Fritillaria unibracteata

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Description

Synonyms

Common Names

Subtypes (subspecies, varieties, subvarieties, forms)

Germination/Propagation

Distribution

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Genome

Scientific Literature

Phytochemical Profile

Biological Material

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Details Top

Internal ID	UUID64402656ed6e1091332092
Scientific name	Fritillaria unibracteata
Authority	Hsiao & K.C.Hsia
First published in	Acta Phytotax. Sin. 15(2): 39 (1977)

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Synonyms Top

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Common names Top

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Filter by language:

Language	Common/alternative name
Chinese	川贝母
Chinese	暗紫贝母
Chinese	冲松贝
Chinese	松贝
Chinese	暗紫貝母

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name	Authority	First published in
Fritillaria unibracteata var. longinectarea	S.Y.Tang & S.C.Yueh	Fl. Sichuanica 7: 60 (1991)
Fritillaria unibracteata var. unibracteata		Unknown
Fritillaria unibracteata var. wabuensis	(S.Y.Tang & S.C.Yueh) Z.D.Liu, Shu Wang & S.C.Chen	Acta Bot. Yunnan. 31: 145 (2009)

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 click to expand
- China
  - China North-central
  - China South-central
  - Qinghai

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000768140
UNII	U7T9NW5821
Tropicos	18406486
KEW	urn:lsid:ipni.org:names:535351-1
The Plant List	kew-306935
Open Tree Of Life	702580
NCBI Taxonomy	152095
IPNI	535351-1
iNaturalist	565537
GBIF	5300797
Freebase	/m/0134lv3g
EOL	1088587
USDA GRIN	423618
Wikipedia	Fritillaria_unibracteata
CMAUP	NPO14849

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

Genome-Wide Identification and Expression Profile Analysis of the Phenylalanine Ammonia-Lyase Gene Family in Hevea brasiliensis

Liu H, He Q, Hu Y, Lu R, Wu S, Feng C, Yuan K, Wang Z

Int J Mol Sci

06-May-2024

PMCID:	PMC11084274
doi:	10.3390/ijms25095052
PMID:	38732270

Investigation the biological activities and the metabolite profiles of endophytic fungi isolated from Gundelia tournefortii L.

Ebadi M, Ahmadi F, Tahmouresi H, Pazhang M, Mollaei S

Sci Rep

25-Mar-2024

PMCID:	PMC10963752
doi:	10.1038/s41598-024-57222-8
PMID:	38528041

Prediction of Potential Suitable Areas and Priority Protection for Cupressus gigantea on the Tibetan Plateau

Zhang H, Wei Y, Yue J, Wang Z, Zou H, Ji X, Zhang S, Liu Z

Plants (Basel)

20-Mar-2024

PMCID:	PMC10974514
doi:	10.3390/plants13060896
PMID:	38592903

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

Explorative study for the rapid detection of Fritillaria using gas chromatography-ion mobility spectrometry

Dai Y, Liu S, Yang L, He Y, Guo X, Ma Y, Li S, Huang D

Front Nutr

06-Feb-2024

PMCID:	PMC10877000
doi:	10.3389/fnut.2024.1361668
PMID:	38379552

Ultrasound-assisted polysaccharide extraction from Fritillaria ussuriensis Maxim. and its structural characterization, antioxidant and immunological activity

Jiang S, Wang Q, Wang Z, Borjigin G, Sun J, Zhao Y, Li Q, Shi X, faizan ali shah S, Wang X, Gan C, Wu Y, Song X, Li Q, Yang C

Ultrason Sonochem

05-Feb-2024

PMCID:	PMC10878995
doi:	10.1016/j.ultsonch.2024.106800
PMID:	38359575

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

The power of magnesium: unlocking the potential for increased yield, quality, and stress tolerance of horticultural crops

Ahmed N, Zhang B, Bozdar B, Chachar S, Rai M, Li J, Li Y, Hayat F, Chachar Z, Tu P

