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Allium chinense

Allium chinense - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

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

Details Top

Internal ID UUID64402488e8229459965510
Scientific name Allium chinense
Authority G.Don
First published in Mem. Wern. Nat. Hist. Soc. 6: 83 (1827)

Description Top

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Synonyms Top

Scientific name Authority First published in
Allium bakeri Regel Trudy Imp. S.-Peterburgsk. Bot. Sada 3(2): 141 (1875)
Allium bodinieri H.Lév. & Vaniot Liliac. & C.Chine : 38 (1905)
Allium exsertum G.Don Mem. Wern. Nat. Hist. Soc. 6: 17 (1827)
Allium martini H.Lév. & Vaniot Liliac. & C.Chine : 40 (1905)
Caloscordum exsertum (G.Don) Herb. Edwards's Bot. Reg. 33: t. 5 (1847)

Common names Top

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Language Common/alternative name
English rakkyo
English chinese onion
Afrikaans chinese ui
Arabic بصل شرقي
Arabic ثوم صيني
Arabic كراث ياباني
Arabic كراث صيني
Arabic كراث جيانغشي
Arabic بصل صيني
Bulgarian китайски лук
Greek Άλλιο το κινεζικό
Persian پیاز شرقی
Finnish valkoruohosipuli
Japanese ガイハク
Japanese ラッキョウ
Japanese 辣韮
Japanese 辣韭
Japanese 薤白
Japanese らっきょう
Japanese ラッキョ
Japanese 薤
Korean 염교
Korean 락교
lzh 薤
Swedish rakkyo
Swedish rakkyolök
tay qusul
Thai กระเทียมจีน
trv qowsun
Uzbek xitoy piyozi
Vietnamese củ kiệu
Vietnamese kiệu
Chinese 藠头
Chinese 薤白
Chinese 洋葱
Chinese 薤
Chinese 蕌头
Chinese 蕗蕎
Chinese 藠头(野薤、薤）
Chinese 麗韭
Chinese 荞头
Chinese 小蒜
Chinese 蕎頭

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
      • Hainan
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Kirgizstan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • Bangladesh
      • West Himalaya
    • Indo-China
      • Thailand

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000755945
UNII 1ZE9U9FY36
USDA Plants ALCH5
Tropicos 18400411
INPN 705799
KEW urn:lsid:ipni.org:names:527818-1
The Plant List kew-295288
Open Tree Of Life 1031181
Observations.org 269807
NCBI Taxonomy 130426
IUCN Red List 44392537
IPNI 527818-1
iNaturalist 122344
GBIF 2856307
Freebase /m/026jgb5
EPPO ALLCH
EOL 1084367
Elurikkus 318140
USDA GRIN 101417
Wikipedia Allium_chinense
CMAUP NPO8321
PFAF Allium chinense

