use can be performed selectively, allowing rapid regrowth and minimizing impact on wild populations.

Synonyms Top

Scientific name Authority First published in
Rosa regeliana Linden & André Ill. Hort. 18: 11 (1871)
Rosa ferox Lawrance Collect. roses nat. t. 42. 1797
Rosa pubescens Baker in Willmott, Genus Rosa 2: 499. 1914
Rosa ferox Sol. Hortus kewensis ; 1810 262 1811
Rosa kamtchatica Vent. Descr. Pl. Nouv. : t. 67 (1802)
Rosa coruscans Waitz ex Link Enum. Hort. Berol. Alt. 2: 57 (1822)
Rosa andreae Lange Index Seminum (C, Hauniensi) 1874: 23 (1874)
Rosa rugosa var. chamissoniana C.A.Mey. Mém. Acad. Imp. Sci. Saint-Pétersbourg, Sér. 6, Sci. Math., Seconde Pt. Sci. Nat. 6(1): 34. 1840
Rosa kamtschatica Vent. Descr. Pl. Nouv. : t. 67 (1802)
Rosa rugosa var. albiflora Koidz. ; 1909 180 1909
Rosa camschatica Lindl. Ros. Monogr. : 6 (1820)
Rosa maikwai H.Hara J. Jap. Bot. 32: 315 (1957)
Rosa fastuosa K.Koch Dendrologie 1: 239 (1869)
Rosa rugosa f. rosea (Rehder) Rehder Bibliogr. Cult. Trees : 306 (1949)
Rosa rugosa f. alboplena (Rehder) Rehder Bibliography of cultivated trees and shrubs ; 1949 306 1949
Rosa cinnamomea Ledeb. Fl. Ross. 2: 76 (1843)
Rosa rugosa var. albaplena Rehder Cycl. Amer. Hort. 4: 1556 (1902)
Rosa calocarpa (André) E.Willm. Rosa 1: 189 (1911)
Rosa rugosa var. rosea Rehder Cycl. Amer. Hort. 4: 1556 (1902)
Rosa rugosa subsp. coruscans (K.F.Waitz ex Link) Juel, R.E.Fr. & Örtendahl Index Seminum (UPS, Upsaliensi) 1910: 15 (1911)
Rosa rugosa var. ventenatiana C.A.Mey. Zimmtrosen : 35 (1847)
Rosa kamtchatica var. nitens Lindl. Bot. Reg. 10: t. 824 (1824)
Rosa kamtchatica var. ferox Van Geel Sert. Bot. 4 (cl. 13): t. (1832)
Rosa rugosa f. amurensis Debeaux Actes Soc. Linn. Bordeaux 1: 152 (1876)
Rosa rugosa unranked calocarpa André Rev. Hort. (Paris) 63: 129 (1891)
Rosa rugosa var. ferox C.A.Mey. Zimmtrosen : 33 (1847)
Rosa rugosa var. glabriuscula Crép. Bull. Soc. Roy. Bot. Belgique 11: 55 (1872)
Rosa rugosa var. lindleyana C.A.Mey. Zimmtrosen : 34 (1847)
Rosa rugosa var. plena Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 5: 310 (1878)
Rosa rugosa unranked repens-alba Anon. Garden (London, 1871-1927) 74: 279 (1910)
Rosa rugosa var. rubra Rehder Cycl. Amer. Hort. 4: 1556 (1902)
Rosa rugosa var. rubroplena Rehder Stand. Cycl. Hort. 5: 2992 (1916)
Rosa rugosa var. subinermis C.A.Mey. Zimmtrosen : 36 (1847)
Rosa rugosa var. thunbergiana C.A.Mey. Zimmtrosen : 32 (1847)
Rosa rugosa var. typica Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 5: 309 (1878)
Rosa rugosa var. kamtchatica (Vent.) Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 5: 310 (1878)
Rosa rugosa var. nitens (Lindl.) Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 5: 310 (1878)
Rosa rugosa var. regeliana (Linden & André) Wittm. Gartenflora 42: 539 (1893)
Rosa kamtchatica var. ferox (Lawrance) Ser. Prodr. 2: 607 (1825)
Rosa rugosa unranked alba T.S.Ware Garden (London, 1871-1927) 6: 262 (1874)
Rosa rugosa var. alba (T.S.Ware) Rehder Cycl. Amer. Hort. 4: 1556 (1902)
Rosa rugosa f. albaplena (Rehder) Rehder Bibliogr. Cult. Trees : 306 (1949)
Rosa rugosa var. chamissoniana Rehder & E.H.Wilson Pl. Wilson. 2: 321 (1915)
Rosa rugosa var. coruscans (K.F.Waitz ex Link) Koehne Deut. Dendrol. : 298 (1893)
Rosa rugosa f. plena (Regel) Bijh. J. Arnold Arbor. 10: 98 (1929)
Rosa rugosa f. rubroplena (Rehder) Rehder J. Arnold Arbor. 5: 204 (1924)
Rosa rugosa f. alba (T.S.Ware) Rehder Bibliogr. Cult. Trees : 306 (1949)

Common names Top

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Language Common/alternative name
English japanese rose
English rugosa rose
Arabic ورد متين
Arabic ورد قوي
Arabic ورد خشن
Azerbaijani qırışıqmeyvəli itburnu
Belarusian Ружа маршчыністая
Bulgarian Азиатска шипка
Tibetan རྒྱ་སེ་མེ་ཏོག
Czech růže svraskalá
Danish rynket rose
German kartoffel-rose
German kartoffelrose
Esperanto terpomrozo
Esperanto sulka rozo
Esperanto kamtĉatka rozo
Estonian kurdlehine kibuvits
Persian رز روگوزا
Finnish kurtturuusu
French rosier rugueux
frr irpelruus
Hungarian japán rózsa
Japanese 浜梨
Japanese 浜茄子
Japanese 玫瑰
Japanese ハマナス
Korean 해당화
Latvian krokainā roze
lzh 玫瑰
Malayalam റോസ റുഗോസ
Norwegian Bokmål rynkerose
Dutch rimpelroos
Polish róża pomarszczona
Punjab رگوسا گلاب
Russian Шиповник морщинистый
Slovenian japonski šipek
Serbian Наборана ружа
Swedish vresros
Thai กุหลาบญี่ปุ่น
za vameizgveiq
Chinese 刺梨叶
Chinese 刺梨
Chinese 玫瑰
Chinese 刺梨根
Chinese 玫瑰（玫瑰花）
Chinese 玫瑰根
Chinese 玫瑰花
Chinese 玫瑰露
Chinese 粗皮蛙
Chinese 滨梨
Chinese 滨茄子

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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No variety added yet.

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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Alternate between 20°C and 4°C for 3 months each, across multiple cycles, acknowledging that germination may be prolonged.
Pulpy Coat Inhibits Germination: Seeds with a pulpy or fleshy outer coat need to have this material removed by soaking and rinsing in clean water daily for about a week. The inhibitory substances in the pulp are thus washed away, and germination rates improve.
soak in hot water for 24 hours to scarify

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Kamchatka
      • Primorye
      • Sakhalin
    • Siberia
      • Altay
  • Europe
    • Eastern Europe
      • Baltic States
      • Belarus
      • Central European Russia
      • East European Russia
      • North European Russia
      • Northwest European Russia
      • South European Russia
      • Ukraine
    • Middle Europe
      • Belgium
      • Czechoslovakia
      • Germany
      • Hungary
      • Netherlands
      • Poland
      • Switzerland
    • Northern Europe
      • Denmark
      • Finland
      • Great Britain
      • Ireland
      • Norway
      • Sweden
    • Southeastern Europe
      • Bulgaria
      • Italy
      • Romania
      • Yugoslavia
    • Southwestern Europe
      • France
  • Northern America
    • Eastern Canada
      • New Brunswick
      • Newfoundland
      • Nova Scotia
      • Ontario
      • Prince Edward Island
      • Québec
    • North-central U.S.A.
      • Illinois
      • Minnesota
      • Missouri
      • Wisconsin
    • Northeastern U.S.A.
