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Scrophularia buergeriana

Scrophularia buergeriana - 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 UUID64404e33b035f870603223
Scientific name Scrophularia buergeriana
Authority Miq.
First published in Ann. Mus. Bot. Lugduno-Batavi 2: 116 (1865)

Description Top

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Synonyms Top

Scientific name Authority First published in
Scrophularia oldhamii Oliv. J. Linn. Soc., Bot. 9: 167 (1867)

Common names Top

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Language Common/alternative name
Arabic غدب برغري
Japanese ゴマノハグサ
Korean 현삼
Chinese 玄参
Chinese 北玄参

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
Scrophularia buergerana var. tsinglingensis P.C.Tsoong Fl. Reipubl. Popularis Sin. 67(2): 395 (1979)

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 North-central
      • China Southeast
      • Manchuria
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Primorye

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001136638
UNII NN0EME99GM
Tropicos 29200379
KEW urn:lsid:ipni.org:names:809070-1
The Plant List tro-29200379
Open Tree Of Life 764427
Observations.org 122029
NCBI Taxonomy 476207
IPNI 809070-1
iNaturalist 1067934
GBIF 3738793
Freebase /m/0nbdf2f
EOL 2894988
Elurikkus 405835
USDA GRIN 423530
CMAUP NPO6541

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
Modulating the RFamide-related peptide-3/G protein-coupled receptor 147 signaling pathway with nourishing Yin-removing fire herbal mixture to alleviate precocious puberty in female rats: An experimental study Dai X, He Y, Li S, Sun Y, Sun W, Tian Z, Ph.D., Yu J, Ph.D., Ablakimova N, Wang Y Int J Reprod Biomed 23-Feb-2024
PMCID:PMC10963877
doi:10.18502/ijrm.v22i1.15240
PMID:38544669
Current Research Status and Implication for Further Study of Real-World Data on East Asian Traditional Medicine for Heart Failure: A Scoping Review Park J, Bak S, Chu H, Kang S, Youn I, Jun H, Sim D, Leem J Healthcare (Basel) 27-Dec-2023
PMCID:PMC10779411
doi:10.3390/healthcare12010061
PMID:38200969
The complete chloroplast genome of Torenia violacea (Azaola) Pennell 1943 (Linderniaceae) Zhu W, Cui H, Xiang X Mitochondrial DNA B Resour 30-Oct-2023
PMCID:PMC10769558
doi:10.1080/23802359.2023.2274619
PMID:38188442
Anti-inflammatory and anti-allergic effects of Cheonwangbosim-dan water extract: An in vitro and in vivo study Jeon WY, Jin SE, Sohn E, Jo K, Ha H, Shin HK, Lee MY Heliyon 11-May-2023
PMCID:PMC10199208
doi:10.1016/j.heliyon.2023.e16172
PMID:37215857
Effects of Scrophularia buergeriana Extract (Brainon®) on Aging-Induced Memory Impairment in SAMP8 Mice Kim HL, Lee SK, Min DE, Bastola T, Chang BY, Bae JH, Lee DR Curr Issues Mol Biol 03-Feb-2023
PMCID:PMC9955813
doi:10.3390/cimb45020084
PMID:36826029
Chemical Characterization, Antioxidant Capacity and Anti-Oxidative Stress Potential of South American Fabaceae Desmodium tortuosum Rodríguez JL, Berrios P, Clavo ZM, Marin-Bravo M, Inostroza-Ruiz L, Ramos-Gonzalez M, Quispe-Solano M, Fernández-Alfonso MS, Palomino O, Goya L Nutrients 01-Feb-2023
PMCID:PMC9921092
doi:10.3390/nu15030746
PMID:36771451
Complete Plastome of Physalis angulata var. villosa, Gene Organization, Comparative Genomics and Phylogenetic Relationships among Solanaceae Zhan X, Zhang Z, Zhang Y, Gao Y, Jin Y, Shen C, Wang H, Feng S Genes (Basel) 05-Dec-2022
PMCID:PMC9778145
doi:10.3390/genes13122291
PMID:36553558