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
Local knowledge of homegarden plants in Miao ethnic communities in Laershan region, Xiangxi area, China Luo J, Li Q, He J, Yan J, Zhang S, Chang X, Wu T J Ethnobiol Ethnomed 18-Mar-2024
PMCID:PMC10946099
doi:10.1186/s13002-024-00676-x
PMID:38500123
Antioxidant activity of spirostanol saponins from Allii Macrostemonis Bulbus and their contents in different origins and processed products Wu J, Cui Y, Liu C, Ding W, Ren S, Zhang J, Wang L Food Chem X 17-Jan-2024
PMCID:PMC10831145
doi:10.1016/j.fochx.2024.101144
PMID:38304049
The complete chloroplast genomes of Allium sacculiferum, A. thunbergii, and A. taquetii (Amaryllidaceae) from Korea Kim KM, Park CY, Lee DH, Jung YH, Kim HM, Na CS Mitochondrial DNA B Resour 18-Oct-2023
PMCID:PMC10588515
doi:10.1080/23802359.2023.2268315
PMID:37869569
Ethnobotanical study on edible flowers in Xishuangbanna, China Zhang Q, Cheng Z, Fan Y, Zhang D, Wang M, Zhang J, Sommano S, Wu X, Long C J Ethnobiol Ethnomed 30-Sep-2023
PMCID:PMC10542681
doi:10.1186/s13002-023-00608-1
PMID:37777741
Two New Compounds from Allii Macrostemonis Bulbus and Their In Vitro Antioxidant Activities Wu J, Li L, Liu C, Li C, Cui Y, Ding W, Zhang J, Shi L Molecules 22-Aug-2023
PMCID:PMC10488416
doi:10.3390/molecules28176176
PMID:37687005
Yao-Shan of traditional Chinese medicine: an old story for metabolic health Yang S, Yang H, Zhang Y Front Pharmacol 16-Aug-2023
PMCID:PMC10468577
doi:10.3389/fphar.2023.1194026
PMID:37663255
Steroidal Saponins: Naturally Occurring Compounds as Inhibitors of the Hallmarks of Cancer Bouabdallah S, Al-Maktoum A, Amin A Cancers (Basel) 31-Jul-2023
PMCID:PMC10417465
doi:10.3390/cancers15153900
PMID:37568716
6-Oxofurostane and (iso)Spirostane Types of Saponins in Smilax sieboldii: UHPLC-QToF-MS/MS and GNPS-Molecular Networking Approach for the Rapid Dereplication and Biodistribution of Specialized Metabolites Avula B, Bae JY, Ahn J, Katragunta K, Wang YH, Wang M, Kwon Y, Khan IA, Chittiboyina AG Int J Mol Sci 14-Jul-2023
PMCID:PMC10380369
doi:10.3390/ijms241411487
PMID:37511246
The Cryopreservation of Medicinal and Ornamental Geophytes: Application and Challenges El Merzougui S, Benelli C, El Boullani R, Serghini MA Plants (Basel) 29-May-2023
PMCID:PMC10255897
doi:10.3390/plants12112143
PMID:37299120
Traditional Chinese medicine for heart failure with preserved ejection fraction: clinical evidence and potential mechanisms Fan Y, Yang Z, Wang L, Liu Y, Song Y, Liu Y, Wang X, Zhao Z, Mao J Front Pharmacol 10-May-2023
PMCID:PMC10206212
doi:10.3389/fphar.2023.1154167
PMID:37234711
Effects of saponins from Chinese herbal medicines on signal transduction pathways in cancer: A review Zhu M, Sun Y, Bai H, Wang Y, Yang B, Wang Q, Kuang H Front Pharmacol 29-Mar-2023
PMCID:PMC10090286
doi:10.3389/fphar.2023.1159985
PMID:37063281
Identification of Potential Lead Compounds Targeting Novel Druggable Cavity of SARS-CoV-2 Spike Trimer by Molecular Dynamics Simulations Zhao Y, Zhao Y, Xie L, Li Q, Zhang Y, Zang Y, Li X, Zhang L, Yang Z Int J Mol Sci 27-Mar-2023
PMCID:PMC10094189
doi:10.3390/ijms24076281
PMID:37047254
The efficacy and safety of Chinese herbal medicine as an add-on therapy for type 2 diabetes mellitus patients with carotid atherosclerosis: An updated meta-analysis of 27 randomized controlled trials Zhang Z, Leng Y, Chen Z, Fu X, Liang Q, Peng X, Xie H, Gao H, Xie C Front Pharmacol 23-Mar-2023
PMCID:PMC10076753
doi:10.3389/fphar.2023.1091718
PMID:37033624
Distribution of Cadmium in Fresh Vegetables Marketed in Southeast China and Its Dietary Exposure Assessment Pan XD, Han JL Foods 12-Mar-2023
PMCID:PMC10048524
doi:10.3390/foods12061204
PMID:36981131
Characterization of volatile organic compounds with anti-atherosclerosis effects in Allium macrostemon Bge. and Allium chinense G. Don by head space solid phase microextraction coupled with gas chromatography tandem mass spectrometry Qin Z, Duan S, Li Y, Li X, Xing H, Yao Z, Zhang X, Yao X, Yang J Front Nutr 01-Feb-2023
PMCID:PMC9929146
doi:10.3389/fnut.2023.996675
PMID:36819690

