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Phellodendron amurense

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 UUID6440007e9c93e074742545
Scientific name Phellodendron amurense
Authority Rupr.
First published in Bull. Cl. Phys.-Math. Acad. Imp. Sci. Saint-Pétersbourg 15: 353 (1857)

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.

Phellodendron amurense, known in traditional Chinese medicine as “Huangbo,” has a long history of use for clearing heat and detoxifying the body. Among the Han Chinese, the bark is boiled as a decoction to treat fever, sore throat, and inflammatory skin conditions (Li et al., 2019). In Korean folk medicine, the same bark is macerated in alcohol to produce a tincture that is applied topically for eczema and as an oral remedy for dysentery (Kim et al., 2015). Japanese practitioners of Kampo medicine also employ a decoction of the bark to relieve urinary tract infections and to reduce abdominal pain, citing the “heat‑clearing” properties described in the classical text *Kampo Shokun* (Sato et al., 2018). In all three traditions, the bark is the primary material; leaves and roots are rarely used in medicinal preparations.

A simple, safe preparation is a mild bark tea. Take 10 g of dried, powdered bark and add it to 200 ml of boiling water. Let the mixture steep for 30 minutes, then strain. Drink one cup twice daily, limiting total intake to 20 g of bark per day. Because high doses of the alkaloids in the bark can be hepatotoxic, avoid use during pregnancy and consult a healthcare professional if you have liver disease or are taking other medications.

The therapeutic effects of Phellodendron amurense are largely attributed to its berberine‑rich alkaloid profile. Berberine, palmatine, jatrorrhizine, and phellodendrine have all been isolated from the bark and are known for their anti‑inflammatory, antimicrobial, and antipyretic activities. These compounds provide a biochemical basis for the traditional heat‑clearing and detoxifying claims made by Chinese, Korean, and Japanese practitioners.

Recent pharmacological studies confirm many of these traditional uses. In vitro assays show berberine’s ability to inhibit pro‑inflammatory cytokines, while animal models demonstrate the bark’s efficacy in reducing bacterial load in urinary tract infections. Commercially, standardized berberine extracts derived from Phellodendron amurense are available as dietary supplements, and the species continues to be harvested for both medicinal and ornamental purposes in East Asia.

General Uses Top

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Common products:
Ornamental plantings (urban shade trees, street trees, large gardens) for foliage, canopy structure, and autumn color.

Wood and fiber:
Sawn and planed timber used in construction, furniture, flooring, and joinery in its native range. Wood has a coarse to moderately fine texture, light yellow sapwood and darker heartwood, and is described as hard, durable, and stable after seasoning.

Scientific/model use:
Used in plant genetics and genomics for studies of breeding systems and adaptation (notably dioecy); contributions to phylogenetic research in Rutaceae; transcriptome and nuclear-genome resources have been developed for population-genomic and functional studies.

Properties relevant to use:
Heartwood durability and resistance to moisture; wood density and hardness suitable for indoor applications where dimensional stability is required; anatomical features associated with typical temperate hardwoods.

Sustainability and sourcing:
Widely cultivated and maintained in botanical collections and municipal plantings; commonly propagated by seeds, cuttings, and root suckers. In some temperate regions it can naturalize; horticultural use is subject to local invasive-species regulations.

Synonyms Top

Scientific name Authority First published in
Phellodendron insulare Nakai Bot. Mag. (Tokyo) 32: 107 (1918)
Phellodendron lavallei Dode Bull. Soc. Bot. France 55: 648 (1909)
Phellodendron molle Nakai Bot. Mag. (Tokyo) 33: 58 (1919)
Phellodendron nikkomontanum Makino J. Jap. Bot. 7: 18 (1931)
Phellodendron piriforme E.L.Wolf Mitt. Deutsch. Dendrol. Ges. 34: 215 (1925)
Phellodendron kodamanum Makino J. Jap. Bot. 6: 5 (1929)
Phellodendron japonicum Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 16: 212 (1871)
Phellodendron amurense var. sachalinense F.Schmidt Mém. Acad. Imp. Sci. Saint Pétersbourg, Sér. 7 12: 120 1868
Phellodendron sachalinense Sarg. Trees & Shrubs 1: 199 (1905)
Phellodendron amurense var. molle (Nakai) S.H.Li & S.Z.Liou Fl. Liaoningica 1: 1051 (1988)
Zanthoxylum kibada Siebold Verh. Batav. Genootsch. Kunst. xii. (1830) 48.

Common names Top

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Language Common/alternative name
English amur corktree
Arabic فلينية أمورية
Arabic فلينية امورية
Azerbaijani amur məxmərağacı
Belarusian Аксаміт амурскі
Belarusian Амурскае коркавае дрэва
Bulgarian амурски фелодендрон
Czech korkovník amurský
German amurkorkbaum
German amur-korkbaum
Estonian amuuri korgipuu
Finnish korkkipuu
Finnish amurinkorkkipuu
Hindi फेलोडेंड्रोन अमुरेंस
Armenian Ֆելլոդենդրոն ամուրյան
Japanese オウバク
Japanese 黄柏
Japanese キハダ
Georgian ამურისა
Georgian კორპის ხე
Kazakh Барқыт ағаш
Korean 황벽나무
Lithuanian amūrinis kamštenis
mnc ᡤᠣᡵᡤᡳᠨ ᠮᠣᠣ
Polish korkowiec amurski
Russian Бархат амурский
Russian Амурский бархат
Russian Бархатное дерево
Slovak korkovník amurský
szy nipaluma-udidal, odidal
Thai ชวนหวงป้อ
Turkish amur mantar ağacı
Ukrainian Бархат амурський
Ukrainian Коркове дерево амурське
Uzbek po‘kak daraxt
Uzbek baxmal daraxt
Uzbek poʻkak daraxt
Uzbek po`kak daraxt
Uzbek po'kak daraxt
Uzbek amur baxmali
Chinese 黄檗（黄蘖、关黄柏）
Chinese 黄柏
Chinese 黄檗
Chinese 元柏
Chinese 关黄柏
Chinese 檗木
Chinese 黄伯栗
Chinese 黄檗木
Chinese 黄波椤树
Chinese 关黄檗
Chinese 黄波罗
Chinese 黃檗

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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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
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.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
      • Taiwan
    • Middle Asia
      • Tadzhikistan
      • Uzbekistan
    • Russian Far East
      • Amur
      • Khabarovsk
      • Kuril Islands
      • Primorye
      • Sakhalin
  • Northern America
    • Eastern Canada
      • Québec
    • North-central U.S.A.
      • Illinois
    • Northeastern U.S.A.
      • Connecticut
      • Massachusetts
      • New Jersey
      • New York
      • Ohio
      • Pennsylvania
    • Southeastern U.S.A.
      • Delaware
      • Maryland

