Hovenia dulcis - Seed
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Author: Sorin

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Internal ID UUID644020e29031a044558996
Scientific name Hovenia dulcis
Authority Thunb.
First published in Nov. Gen. Pl. : 8 (1781)

Description Top

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Hovenia dulcis, also known as the Japanese or oriental raisin tree, is a hardy tree found in Asia. It can grow up to 30 meters tall and is typically found in sunny, moist areas with sandy or loamy soil. The tree is known for its health benefits when consumed in tea and is also grown as an ornamental tree. It produces small, cream-colored flowers and edible fruit. The fruit stalks are sweet and can be eaten raw or dried, resembling raisins. The tree's timber is used for construction and furniture. In traditional medicine, it has been used to treat various ailments. In Thailand, it is being considered as a substitute for Eucalyptus trees in reforestation efforts due to its rapid growth and ability to promote biodiversity and soil fertility. It has also been given various scientific names, including Hovenia acerba and Hovenia inequalis.

Synonyms Top

Scientific name Authority First published in
Hovenia dulcis var. glabra Makino Bot. Mag. (Tokyo) 28: 155 1914
Hovenia dulcis var. tomentella Makino Bot. Mag. (Tokyo) 28: 156 1914
Hovenia pubescens Sweet Hort. Brit. : 91 (1826)
Hovenia dulcis var. latifolia Nakai ex Y.Kimura Fl. Jap. 476 1939

Common names Top

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Language Common/alternative name
English japanese raisin tree
English japanese raisintree
English oriental raisin tree
Spanish oriental raisin tree
Spanish japanese raisin tree
ab Акамфеҭҵла
Afrikaans japanse rosyntjieboom
Arabic هوفينية حلوة
Azerbaijani Şirin hoveniya
Catalan arbre de les panses
German japanischer rosinenbaum
Finnish japanillainen rusinapuu
Finnish itämainen rusinapuu
Finnish hovenia
French raisinier de chine
Hebrew עץ הצימוק היפני
Armenian Կոնֆետի ծառ
Italian albero dell'uva passa
Japanese ケンポナシ
Korean 헛개나무
Polish drzewo rodzynkowe
Polish howenia słodka
Portuguese cajueiro-japonês
Russian Конфетное дерево
Russian говения сладкая
Russian конфетное дерево
Serbian Ховенија
Swedish japanskt russinträd
Swedish orientaliskt russinträd
Turkish Şeker ağacı
Uzbek konfet daraxti
xmf ჰოვენია გემუანი
xmf კამფეტიშ ჯა
Chinese 鸡爪梨
Chinese 甜半夜
Chinese 枳椇子
Chinese 拐枣
Chinese 枳椇
Chinese 枳棋子
Chinese 北枳椇

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Hovenia dulcis var. crassifolia Konta Bull. Natl. Sci. Mus. Tokyo, B 31: 147 (2005)

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • East Himalaya
      • India
      • West Himalaya
    • Indo-China
      • Thailand
      • Vietnam
  • Northern America
    • South-central U.S.A.
      • Texas
    • Southeastern U.S.A.
      • North Carolina
  • Southern America
    • Brazil
      • Brazil Northeast
      • Brazil South
      • Brazil Southeast
    • Central America
      • Honduras
    • Southern South America
      • Argentina Northeast
      • Paraguay
    • Western South America
      • Peru

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000725083
UNII 1DM83BAP2N
USDA Plants HODU2
UConn 206
Tropicos 27500165
INPN 448325
KEW urn:lsid:ipni.org:names:717558-1
The Plant List kew-2853957
PFAF Hovenia dulcis
PaleoBotany 49819
Open Tree Of Life 870613
NCBI Taxonomy 99292
Nature Serve 2.129573
IUCN Red List 147482976
IPNI 717558-1
iNaturalist 163847
GBIF 3039410
Freebase /m/02q6_7r
EPPO HOVDU
EOL 582359
USDA GRIN 19387
Wikipedia Hovenia_dulcis

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
The complete chloroplast genome sequence of Rhamnella wilsonii Schneid (Rhamnaceae) Wang G, An J, Si J Mitochondrial DNA B Resour 12-Apr-2024