      • Connecticut
      • Maine
      • Massachusetts
      • Michigan
      • New Hampshire
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
      • Rhode Island
      • Vermont
      • West Virginia
    • Northwestern U.S.A.
      • Washington
    • Southeastern U.S.A.
      • Delaware
      • Kentucky
      • Maryland
      • Virginia
    • Southwestern U.S.A.
      • Utah
    • Subarctic America
      • Alaska
    • Western Canada
      • British Columbia

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001017421
UNII UC8FI8PY9F
Cornell Woody Plants 225
Canadensys 8911
USDA Plants RORU
UConn 441
Tropicos 27800162
INPN 118477
Flora of Italy 8600
KEW urn:lsid:ipni.org:names:927373-1
The Plant List rjp-8096
Plantarium 32402
Missouri Botanical Garden 286364
Open Tree Of Life 1054790
Observations.org 7335
NCBI Taxonomy 74645
NBN Atlas NHMSYS0000462477
Nature Serve 2.146729
IPNI 927373-1
iNaturalist 83653
GBIF 3003979
Freebase /m/01sh9p
WisFlora 4845
EPPO ROSRG
EOL 631307
Elurikkus 6931
Calflora (Californian flora) 9406
USDA GRIN 32156
Wikipedia Rosa_rugosa
CMAUP NPO1524

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
GCF_958449725.1 drRosRugo1.1 Chromosome WELLCOME SANGER INSTITUTE 2023-07-18 54 397.80 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
Commodity risk assessment of Tilia cordata and Tilia platyphyllos plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 03-May-2024
PMCID:PMC11066761
doi:10.2903/j.efsa.2024.8803
PMID:38707495
Rosarugosides A and D from Rosa rugosa Flower Buds: Their Potential Anti-Skin-Aging Effects in TNF-α-Induced Human Dermal Fibroblasts Kim KS, Son SR, Choi YJ, Kim Y, Ahn SY, Jang DS, Lee S Plants (Basel) 02-May-2024
PMCID:PMC11085274
doi:10.3390/plants13091266
PMID:38732481
Genome-Wide Analysis of MYB Gene Family in Chrysanthemum ×morifolium Provides Insights into Flower Color Regulation Wang B, Wen X, Fu B, Wei Y, Song X, Li S, Wang L, Wu Y, Hong Y, Dai S Plants (Basel) 28-Apr-2024
PMCID:PMC11085527
doi:10.3390/plants13091221
PMID:38732436
Natural products in atherosclerosis therapy by targeting PPARs: a review focusing on lipid metabolism and inflammation Zhang Y, Zhang XY, Shi SR, Ma CN, Lin YP, Song WG, Guo SD Front Cardiovasc Med 18-Apr-2024
PMCID:PMC11064802
doi:10.3389/fcvm.2024.1372055
PMID:38699583
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
Phylogeny of genera in Maleae (Rosaceae) based on chloroplast genome analysis Sun J, Zhao D, Qiao P, Wang Y, Wu P, Wang K, Guo L, Huang L, Zhou S Front Plant Sci 26-Mar-2024
PMCID:PMC11002139
doi:10.3389/fpls.2024.1367645
PMID:38595768
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
Argentinian Rose Petals as a Source of Antioxidant and Antimicrobial Compounds Baibuch SY, Schelegueda LI, Bonifazi E, Cabrera G, Mondragón Portocarrero AC, Franco CM, Malec LS, Campos CA Foods 22-Mar-2024
PMCID:PMC11012100
doi:10.3390/foods13070977
PMID:38611283
Identification of the lateral organ boundary domain gene family and its preservation by exogenous salicylic acid in Cerasus humilis Jiang S, Ren W, Ma L, Wu J, Zhang X, Wu W, Kong L, He J, Ma W, Liu X Physiol Mol Biol Plants 20-Mar-2024
PMCID:PMC11018595
doi:10.1007/s12298-024-01438-5
PMID:38633270
FvMYB108, a MYB Gene from Fragaria vesca, Positively Regulates Cold and Salt Tolerance of Arabidopsis Song P, Yang R, Jiao K, Guo B, Zhang L, Li Y, Zhang K, Zhou S, Wu X, Li X Int J Mol Sci 17-Mar-2024
PMCID:PMC10970457
doi:10.3390/ijms25063405
PMID:38542376
Revealing a Novel Potential Pest of Plum Trees in the Caucasus: A Species Resembling the European Leaf-Mining Stigmella plagicolella, Nepticulidae Stonis JR, Diškus A, Orlovskytė S, Dobrynina V Insects 15-Mar-2024
PMCID:PMC10971272
doi:10.3390/insects15030198
PMID:38535393
Chromosome‐scale genome assembly of Poa trivialis and population genomics reveal widespread gene flow in a cool‐season grass seed production system Brunharo CA, Benson CW, Huff DR, Lasky JR Plant Direct 13-Mar-2024
PMCID:PMC10934236
doi:10.1002/pld3.575
PMID:38481436
Commodity risk assessment of plants of 12 selected Prunus species from Moldova Bragard C, Baptista P, Chatzivassiliou E, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Zappalà L, Di Serio F, Gómez P, Urek G, Lucchi A, Carluccio AV, Chiumenti M, Fanelli E, Bernardo U, Marzachì C, Bubici G, Dimitropoulou S, Correia CD, Mosbach‐Schulz O, Kaczmarek A, Yuen J EFSA J 12-Mar-2024
PMCID:PMC10928764
doi:10.2903/j.efsa.2024.8647
PMID:38476321
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
Commodity risk assessment of Ligustrum ovalifolium and Ligustrum vulgare plants from the UK Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Civera AV, Yuen J, Zappalà L, Battisti A, Mas H, Rigling D, Faccoli M, Mikulová A, Mosbach‐Schulz O, Stergulc F, Streissl F, Gonthier P EFSA J 07-Mar-2024
PMCID:PMC10918603
doi:10.2903/j.efsa.2024.8648
PMID:38455154

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
2-Phenylethyl Acetate 7654 Click to see 164.20 unknown via CMAUP database
Phenylethyl Alcohol 6054 Click to see C1=CC=C(C=C1)CCO 122.16 unknown via CMAUP database
> 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
2,5-Dihydroxybenzoic acid 3469 Click to see 154.12 unknown via CMAUP database
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
Protocatechuic Acid 72 Click to see 154.12 unknown https://doi.org/10.1007/S10600-006-0267-3
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid 10742 Click to see 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Gallic acids
Gallic Acid 370 Click to see 170.12 unknown https://doi.org/10.1007/S10600-006-0267-3
https://doi.org/10.1139/O04-100
https://doi.org/10.1016/J.LFS.2004.12.024
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / O-methoxybenzoic acids and derivatives
Ethyl 2-Methoxybenzoate 81784 Click to see CCOC(=O)C1=CC=CC=C1OC 180.20 unknown via CMAUP database
Methyl 2-Methoxybenzoate 61151 Click to see 166.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Salicylic acid and derivatives / Salicylic acids
Salicylic Acid 338 Click to see 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyloxycarbonyls
Benzyl acetate 8785 Click to see 150.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
1,4-Dimethoxybenzene 9016 Click to see 138.16 unknown via CMAUP database
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
2,3-dimethoxy-4-[(E)-3-(7-methoxy-1,3-benzodioxol-5-yl)prop-2-enyl]phenol 72701898 Click to see COC1=CC(=CC2=C1OCO2)C=CCC3=C(C(=C(C=C3)O)OC)OC 344.40 unknown https://doi.org/10.1021/NP4004068
4-[(E)-3-(1,3-benzodioxol-5-yl)prop-2-enyl]-2,3-dimethoxyphenol 72701897 Click to see COC1=C(C=CC(=C1OC)O)CC=CC2=CC3=C(C=C2)OCO3 314.30 unknown https://doi.org/10.1021/NP4004068
Eugenol 3314 Click to see 164.20 unknown https://doi.org/10.1016/J.FCT.2012.12.050
> Hydrocarbons / Saturated hydrocarbons
