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Details Top

Internal ID UUID64402655e744c346925268
Scientific name Fritillaria taipaiensis
Authority P.Y.Li
First published in Acta Phytotax. Sin. 11: 251 (1966)

Description Top

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Synonyms Top

Scientific name Authority First published in
Fritillaria cirrhosa f. glabra P.Y.Li Acta Phytotax. Sin. 11: 251 1966
Fritillaria glabra (P.Y.Li) S.C.Chen Acta Bot. Yunnan. 5: 372 (1983)
Fritillaria shaanxiica Y.K.Yang, S.X.Zhang & D.K.Zhang J. Wuhan Bot. Res. 5: 133 (1987)
Fritillaria shennongjiaensis Y.K.Yang & Z.Zheng J. Wuhan Bot. Res. 5: 136 (1987)
Fritillaria taipaiensis var. fengxianensis Y.K.Yang & J.K.Wu J. Wuhan Bot. Res. 5: 134 (1987)
Fritillaria taipaiensis f. platyphylla Y.K.Yang & S.X.Zhang J. Wuhan Bot. Res. 5: 134 (1987)
Fritillaria chuanganensis var. glabra (P.Y.Li) Y.K.Yang & J.K.Wu Acta Bot. Boreal.-Occid. Sin. 5(1): 30 (1985):.
Fritillaria shennongjiaensis var. zhengbaensis Y.K.Yang & J.X.Yang J. Wuhan Bot. Res. 5(2): 137 (1987).
Fritillaria taipaiensis var. wanyuanensis Y.K.Yang & J.K.Wu Acta Bot. Boreal.-Occid. Sin. 5: 32 (1985)

Common names Top

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Language Common/alternative name
Chinese 太白贝母
Chinese 川贝母

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

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000768098
Tropicos 18406484
KEW urn:lsid:ipni.org:names:535333-1
The Plant List kew-306895
Open Tree Of Life 702591
NCBI Taxonomy 152093
IPNI 535333-1
iNaturalist 565532
GBIF 5300591
Freebase /m/0134rd7v
EOL 1088582
Wikipedia Fritillaria_taipaiensis
CMAUP NPO25808

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
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
Characterization of endophytic bacteriome diversity and associated beneficial bacteria inhabiting a macrophyte Eichhornia crassipes Fan D, Schwinghamer T, Liu S, Xia O, Ge C, Chen Q, Smith DL Front Plant Sci 19-Jun-2023
PMCID:PMC10316030
doi:10.3389/fpls.2023.1176648
PMID:37404529
Authenticity and species identification of Fritillariae cirrhosae: a data fusion method combining electronic nose, electronic tongue, electronic eye and near infrared spectroscopy Gui XJ, Li H, Ma R, Tian LY, Hou FG, Li HY, Fan XH, Wang YL, Yao J, Shi JH, Zhang L, Li XL, Liu RX Front Chem 28-Apr-2023
PMCID:PMC10175593
doi:10.3389/fchem.2023.1179039
PMID:37188096
Morphological and anatomical changes during dormancy break of the seeds of Fritillaria taipaiensis Luo M, Gao J, Liu R, Wang S, Wang G Plant Signal Behav 31-Mar-2023
PMCID:PMC10072057
doi:10.1080/15592324.2023.2194748
PMID:36999406
Application of third-generation sequencing to herbal genomics Gao L, Xu W, Xin T, Song J Front Plant Sci 07-Mar-2023
PMCID:PMC10027759
doi:10.3389/fpls.2023.1124536
PMID:36959935
A distinction between Fritillaria Cirrhosa Bulbus and Fritillaria Pallidiflora Bulbus via LC–MS/MS in conjunction with principal component analysis and hierarchical cluster analysis Liu C, Liu S, Tse WM, Tse KW, Erbu A, Xiong H, Lanzi G, Liu Y, Ye B Sci Rep 15-Feb-2023
PMCID:PMC9931167
doi:10.1038/s41598-023-29631-8
PMID:36792675
The rhizospheric bacterial diversity of Fritillaria taipaiensis under single planting pattern over five years Zhou Y, Mu M, Yang M, Yang X, Zhang H, Guo D, Zhou N Sci Rep 29-Dec-2022
PMCID:PMC9800406
doi:10.1038/s41598-022-26810-x
PMID:36581656
Medicinal herbs and multiple sclerosis: Overview on the hard balance between new therapeutic strategy and occupational health risk Costantini E, Masciarelli E, Casorri L, Di Luigi M, Reale M Front Cell Neurosci 10-Nov-2022
PMCID:PMC9688751
doi:10.3389/fncel.2022.985943
PMID:36439198
Research progress of rhizosphere microorganisms in Fritillaria L. medicinal plants Zhou N, Mei CM, Zhu XY, Zhao JJ, Ma MG, Li WD Front Bioeng Biotechnol 07-Nov-2022
PMCID:PMC9676442
doi:10.3389/fbioe.2022.1054757
PMID:36420438
Biological Control of Melon Continuous Cropping Obstacles: Weakening the Negative Effects of the Vicious Cycle in Continuous Cropping Soil Ku Y, Li W, Mei X, Yang X, Cao C, Zhang H, Cao L, Li M Microbiol Spectr 27-Oct-2022
PMCID:PMC9769590
doi:10.1128/spectrum.01776-22
PMID:36301101
Integrative analysis of the steroidal alkaloids distribution and biosynthesis of bulbs Fritillariae Cirrhosae through metabolome and transcriptome analyses Lu Q, Li R, Liao J, Hu Y, Gao Y, Wang M, Li J, Zhao Q BMC Genomics 14-Jul-2022
PMCID:PMC9284883
doi:10.1186/s12864-022-08724-0
PMID:35836113
Chemistry and bioactivities of natural steroidal alkaloids Xiang ML, Hu BY, Qi ZH, Wang XN, Xie TZ, Wang ZJ, Ma DY, Zeng Q, Luo XD Nat Prod Bioprospect 15-Jun-2022
PMCID:PMC9198197
doi:10.1007/s13659-022-00345-0
PMID:35701630
Corrigendum: Biocontrol Mechanism of Bacillus subtilis C3 Against Bulb Rot Disease in Fritillaria taipaiensis P.Y.Li Ku Y, Yang N, Pu P, Mei X, Cao L, Yang X, Cao C Front Microbiol 09-Feb-2022
PMCID:PMC8865616
doi:10.3389/fmicb.2022.855980
PMID:35222349
Levels and Health Risk of Pesticide Residues in Chinese Herbal Medicines Wang Y, Gou Y, Zhang L, Li C, Wang Z, Liu Y, Geng Z, Shen M, Sun L, Wei F, Zhou J, Gu L, Jin H, Ma S Front Pharmacol 01-Feb-2022
PMCID:PMC8844025
doi:10.3389/fphar.2021.818268
PMID:35177984
Bulbus Fritillariae Cirrhosae as a Respiratory Medicine: Is There a Potential Drug in the Treatment of COVID-19? Quan Y, Li L, Yin Z, Chen S, Yi J, Lang J, Zhang L, Yue Q, Zhao J Front Pharmacol 20-Jan-2022
PMCID:PMC8811224
doi:10.3389/fphar.2021.784335
PMID:35126123

