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 click to expand
- Caucasus
  - Transcaucasus
- China
  - Xinjiang
- Middle Asia
  - Kazakhstan
  - Kirgizstan
  - Tadzhikistan
  - Turkmenistan
  - Uzbekistan
- Mongolia
  - Mongolia
- Western Asia
  - Afghanistan
  - Iran
  - Iraq
  - Lebanon-Syria
  - Palestine
  - Turkey

Asia-tropical click to expand
- Indian Subcontinent
  - Pakistan

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

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

Add a new one!

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
(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 CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C5C(=C2OC)OCO5)OC)O	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 CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)OC)OC)O	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 CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2O)OC)OC)OC)O	357.40	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 CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2O)OC)OC)OC)O	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
2,9,10-trimethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-1-ol	100020	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)O)OC	341.40	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 CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)OC)OC)O	371.40	unknown	https://doi.org/10.1007/BF00565243
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/10.1016/0031-9422(86)80030-9
Dehydroocoteine	21769946	Click to see CN1CCC2=C(C3=C(C4=C5C=C(C(=CC5=CC1=C24)OC)OC)OCO3)OC	367.40	unknown	https://doi.org/10.1016/0031-9422(86)80030-9
Isoboldine	133323	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
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/10.1016/0031-9422(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 CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C5C(=C2OC)OCO5)OC)OC	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 COC1=C(C=C2C(=C1)C3=C4C(=C(C5=C3C(=NC=C5)C2=O)OC)OCO4)OC	365.30	unknown	https://doi.org/10.1016/0031-9422(86)80030-9
Thaliporphine	6992288	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)O)OC	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 CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)O)C=C5)OC	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 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
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 CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)O)C=C5)OC	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 CN1C=CC2=CC(=C(C=C2C1=O)OC)OC	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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Thalictrum isopyroides

Table of Contents

Details Top

Description Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top