CID 172416 172416 Click to see CCCCCCCCCCCCCCC[CH2] 225.43 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hexadecane 11006 Click to see CCCCCCCCCCCCCCCC 226.44 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(4E)-3,5,5-trimethyl-4-[3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutylidene]cyclohex-2-en-1-one 76335966 Click to see CC1=CC(=O)CC(C1=CCC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 370.40 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
(4Z)-3,5,5-trimethyl-4-[3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutylidene]cyclohex-2-en-1-one 76310564 Click to see 370.40 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
(6R,9R)-3-Oxo-Alpha-Ionol-Beta-D-Glucopyranoside 9820702 Click to see 370.40 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
3Eec4Q65S4 21630888 Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 370.40 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohol esters
Citronellol acetate, (S)- 6999975 Click to see 198.30 unknown via CMAUP database
Citronellyl acetate 9017 Click to see CC(CCC=C(C)C)CCOC(=O)C 198.30 unknown https://doi.org/10.1002/FFJ.2730050406
Geranyl acetate 1549026 Click to see CC(=CCCC(=CCOC(=O)C)C)C 196.29 unknown via CMAUP database
Hexacosyl 3-(4-hydroxyphenyl)propanoate 163033718 Click to see 530.90 unknown https://doi.org/10.1016/0031-9422(92)83497-M
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
3,7-Dimethyl-2,6-octadienol 4458 Click to see 154.25 unknown https://doi.org/10.1016/J.PLANTSCI.2012.12.013
beta-CITRONELLOL, (R)- 101977 Click to see 156.26 unknown via CMAUP database
beta-Ocimene, (3Z)- 5320250 Click to see 136.23 unknown via CMAUP database
Citronellol 8842 Click to see 156.26 unknown https://doi.org/10.1002/FFJ.2730050406
Geraniol 637566 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1002/FFJ.2730050406
Linalool 6549 Click to see 154.25 unknown https://doi.org/10.1080/10412905.1995.9698565
Nerol 643820 Click to see CC(=CCCC(=CCO)C)C 154.25 unknown https://doi.org/10.1080/10412905.1995.9698565
https://doi.org/10.1002/FFJ.2730050406
https://doi.org/10.1016/J.PLANTSCI.2012.12.013
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
p-Menth-1-ene 21671 Click to see 138.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
(4R)-4-methyl-4-(4-methyl-3-oxopentyl)-5-oxocycloheptene-1-carbaldehyde 162989011 Click to see 250.33 unknown https://doi.org/10.1016/S0031-9422(00)95000-3
4-Methyl-4-(4-methyl-3-oxopentyl)-5-oxocycloheptene-1-carbaldehyde 162989010 Click to see CC(C)C(=O)CCC1(CC=C(CCC1=O)C=O)C 250.33 unknown https://doi.org/10.1016/S0031-9422(00)95000-3
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Epi-alpha-bisabolol 1201551 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/0031-9422(92)80384-Q
(1R,3aR,5S,8S,8aR)-5,8,8a-trihydroxy-3a-methyl-1-propan-2-yl-1,2,3,4,5,8-hexahydroazulene-6-carboxylic acid 101606460 Click to see 284.35 unknown https://doi.org/10.1271/BBB1961.55.1049
(1R,3aR,8aR)-3a,6-dimethyl-1-prop-1-en-2-yl-2,3,4,7,8,8a-hexahydroazulen-1-ol 9991038 Click to see CC1=CCC2(CCC(C2CC1)(C(=C)C)O)C 220.35 unknown https://doi.org/10.1016/0031-9422(92)80384-Q
(1R,3aR)-3a-methyl-1-propan-2-yl-2,3,4,7-tetrahydro-1H-azulene-6-carbaldehyde 14543558 Click to see 218.33 unknown https://doi.org/10.1016/0031-9422(90)80035-F
https://doi.org/10.1016/S0031-9422(00)95000-3
https://doi.org/10.1016/0031-9422(92)80013-5
(1R,3aR)-3a-methyl-1-propan-2-yl-2,3,4,7-tetrahydro-1H-azulene-6-carboxylic acid 14543560 Click to see 234.33 unknown https://doi.org/10.1016/0031-9422(90)80035-F
https://doi.org/10.1016/0031-9422(92)80013-5
(1R,7R,10R)-7-methyl-10-propan-2-yl-11-oxatricyclo[5.4.0.01,10]undec-4-ene-4-carbaldehyde 101617541 Click to see CC(C)C12CCC3(C1(O2)CCC(=CC3)C=O)C 234.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
(1R,7S,10R)-7-methyl-10-propan-2-yl-11-oxatricyclo[5.4.0.01,10]undec-4-ene-4-carbaldehyde 162854128 Click to see 234.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
(1R,7S,10R)-7-methyl-10-propan-2-yl-11-oxatricyclo[5.4.0.01,10]undeca-3,5-diene-4-carbaldehyde 163048369 Click to see CC(C)C12CCC3(C1(O2)CC=C(C=C3)C=O)C 232.32 unknown https://doi.org/10.1016/0031-9422(91)80099-M
(1S,7R,10S)-7-methyl-10-propan-2-yl-11-oxatricyclo[5.4.0.01,10]undec-4-ene-4-carbaldehyde 101617540 Click to see 234.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
(1S,7R,10S)-7-methyl-10-propan-2-yl-11-oxatricyclo[5.4.0.01,10]undeca-3,5-diene-4-carbaldehyde 101617542 Click to see CC(C)C12CCC3(C1(O2)CC=C(C=C3)C=O)C 232.32 unknown https://doi.org/10.1016/0031-9422(91)80099-M
(3aR,8aR)-3-hydroxy-8a-methyl-3-prop-1-en-2-yl-1,2,3a,4,5,8-hexahydroazulene-6-carbaldehyde 15109135 Click to see 234.33 unknown via CMAUP database
(3R,3aS,8aS)-3-hydroxy-8a-methyl-3-prop-1-en-2-yl-1,2,3a,4,5,8-hexahydroazulene-6-carbaldehyde 163073065 Click to see 234.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
(3S,3aR,8aS)-3-(2-hydroxypropan-2-yl)-8a-methyl-2,3,3a,4,5,8-hexahydro-1H-azulene-6-carbaldehyde 162858911 Click to see CC12CCC(C1CCC(=CC2)C=O)C(C)(C)O 236.35 unknown https://doi.org/10.1016/0031-9422(91)80099-M
(3S,3aR,8aS)-8a-methyl-3-prop-1-en-2-yl-2,3,3a,4,5,8-hexahydro-1H-azulene-6-carbaldehyde 162981325 Click to see CC(=C)C1CCC2(C1CCC(=CC2)C=O)C 218.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
(3S,3aR,8aS)-8a-methyl-3-prop-1-en-2-yl-2,3,3a,4,5,8-hexahydro-1H-azulene-6-carboxylic acid 163187122 Click to see 234.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
(3S,3aS,8aR)-3-(2-hydroxypropan-2-yl)-8a-methyl-2,3,3a,4,5,8-hexahydro-1H-azulene-6-carbaldehyde 15109132 Click to see 236.35 unknown via CMAUP database
(3S,3aS,8aR)-8a-methyl-3-prop-1-en-2-yl-2,3,3a,4,5,8-hexahydro-1H-azulene-6-carboxylic acid 15109130 Click to see CC(=C)C1CCC2(C1CCC(=CC2)C(=O)O)C 234.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
https://doi.org/10.1016/0031-9422(92)80013-5
(8a-methyl-3-prop-1-en-2-yl-2,3,3a,4,5,8-hexahydro-1H-azulen-6-yl)methanol 162843182 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)95000-3
(8aR)-8a-methyl-3-propan-2-yl-2,4,5,8-tetrahydro-1H-azulene-6-carbaldehyde 15109127 Click to see 218.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
(8aS)-8a-methyl-3-prop-1-en-2-yl-2,4,5,8-tetrahydro-1H-azulene-6-carbaldehyde 162957848 Click to see 216.32 unknown https://doi.org/10.1016/0031-9422(91)80099-M
(8aS)-8a-methyl-3-prop-1-en-2-yl-2,4,5,8-tetrahydro-1H-azulene-6-carboxylic acid 162984424 Click to see 232.32 unknown https://doi.org/10.1016/0031-9422(91)80099-M
(8aS)-8a-methyl-3-propan-2-yl-2,4,5,8-tetrahydro-1H-azulene-6-carbaldehyde 162947577 Click to see CC(C)C1=C2CCC(=CCC2(CC1)C)C=O 218.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
[(3S,3aS,8aR)-8a-methyl-3-prop-1-en-2-yl-2,3,3a,4,5,8-hexahydro-1H-azulen-6-yl]methanol 162843183 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)95000-3
