Thalictrum lucidum is a type of flowering plant that is part of the Ranunculaceae family. It is found naturally in Europe, Western Siberia, and Turkey.

Synonyms Top

Scientific name	Authority	First published in
Thalictrum longifolium	Krock.	Fl. Siles. 2(1): 242 (1790)
Thalictrum nigrescens	hort. ex Lecoy.	Bull. Soc. Roy. Bot. Belgique 24: 297 (1885)
Thalictrum nestleri	F.W.Schultz	Fl. Pfalz : 4 (1845)
Thalictrum peucedanifolium	Griseb. & Schenk	Arch. Naturgesch. 18(1): 312 (1852)
Thalictrum divaricatum	Spreng.	Index Seminum (HAL, Halensis) 1807: 61 (1807)
Thalictrum galiiforme	Schur	Verh. Naturf. Vereins Brünn 15(2): 19 (1877)
Thalictrum speciosum	Mill.	Gard. Dict. ed. 8 : n.º 2 (1768)
Thalictrum stenophyllum	Schur	Verh. Naturf. Vereins Brünn 15(2): 19 (1877)
Thalictrum rosmarinifolium	Pollini	Giorn. Fis. 9: 32 (1816)
Thalictrum bulgaricum	Velen.	Fl. Bulg. : 4 (1891)
Thalictrum angustissimum	Crantz	Stirp. Austr. Fasc. 2: 76 (1763)
Thalictrum angustifolium	L.	Sp. Pl. : 546 (1753)
Thalictrum ammophilum	Schur	Verh. Naturf. Vereins Brünn 15(2): 21 (1877)
Thalictrum lucidum var. angustissimum	(Crantz) Osvač.	Fl. Slovenska 3: 246 (1982)

Common names Top

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Filter by language:

Language	Common/alternative name
Belarusian	Пылюшнік светлы
Belarusian	Сузіц
Belarusian	Сузік
Belarusian	Расходнік
Belarusian	Балотная мятла
Belarusian	Мядуніца
Belarusian	Мядуніца лугавая
Belarusian	Пажытнік
Belarusian	Пылюшнік вузкалісты
Belarusian	Руцьвянка
Bulgarian	теснолистно обичниче
Czech	žluťucha lesklá
German	glanz-wiesenraute
German	glänzende wiesenraute
Estonian	ahtaleheline ängelhein
Estonian	ahtalehine ängelhein
Finnish	kaitaängelmä
Finnish	kiiltoängelmä
Upper Sorbian	bahnowy žiwotnik
Lithuanian	siauralapis vingiris
Latvian	spožais saulkrēsliņš
Polish	rutewka wąskolistna
Russian	Василистник узколистный
Russian	Василисник светлый
Russian	Василистник светлый
Russian	Василистник блестящий
Russian	Василисник узколистный
Russian	Василисник блестящий
Slovak	Žltuška lesklá
Swedish	glansruta
Chinese	保加利亚唐松草

Subspecies (abbr. subsp./ssp.) Top

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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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Alternate between 20°C and 4°C for 3 months each, across multiple cycles, acknowledging that germination may be prolonged.

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

Asia-temperate click to expand
- Russian Far East
  - Magadan
- Siberia
  - West Siberia
- Western Asia
  - East Aegean Islands
  - Turkey

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Central European Russia
  - Krym
  - North European Russia
  - Northwest European Russia
  - South European Russia
  - Ukraine
- Middle Europe
  - Austria
  - Czechoslovakia
  - Germany
  - Hungary
  - Poland
- Northern Europe
  - Finland
- Southeastern Europe
  - Albania
  - Bulgaria
  - Greece
  - Italy
  - Romania
  - Turkey-in-Europe
  - Yugoslavia

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000453840
Tropicos	27100246
INPN	126150
Flora of Italy	1208
KEW	urn:lsid:ipni.org:names:714579-1
The Plant List	kew-2512323
Open Tree Of Life	977702
Observations.org	132586
NCBI Taxonomy	1084680
NBN Atlas	NBNSYS0000014996
IPNI	714579-1
iNaturalist	485803
GBIF	7277720
EPPO	THCLU
EOL	5529584
Elurikkus	7903
USDA GRIN	36441
Wikipedia	Thalictrum_lucidum
CMAUP	NPO547

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

Examination of the Effects of Domestic Water Buffalo (Bubalus bubalis) Grazing on Wetland and Dry Grassland Habitats

Fűrész A, Penksza K, Sipos L, Turcsányi-Járdi I, Szentes S, Fintha G, Penksza P, Viszló L, Szalai F, Wagenhoffer Z

Plants (Basel)

31-May-2023

PMCID:	PMC10255522
doi:	10.3390/plants12112184
PMID:	37299162

Treatment Effects of Natural Products on Inflammatory Bowel Disease In Vivo and Their Mechanisms: Based on Animal Experiments

