Fritillaria cirrhosa - Unknown
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Internal ID UUID6440264778404332084024
Scientific name Fritillaria cirrhosa
Authority D.Don
First published in Prodr. Fl. Nepal. : 51 (1825)

Description Top

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Synonyms Top

Scientific name Authority First published in
Lilium bonatii H.Lév. Repert. Spec. Nov. Regni Veg. 11: 303 (1912)
Melorima cirrhosa Raf. Fl. Tellur. 4: 53 (1838)
Baimo cirrhosa Raf. Fl. Tellur. 4: 27 (1838)
Fritillaria cirrhosa var. bonatii (Lèvl.) S.C.Chen Acta Bot. Yunnan. 5: 374 (1983)
Fritillaria cirrhosa var. brachyantha C.Marquand & Airy Shaw J. Linn. Soc., Bot. 48: 227. 1929
Fritillaria cirrhosa var. dingriensis Y.K.Yang & J.Z.Zhang Acta Bot. Boreal.-Occid. Sin. 5: 34 (1985)
Fritillaria cirrhosa var. viridiflava S.C.Chen Acta Bot. Yunnan. 5: 373 (1983)
Fritillaria duilongdeqingensis Y.K.Yang & Gesang Acta Bot. Boreal.-Occid. Sin. 5: 30 (1985)
Fritillaria guilelmi-waldemarii Klotzsch Bot. Ergebn. Reise Waldemar [Klotzsch & Garcke] 52. 1862 [Jan 1862]
Fritillaria lhiinzeensis Y.K.Yang & Y.Q.Ye et al. J. Wuhan Bot. Res. 5: 126 (1987)
Fritillaria roylei Hook. Hooker's Icon. Pl. 9: t. 860 (1852)
Fritillaria zhufenensis Y.K.Yang & J.Z.Zhang Acta Bot. Boreal.-Occid. Sin. 5: 21 (1985)
Fritillaria cirrhosa subsp. roylei (Hook.) Ali Fl. Pakistan 215: 10 (2007)
Fritillaria polyphylla Fortune Journey China : 366 (1852)
Fritillaria cirrhosa var. jilongensis Y.K.Yang & Gesang Acta Bot. Boreal.-Occid. Sin. 5(1): 34. 1985

Common names Top

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Language Common/alternative name
Spanish fritillaria roylei
Czech řebčík úponkovitý
Persian لاله واژگون سیرهوزا
Malayalam കാകോളി
Burmese မချစ်ဥ
Chinese 贝母
Chinese 香雪兰
Chinese 川贝母(卷叶贝母)
Chinese 罗氏贝母
Chinese 卷叶贝母
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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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 North-central
      • China South-central
      • Qinghai
      • Tibet
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000767733
UNII LEP1GUV1GB
Tropicos 18404308
KEW urn:lsid:ipni.org:names:535094-1
The Plant List kew-306560
Open Tree Of Life 935705
NCBI Taxonomy 108544
IUCN Red List 215323195
IPNI 535094-1
iNaturalist 565475
GBIF 5300358
Freebase /m/0k8fhht
EOL 1088491
USDA GRIN 402589
Wikipedia Fritillaria_cirrhosa
CMAUP NPO1279

