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Thalictrum baicalense

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 UUID64404d216b7c3857232378
Scientific name Thalictrum baicalense
Authority Turcz.
First published in Uebers. Thalictrum : 11 (1861)

Ethnobotanical Use Top

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General Uses Top

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Common products:
• Dried plant material for scientific reference collections and research herbaria; voucher specimens in botanical databases (e.g., eFloras, GBIF, iDigBio).

Industrial and craft applications:
• No documented industrial or craft applications identified.

Food and beverages (non-medicinal):
• No documented food or beverage uses identified.

Colorants and tanning:
• No documented colorant or tanning uses identified.

Wood and fiber:
• No documented timber or fiber applications identified.

Fragrance and cosmetics:
• No documented fragrance or cosmetic applications identified.

Properties relevant to use:
• Chemical profiling (e.g., isoquinoline alkaloids, flavonoids) has been performed for chemotaxonomy, but no use-specific properties are established.

Standards and regulation:
• No species-specific standards or regulatory frameworks identified.

Sustainability and sourcing:
• No sustainability or sourcing practices documented.

Synonyms Top

Scientific name Authority First published in
Thalictrum franchetii Huth Bull. Herb. Boissier 5: 1069 (1897)
Thalictrum giraldii Ulbr. Notizbl. Bot. Gart. Berlin-Dahlem 9: 224 (1925)

Common names Top

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Language Common/alternative name
Japanese ハルカラマツ
Japanese ニッコウカラマツ
Japanese ニッコウカラマツソウ
Chinese 马尾连
Chinese 马尾黄连
Chinese 西藏水黄连
Chinese 贝加尔唐松草

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

Forms (abbr. f.) Top

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No forms added yet.

Germination/Propagation Top

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Expose seeds to natural outdoor winter conditions for 3 months, then gradually increase light and temperature in the spring.
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
    • China
      • China North-central
      • China Southeast
      • Inner Mongolia
      • Manchuria
      • Qinghai
      • Tibet
    • Eastern Asia
      • Japan
      • Korea
    • Mongolia
      • Mongolia
    • Russian Far East
      • Amur
      • Khabarovsk
      • Primorye
    • Siberia
      • Buryatiya
      • Chita
      • Irkutsk
      • Krasnoyarsk
      • Tuva
      • Yakutskiya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001129324
Tropicos 27100516
KEW urn:lsid:ipni.org:names:714256-1
The Plant List tro-27100516
Open Tree Of Life 1045100
NCBI Taxonomy 1264565
IPNI 714256-1
GBIF 3930659
EOL 2873962

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
First study on in vitro antiviral and virucidal effects of flavonoids against feline infectious peritonitis virus at the early stage of infection Triratapiban C, Lueangaramkul V, Phecharat N, Pantanam A, Lekcharoensuk P, Theerawatanasirikul S Vet World 26-Mar-2023
PMCID:PMC10082729
doi:10.14202/vetworld.2023.618-630
PMID:37041840
Autophagy Induction by Scutellaria Flavones in Cancer: Recent Advances Tuli HS, Bhushan S, Kumar A, Aggarwal P, Sak K, Ramniwas S, Vashishth K, Behl T, Rana R, Haque S, Prieto MA Pharmaceuticals (Basel) 15-Feb-2023
PMCID:PMC9962484
doi:10.3390/ph16020302
PMID:37259445
Identification of bioactive components behind the antimicrobial activity of cow urine by peptide and metabolite profiling Kumar R, Kaushik JK, Mohanty AK, Kumar S Anim Biosci 11-Jan-2023
PMCID:PMC10330998
doi:10.5713/ab.22.0249
PMID:36634651
Organization, Phylogenetic Marker Exploitation, and Gene Evolution in the Plastome of Thalictrum (Ranunculaceae) Xiang KL, Mao W, Peng HW, Erst AS, Yang YX, He WC, Wu ZQ Front Plant Sci 20-May-2022
PMCID:PMC9166237
doi:10.3389/fpls.2022.897843
PMID:35668810
Complete chloroplast genome of Stephania tetrandra (Menispermaceae) from Zhejiang Province: insights into molecular structures, comparative genome analysis, mutational hotspots and phylogenetic relationships Dong S, Ying Z, Yu S, Wang Q, Liao G, Ge Y, Cheng R BMC Genomics 06-Dec-2021
PMCID:PMC8647421
doi:10.1186/s12864-021-08193-x
PMID:34872502
The complete chloroplast genome of Thalictrum baicalense Turcz. ex Ledeb He Y, Wang R, Gai X, Lin P, Li Y, Wang J Mitochondrial DNA B Resour 11-Feb-2021
PMCID:PMC7889159
doi:10.1080/23802359.2020.1870896
PMID:33628881
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
Alkaloids ofThalictrum baicalense S. Kh. Maekh, S. Yu. Yunusov, É. V. Boiko, V. M. Starchenko Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00579453
Baicaline — A new aporphine alkaloid fromThalictrum baicalense S. Kh. Maekh, S. Yu. Yunusov, É. V. Boiko, V. M. Starchenko Springer Science and Business Media LLC 21-Nov-2004
doi:10.1007/BF00577196
Aporphine alkaloids ofThalictrum baicalense S. Kh. Maekh, S. Yu. Yunusov, É. V. Boiko, V. M. Starchenko Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00575733
Alkaloids of Thalictrum. X. Two new alkaloids from T. minus var. adiantifolium: noroxyhydrastinine and thalifoline. Doskotch RW, Schiff PL Jr, Beal JL Tetrahedron 01-Jan-1970
doi:10.1016/S0040-4020(01)82640-5
PMID:5351614

