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Thalictrum isopyroides

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 UUID64404d2fba888894597574
Scientific name Thalictrum isopyroides
Authority C.A.Mey.
First published in Fl. Altaic. 2: 346 (1830)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
English dwarf meadow rue
English dwarf meadow-rue
English isopyrum-like meadow rue
English isopyrum-like meadow-rue
Armenian Քնձմնձուկ իզոպիրոնման
Chinese 紫堇叶唐松草

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.
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

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001130018
Tropicos 27102820
KEW urn:lsid:ipni.org:names:714523-1
The Plant List tro-27102820
Open Tree Of Life 98291
Observations.org 129500
NCBI Taxonomy 1084678
IPNI 714523-1
iNaturalist 493058
GBIF 3928466
EOL 2873986
Elurikkus 441462
Wikipedia Thalictrum_isopyroides

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
Phytochemicals as Invaluable Sources of Potent Antimicrobial Agents to Combat Antibiotic Resistance Jadimurthy R, Jagadish S, Nayak SC, Kumar S, Mohan CD, Rangappa KS Life (Basel) 04-Apr-2023
PMCID:PMC10145550
doi:10.3390/life13040948
PMID:37109477
A Review of Medicinal Plants with Renoprotective Activity in Diabetic Nephropathy Animal Models Putra IM, Fakhrudin N, Nurrochmad A, Wahyuono S Life (Basel) 16-Feb-2023
PMCID:PMC9963806
doi:10.3390/life13020560
PMID:36836916
The Analgesic Properties of Corydalis yanhusuo Alhassen L, Dabbous T, Ha A, Dang LH, Civelli O Molecules 10-Dec-2021
PMCID:PMC8704877
doi:10.3390/molecules26247498
PMID:34946576
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
The alkaloids ofThalictrum isopyroides. Structure of thalisopine Kh. G. Pulatova, S. Kh. Maekh, Z. F. Ismailov, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00569839
Alkaloids ofThalictrum isopyroides S. Abduzhabbarova, S. Kh. Maekh, S. Yu. Yunusov, M. R. Yagudaev, D. Kurbakov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565243
Alkaloids of Jordanian Thalictrum isopyroides Suleiman Al-Khalil, Paul L. Schiff Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(86)80030-9

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 / Aporphines
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
(12S)-7,17-dimethoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),14,16,18-hexaen-16-ol 155806685 Click to see 355.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
(6aR)-1,2,3,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-ol 7786052 Click to see 371.40 unknown https://doi.org/10.1007/BF00565243
(6aS)-1,2,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-3,9-diol 162985663 Click to see 357.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
(6As)-2,9,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol 6992288 Click to see 341.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
1-Hydroxy-2,3,9,10-tetramethoxyaporphine 12305718 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)O)OC)OC 371.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
1,2,10-Trimethoxy-3,9-dihydroxy-aporphine 21769949 Click to see 357.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
2,10-Dimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline-1,9-diol 98369 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)O)OC 327.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
7,17-Dimethoxy-11-methyl-3,5-dioxa-11-azapentacyclo[10.7.1.02,6.08,20.014,19]icosa-1,6,8(20),14,16,18-hexaen-16-ol 162927817 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C5C(=C2OC)OCO5)OC)O 355.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
9-Hydroxy-1,2,3,10-tetramethoxyaporphine 3905924 Click to see 371.40 unknown https://doi.org/10.1007/BF00565243
Dehydroocoteine 21769946 Click to see 367.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
Isoboldine 133323 Click to see 327.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
N-Methyllaurotetanine 16573 Click to see 341.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
N-Methyllaurotetanine; NSC 247506; NSC 247564 631015 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)O)OC)OC 341.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
Ocotein 3083793 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C5C(=C2OC)OCO5)OC)OC 369.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
Ocoteine 52499 Click to see 369.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
Preocoteine 176968 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)O)OC)OC 371.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
Thalicminine 167534 Click to see 365.30 unknown https://doi.org/10.1016/0031-9422(86)80030-9
Thaliporphine 100020 Click to see 341.40 unknown https://doi.org/10.1016/0031-9422(86)80030-9
> Lignans, neolignans and related compounds
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(33),19,21,24,26,31-dodecaene-6,19-diol 163022622 Click to see 624.70 unknown https://doi.org/10.1016/0031-9422(86)80030-9
6,20,21,25-Tetramethoxy-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(33),19,21,24,26,31-dodecaen-19-ol 3696942 Click to see 638.70 unknown https://doi.org/10.1007/BF00569839
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/10.1007/BF00569839
Thalisopidine 76319466 Click to see 624.70 unknown https://doi.org/10.1016/0031-9422(86)80030-9
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
6,7-Dimethoxy-2-methylisoquinolin-1(2H)-one 11367984 Click to see 219.24 unknown https://doi.org/10.1007/BF00565243
> Phenylpropanoids and polyketides / Tannins
19,20,21,25-Tetramethoxy-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(33),19,21,24,26,31-dodecaen-6-ol 75051851 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)OC)C=C5)OC 638.70 unknown https://doi.org/10.1016/0031-9422(86)80030-9
Thaligosinine 44584028 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)OC)C=C5)OC 638.70 unknown https://doi.org/10.1016/0031-9422(86)80030-9

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