Paeonia × suffruticosa (Moutan Peony)—A Review of the Chemical Composition, Traditional and Professional Use in Medicine, Position in Cosmetics Industries, and Biotechnological Studies Ekiert H, Klimek-Szczykutowicz M, Szopa A Plants (Basel) 05-Dec-2022
PMCID:PMC9739549
doi:10.3390/plants11233379
PMID:36501418
Harpagoside attenuates local bone Erosion and systemic osteoporosis in collagen-induced arthritis in mice Kim JY, Cheon YH, Ahn SJ, Kwak SC, Chung CH, Lee CH, Lee MS BMC Complement Med Ther 10-Aug-2022
PMCID:PMC9364518
doi:10.1186/s12906-022-03694-y
PMID:35948905
Taxonomy, comparative genomics of Mullein (Verbascum, Scrophulariaceae), with implications for the evolution of Verbascum and Lamiales Dong X, Mkala EM, Mutinda ES, Yang JX, Wanga VO, Oulo MA, Onjolo VO, Hu GW, Wang QF BMC Genomics 08-Aug-2022
PMCID:PMC9358837
doi:10.1186/s12864-022-08799-9
PMID:35941527
Characterization of the complete chloroplast genome of the medicinal herb Veronica polita Fr. 1819 (Lamiales: Plantaginaceae) Jia S, Chen W, Zhao G, Wang S, Xu Z, Li Q Mitochondrial DNA B Resour 30-Jun-2022
PMCID:PMC9255118
doi:10.1080/23802359.2022.2086074
PMID:35801139
Special Issue “Bioactive Compounds from Natural Sources (2020, 2021)” Sytar O, Smetanska I Molecules 16-Mar-2022
PMCID:PMC8954983
doi:10.3390/molecules27061929
PMID:35335293
Improving phylogenetic resolution of the Lamiales using the complete plastome sequences of six Penstemon species Stettler JM, Stevens MR, Meservey LM, Crump WW, Grow JD, Porter SJ, Love LS, Maughan PJ, Jellen EN PLoS One 15-Dec-2021
PMCID:PMC8673674
doi:10.1371/journal.pone.0261143
PMID:34910738
Scrophulariae Radix: An Overview of Its Biological Activities and Nutraceutical and Pharmaceutical Applications Lee HJ, Kim HL, Lee DR, Choi BK, Yang SH Molecules 30-Aug-2021
PMCID:PMC8434300
doi:10.3390/molecules26175250
PMID:34500684
Recent Developments in Therapeutic and Nutraceutical Applications of p-Methoxycinnamic Acid from Plant Origin Płowuszyńska A, Gliszczyńska A Molecules 23-Jun-2021
PMCID:PMC8270276
doi:10.3390/molecules26133827
PMID:34201697

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
> Alkaloids and derivatives / Cephalotaxus alkaloids
1-O-[(2S,3S,6R)-4-methoxy-16,18-dioxa-10-azapentacyclo[11.7.0.02,6.06,10.015,19]icosa-1(20),4,13,15(19)-tetraen-3-yl] 4-O-methyl (2S)-2-hydroxy-2-(3-hydroxy-3-methylbutyl)butanedioate 29927670 Click to see CC(C)(CCC(CC(=O)OC)(C(=O)OC1C2C3=CC4=C(C=C3CCN5C2(CCC5)C=C1OC)OCO4)O)O 531.60 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
Dibutyl Phthalate 3026 Click to see CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC 278.34 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acids
Benzoic Acid 243 Click to see C1=CC=C(C=C1)C(=O)O 122.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic acid 10742 Click to see COC1=CC(=CC(=C1O)OC)C(=O)O 198.17 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
Methylisoeugenol 637776 Click to see CC=CC1=CC(=C(C=C1)OC)OC 178.23 unknown via CMAUP database
> Benzenoids / Phenols / 1-hydroxy-4-unsubstituted benzenoids
Phenol 996 Click to see C1=CC=C(C=C1)O 94.11 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
> Benzenoids / Phenols / Methoxyphenols
Eugenol 3314 Click to see COC1=C(C=CC(=C1)CC=C)O 164.20 unknown via CMAUP database
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives
5-(2-Hydroxyethyl)-2-methoxyphenol 10034991 Click to see COC1=C(C=C(C=C1)CCO)O 168.19 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Oleic Acid 445639 Click to see CCCCCCCCC=CCCCCCCCC(=O)O 282.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl linoleate 5284421 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OC 294.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Trilaurin 10851 Click to see CCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCC)OC(=O)CCCCCCCCCCC 639.00 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
