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Vincetoxicum stauntonii

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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 UUID64404be6c2b16264262288
Scientific name Vincetoxicum stauntonii
Authority (Decne.) C.Y.Wu & D.Z.Li
First published in Acta Bot. Yunnan. 11: 47 (1989)

Description Top

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Synonyms Top

Scientific name Authority First published in
Cynanchum linearifolium Hemsl. J. Linn. Soc., Bot. 26: 107 (1889)
Pentasacme stauntonii Decne. Prodr. 8: 627 (1844)
Vincetoxicum linearifolium (Hemsl.) Kuntze Revis. Gen. Pl. 2: 424 (1891)

Common names Top

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Language Common/alternative name
Chinese 柳叶白前

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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 North-central
      • China South-central
      • China Southeast

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001104846
Tropicos 2610850
KEW urn:lsid:ipni.org:names:946561-1
Open Tree Of Life 365890
NCBI Taxonomy 516547
IPNI 946561-1
GBIF 5525315
USDA GRIN 432067
CMAUP NPO10366

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
Integrating UPLC-Q-Orbitrap MS with serum pharmacochemistry network and experimental verification to explore the pharmacological mechanisms of Cynanchi stauntonii rhizoma et radix against sepsis-induced acute lung injury Gao H, Yuan Z, Liang H, Liu Y Front Pharmacol 22-Mar-2024
PMCID:PMC10995315
doi:10.3389/fphar.2024.1261772
PMID:38584603
Development of EST-SSR primers and genetic diversity analysis of the southern blight pathogen Sclerotium rolfsii using transcriptome data Wang F, Tang T, Mao T, Duan Y, Guo X, You J Front Microbiol 30-May-2023
PMCID:PMC10267981
doi:10.3389/fmicb.2023.1152865
PMID:37323912
The pharmacology and mechanisms of platycodin D, an active triterpenoid saponin from Platycodon grandiflorus Xie L, Zhao YX, Zheng Y, Li XF Front Pharmacol 06-Apr-2023
PMCID:PMC10117678
doi:10.3389/fphar.2023.1148853
PMID:37089949
Therapeutic drug combinations against COVID-19 obtained by employing a collaborative filtering method Yao R, Yang F, Liu J, Jiao Q, Yu H, Nie X, Li H, Wang X, Xue F Heliyon 25-Feb-2023
PMCID:PMC9958039
doi:10.1016/j.heliyon.2023.e14023
PMID:36873530
Essential Oils and Their Compounds as Potential Anti-Influenza Agents Oriola AO, Oyedeji AO Molecules 12-Nov-2022
PMCID:PMC9693178
doi:10.3390/molecules27227797
PMID:36431899
Ethnobotanical study of Hakka traditional medicine in Ganzhou, China and their antibacterial, antifungal, and cytotoxic assessments Hu H, Yang Y, Aissa A, Tekin V, Li J, Panda SK, Huang H, Luyten W BMC Complement Med Ther 19-Sep-2022
PMCID:PMC9484230
doi:10.1186/s12906-022-03712-z
PMID:36123737
The phytochemical properties, pharmacological effects and traditional uses of Actinidia eriantha Benth.: A review Wang S, Gao X, Sun Q, Zhu Y, Qin L, Zhu B Front Pharmacol 19-Aug-2022
PMCID:PMC9437332
doi:10.3389/fphar.2022.959900
PMID:36059997
Drosophila melanogaster diabetes models and its usage in the research of anti-diabetes management with traditional Chinese medicines Miao Y, Chen R, Wang X, Zhang J, Tang W, Zhang Z, Liu Y, Xu Q Front Med (Lausanne) 11-Aug-2022
PMCID:PMC9403128
doi:10.3389/fmed.2022.953490
PMID:36035393
Antiparasitic Efficacy of Herbal Extracts and Active Compound Against Gyrodactylus kobayashii in Carassius auratus Zhou S, Dong J, Liu Y, Yang Q, Xu N, Yang Y, Ai X Front Vet Sci 06-Apr-2021
PMCID:PMC8056006
doi:10.3389/fvets.2021.665072
PMID:33889606
Complete plastid genome characterization and phylogenetic analysis of Pentasachme caudatum Wallich ex Wight (Gentianales: Apocynaceae) from Guangdong, China Miao S, Luo Y, Bautista MA, Chen T Mitochondrial DNA B Resour 15-Mar-2021
PMCID:PMC7971266
doi:10.1080/23802359.2021.1885319
PMID:33796657
Research Progress on Main Symptoms of Novel Coronavirus Pneumonia Improved by Traditional Chinese Medicine Luo CH, Ma LL, Liu HM, Liao W, Xu RC, Ci ZM, Lin JZ, Han L, Zhang DK Front Pharmacol 11-Sep-2020
PMCID:PMC7516165
doi:10.3389/fphar.2020.556885
PMID:33013395
A robust and miniaturized screening platform to study natural products affecting metabolism and survival in Caenorhabditis elegans Zwirchmayr J, Kirchweger B, Lehner T, Tahir A, Pretsch D, Rollinger JM Sci Rep 23-Jul-2020
PMCID:PMC7378205
doi:10.1038/s41598-020-69186-6
PMID:32704017
Cynanchum paniculatum and Its Major Active Constituents for Inflammatory-Related Diseases: A Review of Traditional Use, Multiple Pathway Modulations, and Clinical Applications Chen JX, Cheng CS, Chen J, Lv LL, Chen ZJ, Chen C, Zheng L Evid Based Complement Alternat Med 22-Jul-2020
PMCID:PMC7396087
doi:10.1155/2020/7259686
PMID:32774428
Essential Oils as Antiviral Agents, Potential of Essential Oils to Treat SARS-CoV-2 Infection: An In-Silico Investigation da Silva JK, Figueiredo PL, Byler KG, Setzer WN Int J Mol Sci 12-May-2020
PMCID:PMC7279430
doi:10.3390/ijms21103426
PMID:32408699
Chemical Constituents of Essential Oils Possessing Anti-Influenza A/WS/33 Virus Activity Choi HJ Osong Public Health Res Perspect 01-Dec-2018
PMCID:PMC6296812
doi:10.24171/j.phrp.2018.9.6.09
PMID:30584499

