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Thalictrum orientale

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ffe88906f5992506615
Scientific name Thalictrum orientale
Authority Boiss.
First published in Ann. Sci. Nat., Bot. , sér. 2, 16: 349 (1841)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Isopyrum aquilegioides Bory & Chaub. Exp. Sci. Morée, Bot. : 35 (1832)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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-0000454017
Tropicos 100350663
KEW urn:lsid:ipni.org:names:714697-1
The Plant List kew-2512604
Open Tree Of Life 6133349
Observations.org 136734
IPNI 714697-1
GBIF 3926798
EPPO THCOR
Elurikkus 441005

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)!
Title Authors Publication Released IDs
Alkaloids of thalictrum orientale growing in Turkey F. Z. Erdemgil, M. V. Telezhenetskaya, K. H. C. Baser, N. Kirimer Springer Science and Business Media LLC 21-Oct-2005
doi:10.1007/BF02236440
Thalictricoside, a new phenolic compound from Thalictrum orientale. Erdemgil FZ, Baser KH, Akbay P, Sticher O, Calis I Z Naturforsch C J Biosci 01-Sep-2003
doi:10.1515/ZNC-2003-9-1005
PMID:14577621

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
> Alkaloids and derivatives / Aporphines
(6aR)-1,2-dimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-10,11-diol 163190058 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)O)O)OC)OC)C 342.40 unknown https://doi.org/10.1007/BF02236440
(6aS)-10-hydroxy-1,2-dimethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium-11-olate 163194783 Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)O)[O-])OC)OC)C 341.40 unknown https://doi.org/10.1007/BF02236440
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see 336.40 unknown https://doi.org/10.1007/BF02236440
> Lignans, neolignans and related compounds
(1R,14S)-9,20,25-Trimethoxy-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),18,20,22(33),24,26,31-dodecaen-21-ol 5458555 Click to see 608.70 unknown https://doi.org/10.1007/BF02236440
Fangchinoline 73481 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 https://doi.org/10.1007/BF02236440
Isofangchinoline 321937 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 https://doi.org/10.1007/BF02236440
Thalrugosine, (+)- 100257 Click to see 608.70 unknown https://doi.org/10.1007/BF02236440
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
Lithospermoside 10065132 Click to see C1=CC(=CC#N)C(C(C1O)O)OC2C(C(C(C(O2)CO)O)O)O 329.30 unknown https://doi.org/10.1515/ZNC-2003-9-1005
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Thalictricoside 45359754 Click to see 461.40 unknown https://doi.org/10.1515/ZNC-2003-9-1005

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