PMCID:PMC11018004
doi:10.1080/23802359.2024.2339492
PMID:38623175
Hovenia dulcis Fruit Peduncle Polysaccharides Reduce Intestinal Dysbiosis and Hepatic Fatty Acid Metabolism Disorders in Alcohol-Exposed Mice Liu L, Zhu S, Zhang Y, Zhu Z, Xue Y, Liu X Foods 09-Apr-2024
PMCID:PMC11049514
doi:10.3390/foods13081145
PMID:38672817
Hovenia dulcis: a Chinese medicine that plays an essential role in alcohol-associated liver disease He YX, Liu MN, Wang YY, Wu H, Wei M, Xue JY, Zou Y, Zhou X, Chen H, Li Z Front Pharmacol 08-Apr-2024
PMCID:PMC11033337
doi:10.3389/fphar.2024.1337633
PMID:38650630
Classification, biosynthesis, and biological functions of triterpene esters in plants Liu J, Yin X, Kou C, Thimmappa R, Hua X, Xue Z Plant Commun 13-Feb-2024
PMCID:PMC11009366
doi:10.1016/j.xplc.2024.100845
PMID:38356259
Application and mechanisms of Sanhua Decoction in the treatment of cerebral ischemia-reperfusion injury Wang YK, Lin H, Wang SR, Bian RT, Tong Y, Zhang WT, Cui YL World J Clin Cases 06-Feb-2024
PMCID:PMC10841129
doi:10.12998/wjcc.v12.i4.688
PMID:38322692
Potential therapeutic target for polysaccharide inhibition of colon cancer progression Fan J, Zhu J, Zhu H, Zhang Y, Xu H Front Med (Lausanne) 08-Jan-2024
PMCID:PMC10804854
doi:10.3389/fmed.2023.1325491
PMID:38264044
Anti-Inflammatory Herbal Extracts and Their Drug Discovery Perspective in Atopic Dermatitis Lee JW, Kim EN, Jeong GS Biomol Ther (Seoul) 01-Jan-2024
PMCID:PMC10762282
doi:10.4062/biomolther.2023.102
PMID:38148551
The complete chloroplast genome of Ziziphus mairei Dode 1908 (Rhamnaceae), an endangered perennial plant in Yunnan, China Wang S, Liu Y, Li R, Wang S, Huang Y Mitochondrial DNA B Resour 24-Dec-2023
PMCID:PMC10763858
doi:10.1080/23802359.2023.2290844
PMID:38173918
Hovenia dulcis Suppresses the Growth of Huh7-Derived Liver Cancer Stem Cells by Inducing Necroptosis and Apoptosis and Blocking c-MET Signaling Kwon M, Jung HJ Cells 21-Dec-2023
PMCID:PMC10778038
doi:10.3390/cells13010022
PMID:38201226
Microwaves and Ultrasound as Emerging Techniques for Lignocellulosic Materials Fernandes A, Cruz-Lopes L, Esteves B, Evtuguin DV Materials (Basel) 25-Nov-2023
PMCID:PMC10706977
doi:10.3390/ma16237351
PMID:38068095
Protective Effects and Mechanism of Polysaccharides from Edible Medicinal Plants in Alcoholic Liver Injury: A Review Su ZW, Yan TY, Feng J, Zhang MY, Han L, Zhang HF, Xiao Y Int J Mol Sci 20-Nov-2023
PMCID:PMC10671977
doi:10.3390/ijms242216530
PMID:38003718
Reactive oxygen species (ROS)-mediated oxidative stress in chronic liver diseases and its mitigation by medicinal plants Sharma P, Nandave M, Nandave D, Yadav S, Vargas-De-La-Cruz C, Singh S, Tandon R, Ramniwas S, Behl T Am J Transl Res 15-Nov-2023
PMCID:PMC10703659
PMID:38074830
Applications and Market of Micro-Organism-Based and Plant-Based Inputs in Brazilian Agriculture Soares CR, Hernández AG, da Silva EP, de Souza JE, Bonfim DF, Zabot GL, Ferreira PA, Brunetto G Plants (Basel) 14-Nov-2023
PMCID:PMC10675046
doi:10.3390/plants12223844
PMID:38005741
Diversity of Leaf Glands and Their Putative Functions in Rhamnaceae Species Iwamoto L, Vicentini TA, Ramos FP, Ribeiro CC, Teixeira SP Plants (Basel) 31-Oct-2023
PMCID:PMC10647809
doi:10.3390/plants12213732
PMID:37960088
Pest categorisation of Pochazia shantungensis Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, 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, Grégoire J, Malumphy C, Kertesz V, Maiorano A, MacLeod A EFSA J 31-Oct-2023
PMCID:PMC10617311
doi:10.2903/j.efsa.2023.8320
PMID:37915980

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Ethyl decyl phthalate 525161 Click to see CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCC 306.40 unknown https://doi.org/10.1016/0031-9422(91)80044-2
