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Morus cathayana

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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 UUID6440545cca398266490769
Scientific name Morus cathayana
Authority Hemsl.
First published in J. Linn. Soc., Bot. 26: 456 (1894)

Description Top

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No description added yet. Help us by writing one.

Synonyms Top

Scientific name Authority First published in
Morus tiliifolia Makino Bot. Mag. (Tokyo) 23: 88 (1909)
Morus cathayana var. japonica (Makino) Koidz. Bot. Mag. (Tokyo) 31: 39 1917
Morus chinlingensis C.L.Min Acta Bot. Boreal.-Occid. Sin. 6: 277 (1986)
Morus rubra var. japonica Makino

Common names Top

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Language Common/alternative name
Arabic توت صيني
Chinese 鸡桑根
Chinese 华桑
Chinese 秦桑
Chinese 花桑
Chinese 葫芦桑

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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Name Authority First published in
Morus cathayana var. gongshanensis (Z.Y.Cao) Z.Y.Cao Acta Bot. Yunnan. 17: 154 (1995)

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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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
    • China
      • China North-central
      • China South-central
      • China Southeast
    • Eastern Asia
      • Japan
      • Korea

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0001228795
Tropicos 50057507
KEW urn:lsid:ipni.org:names:854633-1
The Plant List tro-50057507
Open Tree Of Life 227175
NCBI Taxonomy 226895
IUCN Red List 135925127
IPNI 854633-1
iNaturalist 521646
GBIF 7262430
EPPO MORCA
EOL 2872509
USDA GRIN 461574
Wikipedia Morus_cathayana
CMAUP NPO14875

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
Combined Treatment of Mori folium and Mori Cortex Radicis Ameliorate Obesity in Mice via UCP-1 in Brown Adipocytes Kim DS, Lee HY, Kim HJ, Lee GH, Lim YJ, Ko BM, Kim JH, Kim TW, Kim HK, Kim TY, Hwang DI, Choi HK, Ju SM, Chung MJ, Chae HJ Nutrients 24-Aug-2023
PMCID:PMC10489681
doi:10.3390/nu15173713
PMID:37686745
Optimized Recovery of Cryostored Dormant Buds of Mulberry Germplasm Choudhary R, Malik SK, Chaudhury R, Rao AA Plants (Basel) 04-Jan-2023
PMCID:PMC9867320
doi:10.3390/plants12020225
PMID:36678937
The complete chloroplast genome sequence of Berchemia racemosa Siebold & Zucc. (Rhamnaceae), a rare plant species in Korea Park JM, Koo J Mitochondrial DNA B Resour 02-Jan-2023
PMCID:PMC9817123
doi:10.1080/23802359.2022.2161329
PMID:36620322
Comparative and phylogenetic analyses of the chloroplast genome reveal the taxonomy of the Morus genus Zeng Q, Chen M, Wang S, Xu X, Li T, Xiang Z, He N Front Plant Sci 24-Nov-2022
PMCID:PMC9729782
doi:10.3389/fpls.2022.1047592
PMID:36507423
Synthesis, Biosynthesis, and Biological Activity of Diels–Alder Adducts from Morus Genus: An Update Tortora C, Pisano L, Vergine V, Ghirga F, Iazzetti A, Calcaterra A, Marković V, Botta B, Quaglio D Molecules 04-Nov-2022
PMCID:PMC9657834
doi:10.3390/molecules27217580
