Scientific name	Authority	First published in
Olfa thalictrifolia	Bubani	Fl. Pyren. 3: 378 (1901)
Thalictrella thalictroides	(L.) E.Nardi	Webbia 47: 227 (1993)
Aquilegia aquilegioides	(L.) H.P.Fuchs ex Janch.	Cat. Fl. Austr., I. Pteridophyt. & Anthophyt. 1(2): 180 (1958)
Aquilegia thalictroides	E.H.L.Krause	Deutschl. Fl. (Sturm), ed. 2. 5: 224. 1901
Fontanella tertiaria	Kluk ex Besser	Prim. Fl. Galiciae Austriac. 2: 363 (1809)
Helleborus thalictroides	Lam.	Fl. Franç. 3: 315 (1779)
Isopyrum album	Dulac	Fl. Hautes-Pyrénées : 221 (1867)
Isopyrum aquilegioides	L.	Sp. Pl. : 557 (1753)
Isopyrum thalictrifolium	Gilib.	Fl. Lit. Inch. 2: 281 (1782)

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Arabic	إصفورن تلكترمي
Belarusian	Раўнаплоднік пылюшнікавы
Bulgarian	кокошка
Czech	zapalice žluťuchovitá
German	wiesenrauten-muschelblümchen
Finnish	vuokkoängelmä
French	isopyre faux pigamon
Upper Sorbian	wšědna wušnička
Hungarian	erdei galambvirág
Hungarian	galambvirág
Lithuanian	trilapė bligna
Polish	zdrojówka rutewkowata
Russian	Равноплодник василистниковый
Russian	Равноплодник василисниковый
Russian	Василисничек василисниковый
Slovenian	navadna polžarka
Swedish	vitsippsruta
Ukrainian	Рутвичка звичайна

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

Begin at 20°C for 6 weeks, cool to 4°C for 6 weeks, then gradually increase to 10°C over 6 weeks. If no germination, the cycle is repeated.

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

Europe click to expand
- Eastern Europe
  - Baltic States
  - Belarus
  - Ukraine
- Middle Europe
  - Austria
  - Czechoslovakia
  - Hungary
  - Poland
  - Switzerland
- Northern Europe
  - Denmark
- Southeastern Europe
  - Bulgaria
  - Italy
  - Romania
  - Yugoslavia
- Southwestern Europe
  - Corse
  - France
  - Spain

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000732818
Tropicos	27102548
INPN	103917
Flora of Italy	1009
KEW	urn:lsid:ipni.org:names:711481-1
The Plant List	kew-2867663
Open Tree Of Life	949657
Observations.org	147571
NCBI Taxonomy	432643
NBN Atlas	NBNSYS0200002390
IPNI	711481-1
iNaturalist	361315
GBIF	5615962
Freebase	/m/0dt9xj
EPPO	ISYTH
Wikipedia	Isopyrum_thalictroides

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

Nontarget catches of traps with chemical lures may refer to the flower‐visitation, probable pollination, and feeding of bush crickets (Ensifera: Tettigoniidae)

Nagy A, Ősz A, Tóth M, Rácz IA, Kovács S, Szanyi S

Ecol Evol

04-Jul-2023

PMCID:	PMC10319520
doi:	10.1002/ece3.10249
PMID:	37415641

Molecular Docking Study of Several Seconder Metabolites from Medicinal Plants as Potential Inhibitors of COVID-19 Main Protease

BİLGİNER S, GÖZCÜ S, GÜVENALP Z

Turk J Pharm Sci

31-Aug-2022

PMCID:	PMC9438759
doi:	10.4274/tjps.galenos.2021.83548
PMID:	36047576

Profiling of secondary metabolites and DNA typing of three different Annona cultivars grown in Egypt

Mohammed MA, Hamed MA, El-Gengaihi SE, Enein AM, Kachlicki P, Hassan EM

Metabolomics

04-Jul-2022

PMCID:	PMC9252975
doi:	10.1007/s11306-022-01911-w
PMID:	35781851

Activity of Alkaloids on Peptic Ulcer: What’s New?

