PlantaeDB Logo
Login Sign-up

Thalictrum cultratum

Thalictrum cultratum - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
Upload a new image!

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 UUID64404d217bd7d755398667
Scientific name Thalictrum cultratum
Authority Wall.
First published in Pl. Asiat. Rar. 2: 26 (1831)

Description Top

Suggest a correction or write a new one!
No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Thalictrum deciternatum B.Boivin J. Arnold Arbor. 26: 112 (1945)
Thalictrum yui B.Boivin J. Arnold Arbor. 26: 115 (1945)

Common names Top

Add a new one! Suggest a correction!

Language Common/alternative name
English knife-like meadow rue
Chinese 马尾连
Chinese 马尾黄连
Chinese 西藏水黄连
Chinese 高原唐松草
Chinese 草黄连

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!
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
    • China
      • China North-central
      • China South-central
      • Tibet
  • Asia-tropical
    • Indian Subcontinent
      • East Himalaya
      • Nepal
      • Pakistan
      • West Himalaya
    • Indo-China
      • Myanmar

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001129326
Tropicos 27100518
KEW urn:lsid:ipni.org:names:714354-1
The Plant List tro-27100518
Open Tree Of Life 583170
Observations.org 506040
NCBI Taxonomy 341022
IPNI 714354-1
GBIF 3929860
EOL 2873967
Elurikkus 441752
USDA GRIN 36427
CMAUP NPO24447

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
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
Screening an In-House Isoquinoline Alkaloids Library for New Blockers of Voltage-Gated Na+ Channels Using Voltage Sensor Fluorescent Probes: Hits and Biases Coquerel Q, Legendre C, Frangieh J, Waard SD, Montnach J, Cmarko L, Khoury J, Hassane CS, Bréard D, Siegler B, Fajloun Z, De Pomyers H, Mabrouk K, Weiss N, Henrion D, Richomme P, Mattei C, Waard MD, Le Ray AM, Legros C Molecules 28-Jun-2022
PMCID:PMC9268414
doi:10.3390/molecules27134133
PMID:35807390
Jatrorrhizine: A Review of Sources, Pharmacology, Pharmacokinetics and Toxicity Zhong F, Chen Y, Chen J, Liao H, Li Y, Ma Y Front Pharmacol 13-Jan-2022
PMCID:PMC8793695
doi:10.3389/fphar.2021.783127
PMID:35095493
Distribution of Therapeutic Efficacy of Ranunculales Plants Used by Ethnic Minorities on the Phylogenetic Tree of Chinese Species Hao DC, Zhang Y, He CN, Xiao PG Evid Based Complement Alternat Med 12-Jan-2022
PMCID:PMC8769838
doi:10.1155/2022/9027727
PMID:35069772
8-, 9-, and 11-Aryloxy Dimeric Aporphines and Their Pharmacological Activities Ali G, Cuny GD Molecules 27-Jul-2021
PMCID:PMC8347945
doi:10.3390/molecules26154521
PMID:34361671
Unraveling Plant Natural Chemical Diversity for Drug Discovery Purposes Lautié E, Russo O, Ducrot P, Boutin JA Front Pharmacol 07-Apr-2020
PMCID:PMC7154113
doi:10.3389/fphar.2020.00397
PMID:32317969
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
Natural Products and Acute Myeloid Leukemia: A Review Highlighting Mechanisms of Action Hwang D, Kim M, Park H, Jeong MI, Jung W, Kim B Nutrients 03-May-2019
PMCID:PMC6567155
doi:10.3390/nu11051010
PMID:31058874
Meiotic abnormalities affect genetic constitution and pollen viability in dicots from Indian cold deserts Kaur D, Singhal VK BMC Plant Biol 07-Jan-2019
PMCID:PMC6323802
doi:10.1186/s12870-018-1596-7
PMID:30616590
Floristic Diversity and Distribution Pattern of Plant Communities along Altitudinal Gradient in Sangla Valley, Northwest Himalaya Sharma P, Rana JC, Devi U, Randhawa SS, Kumar R ScientificWorldJournal 14-Oct-2014
PMCID:PMC4212538
doi:10.1155/2014/264878
PMID:25383363
Antiviral Activity of Some Plants Used in Nepalese Traditional Medicine Rajbhandari M, Mentel R, Jha PK, Chaudhary RP, Bhattarai S, Gewali MB, Karmacharya N, Hipper M, Lindequist U Evid Based Complement Alternat Med 25-Oct-2007
PMCID:PMC2781767
doi:10.1093/ecam/nem156
PMID:18955262
Nine Bisbenzylisoquinoline Alkaloids from Thalictrum cultratum Wasala H. M. W. Herath, S. Fazal Hussain, Alan J. Freyer, Hélène Guinaudeau, Maurice Shamma American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50052A024
Bisbenzylisoquinoline Alkaloids from Thalictrum cultratum. The Structures of Thalrugosinone and Thalpindione S. Fazal Hussain, Hélène Guinaudeau, Alan J. Freyer, Maurice Shamma American Chemical Society (ACS) 17-Mar-2005
doi:10.1021/NP50042A014
Five New Bisbenzylisoquinoline Alkaloids from Thalictrum cultratum S. Fazal Hussain, Alan J. Freyer, Hélène Guinaudeau, Maurice Shamma American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50045A018
Seven New Aporphine-Benzylisoquinoline Alkaloids from Thalictrum cultratum S. Fazal Hussain, Alan J. Freyer, Hélène Guinaudeau, Maurice Shamma, M. Tariq Siddiqui American Chemical Society (ACS) 11-Mar-2005
doi:10.1021/NP50045A019