PMID:36364405
The complete chloroplast genome sequences of three Broussonetia species and comparative analysis within the Moraceae Yang J, Chu Q, Meng G, Kong W PeerJ 31-Oct-2022
PMCID:PMC9632464
doi:10.7717/peerj.14293
PMID:36340196
The complete chloroplast genome sequence of Ficus pandurata Hance var. angustifolia W.C. Cheng (Moraceae) Zhang X, Xu F, Guo L Mitochondrial DNA B Resour 22-Aug-2022
PMCID:PMC9415532
doi:10.1080/23802359.2022.2110005
PMID:36034529
Physicochemical Properties and Elimination of the Activity of Anti-Nutritional Serine Protease Inhibitors from Mulberry Leaves Luo Z, Yang J, Zhang J, Meng G, Lu Q, Yang X, Zhao P, Li Y Molecules 11-Mar-2022
PMCID:PMC8948906
doi:10.3390/molecules27061820
PMID:35335184
Phytochemical Composition of Different Botanical Parts of Morus Species, Health Benefits and Application in Food Industry Memete AR, Timar AV, Vuscan AN, Miere (Groza) F, Venter AC, Vicas SI Plants (Basel) 06-Jan-2022
PMCID:PMC8777750
doi:10.3390/plants11020152
PMID:35050040
Molecular Mechanisms Underlying the Biosynthesis of Melatonin and Its Isomer in Mulberry Zheng S, Zhu Y, Liu C, Zhang S, Yu M, Xiang Z, Fan W, Wang S, Zhao A Front Plant Sci 06-Oct-2021
PMCID:PMC8526549
doi:10.3389/fpls.2021.708752
PMID:34691094
Pharmacological Activities for Morus alba L., Focusing on the Immunostimulatory Property from the Fruit Aqueous Extract Chang BY, Koo BS, Kim SY Foods 23-Aug-2021
PMCID:PMC8393821
doi:10.3390/foods10081966
PMID:34441742
The complete chloroplast genome of Humulus lupulus cv. ‘Fubei-1’ (Rosales: Cannabaceae) Wang G, Fan C, Qiu Y, Zhao Y, Zhang J, Xin H, Li X Mitochondrial DNA B Resour 20-Jul-2021
PMCID:PMC8297399
doi:10.1080/23802359.2021.1926352
PMID:34350360
Oxyresveratrol: Sources, Productions, Biological Activities, Pharmacokinetics, and Delivery Systems Likhitwitayawuid K Molecules 11-Jul-2021
PMCID:PMC8307110
doi:10.3390/molecules26144212
PMID:34299485
Deciphering potential pharmacological mechanism of Sha-Shen-Mai-Dong decoction on primary Sjogren’s syndrome Jiang Y, Zhao X, Yu J, Wang Q, Wen C, Huang L BMC Complement Med Ther 01-Mar-2021
PMCID:PMC7923330
doi:10.1186/s12906-021-03257-7
PMID:33648502
Complete plastome sequence of Prunus hypoxantha (Rosaceae), a species endemic in west of China Wang JR, Guo YH, Yang JQ, Tong RC, Cao Z, Zhao L Mitochondrial DNA B Resour 20-Jan-2021
PMCID:PMC7832505
doi:10.1080/23802359.2020.1861995
PMID:33537453

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 / Lupin alkaloids / Sparteine, lupanine, and related alkaloids
Lupanine(1+) 6987464 Click to see C1CC[NH+]2CC3CC(C2C1)CN4C3CCCC4=O 249.37 unknown via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives / Galloyl esters
Methyl gallate 7428 Click to see COC(=O)C1=CC(=C(C(=C1)O)O)O 184.15 unknown via CMAUP database
> Benzenoids / Phenols / Benzenediols / Resorcinols
5-(6-Hydroxy-7,7-dimethyl-3a,4,5,6-tetrahydrofuro[3,2-g]chromen-2-yl)benzene-1,3-diol 480776 Click to see CC1(C(CC2=C(O1)C=C3C(C2)C=C(O3)C4=CC(=CC(=C4)O)O)O)C 328.40 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
