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Thalictrum revolutum

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Table of Contents

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 UUID64404d27c456c224050323
Scientific name Thalictrum revolutum
Authority DC.
First published in Syst. Nat. 1: 173 (1817)

Description Top

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Synonyms Top

Scientific name Authority First published in
Thalictrum praealtum Greene Leafl. Bot. Observ. Crit. 2: 89 (1910)
Thalictrum amabile Greene Amer. Midl. Naturalist 2: 294 (1912)
Thalictrum amphibolum Greene Repert. Spec. Nov. Regni Veg. 7: 255 (1909)
Thalictrum moseleyi Greene Amer. Midl. Naturalist 2: 294 (1912)
Thalictrum revolutum var. glandulosior B.Boivin Amer. Midl. Naturalist 60: 255 (1958)
Thalictrum revolutum var. subglabrum DC. Syst. Nat. 1: 173 (1817)

Common names Top

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Language Common/alternative name
English waxyleaf meadow-rue

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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Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Sow at 4°C for 3 weeks, then increase to 20°C.
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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001129472
Florida Plant Atlas 3973
Flora of Alabama 3081
Canadensys 8576
USDA Plants THRE
Tropicos 27100852
KEW urn:lsid:ipni.org:names:714816-1
The Plant List tro-27100852
Open Tree Of Life 421843
NCBI Taxonomy 46972
Nature Serve 2.152762
IPNI 714816-1
iNaturalist 143040
GBIF 3033127
WisFlora 5218
EPPO THCRE
EOL 594415
USDA GRIN 36451

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
8-, 9-, and 11-Aryloxy Dimeric Aporphines and Their Pharmacological Activities Ali G, Cuny GD Molecules 27-Jul-2021
PMCID:PMC8347945
doi:10.3390/molecules26154521
PMID:34361671
Diversity in Chemical Structures and Biological Properties of Plant Alkaloids Bhambhani S, Kondhare KR, Giri AP Molecules 03-Jun-2021
PMCID:PMC8199754
doi:10.3390/molecules26113374
PMID:34204857
Ethnobotanical survey of the medicinal flora of Harighal, Azad Jammu & Kashmir, Pakistan Amjad MS, Zahoor U, Bussmann RW, Altaf M, Gardazi SM, Abbasi AM J Ethnobiol Ethnomed 27-Oct-2020
PMCID:PMC7590686
doi:10.1186/s13002-020-00417-w
PMID:33109243
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
In vitro anti-proliferative activity of Argemone gracilenta and identification of some active components Leyva-Peralta MA, Robles-Zepeda RE, Garibay-Escobar A, Ruiz-Bustos E, Alvarez-Berber LP, Gálvez-Ruiz JC BMC Complement Altern Med 05-Feb-2015
PMCID:PMC4321710
doi:10.1186/s12906-015-0532-8
PMID:25652581
Alkaloids of Thalictrum. XIX. Revolutopine and Thelipine, New Arophinebenzylisoquinoline Dimers from Thalictrum revolutum Raymond W. Doskotch, Jinn Wu, Jack L. Beal, Wu-Nan Wu, Raymond W. Deskotch The Japan Institute of Heterocyclic Chemistry 05-Mar-2009
doi:10.3987/R-1977-04-0405
The Isoquinolone Alkaloids Barry D. Krane, Maurice Shamma American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50022A001
Alkaloids of Thalictrum XXXV. Northalicarpine, A New Aporphine-Benzylisoquinoline Dimer, N-Methyllaurotetanine and Thalflavidine From the Roots of Thalictrum revolutum Wu-Nan Wu, Jack L. Beal, Raymond W. Doskotch American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50011A006
Fatty Acids of Thalictrum revolutum Fruit Lipid Jinn Wu, Amitabha Ghosh, Jack L. Beal American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50009A007
Alkaloids of Thalictrum. XXXII. Isolation and Identification of Alkaloids From Thalictrum revolutum DC. Fruit Jinn Wu, Jack L. Beal, Wu-Nan Wu, Raymond W. Doskotch American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50008A005
Alkaloids of thalictrum—XXIII W.-N. Wu, J.L. Beal, R.W. Doskotch Elsevier BV 25-Jul-2002
doi:10.1016/0040-4020(77)88023-X