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Methyl vanillate 19844 Click to see COC1=C(C=CC(=C1)C(=O)OC)O 182.17 unknown https://doi.org/10.1007/BF02977346
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown https://doi.org/10.1007/BF02977346
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides
(2S,3R,4S,5S,6R)-2-[(2E)-3,7-dimethylocta-2,6-dienoxy]-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxane-3,4,5-triol 6439502 Click to see CC(=CCCC(=CCOC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O)C)C 448.50 unknown https://doi.org/10.1016/0031-9422(91)80044-2
Kenposide B 192589 Click to see CC(=CCC(COC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O)C(=C)C)C 448.50 unknown https://doi.org/10.1016/0031-9422(91)80044-2
Lavandulyl 1-O-arabinopyranosyl-1-6-glucopyranoside 73753502 Click to see CC(=CCC(COC1C(C(C(C(O1)COC2C(C(C(CO2)O)O)O)O)O)O)C(=C)C)C 448.50 unknown https://doi.org/10.1016/0031-9422(91)80044-2
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
(1S,2S,4aR,4bR,7S,8aR,10aR)-2-[(2R,3S)-3-[(2R)-2-hydroxy-4-methylpent-3-enyl]-3-methyloxiran-2-yl]-4b,8,8,10a-tetramethyl-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[2,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene-1,4'-oxolane]-2'-one 162848719 Click to see CC(=CC(CC1(C(O1)C2CCC3C4(CCC(C(C4CCC3(C25CC(=O)OC5)C)(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C 650.80 unknown https://doi.org/10.1248/CPB.40.2287
(1S,2S,4aR,4bR,7S,8aR,10aR)-7-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-[(2S,3S)-3-[(2R)-2-hydroxy-4-methylpent-3-enyl]-3-methyloxiran-2-yl]-4b,8,8,10a-tetramethylspiro[2,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene-1,4'-oxolane]-2'-one 101634396 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC(C6(C5(CCC4C3(C)C)C)CC(=O)OC6)C7C(O7)(C)CC(C=C(C)C)O)C)CO)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O 959.10 unknown https://doi.org/10.1248/CPB.40.2287
(1S,2S,4aR,4bR,7S,8aR,10aR)-7-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-2-[(2S,3S)-3-[(2R)-2-hydroxy-4-methylpent-3-enyl]-3-methyloxiran-2-yl]-4b,8,8,10a-tetramethylspiro[2,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene-1,4'-oxolane]-2'-one 101634401 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC(C6(C5(CCC4C3(C)C)C)CC(=O)OC6)C7C(O7)(C)CC(C=C(C)C)O)C)CO)O)O)O)O)O 797.00 unknown https://doi.org/10.1248/CPB.40.2287
(1S,2S,4aR,4bR,7S,8aR,10aR)-7-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4b,8,8,10a-tetramethyl-2-[(2S,3S)-3-methyl-3-[(2R)-4-methyl-2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypent-3-enyl]oxiran-2-yl]spiro[2,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene-1,4'-oxolane]-2'-one 101634395 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC(C6(C5(CCC4C3(C)C)C)CC(=O)OC6)C7C(O7)(C)CC(C=C(C)C)OC8C(C(C(C(O8)CO)O)O)O)C)CO)O)O)O)O)O 959.10 unknown https://doi.org/10.1248/CPB.40.2287
[(2S,3R)-3-[(1S,2R,4aR,4bR,7S,8aR,10aR)-4b,8,8,10a-tetramethyl-2'-oxo-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[2,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene-1,4'-oxolane]-2-yl]-1-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]butan-2-yl] acetate 101998900 Click to see CC1=CC(OC1=O)CC(C(C)C2CCC3C4(CCC(C(C4CCC3(C25CC(=O)OC5)C)(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)OC(=O)C 706.90 unknown https://doi.org/10.1248/CPB.43.532
[(2S,3R)-3-[(1S,2R,4aR,4bR,7S,8aR,10aR)-7-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4b,8,8,10a-tetramethyl-2'-oxospiro[2,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene-1,4'-oxolane]-2-yl]-1-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]butan-2-yl] acetate 101998899 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC(C6(C5(CCC4C3(C)C)C)CC(=O)OC6)C(C)C(CC7C=C(C(=O)O7)C)OC(=O)C)C)CO)O)O)O)O)O 853.00 unknown https://doi.org/10.1248/CPB.43.532
