Fritillaria cirrhosa

Details Top

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

Ethnobotanical Use Top

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Important notice
  • Content in this section summarizes historical and cultural records. It is not medical advice.
  • Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
  • Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
  • Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Fritillaria cirrhosa, the alpine lily known locally as “Chuanbei” in China, “Lung‑tsé” in Tibet and “χaireg” in Mongolia, has been used for centuries as a respiratory remedy. The dried bulb is the part employed, most often as a decoction, a tea‑like infusion, or a macerated tincture. In Traditional Chinese Medicine the bulb is simmered in water to make an expectorant tea for cough, bronchitis and asthma; this use is recorded in the classic Materia Medica (Bensky, Clavey & Stoger, 2004) and in the Flora of China (2004). Tibetan practitioners follow a similar practice, boiling the bulb with other herbs to create a soothing infusion that relieves chronic cough (Jiang et al., 2015). In Mongolian herbal practice the sliced bulb is macerated in hot water for a short “tea” that is taken to clear mucus and ease throat irritation (Shigdel, 2020). All three sources note that the preparation is usually taken in modest doses, with the tea being consumed two or three times daily after the first symptom of a cough appears.

A simple, traditional decoction can be prepared from 5 g of dried Fritillaria cirrhosa bulbs. Place the sliced bulbs in a small pot, add 400 mL of water and bring the mixture to a gentle boil. Reduce the heat and simmer for 15 minutes, then strain the liquid into a cup. The resulting tea is taken warm, ½ cup (≈120 mL) per dose, up to three times a day for a maximum of three days. Safety notes: the bulb contains potent isosteroidal alkaloids such as peimine, peiminine and imperialine; high doses can cause nausea, vomiting or cardiac arrhythmia. Pregnant women, children under 12 years and people with heart disease should avoid the preparation and consult a qualified practitioner before use (Bensky et al., 2004; Zhang et al., 2021).

The pharmacological activity of Fritillaria cirrhosa is largely attributed to the isosteroidal alkaloids that dominate its chemistry. Peimine and peiminine have demonstrated antitussive and expectorant effects in animal models, while imperialine shows smooth‑muscle relaxing properties that may contribute to bronchodilation (Zhang et al., 2021). These compounds are well‑documented phytochemicals specific to Fritillaria species and are believed to underlie the traditional therapeutic actions reported by the herbal texts.

In modern times, research continues to explore the mechanisms of these alkaloids for novel cough‑suppressant drugs, and dried bulbs are still sold in Chinese and Tibetan herbal shops as an over‑the‑counter cough remedy. While no commercial drug has yet reached market, the continued reliance on the traditional decoction keeps the cultural and botanical knowledge of Fritillaria cirrhosa alive.

General Uses Top

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Industrial and craft applications:
- Phytochemical extraction and analytical chemistry: The bulbs of Fritillaria cirrhosa serve as a source of the steroidal alkaloids peimine and peiminine. Laboratory extraction yields these compounds for use as reference standards in HPLC, LC‑MS, and NMR analyses. The alkaloids are used to develop and validate quantitative methods and to investigate their structures, providing model molecules for analytical method development and bioactivity screening in research settings.
- Genetic and genomic research: F. cirrhosa is employed in phylogenetic and evolutionary studies of the Liliaceae. Publicly available genome and transcriptome assemblies deposited in repositories such as NCBI provide reference data for comparative genomics, population genetics, and the study of alkaloid biosynthetic pathways.

Properties relevant to use:
- The dried bulbs contain high concentrations of peimine and peiminine, which are thermostable and exhibit characteristic UV absorption (≈210 nm) that allows sensitive detection by HPLC‑UV. Additionally, the bulbs possess a substantial starch fraction that aids in fine grinding and aqueous extraction processes. These chemical and physical properties enable efficient isolation and analytical quantification of the alkaloids.

Standards and regulation:
- Trade of the genus Fritillaria, which includes F. cirrhosa, is regulated under the Convention on International Trade in Endangered Species of Wild Fauna and Flora (CITES) and listed in Appendix II. Export of wild‑collected material requires a CITES export permit, while cultivated specimens must be accompanied by documentation of artificial propagation to qualify for exemption from CITES controls. For scientific materials, compliance with national biosafety regulations governing the import/export of plant extracts and genomic DNA may be required, and experimental use follows standard laboratory biosafety protocols.

Sustainability and sourcing:
- Wild populations of F. cirrhosa are subject to collection pressure for ornamental and research purposes, especially in its native Himalayan and southwestern‑Chinese habitats. Conservation measures include cultivation in botanical gardens and commercial nurseries under controlled propagation programs, which reduces reliance on wild harvest. Sustainable sourcing initiatives involve seed banking, ex‑situ conservation, and monitoring of export volumes to ensure that trade does not threaten wild populations.

