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Aconitum vilmorinianum

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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 UUID6440071b89291618851951
Scientific name Aconitum vilmorinianum
Authority Kom.
First published in Repert. Spec. Nov. Regni Veg. 7: 145 (1909)

Description Top

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Synonyms Top

Scientific name Authority First published in
Aconitum mairei H.Lév. Repert. Spec. Nov. Regni Veg. 13: 341 (1914)
Aconitum vilmorinianum var. spreadingipilum W.T.Wang Acta Phytotax. Sin., Addit. 1: 82 1965

Common names Top

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Language Common/alternative name
Chinese 深裂黄草乌
Chinese 黄草乌
Chinese 大草乌
Chinese 昆明乌头
Chinese 昆明堵喇
Chinese 草乌

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000518298
Tropicos 27102959
KEW urn:lsid:ipni.org:names:707943-1
The Plant List kew-2619734
Open Tree Of Life 976183
NCBI Taxonomy 226101
IPNI 707943-1
GBIF 3930629
EOL 2873412
USDA GRIN 410030
CMAUP NPO651

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
Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X J Ethnobiol Ethnomed 23-Feb-2024
PMCID:PMC10893717
doi:10.1186/s13002-024-00656-1
PMID:38395900
A strategy for quality evaluation of complex herbal preparations based on multi-color scale and efficacy-oriented high-performance thin-layer chromatography characteristic fingerprint combined with chemometric method: Sanwujiao Pills as an example Pei W, Huang Y, Qu Y, Cui X, Zhou L, Yang H, Zhao M, Zhang Z, He F, Zhou H Heliyon 08-Nov-2023
PMCID:PMC10694152
doi:10.1016/j.heliyon.2023.e22098
PMID:38053910
Cloning and Functional Characterization of NADPH-Cytochrome P450 Reductases in Aconitum vilmorinianum Cheng J, Li G, Wang X, Yang C, Xu F, Qian Z, Ma X Molecules 03-Nov-2023
PMCID:PMC10648341
doi:10.3390/molecules28217409
PMID:37959828
Microbial fortification of pharmacological metabolites in medicinal plants Wu X, Yang Y, Zhang H Comput Struct Biotechnol J 13-Oct-2023
PMCID:PMC10589376
doi:10.1016/j.csbj.2023.10.024
PMID:37867972
Bioactive Steroids Bearing Oxirane Ring Dembitsky VM Biomedicines 09-Aug-2023
PMCID:PMC10452232
doi:10.3390/biomedicines11082237
PMID:37626733
Revealing ecotype influences on Cistanche sinensis: from the perspective of endophytes to metabolites characteristics Zhang M, Miao Y, Zhang X, Sun X, Li M, Huang L Front Microbiol 27-Jun-2023
PMCID:PMC10394521
doi:10.3389/fmicb.2023.1154688
PMID:37538848
Fungal Endophytes: Microfactories of Novel Bioactive Compounds with Therapeutic Interventions; A Comprehensive Review on the Biotechnological Developments in the Field of Fungal Endophytic Biology over the Last Decade Gupta A, Meshram V, Gupta M, Goyal S, Qureshi KA, Jaremko M, Shukla KK Biomolecules 25-Jun-2023
PMCID:PMC10377637
doi:10.3390/biom13071038
PMID:37509074
Bioactive compounds and biomedical applications of endophytic fungi: a recent review Hashem AH, Attia MS, Kandil EK, Fawzi MM, Abdelrahman AS, Khader MS, Khodaira MA, Emam AE, Goma MA, Abdelaziz AM Microb Cell Fact 06-Jun-2023
PMCID:PMC10243280
doi:10.1186/s12934-023-02118-x
PMID:37280587
Endophytic fungi: a potential source for drugs against central nervous system disorders Pant A, Vasundhara M Braz J Microbiol 11-May-2023
PMCID:PMC10485218
doi:10.1007/s42770-023-00997-1
PMID:37165297
Overview of Bioactive Fungal Secondary Metabolites: Cytotoxic and Antimicrobial Compounds Conrado R, Gomes TC, Roque GS, De Souza AO Antibiotics (Basel) 11-Nov-2022
PMCID:PMC9687038
doi:10.3390/antibiotics11111604
PMID:36421247
Tapping into Plant–Microbiome Interactions through the Lens of Multi-Omics Techniques Mishra AK, Sudalaimuthuasari N, Hazzouri KM, Saeed EE, Shah I, Amiri KM Cells 17-Oct-2022
PMCID:PMC9600287
doi:10.3390/cells11203254
PMID:36291121
Research progress on the antiviral activities of natural products and their derivatives: Structure–activity relationships Guo Y, Ma A, Wang X, Yang C, Chen X, Li G, Qiu F Front Chem 12-Oct-2022
PMCID:PMC9596788
doi:10.3389/fchem.2022.1005360
PMID:36311429
The Manchurian Walnut Genome: Insights into Juglone and Lipid Biosynthesis Li X, Cai K, Zhang Q, Pei X, Chen S, Jiang L, Han Z, Zhao M, Li Y, Zhang X, Li Y, Zhang S, Chen S, Qu G, Tigabu M, Chiang VL, Sederoff R, Zhao X Gigascience 28-Jun-2022
PMCID:PMC9239856
doi:10.1093/gigascience/giac057
PMID:35764602
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
Promising antimicrobials from Phoma spp.: progress and prospects Rai M, Zimowska B, Gade A, Ingle P AMB Express 23-May-2022
PMCID:PMC9125353
doi:10.1186/s13568-022-01404-y
PMID:35604500