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
(+)-Glaucine 16754 Click to see 355.40 unknown https://doi.org/10.1016/S0040-4020(01)82640-5
https://doi.org/10.1007/BF00579453
(+)-Magnoflorine 73337 Click to see 342.40 unknown https://doi.org/10.1007/BF00577196
(12R)-2,16,17-trimethoxy-4,6-dioxa-11-azapentacyclo[10.7.1.03,7.08,20.014,19]icosa-1,3(7),8(20),14,16,18-hexaene 162953809 Click to see 355.40 unknown https://doi.org/10.1007/BF00579453
(12S)-2,16,17-trimethoxy-11-methyl-4,6-dioxa-11-azapentacyclo[10.7.1.03,7.08,20.014,19]icosa-1,3(7),8(20),14,16,18-hexaene 162916962 Click to see 369.40 unknown https://doi.org/10.1007/BF00579453
(12S)-2,16,17-trimethoxy-4,6-dioxa-11-azapentacyclo[10.7.1.03,7.08,20.014,19]icosa-1,3(7),8(20),14,16,18-hexaene 13647316 Click to see 355.40 unknown https://doi.org/10.1007/BF00579453
https://doi.org/10.1007/BF00577196
(6aS)-1,2,9,10-tetramethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-3-ol 6352241 Click to see 357.40 unknown https://doi.org/10.1007/BF00575733
https://doi.org/10.1007/BF00579453
(6aS)-1,2,9,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-3-ol 100927112 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2O)OC)OC)OC)OC 371.40 unknown https://doi.org/10.1007/BF00575733
(R)-5,6,6a,7-Tetrahydro-1,2,9,10-tetramethoxy-6-methyl-4H-dibenzo(de,g)quinoline 1078819 Click to see 355.40 unknown https://doi.org/10.1007/BF00579453
1,2,9,10-tetramethoxy-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-3-ol 3734385 Click to see 357.40 unknown https://doi.org/10.1007/BF00579453
https://doi.org/10.1007/BF00575733
1,2,9,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-3-ol 21770003 Click to see 371.40 unknown https://doi.org/10.1007/BF00575733
1,9,10-Trimethoxy-2,3-methylenedioxyaporphine 21769907 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C5=C2OCO5)OC)OC)OC 369.40 unknown https://doi.org/10.1007/BF00579453
1,9,10-Trimethoxy-2,3-methylenedioxynoraporphine 13647315 Click to see 355.40 unknown https://doi.org/10.1007/BF00577196
https://doi.org/10.1007/BF00579453
2,16,17-Trimethoxy-4,6-dioxa-11-azapentacyclo[10.7.1.03,7.08,20.014,19]icosa-1,3(7),8(20),9,11,14,16,18-octaen-13-one 21769994 Click to see COC1=C(C=C2C(=C1)C3=C(C4=C(C5=C3C(=NC=C5)C2=O)OCO4)OC)OC 365.30 unknown https://doi.org/10.1007/BF00579453
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Berberine 2353 Click to see 336.40 unknown https://doi.org/10.1007/BF00577196
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Kaurane diterpenoids
Excisanin H 10066342 Click to see CC1(CCC(C23C1CC(C45C2CCC(C4(OC3)O)C(=C)C5=O)O)O)C 348.40 unknown https://doi.org/10.1007/BF00579453
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glucuronides / Flavonoid-7-O-glucuronides
Baicalin 64982 Click to see C1=CC=C(C=C1)C2=CC(=O)C3=C(C(=C(C=C3O2)OC4C(C(C(C(O4)C(=O)O)O)O)O)O)O 446.40 unknown https://doi.org/10.1016/S0040-4020(01)82640-5
https://doi.org/10.1007/BF00577196

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