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!

Filter by language:

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

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

Asia-temperate click to expand
- China
  - China South-central
  - Qinghai
  - Tibet

Asia-tropical click to expand
- Indian Subcontinent
  - East Himalaya

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

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

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

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

Identification of evolutionary relationships and DNA markers in the medicinally important genus Fritillaria based on chloroplast genomics

Zhang T, Huang S, Song S, Zou M, Yang T, Wang W, Zhou J, Liao H

PeerJ

16-Dec-2021

PMCID:	PMC8684722
doi:	10.7717/peerj.12612
PMID:	35003925

Potential geographical distribution and environmental explanations of rare and endangered plant species through combined modeling: A case study of Northwest Yunnan, China

Ye P, Zhang G, Zhao X, Chen H, Si Q, Wu J

Ecol Evol

04-Sep-2021

PMCID:	PMC8495784
doi:	10.1002/ece3.7999
PMID:	34646452

Evaluation and application of an efficient plant DNA extraction protocol for laboratory and field testing

WANG Q, SHEN X, QIU T, WU W, LI L, WANG Z, SHOU H

J Zhejiang Univ Sci B

15-Feb-2021

PMCID:	PMC7897602
doi:	10.1631/jzus.B2000465
PMID:	33615751

Simultaneous determination of 114 pesticides in complex Chinese herbal medicine Fritillaria using ordered mesoporous carbon CMK-3 as a reversed-dispersive solid phase extraction sorbent

Wu T, Qi P, Wang J, Wang Z, Di S, Xu H, Zhao H, Zhao C, Wang X

RSC Adv

20-Jan-2021

PMCID:	PMC8694350
doi:	10.1039/d0ra07229j
PMID:	35424355

A Systematic Review on Traditional Uses, Sources, Phytochemistry, Pharmacology, Pharmacokinetics, and Toxicity of Fritillariae Cirrhosae Bulbus

Chen T, Zhong F, Yao C, Chen J, Xiang Y, Dong J, Yan Z, Ma Y

Evid Based Complement Alternat Med

12-Nov-2020

PMCID:	PMC7676930
doi:	10.1155/2020/1536534
PMID:	33273948

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 CCN1CC2(CCC(C34C2C(C5(C31)C6(CC(C7CC4C6C7O)OC)OCO5)OC)O)COC	465.60	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Gummosogenin	15560274	Click to see CC1(CCC2(C(C1)C3=CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C=O)C	456.70	unknown	via CMAUP database
Machaeric 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 CC1(CC2C3=CCC4C5(CCC(C(C5CCC4(C3(CCC2(CC1O)C(=O)OC)C)C)(C)C)O)C)C	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 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,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 CC1CCC2C(C3C(CC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)O)C	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 CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C	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 CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C	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 CC1CCC2C(C3C(CC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)O)C	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 CC1CCC2C(C3C(CC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)O)C	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 CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)C	415.70	unknown	https://doi.org/10.1248/CPB.36.4700 https://doi.org/10.1248/CPB.33.2614
(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)-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
(2S,6S,10S,15S,20S,23R)-10,20-dihydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one	5320446	Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O	429.60	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
(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 CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)C	415.70	unknown	https://doi.org/10.1248/CPB.33.2614 https://doi.org/10.1248/CPB.36.4700
(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 CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C	413.60	unknown	https://doi.org/10.1248/CPB.36.4700 https://doi.org/10.1248/CPB.33.2614
(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/10.1016/S0040-4039(00)84536-0 https://doi.org/10.1248/CPB.36.4700
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 CC1CCC2C(C3C(CC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)O)C	429.60	unknown	https://doi.org/10.1248/CPB.33.2614 https://doi.org/10.1248/CPB.36.4700
20-Hydroxy-6,10,23-trimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one	14240939	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
3,20-Dihydroxycevan-6-one	5221	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
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 CC1CCC2C(C3C(CC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)O)C	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
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
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
Peimine	131900	Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(C6C5(CCC(C6)O)C)O)(C)O	431.70	unknown	via CMAUP database
Peiminine	167691	Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)(C)O	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
Puqiedinone	126149	Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C	413.60	unknown	via CMAUP database
Raddeamine	102063129	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,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
CID 21123947	21123947	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 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 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
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 CC1CCC2C(C3C(N2C1)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C	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 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
> 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 / Benzopyrans / 2-benzopyrans
1-Butylidene-8-hydroxy-1H-2-benzopyran-4(3H)-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 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

Biological Material Top

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.

Fritillaria delavayi

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top