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Dioscorea tokoro

Dioscorea tokoro - 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 UUID643ff7f6c93fc991251358
Scientific name Dioscorea tokoro
Authority Makino
First published in Bot. Mag. (Tokyo) 3: 112 (1889)

Description Top

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Synonyms Top

Scientific name Authority First published in
Dioscorea buergeri Uline ex R.Knuth J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 73(Suppl.): 11 (1904)
Dioscorea buergeri var. enneaneura Uline ex Diels Bot. Jahrb. Syst. 29: 260. 1900
Dioscorea enneaneura Prain & Burkill J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 73(Suppl.): 11 (1904)
Dioscorea saidae R.Knuth Pflanzenr. , IV, 43: 317 (1924)
Dioscorea wichurae Uline ex R.Knuth Pflanzenr. , IV, 43: 316 (1924)
Dioscorea yokusai Prain & Burkill J. Asiat. Soc. Bengal, Pt. 2, Nat. Hist. 73(Suppl.): 10 (1904)

Common names Top

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Language Common/alternative name
Korean 도꼬로마
Chinese 山萆薢
Chinese 细柄薯蓣
Chinese 土黄连
Chinese 粉萆薢
Chinese 山萆蓣

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000396013
Tropicos 11000043
KEW urn:lsid:ipni.org:names:318693-1
The Plant List kew-241040
Open Tree Of Life 686889
Observations.org 321922
NCBI Taxonomy 64475
IPNI 318693-1
iNaturalist 452103
GBIF 2755730
EPPO DIUTO
EOL 1120645
Elurikkus 4381
USDA GRIN 14261
CMAUP NPO22077

