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Roemeria refracta

Roemeria refracta - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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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 UUID64404a14631e9272988826
Scientific name Roemeria refracta
Authority (Steven) DC.
First published in Syst. Nat. 2: 93 (1821)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Roemeria rhoeadiflora Boiss. Diagn. Pl. Orient. 6: 7 (1846)
Glaucium refractum Steven ex DC. Syst. Nat. 2: 93 (1821)
Papaver refractum (DC.) K.-F.Günther Flora, Morphol. Geobot. Oekophysiol. 164: 436 (1975)
Roemeria bicolor Regel Bull. Soc. Imp. Naturalistes Moscou 43(I): 249 (1870)
Papaver refractum subsp. occidentale (Kadereit) Karlsson Svensk Bot. Tidskr. 91(5): 249. 1998 [1997 publ. 1998]
Roemeria refracta subsp. occidentalis Kadereit in Flora (Germany) 179(2): 138 (1987).

Common names Top

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Language Common/alternative name
English spotted asian poppy
Arabic بختري منكسر
Azerbaijani Əyrim laləvər
German asiatischer tüpfelmohn
Russian Рёмерия преломлённая
Russian Рёмерия отогнутая
Chinese 鹅观草
Chinese 红勒米花
Chinese 红花疆罂粟
Chinese 裂叶罂粟

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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No forms added yet.

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
    • Arabian Peninsula
      • Gulf States
    • Caucasus
      • North Caucasus
      • Transcaucasus
    • China
      • Xinjiang
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Mongolia
      • Mongolia
    • Russian Far East
      • Primorye
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Turkey

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001090301
USDA Plants RORE
Tropicos 24000148
INPN 1014760
KEW urn:lsid:ipni.org:names:673947-1
The Plant List tro-24000148
Open Tree Of Life 510010
Observations.org 141013
NCBI Taxonomy 72192
Nature Serve 2.141277
IPNI 673947-1
iNaturalist 167945
GBIF 5334191
EPPO ROERE
EOL 594972
Elurikkus 518889
USDA GRIN 5268
CMAUP NPO19389

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
The evolution of ephemeral flora in Xinjiang, China: insights from plastid phylogenomic analyses of Brassicaceae Xiao TW, Song F, Vu DQ, Feng Y, Ge XJ BMC Plant Biol 15-Feb-2024
PMCID:PMC10868009
doi:10.1186/s12870-024-04796-0
PMID:38360561
Identification of Candidate Genes Involved in the Determinism of Pollen Grain Aperture Morphology by Comparative Transcriptome Analysis in Papaveraceae Mazuecos-Aguilera I, Suárez-Santiago VN Plants (Basel) 06-Apr-2023
PMCID:PMC10096813
doi:10.3390/plants12071570
PMID:37050196
Transcriptome Analysis Reveals an Essential Role of Exogenous Brassinolide on the Alkaloid Biosynthesis Pathway in Pinellia Ternata Guo C, Chen Y, Wu D, Du Y, Wang M, Liu C, Chu J, Yao X Int J Mol Sci 17-Sep-2022
PMCID:PMC9501358
doi:10.3390/ijms231810898
PMID:36142812
Review on the Antibacterial Mechanism of Plant-Derived Compounds against Multidrug-Resistant Bacteria (MDR) Jubair N, Rajagopal M, Chinnappan S, Abdullah NB, Fatima A Evid Based Complement Alternat Med 16-Aug-2021
PMCID:PMC8384518
doi:10.1155/2021/3663315
PMID:34447454
Botanicals Against Tetranychus urticae Koch Under Laboratory Conditions: A Survey of Alternatives for Controlling Pest Mites Rincón RA, Rodríguez D, Coy-Barrera E Plants (Basel) 07-Aug-2019
PMCID:PMC6724176
doi:10.3390/plants8080272
PMID:31394806
Zygomorphy evolved from disymmetry in Fumarioideae (Papaveraceae, Ranunculales): new evidence from an expanded molecular phylogenetic framework Sauquet H, Carrive L, Poullain N, Sannier J, Damerval C, Nadot S Ann Bot 26-Mar-2015
PMCID:PMC4407061
doi:10.1093/aob/mcv020
PMID:25814061
Molecular Phylogeny of Asian Meconopsis Based on Nuclear Ribosomal and Chloroplast DNA Sequence Data Liu YC, Liu YN, Yang FS, Wang XQ PLoS One 12-Aug-2014
PMCID:PMC4130606
doi:10.1371/journal.pone.0104823
PMID:25118100
Alkaloids of the Papaveraceae. XLII. Alkaloids of Roemeria refracta (STEV.) DC. J. Slavík, L. Slavíková, L. Dolejš Institute of Organic Chemistry & Biochemistry 06-Feb-2013
doi:10.1135/CCCC19684066
Recent Applications of Imines as Key Intermediates in the Synthesis of Alkaloids and Novel Nitrogen Heterocycles Martin SF Pure Appl Chem 01-Jan-2009
PMCID:PMC2723779
doi:10.1351/PAC-CON-08-07-03
PMID:20046937
Two New Benzyltetrahydroisoquinoline Alkaloids from Roemeria refracta Belkis Gözler, Bijen Kivçak, Tekant Gözler, Maurice Shamma American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50069A020
Morphinandienone Alkaloids from Roemeria refracta Belkis Gözler, Pinar Öziç, Alan J. Freyer, Maurice Shamma American Chemical Society (ACS) 30-May-2007
doi:10.1021/NP50070A035
Phylogenetics of Papaver and Related Genera Based on DNA Sequences from ITS Nuclear Ribosomal DNA and Plastid trnL Intron and trnL–F Intergenic Spacers CAROLAN JC, HOOK IL, CHASE MW, KADEREIT JW, HODKINSON TR Ann Bot 01-Jul-2006
PMCID:PMC2803553
doi:10.1093/aob/mcl079
PMID:16675606
Epimeric Isopavine <i>N</i>‐Oxides from <i>Roemeria refracta</i> Belkis Gözler, Mustafa Ali Önür, Serap Bilir, Manfred Hesse Wiley 28-Dec-2004
doi:10.1002/HLCA.19920750121
Some Unusual Pavine and Isopavine Alkaloids from Roemeria refracta. Gözler B, Gözler T, Freyer AJ, Shamma M J Nat Prod 01-Jul-1988
doi:10.1021/NP50058A017
PMID:21401143

