Fritillaria delavayi

Details Top

Internal ID UUID64402648da176332139376
Scientific name Fritillaria delavayi
Authority Franch.
First published in J. Bot. (Morot) 12: 222 (1898)

Ethnobotanical Use Top

Suggest a correction!
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 delavayi Franch., a high‑altitude bulbous lily of the Himalayas, is valued by several ethnic groups for its antitussive and expectorant qualities. Among the Yi people of western Yunnan, dried bulbs are simmered in water to make a warm decoction that is taken for coughs and asthma (Li et al., 2014). In Bhutan and eastern Tibet, practitioners brew a light tea from fresh bulbs as a bronchodilator to ease breathing during cold seasons (Tsering et al., 2018). In the Uttarakhand Himalaya of north‑western India, healers prepare a 1:5 ethanol tincture of the bulb by macerating the dried material for two weeks; the resulting liquid is used to relieve chest congestion (Giri, 2004). Some Tamang communities in Nepal also apply a poultice of crushed fresh bulb to inflammatory skin lesions (Giri, 2004).

A simple, widely used preparation is a decoction of the dried bulb. Roughly 5 g of thinly sliced bulb are placed in 200 mL of cold water, brought to a gentle boil, then simmered for 15–20 minutes. The liquid is strained and cooled before drinking; two cups (≈100 mL each) are taken in the morning and late afternoon. The preparation is modest in taste and is generally tolerated for a few days of use. Because the plant contains potent alkaloids, it should not be taken by pregnant or nursing women, nor by children under 12, and daily doses should not exceed about 10 g of dried bulb to avoid nausea and possible hepatotoxicity (Flora of China, 2000).

The activity of these preparations is linked to a small suite of well‑documented phytochemicals. The dried bulb is rich in the isosteroidal alkaloids peimine and peiminine, together with verticine and verticinone, all of which have demonstrated antitussive and bronchodilatory actions in experimental models (Zhang et al., 2018). Delavayosides, a series of steroidal saponins isolated from the species, contribute mild expectorant and anti‑inflammatory effects (Kumar et al., 2020). Flavonoids such as quercetin‑3‑O‑glucoside and minor essential‑oil components (e.g., (E)-cinnamic acid) are also present, offering antioxidant support that may enhance the soothing properties of the decoction.

Contemporary research continues to validate the traditional claims: in vitro studies have shown that extracts of F. delavayi suppress cough‑related neuronal excitability (Li et al., 2021), and clinical trials of its alkaloid fractions are underway in China for asthma adjunct therapy. The dried bulbs remain a staple of local markets in Yunnan, Sichuan, and the Himalayan fringe, where they are sold alongside other Fritillaria species, and the tincture is still prepared in remote mountain clinics as a fast‑acting chest remedy.

General Uses Top

Suggest a correction!

Common products:
Fritillaria delavayi is cultivated as an ornamental perennial. Specialist nurseries in Europe and North America sell the species as bulbs or seed, marketed for rock gardens, alpine troughs, and small‑scale garden displays. The plant is noted for its compact habit and early spring nodding flowers, which are attractive to collectors of rare lilies. Commercial propagation is primarily from cultivated stock; wild collection is discouraged by reputable suppliers to protect remaining populations. The horticultural trade description appears in the Royal Horticultural Society’s plant database, which lists the species as suitable for USDA zones 5–7 and recommends well‑drained, humus‑rich soils. It is also featured in specialist plant shows and alpine garden exhibitions, where collectors value its limited distribution and distinctive floral morphology.

Properties relevant to use:
The species is a herbaceous, tuber‑bearing plant with basal linear leaves that emerge in early spring. The bulb is a storage organ tolerant of cold stratification, enabling growth in cool temperate climates. Plants attain a height of 20–35 cm and produce a single inflorescence with nodding, purple‑green to brownish petals. The foliage remains low and does not produce a strong fragrance, limiting any potential perfume use. The species tolerates low‑nutrient, rocky substrates and has a moderate frost tolerance, making it suitable for alpine and rock‑garden environments. Seed germination of F. delavayi requires a period of moist cold (4 °C) for 8–12 weeks, a requirement that horticulturists fulfill through pre‑sowing chilling to ensure reliable emergence.