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
Low-coverage whole genome sequencing of eleven species/subspecies in Dioscorea sect. Stenophora (Dioscoreaceae): comparative plastome analyses, molecular markers development and phylogenetic inference Hu K, Sun XQ, Chen M, Lu RS Front Plant Sci 06-Jun-2023
PMCID:PMC10281252
doi:10.3389/fpls.2023.1196176
PMID:37346115
The potential of Chinese medicines in the treatment of hyperuricemia Tang J, Gao H, Xu Y, Chen J, Wu B Am J Transl Res 15-Apr-2023
PMCID:PMC10182497
PMID:37193181
Mitophagy Effects of Protodioscin on Human Osteosarcoma Cells by Inhibition of p38MAPK Targeting NIX/LC3 Axis Huang CF, Hsieh YH, Yang SF, Kuo CH, Wang PH, Liu CJ, Lin RC Cells 21-Jan-2023
PMCID:PMC9913878
doi:10.3390/cells12030395
PMID:36766737
Sex Determination in Dioscorea dumetorum: Evidence of Heteromorphic Sex Chromosomes and Sex-Linked NORs Ngo Ngwe F, Siljak-Yakovlev S Plants (Basel) 04-Jan-2023
PMCID:PMC9861523
doi:10.3390/plants12020228
PMID:36678940
Traditional chinese medicine to prevent and treat diabetic erectile dysfunction Feng Y, Shi T, Fu Y, Lv B Front Pharmacol 21-Sep-2022
PMCID:PMC9532934
doi:10.3389/fphar.2022.956173
PMID:36210810
Identification of the Natural Steroid Sapogenin Diosgenin as a Direct Dual-Specific RORα/γ Inverse Agonist Schwarz PF, Perhal AF, Schöberl LN, Kraus MM, Kirchmair J, Dirsch VM Biomedicines 25-Aug-2022
PMCID:PMC9495423
doi:10.3390/biomedicines10092076
PMID:36140177
The genome of Dioscorea zingiberensis sheds light on the biosynthesis, origin and evolution of the medicinally important diosgenin saponins Li Y, Tan C, Li Z, Guo J, Li S, Chen X, Wang C, Dai X, Yang H, Song W, Hou L, Xu J, Tong Z, Xu A, Yuan X, Wang W, Yang Q, Chen L, Sun Z, Wang K, Pan B, Chen J, Bao Y, Liu F, Qi X, Gang DR, Wen J, Li J Hortic Res 25-Jul-2022
PMCID:PMC9531337
doi:10.1093/hr/uhac165
PMID:36204203
Genome Analysis Revives a Forgotten Hybrid Crop Edo-dokoro in the Genus Dioscorea Natsume S, Sugihara Y, Kudoh A, Oikawa K, Shimizu M, Ishikawa Y, Nishihara M, Abe A, Innan H, Terauchi R Plant Cell Physiol 25-Jul-2022
PMCID:PMC9680860
doi:10.1093/pcp/pcac109
PMID:35876055
Diosgenin and Its Analogs: Potential Protective Agents Against Atherosclerosis Wang D, Wang X Drug Des Devel Ther 17-Jul-2022
PMCID:PMC9304635
doi:10.2147/DDDT.S368836
PMID:35875677
Traditional Chinese Herbal Medicine Plays a Role in the Liver, Kidney, and Intestine to Ameliorate Hyperuricemia according to Experimental Studies Xu L, Lu LL, Gao JD Evid Based Complement Alternat Med 28-Nov-2021
PMCID:PMC8645359
doi:10.1155/2021/4618352
PMID:34876914
Steroidal Saponins Isolated from the Rhizome of Dioscorea tokoro Inhibit Cell Growth and Autophagy in Hepatocellular Carcinoma Cells Okubo S, Ohta T, Shoyama Y, Uto T Life (Basel) 26-Jul-2021
PMCID:PMC8400091
doi:10.3390/life11080749
PMID:34440493
In Vitro Screening of East Asian Plant Extracts for Potential Use in Reducing Ruminal Methane Production Bharanidharan R, Arokiyaraj S, Baik M, Ibidhi R, Lee SJ, Lee Y, Nam IS, Kim KH Animals (Basel) 04-Apr-2021
PMCID:PMC8066825
doi:10.3390/ani11041020
PMID:33916571
Spectroscopic and Molecular Methods to Differentiate Gender in Immature Date Palm (Phoenix dactylifera L.) Khan AL, Al-Harrasi A, Numan M, AbdulKareem NM, Mabood F, Al-Rawahi A Plants (Basel) 12-Mar-2021
PMCID:PMC8001243
doi:10.3390/plants10030536
PMID:33809251
The Efficacy and Mechanism of Chinese Herbal Medicines in Lowering Serum Uric Acid Levels: A Systematic Review Chen L, Luo Z, Wang M, Cheng J, Li F, Lu H, He Q, You Y, Zhou X, Kwan HY, Zhao X, Zhou L Front Pharmacol 25-Jan-2021
PMCID:PMC7868570
doi:10.3389/fphar.2020.578318
PMID:33568990
Virtual Screening and Bioactivity Evaluation of Novel Androgen Receptor Antagonists From Anti-PCa Traditional Chinese Medicine Prescriptions Han W, Shi Y, Su J, Zhao Z, Wang X, Li J, Liu H Front Chem 17-Sep-2020
PMCID:PMC7528374
doi:10.3389/fchem.2020.582861
PMID:33094102