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 / 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.35.2668
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(+)-alpha-Pinene 82227 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene 12223113 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
alpha-PINENE 6654 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
beta-Pinene 14896 Click to see CC1(C2CCC(=C)C1C2)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
Limonene, (-)- 439250 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Limonene, (+)- 440917 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
Limonene, (+/-)- 22311 Click to see CC1=CCC(CC1)C(=C)C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
Calenduloside E 176079 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 632.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(25R)-5alpha-Spirostan-3beta-ol 219836 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown https://doi.org/10.1016/0031-9422(95)00553-6
(2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one 11743436 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)O)C)C)C)OC1 430.60 unknown via CMAUP database
(9S,13R,16S)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one 5318958 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)O)C)C)C)OC1 430.60 unknown https://doi.org/10.1016/0031-9422(95)00553-6
https://doi.org/10.1248/BPB.23.660
6-Oxotigogenin 90450918 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)O)C)C)C)OC1 430.60 unknown via CMAUP database
6-Oxotigogenin 4669449 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)O)C)C)C)OC1 430.60 unknown https://doi.org/10.1248/BPB.23.660
Laxogenin 10950057 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)O)C)C)C)OC1 430.60 unknown https://doi.org/10.1016/0031-9422(95)00553-6
https://doi.org/10.1248/BPB.23.660
Tigogenin 99516 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CCC(C6)O)C)C)C)OC1 416.60 unknown https://doi.org/10.1016/0031-9422(95)00553-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1R,2S,4R,8R,9S,12S,13R,16S,18S)-6-[(2S,4R)-1-hydroxy-4-methyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypentan-2-yl]-7,9,13-trimethyl-16-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-19-one 162906230 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)O)O)O)C)C)C(CC(C)COC8C(C(C(C(O8)CO)O)O)O)CO 917.00 unknown https://doi.org/10.1055/S-2006-957941
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S)-16-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one 11331926 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)OC9C(C(C(CO9)O)O)O)O)O)C)C)C)OC1 857.00 unknown https://doi.org/10.1016/0031-9422(95)00423-5
https://doi.org/10.1248/BPB.23.660
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S)-16-[(2S,3S,4S,5R,6S)-3,4-dihydroxy-5-[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-6-[[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one 162937067 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)OC9C(C(C(CO9)O)O)O)O)O)C)C)C)OC1 857.00 unknown https://doi.org/10.1248/BPB.23.660
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S)-5',7,9,13-tetramethyl-16-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one 21636289 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)O)O)O)C)C)C)OC1 724.90 unknown https://doi.org/10.1016/0031-9422(95)00423-5
(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S)-5',7,9,13-tetramethyl-16-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-[[(2R,3S,4R,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one 162952884 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)O)O)O)C)C)C)OC1 724.90 unknown https://doi.org/10.1248/BPB.23.660
(1R,2S,4S,6S,7S,8R,9S,12S,13R,16S,18S)-16-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-6-[[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-6-hydroxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-19-one 162995168 Click to see CC1C2C(CC3C2(CCC4C3CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1037.10 unknown https://doi.org/10.1248/CPB.37.1390