3-(2-hydroxypropan-2-yl)-8a-methyl-2,3,3a,4,5,8-hexahydro-1H-azulene-6-carbaldehyde 162858910 Click to see CC12CCC(C1CCC(=CC2)C=O)C(C)(C)O 236.35 unknown https://doi.org/10.1016/0031-9422(91)80099-M
3-Hydroxy-8a-methyl-3-prop-1-en-2-yl-1,2,3a,4,5,8-hexahydroazulene-6-carbaldehyde 163073064 Click to see 234.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
3a-methyl-1-propan-2-yl-2,3,4,7-tetrahydro-1H-azulene-6-carbaldehyde 14543557 Click to see 218.33 unknown https://doi.org/10.1016/0031-9422(90)80035-F
https://doi.org/10.1016/S0031-9422(00)95000-3
https://doi.org/10.1016/0031-9422(92)80013-5
3a-methyl-1-propan-2-yl-2,3,4,7-tetrahydro-1H-azulene-6-carboxylic acid 14543559 Click to see 234.33 unknown https://doi.org/10.1016/0031-9422(90)80035-F
https://doi.org/10.1016/0031-9422(92)80013-5
3a,6-Dimethyl-1-prop-1-en-2-yl-2,3,4,7,8,8a-hexahydroazulen-1-ol 85085646 Click to see 220.35 unknown https://doi.org/10.1016/0031-9422(92)80384-Q
4-[(E)-6-hydroperoxy-3-hydroxy-6-methylhept-4-en-2-yl]cyclohexene-1-carboxylic acid 101608764 Click to see 284.35 unknown https://doi.org/10.1515/ZNC-1991-5-605
5,8,8a-Trihydroxy-3a-methyl-1-propan-2-yl-1,2,3,4,5,8-hexahydroazulene-6-carboxylic acid 162896855 Click to see CC(C)C1CCC2(C1(C(C=C(C(C2)O)C(=O)O)O)O)C 284.35 unknown https://doi.org/10.1271/BBB1961.55.1049
7-Methyl-10-propan-2-yl-11-oxatricyclo[5.4.0.01,10]undec-4-ene-4-carbaldehyde 162854127 Click to see CC(C)C12CCC3(C1(O2)CCC(=CC3)C=O)C 234.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
7-Methyl-10-propan-2-yl-11-oxatricyclo[5.4.0.01,10]undeca-3,5-diene-4-carbaldehyde 163048368 Click to see 232.32 unknown https://doi.org/10.1016/0031-9422(91)80099-M
8a-methyl-3-prop-1-en-2-yl-2,3,3a,4,5,8-hexahydro-1H-azulene-6-carbaldehyde 73880777 Click to see 218.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
8a-methyl-3-prop-1-en-2-yl-2,3,3a,4,5,8-hexahydro-1H-azulene-6-carboxylic acid 162842999 Click to see CC(=C)C1CCC2(C1CCC(=CC2)C(=O)O)C 234.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
https://doi.org/10.1016/0031-9422(92)80013-5
8a-methyl-3-prop-1-en-2-yl-2,4,5,8-tetrahydro-1H-azulene-6-carbaldehyde 162957847 Click to see CC(=C)C1=C2CCC(=CCC2(CC1)C)C=O 216.32 unknown https://doi.org/10.1016/0031-9422(91)80099-M
8a-methyl-3-prop-1-en-2-yl-2,4,5,8-tetrahydro-1H-azulene-6-carboxylic acid 162984423 Click to see 232.32 unknown https://doi.org/10.1016/0031-9422(91)80099-M
8a-methyl-3-propan-2-yl-2,4,5,8-tetrahydro-1H-azulene-6-carbaldehyde 162947576 Click to see CC(C)C1=C2CCC(=CCC2(CC1)C)C=O 218.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
alpha-Bisabolol 10586 Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O 222.37 unknown https://doi.org/10.1016/0031-9422(92)80384-Q
Bisaborosaol A 195819 Click to see CC(=CCCC(C)(C1CCC(=CC1)C(=O)OC)O)C 266.38 unknown https://doi.org/10.1515/ZNC-1991-5-604
Daucene 177773 Click to see CC1=CCC2(CCC(=C2CC1)C(C)C)C 204.35 unknown https://doi.org/10.1515/ZNC-1992-0606
ethyl (1R,3aR,5R)-5-hydroxy-3a-methyl-1-propan-2-yl-2,3,4,5-tetrahydro-1H-azulene-6-carboxylate 10084964 Click to see CCOC(=O)C1=CC=C2C(CCC2(CC1O)C)C(C)C 278.40 unknown https://doi.org/10.1016/0031-9422(92)80384-Q
ethyl 5-hydroxy-3a-methyl-1-propan-2-yl-2,3,4,5-tetrahydro-1H-azulene-6-carboxylate 162987972 Click to see 278.40 unknown https://doi.org/10.1016/0031-9422(92)80384-Q
Isodaucene 73809332 Click to see 204.35 unknown https://doi.org/10.1515/ZNC-1992-0606
methyl (4R)-4-[(2S,5R)-2,5-dihydroxy-6-methylhept-6-en-2-yl]cyclohexene-1-carboxylate 162913173 Click to see CC(=C)C(CCC(C)(C1CCC(=CC1)C(=O)OC)O)O 282.37 unknown https://doi.org/10.1016/S0031-9422(00)95000-3
methyl (4R)-4-[(E,2S)-2,6-dihydroxy-6-methylhept-4-en-2-yl]cyclohexene-1-carboxylate 162868516 Click to see 282.37 unknown https://doi.org/10.1016/S0031-9422(00)95000-3
Methyl 4-(2,5-dihydroxy-6-methylhept-6-en-2-yl)cyclohexene-1-carboxylate 162913172 Click to see 282.37 unknown https://doi.org/10.1016/S0031-9422(00)95000-3
Methyl 4-(2,6-dihydroxy-6-methylhept-4-en-2-yl)cyclohexene-1-carboxylate 162868515 Click to see 282.37 unknown https://doi.org/10.1016/S0031-9422(00)95000-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
[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/10.1248/BPB.28.101
Kajiichigoside F1 14019178 Click to see 650.80 unknown https://doi.org/10.1248/BPB.28.101
Rosamultin 21122581 Click to see 650.80 unknown https://doi.org/10.1248/BPB.28.101
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
8-Geranyloxypsoralen 5317564 Click to see 338.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
Rabdosin B 14109027 Click to see 448.50 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Carotenes
Beta-Carotene 5280489 Click to see 536.90 unknown https://doi.org/10.1111/J.1365-2621.1989.TB04709.X
Zeta-Carotene 6440490 Click to see 540.90 unknown https://doi.org/10.1111/J.1365-2621.1989.TB04709.X
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
(3S,6S)-6-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1S,4S)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol 51346155 Click to see 600.90 unknown https://doi.org/10.1111/J.1365-2621.1989.TB04709.X
Cryptoxanthin 5281235 Click to see CC1=C(C(CCC1)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC2=C(CC(CC2(C)C)O)C)C)C 552.90 unknown https://doi.org/10.1111/J.1365-2621.1989.TB04709.X
Rubixanthin 5281252 Click to see 552.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
(1R,2R,4aS,6aS,6bR,10R,12aR)-1,10-dihydroxy-1,2,6a,6b,9,9,12a-heptamethyl-11-oxo-3,4,5,6,6a,7,8,8a,10,12,13,14b-dodecahydro-2H-picene-4a-carboxylic acid 470711 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(=O)C(C5(C)C)O)C)C)C2C1(C)O)C)C(=O)O 486.70 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
2-Oxopomolic Acid 44593379 Click to see 486.70 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
Betulinic Acid 64971 Click to see 456.70 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
Euscaphic Acid 471426 Click to see 488.70 unknown https://doi.org/10.1248/BPB.28.101
Fupenzic Acid 12045007 Click to see 484.70 unknown via CMAUP database
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/10.1248/BPB.28.101
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/10.1248/BPB.28.101
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-beta-hydroxysteroids
3Beta,15Alpha-Dihydroxymansumbinol 76317773 Click to see 332.50 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids / 3-carboxy steroids
(3aS,5aR,5bS,7aR,11S,11aS,13aS,13bS)-1-formyl-11-hydroxy-3,3,5a,5b,10,10,13b-heptamethyl-4,5,6,7,8,9,11,11a,13,13a-decahydro-3aH-cyclopenta[a]chrysene-7a-carboxylic acid 76321490 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(C(=CC5(C)C)C=O)C)C)C2C1O)C)C(=O)O)C 468.70 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters / Enol esters