Zhou Y, Wang D, Yan W

Nutrients

18-Feb-2023

PMCID:	PMC9967064
doi:	10.3390/nu15041031
PMID:	36839389

Traditional Uses of Medicinal Plants in South-Western Part of Lithuania

Karpavičienė B

Plants (Basel)

11-Aug-2022

PMCID:	PMC9413674
doi:	10.3390/plants11162093
PMID:	36015397

Nanoformulation and Evaluation of Oral Berberine-Loaded Liposomes

Duong TT, Isomäki A, Paaver U, Laidmäe I, Tõnisoo A, Yen TT, Kogermann K, Raal A, Heinämäki J, Pham TM

Molecules

29-Apr-2021

PMCID:	PMC8125214
doi:	10.3390/molecules26092591
PMID:	33946815

In Vitro and In Vivo Biological Activity of Berberine Chloride against Uropathogenic E. coli Strains Using Galleria mellonella as a Host Model

Petronio Petronio G, Cutuli MA, Magnifico I, Venditti N, Pietrangelo L, Vergalito F, Pane A, Scapagnini G, Di Marco R

Molecules

29-Oct-2020

PMCID:	PMC7662377
doi:	10.3390/molecules25215010
PMID:	33137930

Chloroplast primers for clade‐wide phylogenetic studies of Thalictrum

Morales‐Briones DF, Arias T, Di Stilio VS, Tank DC

Appl Plant Sci

16-Oct-2019

PMCID:	PMC6814179
doi:	10.1002/aps3.11294
PMID:	31667022

Ecology, threats and conservation status of Carex buekii (Cyperaceae) in Central Europe

Więcław H, Šumberová K, Bosiacka B, Hrivnák R, Dajdok Z, Mesterházy A, Minuzzo C, Martinetto E, Koopman J

Sci Rep

01-Aug-2019

PMCID:	PMC6671956
doi:	10.1038/s41598-019-47563-0
PMID:	31371740

Karst dolines provide diverse microhabitats for different functional groups in multiple phyla

Bátori Z, Vojtkó A, Maák IE, Lőrinczi G, Farkas T, Kántor N, Tanács E, Kiss PJ, Juhász O, Módra G, Tölgyesi C, Erdős L, Aguilon DJ, Keppel G

Sci Rep

09-May-2019

PMCID:	PMC6509348
doi:	10.1038/s41598-019-43603-x
PMID:	31073136

Scent matters: differential contribution of scent to insect response in flowers with insect vs. wind pollination traits

Wang TN, Clifford MR, Martínez-Gómez J, Johnson JC, Riffell JA, Di Stilio VS

Ann Bot

20-Jul-2018

PMCID:	PMC6344221
doi:	10.1093/aob/mcy131
PMID:	30052759

Root Foraging Performance and Life-History Traits

Weiser M, Koubek T, Herben T

Front Plant Sci

09-Jun-2016

PMCID:	PMC4899455
doi:	10.3389/fpls.2016.00779
PMID:	27375639

Alkaloids of Thalictrum angustifolium

Tawfeq Alhowiriny, Michael Zemaitis, Fu-Tyan Lin, Jack Beal, Paul Schiff

Informa UK Limited

27-Oct-2003

doi:	10.1300/J157V02N02_01

Enzymic 12-hydroxylation and 12-O-methylation of dihydrochelirubine in dihydromacarpine formation by Thalictrum bulgaricum

