Tricyrtis formosana - Entire plant
Part: Entire plant
Author: Sorin

Tricyrtis formosana - Entire plant
Part: Entire plant
Author: Sorin

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Details Top

Internal ID UUID644024010e22d235160948
Scientific name Tricyrtis formosana
Authority Baker
First published in J. Linn. Soc., Bot. 17: 465 (1879)

Description Top

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Synonyms Top

Scientific name Authority First published in
Compsoa formosana (Baker) Kuntze Revis. Gen. Pl. 2: 708 (1891)

Common names Top

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Language Common/alternative name
Persian سوسن غوک تایوانی
Japanese タイワンホトトギス
Swedish taiwanskugglilja
szy nipaluma-yutiancaw
Chinese 台湾油点草

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Tricyrtis formosana var. formosana Unknown
Tricyrtis formosana var. glandosa (T.Shimizu) T.S.Liu & S.S.Ying Fl. Taiwan 5: 79 (1978)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Sow at 4°C for 3 weeks, then increase to 20°C.
Requires Light or Surface Sowing: These seeds need light to germinate and should not be covered with soil or only very lightly. They are often very small and sown directly on the surface of the growing medium.
Sow seeds immediately as their viability decreases rapidly, or they best germinate when fresh. If stored, seeds might need temperature cycling and patience to germinate.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000750552
Tropicos 18406406
KEW urn:lsid:ipni.org:names:542477-1
The Plant List kew-290590
Missouri Botanical Garden 282436
Open Tree Of Life 554851
NCBI Taxonomy 1126413
IPNI 542477-1
iNaturalist 452312
GBIF 2752120
Freebase /m/0135zljs
EPPO TCYFO
EOL 1083240
USDA GRIN 40133
Wikipedia Tricyrtis_formosana

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
Flower colour and size-signals vary with altitude and resulting climate on the tropical-subtropical islands of Taiwan Shrestha M, Tai KC, Dyer AG, Garcia JE, Yang EC, Jentsch A, Wang CN Front Plant Sci 01-Feb-2024
PMCID:PMC10867191
doi:10.3389/fpls.2024.1304849
PMID:38362451
Double migration of the endangered Tricyrtis formosana (Liliaceae) in Japan Tsunenari K, Ito T, Yokota M, Shibabayashi M, Endo C, Chung KF, Suyama Y, Matsuo A, Abe A, Naiki A, Setoguchi H, Makino T, Isagi Y Sci Rep 10-Jan-2024
PMCID:PMC10781951
doi:10.1038/s41598-024-51431-x
PMID:38200076
Complete chloroplast genome of Tricyrtis xianjuensis Li, Chen & Ma 2014 (Liliaceae): a species endemic to Zhejiang province, China Huang L, Lu Z, Wang J, Bao H, Zhang H, Jiang M Mitochondrial DNA B Resour 08-Jan-2024
PMCID:PMC10776049
doi:10.1080/23802359.2023.2301021
PMID:38197054
Physicochemical properties and homology studies of the floral meristem identity gene LFY in nonflowering and flowering plants Thekkeveedu RP, Hegde S BioTechnologia (Pozn) 29-Jun-2022
PMCID:PMC9642948
doi:10.5114/bta.2022.116205
PMID:36606070
A Novel Botrytis Species Is Associated with a Newly Emergent Foliar Disease in Cultivated Hemerocallis Grant-Downton RT, Terhem RB, Kapralov MV, Mehdi S, Rodriguez-Enriquez MJ, Gurr SJ, van Kan JA, Dewey FM PLoS One 02-Jun-2014
PMCID:PMC4041564
doi:10.1371/journal.pone.0089272
PMID:24887415
Phytochemical study of polyphenols in Perilla Frutescens as an antioxidant Asif M Avicenna J Phytomed 01-Sep-2012
PMCID:PMC4075683
PMID:25050247
Phenolics: From Chemistry to Biology Pereira DM, Valentão P, Pereira JA, Andrade PB Molecules 17-Jun-2009
PMCID:PMC6254163
doi:10.3390/molecules14062202
Diacylated 8‐C‐Glucosylcyanidin 3‐Glucoside from the Flowers of Tricyrtis formosana. Fumi Tatsuzawa, Norio Saito, Kazumitsu Miyoshi, Koichi Shinoda, Atsushi Shigihara, Toshio Honda Wiley 12-Oct-2004
doi:10.1002/CHIN.200444199
Diacylated 8-C-glucosylcyanidin 3-glucoside from the flowers of Tricyrtis formosana. Tatsuzawa F, Saito N, Miyoshi K, Shinoda K, Shigihara A, Honda T Chem Pharm Bull (Tokyo) 01-May-2004
doi:10.1248/CPB.52.631
PMID:15133223
The first isolation of C-glycosylanthocyanin from the flowers of Tricyrtis formosana Norio Saito, Fumi Tatsuzawa, Kazumitsu Miyoshi, Atsushi Shigihara, Toshio Honda Elsevier BV 03-Sep-2003
doi:10.1016/S0040-4039(03)01747-7
Constituents of Couepia paraensis. Sanduja R, Alam M, Euler KL J Nat Prod 01-Jan-1983
doi:10.1021/NP50025A019
PMID:6854338

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 / Triterpenoids
Isoarborinol 12305182 Click to see CC(C)C1CCC2C1(CCC3(C2(CC=C4C3CCC5C4(CCC(C5(C)C)O)C)C)C)C 426.70 unknown https://doi.org/10.1248/CPB.52.631
https://doi.org/10.1002/CHIN.200444199
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Pregnane steroids / Gluco/mineralocorticoids, progestogins and derivatives
[(3R,5S,8S,9S,10S,11R,13R,14S,17R)-17-ethenyl-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-11-yl] acetate 25180961 Click to see CC(=O)OC1CC2(C(CCC2C3C1C4(CCC(CC4CC3)O)C)C=C)C 360.50 unknown https://doi.org/10.1002/CHIN.200444199
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Anthocyanins / Anthocyanidin-3-O-glycosides
(2R,3R,4S,5R,6S)-2-[[(2R,3S,4R,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-6-methyloxane-3,4,5-triol 154496406 Click to see CC1C(C(C(C(O1)OCC2C(C(C(C(O2)OC3=CC4=C(C=C(C=C4[O+]=C3C5=CC(=C(C=C5)O)O)O)O)O)O)O)O)O)O 595.50 unknown https://doi.org/10.1248/CPB.52.631
(2S,5S)-2-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 44256715 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1002/CHIN.200444199
3-[[(2R,3S,4R,5R,6S)-6-[2-(3,4-dihydroxyphenyl)-5,7-dihydroxychromenylium-3-yl]oxy-3,4,5-trihydroxyoxan-2-yl]methoxy]-3-oxopropanoic acid 154496402 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)COC(=O)CC(=O)O)O)O)O)O)O)O)O 535.40 unknown https://doi.org/10.1248/CPB.52.631
Cyanidin 3-(6-malonylglucoside)-8-C-glucoside 163184513 Click to see C1=CC(=C(C=C1C2=C(C=C3C(=CC(=C(C3=[O+]2)C4C(C(C(C(O4)CO)O)O)O)O)O)OC5C(C(C(C(O5)COC(=O)CC(=O)[O-])O)O)O)O)O 696.60 unknown https://doi.org/10.1016/S0040-4039(03)01747-7
Kuromanin 441667 Click to see C1=CC(=C(C=C1C2=[O+]C3=CC(=CC(=C3C=C2OC4C(C(C(C(O4)CO)O)O)O)O)O)O)O 449.40 unknown https://doi.org/10.1248/CPB.52.631

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