(1R,2S,4S,8S,9S,12S,13R,16S,18S)-16-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-6-[[(2R,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-19-one 162856783 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)C)CCC(C)COC9C(C(C(C(O9)CO)O)O)O 1019.10 unknown https://doi.org/10.1016/0031-9422(95)00553-6
(1R,2S,4S,8S,9S,12S,13R,16S,18S)-16-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2S,3S,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxy-6-[[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-19-one 162856786 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)C)CCC(C)COC9C(C(C(C(O9)CO)O)O)O 1019.10 unknown https://doi.org/10.1016/0031-9422(95)00553-6
(1R,2S,4S,8S,9S,12S,13R,16S,18S)-16-[(2R,3S,4S,5S,6R)-3,4-dihydroxy-5-[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-6-[[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-6-[(2R,4R)-1-hydroxy-4-methyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypentan-2-yl]-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-19-one 163044061 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)C)C(CC(C)COC9C(C(C(C(O9)CO)O)O)O)CO 1049.20 unknown https://doi.org/10.1055/S-2006-957941
(1R,2S,4S,8S,9S,12S,13R,16S,18S)-6-[(2S,4R)-1-hydroxy-4-methyl-5-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypentan-2-yl]-7,9,13-trimethyl-16-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-19-one 162906229 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)O)O)O)C)C)C(CC(C)COC8C(C(C(C(O8)CO)O)O)O)CO 917.00 unknown https://doi.org/10.1055/S-2006-957941
(1R,2S,4S,8S,9S,12S,13R,16S,18S)-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-16-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-[[(2S,3S,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-19-one 162897656 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)O)O)O)C)C)CCC(C)COC8C(C(C(C(O8)CO)O)O)O 887.00 unknown https://doi.org/10.1016/0031-9422(95)00553-6
(1R,2S,4S,8S,9S,12S,13R,16S,18S)-7,9,13-trimethyl-6-[(3S)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-16-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3S,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-19-one 162897655 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)O)O)O)C)C)CCC(C)COC8C(C(C(C(O8)CO)O)O)O 887.00 unknown https://doi.org/10.1016/0031-9422(95)00553-6
(2R,3S,4R,5R,6S)-2-[(2R,3S,4R,5R,6S)-2-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'S,6S,7S,8R,9R,12S,13R,15S,16S,18S)-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 163035125 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)OC1 919.10 unknown https://doi.org/10.1016/0031-9422(95)00423-5
(2R,3S,4R,5R,6S)-2-[(2R,3S,4R,5S,6S)-2-[(2S,3R,4S,5S,6S)-4,5-dihydroxy-2-(hydroxymethyl)-6-[(1R,2S,4S,5'S,6S,7S,8R,9R,12S,13R,15S,16S,18S)-15-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-3-yl]oxy-5-hydroxy-6-(hydroxymethyl)-3-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 162933812 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)C)C)OC1 1081.20 unknown https://doi.org/10.1016/0031-9422(95)00423-5
(3b,5a,25R)-3-Hydroxyspirostan-6-one 3-[2-acetylarabinosyl-(1->6)-glucoside] 74029744 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)OC(=O)C)O)O)O)C)C)C)OC1 766.90 unknown https://doi.org/10.1016/0031-9422(95)00423-5
(9S,13R,16S,18S)-16-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2R,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-6-[[(2R,3R,4R,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-7,9,13-trimethyl-6-[(3R)-3-methyl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-ene-10,19-dione 23304295 Click to see CC1=C(OC2C1C3(C(C2)C4CC(=O)C5CC(CCC5(C4CC3=O)C)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)CCC(C)COC9C(C(C(C(O9)CO)O)O)O 1033.10 unknown via CMAUP database