do Nascimento RF, de Sales IR, Formiga RD, Barbosa-Filho JM, Sobral MV, Tavares JF, Diniz MD, Batista LM

Molecules

08-Jan-2015

PMCID:	PMC6272740
doi:	10.3390/molecules20010929
PMID:	25580688

Nutrient reserves may allow for genome size increase: evidence from comparison of geophytes and their sister non-geophytic relatives

Veselý P, Bureš P, Šmarda P

Ann Bot

19-Aug-2013

PMCID:	PMC3783246
doi:	10.1093/aob/mct185
PMID:	23960044

Complement Activation and Inhibition in Wound Healing

Cazander G, Jukema GN, Nibbering PH

Clin Dev Immunol

30-Dec-2012

PMCID:	PMC3546472
doi:	10.1155/2012/534291
PMID:	23346185

Alkaloids from Isopyrum thalictroides L.

Istatkova R, Philipov S

Nat Prod Res

01-Jun-2004

doi:	10.1080/14786410310001620510
PMID:	15143837

Alkaloids from Isopyrum thalictroides

Stefan A. Philipov, Ralitsa S. Istatkova

Elsevier BV

05-Apr-2003

doi:	10.1016/S0031-9422(96)00696-6

Alcaloïdes de l' Isopyrum thalictroïdes—bases quaternaires des feuilles—isolement et identification de quatre pseudoprotoberberines

C. Moulis, J. Gleye, E. Stanislas

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(00)94375-9

Alkaloids from Isopyrum thalictroides*1

S PHILIPOV, R ISTATKOVA

Elsevier BV

25-Jul-2002

doi:	10.1016/S0031-9422(99)00012-6

Alkaloids from Isopyrum thalictroides L.

Istatkova RS, Philipov SA

Phytochemistry

01-Aug-2000

doi:	10.1016/S0031-9422(00)00068-6
PMID:	11014297

Complement-mediated antiinflammatory effect of bisbenzylisoquinoline alkaloid fangchinoline.

Hristova M, Istatkova R

Phytomedicine

01-Nov-1999

doi:	10.1016/S0944-7113(99)80059-2
PMID:	11962544

Potentiation of Artemisinin Activity against Chloroquine-Resistant Plasmodium falciparum Strains by Using Heme Models

Benoit-Vical F, Robert A, Meunier B

Antimicrob Agents Chemother

01-Oct-1999

PMCID:	PMC89520
doi:	10.1128/aac.43.10.2555
PMID:	10508044

Plant Products as Antimicrobial Agents

Cowan MM

Clin Microbiol Rev

01-Oct-1999

PMCID:	PMC88925
doi:	10.1128/cmr.12.4.564
PMID:	10515903

In vitro antimalarial activity of penduline, a bisbenzylisoquinoline from Isopyrum thalictroides.

Valentin A, Benoit-Vical F, Moulis C, Stanislas E, Mallié M, Fouraste I, Bastide JM