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
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
3alpha-Hydroxyfriedelane-2-one 14465808 Click to see CC1C(C(=O)CC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C)O 442.70 unknown via CMAUP database
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown via CMAUP database
Neoruscogenin 9910474 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)O)C)C)OC16CCC(=C)CO6 428.60 unknown via CMAUP database
Ruscogenin 441893 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)O)C)C)C)OC1 430.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Bile acids, alcohols and derivatives / Hydroxy bile acids, alcohols and derivatives / Dihydroxy bile acids, alcohols and derivatives
(22r)-22-Hydroxycholes-terol 13754059 Click to see CC(C)CCC(C(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)O 402.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / 22,26-epiminocholestanes
(3S,5S,8S,9S,10R,13S,14S,17R)-17-[(1S)-1-[(2R,5S)-1,5-dimethylpiperidin-2-yl]ethyl]-3-hydroxy-10,13-dimethyl-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 10693900 Click to see CC1CCC(N(C1)C)C(C)C2CCC3C2(CCC4C3CC(=O)C5C4(CCC(C5)O)C)C 429.70 unknown via CMAUP database
N-Desmethylpuqietinone 11304576 Click to see CC1CCC(NC1)C(C)C2CCC3C2(CCC4C3CC(=O)C5C4(CCC(C5)O)C)C 415.70 unknown via CMAUP database
Puqietinone 44583920 Click to see CC1CCC(N(C1)C)C(C)C2CCC3C2(CCC4C3CC(=O)C5C4(CCC(C5)O)C)C 429.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
(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,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 via CMAUP database
(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 via CMAUP database
(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
(5alpha,8xi,10xi,13xi,25xi)-Cevane-3,6,20-triol 139291898 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown https://doi.org/10.4028/WWW.SCIENTIFIC.NET/AMR.781-784.1134
Imperialine 442977 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 429.60 unknown https://doi.org/10.4028/WWW.SCIENTIFIC.NET/AMR.781-784.1134
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 via CMAUP database
Peiminine 167691 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 429.60 unknown via CMAUP database
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 via CMAUP database
Taipaienine 192522 Click to see CC1C2CCC3C(C2CN4C1CCC(C4)(C)O)CC5C3CC(=O)C6C5(CCC(C6)O)C 429.60 unknown https://doi.org/10.4028/WWW.SCIENTIFIC.NET/AMR.781-784.1134
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Jerveratrum-type alkaloids
(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
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
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/10.4028/WWW.SCIENTIFIC.NET/AMR.781-784.1134
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
Puqietinonoside 21575476 Click to see CC1CCC(N(C1)C)C(C)C2CCC3C2(CCC4C3CC(=O)C5C4(CCC(C5)OC6C(C(C(C(O6)CO)O)O)O)C)C 591.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(23S,25R)-23-[6-O-(beta-D-Glucopyranosyl)-beta-D-glucopyranosyloxy]spirosta-5-ene-3beta-ol 100982641 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1)OC7C(C(C(C(O7)COC8C(C(C(C(O8)CO)O)O)O)O)O)O 754.90 unknown via CMAUP database
(23S)-1beta-[[2-O-[3-O-(beta-D-Glucopyranosyl)-alpha-L-rhamnopyranosyl]-alpha-L-arabinopyranosyl]oxy]-23-(beta-D-glucopyranosyloxy)spirosta-5,25(27)-diene-3beta-ol 10581939 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19C(CC(=C)CO9)OC1C(C(C(C(O1)CO)O)O)O 1047.10 unknown via CMAUP database
