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
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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 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 |
Germination/Propagation Top
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No germination or propagation data was added yet.
Distribution (via POWO/KEW) Top
Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
-
Asia-temperate click to expand
-
China
- China South-central
- Qinghai
- Tibet
-
China
-
Asia-tropical click to expand
-
Indian Subcontinent
- East Himalaya
-
Indian Subcontinent
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)!
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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 / 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 |
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