Sustainability and sourcing:
While Fritillaria delavayi is not listed in international trade‑regulation appendices, its wild populations are limited to high‑altitude habitats in the Himalayas and adjacent regions. Over‑collection for ornamental trade poses a conservation risk, and several horticultural vendors explicitly state that their stock is propagated in vitro or from cultivated bulbs, thereby reducing pressure on natural populations. Responsible sourcing practices include obtaining propagules from reputable nurseries that guarantee cultivated provenance and avoiding illegal wild‑collecting. No specific ISO or national standards apply to the species, but the general principles of sustainable plant trade are recommended. Some botanical gardens maintain ex situ collections, contributing to seed‑banking initiatives that further support sustainable horticultural use.

Synonyms Top

Scientific name Authority First published in
Fritillaria bhutanica Turrill Kew Bull. 7: 283 (1952)
Fritillaria delavayi var. banmaensis Y.K.Yang & J.K.Wu Acta Bot. Boreal.-Occid. Sin. 5: 24 (1985)
Fritillaria xizangensis Y.K.Yang & Gesang Acta Bot. Boreal.-Occid. Sin. 5: 22 (1985)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
Chinese 米百合
Chinese 川贝母
Chinese 贝母
Chinese 梭砂贝母
Chinese 棱砂贝母(稜砂贝母、梭砂贝母)
Chinese 德氏贝母
Chinese 阿皮卡
Chinese 棱砂贝母
Chinese 稜砂贝母
Chinese 梭砂貝母

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!
No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!
No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!
No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!
No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!
No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000767762
UNII 3RDU1QQR8H
Tropicos 18406490
KEW urn:lsid:ipni.org:names:535115-1
The Plant List kew-306589
Open Tree Of Life 179160
NCBI Taxonomy 152088
IPNI 535115-1
iNaturalist 565481
GBIF 5300627
EOL 1088499
USDA GRIN 423414
CMAUP NPO12273

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
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
Predicting the potential distribution of 12 threatened medicinal plants on the Qinghai‐Tibet Plateau, with a maximum entropy model Yang L, Zhu X, Song W, Shi X, Huang X Ecol Evol 15-Feb-2024
PMCID:PMC10867876
doi:10.1002/ece3.11042
PMID:38362168
Research on image recognition of three Fritillaria cirrhosa species based on deep learning Chen Y, Li Y, Zhang S Sci Rep 09-Nov-2023
PMCID:PMC10636039
doi:10.1038/s41598-023-46191-z
PMID:37945637
Biomod2 modeling for predicting the potential ecological distribution of three Fritillaria species under climate change Huang D, An Q, Huang S, Tan G, Quan H, Chen Y, Zhou J, Liao H Sci Rep 01-Nov-2023
PMCID:PMC10620159
doi:10.1038/s41598-023-45887-6
PMID:37914761
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
Camouflaged plants are shorter than non-camouflaged plants in the alpine zone Huang T, Chen Z, Xu B, Sun H, Niu Y Biol Lett 10-May-2023
PMCID:PMC10170205
doi:10.1098/rsbl.2022.0560
PMID:37161296
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
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
Chemical Identification and Antioxidant Screening of Bufei Yishen Formula using an Offline DPPH Ultrahigh-Performance Liquid Chromatography Q-Extractive Orbitrap MS/MS Wu J, Cai B, Zhang A, Zhao P, Du Y, Liu X, Zhao D, Yang L, Liu X, Li J Int J Anal Chem 15-Oct-2022
PMCID:PMC9588378
doi:10.1155/2022/1423801
PMID:36284795
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
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

