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Thalictrum sachalinense

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 UUID64404d2bb0115822632035
Scientific name Thalictrum sachalinense
Authority Lecoy.
First published in Bull. Soc. Roy. Bot. Belgique 24: 152 (1885)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Thalictrum spirostigmum Nakai Bot. Mag. (Tokyo) 33: 51 (1919)
Thalictrum akanense Huth Bull. Herb. Boissier 5: 1069 (1897)
Thalictrum neosachalinense H.Lév. Repert. Spec. Nov. Regni Veg. 7: 101 (1909)

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
  • Asia-temperate
    • Eastern Asia
      • Japan
      • Korea
    • Russian Far East
      • Kuril Islands
      • Sakhalin

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001129816
Tropicos 27102000
KEW urn:lsid:ipni.org:names:714849-1
The Plant List tro-27102000
Open Tree Of Life 338815
Observations.org 142167
NCBI Taxonomy 1264570
IPNI 714849-1
GBIF 3925470
Elurikkus 440656

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)!
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Title Authors Publication Released IDs
Alkaloids ofThalictrum sachalinense. V D. Umarova, S. Kh. Maekh, S. Yu. Yunusov, N. M. Zaitseva, S. A. Volkova, P. G. Gorovoi Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567144
Alkaloids of Thalictrum. X. Two new alkaloids from T. minus var. adiantifolium: noroxyhydrastinine and thalifoline. Doskotch RW, Schiff PL Jr, Beal JL Tetrahedron 01-Jan-1970
doi:10.1016/S0040-4020(01)82640-5
PMID:5351614

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
Nantenine 197001 Click to see 339.40 unknown https://doi.org/10.1016/S0040-4020(01)82640-5
> 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/10.1016/S0040-4020(01)82640-5
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/BF00567144
Thalrugosine, (+)- 100257 Click to see 608.70 unknown https://doi.org/10.1007/BF00567144

Gallery Top

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Collections Top

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