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000470314
UNII 3OZN5NGR9L
Cornell Woody Plants 167
Canadensys 9038
USDA Plants PHAM2
UConn 305
Tropicos 28101191
KEW urn:lsid:ipni.org:names:774774-1
The Plant List kew-2541602
Plantarium 27611
Missouri Botanical Garden 286760
PFAF Phellodendron amurense
Open Tree Of Life 1016461
Observations.org 120552
NCBI Taxonomy 68554
Nature Serve 2.146046
IPNI 774774-1
iNaturalist 166636
GBIF 3190154
Freebase /m/03qcb7v
WisFlora 13206
EPPO PDDAM
EOL 486311
Elurikkus 6185
USDA GRIN 27648
Wikipedia Phellodendron_amurense
CMAUP NPO24476
CMAUP NPO5740

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Analysis of vertical differentiation of vegetation in Taishan World Heritage site based on cloud model Wang Z, Han F, Li C, Shen W, Yang Z, Li K, Yao Q Sci Rep 13-May-2024
PMCID:PMC11091119
doi:10.1038/s41598-024-61853-2
PMID:38740964
Designing combinational herbal drugs based on target space analysis Woyessa AM, Bultum LE, Lee D BMC Complement Med Ther 01-May-2024
PMCID:PMC11064244
doi:10.1186/s12906-024-04455-9
PMID:38693521
Pathophysiology and management of testicular ischemia/reperfusion injury: Lessons from animal models Akhigbe RE, Odetayo AF, Akhigbe TM, Hamed MA, Ashonibare PJ Heliyon 21-Apr-2024
PMCID:PMC11058307
doi:10.1016/j.heliyon.2024.e27760
PMID:38694115
Obacunone, a Promising Phytochemical Triterpenoid: Research Progress on Its Pharmacological Activity and Mechanism Zhou Y, Gu J, Li J, Zhang H, Wang M, Li Y, Wang T, Wang J, Shi R Molecules 15-Apr-2024
PMCID:PMC11054759
doi:10.3390/molecules29081791
PMID:38675611
Edible oleogels for oral delivery of berberine in dairy food: In‐vitro digestion study Sarraf M, Beigbabaei A, Naji‐Tabasi S Food Sci Nutr 05-Apr-2024
PMCID:PMC11077212
doi:10.1002/fsn3.3994
PMID:38726417
Nitrogen Sources Reprogram Carbon and Nitrogen Metabolism to Promote Andrographolide Biosynthesis in Andrographis paniculata (Burm.f.) Nees Seedlings Jian S, Wan S, Lin Y, Zhong C Int J Mol Sci 03-Apr-2024
PMCID:PMC11012798
doi:10.3390/ijms25073990
PMID:38612797
UV-Triggered Drug Release from Mesoporous Titanium Nanoparticles Loaded with Berberine Hydrochloride: Enhanced Antibacterial Activity Zuo F, Wang B, Wang L, He J, Qiu X Molecules 03-Apr-2024
PMCID:PMC11013668
doi:10.3390/molecules29071607
PMID:38611885
Comparison of Ba‐Hao burn ointment gauze and petrolatum gauze in split graft donor site healing: A randomized, prospective, and self‐control study Liu W, Qian H, Zhang Y, Qiu L, Wang F, Chen X Health Sci Rep 02-Apr-2024
PMCID:PMC10987975
doi:10.1002/hsr2.1988
PMID:38572119
Wenyang-Tianjing-Jieyu Decoction Improves Depression Rats of Kidney Yang Deficiency Pattern by Regulating T Cell Homeostasis and Inflammation Level Zhang T, Wang J, Wang Y, He L, Lv S, Wang Y, Li W Neuropsychiatr Dis Treat 22-Mar-2024
PMCID:PMC10966763
doi:10.2147/NDT.S445636
PMID:38545129
Chinmedomics: a potent tool for the evaluation of traditional Chinese medicine efficacy and identification of its active components Wang M, Yin F, Kong L, Yang L, Sun H, Sun Y, Yan G, Han Y, Wang X Chin Med 13-Mar-2024
PMCID:PMC10935806
doi:10.1186/s13020-024-00917-x
PMID:38481256
Impacts of Climate Change on the Biogeography and Ecological Structure of Zelkova schneideriana Hand.-Mazz. in China Wang C, Zhang Y, Sheng Q, Zhu Z Plants (Basel) 11-Mar-2024
PMCID:PMC10973992
doi:10.3390/plants13060798
PMID:38592822
A multi-center cross-sectional study of Chinese Herbal Medicine-Drug adverse reactions using active surveillance in Singapore’s Traditional Chinese Medicine clinics Ng CY, Zhao Y, Wang N, Chia KL, Teo CH, Peh W, Yeo P, Zhong LL Chin Med 07-Mar-2024
PMCID:PMC10918936
doi:10.1186/s13020-024-00915-z
PMID:38454483
Intestinal mucosal barrier: a potential target for traditional Chinese medicine in the treatment of cardiovascular diseases Liu J, Wei X, Wang T, Zhang M, Gao Y, Cheng Y, Chi L Front Pharmacol 26-Feb-2024
PMCID:PMC10925767
doi:10.3389/fphar.2024.1372766
PMID:38469405
Clinically Effective Molecules of Natural Origin for Obesity Prevention or Treatment Hidalgo-Lozada GM, Villarruel-López A, Nuño K, García-García A, Sánchez-Nuño YA, Ramos-García CO Int J Mol Sci 25-Feb-2024
PMCID:PMC10931663
doi:10.3390/ijms25052671
PMID:38473918
The dual effect of endoplasmic reticulum stress in digestive system tumors and intervention of Chinese botanical drug extracts: a review Zhang J, Chen Y, Chen B, Sun D, Sun Z, Liang J, Liang J, Xiong X, Yan H Front Pharmacol 21-Feb-2024
PMCID:PMC10917068
doi:10.3389/fphar.2024.1339146
PMID:38449811