Antimicrob Agents Chemother

01-Oct-1997

PMCID:	PMC164116
doi:	10.1128/AAC.41.10.2305
PMID:	9333071

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
(15R)-18-[4,5-dimethoxy-2-[[(1R)-5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-11,19-dimethoxy-4,6-dioxa-13-azapentacyclo[10.7.1.02,10.03,7.016,20]icosa-1(20),2(10),3(7),8,11,16,18-heptaen-15-ol	163106775	Click to see CN1CCC2=C(C(=C(C=C2C1CC3=CC(=C(C=C3OC4=C(C5=C6C(=C4)C(CNC6=C(C7=C5C8=C(C=C7)OCO8)OC)O)OC)OC)OC)OC)OC)OC	740.80	unknown	https://doi.org/10.1080/14786410310001620510
(15R)-18-[4,5-dimethoxy-2-[[(1S)-5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-11,19-dimethoxy-4,6-dioxa-13-azapentacyclo[10.7.1.02,10.03,7.016,20]icosa-1(20),2(10),3(7),8,11,16,18-heptaen-15-ol	163106774	Click to see CN1CCC2=C(C(=C(C=C2C1CC3=CC(=C(C=C3OC4=C(C5=C6C(=C4)C(CNC6=C(C7=C5C8=C(C=C7)OCO8)OC)O)OC)OC)OC)OC)OC)OC	740.80	unknown	https://doi.org/10.1080/14786410310001620510
(6aS)-1,2,9,10-tetramethoxy-6,6-dimethyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-6-ium	1119124	Click to see C[N+]1(CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C43)OC)OC)OC)OC)C	370.50	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
18-[4,5-dimethoxy-2-[(5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]-11,19-dimethoxy-4,6-dioxa-13-azapentacyclo[10.7.1.02,10.03,7.016,20]icosa-1(20),2(10),3(7),8,11,16,18-heptaen-15-ol	163106773	Click to see CN1CCC2=C(C(=C(C=C2C1CC3=CC(=C(C=C3OC4=C(C5=C6C(=C4)C(CNC6=C(C7=C5C8=C(C=C7)OCO8)OC)O)OC)OC)OC)OC)OC)OC	740.80	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
Artabotrine	48704	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC	341.40	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
Isocorydine	10143	Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C3C(=C(C=C4)OC)O)OC)OC	341.40	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
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/S0031-9422(00)00068-6
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
Columbamine	72310	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)O)OC	338.40	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
Palmatine	19009	Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC(=C(C=C4CC3)OC)OC)OC	352.40	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
Pseudocolumbamine	182406	Click to see COC1=C(C=C2C(=C1)CC[N+]3=CC4=CC(=C(C=C4C=C23)OC)OC)O	338.40	unknown	https://doi.org/10.1016/S0031-9422(00)94375-9
> Lignans, neolignans and related compounds
(1R,14S)-9,20,25-Trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-21-ol	5458555	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC	608.70	unknown	https://doi.org/10.1016/S0031-9422(99)00012-6 https://doi.org/10.1016/S0944-7113(99)80059-2
(1S,14S)-20,21,25-trimethoxy-15,30-dimethyl-7,23-dioxa-15,30-diazaheptacyclo[22.6.2.23,6.18,12.114,18.027,31.022,33]hexatriaconta-3(36),4,6(35),8,10,12(34),18,20,22(33),24,26,31-dodecaen-9-ol	6330552	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC	608.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC164116/
(9R,22R)-17,29-dihydroxy-6,28,35-trimethoxy-23-methyl-15-oxa-8,23-diazaheptacyclo[20.6.2.22,5.211,14.116,20.04,9.026,30]pentatriaconta-1(28),2,4,6,11,13,16,18,20(31),26,29,32,34-tridecaene-8-carbaldehyde	637189	Click to see CN1CCC2=CC(=C3C4=CC5=C(C=C4OC)C(=CN(C5CC6=CC=C(C=C6)OC7=C(C=CC(=C7)CC1C2=C3O)O)C=O)OC)OC	620.70	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