(Z)-alpha-ocimene 5463455 Click to see CC(=C)CCC=C(C)C=C 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Iridoids and derivatives
6-Methoxy-2,10-dioxatricyclo[5.3.1.04,11]undecane-4,5-diol 162953054 Click to see COC1C2CCOC3C2C(C1O)(CO3)O 216.23 unknown https://doi.org/10.1002/HLCA.200690250
Buergerinin E 102153621 Click to see COC1C2CCOC3C2C(C1O)(CO3)O 216.23 unknown https://doi.org/10.1002/HLCA.200690250
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
Beta-Elemene 6918391 Click to see CC(=C)C1CCC(C(C1)C(=C)C)(C)C=C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
(1S,4aR,5R,7S,7aR)-7-methyl-1-[(2R,3S,4R,5S,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol 162989826 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown https://doi.org/10.1021/NP0202172
(1S,4aS,5R,7S,7aR)-7-methyl-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol 44438955 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown https://doi.org/10.1021/NP0202172
(1S,4aS,5R,7S)-7-methyl-1-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol 91973789 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown via CMAUP database
(1S,4aS,5R)-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol 54748480 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown via CMAUP database
(4aS,5R,7S,7aR)-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-4a,5,7-triol 101286236 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown via CMAUP database
[(1R,4aR,5S,7R)-4a,5-dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] (Z)-3-phenylprop-2-enoate 24085834 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=CC=C4 494.50 unknown via CMAUP database
[(1S,4aR,5R,7S,7aS)-4a,5-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] (E)-3-(4-methoxyphenyl)prop-2-enoate 162902459 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)OC 524.50 unknown https://doi.org/10.1021/NP0202172
[(1S,4aR,5R,7S,7aS)-4a,5-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] (Z)-3-(4-methoxyphenyl)prop-2-enoate 162902460 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)OC 524.50 unknown https://doi.org/10.1021/NP0202172
[(1S,4aR,5R,7S,7aS)-4a,5-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] (Z)-3-phenylprop-2-enoate 162989217 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=CC=C4 494.50 unknown https://doi.org/10.1021/NP0202172
[(1S,4aS,5R,7S,7aS)-4a,5-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] 3-(4-methoxyphenyl)prop-2-enoate 162902462 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)OC 524.50 unknown https://doi.org/10.1021/NP0202172
[(1S,4aS,5R,7S,7aS)-4a,5-dihydroxy-7-methyl-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] 3-phenylprop-2-enoate 87959 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=CC=C4 494.50 unknown https://doi.org/10.1021/NP0202172
[(2R,3S,4S,5R,6S)-6-[[(1S,4aR,5R,7S,7aR)-4a,5,7-trihydroxy-7-methyl-1,5,6,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (E)-3-(4-methoxyphenyl)prop-2-enoate 162947774 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)OC)O)O)O)O)O)O 524.50 unknown https://doi.org/10.1021/NP0202172
[(2R,3S,4S,5R,6S)-6-[[(1S,4aR,5R,7S,7aR)-4a,5,7-trihydroxy-7-methyl-1,5,6,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl (Z)-3-(4-methoxyphenyl)prop-2-enoate 162947775 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)OC)O)O)O)O)O)O 524.50 unknown https://doi.org/10.1021/NP0202172