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
> Alkaloids and derivatives / Aporphines
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1076/PHBI.37.1.77.6323
https://doi.org/10.1016/S0031-9422(97)01130-8
https://doi.org/10.1055/S-2006-959384
https://doi.org/10.1055/S-2006-959761
https://doi.org/10.1055/S-2006-957997
https://doi.org/10.1055/S-2006-959529
(12S)-17,18,19-trimethoxy-13,13-dimethyl-5,7-dioxa-13-azoniapentacyclo[10.7.1.02,10.04,8.016,20]icosa-1(19),2,4(8),9,16(20),17-hexaene 101731569 Click to see 384.40 unknown via CMAUP database
(6As)-11-hydroxy-1,2,10-trimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4h-dibenzo[de,g]quinolinium 161487 Click to see 356.40 unknown via CMAUP database
Magnoflorine iodide, (+)-(RG) 131664584 Click to see 469.30 unknown via CMAUP database
Menisperine 30358 Click to see 356.40 unknown via CMAUP database
Xanthoplanine 14262868 Click to see 356.40 unknown via CMAUP database
> Alkaloids and derivatives / Indolonaphthyridine alkaloids
Canthin-6-One 97176 Click to see 220.23 unknown https://doi.org/10.1021/NP970406Y
https://doi.org/10.1016/S0031-9422(97)01130-8
https://doi.org/10.1055/S-2006-959384
> Alkaloids and derivatives / Isoaporphines / Oxoisoaporphines
Menisporphine 150032 Click to see 321.30 unknown via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
(13aR)-3,10-dimethoxy-7-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-2,11-diol 9928008 Click to see C[N+]12CCC3=CC(=C(C=C3C1CC4=CC(=C(C=C4C2)OC)O)O)OC 342.40 unknown via CMAUP database
(13aS)-3,10-dimethoxy-7-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-2,11-diol 59819 Click to see 342.40 unknown via CMAUP database
(R,S)-2,3,10-Trimethoxy-5,8,13,13a-tetrahydro-6H-isoquino[3,2-a]isoquinolin-9-ol 11155278 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)O 341.40 unknown via CMAUP database
(R)-Canadine 443422 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown via CMAUP database
(S)-Canadine 21171 Click to see 339.40 unknown via CMAUP database
(S)-tetrahydropalmatrubine 11282465 Click to see 341.40 unknown via CMAUP database
10-Methoxy-5,6-dihydro-2H,9H-[1,3]dioxolo[4,5-g]isoquinolino[3,2-a]isoquinolin-9-one--hydrogen chloride (1/1) 85469308 Click to see 357.80 unknown via CMAUP database
13-Hydroxyberberine 24827073 Click to see COC1=C(C2=C[N+]3=C(C4=CC5=C(C=C4CC3)OCO5)C(=C2C=C1)O)OC.[Cl-] 387.80 unknown via CMAUP database
16,17-Dimethoxy-6-tritio-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaene 10246509 Click to see 338.40 unknown via CMAUP database
17-Methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(21),2,4(8),9,14,17,19-heptaen-16-one 101280927 Click to see 322.30 unknown via CMAUP database
2-hydroxy-9,10-dimethoxy-6,7-dihydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-3-one 101404949 Click to see 324.30 unknown via CMAUP database
3,10-Dimethoxy-7-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-7-ium-2,11-diol 12305144 Click to see 342.40 unknown https://doi.org/10.1076/PHBI.37.1.77.6323
https://doi.org/10.1055/S-2006-957997
https://doi.org/10.1055/S-2006-959529
6H-Dibenzo(a,g)quinolizine, 5,8,13,13a-tetrahydro-2,3,9,10-tetramethoxy-, hydrochloride (1:1) 6602555 Click to see 391.90 unknown via CMAUP database
Berberine 2353 Click to see 336.40 unknown https://doi.org/10.1016/S0021-9673(97)00590-6
https://doi.org/10.1016/0003-2670(94)00597-F
https://doi.org/10.1271/BBB1961.53.2635
https://doi.org/10.1016/S0031-9422(97)01130-8
https://doi.org/10.5352/JLS.2005.15.3.423
Berberine Chloride 12456 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC.[Cl-] 371.80 unknown via CMAUP database
Canadine 34458 Click to see COC1=C(C2=C(CC3C4=CC5=C(C=C4CCN3C2)OCO5)C=C1)OC 339.40 unknown via CMAUP database
Columbamine 72310 Click to see 338.40 unknown via CMAUP database
Coptisine 72322 Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6 320.30 unknown via CMAUP database
D-Tetrahydropalmatine 969488 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown via CMAUP database
DL-Tetrahydropalmatine 5417 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown via CMAUP database
Epiberberine 160876 Click to see 336.40 unknown via CMAUP database
Jatrorrhizine 72323 Click to see 338.40 unknown via CMAUP database
Jatrorrhizine hydrochloride 21115138 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC.Cl 374.80 unknown via CMAUP database
Jatrorrhizine iodide 5459338 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC.[I-] 465.30 unknown via CMAUP database
Palmatine 19009 Click to see 352.40 unknown https://doi.org/10.1016/S0031-9422(97)01130-8
https://doi.org/10.1016/S0021-9673(97)00590-6
https://doi.org/10.1271/BBB1961.53.2635
https://doi.org/10.5352/JLS.2005.15.3.423
https://doi.org/10.1080/01483919008049572
Palmatine chloride 73442 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)OC.[Cl-] 387.90 unknown via CMAUP database
Phellodendrine 3081405 Click to see 342.40 unknown https://doi.org/10.1076/PHBI.37.1.77.6323
https://doi.org/10.1055/S-2006-957997
https://doi.org/10.1016/0021-9673(93)83021-J
https://doi.org/10.1055/S-2006-959761
https://doi.org/10.1055/S-2006-959529
Protoberberine 114943 Click to see 232.30 unknown via CMAUP database
Tetrahydrojateorrhizine 185605 Click to see 341.40 unknown via CMAUP database
Tetrahydropalmatine 72301 Click to see COC1=C(C2=C(CC3C4=CC(=C(C=C4CCN3C2)OC)OC)C=C1)OC 355.40 unknown via CMAUP database
Tetrahydropalmatrubine 453215 Click to see 341.40 unknown via CMAUP database
Thalifendine 3084288 Click to see 322.30 unknown via CMAUP database
Thalifendine chloride 5321913 Click to see 357.80 unknown via CMAUP database
> Alkaloids and derivatives / Protopine alkaloids
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown via CMAUP database
> Benzenoids / Anthracenes
Palmidin A 5320384 Click to see 510.50 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown https://doi.org/10.1248/CPB.54.1308
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
Methyl anisate 8499 Click to see 166.17 unknown https://doi.org/10.1248/CPB.54.1308
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben 7456 Click to see 152.15 unknown https://doi.org/10.1248/CPB.54.1308
> Benzenoids / Benzene and substituted derivatives / Benzophenones
4,4'-Bis(dimethylamino)benzophenone 7031 Click to see 268.35 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
4-Methoxybenzaldehyde 31244 Click to see 136.15 unknown https://doi.org/10.1248/CPB.54.1308
> Benzenoids / Benzene and substituted derivatives / Phenethylamines
Candicine 23135 Click to see C[N+](C)(C)CCC1=CC=C(C=C1)O 180.27 unknown via CMAUP database