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 / Phenylpropanes
Butylated Hydroxytoluene 31404 Click to see CC1=CC(=C(C(=C1)C(C)(C)C)O)C(C)(C)C 220.35 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
beta-Asarone 5281758 Click to see CC=CC1=CC(=C(C=C1OC)OC)OC 208.25 unknown via CMAUP database
> Benzenoids / Phenols / Cresols / Ortho cresols
2-Butyl-6-methylphenol 15570435 Click to see CCCCC1=CC=CC(=C1O)C 164.24 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Docosane 12405 Click to see CCCCCCCCCCCCCCCCCCCCCC 310.60 unknown via CMAUP database
Eicosane 8222 Click to see CCCCCCCCCCCCCCCCCCCC 282.50 unknown via CMAUP database
Heneicosane 12403 Click to see CCCCCCCCCCCCCCCCCCCCC 296.60 unknown via CMAUP database
Heptadecane 12398 Click to see CCCCCCCCCCCCCCCCC 240.50 unknown via CMAUP database
Hexadecane 11006 Click to see CCCCCCCCCCCCCCCC 226.44 unknown via CMAUP database
Nonadecane 12401 Click to see CCCCCCCCCCCCCCCCCCC 268.50 unknown via CMAUP database
Octadecane 11635 Click to see CCCCCCCCCCCCCCCCCC 254.50 unknown via CMAUP database
Pentacosane 12406 Click to see CCCCCCCCCCCCCCCCCCCCCCCCC 352.70 unknown via CMAUP database
Tetracosane 12592 Click to see CCCCCCCCCCCCCCCCCCCCCCCC 338.70 unknown via CMAUP database
Tetradecane 12389 Click to see CCCCCCCCCCCCCC 198.39 unknown via CMAUP database
Tricosane 12534 Click to see CCCCCCCCCCCCCCCCCCCCCCC 324.60 unknown via CMAUP database
Tridecane 12388 Click to see CCCCCCCCCCCCC 184.36 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters
Ethyl palmitate 12366 Click to see CCCCCCCCCCCCCCCC(=O)OCC 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
Methyl palmitate 8181 Click to see CCCCCCCCCCCCCCCC(=O)OC 270.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
1-Octanol 957 Click to see CCCCCCCCO 130.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
(9Z,12Z)-Ethyl octadeca-9,12-dienoate 11001 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC 308.50 unknown via CMAUP database
Ethyl Linoleate 5282184 Click to see CCCCCC=CCC=CCCCCCCCC(=O)OCC 308.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Linalool, (-)- 443158 Click to see CC(=CCCC(C)(C=C)O)C 154.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-beta-Caryophyllene 20831623 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
(+)-tau-Muurolol 51394521 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
(4Z)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene 5322111 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
(Z)-caryophyllene 6429301 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
4,11,11-Trimethyl-8-methylene-5-oxatricyclo(8.2.0.0(4,6))dodecane, (1R,4R,6R,10S)- 6604672 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
6,10,14-Trimethylpentadecan-2-one 10408 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=O)C 268.50 unknown via CMAUP database
beta-CARYOPHYLLENE OXIDE 1742210 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Caryophyllene 5281515 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Caryophyllene epoxide 14350 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Caryophyllene oxide 2 13240188 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
Caryophyllene,alpha + beta mixt. 5354499 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Isocaryophyllene 5281522 Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C 204.35 unknown via CMAUP database
