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Aconitum episcopale

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID644006f96a081726051931
Scientific name Aconitum episcopale
Authority H.Lév.
First published in Repert. Spec. Nov. Regni Veg. 13: 341 (1914)

Ethnobotanical Use Top

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No ethnobotanical data added yet. Help us by writing one.

General Uses Top

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Common products:
* None documented beyond scientific research materials.

Industrial and craft applications:
* No industrial or craft applications are documented.

Food and beverages (non-medicinal):
* No food or beverage uses are documented.

Colorants and tanning:
* No colorant or tanning applications are documented.

Wood and fiber:
* No wood or fiber applications are documented.

Fragrance and cosmetics:
* No fragrance or cosmetic applications are documented.

Properties relevant to use:
* Highly toxic alkaloids (e.g., aconitine) are the primary chemical constituents. These potent neurotoxins render the plant unsuitable for non-scientific applications due to extreme hazard.

Scientific and model organism use:
* Used as a model organism in phytochemistry and alkaloid biosynthesis research. It provides a source of diterpenoid alkaloids for studies into their chemical structures, biosynthesis pathways, and biological activities. This research contributes to understanding the evolution and pharmacology of these compounds within the Ranunculaceae family.

Sustainability and sourcing:
* Wild-harvesting poses conservation risks due to limited distribution and slow propagation. Cultivation is challenging due to toxicity requirements and specific habitat needs. Research materials typically originate from botanical gardens or specialized collections.

Synonyms Top

Scientific name Authority First published in
Aconitum vilmorianum var. altifidum W.T.Wang Acta Phytotax. Sin., Addit. 1: 82 1965
Aconitum vilmorinianum var. altifidum W.T.Wang Acta Phytotax. Sin., Addit. 1: 82 1965

Common names Top

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Language Common/alternative name
Chinese 堵喇
Chinese 小黑牛
Chinese 紫乌头
Chinese 紫草乌
Chinese 西南乌头
Chinese 西南烏頭

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000517218
Tropicos 27102951
KEW urn:lsid:ipni.org:names:707335-1
The Plant List kew-2618671
Open Tree Of Life 50065
NCBI Taxonomy 226106
IPNI 707335-1
GBIF 7277368
EOL 2873279
CMAUP NPO16877

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
Exploring the Biomedical Potential of Terpenoid Alkaloids: Sources, Structures, and Activities Wang X, Xin J, Sun L, Sun Y, Xu Y, Zhao F, Niu C, Liu S Molecules 25-Apr-2024
PMCID:PMC11085545
doi:10.3390/molecules29091968
PMID:38731459
Neuropharmacological Potential of Diterpenoid Alkaloids Salehi A, Ghanadian M, Zolfaghari B, Jassbi AR, Fattahian M, Reisi P, Csupor D, Khan IA, Ali Z Pharmaceuticals (Basel) 14-May-2023
PMCID:PMC10223254
doi:10.3390/ph16050747
PMID:37242531
Sequencing and characterization of the chloroplast genome of Aconitum forrestii Stapf provide insights into phylogenetics in Aconitum Yang MH, Xia CL, Guan YH, Zhang HZ, Chen XB, Wang Y Mitochondrial DNA B Resour 24-Jun-2022
PMCID:PMC9246018
doi:10.1080/23802359.2022.2088307
PMID:35783038
Comparative analysis of complete chloroplast genome of ethnodrug Aconitum episcopale and insight into its phylogenetic relationships Xia C, Wang M, Guan Y, Li Y, Li J Sci Rep 08-Jun-2022
PMCID:PMC9178047
doi:10.1038/s41598-022-13524-3
PMID:35676401
Characterization of the complete chloroplast genome of Aconitum flavum (Ranunculaceae) Liu Y, Yu S, You F Mitochondrial DNA B Resour 25-Jul-2020
PMCID:PMC7781867
doi:10.1080/23802359.2020.1787894
PMID:33458024
The complete chloroplast genome of Aconitum coreanum (H. Lév.) Rapaics (Ranunculaceae) Kim Y, Yi JS, Min J, Xi H, Kim DY, Son J, Park J, Jeon JI Mitochondrial DNA B Resour 09-Oct-2019
PMCID:PMC7707295
doi:10.1080/23802359.2019.1674213
PMID:33366014
Comparative Analysis of the Complete Chloroplast Genomes of Four Aconitum Medicinal Species Meng J, Li X, Li H, Yang J, Wang H, He J Molecules 26-Apr-2018
PMCID:PMC6102581
doi:10.3390/molecules23051015
PMID:29701675
Feeding deterrents from Aconitum episcopale roots against the red flour beetle, Tribolium castaneum. Liu ZL, Cao J, Zhang HM, Lin LL, Liu HJ, Du SS, Zhou L, Deng ZW J Agric Food Chem 27-Apr-2011
doi:10.1021/JF104879H
PMID:21417277
A New Diterpenoid Alkaloid from <i>Aconitum episcopale</i> Zi Yan Li, Jingfeng Zhao, Jing‐Hua Yang, Hong Bin Zhang, Liang Li Wiley 27-Aug-2004
doi:10.1002/HLCA.200490187
Diterpenoid alkaloids from aconitum episcopale Jing-Hua Yang, Zi-Yan Li, Liang Li, Yun-Song Wang Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(98)00387-2