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
(6aS)-8-[4-[[(1S)-7-hydroxy-6-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]-1,2,3,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-ol 10484580 Click to see CN1CCC2=C3C1CC4=C(C(=C(C=C4C3=C(C(=C2OC)OC)OC)OC)O)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O 668.80 unknown https://doi.org/10.1021/NP50045A019
1-[[4,5-dimethoxy-2-[(1,2,3,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-9-yl)oxy]phenyl]methyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-5-ol 3420841 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)OC)OC)OC5=CC(=C(C=C5CC6C7=CC(=C(C(=C7CCN6C)O)OC)OC)OC)OC 742.90 unknown https://doi.org/10.1021/NP50045A019
6-methoxy-2-methyl-1-[[4-[(1,2,9,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-8-yl)oxy]phenyl]methyl]-3,4-dihydro-1H-isoquinolin-7-ol 13892252 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C(C(=C(C=C43)OC)OC)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O)OC)OC 652.80 unknown https://doi.org/10.1021/NP50045A019
6-methoxy-2-methyl-1-[[4-[(14,15,16-trimethoxy-10-methyl-10-azatetracyclo[7.7.1.02,7.013,17]heptadeca-1,3,5,7,9(17),13,15-heptaen-6-yl)oxy]phenyl]methyl]-3,4-dihydro-1H-isoquinolin-7-ol 101216513 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC4=CC=CC5=C6C7=C(C=C54)N(CCC7=C(C(=C6OC)OC)OC)C)O)OC 620.70 unknown https://doi.org/10.1021/NP50045A019
7-methoxy-2-methyl-1-[[4-[(1,2,3,9,10-pentamethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinolin-8-yl)oxy]phenyl]methyl]-3,4-dihydro-1H-isoquinolin-6-ol 13892256 Click to see CN1CCC2=C3C1CC4=C(C(=C(C=C4C3=C(C(=C2OC)OC)OC)OC)OC)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)O)OC 682.80 unknown https://doi.org/10.1021/NP50045A019
8-[4-[(6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl)methyl]phenoxy]-1,2,9,10-tetramethoxy-6-methyl-5,6,6a,7-tetrahydro-4H-dibenzo[de,g]quinoline 13892251 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=C(C(=C(C=C43)OC)OC)OC5=CC=C(C=C5)CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC 666.80 unknown https://doi.org/10.1021/NP50045A019
Adiantifoline 167937 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)OC)OC)OC5=CC(=C(C=C5CC6C7=CC(=C(C=C7CCN6C)OC)OC)OC)OC 726.90 unknown https://doi.org/10.1021/NP50045A019
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)84580-X
Thalmelatidine 56842063 Click to see CN1CCC2=C3C1CC4=CC(=C(C=C4C3=C(C(=C2OC)OC)OC)OC)OC5=CC(=C(C=C5CC6C7=CC(=C8C(=C7CCN6C)OCO8)OC)OC)OC 740.80 unknown https://doi.org/10.1021/NP50045A019
> Alkaloids and derivatives / Protoberberine alkaloids and derivatives
16-Methoxy-5,7-dioxa-13-azoniapentacyclo[11.8.0.02,10.04,8.015,20]henicosa-1(13),2,4(8),9,14,16,18,20-octaen-17-olate 10426199 Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)[O-] 321.30 unknown https://doi.org/10.1016/S0031-9422(00)84580-X
Berberine 2353 Click to see COC1=C(C2=C[N+]3=C(C=C2C=C1)C4=CC5=C(C=C4CC3)OCO5)OC 336.40 unknown https://doi.org/10.1016/S0031-9422(00)84580-X
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)84580-X
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)84580-X
Thalifendine 3084288 Click to see COC1=C(C=CC2=CC3=[N+](CCC4=CC5=C(C=C43)OCO5)C=C21)O 322.30 unknown https://doi.org/10.1016/S0031-9422(00)84580-X
> Lignans, neolignans and related compounds
(-)-5-Hydroxythalmine 184486 Click to see CN1CCC2=C3C(=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C(=C7CCN6C)O)OC)O3)OC)OC)O 624.70 unknown https://doi.org/10.1021/NP50045A018
(-)-Thalmiculimine 184489 Click to see CN1CCC2=C(C(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6=NCCC7=C(O3)C(=C(C=C76)OC)OC)C=C5)OC)O 622.70 unknown https://doi.org/10.1021/NP50045A018
(-)-Thalmiculine 184621 Click to see CN1CCC2=C3C(=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C(=C7CCN6C)O)OC)O3)OC)OC)OC 638.70 unknown https://doi.org/10.1021/NP50045A018