Isocaryophyllene oxide 1742211 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
T-Muurolol 3084331 Click to see CC1=CC2C(CCC(C2CC1)(C)O)C(C)C 222.37 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
Eremophilene 12309744 Click to see CC1CCC=C2C1(CC(CC2)C(=C)C)C 204.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives
(1S,3aS,5aS,5bR,9S,11aS,11bR,13aR)-3a,5a,8,8,11b,13a-hexamethyl-1-propan-2-yl-1,2,3,4,5,5b,6,9,10,11,11a,12,13,13b-tetradecahydrocyclopenta[a]chrysen-9-ol 50990037 Click to see CC(C)C1CCC2(C1C3(CCC4(C5CCC(C(C5=CCC4C3(CC2)C)(C)C)O)C)C)C 426.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cholestane steroids / Cholesterols and derivatives
3b-Acetoxycholest-5,24-diene 10916916 Click to see CC(CCC=C(C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC(=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,7S,8S,11S,12S,15R,16R)-7,12,16-trimethyl-15-[(Z,2R)-5-propan-2-ylhept-5-en-2-yl]pentacyclo[9.7.0.01,3.03,8.012,16]octadecan-6-ol 101614311 Click to see CC=C(CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5C)O)C)C)C(C)C 440.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids
5,19-Dimethyl-15,18,20-trioxahexacyclo[14.5.1.01,14.04,13.05,10.019,22]docosa-10,13-dien-8-ol 163009485 Click to see CC12CCC(CC1=CCC3=C4C5(CCC23)COC6(C5C(O4)CO6)C)O 344.40 unknown https://doi.org/10.1055/S-2004-832650
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Hydroxysteroids / 3-hydroxysteroids / 3-beta-hydroxysteroids
Anhydrohirundigenin 102060418 Click to see CC12CCC(CC1=CCC3=C4C5(CCC23)COC6(C5C(O4)CO6)C)O 344.40 unknown https://doi.org/10.1055/S-2004-832650
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Oxasteroids and derivatives
(2R,3R,4S,5R,6R)-2-[[(1R,4R,5R,8S,16S,19S,22R)-5,19-dimethyl-15,18,20-trioxahexacyclo[14.5.1.01,14.04,13.05,10.019,22]docosa-10,13-dien-8-yl]oxy]-4-methoxy-6-methyloxane-3,5-diol 162911141 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC56COC7(C5C(CO7)OC6=C4CC=C3C2)C)C)O)OC)O 504.60 unknown https://doi.org/10.1055/S-2004-832650
2-[(5,19-Dimethyl-15,18,20-trioxahexacyclo[14.5.1.01,14.04,13.05,10.019,22]docosa-10,13-dien-8-yl)oxy]-4-methoxy-6-methyloxane-3,5-diol 162911140 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC56COC7(C5C(CO7)OC6=C4CC=C3C2)C)C)O)OC)O 504.60 unknown https://doi.org/10.1055/S-2004-832650
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids
Funtumine 101702 Click to see CC(=O)C1CCC2C1(CCC3C2CCC4C3(CCC(C4)N)C)C 317.50 unknown via CMAUP database
Irehdiamine A 92198 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)N)C)C)N 316.50 unknown via CMAUP database
Irehdiamine B 15560372 Click to see CC(C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)NC)C)C)N 330.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Conanine-type alkaloids
[(1R,2S,5S,6S,9S,10R,12S,13R,16S)-6,7,13-trimethyl-16-(methylamino)-7-azapentacyclo[10.8.0.02,9.05,9.013,18]icos-18-en-10-yl] 4-methylpent-3-enoate 11178537 Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)NC)C)OC(=O)CC=C(C)C 454.70 unknown via CMAUP database
Con-5-enin-12-ol, 3-(dimethylamino)-, 4-methyl-3-pentenoate (ester), (3beta,12beta)- 11225162 Click to see CC1C2CCC3C2(CN1C)C(CC4C3CC=C5C4(CCC(C5)N(C)C)C)OC(=O)CC=C(C)C 468.70 unknown via CMAUP database