[(1E)-2,6-dimethylhepta-1,5-dienyl] acetate 24832062 Click to see 182.26 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Amines / Primary amines / Monoalkylamines
Isoamylamine 7894 Click to see CC(C)CCN 87.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
(1R,3R,5R)-8-methyl-4-methylidene-1-propan-2-ylspiro[4.5]dec-8-en-3-ol 15109138 Click to see 220.35 unknown https://doi.org/10.1016/S0031-9422(00)95000-3
8-Methyl-4-methylidene-1-propan-2-ylspiro[4.5]dec-8-en-3-ol 101418948 Click to see CC1=CCC2(CC1)C(CC(C2=C)O)C(C)C 220.35 unknown https://doi.org/10.1016/S0031-9422(00)95000-3
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
Chlorogenic Acid 1794427 Click to see C1C(C(C(CC1(C(=O)O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 354.31 unknown via CMAUP database
cis-Chlorogenic acid 1794425 Click to see 354.31 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
Isoamyl alcohol 31260 Click to see CC(C)CCO 88.15 unknown https://doi.org/10.1016/S0031-9422(00)82464-4
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(2R)-2-[(1S)-cyclohex-3-en-1-yl]-6-methylhept-5-en-2-ol 162946021 Click to see 208.34 unknown https://doi.org/10.1016/0031-9422(92)80384-Q
2-Cyclohex-3-en-1-yl-6-methylhept-5-en-2-ol 9990645 Click to see CC(=CCCC(C)(C1CCC=CC1)O)C 208.34 unknown https://doi.org/10.1016/0031-9422(92)80384-Q
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-phenylethyl beta-D-glucopyranoside 468284 Click to see 284.30 unknown https://doi.org/10.1007/S10600-006-0267-3
Phenylethyl beta-D-glucopyranoside 11289099 Click to see C1=CC=C(C=C1)CCOC2C(C(C(C(O2)CO)O)O)O 284.30 unknown https://doi.org/10.1007/S10600-006-0267-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[(7-methoxy-1-methyl-9H-pyrido[3,4-b]indol-8-yl)oxy]oxane-3,4,5-triol 11972453 Click to see 390.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
Echinacoside 5281771 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(C(O4)CO)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 786.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
(1R,5R)-8-methyl-4-methylidene-1-propan-2-ylspiro[4.5]dec-8-en-3-one 15109126 Click to see 218.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
8-Methyl-4-methylidene-1-propan-2-ylspiro[4.5]dec-8-en-3-one 101418824 Click to see CC1=CCC2(CC1)C(CC(=O)C2=C)C(C)C 218.33 unknown https://doi.org/10.1016/0031-9422(91)80099-M
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
2-Tridecanone 11622 Click to see 198.34 unknown https://doi.org/10.1002/FFJ.2730050406
> Organoheterocyclic compounds / Dioxanes / 1,2-dioxanes
(1R,2R,5R,7S,10S)-10-hydroperoxy-5-methyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-8-ene-8-carbaldehyde 14829220 Click to see 282.33 unknown https://doi.org/10.1016/0031-9422(92)80013-5
(1R,2R,5R,7S,10S)-10-hydroperoxy-5-methyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-8-ene-8-carboxylic acid 15736713 Click to see 298.33 unknown https://doi.org/10.1016/0031-9422(92)80013-5
(1R,2R,5R,7S,10S)-10-hydroxy-5-methyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-8-ene-8-carboxylic acid 14543564 Click to see CC(C)C1CCC2(C13C(C=C(C(C2)OO3)C(=O)O)O)C 282.33 unknown https://doi.org/10.1016/0031-9422(89)80026-3
https://doi.org/10.1016/0031-9422(92)80013-5
https://doi.org/10.1016/0031-9422(92)80159-C
(1R,2R,5R,7S,10S)-5,8-dimethyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-8-en-10-ol 10399977 Click to see CC1=CC(C23C(CCC2(CC1OO3)C)C(C)C)O 252.35 unknown https://doi.org/10.1016/0031-9422(92)80384-Q
(1R,2R,5R,7S,8R)-8-hydroperoxy-5,8-dimethyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-9-ene 10015863 Click to see CC(C)C1CCC2(C13C=CC(C(C2)OO3)(C)OO)C 268.35 unknown https://doi.org/10.1016/0031-9422(92)80384-Q
(1R,2R,5R,7S)-5-methyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-9-en-8-one 163055467 Click to see 236.31 unknown https://doi.org/10.1016/0031-9422(92)80013-5
(3R,3aR,4S,7S,8aR)-2,3,4,7,8,8a-Hexahydro-4-hydroxy-8a-methyl-3-(1-methylethyl)-1H-3a,7-epidioxyazulene-6-carboxaldehyde 442391 Click to see 266.33 unknown https://doi.org/10.1016/0031-9422(89)80026-3
https://doi.org/10.1271/NOGEIKAGAKU1924.65.1483
https://doi.org/10.1016/0031-9422(92)80159-C
https://doi.org/10.1016/0031-9422(92)80013-5
10-Hydroperoxy-5-methyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-8-ene-8-carbaldehyde 14829219 Click to see CC(C)C1CCC2(C13C(C=C(C(C2)OO3)C=O)OO)C 282.33 unknown https://doi.org/10.1016/0031-9422(92)80013-5
10-Hydroperoxy-5-methyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-8-ene-8-carboxylic acid 163040555 Click to see 298.33 unknown https://doi.org/10.1016/0031-9422(92)80013-5
10-Hydroxy-5-methyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-8-ene-8-carbaldehyde 3508641 Click to see CC(C)C1CCC2(C13C(C=C(C(C2)OO3)C=O)O)C 266.33 unknown https://doi.org/10.1016/0031-9422(89)80026-3
https://doi.org/10.1016/0031-9422(92)80013-5
5-Methyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-9-en-8-one 14829225 Click to see 236.31 unknown https://doi.org/10.1016/0031-9422(92)80013-5
5,8-Dimethyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-8-en-10-ol 74022541 Click to see 252.35 unknown https://doi.org/10.1016/0031-9422(92)80384-Q
8-Hydroperoxy-5,8-dimethyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-9-ene 74041632 Click to see 268.35 unknown https://doi.org/10.1016/0031-9422(92)80384-Q
methyl (1R,2R,5R,7S,10S)-10-hydroxy-5-methyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-8-ene-8-carboxylate 14878564 Click to see CC(C)C1CCC2(C13C(C=C(C(C2)OO3)C(=O)OC)O)C 296.36 unknown https://doi.org/10.1271/BBB1961.55.1049
https://doi.org/10.1016/0031-9422(92)80013-5
Methyl 10-hydroxy-5-methyl-2-propan-2-yl-11,12-dioxatricyclo[5.3.2.01,5]dodec-8-ene-8-carboxylate 14878562 Click to see 296.36 unknown https://doi.org/10.1271/BBB1961.55.1049
https://doi.org/10.1016/0031-9422(92)80013-5
> Organoheterocyclic compounds / Furopyrans
(1R,3R,6R,8S,11S)-11-hydroxy-6-methyl-3-propan-2-yl-2,12-dioxatricyclo[6.3.1.01,6]dodec-9-ene-9-carbaldehyde 163063067 Click to see 266.33 unknown https://doi.org/10.1016/S0031-9422(00)95000-3
(1R,3S,6R,8S,11S)-11-hydroxy-6-methyl-3-propan-2-yl-2,12-dioxatricyclo[6.3.1.01,6]dodec-9-ene-9-carbaldehyde 163063068 Click to see 266.33 unknown https://doi.org/10.1016/S0031-9422(00)95000-3
(1R,3S,6R,8S,11S)-11-hydroxy-6-methyl-3-propan-2-yl-2,12-dioxatricyclo[6.3.1.01,6]dodec-9-ene-9-carboxylic acid 101607239 Click to see 282.33 unknown https://doi.org/10.1271/BBB1961.55.1049
11-Hydroxy-6-methyl-3-propan-2-yl-2,12-dioxatricyclo[6.3.1.01,6]dodec-9-ene-9-carbaldehyde 163063066 Click to see 266.33 unknown https://doi.org/10.1016/S0031-9422(00)95000-3
11-Hydroxy-6-methyl-3-propan-2-yl-2,12-dioxatricyclo[6.3.1.01,6]dodec-9-ene-9-carboxylic acid 162907305 Click to see 282.33 unknown https://doi.org/10.1271/BBB1961.55.1049
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
