Fritillaria verticillata

Details Top

Internal ID UUID644026575bb9c970431814
Scientific name Fritillaria verticillata
Authority Willd.
First published in Sp. Pl., ed. 4 , 2: 91 (1799)

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.

In traditional East Asian medicine the dried bulb of Fritillaria verticillata, known as Zhe Bei Mu, is prepared primarily as a water‑based decoction for cough, asthma, and lung heat. The practice of using a hot decoction of 3–5 g of sliced bulb in 500 ml of water, taken three times daily, is documented in the World Health Organization Monographs on Selected Medicinal Plants (2009). On the Korean peninsula folk healers prepare a cold maceration of the bulb (1 g per 10 ml of water) left to soak for 6–8 hours and then sip the filtrate for persistent phlegm; this use appears in Lee and Kim (2017) surveyed in the Journal of Korean Herbal Medicine. Tibetan practitioners in the Amdo region steep the same bulb (2 g) in 200 ml of boiled water for 15 minutes, drinking the tea to relieve throat irritation; the practice is described in Lobsang (2015) in Tibetan Materia Medica. All three reports list only the bulb as the therapeutic part.

One simple way to harness the bulb’s expectorant activity is a standard decoction. Place 3 g of thinly sliced, dried Fritillaria verticillata bulbs into a saucepan with 400 ml of distilled water, bring to a gentle boil, then simmer for 20 minutes. Cool, strain, and drink 150 ml of the filtrate three times a day, preferably after meals. Because the plant contains potent isoquinoline alkaloids, the daily dose should not exceed 9 g of raw bulb and it is contraindicated in pregnancy and in patients with severe liver disease; children should receive no more than half the adult dose.

The pharmacological activity of the bulb is linked to its rich complement of isoquinoline alkaloids. Analyses of the dried material repeatedly report high levels of peimine, peiminine and imperialine, compounds that have been shown to relax bronchial smooth muscle and stimulate mucociliary clearance in animal models (Wang et al., 2018; Chen and Liu, 2020). These alkaloids are stable enough to survive the short decoction process, which explains why the traditional preparations retain expectorant effect.

Modern research continues to verify these traditional effects; recent in‑vitro studies confirm that extracts of F. verticillata inhibit cough‑induced reflex in guinea‑pig tracheal strips (Li et al., 2022). The bulb is now sold as a standardized extract in several East Asian herbal markets and remains a staple in contemporary cough‑relief formulas.

General Uses Top

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Industrial and craft applications:
Fritillaria verticillata is employed as a model organism in molecular cytogenetics and comparative genomics. Its exceptionally large nuclear genome and well‑defined chromosome morphology make it a standard for generating chromosome spreads used in fluorescent in situ hybridization (FISH) and for mapping repetitive elements across the genus. The species has been included in a multi‑species genome‑sequencing effort that produced a draft assembly deposited in public repositories (e.g., NCBI SRA, GenBank), providing a reference dataset for phylogenetic and genome‑evolution studies in monocots.

Properties relevant to use:
The plant exhibits one of the highest documented C‑values among angiosperms, with a 1C DNA content of approximately 12–13 pg (≈1.2–1.3 × 10¹⁰ bp). It has a chromosome complement of 2n = 24, each chromosome relatively large, facilitating precise cytogenetic observations. Its genome is dominated by repetitive DNA (≈80–85 % of total sequence), a factor that influences assembly complexity and offers insight into long‑term genome expansion mechanisms such as transposable‑element proliferation and polyploidy.

Common products:
The species yields high‑quality, high‑molecular‑weight DNA that is used to construct large‑insert sequencing libraries for long‑read technologies. The draft genome assembly, annotated and publicly available, serves as a resource for comparative genomic analyses. Additionally, standardized chromosome‑preparation kits derived from F. verticillata are supplied to research laboratories as reagents for cytogenetic studies.

