Fritillaria thunbergii - Unknown
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Internal ID UUID644026562a72b519328730
Scientific name Fritillaria thunbergii
Authority Miq.
First published in Ann. Mus. Bot. Lugduno-Batavi 3: 157 (1867)

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Synonyms Top

Scientific name Authority First published in
Uvularia cirrhosa Thunb. Syst. Veg. ed. 14 : 325 (1784)
Fritillaria austroanhuiensis Y.K.Yang & J.K.Wu Acta Bot. Boreal.-Occid. Sin. 5: 44 (1985)
Fritillaria chekiangensis (Hsiao & K.C.Hsia) Y.K.Yang, Z.H.Lin & C.Lin J. Wuhan Bot. Res. 5: 143 (1987)
Fritillaria collicola Hance J. Bot. 8: 76 (1870)
Fritillaria thunbergii var. chekiangensis Hsiao & K.C.Hsia Acta Phytotax. Sin. 15(2): 42 (1977)
Fritillaria verticillata var. thunbergii (Miq.) Baker J. Linn. Soc., Bot. 14: 258. 1874
Fritillaria xiaobeimu Y.K.Yang, J.Z.Shao & M.M.Fang J. Wuhan Bot. Res. 5: 142 (1987)

Common names Top

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Language Common/alternative name
Chinese 浙贝母
Chinese 浙貝母

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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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.
grow seedlings at cool temperature; leave in pot for 2 years

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China Southeast
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Kazakhstan

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000768116
UNII 8V19OM31TK
Tropicos 18404501
KEW urn:lsid:ipni.org:names:535342-1
The Plant List kew-306913
Open Tree Of Life 935709
NCBI Taxonomy 108546
IPNI 535342-1
iNaturalist 565533
GBIF 5300784
EOL 1088584
USDA GRIN 402590
Wikipedia Fritillaria_thunbergii
CMAUP NPO4487

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
A multi-center cross-sectional study of Chinese Herbal Medicine-Drug adverse reactions using active surveillance in Singapore’s Traditional Chinese Medicine clinics Ng CY, Zhao Y, Wang N, Chia KL, Teo CH, Peh W, Yeo P, Zhong LL Chin Med 07-Mar-2024
PMCID:PMC10918936
doi:10.1186/s13020-024-00915-z
PMID:38454483
Antitumour mechanisms of traditional Chinese medicine elicited by regulating tumour-associated macrophages in solid tumour microenvironments Gao J, Tan W, Yuan L, Wang H, Wen J, Sun K, Chen X, Wang S, Deng W Heliyon 02-Mar-2024
PMCID:PMC10923716
doi:10.1016/j.heliyon.2024.e27220
PMID:38463777
Lianhua Qingke Preserves Mucociliary Clearance in Rat with Acute Exacerbation of Chronic Obstructive Pulmonary Disease by Maintaining Ciliated Cells Proportion and Protecting Structural Integrity and Beat Function of Cilia Wang X, Hao Y, Yin Y, Hou Y, Han N, Liu Y, Li Z, Wei Y, Ma K, Gu J, Ma Y, Qi H, Jia Z Int J Chron Obstruct Pulmon Dis 07-Feb-2024
PMCID:PMC10859105
doi:10.2147/COPD.S436323
PMID:38343495
Explorative study for the rapid detection of Fritillaria using gas chromatography-ion mobility spectrometry Dai Y, Liu S, Yang L, He Y, Guo X, Ma Y, Li S, Huang D Front Nutr 06-Feb-2024
PMCID:PMC10877000
doi:10.3389/fnut.2024.1361668
PMID:38379552
Peiminine Exerts Its Anti-Acne Effects by Regulating the NF-κB Pathway Cha SJ, Kim SS, Shin JH, Seo SR Antioxidants (Basel) 22-Jan-2024
PMCID:PMC10812726
doi:10.3390/antiox13010131
PMID:38275656
Suppressing inflammatory signals and apoptosis-linked sphingolipid metabolism underlies therapeutic potential of Qing-Jin-Hua-Tan decoction against chronic obstructive pulmonary disease Yang J, Shen X, Qin M, Zhou P, Huang FH, You Y, Wang L, Wu JM Heliyon 18-Jan-2024
PMCID:PMC10839876
doi:10.1016/j.heliyon.2024.e24336
PMID:38318072
Modified Qing-Zao-Jiu-Fei decoction attenuated pulmonary fibrosis induced by bleomycin in rats via modulating Nrf2/NF-κB and MAPKs pathways Zhu JQ, Tian YY, Chan KL, Hu Z, Xu QQ, Lin ZX, Xian YF Chin Med 16-Jan-2024
PMCID:PMC10790405
doi:10.1186/s13020-024-00882-5
PMID:38229198
Identification and Functional Characterization of Oxidosqualene Cyclases from Medicinal Plant Hoodia gordonii Parveen I, Wang M, Lee J, Zhao J, Zhu Y, Chittiboyina AG, Khan IA, Pan Z Plants (Basel) 14-Jan-2024
PMCID:PMC10818575
