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Dracaena cambodiana

Dracaena cambodiana - 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 UUID644025eacf12b731136531
Scientific name Dracaena cambodiana
Authority Pierre ex Gagnep.
First published in Bull. Soc. Bot. France 81: 286 (1934)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Pleomele cambodiana (Pierre ex Gagnep.) Merr. & Chun Sunyatsenia 5: 31 (1940)

Common names Top

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Language Common/alternative name
Chinese 葶苈
Chinese 龙血树
Chinese 山铁树叶
Chinese 柬埔寨龙血树
Chinese 山铁树
Chinese 海南龙血树（柬埔寨龙血树）
Chinese 海南龙血树
Chinese 海南龍血树

Subspecies (abbr. subsp./ssp.) Top

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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-tropical
    • Indian Subcontinent
      • Assam
    • Indo-China
      • Cambodia
      • Laos
      • Thailand
      • Vietnam

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000765700
UNII 8GEJ16838B
Tropicos 18406767
KEW urn:lsid:ipni.org:names:534134-1
The Plant List kew-304598
Open Tree Of Life 330864
NCBI Taxonomy 580341
IPNI 534134-1
iNaturalist 480222
GBIF 5304576
EOL 1087611
USDA GRIN 423614

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.
Accession Assembly
Name Level Submitter Released Coverage Size
GCA_036321105.2 ASM3632110v2 Chromosome Yun nan agricultural university 2024-10-30 75.0x 0.95 Gb

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
Screening and validation of reference genes in Dracaena cochinchinensis using quantitative real-time PCR Gao S, Peng J, Rong M, Liu Y, Xu Y, Wei J Sci Rep 14-Mar-2024
PMCID:PMC10940652
doi:10.1038/s41598-024-52754-5
PMID:38486003
Characterization of phenylalanine ammonia lyase and revealing flavonoid biosynthesis in Gymnema sylvestre R. Br through transcriptomic approach Kalariya KA, Mevada RR, Das M J Genet Eng Biotechnol 13-Feb-2024
PMCID:PMC10903758
doi:10.1016/j.jgeb.2023.100344
PMID:38494263
The chromosome-scale genome of Magnolia sinica (Magnoliaceae) provides insights into the conservation of plant species with extremely small populations (PSESP) Cai L, Liu D, Yang F, Zhang R, Yun Q, Dao Z, Ma Y, Sun W Gigascience 11-Jan-2024
PMCID:PMC10999834
doi:10.1093/gigascience/giad110
PMID:38206588
Designing plant flavonoids: harnessing transcriptional regulation and enzyme variation to enhance yield and diversity Jiang L, Gao Y, Han L, Zhang W, Fan P Front Plant Sci 28-Jul-2023
PMCID:PMC10420081
doi:10.3389/fpls.2023.1220062
PMID:37575923
Fulvifomes wrightii (Hymenochaetales), a new species related to F. robiniae from Argentina and Paraguay Martínez M, Salvador-Montoya CA, de Errasti A, Popoff OF, Rajchenberg M Fungal Syst Evol 28-Jul-2023
PMCID:PMC10976966
doi:10.3114/fuse.2023.12.03
PMID:38550752
Regulatory ligand binding in plant chalcone isomerase–like (CHIL) proteins Wolf-Saxon ER, Moorman CC, Castro A, Ruiz-Rivera A, Mallari JP, Burke JR J Biol Chem 10-May-2023
PMCID:PMC10276294
doi:10.1016/j.jbc.2023.104804
PMID:37172720
Integration of mRNA and miRNA Analysis Reveals the Post-Transcriptional Regulation of Salt Stress Response in Hemerocallis fulva Zhou B, Gao X, Zhao F Int J Mol Sci 14-Apr-2023
PMCID:PMC10139057
doi:10.3390/ijms24087290
PMID:37108448
Phenolic Compounds from New Natural Sources—Plant Genotype and Ontogenetic Variation Nurzyńska-Wierdak R Molecules 11-Feb-2023
PMCID:PMC9959341
doi:10.3390/molecules28041731
PMID:36838719
Flavonoid Production: Current Trends in Plant Metabolic Engineering and De Novo Microbial Production Tariq H, Asif S, Andleeb A, Hano C, Abbasi BH Metabolites 13-Jan-2023
PMCID:PMC9864322
doi:10.3390/metabo13010124
PMID:36677049
Comprehensive identification of bHLH transcription factors in Litsea cubeba reveals candidate gene involved in the monoterpene biosynthesis pathway Yang J, Chen Y, Gao M, Wu L, Xiong S, Wang S, Gao J, Zhao Y, Wang Y Front Plant Sci 21-Dec-2022
PMCID:PMC9811127
doi:10.3389/fpls.2022.1081335
PMID:36618662
Pest categorisation of Colletotrichum aenigma , C. alienum , C. perseae , C. siamense and C. theobromicola Bragard C, Baptista P, Chatzivassiliou E, Di Serio F, Gonthier P, Jaques Miret JA, Justesen AF, MacLeod A, Magnusson CS, Milonas P, Navas‐Cortes JA, Parnell S, Potting R, Reignault PL, Stefani E, Thulke H, Van der Werf W, Vicent Civera A, Yuen J, Zappalà L, Migheli Q, Vloutoglou I, Czwienczek E, Maiorano A, Streissl F, Reignault PL EFSA J 25-Aug-2022
PMCID:PMC9405523
doi:10.2903/j.efsa.2022.7529
PMID:36034322
Genome-Wide Classification and Evolutionary Analysis Reveal Diverged Patterns of Chalcone Isomerase in Plants Wang J, Jiang Y, Sun T, Zhang C, Liu X, Li Y Biomolecules 08-Jul-2022
PMCID:PMC9313115
doi:10.3390/biom12070961
PMID:35883518
The Transcriptome Profiling of Flavonoids and Bibenzyls Reveals Medicinal Importance of Rare Orchid Arundina graminifolia Ahmad S, Gao J, Wei Y, Lu C, Zhu G, Yang F Front Plant Sci 23-Jun-2022
PMCID:PMC9260279
doi:10.3389/fpls.2022.923000
PMID:35812923
Integrative analysis of transcriptome and metabolome reveals the effect of DNA methylation of chalcone isomerase gene in promoter region on Lithocarpus polystachyus Rehd flavonoids Lin L, Wang S, Zhang J, Song X, Zhang D, Cheng W, Cui M, Long Y, Xing Z Synth Syst Biotechnol 20-May-2022
PMCID:PMC9149025
doi:10.1016/j.synbio.2022.05.003
PMID:35664927
Functional Characterization of MtrGSTF7, a Glutathione S-Transferase Essential for Anthocyanin Accumulation in Medicago truncatula Panara F, Passeri V, Lopez L, Porceddu A, Calderini O, Paolocci F Plants (Basel) 16-May-2022
PMCID:PMC9147808
doi:10.3390/plants11101318
PMID:35631744