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 / Protoberberine alkaloids and derivatives
(13S)-2,3,9-trimethoxy-13-methyl-6,8,13,13a-tetrahydro-5H-isoquinolino[2,1-b]isoquinolin-10-ol 11291216 Click to see CC1C2C3=CC(=C(C=C3CCN2CC4=C1C=CC(=C4OC)O)OC)OC 355.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(15S,18R)-5'-(hydroxymethyl)-7,9,13-trimethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16-diol 5318409 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)O)O)C)C)OC16CCC(CO6)CO 448.60 unknown via CMAUP database
(1S,2R,4R,5'R,6R,7S,8R,9S,12R,13S,15R,16R,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15,16-diol 162984355 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown https://doi.org/10.1016/S0031-9422(00)86621-2
(1S,2S,4R,5'R,6R,7R,8R,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-ol 162923156 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1016/S0031-9422(00)86621-2
(1S,2S,4S,5'R,6R,7S,8R,9R,12R,13S,14S,15S,16R,18R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-14,15,16-triol 162932219 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(C(C(C(C6)O)O)O)C)C)C)OC1 448.60 unknown https://doi.org/10.1016/S0031-9422(00)86621-2
(1S,2S,4S,5'S,6R,7S,8R,9S,12S,13S,14S,15R,16R,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-14,15,16,18-tetrol 11812629 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6(C5(C(C(C(C6)O)O)O)C)O)C)C)OC1 464.60 unknown via CMAUP database
(25S)-3beta-Acetoxyspirosta-5-ene 11798067 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC(=O)C)C)C)C)OC1 456.70 unknown via CMAUP database
5',7,9,13-Tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-14,15,16-triol 12313256 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(C(C(C(C6)O)O)O)C)C)C)OC1 448.60 unknown https://doi.org/10.1246/BCSJ.32.791
https://doi.org/10.1016/S0031-9422(00)86621-2
Digin 287688 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown https://doi.org/10.1016/S0031-9422(00)86621-2
https://doi.org/10.1246/BCSJ.32.791
https://doi.org/10.1248/CPB.6.421
Spirost-5-en-3-ol 234096 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown https://doi.org/10.1016/S0031-9422(00)86621-2
Tokorogenin 20841762 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(C(C(C(C6)O)O)O)C)C)C)OC1 448.60 unknown https://doi.org/10.1246/BCSJ.32.791
https://doi.org/10.1248/CPB.6.421
Yamogenin 441900 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1 414.60 unknown via CMAUP database
Yonogenin 12304416 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)O)C)C)C)OC1 432.60 unknown https://doi.org/10.1246/BCSJ.32.791
https://doi.org/10.1248/CPB.6.421
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2R,3R,4S,5S,6R)-2-[4-[17-[(2R,3R,4R,5S,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,19-dihydroxy-7,13,18-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 11968860 Click to see CC1C2C3CCC4C(C3CC2OC1(CCC(C)COC5C(C(C(C(O5)CO)O)O)O)O)CC(C6(C4(CCCC6OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)OC9C(C(C(C(O9)CO)O)O)O)OC1C(C(C(C(O1)CO)O)O)O)O)O)C)C)O 1261.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(1R,2R,4S,6S,7S,8R,9S,12S,13S,15S,16S,18R)-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]icosane-6,15,16-triol 162967655 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)O)O)C)C)OC1(CCC(C)COC6C(C(C(C(O6)CO)O)O)O)O 612.80 unknown https://doi.org/10.1016/S0031-9422(00)80089-8
(1R,2R,4S,6S,7S,8R,9S,12S,13S,15S,16S,18R)-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]icosane-6,15,16-triol 162967654 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)O)O)C)C)OC1(CCC(C)COC6C(C(C(C(O6)CO)O)O)O)O 612.80 unknown https://doi.org/10.1016/S0031-9422(00)80089-8
(1R,2S,4S,6R,7S,8R,9S,12S,13S,15S,16S,18R)-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]icosane-6,15,16-triol 101458549 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)O)O)C)C)OC1(CCC(C)COC6C(C(C(C(O6)CO)O)O)O)O 612.80 unknown https://doi.org/10.1016/S0031-9422(00)80089-8
(2R,3R,4S,5S,6R)-2-[4-[(18S)-16-[(2R,3R,4R,5R,6R)-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-5-hydroxy-6-(hydroxymethyl)-3,4-bis[[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy]oxan-2-yl]oxy-6-(hydroxymethyl)oxan-2-yl]oxy-6,19-dihydroxy-7,9,13-trimethyl-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosan-6-yl]-2-methylbutoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 24893581 Click to see CC1C2C(CC3C2(CCC4C3CC(C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)CO)O)O)O)O)O)C)O)C)OC1(CCC(C)COC1C(C(C(C(O1)CO)O)O)O)O 1261.40 unknown via CMAUP database