[(2R,3S,4S,5R,6S)-6-[[(1S,4aS,5R,7S,7aR)-4a,5,7-trihydroxy-7-methyl-1,5,6,7a-tetrahydrocyclopenta[c]pyran-1-yl]oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-methoxyphenyl)prop-2-enoate 162947771 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)OC)O)O)O)O)O)O 524.50 unknown https://doi.org/10.1021/NP0202172
[4a,5-Dihydroxy-7-methyl-1-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-1,5,6,7a-tetrahydrocyclopenta[c]pyran-7-yl] 3-(4-methoxyphenyl)prop-2-enoate 78385276 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)OC 524.50 unknown https://doi.org/10.1021/NP0202172
[6-[(4a,5,7-Trihydroxy-7-methyl-1,5,6,7a-tetrahydrocyclopenta[c]pyran-1-yl)oxy]-3,4,5-trihydroxyoxan-2-yl]methyl 3-(4-methoxyphenyl)prop-2-enoate 75178641 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)OC)O)O)O)O)O)O 524.50 unknown https://doi.org/10.1021/NP0202172
6'-O-p-Methoxy-cis-cinnamoylharpagide 10896666 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)OC)O)O)O)O)O)O 524.50 unknown https://doi.org/10.1021/NP0202172
6'-O-p-Methoxy-trans-cinnamoylharpagide 10984208 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)COC(=O)C=CC4=CC=C(C=C4)OC)O)O)O)O)O)O 524.50 unknown https://doi.org/10.1021/NP0202172
8-O-Feruloylharpagide 101402541 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC(=C(C=C4)O)OC 540.50 unknown via CMAUP database
8-O-p-Methoxy-cis-cinnamoylharpagide 10875054 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)OC 524.50 unknown https://doi.org/10.1021/NP0202172
8-O-p-Methoxy-trans-cinnamoylharpagide 11049658 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=C(C=C4)OC 524.50 unknown https://doi.org/10.1021/NP0202172
Aucubin 91458 Click to see C1=COC(C2C1C(C=C2CO)O)OC3C(C(C(C(O3)CO)O)O)O 346.33 unknown via CMAUP database
CID 10044294 10044294 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown via CMAUP database
Harpagide 93045 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)O 364.34 unknown https://doi.org/10.1021/NP0202172
Harpagoside 5281542 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=CC=C4 494.50 unknown https://doi.org/10.1021/NP0202172
Z-harpagoside 13889700 Click to see CC1(CC(C2(C1C(OC=C2)OC3C(C(C(C(O3)CO)O)O)O)O)O)OC(=O)C=CC4=CC=CC=C4 494.50 unknown https://doi.org/10.1021/NP0202172
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
(4aR,5S,7aS)-5-hydroxy-7-(hydroxymethyl)-4,4a,5,7a-tetrahydro-1H-cyclopenta[c]pyran-3-one 10866992 Click to see C1C2C(COC1=O)C(=CC2O)CO 184.19 unknown https://doi.org/10.1002/HLCA.200690250
(4aR,5S,7aS)-7-(hydroxymethyl)-5-methoxy-4,4a,5,7a-tetrahydro-1H-cyclopenta[c]pyran-3-one 130929387 Click to see COC1C=C(C2C1CC(=O)OC2)CO 198.22 unknown https://doi.org/10.1002/HLCA.200690250
4a,5,7-trihydroxy-7-methyl-4,5,6,7a-tetrahydro-1H-cyclopenta[c]pyran-3-one 124222328 Click to see CC1(CC(C2(C1COC(=O)C2)O)O)O 202.20 unknown https://doi.org/10.1002/HLCA.200690250
5-hydroxy-7-(hydroxymethyl)-4,4a,5,7a-tetrahydro-1H-cyclopenta[c]pyran-3-one 85294993 Click to see C1C2C(COC1=O)C(=CC2O)CO 184.19 unknown https://doi.org/10.1002/HLCA.200690250
7-(hydroxymethyl)-5-methoxy-4,4a,5,7a-tetrahydro-1H-cyclopenta[c]pyran-3-one 130145400 Click to see COC1C=C(C2C1CC(=O)OC2)CO 198.22 unknown https://doi.org/10.1002/HLCA.200690250
Buergerinin B 91885076 Click to see CC1(CC(C2(C1COC(=O)C2)O)O)O 202.20 unknown https://doi.org/10.1002/HLCA.200690250
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Lupeol 259846 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