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
The influence of climate change on the future distribution of two Thymus species in Iran: MaxEnt model-based prediction Hosseini N, Ghorbanpour M, Mostafavi H BMC Plant Biol 11-Apr-2024
PMCID:PMC11007882
doi:10.1186/s12870-024-04965-1
PMID:38605338
The traditional uses, pharmacology, and phytochemistry of Peucedanum praeruptorum Dunn Wang Q, Sun Q, Huang Q, Qin L, Zhu B Front Pharmacol 03-Apr-2024
PMCID:PMC11021687
doi:10.3389/fphar.2024.1352657
PMID:38633612
Traditional Tibetan medicine: therapeutic potential in lung diseases Li C, Li Y, Huang X, Li S, Sangji K, Gu R Front Pharmacol 18-Mar-2024
PMCID:PMC10986185
doi:10.3389/fphar.2024.1365911
PMID:38567353
Advantages of Chinese herbal medicine in treating rheumatoid arthritis: a focus on its anti-inflammatory and anti-oxidative effects Wang X, Kong Y, Li Z Front Med (Lausanne) 07-Mar-2024
PMCID:PMC10954842
doi:10.3389/fmed.2024.1371461
PMID:38515982
Determination of ITS1 haplotypes of Fritillariae Cirrhosae Bulbus by amplicon sequencing Wu HY, Wong KL, Law ST, Nong W, Chan KT, Hui JH, Lin G, Chan WH, Shaw PC Chin Med 28-Feb-2024
PMCID:PMC10900738
doi:10.1186/s13020-024-00911-3
PMID:38419104
Non-Volatile Component and Antioxidant Activity: A Comparative Analysis between Litsea cubeba Branches and Leaves Dai W, Li B, Xiong Y, Dai L, Tian Y, Zhang L, Wang Q, Qian G Molecules 08-Feb-2024
PMCID:PMC10892920
doi:10.3390/molecules29040788
PMID:38398540
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
Study on medicinal food plants in the Gaoligongshan Biosphere Reserve, the richest biocultural diversity center in China Cheng Z, Lin S, Wu Z, Lin C, Zhang Q, Xu C, Li J, Long C J Ethnobiol Ethnomed 15-Jan-2024
PMCID:PMC10790445
doi:10.1186/s13002-023-00638-9
PMID:38225656
Total alkaloids of bulbus of Fritillaria cirrhosa alleviate bleomycin-induced inflammation and pulmonary fibrosis in rats by inhibiting TGF-β and NF-κB signaling pathway Pai M, Er-bu A, Wu Y, Ming TW, Gaun TK, Ye B Food Nutr Res 29-Dec-2023
PMCID:PMC10770707
doi:10.29219/fnr.v67.10292
PMID:38187805
Tibetan medicine Bang Jian: a comprehensive review on botanical characterization, traditional use, phytochemistry, and pharmacology Li Y, Zhang J, Fan JY, Zhong SH, Gu R Front Pharmacol 14-Dec-2023
PMCID:PMC10757618
doi:10.3389/fphar.2023.1295789
PMID:38161696
The local medicinal plant knowledge in Kashmir Western Himalaya: a way to foster ecological transition via community-centred health seeking strategies Manzoor M, Ahmad M, Zafar M, Gillani SW, Shaheen H, Pieroni A, Al-Ghamdi AA, Elshikh MS, Saqib S, Makhkamov T, Khaydarov K J Ethnobiol Ethnomed 30-Nov-2023
PMCID:PMC10688143
doi:10.1186/s13002-023-00631-2
PMID:38037066
Effects of climate warming and human activities on the distribution patterns of Fritillaria unibracteata in eastern Qinghai-Tibetan Plateau Zhao D, Wang J, Dai W, Ye K, Chen J, Lai Q, Li H, Zhong B, Yu X Sci Rep 22-Sep-2023
PMCID:PMC10516939
doi:10.1038/s41598-023-42988-0
PMID:37737302
Progress in application of terahertz time-domain spectroscopy for pharmaceutical analyses Huang S, Deng H, Wei X, Zhang J Front Bioeng Biotechnol 18-Jul-2023
PMCID:PMC10393043
doi:10.3389/fbioe.2023.1219042
PMID:37533693
Natural products modulate cell apoptosis: a promising way for treating endometrial cancer Zhou X, Zeng Y, Zheng R, Wang Y, Li T, Song S, Zhang S, Huang J, Ren Y Front Pharmacol 08-Jun-2023
PMCID:PMC10285317
doi:10.3389/fphar.2023.1209412
PMID:37361222
The Cryopreservation of Medicinal and Ornamental Geophytes: Application and Challenges El Merzougui S, Benelli C, El Boullani R, Serghini MA Plants (Basel) 29-May-2023
PMCID:PMC10255897
doi:10.3390/plants12112143
PMID:37299120