(21S)-10,15,26-trimethoxy-20-methyl-12,28-dioxa-4,20-diazaheptacyclo[27.2.2.17,11.113,17.123,27.03,8.021,35]hexatriaconta-1(31),3,7(36),8,10,13(35),14,16,23(34),24,26,29,32-tridecaen-14-ol 101428567 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6=NCCC7=CC(=C(C=C76)OC)O3)C=C5)O)OC 592.70 unknown https://doi.org/10.1021/NP50045A018
(3S,21S)-10,15,26-trimethoxy-4,20-dimethyl-12,28-dioxa-4,20-diazaheptacyclo[27.2.2.17,11.113,17.123,27.03,8.021,35]hexatriaconta-1(32),7(36),8,10,13(35),14,16,23(34),24,26,29(33),30-dodecaen-14-ol 102148178 Click to see CN1CCC2=CC3=C(C=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/10.1021/NP50045A018
https://doi.org/10.1021/NP50052A024
10,11,15,16,27-Pentamethoxy-4-methyl-13,29-dioxa-4,21-diazaheptacyclo[28.2.2.114,18.124,28.03,8.07,12.022,36]hexatriaconta-1(32),7(12),8,10,14(36),15,17,24(35),25,27,30,33-dodecaene-21-carbaldehyde 13892231 Click to see CN1CCC2=C3C(=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(O3)C(=C(C=C7CCN6C=O)OC)OC)OC)OC)OC 666.80 unknown https://doi.org/10.1021/NP50042A014
2-Northalmine 180979 Click to see CN1CCC2=C3C(=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6)OC)O3)OC)OC)O 594.70 unknown https://doi.org/10.1021/NP50042A014
5-Hydroxythalidasine 184487 Click to see CN1CCC2=C3C(=C(C=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)O)OC)OC)OC 668.80 unknown https://doi.org/10.1021/NP50052A024
https://doi.org/10.1021/NP50045A018
Aromoline 362574 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)O)OC 594.70 unknown https://doi.org/10.1021/NP50052A024
Obaberine 100231 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)OC)OC)OC 622.70 unknown https://doi.org/10.1021/NP50052A024
Oxyacanthine 442333 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC=C(C=C4)OC5=C(C=CC(=C5)CC6C7=CC(=C(C=C7CCN6C)OC)O3)O)OC)OC 608.70 unknown https://doi.org/10.1021/NP50052A024
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/10.1021/NP50045A018
https://doi.org/10.1021/NP50052A024
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/NP50045A018
Thalidasine 159795 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)OC)OC 652.80 unknown https://doi.org/10.1021/NP50042A014
https://doi.org/10.1021/NP50052A024
Thalmiculatimine 184485 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)O)OC5=CC=C(CC6=NCCC7=C(O3)C(=C(C=C76)OC)OC)C=C5)OC 592.70 unknown https://doi.org/10.1021/NP50045A018
Thalmidine 100230 Click to see CN1CCC2=CC3=C(C=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/10.1021/NP50045A018
Thalmine 442366 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)O)OC)C=C5)OC 608.70 unknown https://doi.org/10.1021/NP50042A014
Thalrugosidine 5321920 Click to see CN1CCC2=CC(=C(C3=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=CC(=C(C(=C7CCN6C)O3)OC)OC)C=C5)O)OC 638.70 unknown https://doi.org/10.1021/NP50045A018
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Thalirugine 44584030 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC4=CC=C(C=C4)CC5C6=CC(=C(C(=C6CCN5C)O)OC)OC)O)OC 640.80 unknown https://doi.org/10.1021/NP50052A024
> Organoheterocyclic compounds / Isoquinolines and derivatives / Isoquinolones and derivatives
2,9,10-Trimethoxy-5,6-dihydroisoquinolino[2,1-b]isoquinolin-3-one 10065647 Click to see COC1=C(C2=CN3CCC4=CC(=O)C(=CC4=C3C=C2C=C1)OC)OC 337.40 unknown https://doi.org/10.1016/S0031-9422(00)84580-X
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
3,5,3',4'-Tetrahydroxy-6,7,8-trimethoxyflavone 44260067 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)OC)OC 376.30 unknown via CMAUP database
3,5,7,3',4'-Pentahydroxy-6,8-dimethoxyflavone 14483219 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)O)OC)O 362.30 unknown via CMAUP database
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown via CMAUP database
Limocitrol 12311234 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)O)O 376.30 unknown via CMAUP database
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides
2-(3,4-dihydroxyphenyl)-5-hydroxy-7-[(2S,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 13871824 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)O)O 432.40 unknown via CMAUP database
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2R,3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one 57511421 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C=C(C(=C3O)C4C(C(C(C(O4)CO)O)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
Orientin 5281675 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O)O 448.40 unknown via CMAUP database
Vitexin 5280441 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4C(C(C(C(O4)CO)O)O)O)O 432.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
Cacticin 5318644 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown via CMAUP database
Hyperoside 5281643 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O)O 464.40 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
3-Methoxyluteolin 5280681 Click to see COC1=C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 316.26 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3-methoxyflavone 5319442 Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC=C(C=C3)O 316.26 unknown via CMAUP database
Gossypetin 3-methyl ether 5386958 Click to see COC1=C(OC2=C(C1=O)C(=CC(=C2O)O)O)C3=CC(=C(C=C3)O)O 332.26 unknown via CMAUP database
Gossypetin 3,3'-dimethyl ether 21676153 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)O)OC)O 346.30 unknown via CMAUP database
Quercetagetin 3-methyl ether 5320475 Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)O)O)C3=CC(=C(C=C3)O)O 332.26 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
4',5,7-Trihydroxy-3,6-dimethoxyflavone 5352032 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O 330.29 unknown via CMAUP database
5,7,2'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44259895 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O)OC 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,4',5'-tetramethoxyflavone 44258045 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 390.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,5'-trimethoxyflavone 44258041 Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC 376.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6-dimethoxyflavone 44259884 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C(=C3)O)O)O)O 362.30 unknown via CMAUP database
5,7,8,3',4'-Pentahydroxy-3,6-dimethoxyflavone 21676156 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)O)O 362.30 unknown via CMAUP database
5,7,8,4'-Tetrahydroxy-3,6-dimethoxyflavone 44260054 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)O)O 346.30 unknown via CMAUP database
Axillarin 5281603 Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O 346.30 unknown via CMAUP database
Jaceidin 5464461 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C=C(C(=C3O)OC)O)OC)O 360.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Benthamitin 44259900 Click to see COC1=CC(=C(C=C1C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)OC)OC)OC)OC 432.40 unknown via CMAUP database
Casticin 5315263 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C=C3O2)OC)OC)O)OC)O 374.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 8-O-methylated flavonoids
3',4',5,7-Tetrahydroxy-3,8-dimethoxyflavone 5748553 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O)O 346.30 unknown via CMAUP database
4H-1-Benzopyran-4-one, 5,7-dihydroxy-2-(4-hydroxyphenyl)-3,6,8-trimethoxy- 5386960 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)OC)O 360.30 unknown via CMAUP database
5-Hydroxy-3,6,7,8,3',4',5'-heptamethoxyflavone 44260077 Click to see COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 448.40 unknown via CMAUP database
5,2'-Dihydroxy-3,6,7,8,4',5'-hexamethoxyflavone 44260086 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O)OC 434.40 unknown via CMAUP database
5,3'-Dihydroxy-3,6,7,8,4'-pentamethoxyflavone 369954 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,3',4'-Trihydroxy-3,6,7,8-tetramethoxyflavone 54799 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)OC 390.30 unknown via CMAUP database