[(2S,3R,4S,5S)-4,5-dihydroxy-2-[[(2R,3S,4S,5R,6R)-3,4,5-trihydroxy-6-[(1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,16S,18S)-5',7,9,13-tetramethyl-19-oxospiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxan-2-yl]methoxy]oxan-3-yl] acetate 101682566 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)OC(=O)C)O)O)O)C)C)C)OC1 766.90 unknown https://doi.org/10.1016/0031-9422(95)00423-5
16-[3,4-Dihydroxy-5-(3,4,5-trihydroxyoxan-2-yl)oxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one 72804845 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)OC9C(C(C(CO9)O)O)O)O)O)C)C)C)OC1 857.00 unknown https://doi.org/10.1016/0031-9422(95)00423-5
https://doi.org/10.1248/BPB.23.660
16-[3,4-Dihydroxy-5-(3,4,5-trihydroxyoxan-2-yl)oxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxy-7,9,13-trimethyl-6-[3-methyl-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-6-en-19-one 131753112 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)C)CCC(C)COC9C(C(C(C(O9)CO)O)O)O 1019.10 unknown https://doi.org/10.1016/0031-9422(95)00553-6
5',7,9,13-Tetramethyl-16-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-19-one 14376401 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(C6)OC7C(C(C(C(O7)COC8C(C(C(CO8)O)O)O)O)O)O)C)C)C)OC1 724.90 unknown https://doi.org/10.1016/0031-9422(95)00423-5
https://doi.org/10.1248/BPB.23.660
Chinenoside I 73817575 Click to see CC1C2C(CC3C2(CCC4C3CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1037.10 unknown https://doi.org/10.1248/CPB.37.1390
Chinenoside II 101687168 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)C)CCC(C)COC9C(C(C(C(O9)CO)O)O)O 1019.10 unknown via CMAUP database
Chinenoside III 131753113 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)O)O)O)C)C)CCC(C)COC8C(C(C(C(O8)CO)O)O)O 887.00 unknown https://doi.org/10.1016/0031-9422(95)00553-6
Chinenoside IV 131751142 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)OC8C(C(C(CO8)O)O)O)O)O)C)C)C(CC(C)COC9C(C(C(C(O9)CO)O)O)O)CO 1049.20 unknown https://doi.org/10.1055/S-2006-957941
Chinenoside V 131751143 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)COC7C(C(C(CO7)O)O)O)O)O)O)C)C)C(CC(C)COC8C(C(C(C(O8)CO)O)O)O)CO 917.00 unknown https://doi.org/10.1055/S-2006-957941
Cistocardin 73157303 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC2C(C(C(C(O2)CO)O)O)O)O)O)O)C)C)C)OC1 1081.20 unknown https://doi.org/10.1016/0031-9422(95)00423-5
Macrostemonoside G 101923511 Click to see CC1C2C(CC3C2(C(CC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)O)C)OC1(CCC(=C)COC8C(C(C(C(O8)CO)O)O)O)O 935.10 unknown via CMAUP database
Macrostemonoside H 101923512 Click to see CC1C2C(CC3C2(C(CC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)O)C)OC1(CCC(=C)COC8C(C(C(C(O8)CO)O)O)O)OC 949.10 unknown via CMAUP database
Macrostemonoside I 101923513 Click to see CC1C2C(CC3C2(C(=O)CC4C3CCC5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)OC1(CCC(=C)COC8C(C(C(C(O8)CO)O)O)O)O 933.00 unknown via CMAUP database
Macrostemonoside J 101669618 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)O 937.10 unknown via CMAUP database
Macrostemonoside K 101669619 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)OC1(CCC(C)COC8C(C(C(C(O8)CO)O)O)O)OC 951.10 unknown via CMAUP database
Macrostemonoside L 101669620 Click to see CC1=C(OC2C1C3(CCC4C(C3C2)CCC5C4(CC(C(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)CCC(C)COC8C(C(C(C(O8)CO)O)O)O 919.10 unknown via CMAUP database
Neogitogenin 3-[glucosyl-(1->2)-glucosyl-(1->4)-galactoside] 73800783 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)O)C)C)C)OC1 919.10 unknown https://doi.org/10.1016/0031-9422(95)00423-5
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/BPB.23.660
Sitogluside 5742590 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 576.80 unknown https://doi.org/10.1248/BPB.23.660
https://doi.org/10.1055/S-2006-961993
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-(6-Aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol 191 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown https://doi.org/10.1016/0031-9422(95)00553-6
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown https://doi.org/10.1016/0031-9422(95)00553-6