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 / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
4-Hydroxybenzoic acid 135 Click to see C1=CC(=CC=C1C(=O)O)O 138.12 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzyl alcohols
4-Hydroxybenzyl alcohol 125 Click to see C1=CC(=CC=C1CO)O 124.14 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dotriacontane 11008 Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC 450.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acid esters / Fatty acid methyl esters
methyl (114C)hexadecanoate 10378565 Click to see CCCCCCCCCCCCCCCC(=O)OC 272.44 unknown via CMAUP database
Methyl behenate 13584 Click to see CCCCCCCCCCCCCCCCCCCCCC(=O)OC 354.60 unknown via CMAUP database
Methyl tetradecanoate 31284 Click to see CCCCCCCCCCCCCC(=O)OC 242.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Rosavin 9823887 Click to see C1C(C(C(C(O1)OCC2C(C(C(C(O2)OCC=CC3=CC=CC=C3)O)O)O)O)O)O 428.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
L-Menthyl acetate 220674 Click to see CC1CCC(C(C1)OC(=O)C)C(C)C 198.30 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Diterpene glycosides
Bacosterol3-O-beta-D-glucopyranoside 101389367 Click to see CCC(CCC(C)C1CC=CC2CCC3CC(CCC3(C2=CCC1C)C)OC4C(C(C(C(O4)CO)O)O)O)C(C)C 576.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Bacopaside I 21599442 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)COS(=O)(=O)O)O)O)O)OC9C(C(C(O9)CO)O)O)C)C)C 979.10 unknown via CMAUP database
bacopaside II 9876264 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(O9)CO)O)O)C)C)C 929.10 unknown via CMAUP database
Bacopaside III 15922618 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)COS(=O)(=O)O)O)O)O)O)C)C)C 847.00 unknown via CMAUP database
Bacopaside IV 10865594 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)(C)O)C 767.00 unknown via CMAUP database
Bacopaside N1 11949626 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)(C)O)C 797.00 unknown via CMAUP database
Bacopaside N2 21574494 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C 797.00 unknown via CMAUP database
Bacopaside V 11072737 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)O)C)C)C 767.00 unknown via CMAUP database
Bacopaside X 10629555 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(O9)CO)O)O)C)(C)O)C 899.10 unknown via CMAUP database
Bacoside A3 91827005 Click to see CC(=CC1CC(C2C3CCC4C5(CCC(C(C5CCC4(C36CC2(O1)OC6)C)(C)C)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(O9)CO)O)O)C)(C)O)C 929.10 unknown via CMAUP database
Bacosine 71312547 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C(=O)O)C)(C)C)O)C)C 456.70 unknown via CMAUP database
Bascopasaponin C 21599443 Click to see CC(=CC1COC23CC4(CO2)C(C3C1(C)O)CCC5C4(CCC6C5(CCC(C6(C)C)OC7C(C(C(CO7)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(O9)CO)O)O)C)C)C 899.10 unknown via CMAUP database
Betulin 72326 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)CO 442.70 unknown via CMAUP database
Lupeol 259846 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2)C)C)(C)C)O)C)C 426.70 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 / Cucurbitacins
[(E,6R)-6-hydroxy-2-methyl-5-oxo-6-[(7S,8S,9S,10R,13R,14S,16R,17R)-2,7,16-trihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]hept-3-en-2-yl] acetate 16216753 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2C(C=C4C3C=C(C(=O)C4(C)C)O)O)C)C)C)O)O 572.70 unknown via CMAUP database
Cucurbitacin E 5281319 Click to see CC(=O)OC(C)(C)C=CC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3C=C(C(=O)C4(C)C)O)C)C)C)O)O 556.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
24-Methyldesmosterol 193567 Click to see CC(CCC(=C(C)C)C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C 398.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / 22,26-epiminocholestanes
(3S,10R,13S)-3-hydroxy-10,13-dimethyl-17-[1-(6-methyl-7-oxa-2-azabicyclo[2.2.1]hept-2-en-3-yl)ethyl]-1,2,3,4,5,7,8,9,11,12,14,15,16,17-tetradecahydrocyclopenta[a]phenanthren-6-one 5318842 Click to see CC1CC2C(=NC1O2)C(C)C3CCC4C3(CCC5C4CC(=O)C6C5(CCC(C6)O)C)C 427.60 unknown via CMAUP database
(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 https://doi.org/10.1021/JS960211V
(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/10.1016/S0021-9673(99)00867-5