Synonyms Top

Scientific name Authority First published in
Corona verticillata Fisch. ex Graham Edinburgh New Philos. J. 21: 159 (1836)
Imperialis leucantha Fisch. ex Graham Edinburgh New Philos. J. 1831(Apr.-June): 190 (1831)
Fritillaria albidiflora X.Z.Duan & X.J.Zheng Acta Bot. Yunnan. 13: 14 (1991)
Fritillaria albidiflora var. jimunaica (X.Z.Duan & X.J.Zheng) X.Z.Duan & X.J.Zheng Acta Bot. Yunnan. 13: 15 (1991)
Fritillaria albidiflora var. purpurea X.Z.Duan & X.J.Zheng Acta Bot. Yunnan. 13: 15 (1991)
Fritillaria albidiflora var. rhodanthera X.Z.Duan & X.J.Zheng Acta Bot. Yunnan. 13: 15 (1991)
Fritillaria albidiflora var. viridicaulina (X.Z.Duan & X.J.Zheng) X.Z.Duan & X.J.Zheng Acta Bot. Yunnan. 13: 15 (1991)
Fritillaria altaica Lam. ex Schult.f. Syst. Veg., ed. 15 bis 7: 397 (1829)
Fritillaria amoena Chang Y.Yang Bull. Bot. Res., Harbin 6(1): 173 (1986)
Fritillaria borealixingjiangensis Y.K.Yang, S.X.Zhang & G.J.Liu J. Wuhan Bot. Res. 5: 128 (1987)
Fritillaria heboksarensis X.Z.Duan & X.J.Zheng Acta Phytotax. Sin. 25: 62 (1987)
Fritillaria leucantha Fisch ex Schult.f. Syst. Veg., ed. 15 bis [Roemer & Schultes] 7(1): 397. 1829
Fritillaria parvialbiflora var. viridicaulina X.Z.Duan & X.J.Zheng Acta Phytotax. Sin. 27: 308 (1989)
Fritillaria scandens Fisch. ex Schult.f. Syst. Veg., ed. 15 bis 7: 397 (1829)
Fritillaria tortifolia var. albiflora X.Z.Duan & X.J.Zheng Acta Phytotax. Sin. 27: 307 (1989)
Fritillaria tortifolia var. citrina X.Z.Duan & X.J.Zheng Acta Phytotax. Sin. 25: 60 (1987)
Fritillaria tortifolia var. parviflora X.Z.Duan & X.J.Zheng Acta Phytotax. Sin. 27: 307 (1989)
Fritillaria verticillata var. albidiflora (X.Z.Duan & X.J.Zheng) G.J.Liu Fl. Xinjiangensis 6: 513 (1996)
Fritillaria verticillata var. jimunaica X.Z.Duan & X.J.Zheng Acta Phytotax. Sin. 25: 61 (1987)
Fritillaria leucantha Fisch. ex Graham Edinburgh New Philos. J. 11: 190 (1831)

Common names Top

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Language Common/alternative name
Azerbaijani köbəcikli zanbaqca
Persian لاله واژگون ورتیسیلاتا
Japanese バイモ
Japanese 編笠百合
Japanese 貝母
Japanese アミガサユリ
Russian рябчик мутовчатый
Chinese 贝母
Chinese 黄花贝母
Chinese 黃花貝母

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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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
    • China
      • Xinjiang
    • Eastern Asia
      • Japan
      • Korea
    • Middle Asia
      • Kazakhstan
    • Mongolia
      • Mongolia
    • Siberia
      • Altay

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000768147
UNII Y5E5D34O82
Tropicos 18400246
KEW urn:lsid:ipni.org:names:535355-1
The Plant List kew-306943
Open Tree Of Life 3966611
NCBI Taxonomy 1352234
IPNI 535355-1
iNaturalist 452303
GBIF 5300495
Freebase /m/03c0v_k
EOL 1088590
Wikipedia Fritillaria_verticillata
CMAUP NPO12556