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
(2S,5R,8S,11R,15S,18S,19S,22R)-8,15-bis[3-(diaminomethylideneamino)propyl]-2-(hydroxymethyl)-22-methoxycarbonyl-18-[(1E,3E,5S,6S)-6-methoxy-3,5-dimethyl-7-phenylhepta-1,3-dienyl]-1,5,19-trimethyl-3,6,9,13,16,20,25-heptaoxo-1,4,7,10,14,17,21-heptazacyclopentacosane-11-carboxylic acid 163189999 Click to see CC1C(NC(=O)C(NC(=O)CC(NC(=O)C(NC(=O)C(NC(=O)C(N(C(=O)CCC(NC1=O)C(=O)OC)C)CO)C)CCCN=C(N)N)C(=O)O)CCCN=C(N)N)C=CC(=CC(C)C(CC2=CC=CC=C2)OC)C 1056.20 unknown https://doi.org/10.1055/S-2006-957941
> Organic acids and derivatives / Thiosulfinic acid esters
Allicin 65036 Click to see C=CCSS(=O)CC=C 162.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996138/
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols / Cyclohexanols
Inositol 892 Click to see C1(C(C(C(C(C1O)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/J.CARBPOL.2014.10.019
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3R,4S,5S)-2,3,4,5-tetrahydroxyhexanal 19233 Click to see CC(C(C(C(C=O)O)O)O)O 164.16 unknown https://doi.org/10.1016/J.CARBPOL.2014.10.019
(2R,3S,4S,5R)-2,3,4,5-tetrahydroxyhexanal 94270 Click to see CC(C(C(C(C=O)O)O)O)O 164.16 unknown via CMAUP database
(2R,3S,4S,5R)-2,3,4,5,6-pentahydroxyhexanal 3037556 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/J.CARBPOL.2014.10.019
(2S,3R,4R,5S)-2,3,4,5-tetrahydroxyhexanal 3034656 Click to see CC(C(C(C(C=O)O)O)O)O 164.16 unknown https://doi.org/10.1016/J.CARBPOL.2014.10.019
(2S,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal 161658 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1016/J.CARBPOL.2014.10.019
(4S,5R)-6-methyloltetrahydropyran-2,3,4,5-tetrol 59083882 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown via CMAUP database
(4S,5S)-6-methyltetrahydropyran-2,3,4,5-tetrol 71315513 Click to see CC1C(C(C(C(O1)O)O)O)O 164.16 unknown via CMAUP database
alpha-D-GALACTOSE 439357 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown via CMAUP database
D-Galactose 6036 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown via CMAUP database
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown via CMAUP database
D-Mannose 18950 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown via CMAUP database
L-Fucose 17106 Click to see CC1C(C(C(C(O1)O)O)O)O 164.16 unknown via CMAUP database
L-Rhamnose 25310 Click to see CC1C(C(C(C(O1)O)O)O)O 164.16 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Pentoses
(2S,3R,4R)-2,3,4,5-tetrahydroxypentanal 66308 Click to see C(C(C(C(C=O)O)O)O)O 150.13 unknown https://doi.org/10.1016/J.CARBPOL.2014.10.019
D-Xylose 135191 Click to see C1C(C(C(C(O1)O)O)O)O 150.13 unknown via CMAUP database
DL-Arabinose 854 Click to see C(C(C(C(C=O)O)O)O)O 150.13 unknown via CMAUP database
DL-Xylose 644160 Click to see C(C(C(C(C=O)O)O)O)O 150.13 unknown https://doi.org/10.1016/J.CARBPOL.2014.10.019
L-Arabinose 439195 Click to see C1C(C(C(C(O1)O)O)O)O 150.13 unknown via CMAUP database
Pentose 229 Click to see C1C(C(C(C(O1)O)O)O)O 150.13 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar alcohols
Erythritol 222285 Click to see C(C(C(CO)O)O)O 122.12 unknown https://doi.org/10.1016/J.CARBPOL.2014.10.019
Glycerin 753 Click to see C(C(CO)O)O 92.09 unknown https://doi.org/10.1016/J.CARBPOL.2014.10.019
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
Ledebouriellol 5318962 Click to see CC=C(C)C(=O)OC1CC2=C(C=C3C(=C2O)C(=O)C=C(O3)CO)OC1(C)C 374.40 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones
(2R)-2-hexyl-5-methylfuran-3-one 162906851 Click to see CCCCCCC1C(=O)C=C(O1)C 182.26 unknown https://doi.org/10.1016/0031-9422(84)83097-6
3(2H)-Furanone, 2-hexyl-5-methyl- 566912 Click to see CCCCCCC1C(=O)C=C(O1)C 182.26 unknown https://doi.org/10.1016/0031-9422(84)83097-6
> Organoheterocyclic compounds / Dithianes
1,3-Dithiane 10451 Click to see C1CSCSC1 120.20 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolyl carboxylic acids and derivatives