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
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
[(1R,2R,3S,5R,7S,10R,11R,12S,16S,17S,18R,19S)-8-ethyl-17-hydroxy-3,12,16-trimethoxy-10-(methoxymethyl)-6-oxa-8-azahexacyclo[15.2.1.02,7.02,11.05,10.014,19]icos-13-en-18-yl] 4-methoxybenzoate 162875555 Click to see 599.70 unknown https://doi.org/10.1002/HLCA.200490187
[8-Ethyl-17-hydroxy-3,12,16-trimethoxy-10-(methoxymethyl)-6-oxa-8-azahexacyclo[15.2.1.02,7.02,11.05,10.014,19]icos-13-en-18-yl] 4-methoxybenzoate 162875554 Click to see CCN1CC2(C3CC(C4(C2C(C=C5CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC)C1O3)OC)COC 599.70 unknown https://doi.org/10.1002/HLCA.200490187
> Benzenoids / Benzene and substituted derivatives / Methoxybenzenes / Dimethoxybenzenes
3,4-Dimethoxycinnamyl alcohol 5387770 Click to see COC1=C(C=C(C=C1)C=CCO)OC 194.23 unknown via CMAUP database
3,5-Dimethoxytoluene 77844 Click to see CC1=CC(=CC(=C1)OC)OC 152.19 unknown via CMAUP database
Methyleugenol 7127 Click to see COC1=C(C=C(C=C1)CC=C)OC 178.23 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
Asarone 636822 Click to see 208.25 unknown via CMAUP database
Elemicin 10248 Click to see 208.25 unknown via CMAUP database
Estragole 8815 Click to see 148.20 unknown via CMAUP database
gamma-Asarone 636750 Click to see COC1=CC(=C(C=C1CC=C)OC)OC 208.25 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Pentadecane 12391 Click to see 212.41 unknown via CMAUP database
> Hydrocarbons / Unsaturated hydrocarbons / Branched unsaturated hydrocarbons
Gamma-Terpinene 7461 Click to see 136.23 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-)-Asarinin 11869417 Click to see 354.40 unknown via CMAUP database
4-[(3R,3aR,6S,6aR)-3-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-6-yl]-2,6-dimethoxyphenol 57404419 Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5 386.40 unknown via CMAUP database
4-[(3S,3aR,6R,6aR)-6-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]benzene-1,2-diol 46917405 Click to see 342.30 unknown via CMAUP database
5-[(3S,3aS,6R,6aS)-6-(1,3-benzodioxol-5-yl)-1,3,3a,4,6,6a-hexahydrofuro[3,4-c]furan-3-yl]-2-methoxyphenol 10089592 Click to see COC1=C(C=C(C=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
Epipinoresinol 637584 Click to see 358.40 unknown via CMAUP database
Pluviatilol 70695727 Click to see COC1=C(C=CC(=C1)C2C3COC(C3CO2)C4=CC5=C(C=C4)OCO5)O 356.40 unknown via CMAUP database
Sesamin 72307 Click to see C1C2C(COC2C3=CC4=C(C=C3)OCO4)C(O1)C5=CC6=C(C=C5)OCO6 354.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 7,9-epoxylignans
Sesaminone 158370 Click to see C1C(C(C(O1)C2=CC3=C(C=C2)OCO3)CO)C(=O)C4=CC5=C(C=C4)OCO5 370.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty amides / N-acyl amines
(2E,4E,8Z)-N-(2-methylpropyl)dodeca-2,4,8,10-tetraenamide 70693621 Click to see CC=CC=CCCC=CC=CC(=O)NCC(C)C 247.38 unknown via CMAUP database
Pellitorine 5318516 Click to see 223.35 unknown via CMAUP database
Sanshool 6440935 Click to see 247.38 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(2R,3R,4S,5S,6S,8S,13S,16S,17R)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 146014457 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
(6S,8S,13S)-11-ethyl-6,16-dimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 5321607 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)COC 421.60 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[(1S,2R,3R,4R,5S,6S,8R,9R,10R,13S,16S,17R,18R)-11-ethyl-5-hydroxy-6,16,18-trimethoxy-8-(4-methoxybenzoyl)oxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 100987532 Click to see 733.80 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[(1S,2R,3R,4R,5S,6S,8R,9R,10R,13S,16S,17R,18R)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 100987531 Click to see CCN1CC2(C=CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)COC 641.70 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[(1S,2R,3R,4R,5S,6S,8R,9R,10R,13S,16S,17R,18R)-8-ethoxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 100987533 Click to see CCN1CC2(C=CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OCC)OC)OC)COC 627.80 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[(1S,2R,3R,4R,5S,6S,8S,9R,10R,13R,16S,17R,18S)-11-ethyl-5-hydroxy-6,16,18-trimethoxy-8-(4-methoxybenzoyl)oxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 162992411 Click to see CCN1CC2(C=CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C8=CC=C(C=C8)OC)OC)OC)COC 733.80 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[(1S,2R,3R,4R,5S,6S,8S,9R,10R,13R,16S,17R,18S)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 162969090 Click to see CCN1CC2(C=CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)COC 641.70 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[(1S,2R,3R,4R,5S,6S,8S,9R,10R,13R,16S,17R,18S)-8-ethoxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 