[(2S,3R)-3-[(1S,2R,4aR,4bR,7S,8aS,10aR)-4b,8,8,10a-tetramethyl-2'-oxo-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[2,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene-1,4'-oxolane]-2-yl]-1-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]butan-2-yl] acetate 162905323 Click to see CC1=CC(OC1=O)CC(C(C)C2CCC3C4(CCC(C(C4CCC3(C25CC(=O)OC5)C)(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)OC(=O)C 706.90 unknown https://doi.org/10.1248/CPB.44.1736
[(2S,3R)-3-[(1S,2R,4aR,4bR,7S,8aS,10aR)-4b,8,8,10a-tetramethyl-2'-oxo-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[2,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene-1,4'-oxolane]-2-yl]-1-[(2S,4R)-4-methyl-5-oxooxolan-2-yl]butan-2-yl] acetate 162876806 Click to see CC1CC(OC1=O)CC(C(C)C2CCC3C4(CCC(C(C4CCC3(C25CC(=O)OC5)C)(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)OC(=O)C 708.90 unknown https://doi.org/10.1248/CPB.44.1736
[(2S,3R)-3-[(1S,2R,4aR,4bR,7S,8aS,10aR)-7-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4b,8,8,10a-tetramethyl-2'-oxospiro[2,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene-1,4'-oxolane]-2-yl]-1-[(2R)-4-methyl-5-oxo-2H-furan-2-yl]butan-2-yl] acetate 124871790 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC(C6(C5(CCC4C3(C)C)C)CC(=O)OC6)C(C)C(CC7C=C(C(=O)O7)C)OC(=O)C)C)CO)O)O)O)O)O 853.00 unknown https://doi.org/10.1248/CPB.44.1736
[(2S,3R)-3-[(1S,2R,4aR,4bR,7S,8aS,10aR)-7-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4b,8,8,10a-tetramethyl-2'-oxospiro[2,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene-1,4'-oxolane]-2-yl]-1-[(2S,4R)-4-methyl-5-oxooxolan-2-yl]butan-2-yl] acetate 162951955 Click to see CC1CC(OC1=O)CC(C(C)C2CCC3C4(CCC(C(C4CCC3(C25CC(=O)OC5)C)(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)C)O)O)O)C)OC(=O)C 855.00 unknown https://doi.org/10.1248/CPB.44.1736
[3-[4b,8,8,10a-Tetramethyl-2'-oxo-7-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[2,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene-1,4'-oxolane]-2-yl]-1-(4-methyl-5-oxooxolan-2-yl)butan-2-yl] acetate 78302484 Click to see CC1CC(OC1=O)CC(C(C)C2CCC3C4(CCC(C(C4CCC3(C25CC(=O)OC5)C)(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)OC(=O)C 708.90 unknown https://doi.org/10.1248/CPB.44.1736
[3-[7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4b,8,8,10a-tetramethyl-2'-oxospiro[2,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene-1,4'-oxolane]-2-yl]-1-(4-methyl-5-oxooxolan-2-yl)butan-2-yl] acetate 78302483 Click to see CC1CC(OC1=O)CC(C(C)C2CCC3C4(CCC(C(C4CCC3(C25CC(=O)OC5)C)(C)C)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)C)O)O)O)C)OC(=O)C 855.00 unknown https://doi.org/10.1248/CPB.44.1736
16,17-Secodammar-24-en-16-oic acid, 3-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-beta-D-glucopyranosyl]oxy]-17,20-epoxy-23,30-dihydroxy-, gamma-lactone, (3beta,17S,23R)- 162907302 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC(C6(C5(CCC4C3(C)C)C)CC(=O)OC6)C7C(O7)(C)CC(C=C(C)C)O)C)CO)O)O)O)O)O 797.00 unknown https://doi.org/10.1248/CPB.40.2287
7-[4,5-Dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4b,8,8,10a-tetramethyl-2-[3-methyl-3-[4-methyl-2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypent-3-enyl]oxiran-2-yl]spiro[2,3,4,4a,5,6,7,8a,9,10-decahydrophenanthrene-1,4'-oxolane]-2'-one 85106192 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC(C6(C5(CCC4C3(C)C)C)CC(=O)OC6)C7C(O7)(C)CC(C=C(C)C)OC8C(C(C(C(O8)CO)O)O)O)C)CO)O)O)O)O)O 959.10 unknown https://doi.org/10.1248/CPB.40.2287
Hoduloside I 131752536 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC(C6(C5(CCC4C3(C)C)C)CC(=O)OC6)C7C(O7)(C)CC(C=C(C)C)OC8C(C(C(C(O8)CO)O)O)O)C)CO)O)O)O)O)O 959.10 unknown https://doi.org/10.1016/0378-8741(95)01248-C
https://doi.org/10.1248/CPB.40.2287