https://doi.org/10.3987/COM-95-7310
> Benzenoids / Phenols / Methoxyphenols
4-Hydroxy-3,5-dimethoxybenzyl alcohol 10741 Click to see COC1=CC(=CC(=C1O)OC)CO 184.19 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(5aS,10aS)-1,3,8,10a-tetrahydroxy-5a-[(2Z,6E)-3,7,11-trimethyldodeca-2,6,10-trienyl]-[1]benzofuro[3,2-b]chromen-11-one 162976554 Click to see CC(=CCCC(=CCCC(=CCC12C3=C(C=C(C=C3)O)OC1(C(=O)C4=C(C=C(C=C4O2)O)O)O)C)C)C 506.60 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
Sanggenol H 52951055 Click to see CC(=CCCC(=CCCC(=CCC12C3=C(C=C(C=C3)O)OC1(C(=O)C4=C(C=C(C=C4O2)O)O)O)C)C)C 506.60 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(1R,2S,12S,13R)-2,6,10-trimethyl-13-prop-1-en-2-yl-15-oxabicyclo[10.2.1]pentadeca-5,9-dien-2-ol 162868745 Click to see CC1=CCCC(C2CC(C(O2)CC(=CCC1)C)C(=C)C)(C)O 304.50 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1S,2R,4S,5R,8R,10S,13R,14R,18S,20S)-10-[(2S,3R,4S,5S)-5-[(2S,3R,4S,5S,6R)-4,5-dihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]-3-[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-4-hydroxy-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-hydroxy-4,5,9,9,13,20-hexamethyl-22-oxahexacyclo[18.3.2.01,18.04,17.05,14.08,13]pentacos-16-en-21-one 102069224 Click to see CC1(C2CCC3(C(C2(CCC1OC4C(C(C(CO4)OC5C(C(C(C(O5)COC6C(C(C(C(O6)CO)O)O)O)O)O)OC7C(C(C(CO7)O)O)O)O)OC8C(C(C(C(O8)CO)O)O)O)C)CC=C9C3(CC(C12C9CC(CC1)(C(=O)OC2)C)O)C)C)C 1221.30 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
[(3S,6aR,8aR,12S,14bR)-4,4,6a,6b,8a,11,12,14b-octamethyl-2,3,4a,5,6,7,8,9,10,11,12,12a,14,14a-tetradecahydro-1H-picen-3-yl] acetate 5318295 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
alpha-Amyrenyl acetate 92842 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)OC(=O)C)C)C)C2C1C)C)C 468.80 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
alpha-Amyrin 73170 Click to see CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1C)C)C 426.70 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / 2,2-dimethyl-1-benzopyrans
(5aS,10aR)-2-[(1S,5S,6R)-5-(2,4-dihydroxyphenyl)-6-(5-hydroxy-2,2-dimethyl-3,4-dihydrochromene-6-carbonyl)-3-methylcyclohex-2-en-1-yl]-1,3,8,10a-tetrahydroxy-5a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 162995413 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C4=C(C=C3)OC(CC4)(C)C)O)C5=C(C6=C(C=C5O)OC7(C8=C(C=C(C=C8)O)OC7(C6=O)O)CC=C(C)C)O 776.80 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
2-[(1S,5S,6R)-5-(2,4-dihydroxyphenyl)-6-(5-hydroxy-2,2-dimethyl-3,4-dihydrochromene-6-carbonyl)-3-methylcyclohex-2-en-1-yl]-1,3,8,10a-tetrahydroxy-5a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 101938900 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C4=C(C=C3)OC(CC4)(C)C)O)C5=C(C6=C(C=C5O)OC7(C8=C(C=C(C=C8)O)OC7(C6=O)O)CC=C(C)C)O 776.80 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
4-(9-Methoxy-5,5,13,13-tetramethyl-6-oxatetracyclo[8.5.0.02,7.012,15]pentadeca-1,3,7,9-tetraen-14-yl)benzene-1,3-diol 162990972 Click to see CC1(C=CC2=C3C4C(CC3=C(C=C2O1)OC)C(C4C5=C(C=C(C=C5)O)O)(C)C)C 392.50 unknown https://doi.org/10.1080/10286020.2010.489817