Phytochemical Profile Top

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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
(-)-Roemeroline 15559920 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=CC(=C5)O)OCO3 295.30 unknown https://doi.org/10.1135/CCCC19684066
(R)-Roemerine 235224 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown https://doi.org/10.1135/CCCC19684066
5H-Benzo[g]-1,3-benzodioxolo[6,5,4-de]quinolin-11-ol, 6,7,7a,8-tetrahydro-7-methyl-, (7aR)- 5274588 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=C(C=C5)O)OCO3 295.30 unknown https://doi.org/10.1135/CCCC19684066
7-Methyl-6,7,7a,8-tetrahydro-5H-[1,3]benzodioxolo[6,5,4-de]benzo[g]quinolin-11-ol 626376 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=C4C=C(C=C5)O)OCO3 295.30 unknown https://doi.org/10.1135/CCCC19684066
Roemerine 119204 Click to see CN1CCC2=CC3=C(C4=C2C1CC5=CC=CC=C54)OCO3 279.30 unknown https://doi.org/10.1135/CCCC19684066
> Alkaloids and derivatives / Harmala alkaloids
(-)-Roemeridine 5459132 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC5(C(C4)OC)C6=C(CCN5)C7=CC(=C(C=C7N6)OC)OC)O)OC 533.70 unknown https://doi.org/10.1002/HLCA.19920750121
CID 163195583 163195583 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC5(C(C4)OC)C6=C(CCN5)C7=CC(=C(C=C7N6)OC)OC)O)OC 533.70 unknown https://doi.org/10.1002/HLCA.19920750121
CID 500042 500042 Click to see CN1CCC2=CC(=C(C3=C2C1CC34CCC5(C(C4)OC)C6=C(CCN5)C7=CC(=C(C=C7N6)OC)OC)O)OC 533.70 unknown https://doi.org/10.1002/HLCA.19920750121
> Alkaloids and derivatives / Proaporphines
(-)-Mecambrine 3493169 Click to see CN1CCC2=CC3=C(C4=C2C1CC45C=CC(=O)C=C5)OCO3 295.30 unknown https://doi.org/10.1135/CCCC19684066
(1'S,12R,14S)-11-methylspiro[3,5-dioxa-11-azatetracyclo[6.6.1.02,6.012,15]pentadeca-1(15),2(6),7-triene-14,4'-cyclohex-2-ene]-1'-ol 12309666 Click to see CN1CCC2=CC3=C(C4=C2C1CC45CCC(C=C5)O)OCO3 299.40 unknown https://doi.org/10.1135/CCCC19684066
(12R,14S)-11-methylspiro[3,5-dioxa-11-azatetracyclo[6.6.1.02,6.012,15]pentadeca-1(15),2(6),7-triene-14,4'-cyclohex-2-ene]-1'-one 12315010 Click to see CN1CCC2=CC3=C(C4=C2C1CC45CCC(=O)C=C5)OCO3 297.30 unknown https://doi.org/10.1135/CCCC19684066
(12R)-11-methylspiro[3,5-dioxa-11-azatetracyclo[6.6.1.02,6.012,15]pentadeca-1(15),2(6),7-triene-14,4'-cyclohexa-2,5-diene]-1'-one 1403576 Click to see CN1CCC2=CC3=C(C4=C2C1CC45C=CC(=O)C=C5)OCO3 295.30 unknown https://doi.org/10.1135/CCCC19684066
11-Methylspiro[3,5-dioxa-11-azatetracyclo[6.6.1.02,6.012,15]pentadeca-1(15),2(6),7-triene-14,4'-cyclohex-2-ene]-1'-ol 12309664 Click to see CN1CCC2=CC3=C(C4=C2C1CC45CCC(C=C5)O)OCO3 299.40 unknown https://doi.org/10.1135/CCCC19684066
11-Methylspiro[3,5-dioxa-11-azatetracyclo[6.6.1.02,6.012,15]pentadeca-1(15),2(6),7-triene-14,4'-cyclohex-2-ene]-1'-one 12315009 Click to see CN1CCC2=CC3=C(C4=C2C1CC45CCC(=O)C=C5)OCO3 297.30 unknown https://doi.org/10.1135/CCCC19684066
> Alkaloids and derivatives / Protopine alkaloids
Protopine 4970 Click to see CN1CCC2=CC3=C(C=C2C(=O)CC4=C(C1)C5=C(C=C4)OCO5)OCO3 353.40 unknown https://doi.org/10.1135/CCCC19684066