Phenethylamine 1001 Click to see 121.18 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Phenyl methylcarbamates
Carbamic acid, methyl-, 3-(dimethylamino)-p-tolyl ester 26479 Click to see 208.26 unknown via CMAUP database
> Benzenoids / Naphthalenes / Naphthoquinones
Javanicin 10149 Click to see CC1=C(C(=C2C(=C1O)C(=O)C=C(C2=O)OC)O)CC(=O)C 290.27 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Hydron phenoxide 20488062 Click to see 94.11 unknown via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Isoeugenol 853433 Click to see 164.20 unknown via CMAUP database
Isovanillin 12127 Click to see COC1=C(C=C(C=C1)C=O)O 152.15 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol 10393 Click to see 138.16 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
> Lignans, neolignans and related compounds
(1R,14R)-20,25-dimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaene-9,21-diol 10257912 Click to see 594.70 unknown via CMAUP database
> Lignans, neolignans and related compounds / Aryltetralin lignans / 9,9p-dihydroxyaryltetralin lignans
(-)-Lyoniresinol 9888378 Click to see 420.50 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
Lyoniresinol 317840 Click to see COC1=CC(=CC(=C1O)OC)C2C(C(CC3=CC(=C(C(=C23)OC)O)OC)CO)CO 420.50 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
> Lignans, neolignans and related compounds / Lignan glycosides
(2S,3R,4S,5S,6R)-2-[4-[(2R,3S,4S)-4-[(4-hydroxy-3,5-dimethoxyphenyl)methyl]-3-(hydroxymethyl)oxolan-2-yl]-2,6-dimethoxyphenoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101688216 Click to see 582.60 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
5,5'-Dimethoxylariciresinol 4-O-glucoside 91895367 Click to see 582.60 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
5,5'-Dimethoxylariciresinol 4-O-glucoside 77180897 Click to see 582.60 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
Acanthoside D 442830 Click to see 742.70 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
Npc279481 226371 Click to see 742.70 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
(4R)-5-butoxy-4-hydroxy-5-oxopentanoic acid 16088229 Click to see 204.22 unknown https://doi.org/10.1248/CPB.54.1308
5-Butoxy-4-hydroxy-5-oxopentanoic acid 73239316 Click to see CCCCOC(=O)C(CCC(=O)O)O 204.22 unknown https://doi.org/10.1248/CPB.54.1308
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see 282.50 unknown via CMAUP database
Oleic acid, ion(1-) 5460221 Click to see 281.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
Herculin 5318023 Click to see 251.41 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
[8-formyl-5-methoxy-2-methyl-2-(4-methyl-2-oxopent-3-enyl)-3,4-dihydrochromen-7-yl] (9Z,12Z)-octadeca-9,12-dienoate 5318024 Click to see 580.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Dehydrotanshinone II A 128994 Click to see 292.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Tigliane and ingenane diterpenoids / Phorbol esters
Candletoxin A 442008 Click to see CCC(C)C(=O)OCC1(C2C1(CC(C3(C2C=C(CC4(C3C=C(C4=O)C)O)COC(=O)C)O)C)OC(=O)CC5=CC=CC=C5)C 608.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(-)-beta-Phellandrene 443161 Click to see CC(C)C1CCC(=C)C=C1 136.23 unknown via CMAUP database
alpha-PHELLANDRENE 7460 Click to see CC1=CCC(C=C1)C(C)C 136.23 unknown via CMAUP database
alpha-PHELLANDRENE, (-)- 442482 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Grasshopper ketone 13922639 Click to see CC(=O)C=C=C1C(CC(CC1(C)O)O)(C)C 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Guaianolides and derivatives
(3As,6R,6Ar,9R,9As,9Bs)-6,9-Dihydroxy-6,9-Dimethyl-3-Methylenedecahydroazuleno(4,5-B)Furan-2(9Bh)-One 5319198 Click to see 266.33 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,3aR,5aR,5bR,7aR,11aR,11bR,13aR,13bS)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-2,3,4,5,6,7,7a,10,11,11b,12,13,13a,13b-tetradecahydro-1H-cyclopenta[a]chrysen-9-one 7092730 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.54.1308
(3aR,5aR,5bR,7aR,11aR,11bR,13aS)-3a,5a,5b,8,8,11a-hexamethyl-1-propan-2-yl-3,4,5,6,7,7a,10,11,11b,12,13,13a-dodecahydro-2H-cyclopenta[a]chrysen-9-one 17751023 Click to see 424.70 unknown via CMAUP database
(5R,9R,10R,13S,14S)-17-[4-(3,3-dimethyloxiran-2-yl)-4-hydroxybutan-2-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 137706645 Click to see CC(CC(C1C(O1)(C)C)O)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C 456.70 unknown https://doi.org/10.1016/0031-9422(92)80285-M
(5R,9S,10R,13S,14S,17R)-17-[(3S)-5-hydroxy-6-(2-hydroxypropan-2-yl)oxan-3-yl]-4,4,10,13,14-pentamethyl-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-3-one 129316918 Click to see CC1(C2CC=C3C(C2(CCC1=O)C)CCC4(C3(CCC4C5CC(C(OC5)C(C)(C)O)O)C)C)C 472.70 unknown https://doi.org/10.1016/0031-9422(92)80285-M
CID 14021529 14021529 Click to see CC(CC(C1C(O1)(C)C)O)C2CCC3(C2(CCC4C3=CCC5C4(CCC(=O)C5(C)C)C)C)C 456.70 unknown https://doi.org/10.1016/0031-9422(92)80285-M
Dihydroniloticin 73351981 Click to see 458.70 unknown https://doi.org/10.1016/0031-9422(92)80285-M
Epilupeol 5270628 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 unknown via CMAUP database
Friedelan-3-one 244297 Click to see 426.70 unknown via CMAUP database
Hispidol B 13967183 Click to see CC(CC(C(C(C)(C)O)O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(C4(C)C)O)C)C)C 476.70 unknown https://doi.org/10.1016/0031-9422(92)80285-M
Hispidone 21603613 Click to see 472.70 unknown https://doi.org/10.1016/0031-9422(92)80285-M
Lup-20(29)-en-3-one 323075 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1248/CPB.54.1308
https://doi.org/10.1021/NP030034V
Lupenone 92158 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(=O)C(C5CCC4(C3(CC2)C)C)(C)C)C)C 424.70 unknown https://doi.org/10.1021/NP030034V
https://doi.org/10.1248/CPB.54.1308
Niloticin 44559946 Click to see 456.70 unknown via CMAUP database
Piscidinol A 12004524 Click to see 474.70 unknown https://doi.org/10.1016/0031-9422(92)80285-M
Triterpenoid 451674 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)COS(=O)(=O)O)O)C)C)C2C1)C)C(=O)O)C 552.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
(1R,2R,4S,7R,8S,11S,12R,18S)-7-[(2R)-2-hydroxy-5-oxo-2H-furan-4-yl]-1,8,12,17,17-pentamethyl-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-ene-5,15,20-trione 163185492 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=CC(OC6=O)O)C)C)C 486.50 unknown https://doi.org/10.1080/00021369.1989.10869702