4-[(12R,14R,15S)-9-methoxy-5,5,13,13-tetramethyl-6-oxatetracyclo[8.5.0.02,7.012,15]pentadeca-1,3,7,9-tetraen-14-yl]benzene-1,3-diol 163188123 Click to see CC1(C=CC2=C3C4C(CC3=C(C=C2O1)OC)C(C4C5=C(C=C(C=C5)O)O)(C)C)C 392.50 unknown https://doi.org/10.1080/10286020.2010.489817
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Chromones
(5aR,10aS)-1,3,8,10a-tetrahydroxy-2-[(1R,9R)-5-hydroxy-9-methyl-8-oxatricyclo[7.3.1.02,7]trideca-2(7),3,5,10-tetraen-11-yl]-5a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 162975653 Click to see CC(=CCC12C3=C(C=C(C=C3)O)OC1(C(=O)C4=C(O2)C=C(C(=C4O)C5=CC6(CC(C5)C7=C(O6)C=C(C=C7)O)C)O)O)C 570.60 unknown https://doi.org/10.1021/NP000317C
(5aR,10aS)-4-[(2E)-3,7-dimethylocta-2,6-dienyl]-1,3,8,10a-tetrahydroxy-5a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 163083967 Click to see CC(=CCCC(=CCC1=C2C(=C(C=C1O)O)C(=O)C3(C(O2)(C4=C(O3)C=C(C=C4)O)CC=C(C)C)O)C)C 506.60 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
(5aR,10aS)-9-[(2E)-3,7-dimethylocta-2,6-dienyl]-1,3,8,10a-tetrahydroxy-5a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 101098714 Click to see CC(=CCCC(=CCC1=C(C=CC2=C1OC3(C2(OC4=CC(=CC(=C4C3=O)O)O)CC=C(C)C)O)O)C)C 506.60 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
2-(5,6-Dihydro-9-hydroxy-2-methyl-2,6-methano-2H-1-benzoxocin-4-yl)-5a,10a-dihydro-1,3,8,10a-tetrahydroxy-5a-(3-methyl-2-butenyl)-11H-benzofuro[3,2-b][1]benzopyran-11-one 44559963 Click to see CC(=CCC12C3=C(C=C(C=C3)O)OC1(C(=O)C4=C(O2)C=C(C(=C4O)C5=CC6(CC(C5)C7=C(O6)C=C(C=C7)O)C)O)O)C 570.60 unknown https://doi.org/10.1021/NP000317C
Sanggenol F 66547332 Click to see CC(=CCC1=C(C2=C(C=C1O)OC3(C4=C(C=C(C=C4)O)OC3(C2=O)O)CC=C(C)C)O)C 438.50 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
sorocein F 44559966 Click to see CC(=CCC1=C(C=CC2=C1OC3(C2(OC4=C(C3=O)C(=C(C(=C4)O)CC=C(C)C)O)CC=C(C)C)O)O)C 506.60 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans / Pyranochromenes
(3R,11R)-3,7,14-trihydroxy-18,18-dimethyl-11,21-bis(3-methylbut-2-enyl)-2,10,19-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),4(9),5,7,14,16,20-heptaen-12-one 157483623 Click to see CC(=CCC1=C2C(=C(C3=C1OC4(C5=C(C=C(C=C5)O)OC4(C3=O)CC=C(C)C)O)O)C=CC(O2)(C)C)C 504.60 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
(3S,11R)-3,7,14-trihydroxy-18,18-dimethyl-11-(3-methylbut-2-enyl)-2,10,19-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),4(9),5,7,14,16,20-heptaen-12-one 158328605 Click to see CC(=CCC12C(=O)C3=C(C=C4C(=C3O)C=CC(O4)(C)C)OC1(C5=C(O2)C=C(C=C5)O)O)C 436.50 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
(3S,11R)-7,11,14-trihydroxy-18,18-dimethyl-3-(3-methylbut-2-enyl)-2,10,17-trioxapentacyclo[11.8.0.03,11.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21),19-heptaen-12-one 162977640 Click to see CC(=CCC12C3=C(C=C(C=C3)O)OC1(C(=O)C4=C(O2)C5=C(C=C4O)OC(C=C5)(C)C)O)C 436.50 unknown https://doi.org/10.1021/NP000317C