doi:10.3390/plants13020231
PMID:38256784
Application of Data Fusion in Traditional Chinese Medicine: A Review Huang R, Ma S, Dai S, Zheng J Sensors (Basel) 25-Dec-2023
PMCID:PMC10781265
doi:10.3390/s24010106
PMID:38202967
Chinese herbal compound for multidrug-resistant or extensively drug-resistant bacterial pneumonia: a meta-analysis and trial sequential analysis with association rule mining to identify core herb combinations Zhao S, Geng Y, Shi J, Qian J, Yang Y, Dai D, Yan Z, Qi W, Yu D, Zhao X Front Pharmacol 20-Dec-2023
PMCID:PMC10761442
doi:10.3389/fphar.2023.1282538
PMID:38174222
Advances in Neuropathic Pain Research: Selected Intracellular Factors as Potential Targets for Multidirectional Analgesics Ciapała K, Mika J Pharmaceuticals (Basel) 17-Nov-2023
PMCID:PMC10675751
doi:10.3390/ph16111624
PMID:38004489
Lianhua Qingke ameliorates lipopolysaccharide‐induced lung injury by inhibiting neutrophil extracellular traps formation and pyroptosis Peng W, Qi H, Zhu W, Tong L, Rouzi A, Wu Y, Han L, He L, Yan Y, Pan T, Liu J, Wang Q, Jia Z, Song Y, Zhu Q, Zhou J Pulm Circ 06-Oct-2023
PMCID:PMC10557103
doi:10.1002/pul2.12295
PMID:37808899
Exploring the potential use of Chinese herbs in regulating the inflammatory microenvironment of tumours based on the concept of ‘state-target identification and treatment’: a scooping review Lian J, Lin D, Huang Y, Chen X, Chen L, Zhang F, Tang P, Xie J, Hou X, Du Z, Deng J, Hao E, Liu J Chin Med 23-Sep-2023
PMCID:PMC10517536
doi:10.1186/s13020-023-00834-5
PMID:37742025
Metabolite profiling and transcriptomic analyses demonstrate the effects of biocontrol agents on alkaloid accumulation in Fritillaria thunbergii Cheng X, Li D, Jiang Z, Qu C, Yan H, Wu Q BMC Plant Biol 18-Sep-2023
PMCID:PMC10506312
doi:10.1186/s12870-023-04459-6
PMID:37723471
Efficacy of Chinese herbal medicine on nasal itching in children with allergic rhinitis: a systematic review and meta-analysis Chen Y, Wang J, Wu L, Zhang Y, Chen H, Zhang Z Front Pharmacol 23-Aug-2023
PMCID:PMC10482051
doi:10.3389/fphar.2023.1240917
PMID:37680707

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 / Naphthalenes / Naphthoquinones
Aethiopinone 157301 Click to see CC1=C(C2=C(C=C1)C=C(C(=O)C2=O)C(C)C)CCCC(=C)C 296.40 unknown via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
O-Ethylcubebin 13939336 Click to see CCOC1C(C(CO1)CC2=CC3=C(C=C2)OCO3)CC4=CC5=C(C=C4)OCO5 384.40 unknown https://doi.org/10.1248/CPB.30.3912
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthren-1-yl)methanol 15586710 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)CO)C)C1)C=C 288.50 unknown https://doi.org/10.1248/CPB.30.3912
1-Phenanthrenemethanol, 7-ethenyl-1,2,3,4,4a,4b,5,6,7,8,10,10a-dodecahydro-1,4a,7-trimethyl-, (1S,4aR,4bS,7S,10aR)- 158539 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)CO)C)C1)C=C 288.50 unknown https://doi.org/10.1248/CPB.30.3912
13-Epimanool 10891602 Click to see CC1(CCCC2(C1CCC(=C)C2CCC(C)(C=C)O)C)C 290.50 unknown via CMAUP database
Elliotinol 12303806 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)CO)C)C=C 288.50 unknown https://doi.org/10.1248/CPB.30.3912
methyl (1S,4aR,4bS,7S,10aR)-7-ethenyl-1,4a,7-trimethyl-3,4,4b,5,6,8,10,10a-octahydro-2H-phenanthrene-1-carboxylate 5318629 Click to see CC1(CCC2C(=CCC3C2(CCCC3(C)C(=O)OC)C)C1)C=C 316.50 unknown https://doi.org/10.1248/CPB.30.3912
methyl 1,4a-dimethyl-6-methylidene-5-(3-methylpenta-2,4-dienyl)-3,4,5,7,8,8a-hexahydro-2H-naphthalene-1-carboxylate 535072 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C)C=C 316.50 unknown https://doi.org/10.1248/CPB.30.3912
Methyl trans-communate 11141639 Click to see CC(=CCC1C(=C)CCC2C1(CCCC2(C)C(=O)OC)C)C=C 316.50 unknown https://doi.org/10.1248/CPB.30.3912
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(1'S,2R,4'R,9'R,10'R,13'R)-5',5',9'-trimethylspiro[oxirane-2,14'-tetracyclo[11.2.1.01,10.04,9]hexadecane] 21670063 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C5(C4)CO5)C)C 288.50 unknown https://doi.org/10.1248/CPB.30.3912