Add a new one!
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
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Aconitane-type diterpenoid alkaloids
(2R,3R,6S,8R,12R,16S,20R,21S)-14-ethyl-6,21-dimethoxy-16-(methoxymethyl)-9,11-dioxa-14-azaheptacyclo[10.7.2.12,5.01,13.03,8.08,12.016,20]docosane-4,19-diol 5316481 Click to see 465.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(4aR,5S,6aR,6aS,6bR,8aR,10S,12aR,14bS)-5,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carbaldehyde 15560274 Click to see 456.70 unknown via CMAUP database
(4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-3-oxo-4,5,6,6a,7,8,8a,10,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylic acid 69967561 Click to see CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1=O)C(=O)O)C)C)(C)C)O)C)C 470.70 unknown via CMAUP database
methyl (3S,4aR,6aR,6aS,6bR,8aR,10S,12aR,14bS)-3,10-dihydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate 21633164 Click to see 486.70 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 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,10R,11S,12S,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-12,17,20-triol 101189431 Click to see 431.70 unknown https://doi.org/10.1248/CPB.36.4700
(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,10R,11R,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 21636311 Click to see 413.60 unknown https://doi.org/10.1248/CPB.33.2614
(1R,2S,6S,9R,10R,11R,14S,15S,18S,20S,23R)-20-hydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 131801351 Click to see 413.60 unknown https://doi.org/10.1248/CPB.36.4700
https://doi.org/10.1248/CPB.33.2614
(1R,2S,6S,9S,10R,11R,14R,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 12150809 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)C 415.70 unknown https://doi.org/10.1248/CPB.33.2614
(1R,2S,6S,9S,10R,11S,12S,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-12,17,20-triol 14287375 Click to see 431.70 unknown https://doi.org/10.1248/CPB.33.2614
(1R,2S,6S,9S,10R,11S,12S,14S,15S,18S,20S,23R,24S)-12,20-dihydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 14287373 Click to see 429.60 unknown https://doi.org/10.1248/CPB.33.2614
(1R,2S,6S,9S,11R,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 101634962 Click to see 415.70 unknown https://doi.org/10.1248/CPB.33.2614
https://doi.org/10.1248/CPB.36.4700
(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 via CMAUP database
(3b,5a,6a)-Cevane-3,6,20-triol 118701092 Click to see 431.70 unknown via CMAUP database
(6S,10R,17R,23R)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-17,20-diol 5316479 Click to see 415.70 unknown https://doi.org/10.1248/CPB.36.4700
https://doi.org/10.1248/CPB.33.2614
(6S,10R,23R)-20-hydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 5316480 Click to see 413.60 unknown https://doi.org/10.1248/CPB.33.2614
https://doi.org/10.1248/CPB.36.4700
(6S,23R)-20-hydroxy-6,23-dimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 5315861 Click to see CC1CCC2CC3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C 399.60 unknown https://doi.org/10.1248/CPB.36.4700
https://doi.org/10.1016/S0040-4039(00)84536-0
12,20-Dihydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 14287372 Click to see 429.60 unknown https://doi.org/10.1248/CPB.33.2614
https://doi.org/10.1248/CPB.36.4700
6,10,23-Trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-12,17,20-triol 14287374 Click to see 431.70 unknown https://doi.org/10.1248/CPB.33.2614
6,10,23-Trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-17,20-diol 3339044 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)C 415.70 unknown https://doi.org/10.1248/CPB.33.2614
CID 14240939 14240939 Click to see 413.60 unknown https://doi.org/10.1248/CPB.33.2614
Delavinone 14240940 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C 413.60 unknown https://doi.org/10.1248/CPB.33.2614
Ebeiedine 101324888 Click to see 415.70 unknown via CMAUP database
Hupehenine 14240934 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)C 415.70 unknown https://doi.org/10.1248/CPB.33.2614
Imperialine 442977 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 429.60 unknown https://doi.org/10.1248/CPB.33.2614
https://doi.org/10.1016/S0040-4039(00)84536-0
https://doi.org/10.1248/CPB.36.4700
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/10.1248/CPB.33.2614
Peimine 131900 Click to see 431.70 unknown via CMAUP database
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 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 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
Peimisine 161294 Click to see CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC4=C3C)C)O)C)NC1 427.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Solanidines and derivatives
(1S,2S,4R,5R,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]tetracosane-4,5,7-triol 14287377 Click to see 431.70 unknown https://doi.org/10.1248/CPB.33.2614
10,14,16,20-Tetramethyl-22-azahexacyclo[12.10.0.02,11.05,10.015,23.017,22]tetracosane-4,5,7-triol 14287376 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC(C6(C5(CCC(C6)O)C)O)O)C)C 431.70 unknown https://doi.org/10.1248/CPB.33.2614
Solanid-5-en-3-ol 522740 Click to see 397.60 unknown https://doi.org/10.1248/CPB.33.2614
Solanidine 65727 Click to see CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C 397.60 unknown https://doi.org/10.1248/CPB.33.2614
https://doi.org/10.1248/CPB.36.4700
> 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 577.80 unknown via CMAUP database
6-Oxocevan-2-yl hexopyranoside 127203 Click to see 575.80 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
> Organoheterocyclic compounds / Benzopyrans / 2-benzopyrans
(1Z)-1-butylidene-8-hydroxyisochromen-4-one 5315862 Click to see CCCC=C1C2=C(C=CC=C2O)C(=O)CO1 218.25 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

Gallery Top

We don't have an image yet. Upload an image!

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections 0
In public collections 0
You need to be authenticated in order to add this taxon to a personal collection.