(9R,22S)-17,29-dihydroxy-6,28,35-trimethoxy-23-methyl-15-oxa-8,23-diazaheptacyclo[20.6.2.22,5.211,14.116,20.04,9.026,30]pentatriaconta-1(28),2,4,6,11,13,16,18,20(31),26,29,32,34-tridecaene-8-carbaldehyde	162936564	Click to see CN1CCC2=CC(=C3C4=CC5=C(C=C4OC)C(=CN(C5CC6=CC=C(C=C6)OC7=C(C=CC(=C7)CC1C2=C3O)O)C=O)OC)OC	620.70	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
1-Isotetrandrine	5351212	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC	622.70	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
17,29-Dihydroxy-6,28,35-trimethoxy-23-methyl-15-oxa-8,23-diazaheptacyclo[20.6.2.22,5.211,14.116,20.04,9.026,30]pentatriaconta-1(28),2,4,6,11,13,16,18,20(31),26,29,32,34-tridecaene-8-carbaldehyde	15549706	Click to see CN1CCC2=CC(=C3C4=CC5=C(C=C4OC)C(=CN(C5CC6=CC=C(C=C6)OC7=C(C=CC(=C7)CC1C2=C3O)O)C=O)OC)OC	620.70	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
6,6',7-Trimethoxy-2,2'-dimethylberbaman-12-ol	10170	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC	608.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC164116/
CID 12300053	12300053	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)O)OC	608.70	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
Fangchinoline	73481	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)O)OC)OC	608.70	unknown	https://doi.org/10.1016/S0031-9422(96)00696-6 https://doi.org/10.1016/S0944-7113(99)80059-2
Isosinomenine A	5422	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC	622.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC164116/ https://doi.org/10.1016/S0031-9422(96)00696-6
Tetrandrine	73078	Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C)OC)OC)OC)OC	622.70	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC164116/ https://doi.org/10.1016/S0031-9422(96)00696-6
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(1R)-7-[5-[[(1S)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2,3-dimethoxyphenoxy]-1-[(3,4-dimethoxyphenyl)methyl]-5,6-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline	162917940	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C(=C3)OC4=C(C(=C5CCN(C(C5=C4)CC6=CC(=C(C=C6)OC)OC)C)OC)OC)OC)OC)OC)OC	728.90	unknown	https://doi.org/10.1016/S0031-9422(99)00012-6
(1S)-7-[2-[[(1R)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-4,5-dimethoxyphenoxy]-1-[(3,4-dimethoxyphenyl)methyl]-5,6-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline	162860215	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3OC4=C(C(=C5CCN(C(C5=C4)CC6=CC(=C(C=C6)OC)OC)C)OC)OC)OC)OC)OC)OC	728.90	unknown	https://doi.org/10.1016/S0031-9422(99)00012-6
(2Z)-2-(6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-ylidene)-2-[4-[[4,5-dimethoxy-2-[[(1R)-5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenyl]methyl]-2,3-dimethoxyphenyl]acetaldehyde	163021594	Click to see CN1CCC2=C(C(=C(C=C2C1CC3=CC(=C(C=C3CC4=C(C(=C(C=C4)C(=C5C6=CC(=C(C=C6CCN5)OC)OC)C=O)OC)OC)OC)OC)OC)OC)OC	768.90	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
(2Z)-2-(6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-ylidene)-2-[4-[[4,5-dimethoxy-2-[[(1S)-5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenyl]methyl]-2,3-dimethoxyphenyl]acetaldehyde	163021595	Click to see CN1CCC2=C(C(=C(C=C2C1CC3=CC(=C(C=C3CC4=C(C(=C(C=C4)C(=C5C6=CC(=C(C=C6CCN5)OC)OC)C=O)OC)OC)OC)OC)OC)OC)OC	768.90	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
(2Z)-2-(6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-ylidene)-2-[4-[4,5-dimethoxy-2-[[(1S)-5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenyl]-2,3-dimethoxyphenyl]acetaldehyde	163047087	Click to see CN1CCC2=C(C(=C(C=C2C1CC3=CC(=C(C=C3C4=C(C(=C(C=C4)C(=C5C6=CC(=C(C=C6CCN5)OC)OC)C=O)OC)OC)OC)OC)OC)OC)OC	754.90	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