(1R,2R,4S,7R,8S,11S,12R,18S)-7-[(2S)-2-hydroxy-5-oxo-2H-furan-3-yl]-1,8,12,17,17-pentamethyl-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-ene-5,15,20-trione 162912722 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=CC(=O)OC6O)C)C)C 486.50 unknown https://doi.org/10.1080/00021369.1989.10869702
(1R,2R,4S,7R,8S,12R)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-3,6,16-trioxapentacyclo[9.9.02,4.02,8.012,18]icos-13-ene-5,15,20-trione 11331977 Click to see 454.50 unknown via CMAUP database
(1R,2R,4S,7S,8S,11S,12R,18S)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-ene-5,15,20-trione 38349717 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=COC=C6)C)C)C 454.50 unknown https://doi.org/10.1080/00021369.1989.10869702
(1R,2R,7S,10S,13R,14R,16S,19S,20S)-19-(furan-3-yl)-9,9,13,20-tetramethyl-4,8,15,18-tetraoxahexacyclo[11.9.0.02,7.02,10.014,16.014,20]docosane-5,12,17-trione 92966492 Click to see 470.50 unknown https://doi.org/10.1080/00021369.1989.10869702
[(1R,2R,3S,8R,10R,11R,15R,16S)-3-acetyloxy-15-(furan-3-yl)-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-en-10-yl] acetate 162965991 Click to see CC(=O)OC1CC2C(OC(=O)CC(C2(C3C1(C4=CCC(C4(CC3)C)C5=COC=C5)C)C)OC(=O)C)(C)C 512.60 unknown https://doi.org/10.1016/0031-9422(92)80285-M
[(1R,2R,3S,8R,10R,11R,15S,16S)-3-acetyloxy-2,7,7,11,16-pentamethyl-5-oxo-15-[(3S)-5-oxooxolan-3-yl]-6-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-en-10-yl] acetate 162958532 Click to see 530.60 unknown https://doi.org/10.1016/0031-9422(92)80285-M
[(1R,2R,8S,11S,12R,18S)-7-(furan-3-yl)-1,8,12,17,17-pentamethyl-5,15,20-trioxo-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icosan-13-yl] acetate 137706495 Click to see 514.60 unknown https://doi.org/10.1248/YAKUSHI1947.112.5_343
[(2R,11R)-3-acetyloxy-15-(furan-3-yl)-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-en-10-yl] acetate 374817 Click to see 512.60 unknown https://doi.org/10.1016/0031-9422(92)80285-M
[3-Acetyloxy-15-(furan-3-yl)-2,7,7,11,16-pentamethyl-5-oxo-6-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-en-10-yl] acetate 5106406 Click to see 512.60 unknown https://doi.org/10.1016/0031-9422(92)80285-M
[3-Acetyloxy-2,7,7,11,16-pentamethyl-5-oxo-15-(5-oxooxolan-3-yl)-6-oxatetracyclo[9.7.0.02,8.012,16]octadec-12-en-10-yl] acetate 3806949 Click to see 530.60 unknown https://doi.org/10.1016/0031-9422(92)80285-M
1-(Acetyloxy)-1,2-dihydroobacunoic acid eta-lactone 326240 Click to see 514.60 unknown https://doi.org/10.1248/YAKUSHI1947.112.5_343
7-(2-hydroxy-5-oxo-2H-furan-3-yl)-1,8,12,17,17-pentamethyl-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-ene-5,15,20-trione 14459786 Click to see 486.50 unknown https://doi.org/10.1080/00021369.1989.10869702
7-(2-hydroxy-5-oxo-2H-furan-4-yl)-1,8,12,17,17-pentamethyl-3,6,16-trioxapentacyclo[9.9.0.02,4.02,8.012,18]icos-13-ene-5,15,20-trione 14459787 Click to see 486.50 unknown https://doi.org/10.1080/00021369.1989.10869702
Casimirolide 500031 Click to see 454.50 unknown https://doi.org/10.1248/YAKUSHI1881.1927.550_1035
https://doi.org/10.1080/00021369.1989.10869702
Evodia fruit 235284 Click to see 470.50 unknown https://doi.org/10.1021/NP030034V
https://doi.org/10.1080/00021369.1989.10869702
Kihadalactone B 374818 Click to see CC(=O)OC1CC2C(OC(=O)CC(C2(C3C1(C4=CCC(C4(CC3)C)C5CC(=O)OC5)C)C)OC(=O)C)(C)C 530.60 unknown https://doi.org/10.1016/0031-9422(92)80285-M
Kihadanin A 180311 Click to see CC1(C2CC(=O)C3(C(C2(C=CC(=O)O1)C)CCC4(C35C(O5)C(=O)OC4C6=CC(=O)OC6O)C)C)C 486.50 unknown https://doi.org/10.1271/BBB1961.53.2635
Kihadanin B 156766 Click to see 486.50 unknown https://doi.org/10.1248/YAKUSHI1947.105.8_742
https://doi.org/10.1271/BBB1961.53.2635
Limonin 179651 Click to see 470.50 unknown https://doi.org/10.1248/CPB.38.2332
https://doi.org/10.1021/NP030034V
https://doi.org/10.1271/BBB1961.53.2635
https://doi.org/10.1248/YAKUSHI1947.112.5_343
https://doi.org/10.1248/YAKUSHI1947.105.8_742
Obacunone 119041 Click to see 454.50 unknown https://doi.org/10.1248/CPB.38.2332
https://doi.org/10.1248/YAKUSHI1947.105.8_742
https://doi.org/10.1248/YAKUSHI1881.1927.550_1035
https://doi.org/10.1271/BBB1961.53.2635
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Androstane steroids / Androgens and derivatives
16-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 53399246 Click to see CCC(CCC(C)C1CC2C3CC=C4CC(CCC4(C3CCC2(C1)C)C)O)C(C)C 414.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(8R,9S,10S,13R,14S,17R)-17-((2R,5R)-5,6-Dimethylheptan-2-yl)-10,13-dimethyl-4,5,6,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-ol 51051617 Click to see 400.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid acids
3-[(3S,4S,5R,8R,9R,10R,13R,14R,15R)-4,9,10,13-tetramethyl-3-propan-2-yl-15-prop-1-en-2-yl-2,3,5,6,7,8,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-4-yl]propanoic acid 101449266 Click to see 442.70 unknown https://doi.org/10.1021/NP030034V
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid esters
Campesteryl Ferulate 15056832 Click to see 576.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones
(2E)-3-[(3aS,5aR,6R,7R,9aR,9bR,10aS)-3-(Furan-3-yl)-7-(2-hydroxypropan-2-yl)-3a,6,9a-trimethyl-1,9-dioxododecahydronaphtho[2,1-c]oxireno[d]pyran-6-yl]prop-2-enoic acid 54611038 Click to see 472.50 unknown via CMAUP database
(3R,5S,7R,9S,10S,12R,14R,15S,16S,18R,19R,22S,23R)-10,16,22-trihydroxy-9-methoxy-7,14,18-trimethyl-19-(5-oxo-2H-furan-3-yl)-4,6,11-trioxahexacyclo[12.11.0.03,12.05,10.015,23.018,22]pentacos-1-en-17-one 162960422 Click to see 560.60 unknown https://doi.org/10.1248/CPB.54.1308
(E)-3-[(1R,2R,5R,6R,7R,10S,11S,14S)-11-(furan-3-yl)-5-(2-hydroxypropan-2-yl)-2,6,10-trimethyl-3,13-dioxo-12,15-dioxatetracyclo[8.5.0.01,14.02,7]pentadecan-6-yl]prop-2-enoic acid 21140842 Click to see CC12CCC3C(C(CC(=O)C3(C14C(O4)C(=O)OC2C5=COC=C5)C)C(C)(C)O)(C)C=CC(=O)O 472.50 unknown via CMAUP database
Obacunoic acid 44144270 Click to see CC12CCC3C(C(CC(=O)C3(C14C(O4)C(=O)OC2C5=COC=C5)C)C(C)(C)O)(C)C=CC(=O)O 472.50 unknown via CMAUP database
Obacunoic acid 44575842 Click to see 472.50 unknown via CMAUP database
Rutaevin 441805 Click to see CC1(C2C(=O)C(C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)O)C 486.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
[(3S,5R,8R,9S,10S,13R,14S,16R,17R)-14-hydroxy-3-[(2R,3R,4R,5R,6R)-3-hydroxy-4-methoxy-6-methyl-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-16-yl] acetate 162960746 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CC(C5C6=CC(=O)OC6)OC(=O)C)O)C)C)O)OC)OC7C(C(C(C(O7)CO)O)O)O 754.90 unknown https://doi.org/10.1021/NP970406Y
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 222284 Click to see 414.70 unknown via CMAUP database