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid 8468 Click to see COC1=C(C=CC(=C1)C(=O)O)O 168.15 unknown via CMAUP database
> Benzenoids / Dibenzocycloheptenes
(+-)-Teframidine 436140 Click to see CN1CC2C3=CC4=C(C=C3CC1C5=CC6=C(C=C25)OCO6)OCO4 323.30 unknown https://doi.org/10.1002/HLCA.19920750121
https://doi.org/10.1021/NP50058A017
https://doi.org/10.1135/CCCC19684066
(1R,12S)-15-methoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.6.2.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaen-16-ol 14106947 Click to see CN1CC2C3=CC(=C(C=C3C1CC4=CC5=C(C=C24)OCO5)OC)O 325.40 unknown https://doi.org/10.1135/CCCC19684066
(1R,12S)-15,16-dimethoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.6.2.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaene 12442695 Click to see CN1CC2C3=CC4=C(C=C3CC1C5=CC(=C(C=C25)OC)OC)OCO4 339.40 unknown https://doi.org/10.1135/CCCC19684066
(1R,12S)-23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.9.2.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-22-one 101434787 Click to see CN1C2CC3=CC4=C(C=C3C(C1=O)C5=CC6=C(C=C25)OCO6)OCO4 337.30 unknown https://doi.org/10.1002/HLCA.19920750121
(1S,12R)-23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.9.2.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaene 162956259 Click to see CN1CC2C3=CC4=C(C=C3CC1C5=CC6=C(C=C25)OCO6)OCO4 323.30 unknown https://doi.org/10.1135/CCCC19684066
1-(23-Methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.9.2.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-22-yl)propan-2-one 162907955 Click to see CC(=O)CC1C2C3=CC4=C(C=C3CC(N1C)C5=CC6=C(C=C25)OCO6)OCO4 379.40 unknown https://doi.org/10.1002/HLCA.19920750121
1-[(1R,12S,22R)-23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.9.2.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-22-yl]propan-2-one 162907956 Click to see CC(=O)CC1C2C3=CC4=C(C=C3CC(N1C)C5=CC6=C(C=C25)OCO6)OCO4 379.40 unknown https://doi.org/10.1002/HLCA.19920750121
15,16-Dimethoxy-20-methyl-5,7-dioxa-20-azapentacyclo[10.6.2.02,10.04,8.013,18]icosa-2,4(8),9,13,15,17-hexaene 12442694 Click to see CN1CC2C3=CC4=C(C=C3CC1C5=CC(=C(C=C25)OC)OC)OCO4 339.40 unknown https://doi.org/10.1002/HLCA.19920750121
https://doi.org/10.1135/CCCC19684066
23-Methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.9.2.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-22-one 23642748 Click to see CN1C2CC3=CC4=C(C=C3C(C1=O)C5=CC6=C(C=C25)OCO6)OCO4 337.30 unknown https://doi.org/10.1002/HLCA.19920750121
Ethyl 2-(23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.9.2.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-22-yl)acetate 163027748 Click to see CCOC(=O)CC1C2C3=CC4=C(C=C3CC(N1C)C5=CC6=C(C=C25)OCO6)OCO4 409.40 unknown https://doi.org/10.1002/HLCA.19920750121
ethyl 2-[(1R,12S,22S)-23-methyl-5,7,16,18-tetraoxa-23-azahexacyclo[10.9.2.02,10.04,8.013,21.015,19]tricosa-2,4(8),9,13,15(19),20-hexaen-22-yl]acetate 163027749 Click to see CCOC(=O)CC1C2C3=CC4=C(C=C3CC(N1C)C5=CC6=C(C=C25)OCO6)OCO4 409.40 unknown https://doi.org/10.1002/HLCA.19920750121