Conessine 441082 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N(C)C)C)CN1C 356.60 unknown via CMAUP database
Isoconessimine 11772257 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)NC)C)CN1C 342.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Primary alcohols
(S)-3-Ethyl-4-methylpentanol 59911029 Click to see CCC(CCO)C(C)C 130.23 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(4S,5R,8S,13S,16S,19R,22R)-8-[(2R,3R,4S,5R,6R)-3,5-dihydroxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 44584779 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5=COC6(C5C(CO6)OC(=O)C4CC=C3C2)C)C)O)OC)O 520.60 unknown https://doi.org/10.1055/S-2004-832650
8-(3,5-Dihydroxy-4-methoxy-6-methyloxan-2-yl)oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 14755283 Click to see CC1C(C(C(C(O1)OC2CCC3(C4CCC5=COC6(C5C(CO6)OC(=O)C4CC=C3C2)C)C)O)OC)O 520.60 unknown https://doi.org/10.1055/S-2004-832650
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
(1E,4S,5R,8S,13R,16S,19R,22R)-8-[(2R,4R,5S,6R)-4-hydroxy-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2S,4R,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1,10-diene-14,21-dione 163048046 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3O)OC4CCC5(C6CC=C7C8C(COC8(OC7=O)C)OC(=O)C6CC=C5C4)C)C)C)OC)O 778.90 unknown https://doi.org/10.1016/S0031-9422(99)00439-2
(1Z,4R,5R,8S,13R,16S,19S,22S)-8-[(2S,4R,5S,6R)-4-hydroxy-5-[(2S,4S,5R,6R)-4-hydroxy-5-[(2S,4R,5R,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1,10-diene-14,21-dione 163048044 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3O)OC4CCC5(C6CC=C7C8C(COC8(OC7=O)C)OC(=O)C6CC=C5C4)C)C)C)OC)O 778.90 unknown https://doi.org/10.1016/S0031-9422(99)00439-2
(1Z,4S,5R,8R,13S,16R,19S,22S)-8-[(2S,3S,4S,5S,6S)-3-hydroxy-5-[(2S,4R,5S,6R)-4-hydroxy-5-[(2S,4R,5R,6R)-5-[(2S,4R,5R,6R)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1,10-diene-14,21-dione 162938793 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3C(OC(CC3O)OC4C(OC(C(C4OC)O)OC5CCC6(C7CC=C8C9C(COC9(OC8=O)C)OC(=O)C7CC=C6C5)C)C)C)C)OC)O 953.10 unknown https://doi.org/10.1016/S0031-9422(99)00439-2
(1Z,4S,5R,8S,13R,16S,19R,22R)-8-[(2R,3R,4R,5R,6R)-3-hydroxy-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2R,4R,5S,6S)-5-[(2S,4S,5R,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1,10-diene-14,21-dione 162938792 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3C(OC(CC3O)OC4C(OC(C(C4OC)O)OC5CCC6(C7CC=C8C9C(COC9(OC8=O)C)OC(=O)C7CC=C6C5)C)C)C)C)OC)O 953.10 unknown https://doi.org/10.1016/S0031-9422(99)00439-2
(1Z,4S,5R,8S,13R,16S,19R,22R)-8-[(2R,4R,5S,6R)-4-hydroxy-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2S,4R,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1,10-diene-14,21-dione 163194948 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3O)OC4CCC5(C6CC=C7C8C(COC8(OC7=O)C)OC(=O)C6CC=C5C4)C)C)C)OC)O 778.90 unknown https://doi.org/10.1016/S0031-9422(99)00439-2
(4E,7S,8R,11S,16R,21S)-11-[(2R,4R,5S,6R)-4-hydroxy-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2R,4R,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-1,8-dimethyl-2,18,22-trioxapentacyclo[17.2.1.04,21.07,16.08,13]docosa-4,13-diene-3,17-dione 101010462 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3O)OC4CCC5(C6CC=C7C8CC(OC(=O)C6CC=C5C4)OC8(OC7=O)C)C)C)C)OC)O 778.90 unknown via CMAUP database
