Fritillaria przewalskii

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

Links to other databases

Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID644026528facb782169072
Scientific name	Fritillaria przewalskii
Authority	Maxim. ex Batalin
First published in	Trudy Imp. S.-Peterburgsk. Bot. Sada 13: 105 (1893)

Description Top

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Fritillaria przewalskii is a species of flowering plant in the lily family Liliaceae, native to China. It produces bulbs up to 15 mm in diameter and has a stem that can reach up to 50 cm tall. The flowers of this species are yellow with deep purple spots and hang down in a nodding fashion. It is named after the Polish-Russian explorer Colonel Nikolai Przhevalsky, who lived from 1839 to 1888.

Synonyms Top

Scientific name	Authority	First published in
Fritillaria gansuensis	S.C.Chen & G.D.Yu	Acta Bot. Yunnan. 7: 148 (1985)
Fritillaria przewalskii var. discolor	Y.K.Yang & Y.S.Zhou	Acta Bot. Boreal.-Occid. Sin. 5: 40 (1985)
Fritillaria przewalskii f. emacula	Y.K.Yang & J.K.Wu	Acta Bot. Boreal.-Occid. Sin. 5: 40 (1985)
Fritillaria przewalskii var. gannanica	Y.K.Yang & J.Z.Ren	J. Wuhan Bot. Res. 5: 132 (1987)
Fritillaria przewalskii var. tessellata	Y.K.Yang & Y.S.Zhou	Acta Bot. Boreal.-Occid. Sin. 5: 39 (1985)

Common names Top

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Language	Common/alternative name
Chinese	伊贝母
Chinese	川贝母
Chinese	甘肃贝母
Chinese	岷贝
Chinese	西北贝母
Chinese	甘肅貝母

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

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 North-central
  - China South-central

Links to other databases Top

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Database	ID/link to page
World Flora Online	wfo-0000768027
UNII	CUB29S3EEF
KEW	urn:lsid:ipni.org:names:535282-1
The Plant List	kew-306829
Open Tree Of Life	702593
NCBI Taxonomy	152092
IPNI	535282-1
iNaturalist	565516
GBIF	5300378
Freebase	/m/0134pv6l
EOL	1088558
USDA GRIN	423416
Wikipedia	Fritillaria_przewalskii
CMAUP	NPO22292

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

Editorial: Plants surviving in extreme environment: harnessing soil-plant–microbial relationship to enhance crop health and productivity

Chandra P, Egamberdieva D, Basak N, Rai AK, Sonth B

Front Microbiol

25-Apr-2024

PMCID:	PMC11080980
doi:	10.3389/fmicb.2024.1388802
PMID:	38725690

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

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

Structural characteristics and diversity of the rhizosphere bacterial communities of wild Fritillaria przewalskii Maxim. in the northeastern Tibetan Plateau

Cui Z, Li R, Li F, Jin L, Wu H, Cheng C, Ma Y, Wang Z, Wang Y

Front Microbiol

17-Feb-2023

PMCID:	PMC9981654
doi:	10.3389/fmicb.2023.1070815
PMID:	36876117

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

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

Correction: Allometric relationships between leaf and bulb traits of Fritillaria przewalskii Maxim. grown at different altitudes

N/A

PLoS One

25-Feb-2022

PMCID:	PMC8880756
doi:	10.1371/journal.pone.0264810
PMID:	35213670

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

Modeling of the Potential Geographical Distribution of Three Fritillaria Species Under Climate Change

Jiang R, Zou M, Qin Y, Tan G, Huang S, Quan H, Zhou J, Liao H

Front Plant Sci

10-Jan-2022

PMCID:	PMC8784777
doi:	10.3389/fpls.2021.749838
PMID:	35082804

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 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
(2Z,4E,6E,8E,10E,12E,14E,16E,18E)-3-hydroxy-1-[(1R,4S)-4-hydroxy-1,2,2-trimethylcyclopentyl]-4,8,13,17-tetramethyl-19-(2,3,4-trimethylphenyl)nonadeca-2,4,6,8,10,12,14,16,18-nonaen-1-one	102117088	Click to see CC1=C(C(=C(C=C1)C=CC(=CC=CC(=CC=CC=C(C)C=CC=C(C)C(=CC(=O)C2(CC(CC2(C)C)O)C)O)C)C)C)C	580.80	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,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
(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/10.1080/01635581.2013.878737
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
> Nucleosides, nucleotides, and analogues / Purine nucleosides
(2R,5R)-2-(6-aminopurin-9-yl)-5-(hydroxymethyl)oxolane-3,4-diol	54732806	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	via CMAUP database
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
Deoxyadenosine	636	Click to see C1C(C(OC1N2C=NC3=C(N=CN=C32)N)CO)O	251.24	unknown	https://doi.org/10.1002/JSSC.201100373
> 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
1-[(2R,4S,5R)-4-deuterio-4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-5-methylpyrimidine-2,4-dione	11085982	Click to see CC1=CN(C(=O)NC1=O)C2CC(C(O2)CO)O	243.23	unknown	via CMAUP database
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 CC1=CN=C(N=C1O)O	126.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Pyrimidones
5-methyl-(211C)1H-pyrimidine-2,4-dione	11557282	Click to see CC1=CNC(=O)NC1=O	125.11	unknown	via CMAUP database
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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Fritillaria przewalskii

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