(3S,11S)-3,7,14-trihydroxy-18,18-dimethyl-11-(3-methylbut-2-enyl)-2,10,17-trioxapentacyclo[11.8.0.03,11.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21),19-heptaen-12-one 159570130 Click to see CC(=CCC12C(=O)C3=C(C4=C(C=C3O)OC(C=C4)(C)C)OC1(C5=C(O2)C=C(C=C5)O)O)C 436.50 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
https://doi.org/10.3987/COM-95-7310
(3S,11S)-3,7,14-trihydroxy-18,18-dimethyl-11-(3-methylbut-2-enyl)-2,10,19-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),4(9),5,7,14,16,20-heptaen-12-one 163189705 Click to see CC(=CCC12C(=O)C3=C(C=C4C(=C3O)C=CC(O4)(C)C)OC1(C5=C(O2)C=C(C=C5)O)O)C 436.50 unknown https://doi.org/10.3987/COM-95-7310
(3S,11S)-3,7,14-trihydroxy-18,18-dimethyl-11,21-bis(3-methylbut-2-enyl)-2,10,19-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),4(9),5,7,14,16,20-heptaen-12-one 162901764 Click to see CC(=CCC1=C2C(=C(C3=C1OC4(C5=C(C=C(C=C5)O)OC4(C3=O)CC=C(C)C)O)O)C=CC(O2)(C)C)C 504.60 unknown https://doi.org/10.3987/COM-95-7310
3,7,14-Trihydroxy-18,18-dimethyl-11-(3-methylbut-2-enyl)-2,10,17-trioxapentacyclo[11.8.0.03,11.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21),19-heptaen-12-one 14334684 Click to see CC(=CCC12C(=O)C3=C(C4=C(C=C3O)OC(C=C4)(C)C)OC1(C5=C(O2)C=C(C=C5)O)O)C 436.50 unknown https://doi.org/10.3987/COM-95-7310
3,7,14-Trihydroxy-18,18-dimethyl-11-(3-methylbut-2-enyl)-2,10,19-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),4(9),5,7,14,16,20-heptaen-12-one 10342974 Click to see CC(=CCC12C(=O)C3=C(C=C4C(=C3O)C=CC(O4)(C)C)OC1(C5=C(O2)C=C(C=C5)O)O)C 436.50 unknown https://doi.org/10.3987/COM-95-7310
3,7,14-Trihydroxy-18,18-dimethyl-11,21-bis(3-methylbut-2-enyl)-2,10,19-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),4(9),5,7,14,16,20-heptaen-12-one 15233698 Click to see CC(=CCC1=C2C(=C(C3=C1OC4(C5=C(C=C(C=C5)O)OC4(C3=O)CC=C(C)C)O)O)C=CC(O2)(C)C)C 504.60 unknown https://doi.org/10.3987/COM-95-7310
7,11,14-Trihydroxy-18,18-dimethyl-3-(3-methylbut-2-enyl)-2,10,17-trioxapentacyclo[11.8.0.03,11.04,9.016,21]henicosa-1(13),4(9),5,7,14,16(21),19-heptaen-12-one 15508130 Click to see CC(=CCC12C3=C(C=C(C=C3)O)OC1(C(=O)C4=C(O2)C5=C(C=C4O)OC(C=C5)(C)C)O)C 436.50 unknown https://doi.org/10.1021/NP000317C
7,11,14-Trihydroxy-18,18-dimethyl-3-(3-methylbut-2-enyl)-2,10,19-trioxapentacyclo[11.8.0.03,11.04,9.015,20]henicosa-1(13),4(9),5,7,14,16,20-heptaen-12-one 15508129 Click to see CC(=CCC12C3=C(C=C(C=C3)O)OC1(C(=O)C4=C(O2)C=C5C(=C4O)C=CC(O5)(C)C)O)C 436.50 unknown https://doi.org/10.1021/NP000317C
sanggenon A 156707 Click to see CC(=CCC12C3=C(C=C(C=C3)O)OC1(C(=O)C4=C(O2)C=C5C(=C4O)C=CC(O5)(C)C)O)C 436.50 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
sanggenon M 44559964 Click to see CC(=CCC12C3=C(C=C(C=C3)O)OC1(C(=O)C4=C(O2)C5=C(C=C4O)OC(C=C5)(C)C)O)C 436.50 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
> Organoheterocyclic compounds / Diazines / Pyrimidines and pyrimidine derivatives / Halopyrimidines
Fluorouracil 3385 Click to see C1=C(C(=O)NC(=O)N1)F 130.08 unknown https://doi.org/10.1021/NP800789Y
> Organoheterocyclic compounds / Pyrans / Pyranones and derivatives / Dihydropyranones
