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Thalictrum javanicum

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Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
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Details Top

Internal ID UUID64404d298d511671047048
Scientific name Thalictrum javanicum
Authority Blume
First published in Bijdr. Fl. Ned. Ind. : 2 (1825)

Description Top

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Synonyms Top

Scientific name Authority First published in
Thalictrum argyi H.Lév. & Vaniot Bull. Herb. Boissier , sér. 2, 6: 504 (1906)
Thalictrum glyphocarpum Wight & Arn. Prodr. Fl. Ind. Orient. : 2 (1834)

Common names Top

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Language Common/alternative name
Chinese 羊不食
Chinese 爪哇唐松草
Chinese 鹅整

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • China
      • China North-central
      • China South-central
      • China Southeast
      • Tibet
    • Eastern Asia
      • Taiwan
  • Asia-tropical
    • Indian Subcontinent
      • Assam
      • East Himalaya
      • India
      • Nepal
      • Sri Lanka
      • West Himalaya
    • Malesia
      • Jawa
      • Lesser Sunda Islands

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001129571
Tropicos 27101364
KEW urn:lsid:ipni.org:names:714529-1
The Plant List tro-27101364
Open Tree Of Life 124737
Observations.org 506065
NCBI Taxonomy 327930
IPNI 714529-1
GBIF 7277787
EOL 2873987
Elurikkus 581832
USDA GRIN 407420

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
Evaluation of Mosquito Repellent Activity of Isolated Oleic Acid, Eicosyl Ester from Thalictrum javanicum Gurunathan A, Senguttuvan J, Paulsamy S Indian J Pharm Sci 01-Jan-2016
PMCID:PMC4852559
doi:10.4103/0250-474x.180259
PMID:27168688
Zygomorphy evolved from disymmetry in Fumarioideae (Papaveraceae, Ranunculales): new evidence from an expanded molecular phylogenetic framework Sauquet H, Carrive L, Poullain N, Sannier J, Damerval C, Nadot S Ann Bot 26-Mar-2015
PMCID:PMC4407061
doi:10.1093/aob/mcv020
PMID:25814061
Dioxygenases Catalyze O-Demethylation and O,O-Demethylenation with Widespread Roles in Benzylisoquinoline Alkaloid Metabolism in Opium Poppy Farrow SC, Facchini PJ J Biol Chem 08-Aug-2013
PMCID:PMC3789997
doi:10.1074/jbc.M113.488585
PMID:23928311
Thalocsessine, a New C20-Diterpenoid Alkaloid from Thalictrum sessile Hayata Yang-Chang Wu, Tian-Shung Wu, Masataka Niwa, Sheng-Teh Lu, Yoshimasa Hirata The Japan Institute of Heterocyclic Chemistry 16-Feb-2009
doi:10.3987/R-1987-04-0943
Additional Alkaloids of Thalictrum javanicum Mahendra Sahai, S. C. Sinha, Anil B. Ray, Sunil K. Chattopadhyay, Suleiman Al-Khalil, David J. Slatkin, Paul L. Schiff American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50040A033
Studies on Native Medicinal Plants, I. The Quaternary Alkaloids of Thalictrum javanicum Surendra Bahadur, Arun K. Shukla American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50028A002
Alkaloids of formosan Thalictrum sessile Yang-Chang Wu, Tian-Shung Wu, Masatake Niwa, Sheng-Teh Lu, Yoshimasa Hirata Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)83052-8
Cytotoxic aporphinoid alkaloids from thalictrum sessile Yang-Chang Wu, Sheng-Teh Lu, Jer-Jang Changi, Kuo-Hsiung Lee Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(88)80247-4