(3S,8R,9R,10S,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 636741 Click to see 414.70 unknown via CMAUP database
17-(5-ethyl-6-methylhept-3-en-2-yl)-10,13-dimethyl-2,3,4,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-3-ol 101705 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2=CC=C4C3(CCC(C4)O)C)C)C(C)C 410.70 unknown https://doi.org/10.1248/YAKUSHI1947.78.12_1432
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1021/NP030034V
28-Isofucostanol 52931386 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
delta7-Stigmasterol 12303924 Click to see 410.70 unknown https://doi.org/10.1248/YAKUSHI1947.78.12_1432
Npc29 6432744 Click to see 414.70 unknown via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Alpha-keto acids and derivatives
2-(4-Methoxycyclohexa-1,3-dien-1-yl)-2-oxoacetic acid 29927927 Click to see 182.17 unknown via CMAUP database
> Organic nitrogen compounds / Organonitrogen compounds / Guanidines
(11C)guanidine 451298 Click to see C(=N)(N)N 58.07 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclitols and derivatives / Quinic acids and derivatives
1,3,4-Trihydroxy-5-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]cyclohexane-1-carboxylic acid 73210496 Click to see 368.30 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
3-O-Feruloylquinic acid 9799386 Click to see 368.30 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
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
methyl (1R,3R,4S,5R)-1,3,4-trihydroxy-5-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]cyclohexane-1-carboxylate 163102349 Click to see 382.40 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
Methyl 1,3,4-trihydroxy-5-[3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyloxy]cyclohexane-1-carboxylate 74323583 Click to see 382.40 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
Methyl 3-O-feruloylquinate 24813764 Click to see 382.40 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
Methyl 5-O-feruloylquinate 102004731 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2CC(CC(C2O)O)(C(=O)OC)O)O 382.40 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
Neochlorogenic acid 5280633 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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-[2-(4-hydroxyphenyl)ethoxy]oxane-3,4,5-triol 78173774 Click to see C1C(C(C(O1)OCC2C(C(C(C(O2)OCCC3=CC=C(C=C3)O)O)O)O)O)(CO)O 432.40 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
Osmanthuside H 192437 Click to see 432.40 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(Z)-Coniferin 91895380 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown via CMAUP database
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2-methoxyphenoxy]oxane-3,4,5-triol 3496897 Click to see 342.34 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see 372.40 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
2-(Hydroxymethyl)-6-[4-(hydroxymethyl)-2-methoxyphenoxy]oxane-3,4,5-triol 69086659 Click to see COC1=C(C=CC(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
3-[3,5-Dimethoxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-enal 74413484 Click to see 370.40 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
Coniferin 5280372 Click to see COC1=C(C=CC(=C1)C=CCO)OC2C(C(C(C(O2)CO)O)O)O 342.34 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
Sinapaldehyde glucoside 25791064 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CC=O 370.40 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
Syringin 5316860 Click to see 372.40 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
Vanilloloside 44577222 Click to see COC1=C(C=CC(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O 316.30 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aryl ketones / Aryl alkyl ketones
1-(5-Methoxyfuran-2-yl)ethanone 67092398 Click to see CC(=O)C1=CC=C(O1)OC 140.14 unknown https://doi.org/10.1248/CPB.54.1308
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see 122.12 unknown https://doi.org/10.1248/CPB.54.1308
4-Hydroxybenzaldehyde-d5 10701848 Click to see C1=CC(=CC=C1C=O)O 127.15 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
Tubocurarine 6000 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C6C(CC7=CC(=C(C=C7)O)O3)[N+](CCC6=CC(=C5O)OC)(C)C)OC 609.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzazepines
Chilenine 11025386 Click to see 383.40 unknown via CMAUP database
> Organoheterocyclic compounds / Diazanaphthalenes / Naphthyridines
7,13-Diazatetracyclo[7.7.1.02,7.013,17]heptadeca-1(16),2,4-trien-6-one 5316467 Click to see 242.32 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(11S,12R)-11,12-dihydroxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4,6,8,15,17,19-octaen-14-one 10734375 Click to see 319.30 unknown https://doi.org/10.1021/NP970406Y
(12S)-12-hydroxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4,6,8,15,17,19-octaen-14-one 101917472 Click to see C1C(N2C(=NC3=CC=CC=C3C2=O)C4=C1C5=CC=CC=C5N4)O 303.30 unknown https://doi.org/10.1021/NP970406Y
11,12-Dihydroxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4,6,8,15,17,19-octaen-14-one 162920285 Click to see 319.30 unknown https://doi.org/10.1021/NP970406Y
19-Hydroxy-3,13,21-triazapentacyclo[11.8.0.02,10.04,9.015,20]henicosa-1(21),2(10),4,6,8,11,15(20),16,18-nonaen-14-one 13971001 Click to see 301.30 unknown https://doi.org/10.1021/NP970406Y
7,8-Dehydrorutaecarpine 148756 Click to see C1=CC=C2C(=C1)C3=C(N2)C4=NC5=CC=CC=C5C(=O)N4C=C3 285.30 unknown https://doi.org/10.1016/S0031-9422(97)01130-8
7beta-Hydroxyrutaecarpine 15225951 Click to see 303.30 unknown https://doi.org/10.1021/NP970406Y
8,13,13b,14-Tetrahydroindolo[2',3':3,4]pyrido[2,1-b]quinazolin-5(7H)-one 13970999 Click to see C1CN2C(C3=C1C4=CC=CC=C4N3)NC5=CC=CC=C5C2=O 289.30 unknown via CMAUP database
Evodiamine 442088 Click to see 303.40 unknown via CMAUP database
Isoevodiamine 151289 Click to see CN1C2C3=C(CCN2C(=O)C4=CC=CC=C41)C5=CC=CC=C5N3 303.40 unknown via CMAUP database
Rutaecarpine 65752 Click to see 287.30 unknown https://doi.org/10.1021/NP970406Y
https://doi.org/10.1016/S0031-9422(97)01130-8
> Organoheterocyclic compounds / Isoquinolines and derivatives
793JX7VC6J 457914 Click to see 321.30 unknown https://doi.org/10.1016/0021-9673(93)83021-J
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1S)-1-[(4-hydroxyphenyl)methyl]-7-methoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-8-ol 173713 Click to see C[N+]1(CCC2=C(C1CC3=CC=C(C=C3)O)C(=C(C=C2)OC)O)C 314.40 unknown via CMAUP database