(14-Methoxy-5,5,9-trimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadecanyl)methanol 73819941 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)OC)C)C 320.50 unknown https://doi.org/10.1248/CPB.30.3912
(1S,4R,9R,10R,13R,14S)-14-(hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-ol 12112093 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)C 306.50 unknown https://doi.org/10.1248/CPB.30.3912
(5,5,9-Trimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl)methanol 14019136 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C4)CO)C)C 288.50 unknown https://doi.org/10.1248/CPB.30.3912
[(1S,4R,9R,10R,13R,14S)-14-methoxy-5,5,9-trimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadecanyl]methanol 21670064 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)OC)C)C 320.50 unknown https://doi.org/10.1248/CPB.30.3912
[(1S,4R,9R,10S,13R)-5,5,9-Trimethyl-14-tetracyclo[11.2.1.01,10.04,9]hexadec-14-enyl]methanol 21670065 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(=C4)CO)C)C 288.50 unknown https://doi.org/10.1248/CPB.30.3912
14-(Hydroxymethyl)-5,5,9-trimethyltetracyclo[11.2.1.01,10.04,9]hexadecan-14-ol 13816758 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)C 306.50 unknown https://doi.org/10.1248/CPB.30.3912
5',5',9'-Trimethylspiro[oxirane-2,14'-tetracyclo[11.2.1.01,10.04,9]hexadecane] 14487105 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C5(C4)CO5)C)C 288.50 unknown https://doi.org/10.1248/CPB.30.3912
Kaurane-16alpha,17-diol 13816761 Click to see CC1(CCCC2(C1CCC34C2CCC(C3)C(C4)(CO)O)C)C 306.50 unknown https://doi.org/10.1248/CPB.30.3912
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
1,7,11-Trimethyl-4-propan-2-yl-15-oxabicyclo[12.1.0]pentadeca-5,10-dien-7-ol 72727937 Click to see CC1=CCCC(C=CC(CCC2(C(O2)CC1)C)C(C)C)(C)O 306.50 unknown https://doi.org/10.3987/S-1981-02-0791
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
13-epi-Manoyl oxide-18-oic acid 44575334 Click to see CC1(CCC2C3(CCCC(C3CCC2(O1)C)(C)C(=O)O)C)C=C 320.50 unknown via CMAUP database
23-Hydroxyursolic Acid 14136881 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Asiatic Acid 119034 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)C)C2C1C)C)C(=O)O 488.70 unknown via CMAUP database
Corosolic acid 6918774 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1C)C)C(=O)O 472.70 unknown via CMAUP database
Hederagenin 73299 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)CO)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Labd-14-ene, 8,13-epoxy-, (13S)- 6432025 Click to see CC1(CCCC2(C1CCC3(C2CCC(O3)(C)C=C)C)C)C 290.50 unknown via CMAUP database
Maslinic Acid 73659 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)C)O)O)C)C)C2C1)C)C(=O)O)C 472.70 unknown via CMAUP database
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
Ursolic Acid 64945 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C(=O)O 456.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
(1R,2S,4S,6S,9S,10S,11S,14R,15S,17S,18S,20S,23R,24S)-6,10,23-trimethyl-4-oxido-4-azoniahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-10,17,20-triol 163188806 Click to see CC1CCC2C(C3CCC4C(C3C[N+]2(C1)[O-])CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 447.60 unknown https://doi.org/10.3987/S-1981-02-0791
(1R,2S,4S,6S,9S,10S,11S,14S,15S,18S,20S,23R,24S)-10,20-dihydroxy-6,10,23-trimethyl-4-oxido-4-azoniahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 163190131 Click to see CC1CCC2C(C3CCC4C(C3C[N+]2(C1)[O-])CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 445.60 unknown https://doi.org/10.3987/S-1981-02-0791
(1R,2S,6R,9S,10S,11S,14S,15S,18S,20S,23R,24S)-20-hydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 162943682 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C 413.60 unknown https://doi.org/10.1016/0031-9422(93)85314-H
(1R,2S,6R,9S,11S,14S,15S,18S,20S,23R,24S)-20-hydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 101687687 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C 413.60 unknown via CMAUP database
(1R,2S,6S,9R,10S,11S,14S,15S,17S,18S,20S,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-10,17,20-triol 21121502 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown https://doi.org/10.1248/CPB.8.302