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
> Benzenoids / Phenols / Benzenediols / Catechols
4-Allylbenzene-1,2-diol 70775 Click to see C=CCC1=CC(=C(C=C1)O)O 150.17 unknown https://doi.org/10.1007/S10600-011-0012-4
> Lipids and lipid-like molecules / Fatty Acyls / Lineolic acids and derivatives
Methyl octadeca-3,9,12-trienoate 71443119 Click to see CCCCCC=CCC=CCCCCC=CCC(=O)OC 292.50 unknown https://doi.org/10.1002/HLCA.200900157
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Pennogenin 12314056 Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)O)C)OC1 430.60 unknown https://doi.org/10.1007/S10600-011-0012-4
Spirost-5-en-3,17-diol 581098 Click to see CC1CCC2(C(C3(C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)O)C)OC1 430.60 unknown https://doi.org/10.1007/S10600-011-0012-4
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Buxus alkaloids
(6S,7R,8R,11R,12S,14S,15S,16R)-6-(dimethylamino)-15-[(1S)-1-(dimethylamino)ethyl]-7-(hydroxymethyl)-7,12,16-trimethyltetracyclo[9.7.0.03,8.012,16]octadeca-1(18),2-dien-14-ol 162871600 Click to see CC(C1C(CC2(C1(CC=C3C2CCC4C(=C3)CCC(C4(C)CO)N(C)C)C)C)O)N(C)C 444.70 unknown https://doi.org/10.1002/HLCA.200900157
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal glycosides / Steroidal saponins
(2R,3S,4S,5R,6R)-2-(hydroxymethyl)-6-[(1R,2S,3'S,4S,5'R,6S,7S,8R,9S,12S,13R,16S,18S,19S)-3'-hydroxy-5',7,9,13-tetramethyl-19-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxane-3,4,5-triol 162987206 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)OC8C(C(C(C(O8)CO)O)O)O)C)C)OC1)O 772.90 unknown https://doi.org/10.1002/HLCA.200900157
(2R)-2-[(2S)-5-hydroxy-6-(hydroxymethyl)-2-[(1R,2R,4R,6R,8S,9S,12R,13R)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-16-yl]oxy-4-[(2R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-3-yl]oxy-6-methyloxane-3,4,5-triol 137705996 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)OC8C(C(C(C(O8)CO)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 885.00 unknown https://doi.org/10.1016/J.FITOTE.2014.01.020
(2S,3R,4R,5R,6S)-2-[(2S,3R,4S,5S)-4,5-dihydroxy-2-[[(1S,2S,4S,6R,7S,8R,9S,12S,13R,14R,16R)-16-hydroxy-6-methoxy-7,9,13-trimethyl-6-[3-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]but-3-enyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-en-14-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 163041046 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC1(CCC(=C)COC8C(C(C(C(O8)CO)O)O)O)OC 901.00 unknown https://doi.org/10.1002/HLCA.200900157
(2S,3R,4S,5R,6R)-2-[(1S,2S,3'S,4S,4'S,5'R,6S,7S,8R,9S,12S,13R,14R,16R)-14-[(2S,3R,4S,5S)-4,5-dihydroxy-3-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-3',16-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-4'-yl]oxy-6-methyloxane-3,4,5-triol 163187698 Click to see CC1COC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)C(C1OC9C(C(C(C(O9)C)O)O)O)O 887.00 unknown https://doi.org/10.1002/HLCA.200900157
[(2S,3S,4S,5R,6S)-4-acetyloxy-6-[(2S,3R,4S,5S)-2-[(1S,2S,3'S,4S,4'S,6S,7S,8R,9S,12S,13R,14R,16R)-3',16-dihydroxy-7,9,13-trimethyl-5'-methylidene-4'-[(2S,3R,4S,5R,6R)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-2-methyloxan-3-yl] acetate 162993448 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)OC(=O)C)OC(=O)C)O)C)C)OC18C(C(C(=C)CO8)OC9C(C(C(C(O9)C)O)O)O)O 969.10 unknown https://doi.org/10.1002/HLCA.200900157
