Anisodus tanguticus - Unknown
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Internal ID UUID644040ef6ee17424348406
Scientific name Anisodus tanguticus
Authority (Maxim.) Pascher
First published in Repert. Spec. Nov. Regni Veg. 7: 167. 1909

Description Top

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Synonyms Top

Scientific name Authority First published in
Anisodus tanguticus var. viridulus C.Y.Wu & C.Chen Acta Phytotax. Sin. 15(2): 65. 1977.
Scopolia tangutica Maxim. Bull. Acad. Imp. Sci. Saint-Pétersbourg 27: 508. 1881
Whitleya tangutica (Maxim.) Sandina Bot. Zhurn. (Moscow & Leningrad) 65(4): 495. 1980

Common names Top

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Language Common/alternative name
Spanish scopolia tangutica
Spanish anisodus tanguticus var viridulus
Spanish anisodus tanguticus var. viridulus
Finnish purppurauurnio
Chinese 三分三
Chinese 东莨菪
Chinese 藏茄
Chinese 山莨菪
Chinese 山莨菪(唐古特莨菪)
Chinese 唐古特莨菪
Chinese 唐川那保
Chinese 樟柳

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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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • Qinghai
      • Tibet

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001019299
UNII 3X5ARV568K
Tropicos 29604696
KEW urn:lsid:ipni.org:names:814269-1
The Plant List kew-2640224
Open Tree Of Life 660902
NCBI Taxonomy 243964
IPNI 814269-1
GBIF 7300202
Freebase /m/03mh0y5
USDA GRIN 457021
Wikipedia Anisodus_tanguticus
CMAUP NPO1540
CMAUP NPO26163

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_034509755.1 ASM3450975v1 Chromosome Kunming Institute of Botany, Chinese Academy of Sciences 2023-12-26 101.7x 1.18 Gb

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
An Overview of the Structure–Activity Relationship in Novel Antimicrobial Thiazoles Clubbed with Various Heterocycles (2017–2023) Ungureanu D, Tiperciuc B, Nastasă C, Ionuț I, Marc G, Oniga I, Oniga O Pharmaceutics 09-Jan-2024
PMCID:PMC10820536
doi:10.3390/pharmaceutics16010089
PMID:38258100
Hairy root culture: a potent method for improved secondary metabolite production of Solanaceous plants Biswas D, Chakraborty A, Mukherjee S, Ghosh B Front Plant Sci 04-Sep-2023
PMCID:PMC10507345
doi:10.3389/fpls.2023.1197555
PMID:37731987
Special Issue—“Bioactive Compounds from Natural Sources II” Sytar O, Smetanska I Molecules 31-May-2023
PMCID:PMC10254469
doi:10.3390/molecules28114450
PMID:37298926
Long-Term Impact of N, P, K Fertilizers in Different Rates on Yield and Quality of Anisodus tanguticus (Maxinowicz) Pascher Chen K, Ma L, Chen C, Liu N, Wang B, Bao Y, Liu Z, Zhou G Plants (Basel) 25-May-2023
PMCID:PMC10255661
doi:10.3390/plants12112102
PMID:37299083
Novel Indane Derivatives with Antioxidant Activity from the Roots of Anisodus tanguticus Meng CW, Zhao HY, Zhu H, Peng C, Zhou QM, Xiong L Molecules 03-Feb-2023
PMCID:PMC9919654
doi:10.3390/molecules28031493
PMID:36771160
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
Characterization of the Evolutionary Pressure on Anisodus tanguticus Maxim. with Complete Chloroplast Genome Sequence Zhou D, Mehmood F, Lin P, Cheng T, Wang H, Shi S, Zhang J, Meng J, Zheng K, Poczai P Genes (Basel) 15-Nov-2022
PMCID:PMC9690199
doi:10.3390/genes13112125
PMID:36421800
A Poisoning Outbreak Caused by Anisodus tanguticus — Maqin County, Qinghai Province, China, July 2021 Guo X, He Q, Qi B, Sun C, Lyu D, Zhang H China CDC Wkly 14-Oct-2022
PMCID:PMC9681605
doi:10.46234/ccdcw2022.189
PMID:36426290
Discovery of TCMs and derivatives against the main protease of SARS-CoV-2 via high throughput screening, ADMET analysis, and inhibition assay in vitro Qi X, Li B, Omarini AB, Gand M, Zhang X, Wang J J Mol Struct 12-Jul-2022
PMCID:PMC9273959
doi:10.1016/j.molstruc.2022.133709
PMID:35846732
Multivariate Statistical Analysis of Metabolites in Anisodus tanguticus (Maxim.) Pascher to Determine Geographical Origins and Network Pharmacology Chen C, Wang B, Li J, Xiong F, Zhou G Front Plant Sci 29-Jun-2022
PMCID:PMC9277180
doi:10.3389/fpls.2022.927336
PMID:35845631
Anisodamine potently inhibits SARS-CoV-2 infection in vitro and targets its main protease Wei W, Kong N, Liu MZ, Han T, Xu JF, Liu C Biochem Biophys Res Commun 13-May-2022
PMCID:PMC9098399
doi:10.1016/j.bbrc.2022.05.024
PMID:35636257
Anisodamine microcirulatory effects in septic shock: be aware of cardiac side effects Honore PM, Redant S, Preseau T, Cismas BV, Kaefer K, Barreto Gutierrez L, Anane S, Attou R, Gallerani A, De Bels D Crit Care 16-Dec-2021
PMCID:PMC8680269
doi:10.1186/s13054-021-03854-5
PMID:34915896
Screening S protein – ACE2 blockers from natural products: Strategies and advances in the discovery of potential inhibitors of COVID-19 Ma LL, Liu HM, Liu XM, Yuan XY, Xu C, Wang F, Lin JZ, Xu RC, Zhang DK Eur J Med Chem 04-Oct-2021
PMCID:PMC8489279
doi:10.1016/j.ejmech.2021.113857
PMID:34628234
The Treatment of Cholecystitis and Cholelithiasis by Tibetan Medicine Pan L, Gao J, Han Y, Shi Y, Tang X, Pu L, Lai X, Dongzhu R, Zhang J, Xiangmao Q, Pengcuo J Evid Based Complement Alternat Med 30-Sep-2021
PMCID:PMC8497101
doi:10.1155/2021/9502609
PMID:34630620
Potential geographical distribution and environmental explanations of rare and endangered plant species through combined modeling: A case study of Northwest Yunnan, China Ye P, Zhang G, Zhao X, Chen H, Si Q, Wu J Ecol Evol 04-Sep-2021
PMCID:PMC8495784
doi:10.1002/ece3.7999
PMID:34646452