162970240 Click to see 627.80 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[(1S,2R,3R,4R,5S,6S,8S,9R,10R,16S,17R,18S)-11-ethyl-5-hydroxy-6,16,18-trimethoxy-8-(4-methoxybenzoyl)oxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 163189987 Click to see 733.80 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[(1S,2R,3R,4R,5S,6S,8S,9R,10R,16S,17R,18S)-8-ethoxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 163187104 Click to see 627.80 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[(1S,2R,3R,4R,5S,6S,8S,9R,16S,17R,18S)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 163195279 Click to see 641.70 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[(2R,3R,5S,6S,8R,13S,17R)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 5316126 Click to see 643.80 unknown https://doi.org/10.1021/JF104879H
[(5S,6S,8R)-11-ethyl-5-hydroxy-6,16,18-trimethoxy-8-(4-methoxybenzoyl)oxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 5318984 Click to see 733.80 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[(5S,6S,8R)-8-acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 5318983 Click to see 641.70 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[(5S,6S,8R)-8-ethoxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 5318985 Click to see 627.80 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[11-Ethyl-5-hydroxy-6,16,18-trimethoxy-8-(4-methoxybenzoyl)oxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 78385199 Click to see CCN1CC2(C=CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C8=CC=C(C=C8)OC)OC)OC)COC 733.80 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[8-Acetyloxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 78385198 Click to see 641.70 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
[8-Ethoxy-11-ethyl-5-hydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadec-14-en-4-yl] 4-methoxybenzoate 78385200 Click to see CCN1CC2(C=CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OCC)OC)OC)COC 627.80 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
Chasmanine 20055812 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6CC4C5C6O)OC)O)OC)OC)COC 451.60 unknown https://doi.org/10.1021/JF104879H
Crassicauline A 20055838 Click to see CCN1CC2(CCC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=C(C=C7)OC)O)OC)OC(=O)C)OC)OC)COC 643.80 unknown https://doi.org/10.1021/JF104879H
Yunaconitine 6918110 Click to see 659.80 unknown https://doi.org/10.1021/JF104879H
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids / Napelline-type diterpenoid alkaloids
(1R,2R,5R,7R,8R,9R,13R,16S,17R)-11-ethyl-7,16-dihydroxy-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-4-one 441755 Click to see 357.50 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
(1R,5S,7R,8R,9R,13R)-11-ethyl-7,16-dihydroxy-13-methyl-6-methylidene-11-azahexacyclo[7.7.2.15,8.01,10.02,8.013,17]nonadecan-4-one 139291804 Click to see 357.50 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1R,3S,5R,8R,9S,11S,14R,17R,18R)-3-hydroxy-5,7-dimethyl-12-methylidene-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadecane-10,16-dione 101685134 Click to see 341.40 unknown https://doi.org/10.1016/S0031-9422(98)00387-2
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Myrcene 31253 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Aromatic monoterpenoids
P-Cymene 7463 Click to see 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Bicyclic monoterpenoids
(-)-alpha-Pinene 440968 Click to see CC1=CCC2CC1C2(C)C 136.23 unknown via CMAUP database
(-)-Camphene 440966 Click to see 136.23 unknown via CMAUP database
(+)-Sabinene 10887971 Click to see 136.23 unknown via CMAUP database
(+/-)-Asarinol A 46174001 Click to see 166.22 unknown via CMAUP database
Bornyl acetate, (-)- 93009 Click to see 196.29 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see 154.25 unknown via CMAUP database
(+)-Limonene 440917 Click to see 136.23 unknown via CMAUP database
(1S,6R)-6-Isopropyl-3-methyl-cyclohex-2-en-1-ol 11367127 Click to see CC1=CC(C(CC1)C(C)C)O 154.25 unknown via CMAUP database
Terpinolene 11463 Click to see 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Monocyclic monoterpenoids
Eucarvone 136330 Click to see CC1=CC=CC(CC1=O)(C)C 150.22 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones
2,7,7-Trimethylcyclohepta-2,4-dienone 85794676 Click to see CC1=CC=CCC(C1=O)(C)C 150.22 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Croweacin 5316141 Click to see 192.21 unknown via CMAUP database
Kakuol 596894 Click to see 194.18 unknown via CMAUP database
Safrole 5144 Click to see 162.18 unknown via CMAUP database
Sarisan 95289 Click to see COC1=CC2=C(C=C1CC=C)OCO2 192.21 unknown via CMAUP database

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