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
(S)-Mandelonitrile 439767 Click to see C1=CC=C(C=C1)C(C#N)O 133.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Branched fatty acids / Methyl-branched fatty acids
(R)-2-Methylbutanoic acid 6950479 Click to see CCC(C)C(=O)O 102.13 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Arachidic Acid 10467 Click to see CCCCCCCCCCCCCCCCCCCC(=O)O 312.50 unknown via CMAUP database
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown via CMAUP database
Palmitoleic Acid 445638 Click to see CCCCCCC=CCCCCCCCC(=O)O 254.41 unknown via CMAUP database
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
2-Hexen-1-OL 5318042 Click to see CCCC=CCO 100.16 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown via CMAUP database
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(1S,2R,3R,4S,5S,6S,8S,9S,10R,13R,16S,17R)-11-ethyl-6,16-dimethoxy-13-methyl-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecane-4,8-diol 101297639 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)OC)C 391.50 unknown https://doi.org/10.6023/CJOC201401013
(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/10.1055/S-2006-960089
https://doi.org/10.1016/0031-9422(90)85312-4
(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/10.1055/S-2006-960089
https://doi.org/10.1016/0031-9422(90)85312-4
[(1S,2R,3R,4R,5R,6S,8R,9R,10R,13R,14R,16S,17S,18R)-8-acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 134715408 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)O)COC 659.80 unknown https://doi.org/10.1016/0031-9422(90)85312-4
https://doi.org/10.6023/CJOC201401013
[(2R,3R,5S,6S,8R,13R,17S)-8-acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] 4-methoxybenzoate 5315414 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)O)COC 659.80 unknown https://doi.org/10.1016/J.JPBA.2007.04.016
https://doi.org/10.1016/0031-9422(90)85312-4
https://doi.org/10.1021/NP0700117
https://doi.org/10.1002/JSSC.201300472
[(2S,3S,5S,8R,13R,17R)-8-acetyloxy-11-ethyl-5,14-dihydroxy-6,16,18-trimethoxy-13-(methoxymethyl)-11-azahexacyclo[7.7.2.12,5.01,10.03,8.013,17]nonadecan-4-yl] benzoate 137706149 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=CC=C7)O)OC)OC(=O)C)OC)OC)O)COC 629.70 unknown https://doi.org/10.1016/0031-9422(90)85312-4
Acoforine 118856031 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6OC(=O)C)OC)OCC)OC)COC 491.70 unknown https://doi.org/10.6023/CJOC201401013
CID 138911429 138911429 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)C 377.50 unknown https://doi.org/10.1055/S-2006-960089
CID 155569 155569 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)O)COC 659.80 unknown https://doi.org/10.1002/JSSC.201300472
https://doi.org/10.1021/JF104879H
Guayewuanine B 6918110 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)O)COC 659.80 unknown https://doi.org/10.1002/JSSC.201300472
Indaconitine 441740 Click to see CCN1CC2(C(CC(C34C2C(C(C31)C5(CC(C6(CC4C5C6OC(=O)C7=CC=CC=C7)O)OC)OC(=O)C)OC)OC)O)COC 629.70 unknown https://doi.org/10.1016/0031-9422(90)85312-4
Isotalatisidine 12304578 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)COC 407.50 unknown https://doi.org/10.1055/S-2006-960089
Talatisidine 139066658 Click to see CCN1CC2(CCC(C34C2CC(C31)C5(CC(C6CC4C5C6O)OC)O)O)COC 407.50 unknown https://doi.org/10.1055/S-2006-960089
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
Vilmorrianone 44566629 Click to see CC(=O)OC1CC2(CN(C3C4C(=O)C5CC6C3(C1)C2C(=O)C(=O)C64CC5=C)C)C 397.50 unknown https://doi.org/10.1055/S-2006-960089
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Acyclic monoterpenoids
Citral 638011 Click to see CC(=CCCC(=CC=O)C)C 152.23 unknown via CMAUP database
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 / Monoterpenoids / Aromatic monoterpenoids
p-CYMENE 7463 Click to see CC1=CC=C(C=C1)C(C)C 134.22 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(+)-alpha-Terpineol 442501 Click to see CC1=CCC(CC1)C(C)(C)O 154.25 unknown via CMAUP database
Terpinolene 11463 Click to see CC1=CCC(=C(C)C)CC1 136.23 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
beta-Ionone 638014 Click to see CC1=C(C(CCC1)(C)C)C=CC(=O)C 192.30 unknown via CMAUP database
Vomifoliol 5280462 Click to see CC1=CC(=O)CC(C1(C=CC(C)O)O)(C)C 224.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
Flavoxanthin 5281238 Click to see CC1=CC(CC(C1C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C2C=C3C(CC(CC3(O2)C)O)(C)C)C)C)(C)C)O 584.90 unknown via CMAUP database