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
1,3-Bis(1-methyl-2beta-pyrrolidinyl)-2-propanone 11816962 Click to see CN1CCCC1CC(=O)CC2CCCN2C 224.34 unknown https://doi.org/10.1007/BF00622431
https://doi.org/10.1007/BF00569026
Cuskhygrine 441070 Click to see CN1CCCC1CC(=O)CC2CCCN2C 224.34 unknown https://doi.org/10.1007/BF00622431
https://doi.org/10.1007/BF00569026
> Alkaloids and derivatives / Tropane alkaloids
(1R,3S,5R,6RS)-6-Hydroxy-8-methyl-8-azabicyclo(3.2.1)oct-3-YL (2S)-3-hydroxy-2-phenylpropanoate 139033153 Click to see CN1C2CC(CC1C(C2)O)OC(=O)C(CO)C3=CC=CC=C3 305.40 unknown https://doi.org/10.1055/S-2006-962674
https://doi.org/10.1007/BF00569615
(1S,5R)-8-(trideuteriomethyl)-8-azabicyclo[3.2.1]octan-3-one 10374559 Click to see CN1C2CCC1CC(=O)C2 142.21 unknown via CMAUP database
(6S)-6-Hydroxyhyoscyamine 183088 Click to see CN1C2CC(CC1C(C2)O)OC(=O)C(CO)C3=CC=CC=C3 305.40 unknown https://doi.org/10.1016/S0021-9673(01)82171-3
https://doi.org/10.1067/MLC.2001.112507
(S)-((1R,3r,5S)-8-methyl-8-azabicyclo[3.2.1]octan-3-yl) 3-hydroxy-2-phenylpropanoate 6931560 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1007/BF00569615
[(1S,3R,5S,6S)-6-hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] (2S)-3-hydroxy-2-phenylpropanoate 929216 Click to see CN1C2CC(CC1C(C2)O)OC(=O)C(CO)C3=CC=CC=C3 305.40 unknown https://doi.org/10.1007/BF00569615
[(1S,3R,5S)-6-hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl] 3-hydroxy-2-phenylpropanoate 51026956 Click to see CN1C2CC(CC1C(C2)O)OC(=O)C(CO)C3=CC=CC=C3 305.40 unknown https://doi.org/10.1016/S0021-9673(01)82171-3
https://doi.org/10.1067/MLC.2001.112507
6-Hydroxy-8-methyl-8-azabicyclo[3.2.1]octan-3-yl 3-hydroxy-2-phenylpropanoate 2198 Click to see CN1C2CC(CC1C(C2)O)OC(=O)C(CO)C3=CC=CC=C3 305.40 unknown https://doi.org/10.1007/BF00569615
Atropine sulfate 3661 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1007/BF00771504
https://doi.org/10.1007/BF00779095
Hyoscyamine 154417 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown via CMAUP database
L-Hyoscyamine 64692 Click to see CN1C2CCC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 289.40 unknown https://doi.org/10.1007/BF00569615
Tropine 449293 Click to see CN1C2CCC1CC(C2)O 141.21 unknown via CMAUP database
> Benzenoids / Phenol ethers / Anisoles
1,2,3-Trimethoxybenzene 12462 Click to see COC1=C(C(=CC=C1)OC)OC 168.19 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
Darutigenol 3037565 Click to see CC1(C2CCC3=CC(CCC3C2(CCC1O)C)(C)C(CO)O)C 322.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Spathulenol 92231 Click to see CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
Darutoside 44715524 Click to see CC1(C2CCC3=CC(CCC3C2(CCC1OC4C(C(C(C(O4)CO)O)O)O)C)(C)C(CO)O)C 484.60 unknown via CMAUP database
Hythiemoside A 44607102 Click to see CC(=O)OCC(C1(CCC2C(=C1)CCC3C2(CCC(C3(C)C)OC4C(C(C(C(O4)CO)O)O)O)C)C)O 526.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Iridoid O-glycosides
6-O-Acetylscandoside 6324968 Click to see CC(=O)OC1C=C(C2C1C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 432.40 unknown via CMAUP database
Scandoside 21602023 Click to see C1=C(C2C(C1O)C(=COC2OC3C(C(C(C(O3)CO)O)O)O)C(=O)O)CO 390.34 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