(2Z)-2-(6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-ylidene)-2-[6-[[2,3-dimethoxy-4-[[(1R)-5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenyl]methyl]-1,3-benzodioxol-5-yl]acetaldehyde	163079536	Click to see CN1CCC2=C(C(=C(C=C2C1CC3=C(C(=C(C=C3)CC4=CC5=C(C=C4C(=C6C7=CC(=C(C=C7CCN6)OC)OC)C=O)OCO5)OC)OC)OC)OC)OC	752.80	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
(6R)-6-[[4-[5-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]-2,3-dimethoxyphenoxy]phenyl]methyl]-4-methoxy-7-methyl-8,9-dihydro-6H-[1,3]dioxolo[4,5-f]isoquinoline	102066464	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C(=C3)OC4=CC=C(C=C4)CC5C6=CC(=C7C(=C6CCN5C)OCO7)OC)OC)OC)OC)OC	682.80	unknown	https://doi.org/10.1016/S0031-9422(99)00012-6
(6R)-6-[[4-[5-[[(1S)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2,3-dimethoxyphenoxy]phenyl]methyl]-4-methoxy-7-methyl-8,9-dihydro-6H-[1,3]dioxolo[4,5-f]isoquinoline	162982586	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C(=C3)OC4=CC=C(C=C4)CC5C6=CC(=C7C(=C6CCN5C)OCO7)OC)OC)OC)OC)OC	682.80	unknown	https://doi.org/10.1016/S0031-9422(96)00696-6
(6S)-4-methoxy-7-methyl-6-[[4-[2,3,4-trimethoxy-5-[(5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]phenyl]methyl]-8,9-dihydro-6H-[1,3]dioxolo[4,5-f]isoquinoline	102066463	Click to see CN1CCC2=C3C(=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C(=C(C(=C5)CC6C7=CC(=C(C(=C7CCN6C)OC)OC)OC)OC)OC)OC)OC)OCO3	742.90	unknown	https://doi.org/10.1016/S0031-9422(99)00012-6
(6S)-4-methoxy-7-methyl-6-[[4-[2,3,4-trimethoxy-5-[[(1S)-5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]phenyl]methyl]-8,9-dihydro-6H-[1,3]dioxolo[4,5-f]isoquinoline	10032952	Click to see CN1CCC2=C3C(=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C(=C(C(=C5)CC6C7=CC(=C(C(=C7CCN6C)OC)OC)OC)OC)OC)OC)OC)OCO3	742.90	unknown	https://doi.org/10.1016/S0031-9422(96)00696-6
(R)-Reticuline	440586	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	329.40	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
2-(6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-ylidene)-2-[4-[[4,5-dimethoxy-2-[(5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenyl]methyl]-2,3-dimethoxyphenyl]acetaldehyde	163021592	Click to see CN1CCC2=C(C(=C(C=C2C1CC3=CC(=C(C=C3CC4=C(C(=C(C=C4)C(=C5C6=CC(=C(C=C6CCN5)OC)OC)C=O)OC)OC)OC)OC)OC)OC)OC	768.90	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
2-(6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-ylidene)-2-[4-[4,5-dimethoxy-2-[(5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenyl]-2,3-dimethoxyphenyl]acetaldehyde	163047086	Click to see CN1CCC2=C(C(=C(C=C2C1CC3=CC(=C(C=C3C4=C(C(=C(C=C4)C(=C5C6=CC(=C(C=C6CCN5)OC)OC)C=O)OC)OC)OC)OC)OC)OC)OC	754.90	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
2-(6,7-dimethoxy-3,4-dihydro-2H-isoquinolin-1-ylidene)-2-[6-[[2,3-dimethoxy-4-[(5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenyl]methyl]-1,3-benzodioxol-5-yl]acetaldehyde	163079535	Click to see CN1CCC2=C(C(=C(C=C2C1CC3=C(C(=C(C=C3)CC4=CC5=C(C=C4C(=C6C7=CC(=C(C=C7CCN6)OC)OC)C=O)OCO5)OC)OC)OC)OC)OC	752.80	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
2-methoxy-5-[[(1S)-6-methoxy-2-methyl-7-[2,3,4-trimethoxy-5-[[(1S)-5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenol	15907629	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC4=C(C(=C(C(=C4)CC5C6=CC(=C(C(=C6CCN5C)OC)OC)OC)OC)OC)OC)OC	744.90	unknown	https://doi.org/10.1016/S0031-9422(99)00012-6