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
Thalflavidine 181848 Click to see CN(C)CCC1=C2C=CC3=CC4=C(C5=C3C2=C(C(=C1OC)OC)OC5=O)OCO4 395.40 unknown https://doi.org/10.1021/NP50011A006
Thaliglucinone 182266 Click to see CN(C)CCC1=CC(=C2C3=C1C=CC4=CC5=C(C(=C43)C(=O)O2)OCO5)OC 365.40 unknown https://doi.org/10.1021/NP50011A006
> Alkaloids and derivatives / Aporphines
(1S)-1-[[2-[[(6aS)-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-yl]oxy]-4-hydroxy-3-methoxyphenyl]methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-ol 163039035 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=C(C=CC(=C5OC)O)CC6C7=CC(=C(C=C7CCN6C)OC)O)OC)OC 668.80 unknown https://doi.org/10.3987/R-1977-04-0405
(1S)-1-[[2-[[(6aS)-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-yl]oxy]-4,5-dimethoxyphenyl]methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 102278103 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=CC(=C(C=C5CC6C7=CC(=C(C=C7CCN6C)O)OC)OC)OC)OC)OC 682.80 unknown https://doi.org/10.1016/0040-4020(77)88023-X
(6aS)-9-[2-[[(1S)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-4,5-dimethoxyphenoxy]-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-3-ol 21763780 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2O)OC)OC)OC)OC5=CC(=C(C=C5CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC 712.80 unknown https://doi.org/10.1016/0040-4020(77)88023-X
(6aS)-9-[6-[[(1S)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2,3-dimethoxyphenoxy]-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline 102077163 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=C(C=CC(=C5OC)OC)CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC 696.80 unknown https://doi.org/10.1016/0040-4020(77)88023-X
1-[[4-hydroxy-3-methoxy-2-[(1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-yl)oxy]phenyl]methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-ol 163039034 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=C(C=CC(=C5OC)O)CC6C7=CC(=C(C=C7CCN6C)OC)O)OC)OC 668.80 unknown https://doi.org/10.3987/R-1977-04-0405
1-[[4,5-dimethoxy-2-[(1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-yl)oxy]phenyl]methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 163014017 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=CC(=C(C=C5CC6C7=CC(=C(C=C7CCN6C)O)OC)OC)OC)OC)OC 682.80 unknown https://doi.org/10.1016/0040-4020(77)88023-X
1-[[5-hydroxy-4-methoxy-2-[(1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-yl)oxy]phenyl]methyl]-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-7-ol 14379242 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=CC(=C(C=C5CC6C7=CC(=C(C=C7CCN6C)OC)O)O)OC)OC)OC 668.80 unknown https://doi.org/10.3987/R-1977-04-0405
3-[[(6aS)-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-yl]oxy]-4-[[(1S)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2-methoxyphenol 102278071 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=C(C=CC(=C5OC)O)CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC 682.80 unknown https://doi.org/10.1016/0040-4020(77)88023-X
4-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]-2-methoxy-3-[(1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-yl)oxy]phenol 162910877 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=C(C=CC(=C5OC)O)CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC 682.80 unknown https://doi.org/10.1016/0040-4020(77)88023-X
7-Isoquinolinol, 1,2,3,4-tetrahydro-1-((5-hydroxy-4-methoxy-2-((5,6,6a,7-tetrahydro-1,2,10-trimethoxy-6-methyl-4H-dibenzo(de,g)quinolin-9-yl)oxy)phenyl)methyl)-6-methoxy-2-methyl-, (S-(R*,R*))- 3085252 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=CC(=C(C=C5CC6C7=CC(=C(C=C7CCN6C)OC)O)O)OC)OC)OC 668.80 unknown https://doi.org/10.3987/R-1977-04-0405
https://doi.org/10.1021/NP50008A005
9-[2-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]-4,5-dimethoxyphenoxy]-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-3-ol 73832276 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2O)OC)OC)OC)OC5=CC(=C(C=C5CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC 712.80 unknown https://doi.org/10.1016/0040-4020(77)88023-X