3beta-(2-O-beta-D-Galactopyranosyl-beta-D-glucurono pyranosyloxy)olean-12-en-28-oic acid 101923141 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)O)C 795.00 unknown via CMAUP database
Araloside A 10079497 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 927.10 unknown via CMAUP database
Calenduloside E 176079 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)O)C 632.80 unknown via CMAUP database
Calenduloside F 13909684 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)O)C)C)C2C1)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C 795.00 unknown via CMAUP database
methyl (2S,3S,4S,5R,6R)-6-[[(3S,4aR,6aR,6bS,8aS,12aS,14aR,14bR)-4,4,6a,6b,11,11,14b-heptamethyl-8a-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-yl]oxy]-3,4-dihydroxy-5-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxane-2-carboxylate 21669007 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)OC)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 971.10 unknown via CMAUP database
Narcissiflorine 162878 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)OC7C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C 764.90 unknown via CMAUP database
Papyrioside LE 11803947 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CCC7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O 941.10 unknown via CMAUP database
Papyrioside LF 10819773 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CCC7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)COC(=O)C)O)O)O 983.10 unknown via CMAUP database
Scheffleraside II 101720880 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC(CC4C6=CCC7C8(CCC(C(C8CCC7(C6(CC5)C)C)(C)C)OC9C(C(C(C(O9)C(=O)O)O)O)O)C)(C)C)O)O)O)CO)O)O)O 1103.20 unknown via CMAUP database
Udosaponin B 21635582 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(C(O6)C(=O)O)O)O)OC7C(C(C(C(O7)CO)O)O)O)C)C)C2C1)C)C(=O)OC8C(C(C(C(O8)CO)O)O)O)C 957.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
[(3aR,4R,6R,9E,11aR)-10-formyl-6-(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,6,7,8,11,11a-octahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 44421659 Click to see CC(=C)C(=O)OC1CC(CCC=C(CC2C1C(=C)C(=O)O2)C=O)CO 348.40 unknown via CMAUP database
[(3aR,4R,6R,9E,11aR)-6,10-bis(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,6,7,8,11,11a-octahydrocyclodeca[b]furan-4-yl] (Z)-2-methylbut-2-enoate 44421658 Click to see CC=C(C)C(=O)OC1CC(CCC=C(CC2C1C(=C)C(=O)O2)CO)CO 364.40 unknown via CMAUP database
[(3aR,4R,6R,9E,11aR)-6,10-bis(hydroxymethyl)-3-methylidene-2-oxo-3a,4,5,6,7,8,11,11a-octahydrocyclodeca[b]furan-4-yl] 2-methylprop-2-enoate 44421660 Click to see CC(=C)C(=O)OC1CC(CCC=C(CC2C1C(=C)C(=O)O2)CO)CO 350.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-2,2,6a,6b,9,9,12a-heptamethyl-10-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid 13878127 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)O)O)C)C)C2C1)C)C(=O)O)C 588.80 unknown via CMAUP database
3-Epipapyriogenin C 16112782 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)O)C)C 468.70 unknown via CMAUP database
3-O-alpha-L-Arabinopyranosylechinocystic acid 15379012 Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)OC6C(C(C(CO6)O)O)O)C)C(=O)O)C 604.80 unknown via CMAUP database
3alpha,21beta,22alpha-Trihydroxyoleana-11,13(18)-diene-28-oic acid 16112781 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(C(C1O)O)C(=O)O)C)C)(C)C)O)C)C 486.70 unknown via CMAUP database