(4S,5R,8S,13S,16S,19R,22R)-8-[(2R,4R,5R,6R)-5-[(2S,4S,5S,6R)-4-hydroxy-5-[(2S,4R,5S,6S)-5-hydroxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1(21),10-dien-14-one 90670869 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3OC)OC4CCC5(C6CCC7=COC8(C7C(CO8)OC(=O)C6CC=C5C4)C)C)C)C)OC)O 778.90 unknown https://doi.org/10.1021/NP4008969
8-[3-Hydroxy-5-[4-hydroxy-5-[5-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy-4-methoxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-4-methoxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1,10-diene-14,21-dione 162938791 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC)OC3C(OC(CC3O)OC4C(OC(C(C4OC)O)OC5CCC6(C7CC=C8C9C(COC9(OC8=O)C)OC(=O)C7CC=C6C5)C)C)C)C)OC)O 953.10 unknown https://doi.org/10.1016/S0031-9422(99)00439-2
8-[4-Hydroxy-5-[4-hydroxy-5-(5-hydroxy-4-methoxy-6-methyloxan-2-yl)oxy-6-methyloxan-2-yl]oxy-6-methyloxan-2-yl]oxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1,10-diene-14,21-dione 163048043 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3O)OC4CCC5(C6CC=C7C8C(COC8(OC7=O)C)OC(=O)C6CC=C5C4)C)C)C)OC)O 778.90 unknown https://doi.org/10.1016/S0031-9422(99)00439-2
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
(E,Z)-2,4-Decadienal 6427087 Click to see CCCCCC=CC=CC=O 152.23 unknown via CMAUP database
(E)-2-butyl-2-octenal 5352696 Click to see CCCCCC=C(CCCC)C=O 182.30 unknown via CMAUP database
2-Butyl-2-octenal 5362697 Click to see CCCCCC=C(CCCC)C=O 182.30 unknown via CMAUP database
2,4-Decadienal 5283349 Click to see CCCCCC=CC=CC=O 152.23 unknown via CMAUP database
Butyloctenal 25610 Click to see CCCCCC=C(CCCC)C=O 182.30 unknown via CMAUP database
Nona-2,4-dienal 23203 Click to see CCCCC=CC=CC=O 138.21 unknown via CMAUP database
Nonanal 31289 Click to see CCCCCCCCC=O 142.24 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Paeonol 11092 Click to see CC(=O)C1=C(C=C(C=C1)OC)O 166.17 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
5-pentyl-3H-furan-2-one 10725569 Click to see CCCCCC1=CCC(=O)O1 154.21 unknown via CMAUP database
> Organoheterocyclic compounds / Epoxides
Humulene epoxide 5352470 Click to see CC1=CCCC2(C(O2)CC(C=CC1)(C)C)C 220.35 unknown via CMAUP database
> Organoheterocyclic compounds / Furofurans
(1E,4S,5R,8S,13R,16S,19R,21S,22R)-21-hydroperoxy-8-hydroxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1,10-dien-14-one 162969149 Click to see CC12CCC(CC1=CCC3C2CC=C4C5C(COC5(OC4OO)C)OC3=O)O 392.40 unknown https://doi.org/10.1055/S-2004-832650
21-Hydroperoxy-8-hydroxy-5,19-dimethyl-15,18,20-trioxapentacyclo[14.5.1.04,13.05,10.019,22]docosa-1,10-dien-14-one 72953614 Click to see CC12CCC(CC1=CCC3C2CC=C4C5C(COC5(OC4OO)C)OC3=O)O 392.40 unknown https://doi.org/10.1055/S-2004-832650
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(R)-5-pentyldihydrofuran-2(3H)-one 11094875 Click to see CCCCCC1CCC(=O)O1 156.22 unknown via CMAUP database
Gamma-nonalactone 7710 Click to see CCCCCC1CCC(=O)O1 156.22 unknown via CMAUP database
> Organoheterocyclic compounds / Pyrrolines
Conckurchine 76330309 Click to see CC1C2CCC3C2(CCC4C3CC=C5C4(CCC(C5)N)C)C=N1 312.50 unknown via CMAUP database

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