(3S)-3beta-(3-Furyl)-4alpha-hydroxy-7alpha,5alpha-(epoxymethano)-5-methyl-3,4,5,6,7,8-hexahydro-1H-2-benzopyran-1,10-dione 21669397 Click to see CC12CC(CC3=C1C(C(OC3=O)C4=COC=C4)O)OC2=O 290.27 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(-)-Moracin P 25208124 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=C(O3)C4=CC(=CC(=C4)O)O)O)C 326.30 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
https://doi.org/10.3987/COM-95-7310
(2R,3S,4S,5S)-2-[3-hydroxy-5-[(6R)-6-hydroxy-7,7-dimethyl-5,6-dihydrofuro[3,2-g]chromen-2-yl]phenoxy]oxane-3,4,5-triol 162982501 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=C(O3)C4=CC(=CC(=C4)OC5C(C(C(CO5)O)O)O)O)O)C 458.50 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
(3S)-5-(6-hydroxy-1-benzofuran-2-yl)-7-methoxy-2,2-dimethyl-6-(3-methylbut-2-enyl)-3,4-dihydrochromen-3-ol 44139124 Click to see CC(=CCC1=C(C=C2C(=C1C3=CC4=C(O3)C=C(C=C4)O)CC(C(O2)(C)C)O)OC)C 408.50 unknown https://doi.org/10.1021/NP800789Y
1,3-Benzenediol, 5-(7-((2E)-3,7-dimethyl-2,6-octadienyl)-6-methoxy-2-benzofuranyl)- 6440635 Click to see CC(=CCCC(=CCC1=C(C=CC2=C1OC(=C2)C3=CC(=CC(=C3)O)O)OC)C)C 392.50 unknown https://doi.org/10.3987/COM-95-7310
4,6-Bis(3,7-dimethylocta-2,6-dienyl)-5-(6-hydroxy-1-benzofuran-2-yl)benzene-1,3-diol 74932298 Click to see CC(=CCCC(=CCC1=C(C(=C(C=C1O)O)CC=C(C)CCC=C(C)C)C2=CC3=C(O2)C=C(C=C3)O)C)C 514.70 unknown https://doi.org/10.1021/NP800789Y
5-(6-Hydroxy-1-benzofuran-2-yl)-7-methoxy-2,2-dimethyl-6-(3-methylbut-2-enyl)-3,4-dihydrochromen-3-ol 74932299 Click to see CC(=CCC1=C(C=C2C(=C1C3=CC4=C(O3)C=C(C=C4)O)CC(C(O2)(C)C)O)OC)C 408.50 unknown https://doi.org/10.1021/NP800789Y
5-[(6S)-6-(2-hydroxypropan-2-yl)-5,6-dihydrofuro[3,2-f][1]benzofuran-2-yl]benzene-1,3-diol 42603436 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=C(O3)C4=CC(=CC(=C4)O)O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
5-[(6S)-6-hydroxy-7,7-dimethyl-5,6-dihydrofuro[3,2-g]chromen-2-yl]benzene-1,3-diol 102424959 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=C(O3)C4=CC(=CC(=C4)O)O)O)C 326.30 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
https://doi.org/10.3987/COM-95-7310
5-[7-[(2E)-3,7-dimethylocta-2,6-dienyl]-4-methoxy-1-benzofuran-2-yl]benzene-1,3-diol 5319926 Click to see CC(=CCCC(=CCC1=C2C(=C(C=C1)OC)C=C(O2)C3=CC(=CC(=C3)O)O)C)C 392.50 unknown https://doi.org/10.3987/COM-95-7310
Cathafuran A 44139122 Click to see CC(=CCCC(=CCC1=C(C(=C(C=C1O)O)CC=C(C)CCC=C(C)C)C2=CC3=C(O2)C=C(C=C3)O)C)C 514.70 unknown https://doi.org/10.1021/NP800789Y
Cathafuran B 44139000 Click to see CC(=CCC1=C(C=CC2=C1OC(=C2)C3=C(C(=CC(=C3)O)O)CC=C(C)C)O)C 378.50 unknown https://doi.org/10.1021/NP800789Y
Cathafuran C 44139123 Click to see CC(=CCC1=C(C2=C(C=C1O)OC(C=C2)(C)C)C3=CC4=C(O3)C=C(C=C4)O)C 376.40 unknown https://doi.org/10.1021/NP800789Y
CID 42604718 42604718 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=C(O3)C4=CC(=CC(=C4)O)O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
Moracin C 155248 Click to see CC(=CCC1=C(C=C(C=C1O)C2=CC3=C(O2)C=C(C=C3)O)O)C 310.30 unknown https://doi.org/10.3987/COM-95-7310
https://doi.org/10.1016/S0031-9422(01)00171-6