(2S)-2-azaniumyl-3-(1H-indol-3-yl)propanoate 6923516 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)[O-])[NH3+] 204.22 unknown via CMAUP database
D-Tryptophan 9060 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 204.22 unknown via CMAUP database
DL-Tryptophan 1148 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 204.22 unknown https://doi.org/10.1016/0031-9422(95)00553-6
Tryptophan 6305 Click to see C1=CC=C2C(=C1)C(=CN2)CC(C(=O)O)N 204.22 unknown https://doi.org/10.1016/0031-9422(95)00553-6
https://doi.org/10.1055/S-2006-961993
> Organoheterocyclic compounds / Indoles and derivatives / Pyridoindoles / Beta carbolines
(3R)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate 6920043 Click to see C1C([NH2+]CC2=C1C3=CC=CC=C3N2)C(=O)[O-] 216.24 unknown via CMAUP database
(3S)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate 6920044 Click to see C1C([NH2+]CC2=C1C3=CC=CC=C3N2)C(=O)[O-] 216.24 unknown via CMAUP database
2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-ium-3-carboxylate 3288669 Click to see C1C([NH2+]CC2=C1C3=CC=CC=C3N2)C(=O)[O-] 216.24 unknown via CMAUP database
> Organosulfur compounds / Allyl sulfur compounds
Allyl methyl disulfide 62434 Click to see CSSCC=C 120.20 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996138/
Allyl methyl tetrasulfide 525329 Click to see CSSSSCC=C 184.40 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996138/
Diallyl disulfide 16590 Click to see C=CCSSCC=C 146.30 unknown https://doi.org/10.1248/CPB.35.2668
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996138/
Diallyl sulfide 11617 Click to see C=CCSCC=C 114.21 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996138/
> Organosulfur compounds / Isothiocyanates
Allyl isothiocyanate 5971 Click to see C=CCN=C=S 99.16 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996138/
> Organosulfur compounds / Organic disulfides / Dialkyldisulfides
Methyl propyl disulfide 16592 Click to see CCCSSC 122.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996138/
> Organosulfur compounds / Organic trisulfides
Allyl methyl trisulfide 61926 Click to see CSSSCC=C 152.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996138/
Diallyl trisulfide 16315 Click to see C=CCSSSCC=C 178.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996138/
Dimethyl trisulfide 19310 Click to see CSSSC 126.30 unknown via CMAUP database
Methyl propyl trisulfide 5319765 Click to see CCCSSSC 154.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996138/
> Organosulfur compounds / Sulfenyl compounds
Dimethyl tetrasulfide 79828 Click to see CSSSSC 158.30 unknown https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996138/
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Cinnamamide, p-hydroxy-N-(p-hydroxyphenethyl)- 89322 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown https://doi.org/10.1248/CPB.35.2668
cis-N-p-coumaroyltyramine 13939145 Click to see C1=CC(=CC=C1CCNC(=O)C=CC2=CC=C(C=C2)O)O 283.32 unknown https://doi.org/10.1248/CPB.35.2668
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1248/CPB.35.2668
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
(E)-1-(2,4-dihydroxyphenyl)-3-[4-[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one 163188672 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 418.40 unknown https://doi.org/10.1248/BPB.23.660
1-(2,4-Dihydroxyphenyl)-3-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]prop-2-en-1-one 72728334 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 418.40 unknown https://doi.org/10.1248/BPB.23.660
Isoliquiritin 5318591 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O 418.40 unknown https://doi.org/10.1248/BPB.23.660
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1248/BPB.23.660
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1248/BPB.23.660
> Phenylpropanoids and polyketides / Stilbenes
Lunularic acid 161413 Click to see C1=CC(=C(C(=C1)O)C(=O)O)CCC2=CC=C(C=C2)O 258.27 unknown https://doi.org/10.1248/CPB.35.2668

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