Front Plant Sci

24-Oct-2023

PMCID:	PMC10628537
doi:	10.3389/fpls.2023.1285512
PMID:	37941670

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

Current status of research on endophytes of traditional Tibetan medicinal plant and their metabolites

Hu D, Long X, Luobu T, Wang Q

3 Biotech

11-Sep-2023

PMCID:	PMC10495306
doi:	10.1007/s13205-023-03720-x
PMID:	37705864

Integrated metagenomics and metabolomics analysis reveals changes in the microbiome and metabolites in the rhizosphere soil of Fritillaria unibracteata

Liu C, Yu J, Ying J, Zhang K, Hu Z, Liu Z, Chen S

Front Plant Sci

04-Aug-2023

PMCID:	PMC10436506
doi:	10.3389/fpls.2023.1223720
PMID:	37600181

Plants as the Extended Phenotype of Endophytes—The Actual Source of Bioactive Compounds

Rutkowska N, Drożdżyński P, Ryngajłło M, Marchut-Mikołajczyk O

Int J Mol Sci

13-Jun-2023

PMCID:	PMC10298476
doi:	10.3390/ijms241210096
PMID:	37373241

Endophytic fungi mediates production of bioactive secondary metabolites via modulation of genes involved in key metabolic pathways and their contribution in different biotechnological sector

Toppo P, Kagatay LL, Gurung A, Singla P, Chakraborty R, Roy S, Mathur P

3 Biotech

14-May-2023

PMCID:	PMC10183385
doi:	10.1007/s13205-023-03605-z
PMID:	37197561

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

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 / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Stearic Acid	5281	Click to see CCCCCCCCCCCCCCCCCC(=O)O	284.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Glycerolipids / Triradylcglycerols / Triacylglycerols
Tristearin	11146	Click to see CCCCCCCCCCCCCCCCCC(=O)OCC(COC(=O)CCCCCCCCCCCCCCCCC)OC(=O)CCCCCCCCCCCCCCCCC	891.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
(5R,19R)-11-ethyl-19-hydroxy-5-methyl-18-methylidene-9-oxa-11-azaheptacyclo[15.2.1.01,14.02,12.04,13.05,10.08,13]icosan-16-one	5321389	Click to see CCN1C2C3CC4C2(C5CCC4(C1O5)C)C6C37CC(C(=C)C7O)C(=O)C6	355.50	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
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/10.1080/10286020.2011.619980
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/10.1080/10286020.2011.619980
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	https://doi.org/10.1080/10286020.2011.619980
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
Zhebeirine	10597859	Click to see CC1CCC2C(C3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C)C	413.60	unknown	https://doi.org/10.1080/10286020.2011.619980
> 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
CID 5320448	5320448	Click to see CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC4=C3C)C)O)C)NC1	427.60	unknown	https://doi.org/10.1080/10286020.2011.619980
Peimisine	161294	Click to see CC1CC2C(C(C3(O2)CCC4C5CC(=O)C6CC(CCC6(C5CC4=C3C)C)O)C)NC1	427.60	unknown	https://doi.org/10.1080/10286020.2011.619980
Songbaisine	197469	Click to see CC1CC2C(C(C3(O2)CCC4C5CCC6CC(CCC6(C5C(=O)C4=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
(3S,8R,9R,10S,13R,14S,17R)-17-[(2R,5S)-5-ethyl-6-methylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol	636741	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	414.70	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
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
D-Alt(a1-2a)L-Psif	53301851	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Suffruticoside A	9986231	Click to see CC(=O)C1=C(C=C(C=C1)OC)OC2C(C(C(C(O2)COC3C(C(CO3)(COC(=O)C4=CC(=C(C(=C4)O)O)O)O)O)O)O)O	612.50	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
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives
Verrucosidin	6437365	Click to see CC1C2(C(O2)C(O1)(C)C=C(C)C=C(C)C3C(O3)(C)C4=C(C(=C(C(=O)O4)C)OC)C)C	416.50	unknown	via CMAUP database

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Fritillaria unibracteata

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