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Thalictrum glandulosissimum

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 UUID64404d3c7a91b791468230
Scientific name Thalictrum glandulosissimum
Authority (Finet & Gagnep.) W.T.Wang & S.H.Wang
First published in Fl. Reipubl. Popularis Sin. 26: 567 (1979)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Thalictrum foetidum var. glandulosissmum Finet & Gagnep. Bull. Soc. Bot. France 50: 619 1903

Common names Top

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Language Common/alternative name
Chinese 马尾连
Chinese 金丝马尾连

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Thalictrum glandulosissimum var. chaotungense W.T.Wang & S.H.Wang Fl. Reipubl. Popularis Sin. 26: 569 (1979)

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-0001130471
Tropicos 27105247
KEW urn:lsid:ipni.org:names:714461-1
The Plant List tro-27105247
Open Tree Of Life 5728052
IPNI 714461-1
GBIF 7277885
EOL 2873981
USDA GRIN 410485
CMAUP NPO15847

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 glandulosissimum. Lou ZC, Gao CY, Lin FT, Zhang J, Lin MC, Sharaf M, Wong LK, Slatkin DJ, Schiff PL Jr Planta Med 01-Feb-1992
doi:10.1055/S-2006-961407
PMID:1620736
Quaternary Alkaloids of Thalictrum glandulosissimum. Lou ZC, Gao CY, Lin FT, Lin MC, Zhang J, Slatkin DJ, Schiff PL Jr Planta Med 01-Oct-1987
doi:10.1055/S-2006-962784
PMID:17269078

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
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1055/S-2006-962784
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
16-Methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaen-17-olate 10426199 Click to see 321.30 unknown https://doi.org/10.1055/S-2006-962784
16,17-Dimethoxy-6-tritio-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaene 10246509 Click to see 338.40 unknown via CMAUP database
Berberine 2353 Click to see 336.40 unknown https://doi.org/10.1055/S-2006-962784
Columbamine 72310 Click to see 338.40 unknown https://doi.org/10.1055/S-2006-962784
Coptisine 72322 Click to see C1C[N+]2=C(C=C3C=CC4=C(C3=C2)OCO4)C5=CC6=C(C=C51)OCO6 320.30 unknown https://doi.org/10.1055/S-2006-962784
Jatrorrhizine 72323 Click to see 338.40 unknown via CMAUP database
Jatrorrhizine 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
Palmatine 19009 Click to see 352.40 unknown https://doi.org/10.1055/S-2006-962784
Thalifendine 3084288 Click to see 322.30 unknown https://doi.org/10.1055/S-2006-962784
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine 98570 Click to see 369.40 unknown via CMAUP database
Pseudoprotopine 185559 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=CC5=C(C=C4C1)OCO5)OCO3 353.40 unknown via CMAUP database
> Lignans, neolignans and related compounds
(1S,14S)-20,21,25-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-6-ol 10031631 Click to see 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 638.70 unknown via CMAUP database
1-Isotetrandrine 5351212 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC 622.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Diarylethers
21,22,26-Trimethoxy-16,31-dimethyl-8,24-dioxa-16,31-diazaheptacyclo[23.6.2.13,7.19,13.115,19.028,32.023,34]hexatriaconta-3(36),4,6,9,11,13(35),19,21,23(34),25,27,32-dodecaen-10-ol 45356938 Click to see 608.70 unknown via CMAUP database
> Organoheterocyclic compounds / Benzodioxoles
11,12-Dimethoxy-6,8,9,15-tetrahydro[1,3]benzodioxolo[4,5-c]benzo[g]azecin-14(7H)-one 371229 Click to see COC1=C(C=C2C(=C1)CCNCC3=C(CC2=O)C=CC4=C3OCO4)OC 355.40 unknown via CMAUP database
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
16-Methoxy-5,7-dioxa-1-azapentacyclo[11.8.0.03,11.04,8.014,19]henicosa-2,4(8),9,11,13,15,18-heptaen-17-one 11723579 Click to see COC1=CC2=C3C=C4C=CC5=C(C4=CN3CCC2=CC1=O)OCO5 321.30 unknown https://doi.org/10.1055/S-2006-962784
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 10065647 Click to see 337.40 unknown https://doi.org/10.1055/S-2006-962784
> Phenylpropanoids and polyketides / Tannins
Hernandezine (7CI, 8CI) 362567 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)OC)OC)OC 652.80 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Gomisin A 68781 Click to see CC1CC2=CC3=C(C(=C2C4=C(C(=C(C=C4CC1(C)O)OC)OC)OC)OC)OCO3 416.50 unknown https://doi.org/10.1055/S-2006-961407

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