9-{6-[(6,7-dimethoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-1-yl)methyl]-2,3-dimethoxyphenoxy}-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline 4365802 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=C(C=CC(=C5OC)OC)CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC 696.80 unknown https://doi.org/10.1016/0040-4020(77)88023-X
Boldine 2-methyl ether 16573 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC 341.40 unknown https://doi.org/10.1021/NP50011A006
Northalicarpine 185830 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=CC(=C(C=C5CC6C7=CC(=C(C=C7CCN6)OC)OC)OC)OC)OC)OC 682.80 unknown https://doi.org/10.1021/NP50011A006
Thalicarpine 21470 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=CC(=C(C=C5CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC)OC)OC 696.80 unknown https://doi.org/10.1021/NP50008A005
Thalmelatine 133562520 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC5=CC(=C(C=C5CC6C7=CC(=C(C=C7CCN6C)OC)O)OC)OC)OC)OC 682.80 unknown https://doi.org/10.1021/NP50008A005
> Alkaloids and derivatives / Pavine alkaloids
(1S,9S)-4,12,13-trimethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2(7),3,5,10,12,14-hexaen-3-ol 162851662 Click to see CN1C2CC3=C(C1CC4=CC(=C(C=C24)OC)OC)C(=C(C=C3)OC)O 341.40 unknown https://doi.org/10.1021/NP50008A005
(1S)-4,5,12,13-tetramethoxy-17-methyl-17-azatetracyclo[7.7.1.02,7.010,15]heptadeca-2,4,6,10,12,14-hexaene 44558920 Click to see CN1C2CC3=CC(=C(C=C3C1CC4=CC(=C(C=C24)OC)OC)OC)OC 355.40 unknown https://doi.org/10.1021/NP50008A005
Eschscholtzidine 442222 Click to see CN1C2CC3=CC4=C(C=C3C1CC5=CC(=C(C=C25)OC)OC)OCO4 339.40 unknown https://doi.org/10.1021/NP50008A005
Platycerine 12314368 Click to see CN1C2CC3=C(C1CC4=CC(=C(C=C24)OC)OC)C(=C(C=C3)OC)O 341.40 unknown https://doi.org/10.1021/NP50008A005
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
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/NP50008A005
> Alkaloids and derivatives / Protopine alkaloids
Allocryptopine 98570 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C(=C(C=C4)OC)OC)OCO3 369.40 unknown https://doi.org/10.1021/NP50008A005
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown https://doi.org/10.1021/NP50008A005
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Myristic Acid 11005 Click to see CCCCCCCCCCCCCC(=O)O 228.37 unknown https://doi.org/10.1021/NP50009A007
Stearic Acid 5281 Click to see CCCCCCCCCCCCCCCCCC(=O)O 284.50 unknown https://doi.org/10.1021/NP50009A007
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Linoleic Acid 5280450 Click to see CCCCCC=CCC=CCCCCCCCC(=O)O 280.40 unknown https://doi.org/10.1021/NP50009A007
Linolenic Acid 5280934 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1021/NP50009A007
Octadeca-9,12,15-trienoic acid 5282822 Click to see CCC=CCC=CCC=CCCCCCCCC(=O)O 278.40 unknown https://doi.org/10.1021/NP50009A007
> Organic nitrogen compounds / Organonitrogen compounds / Quaternary ammonium salts / Cholines
Choline 305 Click to see C[N+](C)(C)CCO 104.17 unknown https://doi.org/10.1021/NP50008A005
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
4-[(6,7-dimethoxy-2,2-dimethyl-3,4-dihydro-1H-isoquinolin-2-ium-1-yl)methyl]phenol 2752261 Click to see C[N+]1(CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC)OC)C 328.40 unknown https://doi.org/10.1021/NP50008A005
4-[5-[[(1S)-6,7-dimethoxy-8-[(7-methoxy-2-methyl-1-oxo-3,4-dihydroisoquinolin-6-yl)oxy]-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2-methoxyphenoxy]benzaldehyde 102401953 Click to see CN1CCC2=CC(=C(C(=C2C1CC3=CC(=C(C=C3)OC)OC4=CC=C(C=C4)C=O)OC5=C(C=C6C(=C5)CCN(C6=O)C)OC)OC)OC 652.70 unknown https://doi.org/10.1021/NP50022A001
https://doi.org/10.1021/NP50008A005
N-Methylcoclaurine 2752274 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://doi.org/10.1021/NP50008A005
> 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/NP50011A006
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/NP50011A006

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