Hoduloside II 131752537 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC(C6(C5(CCC4C3(C)C)C)CC(=O)OC6)C7C(O7)(C)CC(C=C(C)C)O)C)CO)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O 959.10 unknown https://doi.org/10.1016/0378-8741(95)01248-C
https://doi.org/10.1248/CPB.40.2287
Hovenidulcioside A1 76401300 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC(C6(C5(CCC4C3(C)C)C)CC(=O)OC6)C(C)C(CC7C=C(C(=O)O7)C)OC(=O)C)C)CO)O)O)O)O)O 853.00 unknown https://doi.org/10.1248/CPB.44.1736
https://doi.org/10.1248/CPB.43.532
Hovenidulcioside A2 85084179 Click to see CC1=CC(OC1=O)CC(C(C)C2CCC3C4(CCC(C(C4CCC3(C25CC(=O)OC5)C)(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)OC(=O)C 706.90 unknown https://doi.org/10.1248/CPB.44.1736
https://doi.org/10.1248/CPB.43.532
Saponin H 131751812 Click to see CC(=CC(CC1(C(O1)C2CCC3C4(CCC(C(C4CCC3(C25CC(=O)OC5)C)(C)C)OC6C(C(C(C(O6)CO)O)O)O)C)C)O)C 650.80 unknown https://doi.org/10.1248/CPB.40.2287
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(3S,5R,8R,9R,10R,13R,14S,17S)-17-[(E,2S)-2,6-dihydroxy-6-methylhept-4-en-2-yl]-3-[(2S,3R,4S,5S)-5-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-4,4,8,10-tetramethyl-14-[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,2,3,5,6,7,9,11,12,13,15,17-dodecahydrocyclopenta[a]phenanthren-16-one 163017572 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C(C(=O)CC6(C5(CCC4C3(C)C)C)COC7C(C(C(C(O7)CO)O)O)O)C(C)(CC=CC(C)(C)O)O)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O 1093.20 unknown https://doi.org/10.1248/CPB.41.1722
Dammar-23-en-16-one, 3-(alpha-L-arabinopyranosyloxy)-20,25-dihydroxy-30-[(6-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl)oxy]-, (3beta,23E)- 163188344 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(CO4)O)O)O)C)CCC5C3(CC(=O)C5C(C)(CC=CC(C)(C)O)O)COC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)O)O)O)C)C 917.10 unknown https://doi.org/10.1248/CPB.41.1722
Dammar-23-en-16-one, 3-(alpha-L-arabinopyranosyloxy)-30-(beta-D-glucopyranosyloxy)-20,25-dihydroxy-, (3beta,23E)- 162883928 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(CO4)O)O)O)C)CCC5C3(CC(=O)C5C(C)(CC=CC(C)(C)O)O)COC6C(C(C(C(O6)CO)O)O)O)C)C 785.00 unknown https://doi.org/10.1248/CPB.41.1722
Dammar-23-en-16-one, 3-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-alpha-L-arabinopyranosyl]oxy]-20,25-dihydroxy-30-[(6-O-beta-D-xylopyranosyl-beta-D-glucopyranosyl)oxy]-, (3beta,23E)- 162940517 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C(C(=O)CC6(C5(CCC4C3(C)C)C)COC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)O)O)O)C(C)(CC=CC(C)(C)O)O)C)O)O)O)O)O 1063.20 unknown https://doi.org/10.1248/CPB.41.1722
Dammar-23-en-16-one, 3-[[2-O-(6-deoxy-alpha-L-mannopyranosyl)-alpha-L-arabinopyranosyl]oxy]-30-(beta-D-glucopyranosyloxy)-20,25-dihydroxy-, (3beta,23E)- 163068805 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C(C(=O)CC6(C5(CCC4C3(C)C)C)COC7C(C(C(C(O7)CO)O)O)O)C(C)(CC=CC(C)(C)O)O)C)O)O)O)O)O 931.10 unknown https://doi.org/10.1248/CPB.41.1722
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-2-[[(1S,2R,5R,7S,10R,11R,14R,15S,16S,18R,20S)-16-hydroxy-2,6,6,10,16-pentamethyl-18-(2-methylprop-1-enyl)-19,21-dioxahexacyclo[18.2.1.01,14.02,11.05,10.015,20]tricosan-7-yl]oxy]-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 101634399 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6C7C(CC(OC78CC6(C5(CCC4C3(C)C)C)CO8)C=C(C)C)(C)O)C)CO)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O 943.10 unknown https://doi.org/10.1016/0378-8741(95)01248-C
https://doi.org/10.1248/CPB.40.2287
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[[(1S,2R,5R,7S,10R,11R,14R,15S,16S,18R,20S)-2,6,6,10,16-pentamethyl-18-(2-methylprop-1-enyl)-16-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-19,21-dioxahexacyclo[18.2.1.01,14.02,11.05,10.015,20]tricosan-7-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 163038309 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6C7C(CC(OC78CC6(C5(CCC4C3(C)C)C)CO8)C=C(C)C)(C)OC9C(C(C(C(O9)C)O)O)O)C)CO)O)O)O)O)O 927.10 unknown https://doi.org/10.1039/P19810001923