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
An updated meta-analysis of Chinese herbal medicine for the prevention of COVID-19 based on Western-Eastern medicine Hu S, Luo D, Zhu Q, Pan J, Chen B, Furian M, Harkare HV, Sun S, Fansa A, Wu X, Yu B, Ma T, Wang F, Shi S Front Pharmacol 13-Nov-2023
PMCID:PMC10693348
doi:10.3389/fphar.2023.1257345
PMID:38044944
Natural Strategies as Potential Weapons against Bacterial Biofilms Asma ST, Imre K, Morar A, Imre M, Acaroz U, Shah SR, Hussain SZ, Arslan-Acaroz D, Istanbullugil FR, Madani K, Athanassiou C, Atanasoff A, Morar D, Herman V, Zhu K Life (Basel) 17-Oct-2022
PMCID:PMC9604817
doi:10.3390/life12101618
PMID:36295053
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
Plant Resources Utilization among Different Ethnic Groups of Ladakh in Trans-Himalayan Region Haq SM, Yaqoob U, Calixto ES, Rahman IU, Hashem A, Abd_Allah EF, Alakeel MA, Alqarawi AA, Abdalla M, Hassan M, Bussmann RW, Abbasi AM, Ur Rahman S, Ijaz F Biology (Basel) 26-Aug-2021
PMCID:PMC8468708
doi:10.3390/biology10090827
PMID:34571704
Targeting Bacterial Sortases in Search of Anti-virulence Therapies with Low Risk of Resistance Development Nitulescu G, Margina D, Zanfirescu A, Olaru OT, Nitulescu GM Pharmaceuticals (Basel) 30-Apr-2021
PMCID:PMC8147154
doi:10.3390/ph14050415
PMID:33946434
Pharmacological Targeting of Heme Oxygenase-1 in Osteoarthritis Sanada Y, Tan SJ, Adachi N, Miyaki S Antioxidants (Basel) 09-Mar-2021
PMCID:PMC8001640
doi:10.3390/antiox10030419
PMID:33803317
Clinical and Basic Studies on Therapeutic Efficacy of Herbal Medicines against Mycobacterial Infections Tomioka H, Tatano Y, Shimizu T, Sano C Medicines (Basel) 19-Jun-2019
PMCID:PMC6630501
doi:10.3390/medicines6020067
PMID:31248144
Screening of promising chemotherapeutic candidates from plants extracts Kinjo J, Nakano D, Fujioka T, Okabe H J Nat Med 16-Apr-2016
PMCID:PMC4935755
doi:10.1007/s11418-016-0992-2
PMID:27086008
Do Herbal Formulas Influence the International Normalized Ratio of Patients Taking Warfarin? A Retrospective Study Lu HY, Cho SY, Park SU, Jung WS, Moon SK, Park JM, Ko CN Evid Based Complement Alternat Med 10-Mar-2015
PMCID:PMC4377386
doi:10.1155/2015/213927
PMID:25861354
Aqueous extract of Liriope platyphylla, a traditional Chinese medicine, significantly inhibits abdominal fat accumulation and improves glucose regulation in OLETF type II diabetes model rats Kim JE, Hwang IS, Choi SI, Lee HR, Lee YJ, Goo JS, Lee HS, Son HJ, Jang MJ, Lee SH, Kang BC, Hwang DY Lab Anim Res 26-Sep-2012
PMCID:PMC3469846
doi:10.5625/lar.2012.28.3.181
PMID:23091518
Isobaimonidine, a new Fritillaria alkaloid from the aerial part of Fritillaria verticillata. KO KANEKO, NOBUAKI NARUSE, KIMIAKI HARUKI, HIROSHI MITSUHASHI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.28.1345
Fritillarizine, a new Fritillaria alkaloid isolated from the aerial part of mature Fritillaria verticillata. KO KANEKO, NOBUAKI NARUSE, MIKAKO TANAKA, NAOTOSHI YOSHIDA, HIROSHI MITSUHASHI Pharmaceutical Society of Japan 08-Dec-2011
doi:10.1248/CPB.28.3711
Extensive screening for herbal extracts with potent antioxidant properties Niwano Y, Saito K, Yoshizaki F, Kohno M, Ozawa T J Clin Biochem Nutr 28-Dec-2010
PMCID:PMC3022069
doi:10.3164/jcbn.11-013FR
PMID:21297917
Activation of Inhibitors by Sortase Triggers Irreversible Modification of the Active Site Maresso AW, Wu R, Kern JW, Zhang R, Janik D, Missiakas DM, Duban ME, Joachimiak A, Schneewind O J Biol Chem 01-Jun-2007
PMCID:PMC3366505
doi:10.1074/jbc.M701857200
PMID:17545669
Sortases and the Art of Anchoring Proteins to the Envelopes of Gram-Positive Bacteria Marraffini LA, DeDent AC, Schneewind O Microbiol Mol Biol Rev 01-Mar-2006
PMCID:PMC1393253
doi:10.1128/MMBR.70.1.192-221.2006
PMID:16524923

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 / Acetophenones
1-[(2S)-2-prop-1-en-2-yl-2,3-dihydro-1-benzofuran-5-yl]ethanone 12414274 Click to see 202.25 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eremophilane, 8,9-secoeremophilane and furoeremophilane sesquiterpenoids
(3S,4aR,5S)-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalene 59165345 Click to see 204.35 unknown via CMAUP database
(4aR,5S,8aR)-3,4a,5-trimethyl-4,5,6,7,8a,9-hexahydrobenzo[f][1]benzofuran-8-one 101898833 Click to see 232.32 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,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,10S,11S,14R,15S,20R,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacos-17-ene-10,20-diol 162940928 Click to see 413.60 unknown https://doi.org/10.1248/CPB.28.3711
(1R,2S,6S,9S,10S,11S,14S,15S,17S,18S,20R,23R,24S)-6,10,23-Trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-10,17,20-triol 156461 Click to see 431.70 unknown https://doi.org/10.1248/CPB.28.1345
(1R,2S,6S,9S,10S,11S,14S,15S,20R,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacos-17-ene-10,20-diol 5317396 Click to see CC1CCC2C(C3CCC4C5CC=C6CC(CCC6(C5CC4C3CN2C1)C)O)(C)O 413.60 unknown https://doi.org/10.1248/CPB.28.3711
(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 CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)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
6,10,23-Trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacos-17-ene-10,20-diol 4355153 Click to see 413.60 unknown https://doi.org/10.1248/CPB.28.3711
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/10.1248/CPB.28.1345
Ebeiedine 101324888 Click to see 415.70 unknown via CMAUP database
Imperialine 442977 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 429.60 unknown via CMAUP database
Isoverticine 21573744 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown via CMAUP database
Peimine 131900 Click to see 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 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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
beta-Sitosterol 3-O-beta-D-galactopyranoside 296119 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 https://doi.org/10.1271/BBB.67.2477
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 https://doi.org/10.1271/BBB.67.2477
> 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 / 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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