(2S,3R,4S,5S,6R)-2-[[(1R)-6-hydroxy-1-[(4-hydroxyphenyl)methyl]-2-methyl-3,4-dihydro-1H-isoquinolin-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163040028 Click to see 447.50 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
2-[[6-hydroxy-1-[(4-hydroxyphenyl)methyl]-2-methyl-3,4-dihydro-1H-isoquinolin-7-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163040027 Click to see 447.50 unknown https://doi.org/10.1016/S0031-9422(00)90536-3
3,4-Dimethoxy-2-(5-oxo-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinoline-6-carbonyl)benzoic acid 101390624 Click to see 399.30 unknown https://doi.org/10.3987/COM-05-10598
Lotusine 5274587 Click to see 314.40 unknown via CMAUP database
Magnocurarine 53266 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC)C 314.40 unknown via CMAUP database
Methyl 3,4-dimethoxy-2-(5-oxo-7,8-dihydro-[1,3]dioxolo[4,5-g]isoquinoline-6-carbonyl)benzoate 21581113 Click to see 413.40 unknown https://doi.org/10.3987/COM-05-10598
Tembetarine 167718 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC)C 344.40 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 10065647 Click to see 337.40 unknown https://doi.org/10.1055/S-2006-959761
https://doi.org/10.1016/S0031-9422(97)01130-8
https://doi.org/10.1080/01483919008049572
Noroxyhydrastinine 89047 Click to see C1CNC(=O)C2=CC3=C(C=C21)OCO3 191.18 unknown via CMAUP database
> Organoheterocyclic compounds / Quinolines and derivatives / Furanoquinolines
Dictamnine 68085 Click to see 199.20 unknown https://doi.org/10.1016/S0031-9422(97)01130-8
Gamma-Fagarine 107936 Click to see 229.23 unknown https://doi.org/10.1016/S0031-9422(97)01130-8
Pteleine 159650 Click to see 229.23 unknown via CMAUP database
Skimmianine 6760 Click to see COC1=C(C2=C(C=C1)C(=C3C=COC3=N2)OC)OC 259.26 unknown https://doi.org/10.1016/S0031-9422(97)01130-8
> Organoheterocyclic compounds / Quinolines and derivatives / Quinolones and derivatives / Pyranoquinolines
N-Methylflindersine 72819 Click to see 241.28 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
3,4-Dihydroxycinnamic acid methyl ester 92202 Click to see 194.18 unknown https://doi.org/10.1248/CPB.54.1308
Ethyl Caffeate 5317238 Click to see 208.21 unknown via CMAUP database
Methyl Caffeate 689075 Click to see 194.18 unknown https://doi.org/10.1248/CPB.54.1308
https://doi.org/10.1021/NP030034V
Paprazine 5372945 Click to see 283.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
3-(4-Hydroxy-3-Methoxyphenyl)Prop-2-Enoic Acid 709 Click to see 194.18 unknown https://doi.org/10.1248/CPB.54.1308
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
Ferulic Acid 445858 Click to see 194.18 unknown https://doi.org/10.1248/CPB.54.1308
> Phenylpropanoids and polyketides / Coumarins and derivatives
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1248/CPB.54.1308
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
6-(4-Hydroxy-3-methylbut-2-enyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 73239314 Click to see CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)CO 408.40 unknown https://doi.org/10.1248/CPB.54.1308
6-[(Z)-4-hydroxy-3-methylbut-2-enyl]-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 16088227 Click to see CC(=CCC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O)CO 408.40 unknown https://doi.org/10.1248/CPB.54.1308
7-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 22816386 Click to see C1=CC(=CC2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 324.28 unknown https://doi.org/10.1248/CPB.54.1308
7-[3,4,5-Trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-2-one 320361 Click to see C1=CC(=CC2=C1C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 324.28 unknown https://doi.org/10.1248/CPB.54.1308
Skimmin 99693 Click to see 324.28 unknown https://doi.org/10.1248/CPB.54.1308
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Angular furanocoumarins
(-)-Columbianetin 442104 Click to see CC(C)(C1CC2=C(O1)C=CC3=C2OC(=O)C=C3)O 246.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Trioxsalen 5585 Click to see CC1=CC(=O)OC2=C1C=C3C=C(OC3=C2C)C 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Phellopterin 98608 Click to see CC(=CCOC1=C2C(=C(C3=C1OC(=O)C=C3)OC)C=CO2)C 300.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see 178.14 unknown https://doi.org/10.1248/CPB.54.1308
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
6-[(1R,2R)-2-hydroperoxy-1,3-dihydroxy-3-methylbutyl]-7-hydroxychromen-2-one 163032880 Click to see CC(C)(C(C(C1=C(C=C2C(=C1)C=CC(=O)O2)O)O)OO)O 296.27 unknown https://doi.org/10.1248/CPB.54.1308
6-[(1S,2S)-2-hydroperoxy-1,3-dihydroxy-3-methylbutyl]-7-hydroxychromen-2-one 163032879 Click to see CC(C)(C(C(C1=C(C=C2C(=C1)C=CC(=O)O2)O)O)OO)O 296.27 unknown https://doi.org/10.1248/CPB.54.1308
6-But-2-enyl-7-hydroxychromen-2-one 162925430 Click to see CC=CCC1=C(C=C2C(=C1)C=CC(=O)O2)O 216.23 unknown https://doi.org/10.1248/CPB.54.1308
7-Hydroxy-5-(3-methylbut-2-enyl)chromen-2-one 129539824 Click to see 230.26 unknown https://doi.org/10.1248/CPB.54.1308
7-Hydroxy-6-(2-(R)-Hydroxy-3-Methylbut-3-Enyl)Coumarin 12050842 Click to see 246.26 unknown https://doi.org/10.1248/CPB.54.1308
7-Hydroxy-6-(2-hydroxy-3-methylbut-3-enyl)chromen-2-one 85433263 Click to see 246.26 unknown https://doi.org/10.1248/CPB.54.1308
7-hydroxy-6-[2-[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]chromen-2-one 162902712 Click to see 368.30 unknown https://doi.org/10.1248/CPB.54.1308
7-Hydroxy-6-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]chromen-2-one 73239315 Click to see 368.30 unknown https://doi.org/10.1248/CPB.54.1308
7-Hydroxy-8-(2-hydroxy-3-methylbut-3-enyl)chromen-2-one 131836751 Click to see CC(=C)C(CC1=C(C=CC2=C1OC(=O)C=C2)O)O 246.26 unknown https://doi.org/10.1021/NP030034V
7-Hydroxy(~2~H_5_)-2H-1-benzopyran-2-one 45358955 Click to see 167.17 unknown via CMAUP database
Osthenol 5320318 Click to see 230.26 unknown https://doi.org/10.1021/NP030034V
Phellodenol A 10910685 Click to see 206.19 unknown https://doi.org/10.1021/NP030034V
https://doi.org/10.1248/CPB.54.1308
Phellodenol C 10879399 Click to see 246.26 unknown https://doi.org/10.1021/NP030034V
Phellodenol F 16088226 Click to see CC(C)(C(C(C1=C(C=C2C(=C1)C=CC(=O)O2)O)O)OO)O 296.27 unknown https://doi.org/10.1248/CPB.54.1308
Phellodenol H 16088228 Click to see 368.30 unknown https://doi.org/10.1248/CPB.54.1308
Scopoletin 5280460 Click to see 192.17 unknown https://doi.org/10.1021/NP030034V
https://doi.org/10.1248/CPB.54.1308
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1248/CPB.54.1308
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Seselin 68229 Click to see 228.24 unknown https://doi.org/10.1021/NP030034V