[4-Acetyloxy-6-[2-[3',16-dihydroxy-7,9,13-trimethyl-5'-methylidene-4'-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-5-hydroxy-2-methyloxan-3-yl] acetate 162993447 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)OC(=O)C)OC(=O)C)O)C)C)OC18C(C(C(=C)CO8)OC9C(C(C(C(O9)C)O)O)O)O 969.10 unknown https://doi.org/10.1002/HLCA.200900157
[6-[2-[3',16-Dihydroxy-7,9,13-trimethyl-5'-methylidene-4'-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-14-yl]oxy-4,5-dihydroxyoxan-3-yl]oxy-4,5-dihydroxy-2-methyloxan-3-yl] acetate 85415847 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)OC(=O)C)O)O)C)C)OC18C(C(C(=C)CO8)OC9C(C(C(C(O9)C)O)O)O)O 927.00 unknown https://doi.org/10.1002/HLCA.200900157
1beta-[(2-O-alpha-L-Rhamnopyranosyl-alpha-L-arabinopyranosyl)oxy]-26-(beta-D-glucopyranosyloxy)furosta-5,20(22),25(27)-trien-3beta-ol 44567205 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CC(CC4=CCC5C(C34C)CCC6(C5CC7C6C(=C(O7)CCC(=C)COC8C(C(C(C(O8)CO)O)O)O)C)C)O)O)O)O)O)O 869.00 unknown https://doi.org/10.1002/HLCA.200900157
2-(Hydroxymethyl)-6-[3'-hydroxy-5',7,9,13-tetramethyl-19-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16-yl]oxyoxane-3,4,5-triol 78172924 Click to see CC1CC(C2(C(C3C(O2)CC4C3(CCC5C4CC(C6C5(CCC(C6)OC7C(C(C(C(O7)CO)O)O)O)C)OC8C(C(C(C(O8)CO)O)O)O)C)C)OC1)O 772.90 unknown https://doi.org/10.1002/HLCA.200900157
2-[14-[4,5-Dihydroxy-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3',16-dihydroxy-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-4'-yl]oxy-6-methyloxane-3,4,5-triol 163041879 Click to see CC1COC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(C(CC(C6)O)OC7C(C(C(CO7)O)O)OC8C(C(C(C(O8)C)O)O)O)C)C)C)C(C1OC9C(C(C(C(O9)C)O)O)O)O 887.00 unknown https://doi.org/10.1002/HLCA.200900157
2-[4,5-Dihydroxy-2-[[16-hydroxy-7,9,13-trimethyl-6-[3-[[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]but-3-enyl]-5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-6,18-dien-14-yl]oxy]oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 74208357 Click to see CC1C(C(C(C(O1)OC2C(C(COC2OC3CC(CC4=CCC5C(C34C)CCC6(C5CC7C6C(=C(O7)CCC(=C)COC8C(C(C(C(O8)CO)O)O)O)C)C)O)O)O)O)O)O 869.00 unknown https://doi.org/10.1002/HLCA.200900157
Dioscin 119245 Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)OC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)OC9C(C(C(C(O9)C)O)O)O)C)C)C)OC1 869.00 unknown https://doi.org/10.1016/J.FITOTE.2014.01.020
Namonin C 10440733 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)O)O)O)C)C)OC18C(C(C(=C)CO8)OC9C(C(C(C(O9)C)O)O)O)O 885.00 unknown https://doi.org/10.1002/HLCA.200900157
Namonin D 11147371 Click to see CC1C2C(CC3C2(CCC4C3CC=C5C4(C(CC(C5)O)OC6C(C(C(CO6)O)O)OC7C(C(C(C(O7)C)OC(=O)C)O)O)C)C)OC18C(C(C(=C)CO8)OC9C(C(C(C(O9)C)O)O)O)O 927.00 unknown https://doi.org/10.1002/HLCA.200900157
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
2-(Hydroxymethyl)-6-[4-(3-hydroxyprop-1-enyl)-2,6-dimethoxyphenoxy]oxane-3,4,5-triol 323959 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1002/HLCA.200900157