(2R,6R,10R,15R,17R,23R)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-14,17,20-triol 5318840 Click to see CC1CCC2C(C3CCC4(C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)O)C 431.70 unknown via CMAUP database
(2R,6R,10R,18R,20S,23S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacos-15(24)-ene-8,20,25-triol 5318843 Click to see CC1CC(C2C(C3CCC4C(C3CN2C1)C(C5=C4CCC6C5(CCC(C6)O)C)O)C)O 429.60 unknown via CMAUP database
(2S,6R,10R,23S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacos-15(24)-ene-17,20-diol 5318841 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5=C4CC(C6C5(CCC(C6)O)C)O)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/10.1021/JS960211V
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/10.1107/S0108270100014499
https://doi.org/10.1021/JA01238A048
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/10.1021/JA01298A067
Imperialine 442977 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 429.60 unknown https://doi.org/10.1006/ABIO.2000.4756
https://doi.org/10.1107/S0108270100014499
Isoverticine 21573744 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown via CMAUP database
Korseveramine 101316984 Click to see CC1CCC2C(C3CCC4(C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)O)C 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/S0021-9673(00)00049-2
https://doi.org/10.1016/S0021-9673(00)01083-9
https://doi.org/10.1021/JA01298A067
https://doi.org/10.1021/JS960211V
Peiminine 167691 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 429.60 unknown https://doi.org/10.1021/JA01238A048
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
> 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
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/10.1002/JPS.3030360707
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/10.1002/JPS.3030360707
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
(3beta)-Solanid-5-en-3-ol 25244262 Click to see CC1CCC2C(C3C([NH+]2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C 398.60 unknown via CMAUP database
> 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
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
Solanine 262500 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C 868.10 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
Stigmasterol glucoside 6602508 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
> 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
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Cyclic alcohols and derivatives
Bacosterol 101389368 Click to see CCC(CCC(C)C1CC=CC2CCC3CC(CCC3(C2=CCC1C)C)O)C(C)C 414.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzofurans
Loliolide 100332 Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C 196.24 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
> Organoheterocyclic compounds / Piperidines
(1R,6R,14S,15S,17R,18S,20S,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacos-2(11)-ene-17,20-diol 101014741 Click to see CC1CCC2C(C3=C(CN2C1)C4CC5C(C4CC3)CC(C6C5(CCC(C6)O)C)O)C 413.60 unknown https://doi.org/10.1016/S0021-9673(00)00049-2
Cev-13(17)-ene-3,6-diol 494801 Click to see CC1CCC2C(C3=C(CN2C1)C4CC5C(C4CC3)CC(C6C5(CCC(C6)O)C)O)C 413.60 unknown https://doi.org/10.1016/S0021-9673(00)00049-2
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
2-Propenoic acid, 3-(3,4-dimethoxyphenyl)- 16848 Click to see COC1=C(C=C(C=C1)C=CC(=O)O)OC 208.21 unknown via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Hydroxycinnamic acid glycosides
Ferulic acid glucoside 53978589 Click to see COC1=C(C=CC(=C1)C=CC(=O)OC2C(C(C(C(O2)CO)O)O)O)O 356.32 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(3R)-2-(2,4-dihydroxyphenyl)-3,5,7-trihydroxy-6-(3-hydroxy-3-methylbutyl)-8-(5-methyl-2-prop-1-en-2-ylhex-4-enyl)-2,3-dihydrochromen-4-one 5318844 Click to see CC(=CCC(CC1=C2C(=C(C(=C1O)CCC(C)(C)O)O)C(=O)C(C(O2)C3=C(C=C(C=C3)O)O)O)C(=C)C)C 526.60 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
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
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-7-O-glycosides
Luteolin 7-O-glucoside 5280637 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O)O 448.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxy-dihydrochalcones
1-[2,4,6-Trihydroxy-3-(3-methyl-2-butenyl)phenyl]-3-(4-hydroxyphenyl)-1-propanone 19744872 Click to see CC(=CCC1=C(C(=C(C=C1O)O)C(=O)CCC2=CC=C(C=C2)O)O)C 342.40 unknown via CMAUP database

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