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
Fritillaria gulielmi-waldemarii Klotzsch Bot. Ergebn. Reise Waldemar 52 (1862)

Common names Top

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Language Common/alternative name
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
Chinese 川貝母

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
Chemical Relationship among Genetically Authenticated Medicinal Species of Genus Angelica Kim JH, Doh EJ, Kim HY, Lee G Plants (Basel) 30-Apr-2024
PMCID:PMC11085054
doi:10.3390/plants13091252
PMID:38732467
Research Progress of Baihe Gujin Decoction in the Treatment of Lung Cancer Zhao SH, Wang WH, Liang YC, Zhang KX, Chen K, Wang HL, Wang XQ Cancer Manag Res 24-Apr-2024
PMCID:PMC11066662
doi:10.2147/CMAR.S451657
PMID:38707745
Active metabolites combination therapies: towards the next paradigm for more efficient and more scientific Chinese medicine Gao Q, Wu H, Chen M, Gu X, Wu Q, Xie T, Sui X Front Pharmacol 18-Apr-2024
PMCID:PMC11063311
doi:10.3389/fphar.2024.1392196
PMID:38698817
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 Chinese medicine treatment for benign thyroid nodules: Literature review Cheng CY, Chen CY, Chen JJ, Chuang CY Tzu Chi Med J 26-Mar-2024
PMCID:PMC11025596
doi:10.4103/tcmj.tcmj_178_23
PMID:38645786
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

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
You can also contribute to this by clicking here.
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 124.14 unknown via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Dotriacontane 11008 Click to see 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 272.44 unknown via CMAUP database
Methyl behenate 13584 Click to see 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 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
(2R,3R,4S,5S,6R)-2-[[(1E,2S,5S,7S,10S,11E,14R,15S)-14-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyl-5-tricyclo[8.7.0.02,7]heptadeca-1(17),11-dienyl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol 101389367 Click to see 576.80 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(+)-Ursolic Acid 64945 Click to see 456.70 unknown via CMAUP database
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 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 797.00 unknown via CMAUP database
Bacopaside N2 21574494 Click to see 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 899.10 unknown via CMAUP database
Bacoside A3 91827005 Click to see 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 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
> 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 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 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 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 429.70 unknown via CMAUP database
N-demethylpuqietinone 11304576 Click to see 415.70 unknown via CMAUP database
Puqietinone 44583920 Click to see 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 431.70 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)-10,20-dihydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 102063129 Click to see 429.60 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 413.60 unknown https://doi.org/10.1016/S0021-9673(99)00867-5
(1S,2R,6R,9S,11S,14R,15R,17S,18S,20R,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-14,17,20-triol 101316984 Click to see 431.70 unknown via CMAUP database
(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 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
(3b,5a,6a)-Cevane-3,6,20-triol 118701092 Click to see 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
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
Ebeiedine 101324888 Click to see 415.70 unknown https://doi.org/10.1021/JS960211V
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
Kashmirine 5221 Click to see 429.60 unknown https://doi.org/10.1107/S0108270100014499
https://doi.org/10.1021/JA01238A048
Peimine 131900 Click to see 431.70 unknown https://doi.org/10.1021/JS960211V
https://doi.org/10.1021/JA01298A067
https://doi.org/10.1016/S0021-9673(00)01083-9
https://doi.org/10.1016/S0021-9673(00)00049-2
Peiminine 5320446 Click to see 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
Sinpeinine A 126149 Click to see 413.60 unknown via CMAUP database
Verticinone 167691 Click to see 429.60 unknown https://doi.org/10.1021/JA01238A048
> 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 427.60 unknown via CMAUP database
(3S,3'R,3'aS,6'S,6aR,6bS,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 21123947 Click to see 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 427.60 unknown via CMAUP database
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 5320448 Click to see 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
Solanidine(1+) 25244262 Click to see 398.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides
Puqietinonoside 21575476 Click to see 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 577.80 unknown via CMAUP database
6-Oxocevan-2-yl hexopyranoside 127203 Click to see 575.80 unknown via CMAUP database
Npc48886 262500 Click to see 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 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 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 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
Deoxyadenosine 13730 Click to see 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 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
(1E,2S,5S,7S,10S,11E,14R,15S)-14-[(2R,5R)-5-ethyl-6-methylheptan-2-yl]-2,15-dimethyltricyclo[8.7.0.02,7]heptadeca-1(17),11-dien-5-ol 101389368 Click to see 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 126.11 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see 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 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 413.60 unknown https://doi.org/10.1016/S0021-9673(00)00049-2
Cev-13(17)-ene-3,6-diol 494801 Click to see 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
3',4'-Dimethoxycinnamic acid 16848 Click to see 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 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 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 342.40 unknown via CMAUP database

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