(1R,2S,6S,9S,10S,11S,14S,15S,18S,20S,23R,24S)-20-hydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 127031870 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C 413.60 unknown https://doi.org/10.1016/0031-9422(93)85314-H
(1R,2S,6S,9S,11S,14S,15S,17R,18S,20S,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-10,17,20-triol 102063130 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown via CMAUP database
(1R,2S,6S,9S,11S,14S,15S,17R,18S,20S,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-17,20-diol 101324888 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)C 415.70 unknown https://doi.org/10.1016/S0021-9673(00)01083-9
https://doi.org/10.1016/S0021-9673(00)00049-2
(1R,2S,6S,9S,11S,14S,15S,17S,18S,20S,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-10,17,20-triol 101297579 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown via CMAUP database
(1R,2S,6S,9S,11S,14S,15S,18S,20S,23R,24S)-20-hydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 102062796 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C 413.60 unknown https://doi.org/10.1021/JS960211V
https://doi.org/10.1016/S0021-9673(00)00049-2
(2S,6S,10S,15S,20S,23R)-10,20-dihydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 5320446 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 429.60 unknown via CMAUP database
(3b,5a,6a)-Cevane-3,6,20-triol 118701092 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown via CMAUP database
20-Hydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 14240939 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C 413.60 unknown https://doi.org/10.1016/0031-9422(93)85314-H
3,20-Dihydroxycevan-6-one 5221 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 429.60 unknown https://doi.org/10.3987/S-1981-02-0791
https://doi.org/10.1016/0031-9422(82)80040-X
6,10,23-Trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-10,17,20-triol 3727034 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown https://doi.org/10.1016/0031-9422(93)85314-H
https://doi.org/10.3987/S-1981-02-0791
https://doi.org/10.1248/CPB.8.302
https://doi.org/10.1016/0031-9422(82)80040-X
Hupehenine 14240934 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)C 415.70 unknown https://doi.org/10.1016/S0021-9673(00)01083-9
Imperialine 442977 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 429.60 unknown https://doi.org/10.1016/S0021-9673(00)01083-9
https://doi.org/10.1016/S0021-9673(99)00867-5
Isoverticine 21573744 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown via CMAUP database
Peimine 131900 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown https://doi.org/10.1016/J.CHROMA.2008.03.093
https://doi.org/10.3987/S-1981-02-0791
https://doi.org/10.1016/0031-9422(82)80040-X
Peiminine 167691 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 429.60 unknown https://doi.org/10.3987/S-1981-02-0791
https://doi.org/10.1016/0031-9422(82)80040-X
Puqiedine 101400593 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)C 415.70 unknown via CMAUP database
Puqiedinone 126149 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C 413.60 unknown via CMAUP database
Raddeamine 102063129 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 429.60 unknown https://doi.org/10.1016/S0021-9673(00)00049-2
Verticine N-oxide 163184365 Click to see CC1CCC2C(C3CCC4C(C3C[N+]2(C1)[O-])CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 447.60 unknown https://doi.org/10.3987/S-1981-02-0791
Verticinone N-oxide 163184364 Click to see CC1CCC2C(C3CCC4C(C3C[N+]2(C1)[O-])CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 445.60 unknown https://doi.org/10.3987/S-1981-02-0791
Zhebeinine 21121503 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown https://doi.org/10.1007/S10600-012-0286-1
https://doi.org/10.1016/0031-9422(93)85314-H
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Jerveratrum-type alkaloids