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5S)-5-hydroxy-2-[[(1S,2R,5R,7S,10R,11R,14R,15S,16S,18R,20S)-16-hydroxy-2,6,6,10,16-pentamethyl-18-(2-methylprop-1-enyl)-19,21-dioxahexacyclo[18.2.1.01,14.02,11.05,10.015,20]tricosan-7-yl]oxy]-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21637212 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C7C(CC(OC78CC6(C5(CCC4C3(C)C)C)CO8)C=C(C)C)(C)O)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O 913.10 unknown https://doi.org/10.1039/P19810001923
https://doi.org/10.1248/CPB.40.2287
(2S,3R,4R,5R,6S)-2-methyl-6-[[(1S,2R,5R,7S,10R,11R,14R,15S,16S,18R,20S)-2,6,6,10,16-pentamethyl-18-(2-methylprop-1-enyl)-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-19,21-dioxahexacyclo[18.2.1.01,14.02,11.05,10.015,20]tricosan-16-yl]oxy]oxane-3,4,5-triol 162989466 Click to see CC1C(C(C(C(O1)OC2(CC(OC34C2C5CCC6C7(CCC(C(C7CCC6(C5(C3)CO4)C)(C)C)OC8C(C(C(C(O8)CO)O)O)O)C)C=C(C)C)C)O)O)O 781.00 unknown https://doi.org/10.1039/P19810001923
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5S)-5-hydroxy-2-[[(1S,2R,5R,7S,10R,11R,14R,15S,16S,18R,20S)-16-hydroxy-2,6,6,10,16-pentamethyl-18-(2-methylprop-1-enyl)-19,21-dioxahexacyclo[18.2.1.01,14.02,11.05,10.015,20]tricosan-7-yl]oxy]-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 101634398 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)O)C 929.10 unknown https://doi.org/10.1248/CPB.40.2287
https://doi.org/10.1016/0378-8741(95)01248-C
(2S,3R,4S,5S,6R)-2-[(2S,3R,4S,5S)-5-hydroxy-2-[[(1S,2R,5R,7S,10R,11R,14S,15R,16S,18R,20S)-16-hydroxy-2,6,6,10,16-pentamethyl-18-(2-methylprop-1-enyl)-19,21-dioxahexacyclo[18.2.1.01,14.02,11.05,10.015,20]tricosan-7-yl]oxy]-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 163085985 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C7C(CC(OC78CC6(C5(CCC4C3(C)C)C)CO8)C=C(C)C)(C)O)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O 913.10 unknown https://doi.org/10.1248/CPB.40.2287
17-(2,6-Dihydroxy-6-methylhept-4-en-2-yl)-3-[4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4,4,8,10-tetramethyl-14-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-1,2,3,5,6,7,9,11,12,13,15,17-dodecahydrocyclopenta[a]phenanthren-16-one 163068804 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C(C(=O)CC6(C5(CCC4C3(C)C)C)COC7C(C(C(C(O7)CO)O)O)O)C(C)(CC=CC(C)(C)O)O)C)O)O)O)O)O 931.10 unknown https://doi.org/10.1248/CPB.41.1722
17-(2,6-Dihydroxy-6-methylhept-4-en-2-yl)-3-[4,5-dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-4,4,8,10-tetramethyl-14-[[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxymethyl]-1,2,3,5,6,7,9,11,12,13,15,17-dodecahydrocyclopenta[a]phenanthren-16-one 162940516 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C(C(=O)CC6(C5(CCC4C3(C)C)C)COC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)O)O)O)C(C)(CC=CC(C)(C)O)O)C)O)O)O)O)O 1063.20 unknown https://doi.org/10.1248/CPB.41.1722
17-(2,6-Dihydroxy-6-methylhept-4-en-2-yl)-4,4,8,10-tetramethyl-14-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3-(3,4,5-trihydroxyoxan-2-yl)oxy-1,2,3,5,6,7,9,11,12,13,15,17-dodecahydrocyclopenta[a]phenanthren-16-one 162883927 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(CO4)O)O)O)C)CCC5C3(CC(=O)C5C(C)(CC=CC(C)(C)O)O)COC6C(C(C(C(O6)CO)O)O)O)C)C 785.00 unknown https://doi.org/10.1248/CPB.41.1722
17-(2,6-Dihydroxy-6-methylhept-4-en-2-yl)-4,4,8,10-tetramethyl-3-(3,4,5-trihydroxyoxan-2-yl)oxy-14-[[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxymethyl]-1,2,3,5,6,7,9,11,12,13,15,17-dodecahydrocyclopenta[a]phenanthren-16-one 162978132 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(CO4)O)O)O)C)CCC5C3(CC(=O)C5C(C)(CC=CC(C)(C)O)O)COC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)O)O)O)C)C 917.10 unknown https://doi.org/10.1248/CPB.41.1722