(25R)-1beta-(2-O-alpha-L-Rhamnopyranosyl-alpha-L-arabinopyranosyloxy)spirosta-5-ene-3beta-ol 44575746 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)OC1 708.90 unknown via CMAUP database
[(2S,3S,4R,5R,6S)-4,5-diacetyloxy-6-[(2S,3R,4S,5S)-2-[(1S,2S,3'S,4S,4'S,6S,7S,8R,9S,12S,13R,14R,16R)-4'-[[(2R,5S,6R,7R,8R,10R)-6,7-dihydroxy-2-[(2S)-2-hydroxybutan-2-yl]-10-methyl-3-oxo-1,4,9-trioxaspiro[4.5]decan-8-yl]oxy]-3',16-dihydroxy-7,9,13-trimethyl-5'-methylidenespiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-2-methyloxan-3-yl] acetate 21590070 Click to see CCC(C)(C1C(=O)OC2(O1)C(OC(C(C2O)O)OC3C(C4(C(C5C(O4)CC6C5(CCC7C6CC=C8C7(C(CC(C8)O)OC9C(C(C(CO9)O)O)OC1C(C(C(C(O1)C)OC(=O)C)OC(=O)C)OC(=O)C)C)C)C)OCC3=C)O)C)O 1139.20 unknown via CMAUP database
1beta-[(2-O-alpha-L-Rhamnopyranosyl-alpha-L-arabinopyranosyl)oxy]-26-(beta-D-glucopyranosyloxy)furosta-5,20(22),25(27)-trien-3beta-ol 44567205 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CC(CC4=CCC5C(C34C)CCC6(C5CC7C6C(=C(O7)CCC(=C)COC8C(C(C(C(O8)CO)O)O)O)C)C)O)O)O)O)O)O 869.00 unknown via CMAUP database
1beta-[2-O-(3-O-beta-D-Glucopyranosyl-alpha-L-rhamnopyranosyl)-4-O-acetyl-alpha-L-arabinopyranosyloxy]spirosta-5,25(27)-dien-3beta-ol 101937241 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)OC(=O)C)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19CCC(=C)CO9 911.00 unknown via CMAUP database
6-Hydroxycevan-2-yl hexopyranoside 127202 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CC(CC6)OC7C(C(C(C(O7)CO)O)O)O)C)O)C 577.80 unknown via CMAUP database
6-Oxocevan-2-yl hexopyranoside 127203 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CC(CC6)OC7C(C(C(C(O7)CO)O)O)O)C)C 575.80 unknown via CMAUP database
Aculeoside B 154169 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(C(O7)COC(=O)C)OC(=O)C)OC(=O)C)OC8C(C(C(C(O8)C)O)OC9C(C(C(C(O9)CO)O)O)O)O)C)C)C)OC1)OC1C(C(C(C(O1)CO)O)O)O 1205.30 unknown via CMAUP database
CID 10462472 10462472 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC18CCC(=C)CO8 706.90 unknown via CMAUP database
Ruscin(P) 13935613 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC19CCC(=C)CO9 869.00 unknown via CMAUP database
Ruscoside [WHO-DD] 91936850 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)OC1(CCC(=C)COC9C(C(C(C(O9)CO)O)O)O)O 1049.20 unknown via CMAUP database
> 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
> 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 via CMAUP database
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 / Purine nucleosides / Purine 2-deoxyribonucleosides
2'-Deoxyadenosine 13730 Click to see C1C(C(OC1N2C=NC3=C(N=CN=C32)N)CO)O 251.24 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 via CMAUP database
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 via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Euparone 104654 Click to see CC(=O)C1=CC2=CC(=C(C=C2O1)O)C(=O)C 218.20 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans / Dibenzofurans
Ruscodibenzofuran 323624 Click to see CC1=C2C3=CC(=C(C=C3OC2=C(C=C1)C)O)C(=O)C 254.28 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydroxypyrimidines
5-methylpyrimidine-2,4-diol 5274265 Click to see CC1=CN=C(N=C1O)O 126.11 unknown via CMAUP database
> 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 via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Purinones / Hypoxanthines
CID 790 790 Click to see C1=NC2=C(N1)C(=O)N=CN2 136.11 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Esculin 5281417 Click to see C1=CC(=O)OC2=CC(=C(C=C21)OC3C(C(C(C(O3)CO)O)O)O)O 340.28 unknown via CMAUP database

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