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
(1S)-1-[[4-[[(6aR)-1,2,3,9,10-pentamethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-8-yl]oxy]phenyl]methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 13892257 Click to see CN1CCC2=C3C1CC4=C(C(=C(C=C4C3=C(C(=C2OC)OC)OC)OC)OC)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)O)OC 682.80 unknown https://doi.org/10.1016/0031-9422(88)83052-8
7-methoxy-2-methyl-1-[[4-[(1,2,3,9,10-pentamethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-8-yl)oxy]phenyl]methyl]-3,4-dihydro-1H-isoquinolin-6-ol 13892256 Click to see CN1CCC2=C3C1CC4=C(C(=C(C=C4C3=C(C(=C2OC)OC)OC)OC)OC)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)O)OC 682.80 unknown https://doi.org/10.1016/0031-9422(88)80247-4
https://doi.org/10.1016/0031-9422(88)83052-8
Liriodenine 10144 Click to see C1OC2=C(O1)C3=C4C(=C2)C=CN=C4C(=O)C5=CC=CC=C53 275.26 unknown https://doi.org/10.1016/0031-9422(88)80247-4
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/10.1021/NP50028A002
https://doi.org/10.1016/0031-9422(88)83052-8
> 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 COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)[O-] 321.30 unknown https://doi.org/10.1021/NP50040A033
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/10.1021/NP50040A033
https://doi.org/10.1016/0031-9422(88)83052-8
https://doi.org/10.1021/NP50028A002
Columbamine 72310 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)O)OC 338.40 unknown https://doi.org/10.1021/NP50028A002
Palmatine 19009 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)OC 352.40 unknown https://doi.org/10.1021/NP50028A002
Thalifendine 3084288 Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)O 322.30 unknown https://doi.org/10.1021/NP50040A033
> Lignans, neolignans and related compounds
Talysopine 179390 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)O)C=C5)OC 638.70 unknown https://doi.org/10.1021/NP50040A033
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids
(1R,5R,6R,11R,12S,14S,17R,20S,21S)-21-hydroxy-5,15-dimethyl-7-oxa-10-azaheptacyclo[12.6.2.01,11.05,20.06,10.012,17.017,21]docos-15-en-19-one 162929144 Click to see CC1=CC23CC(=O)C4C5(CCCC46C2(CC1CC3C6N7C5OCC7)O)C 355.50 unknown https://doi.org/10.1016/0031-9422(88)83052-8
(1R,5R,6S,11R,12S,14S,17S,20S,21S)-21-hydroxy-5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.01,11.05,20.06,10.012,17.017,21]docosan-19-one 162843954 Click to see CC12CCCC34C1C(=O)CC56C3(CC(CC5C4N7C2OCC7)C(=C)C6)O 355.50 unknown https://doi.org/10.1016/0031-9422(88)83052-8
(1S,5R,6S,11R,12S,14R,17S,20S,21R)-5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.01,11.05,20.06,10.012,17.017,21]docosane-19,22-dione 163006444 Click to see CC12CCCC34C1C(=O)CC56C3C(=O)C(CC5C4N7C2OCC7)C(=C)C6 353.50 unknown https://doi.org/10.1016/0031-9422(88)83052-8
(1S,5R,8R,9S,11R,14S,16R,17R,18R)-16-hydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.17,16.01,8.05,17.09,14.014,18]icosan-19-one 162930479 Click to see CC12CCCC34C1C5(CC67C3C(=O)C(CC6C4N(C2)C5)C(=C)C7)O 325.40 unknown https://doi.org/10.1016/0031-9422(88)83052-8
(1S,5R,8R,9S,11R,14S,17S,18R)-7-(2-hydroxyethyl)-5-methyl-12-methylidene-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadecane-6,16,19-trione 102482182 Click to see CC12CCCC34C1C(=O)CC56C3C(=O)C(CC5C4N(C2=O)CCO)C(=C)C6 369.50 unknown https://doi.org/10.3987/R-1987-04-0943
https://doi.org/10.1016/0031-9422(88)83052-8
(4-Hydroxy-4,12-dimethyl-14,19-dioxa-17-azaheptacyclo[10.7.2.22,5.02,7.08,18.08,21.013,17]tricosan-20-yl) acetate 14191508 Click to see CC(=O)OC1C2C3(CCCC24C5CC6CCC5(C1OC4N7C3OCC7)CC6(C)O)C 417.50 unknown https://doi.org/10.1016/0031-9422(88)83052-8
[(1R,2R,4S,5S,7S,8S,12S,13S,18S,20R,21S)-4-hydroxy-4,12-dimethyl-14,19-dioxa-17-azaheptacyclo[10.7.2.22,5.02,7.08,18.08,21.013,17]tricosan-20-yl] acetate 154497801 Click to see CC(=O)OC1C2C3(CCCC24C5CC6CCC5(C1OC4N7C3OCC7)CC6(C)O)C 417.50 unknown https://doi.org/10.1016/0031-9422(88)83052-8