2-[2-[2-[4,5-dihydroxy-2-[[(1S,2R,7S,10R,11R,14R,15S,16S,20S)-16-hydroxy-2,6,6,10,16-pentamethyl-18-(2-methylprop-1-enyl)-19,21-dioxahexacyclo[18.2.1.01,14.02,11.05,10.015,20]tricosan-7-yl]oxy]-6-methyloxan-3-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-4-yl]oxyoxane-3,4,5-triol 11970116 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5C6C(CC(OC67CC5(C4(CCC3C2(C)C)C)CO7)C=C(C)C)(C)O)C)OC8C(C(C(CO8)O)O)OC9C(C(C(C(O9)CO)O)OC1C(C(C(CO1)O)O)O)O)O)O 1045.20 unknown https://doi.org/10.1248/CPB.40.2287
alpha-L-Arabinopyranoside, (3beta,16beta,23R)-16,23:16,30-diepoxy-20-hydroxydammar-24-en-3-yl O-6-deoxy-beta-D-glucopyranosyl-(1-->2)-O-[beta-D-glucopyranosyl-(1-->3)]- 101634397 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C7C(CC(OC78CC6(C5(CCC4C3(C)C)C)CO8)C=C(C)C)(C)O)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O 913.10 unknown https://doi.org/10.1016/0378-8741(95)01248-C
https://doi.org/10.1248/CPB.40.2287
alpha-L-Arabinopyranoside, (3beta,16beta,23R)-16,23:16,30-diepoxy-20-hydroxydammar-24-en-3-yl O-beta-D-glucopyranosyl-(1-->3)-O-[beta-D-xylopyranosyl-(1-->2)]- 101634400 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(CO9)O)O)O)C)(C)O)C 899.10 unknown https://doi.org/10.1248/CPB.40.2287
Dammar-23-en-16-one, 3-[(O-6-deoxy-alpha-L-mannopyranosyl-(1-->2)-O-[beta-D-glucopyranosyl-(1-->3)]-alpha-L-arabinopyranosyl)oxy]-30-(beta-D-glucopyranosyloxy)-20,25-dihydroxy-, (3beta,23E)- 163017571 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C(C(=O)CC6(C5(CCC4C3(C)C)C)COC7C(C(C(C(O7)CO)O)O)O)C(C)(CC=CC(C)(C)O)O)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)O)O 1093.20 unknown https://doi.org/10.1248/CPB.41.1722
Hoduloside III 73156986 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C7C(CC(OC78CC6(C5(CCC4C3(C)C)C)CO8)C=C(C)C)(C)O)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O 913.10 unknown https://doi.org/10.1039/P19810001923
https://doi.org/10.1248/CPB.40.2287
Hoduloside IV 85137972 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)C)(C)O)C 929.10 unknown https://doi.org/10.1248/CPB.40.2287
Hoduloside IX 131752895 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C(C(=O)CC6(C5(CCC4C3(C)C)C)COC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)O)O)O)C(C)(CC=CC(C)(C)O)O)C)O)O)O)O)O 1063.20 unknown https://doi.org/10.1248/CPB.41.1722
https://doi.org/10.1016/0378-8741(95)01248-C
Hoduloside V 73204031 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6C7C(CC(OC78CC6(C5(CCC4C3(C)C)C)CO8)C=C(C)C)(C)O)C)CO)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O 943.10 unknown https://doi.org/10.1248/CPB.40.2287
Hoduloside VII 131752893 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C(C(=O)CC6(C5(CCC4C3(C)C)C)COC7C(C(C(C(O7)CO)O)O)O)C(C)(CC=CC(C)(C)O)O)C)O)O)O)O)O 931.10 unknown https://doi.org/10.1016/0378-8741(95)01248-C
https://doi.org/10.1248/CPB.41.1722
Hoduloside VIII 131752894 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(CO4)O)O)O)C)CCC5C3(CC(=O)C5C(C)(CC=CC(C)(C)O)O)COC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)O)O)O)C)C 917.10 unknown https://doi.org/10.1016/0378-8741(95)01248-C
https://doi.org/10.1248/CPB.41.1722
Hoduloside X 131752896 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C(C(=O)CC6(C5(CCC4C3(C)C)C)COC7C(C(C(C(O7)CO)O)O)O)C(C)(CC=CC(C)(C)O)O)C)O)O)OC8C(C(C(C(O8)CO)O)O)O)O)O 1093.20 unknown https://doi.org/10.1248/CPB.41.1722
Hovenoside I 131751657 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(CO9)O)O)O)C)(C)O)C 899.10 unknown https://doi.org/10.1248/CPB.40.2287
https://doi.org/10.1016/0378-8741(95)01248-C