Parkeol 12313974 Click to see CC(CCC=C(C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
(1S,3R,6S,8R,11S,12S,15R,16R)-15-[(2R,5S)-5-ethyl-6-methylhept-6-en-2-yl]-7,7,12,16-tetramethylpentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 44423569 Click to see CCC(CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C)C(=C)C 454.80 unknown via CMAUP database
Cycloneolitsol 101306728 Click to see CC(CCC(C)(C)C(=C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C 454.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
(24S)-24-Methyl-5alpha-lanosta-9(11),25-dien-3beta-ol 101630502 Click to see CC(CCC(C)C(=C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 440.70 unknown via CMAUP database
24,24-Dimethyllanosta-9(11),25-dien-3beta-ol 102504569 Click to see CC(CCC(C)(C)C(=C)C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 454.80 unknown via CMAUP database
4alpha,14alpha-Dimethyl-24-methylene-cholest-9(11)-en-3beta-ol 5283648 Click to see CC1C2CCC3C(=CCC4(C3(CCC4C(C)CCC(=C)C(C)C)C)C)C2(CCC1O)C 426.70 unknown via CMAUP database
Agrostophyllinol 489917 Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol 6432744 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
(24S)-24-Ethyl-5alpha-lanosta-9(11),25-dien-3beta-ol 101630504 Click to see CCC(CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4(C)C)O)C)C)C)C(=C)C 454.80 unknown via CMAUP database
(24S)-4alpha,14-Dimethyl-5alpha-stigmasta-9(11),25-dien-3beta-ol 101630497 Click to see CCC(CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4C)O)C)C)C)C(=C)C 440.70 unknown via CMAUP database
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 via CMAUP database
4alpha,14-Dimethyl-5alpha-stigmast-9(11)-en-3beta-ol 101630496 Click to see CCC(CCC(C)C1CCC2(C1(CC=C3C2CCC4C3(CCC(C4C)O)C)C)C)C(C)C 442.80 unknown via CMAUP database
alpha1-Sitosterol 9548595 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2=CCC4C3(CCC(C4C)O)C)C)C(C)C 426.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
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 via CMAUP database
Stigmast-4-en-3-one 5484202 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CCC4=CC(=O)CCC34C)C)C(C)C 412.70 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5R,6R)-2-ethoxy-3,5-dihydroxy-3-(3-hydroxy-4-methoxyphenyl)-6-(hydroxymethyl)oxan-4-yl]oxy-6-methyloxane-3,4,5-triol 192240 Click to see CCOC1C(C(C(C(O1)CO)O)OC2C(C(C(C(O2)C)O)O)O)(C3=CC(=C(C=C3)OC)O)O 476.50 unknown via CMAUP database
Catapol 24721256 Click to see C1=COC(C2C1C(C3C2(O3)CO)O)OC4C(C(C(C(O4)CO)O)O)O 362.33 unknown via CMAUP database
Decaffeoyl-acteoside 13889681 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2O)OCCC3=CC(=C(C=C3)O)O)CO)O)O)O)O 462.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(3-Acetyloxy-2,5-dihydroxy-6-methyloxan-4-yl) 3-(4-methoxyphenyl)prop-2-enoate 85121387 Click to see CC1C(C(C(C(O1)O)OC(=O)C)OC(=O)C=CC2=CC=C(C=C2)OC)O 366.40 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
(4,5,6-Trihydroxy-2-methyloxan-3-yl) 3-(4-methoxyphenyl)prop-2-enoate 85101415 Click to see CC1C(C(C(C(O1)O)O)O)OC(=O)C=CC2=CC=C(C=C2)OC 324.32 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
[(2R,3R,4R,5S,6S)-3-acetyloxy-2,5-dihydroxy-6-methyloxan-4-yl] (E)-3-(4-methoxyphenyl)prop-2-enoate 10361522 Click to see CC1C(C(C(C(O1)O)OC(=O)C)OC(=O)C=CC2=CC=C(C=C2)OC)O 366.40 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