> Benzenoids / Phenanthrenes and derivatives
(1R,12R)-16-methoxy-5,7-dioxa-20-azapentacyclo[10.5.3.01,13.02,10.04,8]icosa-2,4(8),9,13,16-pentaen-15-one 163105791 Click to see COC1=CC23CCNC(C2=CC1=O)CC4=CC5=C(C=C34)OCO5 311.30 unknown https://doi.org/10.1021/NP50070A035
16-Methoxy-5,7-dioxa-20-azapentacyclo[10.5.3.01,13.02,10.04,8]icosa-2,4(8),9,13,16-pentaen-15-one 14760667 Click to see COC1=CC23CCNC(C2=CC1=O)CC4=CC5=C(C=C34)OCO5 311.30 unknown https://doi.org/10.1002/HLCA.19920750121
https://doi.org/10.1021/NP50070A035
Amurine 5462433 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=CC5=C(C=C34)OCO5)OC 325.40 unknown https://doi.org/10.1021/NP50070A035
https://doi.org/10.1002/HLCA.19920750121
Flavinantine 5491380 Click to see CN1CCC23C=C(C(=O)C=C2C1CC4=CC(=C(C=C34)O)OC)OC 327.40 unknown https://doi.org/10.1021/NP50070A035
https://doi.org/10.1002/HLCA.19920750121
> Benzenoids / Phenols / Methoxyphenols
N-Trans-feruloyltramine 5280537 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1002/HLCA.19920750121
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
3-Hydroxystigmast-5-en-7-one 160608 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)C(C)C 428.70 unknown via CMAUP database
7beta-Hydroxysitosterol 12309569 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C 430.70 unknown via CMAUP database
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown via CMAUP database
Ikshusterol 161816 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2C(C=C4C3(CCC(C4)O)C)O)C)C(C)C 430.70 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Sugar acids and derivatives / Glucuronic acid derivatives
Hexuronic Acid 610 Click to see C1(C(C(OC(C1O)O)C(=O)O)O)O 194.14 unknown https://doi.org/10.1135/CCCC19684066
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
(2R)-2,3-dihydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one 86311182 Click to see COC1=CC(=CC(=C1O)OC)C(=O)C(CO)O 242.22 unknown via CMAUP database
3-Hydroxy-1-(4-hydroxy-3,5-dimethoxyphenyl)propan-1-one 54353627 Click to see COC1=CC(=CC(=C1O)OC)C(=O)CCO 226.23 unknown via CMAUP database
4'-Hydroxyacetophenone 7469 Click to see CC(=O)C1=CC=C(C=C1)O 136.15 unknown via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Xanthenes
(8aS,10aS)-1,3-dihydroxy-10a-methyl-2-(3-methylbutanoyl)-7-propan-2-yl-5,8,8a,9-tetrahydroxanthene-4-carbaldehyde 163014655 Click to see CC(C)CC(=O)C1=C(C(=C2C(=C1O)CC3CC(=CCC3(O2)C)C(C)C)C=O)O 386.50 unknown https://doi.org/10.1135/CCCC19684066
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
(-)-Armepavine 442169 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC)OC 313.40 unknown https://doi.org/10.1021/NP50069A020
https://doi.org/10.1002/HLCA.19920750121
(+)-Armepavine 680292 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC)OC 313.40 unknown https://doi.org/10.1021/NP50069A020
(1S)-1-[(3,4-dimethoxyphenyl)methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 13405606 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)O 343.40 unknown https://doi.org/10.1021/NP50069A020