Jujuboside B 24721031 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C7C(CC(OC78CC6(C5(CCC4C3(C)C)C)CO8)C=C(C)C)(C)O)C)O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(CO1)O)O)O)O)O)O 1045.20 unknown https://doi.org/10.1248/CPB.40.2287
Jujuboside B1 73156987 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CCC4(C5CCC6C7C(CC(OC78CC6(C5(CCC4C3(C)C)C)CO8)C=C(C)C)(C)O)C)O)OC9C(C(C(C(O9)CO)O)O)OC1C(C(C(CO1)O)O)O)O)O)O 1045.20 unknown https://doi.org/10.1248/CPB.40.2287
Saponin D 131752825 Click to see CC1C(C(C(C(O1)OC2C(C(C(OC2OC3CCC4(C5CCC6C7C(CC(OC78CC6(C5(CCC4C3(C)C)C)CO8)C=C(C)C)(C)OC9C(C(C(C(O9)C)O)O)O)C)CO)O)O)O)O)O 927.10 unknown https://doi.org/10.1039/P19810001923
Saponin G 131752826 Click to see CC1C(C(C(C(O1)OC2(CC(OC34C2C5CCC6C7(CCC(C(C7CCC6(C5(C3)CO4)C)(C)C)OC8C(C(C(C(O8)CO)O)O)O)C)C=C(C)C)C)O)O)O 781.00 unknown https://doi.org/10.1039/P19810001923
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Cyclic peptides
(2S,3S)-3-methyl-2-(methylamino)-N-[(3S,4R,7R,10Z)-7-(2-methylpropyl)-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]pentanamide 163187639 Click to see CCC(C)C(C(=O)NC1C(OC2=CC=C(C=C2)C=CNC(=O)C(NC1=O)CC(C)C)C(C)C)NC 486.60 unknown https://doi.org/10.1016/0031-9422(73)80519-9
3-methyl-2-(methylamino)-N-[7-(2-methylpropyl)-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]pentanamide 78385035 Click to see CCC(C)C(C(=O)NC1C(OC2=CC=C(C=C2)C=CNC(=O)C(NC1=O)CC(C)C)C(C)C)NC 486.60 unknown https://doi.org/10.1016/0031-9422(73)80519-9
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Peptides / Oligopeptides
(2S,3S)-2-(dimethylamino)-3-methyl-N-[(3S,4R,7R,10Z)-7-(2-methylpropyl)-5,8-dioxo-3-propan-2-yl-2-oxa-6,9-diazabicyclo[10.2.2]hexadeca-1(14),10,12,15-tetraen-4-yl]pentanamide 163194560 Click to see CCC(C)C(C(=O)NC1C(OC2=CC=C(C=C2)C=CNC(=O)C(NC1=O)CC(C)C)C(C)C)N(C)C 500.70 unknown https://doi.org/10.1016/0031-9422(73)80519-9
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives / Glucuronic acid derivatives
D-Glucuronic Acid Methyl Ester 71771920 Click to see COC(=O)C(C(C(C(C=O)O)O)O)O 208.17 unknown https://doi.org/10.1016/0378-8741(90)90067-4
> Organoheterocyclic compounds / Diazanaphthalenes / Benzodiazines / Quinazolines
Fumiquinazoline O 71605144 Click to see CC(=O)N1C2C(C3=CC=CC=C3N2C(=O)C14CC4)(CC5C(=O)N(C(C6=NC7=CC=CC=C7C(=O)N56)(C)OC)C)O 543.60 unknown https://doi.org/10.1248/CPB.41.1722
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1007/BF02977346
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins
Cianidanol 9064 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC(=C(C=C3)O)O)O 290.27 unknown https://doi.org/10.1007/BF02977346
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)chroman-4-one 5153580 Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 320.25 unknown https://doi.org/10.1248/BPB.20.381
Dihydromyricetin 161557 Click to see C1=C(C=C(C(=C1O)O)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O 320.25 unknown https://doi.org/10.1248/BPB.20.381
https://doi.org/10.1016/J.FOODCHEM.2012.09.098
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavan-3-ols
Afzelechin 442154 Click to see C1C(C(OC2=CC(=CC(=C21)O)O)C3=CC=C(C=C3)O)O 274.27 unknown https://doi.org/10.1007/BF02977346
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
2,3-Dihydroflavon-3-ol 147806 Click to see C1=CC=C(C=C1)C2C(C(=O)C3=CC=CC=C3O2)O 240.25 unknown https://doi.org/10.1016/J.FOODCHEM.2012.09.098
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 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/10.1007/BF02977346
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/10.1007/BF02977346
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Myricetin 5281672 Click to see C1=C(C=C(C(=C1O)O)O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O 318.23 unknown https://doi.org/10.1248/BPB.20.381

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