[(2R,3R,4R,5S,6S)-3-acetyloxy-2,5-dihydroxy-6-methyloxan-4-yl] (Z)-3-(4-methoxyphenyl)prop-2-enoate 10361523 Click to see CC1C(C(C(C(O1)O)OC(=O)C)OC(=O)C=CC2=CC=C(C=C2)OC)O 366.40 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
[(2S,3R,4S,5R,6R)-4,5,6-trihydroxy-2-methyloxan-3-yl] (E)-3-(4-methoxyphenyl)prop-2-enoate 10041914 Click to see CC1C(C(C(C(O1)O)O)O)OC(=O)C=CC2=CC=C(C=C2)OC 324.32 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
[(2S,3S,4R,5R,6R)-5-acetyloxy-6-hydroxy-4-[(E)-3-(4-methoxyphenyl)prop-2-enoyl]oxy-2-methyloxan-3-yl] (E)-3-(4-methoxyphenyl)prop-2-enoate 10075559 Click to see CC1C(C(C(C(O1)O)OC(=O)C)OC(=O)C=CC2=CC=C(C=C2)OC)OC(=O)C=CC3=CC=C(C=C3)OC 526.50 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
[(2S,3S,4S,5R,6R)-5-acetyloxy-6-hydroxy-4-[(E)-3-(4-methoxyphenyl)prop-2-enoyl]oxy-2-methyloxan-3-yl] (E)-3-(4-methoxyphenyl)prop-2-enoate 162981039 Click to see CC1C(C(C(C(O1)O)OC(=O)C)OC(=O)C=CC2=CC=C(C=C2)OC)OC(=O)C=CC3=CC=C(C=C3)OC 526.50 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
[5-Acetyloxy-6-hydroxy-4-[3-(4-methoxyphenyl)prop-2-enoyloxy]-2-methyloxan-3-yl] 3-(4-methoxyphenyl)prop-2-enoate 162981038 Click to see CC1C(C(C(C(O1)O)OC(=O)C)OC(=O)C=CC2=CC=C(C=C2)OC)OC(=O)C=CC3=CC=C(C=C3)OC 526.50 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[5-hydroxy-6-[2-(3-hydroxy-4-methoxyphenyl)ethoxy]-4-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-2-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-3-yl] (E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoate 14413436 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)OC)O)O)O)O)O 784.80 unknown via CMAUP database
Angoroside C 23757181 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)OC)O)O)O)O)O 784.80 unknown via CMAUP database
Angoroside-C 6444153 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)OC)O)O)O)O)O 784.80 unknown via CMAUP database
Angroside C 102309024 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)OC)O)O)O)O)O 784.80 unknown via CMAUP database
Isoangoroside C 71433809 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)OC)O)O)O)O)O 784.80 unknown via CMAUP database
Stachysoside A 14034195 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)OC5C(C(C(CO5)O)O)O)O)O 756.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural 237332 Click to see C1=C(OC(=C1)C=O)CO 126.11 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
5H-7,4-Methenofuro(3,2-c)oxireno(f)oxacycloundecin-5-one,1a,2,3,7,11,11a-hexahydro-8,11a-dimethyl-, (1aS,7R,11aS)- 497202 Click to see CC1=COC2=C1C3C=C(CCC4C(C2)(O4)C)C(=O)O3 260.28 unknown via CMAUP database
Linderalactone 6450191 Click to see CC1=CCCC2=CC(C3=C(C1)OC=C3C)OC2=O 244.28 unknown via CMAUP database
Pseudoneolinderane 57400551 Click to see CC1=COC2=C1C3C=C(CCC4C(C2)(O4)C)C(=O)O3 260.28 unknown via CMAUP database
Zeylanin 12445041 Click to see CC1=CC2=C(C3C=C(CCC1OC(=O)C)C(=O)O3)C(=CO2)C 302.32 unknown via CMAUP database
> Organoheterocyclic compounds / Dioxanes / 1,4-dioxanes
2H-10,1a-(Epoxymethano)oxireno(4,5)cyclodeca(1,2-b)furan-12-one, 3,6,10,10a-tetrahydro-5,9-methyl-, (1aS-(1aR*,4E,10R*,10aR*))- 6450227 Click to see CC1=CCCC23C(O2)C(C4=C(C1)OC=C4C)OC3=O 260.28 unknown via CMAUP database
> Organoheterocyclic compounds / Furofurans
(1S,5S,7R)-7-methyl-4,8,11-trioxatricyclo[5.3.1.01,5]undecan-3-one 133561877 Click to see CC12CC3C(O1)(CCO2)CC(=O)O3 184.19 unknown https://doi.org/10.1016/S0040-4039(99)02244-3
7-Methyl-4,8,11-trioxatricyclo[5.3.1.01,5]undecan-3-one 72755635 Click to see CC12CC3C(O1)(CCO2)CC(=O)O3 184.19 unknown https://doi.org/10.1016/S0040-4039(99)02244-3