Guaianin N 10395290 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC6C(C(C(CO6)O)OC7C(C(C(C(O7)CO)O)O)O)O)C)C)C2C1)C)C(=O)O)C 751.00 unknown via CMAUP database
Papyriogenin A 3081523 Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)C)C 466.70 unknown via CMAUP database
Papyriogenin C 3081568 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)O)C)C 468.70 unknown via CMAUP database
Papyriogenin D 101277260 Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)C)C 468.70 unknown via CMAUP database
Papyriogenin E 101277261 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C(=O)O)C)C)(C)C)O)C)C 470.70 unknown via CMAUP database
Papyriogenin F 102239749 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)O)C)C 470.70 unknown via CMAUP database
Papyrioside LG 10605857 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CC=C7C6(CCC8C7(CCC(C8(C)C)O)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O 939.10 unknown via CMAUP database
Papyrioside LH 10748397 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OCC3C(C(C(C(O3)OC(=O)C45CCC6(C(=CC=C7C6(CCC8C7(CCC(=O)C8(C)C)C)C)C4CC(C(=O)C5)(C)C)C)O)O)O)CO)O)O)O 937.10 unknown via CMAUP database
> Lipids and lipid-like molecules / Saccharolipids / Acyltrehaloses
stearoyl(-2)Hex6Ac(?1-1?)Hex 85149698 Click to see CCCCCCCCCCCCCCCCCC(=O)OC1C(C(C(OC1OC2C(C(C(C(O2)CO)O)O)O)COC(=O)C)O)O 650.80 unknown https://doi.org/10.1007/BF00779095
https://doi.org/10.1007/BF00771504
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
(-)-Scopolamine 5184 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown https://doi.org/10.1007/BF00779095
(9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl) (2R)-2,3-dihydroxy-2-phenylpropanoate 44386560 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)(C4=CC=CC=C4)O 319.40 unknown https://doi.org/10.1016/S0021-9673(01)82171-3
https://doi.org/10.1007/BF00569615
[(2R,4S)-9-methyl-3-oxa-9-azatricyclo[3.3.1.02,4]nonan-7-yl] (2R)-3-hydroxy-2-phenylpropanoate 134767951 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown https://doi.org/10.1007/BF00569615
3-Bicyclo[3.2.1]octanyl 3-hydroxy-2-phenylpropanoate 45357570 Click to see C1CC2CC1CC(C2)OC(=O)C(CO)C3=CC=CC=C3 274.35 unknown via CMAUP database
Anisodine 11616712 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)(C4=CC=CC=C4)O 319.40 unknown via CMAUP database
Atroscine 452977 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown via CMAUP database
CID 4105431 4105431 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)(C4=CC=CC=C4)O 319.40 unknown https://doi.org/10.1007/BF00569615
https://doi.org/10.1016/S0021-9673(01)82171-3
Tropic acid ester with scopine 153311 Click to see CN1C2CC(CC1C3C2O3)OC(=O)C(CO)C4=CC=CC=C4 303.35 unknown https://doi.org/10.1007/BF00569615
> Organic acids and derivatives / Peptidomimetics / Hybrid peptides
[NMe-Ser7]MC-RY 146684759 Click to see CC1C(NC(=O)C(NC(=O)C(C(NC(=O)C(NC(=O)C(NC(=O)C(N(C(=O)CCC(NC1=O)C(=O)O)C)CO)C)CCCN=C(N)N)C(=O)O)C)CC2=CC=C(C=C2)O)C=CC(=CC(C)C(CC3=CC=CC=C3)OC)C 1063.20 unknown https://doi.org/10.1007/BF00779095
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Asperuloside 84298 Click to see CC(=O)OCC1=CC2C3C1C(OC=C3C(=O)O2)OC4C(C(C(C(O4)CO)O)O)O 414.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Lapachol 1,4-di-O-glucopyranoside 16216283 Click to see CC(=CCC1=C(C2=CC=CC=C2C(=C1O)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)C 568.60 unknown via CMAUP database