(3'aR,4aR,6aS,6bR,7'aR,9R,11aS,11bR)-3-hydroxy-3',6',10,11b-tetramethylspiro[1,2,3,4,4a,6,6a,6b,7,8,11,11a-dodecahydrobenzo[a]fluorene-9,2'-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine]-5-one 138114701 Click to see CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC4=C3C)C)O)C)NC1 427.60 unknown https://doi.org/10.1007/S10600-012-0286-1
(3S,3'R,3'aS,6'S,6aR,6bS,7'aR,9R,11aS,11bR)-3-hydroxy-3',6',10,11b-tetramethylspiro[1,2,3,4,4a,6,6a,6b,7,8,11,11a-dodecahydrobenzo[a]fluorene-9,2'-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine]-5-one 102119835 Click to see CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC4=C3C)C)O)C)NC1 427.60 unknown via CMAUP database
(3S,3'R,4aS,6'S,6aR,6bS,7'aR,9R,11aS,11bR)-3-hydroxy-3',6',10,11b-tetramethylspiro[1,2,3,4,4a,6,6a,6b,7,8,11,11a-dodecahydrobenzo[a]fluorene-9,2'-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine]-5-one 71751476 Click to see CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC4=C3C)C)O)C)NC1 427.60 unknown via CMAUP database
(4-Acetyl-3,6,6',11'-tetramethyl-17'-oxospiro[3,3a,5,6,7,7a-hexahydrofuro[3,2-b]pyridine-2,5'-7-oxapentacyclo[8.8.0.02,8.06,8.011,16]octadecane]-14'-yl) acetate 162844193 Click to see CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC47C3(O7)C)C)OC(=O)C)C)N(C1)C(=O)C 527.70 unknown https://doi.org/10.3987/S-1981-02-0791
[(1'R,2R,2'S,3R,3aS,6S,6'S,7aR,8'S,10'S,11'R,14'S,16'S)-4-acetyl-3,6,6',11'-tetramethyl-17'-oxospiro[3,3a,5,6,7,7a-hexahydrofuro[3,2-b]pyridine-2,5'-7-oxapentacyclo[8.8.0.02,8.06,8.011,16]octadecane]-14'-yl] acetate 162844194 Click to see CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC47C3(O7)C)C)OC(=O)C)C)N(C1)C(=O)C 527.70 unknown https://doi.org/10.3987/S-1981-02-0791
CID 21123947 21123947 Click to see CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC4=C3C)C)O)C)NC1 427.60 unknown via CMAUP database
CID 5320448 5320448 Click to see CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC4=C3C)C)O)C)NC1 427.60 unknown https://doi.org/10.3987/S-1981-02-0791
Peimisine 161294 Click to see CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC4=C3C)C)O)C)NC1 427.60 unknown https://doi.org/10.3987/S-1981-02-0791
https://doi.org/10.1016/J.PHYMED.2011.12.010
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-2-[[(3S,8S,9S,10R,13S,14S,16S,17R)-17-[(1S)-1-[(2S,5S)-1,5-dimethylpiperidin-2-yl]ethyl]-16-hydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21575049 Click to see CC1CCC(N(C1)C)C(C)C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)O 738.00 unknown https://doi.org/10.1016/0031-9422(82)80040-X
2-[2-[[17-[1-(1,5-dimethylpiperidin-2-yl)ethyl]-16-hydroxy-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-yl]oxy]-4,5-dihydroxy-6-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 73157126 Click to see CC1CCC(N(C1)C)C(C)C2C(CC3C2(CCC4C3CC=C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)O 738.00 unknown https://doi.org/10.1016/0031-9422(82)80040-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3R,4S,5S,6R)-2-[[(1S,2S,6S,9R,10S,11S,14S,15S,17S,18S,20S,23R,24S)-10,17-dihydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-20-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 162857121 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)O)(C)O 593.80 unknown https://doi.org/10.1248/CPB.8.302
(2S,3R,4R,5R,6S)-2-[(2R,3R,4S,5S,6R)-4-hydroxy-6-(hydroxymethyl)-2-[[(1S,2S,7S,10R,11S,14S,15R,16S,17R,20S,23S)-10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-7-yl]oxy]-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 21573770 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C 868.10 unknown https://doi.org/10.1016/0031-9422(82)80040-X
2-[(10,17-Dihydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-20-yl)oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 73656859 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)O)(C)O 593.80 unknown https://doi.org/10.1248/CPB.8.302
2-[4-Hydroxy-6-(hydroxymethyl)-2-[(10,14,16,20-tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracos-4-en-7-yl)oxy]-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 14609331 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)CO)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C 868.10 unknown https://doi.org/10.1016/0031-9422(82)80040-X