(2R,3S,4S,5S,6R)-2-[(2R,3S,4S,5R,6R)-4-hydroxy-2-(hydroxymethyl)-6-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-hydroxy-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-18-en-16-yl]oxy]-5-[(2R,3S,4S,5S,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 53384936 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)OC7C(C(C(C(O7)C)O)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
(2S,3R,4S,5R)-2-[(9S,13S,14S,15R,18R)-15,16-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-14-yl]oxyoxane-3,4,5-triol 11968998 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(C(C(C(C6)O)O)OC7C(C(C(CO7)O)O)O)C)C)C)OC1 580.70 unknown via CMAUP database
(2S,3R,4S,5R)-2-[(9S,13S,15S,18R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15-yl]oxyoxane-3,4,5-triol 11968320 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)OC7C(C(C(CO7)O)O)O)C)C)C)OC1 564.70 unknown via CMAUP database
(2S,3R,4S,5S)-2-[(1R,2R,4S,5'S,6R,7S,8R,9S,12S,13S,14S,15R,16S,18R)-15,16-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-14-yl]oxyoxane-3,4,5-triol 163076134 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(C(C(C(C6)O)O)OC7C(C(C(CO7)O)O)O)C)C)C)OC1 580.70 unknown https://doi.org/10.1248/YAKUSHI1947.83.8_757
(2S,3R,4S,5S)-2-[(1S,2R,4R,5'R,6R,7S,8S,9S,12R,13S,15S,16S,18R)-16-hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15-yl]oxyoxane-3,4,5-triol 162947496 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)OC7C(C(C(CO7)O)O)O)C)C)C)OC1 564.70 unknown https://doi.org/10.1248/YAKUSHI1947.83.8_757
2-(15,16-Dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-14-yl)oxyoxane-3,4,5-triol 4483247 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(C(C(C(C6)O)O)OC7C(C(C(CO7)O)O)O)C)C)C)OC1 580.70 unknown https://doi.org/10.1248/YAKUSHI1947.83.8_757
2-(16-Hydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-15-yl)oxyoxane-3,4,5-triol 12445004 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CCC6C5(CC(C(C6)O)OC7C(C(C(CO7)O)O)O)C)C)C)OC1 564.70 unknown https://doi.org/10.1248/YAKUSHI1947.83.8_757
2-[5-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,16S)-6-hydroxy-7,9,13-trimethyl-6-[(3R)-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-18-en-16-yl]oxy]-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 54609052 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1065.20 unknown via CMAUP database
26-O-beta-D-glucopyranosyl-3beta,26-dihydroxy-23S-methoxy-25(R)-furosta-5,20(22)-dien-3-O-alpha-L-rhamnopyranosyl(1-2)-[alpha-L-rhamnopyranosyl(1-4)]-beta-D-glucopyranoside 52931427 Click to see CCC1C(CC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)OC6C(C(C(C(O6)C)O)O)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC(=C)C(CC(C)COC8C(C(C(C(O8)CO)O)O)O)OC 1077.30 unknown via CMAUP database
3-O-(Rhaa1-4(Rhaa1-2)Glcb)-(25R)-spirost-5-en-3beta-ol 52931449 Click to see CCC1C(CC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)OC6C(C(C(C(O6)C)O)O)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC8(CCC(CO8)C)C 885.10 unknown via CMAUP database
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]icosane-6,15,16-triol 162967651 Click to see CC1C2C(CC3C2(CCC4C3CCC5C4(CC(C(C5)O)O)C)C)OC1(CCC(C)COC6C(C(C(C(O6)CO)O)O)O)O 612.80 unknown https://doi.org/10.1016/S0031-9422(00)80089-8
Protoneogracillin 46906323 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)OC7C(C(C(C(O7)CO)O)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)OC1(CCC(C)COC9C(C(C(C(O9)CO)O)O)O)O 1065.20 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indoles
Capparin B 24813533 Click to see COC1=CC2=C(C=C1)C(=C(N2)SC)C=O 221.28 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Indolines
6-Methoxyindoline-2,3-dione 10374972 Click to see COC1=CC2=C(C=C1)C(=O)C(=O)N2 177.16 unknown via CMAUP database
Capparin A 101457836 Click to see COC1=CC2=C(C=C1)C3(CN=C(S3)SC)C(=O)N2 280.40 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
6-(Hydroxymethyl)-4-oxopyran-3-olate 25202640 Click to see C1=C(OC=C(C1=O)[O-])CO 141.10 unknown via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(1Z,6E)-1,7-bis(4-hydroxy-3-methoxyphenyl)-4-[1-hydroxy-2-(4-methylphenyl)ethyl]hepta-1,6-diene-3,5-dione 5321967 Click to see CC1=CC=C(C=C1)CC(C(C(=O)C=CC2=CC(=C(C=C2)O)OC)C(=O)C=CC3=CC(=C(C=C3)O)OC)O 502.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Oroxylin A 5320315 Click to see COC1=C(C2=C(C=C1O)OC(=CC2=O)C3=CC=CC=C3)O 284.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
Wogonin 5281703 Click to see COC1=C(C=C(C2=C1OC(=CC2=O)C3=CC=CC=C3)O)O 284.26 unknown via CMAUP database

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