CID 162977223 162977223 Click to see 416.40 unknown https://doi.org/10.1111/J.1365-2621.1989.TB04709.X
> Organoheterocyclic compounds / Pyrans
Rugosic acid B 101606459 Click to see CC(C)C1CCC2(C13C(C=C(C(C2)(O3)O)C(=O)O)O)C 282.33 unknown https://doi.org/10.1271/BBB1961.55.1049
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
methyl (5R,6S)-5,6-dihydroxy-2-(4-hydroxyphenyl)-4-oxo-6H-pyrano[2,3-b]oxepine-5-carboxylate 72701620 Click to see COC(=O)C1(C(C=COC2=C1C(=O)C=C(O2)C3=CC=C(C=C3)O)O)O 346.30 unknown https://doi.org/10.1021/NP4004068
> Phenylpropanoids and polyketides / Cinnamaldehydes
Cinnamaldehyde 637511 Click to see 132.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(6-(2-(3,4-Dihydroxyphenyl)Ethoxy)-5-Hydroxy-2-(Hydroxymethyl)-4-((2S,3R,4R,5R,6S)-3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxyoxan-3-Yl) (E)-3-(3,4-Dihydroxyphenyl)Prop-2-Enoate 24978601 Click to see 624.60 unknown via CMAUP database
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 44429837 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
[(2R,3R,4R,5R,6R)-6-[2-(3,4-Dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (Z)-3-(3,4-dihydroxyphenyl)prop-2-enoate 10258386 Click to see 624.60 unknown via CMAUP database
[(2S,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-2-(hydroxymethyl)-4-[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 90474101 Click to see 624.60 unknown via CMAUP database
2-Acetylacteoside 21629996 Click to see 666.60 unknown via CMAUP database
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
(Z)-3-(4-Hydroxyphenyl)acrylic acid docosylester 12083115 Click to see 472.70 unknown https://doi.org/10.1016/0031-9422(92)83497-M
2-Propenoic acid, 3-(4-hydroxyphenyl)-, hexacosyl ester 516554 Click to see 528.80 unknown https://doi.org/10.1016/0031-9422(92)83497-M
Docosyl 3-(4-hydroxyphenyl)prop-2-enoate 53396120 Click to see CCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O 472.70 unknown https://doi.org/10.1016/0031-9422(92)83497-M
Hexacosyl (z)-p-coumarate 129685588 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O 528.80 unknown https://doi.org/10.1016/0031-9422(92)83497-M
Octacosyl (z)-p-coumarate 101915969 Click to see 556.90 unknown https://doi.org/10.1016/0031-9422(92)83497-M
Octacosyl 3-(4-hydroxyphenyl)prop-2-enoate 71332701 Click to see 556.90 unknown https://doi.org/10.1016/0031-9422(92)83497-M
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Caffeic Acid 689043 Click to see 180.16 unknown via CMAUP database
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
Cis-P-Coumaric Acid 1549106 Click to see 164.16 unknown via CMAUP database
P-Coumaric Acid 637542 Click to see 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Cinnamyl Alcohol 5315892 Click to see 134.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-methoxyphenoxy)- 5316512 Click to see 300.26 unknown https://doi.org/10.1016/0031-9422(91)80131-J
6-Demethoxycapillarisin 5316511 Click to see C1=CC(=CC=C1O)OC2=CC(=O)C3=C(C=C(C=C3O2)O)O 286.24 unknown https://doi.org/10.1016/0031-9422(91)80131-J
8-[3-[(2S,3S,6S)-6-[[(2R,3R)-3,4-dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-3,4,4-trihydroxyoxan-2-yl]oxy-2-hydroxy-3-methylbutyl]-5,7-dimethoxychromen-2-one 6325929 Click to see 602.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(2R,3R)-8-[(2R,3R,4R)-3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 14353359 Click to see 546.50 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
(2R,3R)-8-[(2S,3R,4R)-3,7-dihydroxy-2-(4-hydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol 14353357 Click to see 546.50 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
(2R,3S)-2-(3,4-dihydroxyphenyl)-6-[(2R,3S,4S)-2-(3,4-dihydroxyphenyl)-3,7-dihydroxy-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol 10325532 Click to see C1C(C(OC2=C1C(=C(C(=C2)O)C3C(C(OC4=C3C=CC(=C4)O)C5=CC(=C(C=C5)O)O)O)O)C6=CC(=C(C=C6)O)O)O 562.50 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
Aescultitannin B 10010849 Click to see 864.80 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
Proanthocyanidin B2 5320711 Click to see 578.50 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
Procyanidin B3 146798 Click to see 578.50 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Catechin 9064 Click to see 290.27 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
Epicatechin 72276 Click to see 290.27 unknown https://doi.org/10.1016/J.BMCL.2013.12.098
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Catechin gallates
Epigallocatechin Gallate 65064 Click to see 458.40 unknown https://doi.org/10.1271/BBB.70645
Tea, ext. 1287 Click to see 458.40 unknown https://doi.org/10.1271/BBB.70645
> Phenylpropanoids and polyketides / Flavonoids / Flavones
2-(3,4-Dihydroxyphenyl)-5,7-dihydroxy-3-[2,4,5-trihydroxy-6-(hydroxymethyl)oxan-3-yl]oxychromen-4-one 57339948 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(OC4O)CO)O)O)O)O 464.40 unknown via CMAUP database
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1016/0031-9422(91)80131-J
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1007/S10600-006-0267-3
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1007/S10600-006-0267-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanidin 3-O-p-coumaroyl glycosides / Anthocyanidin 3-O-6-p-coumaroyl glycosides
[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[7-hydroxy-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-(3,4,5-trihydroxyphenyl)chromenylium-3-yl]oxyoxan-2-yl]methyl 3-(4-hydroxyphenyl)prop-2-enoate 101633884 Click to see 773.70 unknown via CMAUP database
3-[[(2R,3S,4S,5R,6S)-6-[2-(3,4-dihydroxy-5-methoxyphenyl)-7-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[3-(4-hydroxyphenyl)prop-2-enoyloxymethyl]oxan-2-yl]oxychromenylium-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid 100921412 Click to see COC1=CC(=CC(=C1O)O)C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)OC5C(C(C(C(O5)COC(=O)C=CC6=CC=C(C=C6)O)O)O)O 873.70 unknown via CMAUP database
4'''-Demalonylsalvianin 5282162 Click to see 843.70 unknown via CMAUP database
Bis(demalonyl)monardaein cation 20054973 Click to see 741.70 unknown via CMAUP database
Bisdemalonylsalvianin 5282161 Click to see C1=CC(=CC=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)COC(=O)C=CC6=CC(=C(C=C6)O)O)O)O)O)O 757.70 unknown via CMAUP database
CID 101586992 101586992 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)COC(=O)CC(=O)O)O)O)O)O)C6=CC(=C(C=C6)O)O)O)O)O)O 843.70 unknown via CMAUP database
Malonylawobanin 5281258 Click to see C1=CC(=CC=C1C=CC(=O)OCC2C(C(C(C(O2)OC3=C([O+]=C4C=C(C=C(C4=C3)OC5C(C(C(C(O5)COC(=O)CC(=O)O)O)O)O)O)C6=CC(=C(C(=C6)O)O)O)O)O)O)O 859.70 unknown via CMAUP database
Shisonin 5282068 Click to see 757.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-5-O-glycosides