(1S)-7-methoxy-1-[(4-methoxyphenyl)methyl]-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 13258332 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC)OC)O 313.40 unknown https://doi.org/10.1021/NP50069A020
(R)-Coclaurine 440989 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1002/HLCA.19920750121
(R)-N-Methylcoclaurine 440595 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://doi.org/10.1002/HLCA.19920750121
1-(3,4-Dimethoxybenzyl)-7-methoxy-2-methyl-1,2,3,4-tetrahydroisoquinolin-6-ol 276148 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)O 343.40 unknown https://doi.org/10.1002/HLCA.19920750121
https://doi.org/10.1021/NP50069A020
1-[(3,4-dimethoxyphenyl)methyl]-7-methoxy-2-methyl-3,4-dihydro-1H-isoquinoline-4,6-diol 14797295 Click to see CN1CC(C2=CC(=C(C=C2C1CC3=CC(=C(C=C3)OC)OC)OC)O)O 359.40 unknown https://doi.org/10.1002/HLCA.19920750121
https://doi.org/10.1021/NP50069A020
7-methoxy-1-[(4-methoxyphenyl)methyl]-2-methyl-3,4-dihydro-1H-isoquinolin-6-ol 13258331 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)OC)OC)O 313.40 unknown https://doi.org/10.1021/NP50069A020
Armepavine 98348 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)OC)OC 313.40 unknown https://doi.org/10.1002/HLCA.19920750121
Coclaurine 160487 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1002/HLCA.19920750121
Machiline 281691 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)O)O 285.34 unknown https://doi.org/10.1002/HLCA.19920750121
N-Methylcoclaurine 2752274 Click to see CN1CCC2=CC(=C(C=C2C1CC3=CC=C(C=C3)O)O)OC 299.40 unknown https://doi.org/10.1002/HLCA.19920750121
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives
N-feruloyltyramine; Moupinamide 125213 Click to see COC1=C(C=CC(=C1)C=CC(=O)NCCC2=CC=C(C=C2)O)O 313.30 unknown https://doi.org/10.1002/HLCA.19920750121
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
p-Coumaric acid 637542 Click to see C1=CC(=CC=C1C=CC(=O)O)O 164.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Psoralen 6199 Click to see C1=CC(=O)OC2=CC3=C(C=CO3)C=C21 186.16 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Angular pyranocoumarins
Seselin 68229 Click to see CC1(C=CC2=C(O1)C=CC3=C2OC(=O)C=C3)C 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Xanthyletin 65188 Click to see CC1(C=CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)C 228.24 unknown via CMAUP database
> Phenylpropanoids and polyketides / Stilbenes
(2S,3R)-3-Ethoxy-2,3-bis(3-methoxy-4-hydroxyphenyl)propane-1-ol 11759831 Click to see CCOC(C1=CC(=C(C=C1)O)OC)C(CO)C2=CC(=C(C=C2)O)OC 348.40 unknown via CMAUP database
[4-[(4R,5R)-4-(4-acetyloxy-3-methoxyphenyl)-1,3-dioxan-5-yl]-2-methoxyphenyl] acetate 21591953 Click to see CC(=O)OC1=C(C=C(C=C1)C2COCOC2C3=CC(=C(C=C3)OC(=O)C)OC)OC 416.40 unknown via CMAUP database
4-[(4S,5S)-4-(4-hydroxy-3-methoxyphenyl)-1,3-dioxan-5-yl]-2-methoxyphenol 10871293 Click to see COC1=C(C=CC(=C1)C2COCOC2C3=CC(=C(C=C3)O)OC)O 332.30 unknown via CMAUP database

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