Lothar Kammerer, Wanchai de-Eknamkul, Meinhart H. Zenk

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)89732-0

Phytochemical Profile Top

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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
> Alkaloids and derivatives / 6,6a-secoaporphines
Thaliglucinone	182266	Click to see CN(C)CCC1=CC(=C2C3=C1C=CC4=CC5=C(C(=C43)C(=O)O2)OCO5)OC	365.40	unknown	via CMAUP database
> Alkaloids and derivatives / Aporphines
Magnoflorine	73337	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)O)OC)C	342.40	unknown	https://doi.org/10.1300/J157V02N02_01
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Dihydrobenzophenanthridine alkaloids
Dihydromacarpine	440631	Click to see CN1CC2=C3C(=CC(=C2C4=C1C5=CC6=C(C=C5C(=C4)OC)OCO6)OC)OCO3	393.40	unknown	https://doi.org/10.1016/S0031-9422(00)89732-0
> Alkaloids and derivatives / Benzophenanthridine alkaloids / Hexahydrobenzophenanthridine alkaloids
1,2-dimethoxy-12-methyl-5,6,11b,13-tetrahydro-4bH-[1,3]benzodioxolo[5,6-c]phenanthridin-5-ol	3446460	Click to see CN1CC2=C(C=CC(=C2OC)OC)C3C1C4=CC5=C(C=C4CC3O)OCO5	369.40	unknown	via CMAUP database
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium-3-ol;iodide	5459338	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC.[I-]	465.30	unknown	via CMAUP database
Berberine	2353	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC	336.40	unknown	https://doi.org/10.1300/J157V02N02_01
Jatrorrhizine	72323	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)O)OC)OC	338.40	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / p-Hydroxybenzoic acid esters / p-Hydroxybenzoic acid alkyl esters
Methylparaben	7456	Click to see COC(=O)C1=CC=C(C=C1)O	152.15	unknown	https://doi.org/10.1300/J157V02N02_01
> Benzenoids / Naphthalenes / Naphthoquinones
Javanicin	10149	Click to see CC1=C(C(=C2C(=C1O)C(=O)C=C(C2=O)OC)O)CC(=O)C	290.27	unknown	via CMAUP database
> Lignans, neolignans and related compounds
(14S)-6,20,25-trimethoxy-15,30-dimethyl-8,23-dioxa-15,30-diazaheptacyclo[22.6.2.29,12.13,7.114,18.027,31.022,33]hexatriaconta-3(36),4,6,9(35),10,12(34),18,20,22(33),24,26,31-dodecaen-21-ol	10054445	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)O)OC	608.70	unknown	via CMAUP database
(1S,14S)-9,20,21,25-tetramethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18(33),19,21,24,26,31-dodecaen-19-ol	10627884	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)O)OC)OC	638.70	unknown	via CMAUP database
(2R,3R,4S,5R)-2-(6-aminopurin-9-yl)-5-methanidyl-tetrahydrofuran-3,4-diol	46173762	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)OC)O)O3)C=C5)OC	594.70	unknown	via CMAUP database
10,14,15-Trimethoxy-4,20-dimethyl-28-oxa-4,20-diazaheptacyclo[27.2.2.17,11.113,17.123,27.03,8.021,35]hexatriaconta-1(31),7(36),8,10,13(35),14,16,23(34),24,26,29,32-dodecaen-26-ol	5321904	Click to see CN1CCC2=CC3=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(C3)C(=C(C=C7CCN6C)OC)OC)O)OC	606.70	unknown	via CMAUP database
6,6',7,12'-Tetramethoxy-2,2'-dimethyloxyacanthan	284692	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)OC)OC	622.70	unknown	via CMAUP database
CID 417377	417377	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)OC)OC	652.80	unknown	via CMAUP database
CID 5458555	5458555	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC	608.70	unknown	via CMAUP database
Homoaromoline	99620	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)O)OC	608.70	unknown	via CMAUP database
Obaberine	100231	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)OC)OC	622.70	unknown	via CMAUP database
Obamegine	441064	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)O)OC	594.70	unknown	via CMAUP database
Repandine	10031631	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC	608.70	unknown	via CMAUP database
Thalmidine	100230	Click to see CN1CCC2=CC3=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC	622.70	unknown	https://doi.org/10.1300/J157V02N02_01
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1S,9R,10R,16R)-14,16-dimethyl-6,14-diazatetracyclo[7.5.3.01,10.02,7]heptadec-2(7)-en-5-one	6916253	Click to see CC1CC2CC3=C(CCC(=O)N3)C4(C1)C2CCCN4C	274.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids / Limonoids
Limonin	179651	Click to see CC1(C2CC(=O)C3(C(C24COC(=O)CC4O1)CCC5(C36C(O6)C(=O)OC5C7=COC=C7)C)C)C	470.50	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans
(3R,4aR)-8-hydroxy-3-methyl-3,4,4a,5,6,7-hexahydroisochromen-1-one	98512254	Click to see CC1CC2CCCC(=C2C(=O)O1)O	182.22	unknown	via CMAUP database
6-Hydroxyramulosin	54707040	Click to see CC1CC2CC(CC(=C2C(=O)O1)O)O	198.22	unknown	via CMAUP database
Ramulosin	54686269	Click to see CC1CC2CCCC(=C2C(=O)O1)O	182.22	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Thalirabine	181902	Click to see CN1CCC2=C(C3=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C(=C7CC[N+]6(C)C)O)OC)OC)OC)OCO3)OC	683.80	unknown	via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one	10065647	Click to see COC1=C(C2=CN3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)OC)OC	337.40	unknown	https://doi.org/10.1300/J157V02N02_01
> Phenylpropanoids and polyketides / Depsides and depsidones
Thamnolic acid	4316933	Click to see CC1=CC(=C(C(=C1C(=O)OC2=C(C(=C(C(=C2C)C(=O)O)O)C=O)O)O)C(=O)O)OC	420.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Oxyayanin A	5281676	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC)C3=CC(=C(C=C3O)OC)O)O	360.30	unknown	via CMAUP database

Biological Material Top

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Thalictrum lucidum

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