(2S,4S,5S)-2-[2-(3,4-dihydroxyphenyl)-7-hydroxy-3-[(2S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-5-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256718 Click to see C1=CC(=C(C=C1C2=C(C=C3C(=CC(=CC3=[O+]2)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O)O 611.50 unknown via CMAUP database
3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[7-hydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromenylium-5-yl]oxyoxan-2-yl]methoxy]propanoic acid 101930173 Click to see 681.60 unknown via CMAUP database
Delphinidin 3,5-diglucoside 10100906 Click to see 627.50 unknown via CMAUP database
Pelargonin 441772 Click to see 595.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid 3-O-p-coumaroyl glycosides
3-[[(2R,3S,4S,5R,6S)-6-[3-[(2S,3R,4S,5S,6R)-6-[3-(3,4-dihydroxyphenyl)prop-2-enoyloxymethyl]-3,4,5-trihydroxyoxan-2-yl]oxy-7-hydroxy-2-(3,4,5-trihydroxyphenyl)chromenylium-5-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid 101633888 Click to see 875.70 unknown via CMAUP database
Tiliroside 5320686 Click to see 594.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
[(2R,3S,4S,5R,6S)-6-[5,7-dihydroxy-2-(4-hydroxyphenyl)-4-oxochromen-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methyl 4-hydroxybenzoate 15409015 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)COC(=O)C5=CC=C(C=C5)O)O)O)O)O 568.50 unknown https://doi.org/10.1021/NP4004068
2-(3,4-Dihydroxyphenyl)-5,7-Dihydroxy-3-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)Oxychromen-4-One 5378597 Click to see 464.40 unknown https://doi.org/10.1007/S10600-006-0267-3
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4S,5R)-3,4,5-trihydroxytetrahydropyran-2-yl]oxy-chromen-4-one 5481217 Click to see 434.30 unknown via CMAUP database
3-(4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxyoxan-2-yl)oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 13647412 Click to see 610.50 unknown https://doi.org/10.1007/S10600-006-0267-3
3-[(2S,3R,4R,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-5,7-dihydroxy-2-(4-hydroxyphenyl)chromen-4-one 13245583 Click to see 418.30 unknown https://doi.org/10.1007/S10600-006-0267-3
3-[(2S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 44144273 Click to see 434.30 unknown via CMAUP database
3-[4,5-Dihydroxy-6-(hydroxymethyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromen-4-one 14185727 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)OC5C(C(C(C(O5)CO)O)O)O)O)O 626.50 unknown https://doi.org/10.1007/S10600-006-0267-3
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-3-(3,4,5-Trihydroxy-6-((3,4,5-Trihydroxy-6-Methyloxan-2-Yl)Oxymethyl)Oxan-2-Yl)Oxychromen-4-One 12313332 Click to see 594.50 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 20055286 Click to see 594.50 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,4R,5S)-3,4,5-trihydroxy-6-[[(2R,4R,5R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one 24211973 Click to see 594.50 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxyphenyl)-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 5462193 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-006-0267-3
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/S10600-006-0267-3
Avicularin 5490064 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O)O 434.30 unknown https://doi.org/10.1007/S10600-006-0267-3
Avicularine 12308704 Click to see 434.30 unknown https://doi.org/10.1007/S10600-006-0267-3
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/10.1007/S10600-006-0267-3
Isoquercetin 5280804 Click to see 464.40 unknown via CMAUP database
Juglanin 5318717 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(O4)CO)O)O)O 418.30 unknown https://doi.org/10.1007/S10600-006-0267-3
Kaempferol-3-O-Rutinoside 5318767 Click to see 594.50 unknown via CMAUP database
Quercetin 3-O-beta-D-glucopyranosyl-(1->2)-beta-D-galactopyranoside 14185728 Click to see 626.50 unknown https://doi.org/10.1007/S10600-006-0267-3
quercetin 3-O-sophoroside 5282166 Click to see 626.50 unknown via CMAUP database
Quercitrin 5280459 Click to see 448.40 unknown via CMAUP database
Rutin 5280805 Click to see 610.50 unknown via CMAUP database
Sophoraflavonoloside 5282155 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 610.50 unknown https://doi.org/10.1007/S10600-006-0267-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
5-hydroxy-2-(4-hydroxyphenyl)-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44257792 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
Apigenin 7-O-glucoside 5280704 Click to see 432.40 unknown via CMAUP database
Apigenin-7-O-Glucoside 12304093 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
Npc85473 5385553 Click to see 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
[5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxochromen-7-yl] (2S,3S,4S,5R,6R)-3,4,5,6-tetrahydroxyoxane-2-carboxylate 162910162 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC(=O)C4C(C(C(C(O4)O)O)O)O)O)O 476.40 unknown https://doi.org/10.1016/0031-9422(89)80026-3
https://doi.org/10.1016/0031-9422(92)80013-5
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 4-O-methylated flavonoids
Methyl 7-hydroxy-2-(4-methoxyphenyl)-4-oxochromene-5-carboxylate 72702311 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)C(=O)OC 326.30 unknown https://doi.org/10.1021/NP4004068
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
4-[(2R)-8-(2-hydroxyethyl)-7-methoxy-3,4-dihydro-2H-chromen-2-yl]benzene-1,3-diol 53468592 Click to see 316.30 unknown https://doi.org/10.1021/NP4004068
8-Acetyl-2-(3,4-dihydroxyphenyl)-6,7-dimethoxychromen-4-one 72701894 Click to see 356.30 unknown https://doi.org/10.1021/NP4004068
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids
(3R,4S)-3-(4-hydroxyphenyl)-6,7-dimethoxy-3,4-dihydro-2H-chromen-4-ol 72701895 Click to see COC1=C(C=C2C(=C1)C(C(CO2)C3=CC=C(C=C3)O)O)OC 302.32 unknown https://doi.org/10.1021/NP4004068
(3R,4S)-7-methoxy-3-(4-methoxyphenyl)-3,4-dihydro-2H-chromene-4,6-diol 72701896 Click to see 302.32 unknown https://doi.org/10.1021/NP4004068
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
[(10R,11S,12R,13S,15R)-3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 2-[[(10R,11S,12R,13R,15R)-3,4,5,13,22,23-hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]-3,4,5-trihydroxybenzoate 16165067 Click to see 1723.20 unknown https://doi.org/10.1248/CPB.38.3341
[(10R,11S,12R,13S,15R)-3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 3,4,5-trihydroxy-2-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,14,29,30,33,34,35-undecahydroxy-4,17,25,38-tetraoxo-20-(3,4,5-trihydroxybenzoyl)oxy-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]benzoate 16174837 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C7C(C(O6)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O7)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1873.30 unknown https://doi.org/10.1248/CPB.38.3341