[(1S,2R,4S,5S,7R,8R,12R,13S,18R,20S,21R)-4-hydroxy-4,12-dimethyl-14,19-dioxa-17-azaheptacyclo[10.7.2.22,5.02,7.08,18.08,21.013,17]tricosan-20-yl] acetate 163013941 Click to see CC(=O)OC1C2C3(CCCC24C5CC6CCC5(C1OC4N7C3OCC7)CC6(C)O)C 417.50 unknown https://doi.org/10.1016/0031-9422(88)83052-8
16-Hydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.17,16.01,8.05,17.09,14.014,18]icosan-19-one 162930478 Click to see CC12CCCC34C1C5(CC67C3C(=O)C(CC6C4N(C2)C5)C(=C)C7)O 325.40 unknown https://doi.org/10.1016/0031-9422(88)83052-8
21-Hydroxy-5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.01,11.05,20.06,10.012,17.017,21]docosan-19-one 14191513 Click to see CC12CCCC34C1C(=O)CC56C3(CC(CC5C4N7C2OCC7)C(=C)C6)O 355.50 unknown https://doi.org/10.1016/0031-9422(88)83052-8
21-Hydroxy-5-methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.01,11.05,20.06,10.012,17.017,21]docosane-19,22-dione 14191515 Click to see CC12CCCC34C1C(=O)CC56C3(C(=O)C(CC5C4N7C2OCC7)C(=C)C6)O 369.50 unknown https://doi.org/10.1016/0031-9422(88)83052-8
21-Hydroxy-5,15-dimethyl-7-oxa-10-azaheptacyclo[12.6.2.01,11.05,20.06,10.012,17.017,21]docos-15-en-19-one 4481793 Click to see CC1=CC23CC(=O)C4C5(CCCC46C2(CC1CC3C6N7C5OCC7)O)C 355.50 unknown https://doi.org/10.1016/0031-9422(88)83052-8
5-Methyl-15-methylidene-7-oxa-10-azaheptacyclo[12.6.2.01,11.05,20.06,10.012,17.017,21]docosane-19,22-dione 4481794 Click to see CC12CCCC34C1C(=O)CC56C3C(=O)C(CC5C4N7C2OCC7)C(=C)C6 353.50 unknown https://doi.org/10.1016/0031-9422(88)83052-8
7-(2-Hydroxyethyl)-5-methyl-12-methylidene-7-azahexacyclo[9.6.2.01,8.05,17.09,14.014,18]nonadecane-6,16,19-trione 4481795 Click to see CC12CCCC34C1C(=O)CC56C3C(=O)C(CC5C4N(C2=O)CCO)C(=C)C6 369.50 unknown https://doi.org/10.3987/R-1987-04-0943
https://doi.org/10.1016/0031-9422(88)83052-8
Spirasine I 11953913 Click to see CC1=CC23CC(=O)C4C5(CCCC46C2(CC1CC3C6N7C5OCC7)O)C 355.50 unknown https://doi.org/10.1016/0031-9422(88)83052-8
Spiredine 11953914 Click to see CC12CCCC34C1C(=O)CC56C3C(=O)C(CC5C4N7C2OCC7)C(=C)C6 353.50 unknown https://doi.org/10.1016/0031-9422(88)83052-8
Thalicsessine 441762 Click to see CC12CCCC34C1C(=O)CC56C3C(=O)C(CC5C4N(C2=O)CCO)C(=C)C6 369.50 unknown https://doi.org/10.3987/R-1987-04-0943
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Villanovane, atisane, trachylobane or helvifulvane diterpenoids / Atisane diterpenoids / Hetisine-type diterpenoid alkaloids
(1S,5R,8R,9S,11R,14S,16R,17R,18R)-16-hydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-19-one 154497495 Click to see CC12CCCC34C1C5(CC67C3C(=O)C(CC6C4N5C2)C(=C)C7)O 311.40 unknown https://doi.org/10.3987/R-1987-04-0943
16-Hydroxy-5-methyl-12-methylidene-7-azaheptacyclo[9.6.2.01,8.05,17.07,16.09,14.014,18]nonadecan-19-one 4481792 Click to see CC12CCCC34C1C5(CC67C3C(=O)C(CC6C4N5C2)C(=C)C7)O 311.40 unknown https://doi.org/10.3987/R-1987-04-0943
Spiradine A 441756 Click to see CC12CCCC34C1C5(CC67C3C(=O)C(CC6C4N5C2)C(=C)C7)O 311.40 unknown https://doi.org/10.3987/R-1987-04-0943
https://doi.org/10.1016/0031-9422(88)83052-8
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2-Hydroxy-9,10-dimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 101404950 Click to see COC1=C(C2=CN3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)O)OC 323.30 unknown https://doi.org/10.1021/NP50028A002
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/10.1021/NP50028A002
Oxyberberine 11066 Click to see COC1=C(C2=C(C=C1)C=C3C4=CC5=C(C=C4CCN3C2=O)OCO5)OC 351.40 unknown https://doi.org/10.1021/NP50040A033
> Phenylpropanoids and polyketides / Tannins
(-)-Thalrugosaminine 5321919 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)OC)C=C5)OC 652.80 unknown https://doi.org/10.1021/NP50040A033
Thalrugosaminine 321938 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)OC)C=C5)OC 652.80 unknown https://doi.org/10.1021/NP50040A033

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