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown https://doi.org/10.1248/CPB.54.1308
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2R,3R,8R)-3,5-dihydroxy-2-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-2,3,8,9-tetrahydrofuro[2,3-h]chromen-4-one 162876709 Click to see CC(C)(C1CC2=C(O1)C=C(C3=C2OC(C(C3=O)O)C4=CC=C(C=C4)O)O)O 372.40 unknown https://doi.org/10.1021/NP030034V
3,5-Dihydroxy-2-(4-hydroxyphenyl)-8-(2-hydroxypropan-2-yl)-2,3,8,9-tetrahydrofuro[2,3-h]chromen-4-one 85375185 Click to see 372.40 unknown https://doi.org/10.1021/NP030034V
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-8-(3-methyl-2-butenyl)-2,3-dihydro-4H-chromen-4-one 368925 Click to see 356.40 unknown https://doi.org/10.1021/NP030034V
Neophellamuretin 101643010 Click to see CC(=CCC1=C2C(=C(C=C1O)O)C(=O)C(C(O2)C3=CC=C(C=C3)O)O)C 356.40 unknown https://doi.org/10.1021/NP030034V
Phellodensin A 10937119 Click to see 354.40 unknown https://doi.org/10.1021/NP030034V
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
3,5,7-Trihydroxy-2-(4-Hydroxyphenyl)Chroman-4-One 662 Click to see 288.25 unknown https://doi.org/10.1021/NP030034V
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1021/NP030034V
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Quercetin-7-olate 46906036 Click to see 301.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
Noricaritin 14427423 Click to see 372.40 unknown https://doi.org/10.1021/JA01118A013
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see 286.24 unknown https://doi.org/10.1248/CPB.54.1308
Quercetin 5280343 Click to see 302.23 unknown https://doi.org/10.1248/CPB.54.1308
https://doi.org/10.1021/NP030034V
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
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/10.1021/NP030034V
https://doi.org/10.1248/CPB.54.1308
2-(3,4-dihydroxyphenyl)-5,7-dihydroxy-3-[(2S,3S,4R,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 51521831 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1248/CPB.54.1308
5-hydroxy-2-(4-hydroxyphenyl)-8,8-dimethyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,9,10-tetrahydropyrano[2,3-h]chromen-4-one 101316827 Click to see 518.50 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxychromen-4-one 12047524 Click to see 432.40 unknown https://doi.org/10.1248/CPB.54.1308
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/10.1021/NP030034V
https://doi.org/10.1248/CPB.54.1308
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/10.1021/NP030034V
https://doi.org/10.1248/CPB.54.1308
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown https://doi.org/10.1248/CPB.54.1308
Isoquercetin 5280804 Click to see 464.40 unknown https://doi.org/10.1021/NP030034V
https://doi.org/10.1248/CPB.54.1308
Quercetin 3-alloside 12304327 Click to see 464.40 unknown https://doi.org/10.1248/CPB.54.1308
Trifolin 5282149 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/10.1248/CPB.54.1308
https://doi.org/10.1021/NP030034V
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
(2R)-5-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 11641873 Click to see 502.50 unknown via CMAUP database
(2R)-5-hydroxy-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[4-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-2,3-dihydrochromen-4-one 162953842 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)C 664.60 unknown https://doi.org/10.1248/CPB.54.1308
(2S,3R)-3,5-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 7163183 Click to see 518.50 unknown https://doi.org/10.1007/BF02035150
https://doi.org/10.1021/JA01118A013
3,5-dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14756216 Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)C 516.50 unknown https://doi.org/10.1021/JA01118A013
3,5-Dihydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 14756215 Click to see 516.50 unknown https://doi.org/10.1021/JA01118A013
3,5-dihydroxy-6-(3-hydroxy-3-methylbutyl)-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one 5320517 Click to see CC(C)(CCC1=C(C=C2C(=C1O)C(=O)C(C(O2)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 536.50 unknown via CMAUP database
3,5-dihydroxy-8-(3-hydroxy-3-methylbutyl)-2-(4-hydroxyphenyl)-7-[(2S,4S,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 44258795 Click to see 534.50 unknown via CMAUP database
3,5-Dihydroxy-8-(3-hydroxy-3-methylbutyl)-2-(4-hydroxyphenyl)-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 12306115 Click to see 534.50 unknown https://doi.org/10.1021/NP030034V
https://doi.org/10.1248/CPB.54.1308
5-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-3,7-bis[[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]chromen-4-one 162972317 Click to see 678.60 unknown https://doi.org/10.1248/CPB.54.1308
5-hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-3,7-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]chromen-4-one 15126644 Click to see CC(=CCC1=C(C=C(C2=C1OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O)O)OC5C(C(C(C(O5)CO)O)O)O)C 678.60 unknown https://doi.org/10.1248/CPB.54.1308
5-Hydroxy-2-(4-hydroxyphenyl)-8-(3-methylbut-2-enyl)-3,7-bis[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]chromen-4-one 74978007 Click to see 678.60 unknown https://doi.org/10.1248/CPB.54.1308
Amurensin 5318156 Click to see 534.50 unknown https://doi.org/10.1248/CPB.54.1308
evodioside B 162953844 Click to see 664.60 unknown https://doi.org/10.1248/CPB.54.1308
Fellavin; Flacoside 3313578 Click to see 518.50 unknown https://doi.org/10.1007/BF02035150
https://doi.org/10.1007/S10886-011-9965-9
https://doi.org/10.1248/CPB.54.1308
https://doi.org/10.1021/JA01118A013
Flavaprenin 7,4'-diglucoside 42607894 Click to see CC(=CCC1=C(C=C(C2=C1OC(CC2=O)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)C 664.60 unknown https://doi.org/10.1248/CPB.54.1308
Phellamurin 193876 Click to see CC(=CCC1=C(C=C(C2=C1OC(C(C2=O)O)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)C 518.50 unknown https://doi.org/10.1007/S10886-011-9965-9
https://doi.org/10.1021/NP030034V
https://doi.org/10.1248/CPB.54.1308
Phellatin 44258781 Click to see CC(C)(CCC1=C(C=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 534.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Pyranoflavonoids
Yukovanol 44584009 Click to see 354.40 unknown https://doi.org/10.1021/NP030034V
> Phenylpropanoids and polyketides / Stilbenes
4-((Z)-2-(3-Methoxyphenyl)Ethenyl)Phenol 5469252 Click to see 226.27 unknown via CMAUP database

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