7-Methyl-4,8,11-trioxatricyclo[5.3.1.01,5]undecane 72819440 Click to see CC12CC3C(O1)(CCO3)CCO2 170.21 unknown https://doi.org/10.1016/S0040-4039(99)02244-3
Buergerinin F 11367239 Click to see CC12CC3C(O1)(CCO3)CCO2 170.21 unknown https://doi.org/10.1016/S0040-4039(99)02244-3
Buergerinin G 11217635 Click to see CC12CC3C(O1)(CCO2)CC(=O)O3 184.19 unknown https://doi.org/10.1016/S0040-4039(99)02244-3
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
6,6a-bis(hydroxymethyl)-4-methoxy-3a,4-dihydro-3H-cyclopenta[b]furan-2-one 163015924 Click to see COC1C=C(C2(C1CC(=O)O2)CO)CO 214.21 unknown https://doi.org/10.1002/HLCA.200690250
Buergerinin D 102153620 Click to see COC1C=C(C2(C1CC(=O)O2)CO)CO 214.21 unknown https://doi.org/10.1002/HLCA.200690250
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acid esters
Methyl 4-methoxycinnamate 641297 Click to see COC1=CC=C(C=C1)C=CC(=O)OC 192.21 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
Methyl p-methoxycinnamate 92841 Click to see COC1=CC=C(C=C1)C=CC(=O)OC 192.21 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Cinnamic acids
4-Methoxycinnamic acid 13245 Click to see COC1=CC=C(C=C1)C=CC(=O)O 178.18 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
Cinnamic acid 444539 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
cis-Cinnamic acid 5372954 Click to see C1=CC=C(C=C1)C=CC(=O)O 148.16 unknown via CMAUP database
trans-4-Methoxycinnamic acid 699414 Click to see COC1=CC=C(C=C1)C=CC(=O)O 178.18 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
cis-Martynoside 10349304 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O 652.60 unknown via CMAUP database
Cistanoside D 5315930 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)O)OC)O)O)O)O 652.60 unknown via CMAUP database
Martynoside 5319292 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)OC)CO)OCCC4=CC(=C(C=C4)OC)O)O)O)O)O 652.60 unknown via CMAUP database
Ningposide A 5315957 Click to see CC1C(C(C(C(O1)O)OC(=O)C=CC2=CC(=C(C=C2)O)OC)OC(=O)C)O 382.40 unknown via CMAUP database
Ningposide B 5320176 Click to see CC1C(C(C(C(O1)O)OC(=O)C=CC2=CC(=C(C=C2)O)OC)O)OC(=O)C 382.40 unknown via CMAUP database
Verbascoside 5281800 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)CO)OCCC4=CC(=C(C=C4)O)O)O)O)O)O 624.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Ningposide C 10498169 Click to see CC1C(C(C(C(O1)O)OC(=O)C=CC2=CC=C(C=C2)O)OC(=O)C)O 352.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
(E)-3-(3,4-dihydroxyphenyl)prop-2-enoic acid 2518 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
3-(4-Hydroxy-3-methoxyphenyl)prop-2-enoic acid 709 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
4-Hydroxycinnamic acid 322 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
Caffeic Acid 689043 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
cis-Caffeic acid 1549111 Click to see C1=CC(=C(C=C1C=CC(=O)O)O)O 180.16 unknown via CMAUP database
cis-p-Coumaric acid 1549106 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
Ferulic acid 445858 Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O 194.18 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown https://doi.org/10.1016/S0031-9422(00)00110-2
> 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 via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(-)-Epitaxifolin 712318 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Populnin 3-O-rhamnopyranoside 90795788 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)OC4C(C(C(C(O4)CO)O)O)O)C5=CC=C(C=C5)O)O)O)O 594.50 unknown via CMAUP database

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