[(10R,11S,12R,13S)-3,4,5,21,22,23-hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 3,4,5-trihydroxy-2-[[(11S,12R,13S,15R)-3,4,5,22,23-pentahydroxy-8,18-dioxo-11,12,13-tris[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]benzoate 118701701 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C(C(C(O6)OC(=O)C7=CC(=C(C(=C7)O)O)O)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1875.30 unknown via CMAUP database
[(10S,11R,12R,15R)-3,4,5,11,12,21,22,23-octahydroxy-8,18-dioxo-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 3,4,5-trihydroxybenzoate 9874083 Click to see 634.50 unknown via CMAUP database
[(1S,2S,19R,20S,22R)-7,8,9,12,13,14,28,29,30,33,34,35-dodecahydroxy-4,17,25,38-tetraoxo-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-20-yl] 3,4,5-trihydroxybenzoate 50990634 Click to see 936.60 unknown via CMAUP database
[1-(3,4,5,11,17,18,19-Heptahydroxy-8,14-dioxo-9,13-dioxatricyclo[13.4.0.02,7]nonadeca-1(19),2,4,6,15,17-hexaen-10-yl)-3-oxo-1-(3,4,5-trihydroxybenzoyl)oxypropan-2-yl] 3,4,5-trihydroxybenzoate 75596264 Click to see 786.60 unknown https://doi.org/10.1271/BBB.70645
[3,4,5,13,21,22,23-Heptahydroxy-8,18-dioxo-12-(3,4,5-trihydroxybenzoyl)oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-11-yl] 3,4,5-trihydroxybenzoate 5153915 Click to see 786.60 unknown https://doi.org/10.1016/J.BMCL.2010.01.084
[3,4,5,21,22,23-Hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 2-[[3,4,5,13,22,23-hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]-3,4,5-trihydroxybenzoate 16165063 Click to see 1723.20 unknown https://doi.org/10.1248/CPB.38.3341
[3,4,5,21,22,23-Hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 3,4,5-trihydroxy-2-[[3,4,5,22,23-pentahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-13-[3,4,5-trihydroxy-2-[[3,4,5,22,23-pentahydroxy-8,18-dioxo-11,12,13-tris[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]benzoyl]oxy-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]benzoate 16174859 Click to see 2811.90 unknown https://doi.org/10.1248/CPB.38.3341
[3,4,5,21,22,23-Hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-13-yl] 3,4,5-trihydroxy-2-[[7,8,9,12,13,14,29,30,33,34,35-undecahydroxy-4,17,25,38-tetraoxo-20-(3,4,5-trihydroxybenzoyl)oxy-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]benzoate 16174836 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3OC4=C(C(=C5C(=C4)C(=O)OCC6C(C7C(C(O6)OC(=O)C8=CC(=C(C(=C8)O)O)O)OC(=O)C9=CC(=C(C(=C9C2=C(C(=C(C=C2C(=O)O7)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C25)O)O)O)O)O)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2)O)O)O)OC(=O)C2=CC(=C(C(=C2C2=C(C(=C(C=C2C(=O)O1)O)O)O)O)O)O 1873.30 unknown https://doi.org/10.1248/CPB.38.3341
1(beta)-O-Galloylpedunculagin 118701062 Click to see 936.60 unknown https://doi.org/10.1248/CPB.38.3308
2-[[(10R,11S,12R,13R,15R)-3,4,5,13,22,23-hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]-3,4,5-trihydroxybenzoic acid 14704616 Click to see 954.70 unknown https://doi.org/10.1248/CPB.38.3308
2-[[3,4,5,13,22,23-Hexahydroxy-8,18-dioxo-11,12-bis[(3,4,5-trihydroxybenzoyl)oxy]-9,14,17-trioxatetracyclo[17.4.0.02,7.010,15]tricosa-1(23),2,4,6,19,21-hexaen-21-yl]oxy]-3,4,5-trihydroxybenzoic acid 14704614 Click to see 954.70 unknown https://doi.org/10.1248/CPB.38.3308
3,4,5-trihydroxy-2-[[(1R,2S,19R,20S,22R)-7,8,9,12,13,14,29,30,33,34,35-undecahydroxy-4,17,25,38-tetraoxo-20-(3,4,5-trihydroxybenzoyl)oxy-3,18,21,24,39-pentaoxaheptacyclo[20.17.0.02,19.05,10.011,16.026,31.032,37]nonatriaconta-5,7,9,11,13,15,26,28,30,32,34,36-dodecaen-28-yl]oxy]benzoic acid 16174833 Click to see 1104.70 unknown https://doi.org/10.1248/CPB.38.3308
beta-D-Glucopyranose, cyclic 4-2':6-2-((1S)-4-(6-(((4,6-O-(((1S)-4,4',5,5',6,6'-hexahydroxy(1,1'-biphenyl)-2,2'-diyl)dicarbonyl)-2,3-bis-O-(3,4,5-trihydroxybenzoyl)-beta-D-glucopyranosyl)oxy)carbonyl)-2,3,4-trihydroxyphenoxy)-4',5,5',6,6'-pentahydroxy(1,1'-biphenyl)-2,2'-dicarboxylate) 1,2,3-tris(3,4,5-trihydroxybenzoate), stereoisomer 16130312 Click to see 1875.30 unknown https://doi.org/10.1248/CPB.38.3341
https://doi.org/10.1271/BBB.70645
Casuarictin 73644 Click to see 936.60 unknown https://doi.org/10.1248/CPB.38.3308
https://doi.org/10.1016/J.BMCL.2010.01.084
CID 11766372 11766372 Click to see 938.70 unknown https://doi.org/10.1248/CPB.38.3308
CID 16170073 16170073 Click to see C1C2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6C7=C(C(=C(C=C7C(=O)O1)OC8=C(C(=C(C=C8C(=O)O)O)O)O)O)O)O)O)O 1106.80 unknown https://doi.org/10.1271/BBB.70645
https://doi.org/10.1248/CPB.38.3308
CID 16174834 16174834 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O3)O)O)O)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)OC9=C(C(=C(C=C9C(=O)O)O)O)O)O)O)O)O)O 1104.70 unknown https://doi.org/10.1248/CPB.38.3308
CID 442690 442690 Click to see C1C2C(C(C(C(O2)O)OC(=O)C3=CC(=C(C(=C3)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5C6=C(C(=C(C=C6C(=O)O1)O)O)O)O)O)O 786.60 unknown https://doi.org/10.1248/CPB.38.3308
https://doi.org/10.1016/0031-9422(92)83451-4
Ellagic Acid 5281855 Click to see 302.19 unknown via CMAUP database
Eugeniin 442679 Click to see 938.70 unknown https://doi.org/10.1248/CPB.38.3308
https://doi.org/10.1016/J.BMCL.2010.01.084
https://doi.org/10.1271/BBB.70645
GlyTouCan:G69718UQ 9918701 Click to see 786.60 unknown https://doi.org/10.1016/J.BMCL.2010.01.084
Isostrictinin 13917513 Click to see 634.50 unknown https://doi.org/10.1248/CPB.38.3308
Pedunculagin 442688 Click to see 784.50 unknown https://doi.org/10.1016/0031-9422(92)83451-4
https://doi.org/10.1248/CPB.38.3308
Potentillin 452242 Click to see 936.60 unknown https://doi.org/10.1016/J.BMCL.2010.01.084
Rugosin A 16132354 Click to see 1106.80 unknown https://doi.org/10.1271/BBB.70645
https://doi.org/10.1248/CPB.38.3308
Rugosin B 54676084 Click to see C1C2C(=C(C(=C1O)O)O)C3=C(C(=C(C=C3C(=O)OCC4C(C(C(C(O4)O)CC(=O)C5=CC(=C(C(=C5)O)O)O)OC(=O)C6=CC(=C(C(=C6)O)O)O)OC2=O)OC7=C(C(=C(C=C7C(=O)O)O)O)O)O)O 954.70 unknown via CMAUP database
Rugosin C 101590860 Click to see C1C2C(C3C(C(O2)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC5=C(C6=C(C(=C(C=C6C(=O)O3)O)O)O)C(=C(C(=C5)O)O)O)OC(=O)C7=CC(=C(C(=C7C8=C(C(=C(C=C8C(=O)O1)OC9=C(C(=C(C=C9C(=O)O)O)O)O)O)O)O)O)O 1076.70 unknown https://doi.org/10.1248/CPB.38.3308
Rugosin D 16129626 Click to see 1875.30 unknown https://doi.org/10.1271/BBB.70645
https://doi.org/10.1248/CPB.38.3341
https://doi.org/10.1021/NP50040A016
Rugosin E 16129738 Click to see 1723.20 unknown https://doi.org/10.1248/CPB.38.3341
Strictinin 73330 Click to see 634.50 unknown https://doi.org/10.1248/CPB.38.3308
Tellimagrandin I 73179 Click to see 786.60 unknown https://doi.org/10.1271/BBB.70645
Tellimagrandin Ii 151590 Click to see 938.70 unknown https://doi.org/10.1016/J.BMCL.2010.01.084
https://doi.org/10.1271/BBB.70645

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