Methyl 1,4-bisglucosyloxy-3-prenyl-2-naphthoate 10031663 Click to see CC(=CCC1=C(C2=CC=CC=C2C(=C1C(=O)OC)OC3C(C(C(C(O3)CO)O)O)O)OC4C(C(C(C(O4)CO)O)O)O)C 610.60 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Cyclic ketones / Cyclohexenones
28-Noroleana-11,13(18),17(22)-triene-3,21-dione 102588576 Click to see CC1(CC2=C3C=CC4C5(CCC(=O)C(C5CCC4(C3(CCC2=CC1=O)C)C)(C)C)C)C 420.60 unknown via CMAUP database
3alpha-Hydroxy-28-noroleana-11,13(18),17(22)-triene-21-one 102588575 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC2=CC1=O)C)C)(C)C)O)C)C 422.60 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
1-Benzofuran-5-carbaldehyde 2773875 Click to see C1=CC2=C(C=CO2)C=C1C=O 146.14 unknown via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives / Pyrroloindoles
[(8bS)-4,8b-dimethyl-3-(methylcarbamoyl)-2,3a-dihydro-1H-pyrrolo[2,3-b]indol-7-yl] N-methylcarbamate 3083935 Click to see CC12CCN(C1N(C3=C2C=C(C=C3)OC(=O)NC)C)C(=O)NC 318.37 unknown via CMAUP database
> Organoheterocyclic compounds / Lactones / Beta propiolactones
Papyriogenin G 101967008 Click to see CC1(CC2=C3C=CC4C5(CCC(C(C5CCC4(C3(CCC26C(C1O)OC6=O)C)C)(C)C)O)C)C 468.70 unknown via CMAUP database
> Organoheterocyclic compounds / Oxazepines / 1,4-oxazepines
(6-Methyl-2-oxa-6-azatricyclo[3.3.1.03,7]nonan-4-yl) 2,3-dihydroxy-2-phenylpropanoate 163041691 Click to see CN1C2CC3CC1C(C2O3)OC(=O)C(CO)(C4=CC=CC=C4)O 319.40 unknown https://doi.org/10.1007/BF00569615
[(1R,3S,4R,5S,7R)-6-methyl-2-oxa-6-azatricyclo[3.3.1.03,7]nonan-4-yl] (2R)-2,3-dihydroxy-2-phenylpropanoate 163041692 Click to see CN1C2CC3CC1C(C2O3)OC(=O)C(CO)(C4=CC=CC=C4)O 319.40 unknown https://doi.org/10.1007/BF00569615
> Organoheterocyclic compounds / Quinolines and derivatives
Cusparine 442893 Click to see COC1=CC(=NC2=CC=CC=C21)CCC3=CC4=C(C=C3)OCO4 307.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
3,4-Dihydrocoumarin 660 Click to see C1CC(=O)OC2=CC=CC=C21 148.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamyl alcohols
Phenylallyl alcohol 308 Click to see C1=CC=C(C=C1)C=CCO 134.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Coumarin 323 Click to see C1=CC=C2C(=C1)C=CC(=O)O2 146.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Kaempferol 3,4',7-triacetate 44584293 Click to see CC(=O)OC1=CC=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC(=O)C)O)OC(=O)C 412.30 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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Afzelin 5316673 Click to see CC1C(C(C(C(O1)OC2=C(OC3=CC(=CC(=C3C2=O)O)O)C4=CC=C(C=C4)O)O)O)O 432.40 unknown via CMAUP database
Astragalin 5282102 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
kaempferol 7-O-(2-E-p-coumaroyl-alpha-L-rhamnopyranoside) 11678667 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)O)O 578.50 unknown via CMAUP database
kaempferol 7-O-(2,3-di-E-p-coumaroyl-alpha-L-rhamnopyranoside) 11607311 Click to see CC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=C(C3=O)O)C4=CC=C(C=C4)O)O)OC(=O)C=CC5=CC=C(C=C5)O)OC(=O)C=CC6=CC=C(C=C6)O)O 724.70 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
3,7-Di-O-methylquercetin 5280417 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O 330.29 unknown via CMAUP database

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