2-methoxy-5-[[6-methoxy-2-methyl-7-[2,3,4-trimethoxy-5-[(5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenol	163003243	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)OC4=C(C(=C(C(=C4)CC5C6=CC(=C(C(=C6CCN5C)OC)OC)OC)OC)OC)OC)OC	744.90	unknown	https://doi.org/10.1016/S0031-9422(99)00012-6
4-[5-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]-2,3,4-trimethoxyphenoxy]-6-(3,4-dimethoxyphenyl)-[1,3]dioxolo[4,5-f]isoquinoline	100981233	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C(=C3OC)OC)OC)OC4=C5C(=C6C=CN=C(C6=C4)C7=CC(=C(C=C7)OC)OC)OCO5)OC)OC	710.80	unknown	https://doi.org/10.1016/S0031-9422(99)00012-6
4-[5-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]-2,3,4-trimethoxyphenoxy]-6-[(3,4-dimethoxyphenyl)methyl]-[1,3]dioxolo[4,5-f]isoquinoline	15907628	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C(=C3OC)OC)OC)OC4=C5C(=C6C=CN=C(C6=C4)CC7=CC(=C(C=C7)OC)OC)OCO5)OC)OC	724.80	unknown	https://doi.org/10.1016/S0031-9422(99)00012-6
4-[5-[[(1R)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2,3,4-trimethoxyphenoxy]-6-[(2,3-dimethoxyphenyl)methyl]-[1,3]dioxolo[4,5-f]isoquinoline	163106912	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C(=C3OC)OC)OC)OC4=C5C(=C6C=CN=C(C6=C4)CC7=C(C(=CC=C7)OC)OC)OCO5)OC)OC	724.80	unknown	https://doi.org/10.1016/S0031-9422(99)00012-6
4-[5-[[(1S)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]-2,3,4-trimethoxyphenoxy]-6-[(3,4-dimethoxyphenyl)methyl]-[1,3]dioxolo[4,5-f]isoquinoline	10395125	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C(=C3OC)OC)OC)OC4=C5C(=C6C=CN=C(C6=C4)CC7=CC(=C(C=C7)OC)OC)OCO5)OC)OC	724.80	unknown	https://doi.org/10.1016/S0031-9422(99)00012-6
4-methoxy-7-methyl-6-[[4-[2,3,4-trimethoxy-5-[(5,6,7-trimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]phenyl]methyl]-8,9-dihydro-6H-[1,3]dioxolo[4,5-f]isoquinoline	85098604	Click to see CN1CCC2=C3C(=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C(=C(C(=C5)CC6C7=CC(=C(C(=C7CCN6C)OC)OC)OC)OC)OC)OC)OC)OCO3	742.90	unknown	https://doi.org/10.1016/S0031-9422(96)00696-6
6-[[4-[5-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]-2,3-dimethoxyphenoxy]phenyl]methyl]-4-methoxy-7-methyl-8,9-dihydro-6H-[1,3]dioxolo[4,5-f]isoquinoline	162982585	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C(=C3)OC4=CC=C(C=C4)CC5C6=CC(=C7C(=C6CCN5C)OCO7)OC)OC)OC)OC)OC	682.80	unknown	https://doi.org/10.1016/S0031-9422(96)00696-6
7-[2-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]-4,5-dimethoxyphenoxy]-1-[(3,4-dimethoxyphenyl)methyl]-5,6-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline	15907630	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3OC4=C(C(=C5CCN(C(C5=C4)CC6=CC(=C(C=C6)OC)OC)C)OC)OC)OC)OC)OC)OC	728.90	unknown	https://doi.org/10.1016/S0031-9422(99)00012-6
Reticulin	10233	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	329.40	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
Reticuline	439653	Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)O)O)OC	329.40	unknown	https://doi.org/10.1016/S0031-9422(00)00068-6
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Pendulin	44259755	Click to see COC1=C(C(=C2C(=C1)OC(=C(C2=O)OC)C3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O)OC	506.50	unknown	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC164116/

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Isopyrum thalictroides

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

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Biological Material Top

Contributors Top

Collections Top