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Thalictrum sultanabadense

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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
Contributors
Collections

Details Top

Internal ID UUID643ffe8c00b18307524283
Scientific name Thalictrum sultanabadense
Authority Stapf
First published in Verh. K. K. Zool.-Bot. Ges. Wien 38: 550 (1888)

Description Top

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Synonyms Top

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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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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
    • Caucasus
      • Transcaucasus
    • Middle Asia
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Iran
      • Iraq
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000454187
Tropicos 27102838
KEW urn:lsid:ipni.org:names:714928-1
Open Tree Of Life 6133383
Observations.org 146646
IPNI 714928-1
iNaturalist 558679
GBIF 3924711
Elurikkus 440496

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 Anatolian Thalictrum sultanabadense Kemal Hüsnü Can Baser, Muzaffer Ögütveren, Norman G. Bisset American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50040A036
Bisbenzylisoquinoline alkaloids ofThalictrum sultanabadense S. Mukhamedova, S. Kh. Maekh, A. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00575784
alkaloids of Thalictrum sultanabadense S. Abdizhabbarova, S. Kh. Maekh, S. Yu. Yunusov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565898

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
> Lignans, neolignans and related compounds
(12R,25R)-4,5,20,31-tetramethoxy-11,26-dimethyl-2,18-dioxa-11,26-diazaheptacyclo[23.6.2.214,17.119,23.03,8.07,12.029,33]hexatriaconta-1(31),3(8),4,6,14(36),15,17(35),19,21,23(34),29,32-dodecaene 162925359 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)OC 622.70 unknown https://doi.org/10.1007/BF00575784
(12S,25R)-4,5,31-trimethoxy-11,26-dimethyl-2,18-dioxa-11,26-diazaheptacyclo[23.6.2.214,17.119,23.03,8.07,12.029,33]hexatriaconta-1(31),3(8),4,6,14(36),15,17(35),19,21,23(34),29,32-dodecaen-20-ol 163187249 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)OC 608.70 unknown https://doi.org/10.1007/BF00575784
4,5,20,31-Tetramethoxy-11,26-dimethyl-2,18-dioxa-11,26-diazaheptacyclo[23.6.2.214,17.119,23.03,8.07,12.029,33]hexatriaconta-1(31),3(8),4,6,14(36),15,17(35),19,21,23(34),29,32-dodecaene 12312821 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)OC 622.70 unknown https://doi.org/10.1007/BF00575784
4,5,31-Trimethoxy-11,26-dimethyl-2,18-dioxa-11,26-diazaheptacyclo[23.6.2.214,17.119,23.03,8.07,12.029,33]hexatriaconta-1(31),3(8),4,6,14(36),15,17(35),19,21,23(34),29,32-dodecaen-20-ol 13892243 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)OC 608.70 unknown https://doi.org/10.1007/BF00575784
Thalbadensine 181849 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)O)OC)C=C5)OC 594.70 unknown https://doi.org/10.1021/NP50040A036
https://doi.org/10.1007/BF00565898
https://doi.org/10.1007/BF00575784
Thalictine 181168 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)OC 608.70 unknown https://doi.org/10.1021/NP50040A036
https://doi.org/10.1007/BF00575784
Thalidezine 320711 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)O)OC)OC 638.70 unknown https://doi.org/10.1007/BF00575784
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
Thalifoline 89048 Click to see CN1CCC2=CC(=C(C=C2C1=O)O)OC 207.23 unknown https://doi.org/10.1021/NP50040A036
> Phenylpropanoids and polyketides / Tannins
Hernandezine 72343 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 https://doi.org/10.1021/NP50040A036
https://doi.org/10.1007/BF00565898
https://doi.org/10.1007/BF00575784

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