5,3',5'-Trihydroxy-3,6,7,8,4'-pentamethoxyflavone 44260074 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 420.40 unknown via CMAUP database
5,4'-Dihydroxy-3,6,7,8,3'-pentamethoxyflavone 100625 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC)O 404.40 unknown via CMAUP database
5,6,3',5'-Tetrahydroxy-3,7,8,4'-tetramethoxyflavone 44260073 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)O)O)OC)O 406.30 unknown via CMAUP database
5,7-Dihydroxy-2-(4-hydroxy-3-methoxy-phenyl)-3,6,8-trimethoxy-chromen-4-one 5386959 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 390.30 unknown via CMAUP database
5,7-Dihydroxy-3,6,8,3',4',5'-hexamethoxyflavone 5386963 Click to see COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 434.40 unknown via CMAUP database
5,7,2'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5487077 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 21676158 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O)O 406.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-3,8,5'-trimethoxyflavone 44260043 Click to see COC1=C(C=C(C(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O)O 376.30 unknown via CMAUP database
5,7,2',4'-Tetrahydroxy-8,5'-dimethoxyflavone 44258626 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)OC)O)O 346.30 unknown via CMAUP database
5,7,2',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260085 Click to see COC1=C(C=C(C(=C1)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4'-tetramethoxyflavone 21599528 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 390.30 unknown via CMAUP database
5,7,3'-Trihydroxy-3,6,8,4',5'-pentamethoxyflavone 5352085 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8-trimethoxyflavone 5386962 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C=C3)O)O)OC)OC)O 376.30 unknown via CMAUP database
5,7,3',4'-Tetrahydroxy-3,6,8,5'-tetramethoxyflavone 44260072 Click to see COC1=CC(=CC(=C1O)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 406.30 unknown via CMAUP database
5,7,3',4',5'-Pentahydroxy-3,6,8-trimethoxyflavone 11383767 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC(=C(C(=C3)O)O)O)OC)OC)O 392.30 unknown via CMAUP database
5,7,3',5'-Tetrahydroxy-3,6,8,4'-tetramethoxyflavone 44260071 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC)O 406.30 unknown via CMAUP database
5,7,4'-Trihydroxy-3,6,8,3',5'-pentamethoxyflavone 21676159 Click to see COC1=CC(=CC(=C1O)OC)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)O)OC)O)OC 420.40 unknown via CMAUP database
5,7,4'-Trihydroxy-3,8-dimethoxyflavone 13983738 Click to see COC1=C(C=C(C2=C1OC(=C(C2=O)OC)C3=CC=C(C=C3)O)O)O 330.29 unknown via CMAUP database
Agecorynin D 14162688 Click to see COC1=C(C=C(C(=C1)C2=CC(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)O)O 390.30 unknown via CMAUP database
Calycopterin 10429470 Click to see COC1=C(C(=C2C(=C1O)C(=O)C(=C(O2)C3=CC=C(C=C3)O)OC)OC)OC 374.30 unknown via CMAUP database
Conyzatin 13916282 Click to see COC1=CC(=CC(=C1OC)OC)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC 404.40 unknown via CMAUP database
Digicitrin 10071564 Click to see COC1=CC(=CC(=C1OC)O)C2=C(C(=O)C3=C(C(=C(C(=C3O2)OC)OC)OC)O)OC 434.40 unknown via CMAUP database
Gossypetin 3,8,3'-trimethyl ether 5386961 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 360.30 unknown via CMAUP database
Hibiscetin 3,8,4'-trimethyl ether 44260037 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(O2)C(=C(C=C3O)O)OC)OC)O 376.30 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins
(-)-Thalrugosaminine 5321919 Click to see CN1CCC2=CC(=C3C=C2C1CC4=CC(=C(C=C4)OC)OC5=CC=C(CC6C7=C(CCN6C)C(=C(C(=C7O3)OC)OC)OC)C=C5)OC 652.80 unknown https://doi.org/10.1021/NP50052A024
https://doi.org/10.1021/NP50045A018

Biological Material Top ebay Auctions

Please wait .. loading items ..

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.