Rubixanthin 5281252 Click to see CC1=C(C(CC(C1)O)(C)C)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C=CC=C(C)CCC=C(C)C)C)C 552.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
alpha-Amyrenyl acetate 92842 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Estrane steroids / Estrogens and derivatives
(8S,9S,13S,14R)-3-hydroxy-13-methyl-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-17-one 670995 Click to see CC12CCC3C(C1CCC2=O)CCC4=C3C=CC(=C4)O 270.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
Poriferasterol 5281330 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
Stigmasteryl-beta-d-glucopyranoside 12895774 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C 574.80 unknown via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
2-(Carboxymethyl)-2-hydroxybutanedioate;hydron 88113319 Click to see [H+].[H+].C(C(=O)O)C(CC(=O)[O-])(C(=O)[O-])O 192.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glucuronides / O-glucuronides
beta-D-GlcpA-(1->6)-beta-D-Galp 70680285 Click to see C(C1C(C(C(C(O1)O)O)O)O)OC2C(C(C(C(O2)C(=O)O)O)O)O 356.28 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Cyanogenic glycosides
Amygdalin 656516 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 457.40 unknown via CMAUP database
Neoamygdalin 441462 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)COC3C(C(C(C(O3)CO)O)O)O)O)O)O 457.40 unknown via CMAUP database
Prunasin 119033 Click to see C1=CC=C(C=C1)C(C#N)OC2C(C(C(C(O2)CO)O)O)O 295.29 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Medium-chain aldehydes
2-Hexenal 5281168 Click to see CCCC=CC=O 98.14 unknown via CMAUP database
2-Nonenal 5283335 Click to see CCCCCCC=CC=O 140.22 unknown via CMAUP database
2,4-Decadienal 5283349 Click to see CCCCCC=CC=CC=O 152.23 unknown via CMAUP database
Hexanal 6184 Click to see CCCCCC=O 100.16 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(5S)-5-butyloxolan-2-one 7057972 Click to see CCCCC1CCC(=O)O1 142.20 unknown via CMAUP database
(R)-gamma-Decalactone 183870 Click to see CCCCCCC1CCC(=O)O1 170.25 unknown via CMAUP database
2(3H)-Furanone, dihydro-5-octyl-, (5R)- 10888889 Click to see CCCCCCCCC1CCC(=O)O1 198.30 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines
(6,16-Dimethoxy-12,14-dimethyl-10-oxo-14-azapentacyclo[10.3.3.12,5.01,11.03,8]nonadec-8-en-4-yl) acetate 163192375 Click to see CC(=O)OC1C2CC3C1C(=CC(=O)C4C35CN(CC4(CCC5OC)C)C)CC2OC 417.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2015.05.002
> Organoheterocyclic compounds / Piperidines / Piperidinecarboxylic acids and derivatives / Piperidinecarboxylic acids
14-Hydroxy-3-methoxycarbonyl-10,12-dimethyl-5-methylidene-7-oxo-10-azapentacyclo[10.3.1.12,6.01,9.03,8]heptadecane-16-carboxylic acid 163106314 Click to see CC12CC(CC3(C1C(=O)O)C4CC5C(=C)CC4(C(C3N(C2)C)C5=O)C(=O)OC)O 403.50 unknown https://doi.org/10.6023/CJOC201401013
> Organoheterocyclic compounds / Tetrahydrofurans
2-[(2R,5S)-5-ethenyl-5-methyloxolan-2-yl]propan-2-ol 6428573 Click to see CC1(CCC(O1)C(C)(C)O)C=C 170.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Biflavonoids and polyflavonoids
(1S,5S,6R,13R,21S)-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaene-6,9,17,19,21-pentol 73353883 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
[(1S,5R,6R,13R,21S)-6,9,17,19-tetrahydroxy-5,13-bis(4-hydroxyphenyl)-4,12,14-trioxapentacyclo[11.7.1.02,11.03,8.015,20]henicosa-2(11),3(8),9,15,17,19-hexaen-21-yl] 4-hydroxybenzoate 10723070 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)OC(=O)C7=CC=C(C=C7)O)O)C8=CC=C(C=C8)O)O 664.60 unknown via CMAUP database
ent-Epiafzelechin-(2alpha-O-7,4alpha-8)-ent-epiafzelechin 5317051 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
Geranin A 5317050 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 unknown via CMAUP database
Mahuannin A 5317052 Click to see C1C(C(OC2=C1C(=CC3=C2C4C(C(O3)(OC5=CC(=CC(=C45)O)O)C6=CC=C(C=C6)O)O)O)C7=CC=C(C=C7)O)O 544.50 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 / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Isoquercetin 5280804 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
Rutin 5280805 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=C(OC4=CC(=CC(=C4C3=O)O)O)C5=CC(=C(C=C5)O)O)O)O)O)O)O)O 610.50 unknown via CMAUP database

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