beta-Chaconine 119393 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C 705.90 unknown https://doi.org/10.1016/0031-9422(82)80040-X
beta1-Chaconine 12302820 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C 705.90 unknown https://doi.org/10.1016/0031-9422(82)80040-X
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
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 https://doi.org/10.1007/S10600-012-0286-1
3beta-(alpha-D-Glucopyranosyloxy)stigmasta-5-ene 12309073 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
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 https://doi.org/10.1007/S10600-012-0286-1
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6802 Click to see C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N 283.24 unknown via CMAUP database
9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6021 Click to see C1=NC(=O)C2=C(N1)N(C=N2)C3C(C(C(O3)CO)O)O 268.23 unknown https://doi.org/10.1002/JSSC.200900866
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
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Cytidine 6175 Click to see C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)O)O 243.22 unknown https://doi.org/10.1002/JSSC.200900866
Uridine 6029 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides / Pyrimidine 2-deoxyribonucleosides
Thymidine 5789 Click to see CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O 242.23 unknown https://doi.org/10.1002/JSSC.200900866
> Organic acids and derivatives / Hydroxy acids and derivatives / Beta hydroxy acids and derivatives
2alpha,3alpha,16alpha-Trihydroxy-23-noroleana-12,4(24)-diene-28-oic acid 101844542 Click to see CC1(CCC2(C(C1)C3=CCC4C(C3(CC2O)C)(CCC5C4(CC(C(C5=C)O)O)C)C)C(=O)O)C 472.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
2alpha,3alpha-Dihydroxy-24-noroleana-4(23),12-diene-28-oic acid 637444 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5=C)O)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
Chrysosporazine G 146684649 Click to see CC(=O)N1CC2C3C4=CC5=C(C(=C4C(C3(C(=O)N2CC1CC6=CC7=C(C(=C6)OC)OCO7)O)C8=CC=CC=C8)OC)OCO5 600.60 unknown https://doi.org/10.1248/CPB.30.3912
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see C1=CNC(=O)NC1=O 112.09 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives
2-amino-3,7-dihydropurin-6-one 764 Click to see C1=NC2=C(N1)C(=O)N=C(N2)N 151.13 unknown https://doi.org/10.1002/JSSC.200900866
> Organoheterocyclic compounds / Naphthopyrans / Naphthopyranones
Ambreinolide 11807560 Click to see CC1(CCCC2(C1CCC3(C2CCC(=O)O3)C)C)C 264.40 unknown via CMAUP database
> Organoheterocyclic compounds / Piperidines / N-acylpiperidines
[5-[1-(1-Acetyl-3-hydroxy-5-methylpiperidin-2-yl)ethyl]-5-hydroxy-6,11-dimethyl-17-oxo-7-oxapentacyclo[8.8.0.02,8.06,8.011,16]octadecan-14-yl] acetate 163008425 Click to see CC1CC(C(N(C1)C(=O)C)C(C)C2(CCC3C4CC(=O)C5CC(CCC5(C4CC36C2(O6)C)C)OC(=O)C)O)O 545.70 unknown https://doi.org/10.3987/S-1981-02-0791
> Phenylpropanoids and polyketides / 3,4-dihydrocoumarins
Salvipalolide 101020948 Click to see CC(C)C1=C(C2=C3C(=C1O)OC(=O)CC3(C(CC2=O)C(=C)C(=O)C)C)O 358.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
(S)-rosmarinic acid 639655 Click to see C1=CC(=C(C=C1CC(C(=O)O)OC(=O)C=CC2=CC(=C(C=C2)O)O)O)O 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
3'-Methoxy-4',5-dihydroxy-7-[(6-O-butyryl-beta-D-glucopyranosyl)oxy]flavone 101453901 Click to see CCCC(=O)OCC1C(C(C(C(O1)OC2=CC(=C3C(=C2)OC(=CC3=O)C4=CC(=C(C=C4)O)OC)O)O)O)O 532.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Cirsimaritin 188323 Click to see COC1=C(C(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O)OC 314.29 unknown via CMAUP database
Fastigenin 162464 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O)O 344.30 unknown via CMAUP database
Salvigenin 161271 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC)OC)O 328.30 unknown via CMAUP database
Velutin 5464381 Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC(=C(C=C3)O)OC)O 314.29 unknown via CMAUP database

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