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Fritillaria verticillata

Fritillaria verticillata - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

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

Description Top

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No description added yet. Help us by writing one.

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)

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

Suggest others/fix!
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 CC(=C)C1CC2=C(O1)C=CC(=C2)C(=O)C 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 CC1CCC=C2C1(CC(CC2)C(=C)C)C 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 CC1CCC(=O)C2C1(CC3=C(C2)OC=C3C)C 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 CC1CCC(N(C1)C)C(C)C2CCC3C2(CCC4C3CC(=O)C5C4(CCC(C5)O)C)C 429.70 unknown via CMAUP database
N-Desmethylpuqietinone 11304576 Click to see CC1CCC(NC1)C(C)C2CCC3C2(CCC4C3CC(=O)C5C4(CCC(C5)O)C)C 415.70 unknown via CMAUP database
Puqietinone 44583920 Click to see CC1CCC(N(C1)C)C(C)C2CCC3C2(CCC4C3CC(=O)C5C4(CCC(C5)O)C)C 429.70 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
(1R,2S,6R,9S,11S,14S,15S,18S,20S,23R,24S)-20-hydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one 101687687 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C 413.60 unknown via CMAUP database
(1R,2S,6S,9S,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 CC1CCC2C(C3CCC4C5CC=C6CC(CCC6(C5CC4C3CN2C1)C)O)(C)O 413.60 unknown https://doi.org/10.1248/CPB.28.3711
(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 CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 unknown via CMAUP database
(1R,2S,6S,9S,11S,14S,15S,17R,18S,20S,23R,24S)-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosane-17,20-diol 101324888 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)C 415.70 unknown 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 CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 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 CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 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 CC1CCC2C(C3CCC4C5CC=C6CC(CCC6(C5CC4C3CN2C1)C)O)(C)O 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
CID 156461 156461 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
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 CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O 431.70 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
Puqiedinone 126149 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C 413.60 unknown via CMAUP database
Verticinone 167691 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 429.60 unknown via CMAUP database
Zhebeinone 5320446 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O 429.60 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Jerveratrum-type alkaloids
(3S,3'R,3'aS,6'S,6aR,6bS,7'aR,9R,11aS,11bR)-3-hydroxy-3',6',10,11b-tetramethylspiro[1,2,3,4,4a,6,6a,6b,7,8,11,11a-dodecahydrobenzo[a]fluorene-9,2'-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine]-5-one 102119835 Click to see CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC4=C3C)C)O)C)NC1 427.60 unknown via CMAUP database
(3S,3'R,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 CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC4=C3C)C)O)C)NC1 427.60 unknown via CMAUP database
(3S,3'R,4aS,6'S,6aR,6bS,7'aR,9R,11aS,11bR)-3-hydroxy-3',6',10,11b-tetramethylspiro[1,2,3,4,4a,6,6a,6b,7,8,11,11a-dodecahydrobenzo[a]fluorene-9,2'-3a,4,5,6,7,7a-hexahydro-3H-furo[3,2-b]pyridine]-5-one 71751476 Click to see CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC4=C3C)C)O)C)NC1 427.60 unknown via CMAUP database
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 CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CC(CC6)OC7C(C(C(C(O7)CO)O)O)O)C)O)C 577.80 unknown via CMAUP database
6-Oxocevan-2-yl hexopyranoside 127203 Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CC(CC6)OC7C(C(C(C(O7)CO)O)O)O)C)C 575.80 unknown via CMAUP database
> 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 C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N 283.24 unknown via CMAUP database
9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one 6021 Click to see C1=NC(=O)C2=C(N1)N(C=N2)C3C(C(C(O3)CO)O)O 268.23 unknown via CMAUP database
Adenosine 60961 Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N 267.24 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides / Purine 2-deoxyribonucleosides
2'-Deoxyadenosine 13730 Click to see C1C(C(OC1N2C=NC3=C(N=CN=C32)N)CO)O 251.24 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Cytidine 6175 Click to see C1=CN(C(=O)N=C1N)C2C(C(C(O2)CO)O)O 243.22 unknown via CMAUP database
Uridine 6029 Click to see C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O 244.20 unknown via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides / Pyrimidine 2-deoxyribonucleosides
Thymidine 5789 Click to see CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O 242.23 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Hydroxypyrimidines
5-methylpyrimidine-2,4-diol 5274265 Click to see CC1=CN=C(N=C1O)O 126.11 unknown via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
Uracil 1174 Click to see C1=CNC(=O)NC1=O 112.09 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives
2-amino-3,7-dihydropurin-6-one 764 Click to see C1=NC2=C(N1)C(=O)N=C(N2)N 151.13 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / 6-aminopurines
Adenine 190 Click to see C1=NC2=NC=NC(=C2N1)N 135.13 unknown via CMAUP database
> Organoheterocyclic compounds / Imidazopyrimidines / Purines and purine derivatives / Purinones / Hypoxanthines
CID 790 790 Click to see C1=NC2=C(N1)C(=O)N=CN2 136.11 unknown via CMAUP database

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