2-[[3,4-Dihydroxy-4-(hydroxymethyl)oxolan-2-yl]oxymethyl]-6-(3,4,5-trimethoxyphenoxy)oxane-3,4,5-triol 13922633 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 478.40 unknown https://doi.org/10.1002/HLCA.200900157
Eleutheroside B 5316860 Click to see COC1=CC(=CC(=C1OC2C(C(C(C(O2)CO)O)O)O)OC)C=CCO 372.40 unknown https://doi.org/10.1002/HLCA.200900157
Kelampayoside A 10552637 Click to see COC1=CC(=CC(=C1OC)OC)OC2C(C(C(C(O2)COC3C(C(CO3)(CO)O)O)O)O)O 478.40 unknown https://doi.org/10.1002/HLCA.200900157
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde 126 Click to see C1=CC(=CC=C1C=O)O 122.12 unknown https://doi.org/10.1007/S10600-011-0012-4
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(2S)-6-[(1R)-3-(4-hydroxy-2-methoxyphenyl)-1-(4-hydroxyphenyl)propyl]-2-(4-hydroxyphenyl)-8-methyl-3,4-dihydro-2H-chromen-7-ol 162887956 Click to see CC1=C2C(=CC(=C1O)C(CCC3=C(C=C(C=C3)O)OC)C4=CC=C(C=C4)O)CCC(O2)C5=CC=C(C=C5)O 512.60 unknown https://doi.org/10.1007/S10600-011-0012-4
> Phenylpropanoids and polyketides / Homoisoflavonoids / Homoisoflavans
(3S)-3-[(4-hydroxyphenyl)methyl]-3,4-dihydro-2H-chromen-7-ol 124350722 Click to see C1C(COC2=C1C=CC(=C2)O)CC3=CC=C(C=C3)O 256.30 unknown https://doi.org/10.1007/S10600-011-0012-4
(3S)-3-[(4-hydroxyphenyl)methyl]-8-methoxy-3,4-dihydro-2H-chromen-7-ol 162989465 Click to see COC1=C(C=CC2=C1OCC(C2)CC3=CC=C(C=C3)O)O 286.32 unknown https://doi.org/10.1007/S10600-011-0012-4
7-Hydroxy-3-(4-hydroxybenzyl)-8-methoxychroman 44445077 Click to see COC1=C(C=CC2=C1OCC(C2)CC3=CC=C(C=C3)O)O 286.32 unknown https://doi.org/10.1007/S10600-011-0012-4
7-Hydroxy-3-(4-hydroxybenzyl)chroman 11708657 Click to see C1C(COC2=C1C=CC(=C2)O)CC3=CC=C(C=C3)O 256.30 unknown https://doi.org/10.1007/S10600-011-0012-4
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 2-Hydroxychalcones
GU17;ISL;Isoliquiritigen 425 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1007/S10600-011-0012-4
Trihydroxychalcone 638278 Click to see C1=CC(=CC=C1C=CC(=O)C2=C(C=C(C=C2)O)O)O 256.25 unknown https://doi.org/10.1007/S10600-011-0012-4
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / Retro-dihydrochalcones
Loureirin C 14157896 Click to see COC1=C(C=CC(=C1)O)CCC(=O)C2=CC=C(C=C2)O 272.29 unknown https://doi.org/10.1007/S10600-011-0012-4
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Cinnamylphenols
(E)-1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-en-1-one 101008497 Click to see COC1=C(C=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)OC)O 300.30 unknown https://doi.org/10.1007/S10600-011-0012-4
1-(4-Hydroxy-2-methoxyphenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one 25201046 Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=C(C=C2)O 270.28 unknown https://doi.org/10.1007/S10600-011-0012-4
2'-O-Methylisoliquiritigenin 5319688 Click to see COC1=C(C=CC(=C1)O)C(=O)C=CC2=CC=C(C=C2)O 270.28 unknown https://doi.org/10.1007/S10600-011-0012-4
4,4'-Dihydroxy-3,2'-dimethoxychalcone 129882371 Click to see COC1=C(C=CC(=C1)C=CC(=O)C2=C(C=C(C=C2)O)OC)O 300.30 unknown https://doi.org/10.1007/S10600-011-0012-4

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