Moracin D 641378 Click to see CC1(C=CC2=C(C=C(C=C2O1)C3=CC4=C(O3)C=C(C=C4)O)O)C 308.30 unknown https://doi.org/10.3987/COM-95-7310
Moracin M 185848 Click to see C1=CC2=C(C=C1O)OC(=C2)C3=CC(=CC(=C3)O)O 242.23 unknown https://doi.org/10.3987/COM-95-7310
Moracin O 14539883 Click to see CC(C)(C1CC2=C(O1)C=C3C(=C2)C=C(O3)C4=CC(=CC(=C4)O)O)O 326.30 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
Moracin P 14539884 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=C(O3)C4=CC(=CC(=C4)O)O)O)C 326.30 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
https://doi.org/10.3987/COM-95-7310
Mulberrofuran V 15233697 Click to see CC(=CCC1=C(C(=C(C=C1O)O)CC=C(C)C)C2=CC3=C(O2)C=C(C=C3)O)C 378.50 unknown https://doi.org/10.3987/COM-95-7310
Mulberroside C 190453 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=C(O3)C4=CC(=CC(=C4)OC5C(C(C(CO5)O)O)O)O)O)C 458.50 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
Sanggenofuran B 131843029 Click to see CC(=CCC1=C(C=C(C=C1O)C2=CC3=C(O2)C=C(C=C3)OC)O)C 324.40 unknown https://doi.org/10.1016/J.FITOTE.2007.06.009
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Scopoletin 5280460 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)O 192.17 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
https://doi.org/10.3987/COM-95-7310
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.3987/COM-95-7310
https://doi.org/10.1016/S0031-9422(01)00171-6
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(5aR,10aR)-2-[(1R,5S,6R)-6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-1,3,5a,8-tetrahydroxy-10a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 154497417 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C5=C(C=C4O)OC6(C7=C(C=C(C=C7)O)OC6(C5=O)CC=C(C)C)O)O 708.70 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
(5aR,10aR)-2-[(1S,5S,6R)-6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-1,3,5a,8-tetrahydroxy-10a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 124596195 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C5=C(C=C4O)OC6(C7=C(C=C(C=C7)O)OC6(C5=O)CC=C(C)C)O)O 708.70 unknown https://doi.org/10.3987/COM-95-7310
(5aR,10aS)-2-[(1R,5S,6R)-6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-1,3,8,10a-tetrahydroxy-5a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 15479639 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C5=C(C=C4O)OC6(C7=C(C=C(C=C7)O)OC6(C5=O)O)CC=C(C)C)O 708.70 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
(5aR,10aS)-2-[6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-1,3,8,10a-tetrahydroxy-5a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 138114872 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C5=C(C=C4O)OC6(C7=C(C=C(C=C7)O)OC6(C5=O)O)CC=C(C)C)O 708.70 unknown https://doi.org/10.3987/COM-95-7310
(5aS,10aR)-2-[(1R,5S,6R)-6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-1,3,8,10a-tetrahydroxy-5a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 92212915 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C5=C(C=C4O)OC6(C7=C(C=C(C=C7)O)OC6(C5=O)O)CC=C(C)C)O 708.70 unknown https://doi.org/10.1021/NP000317C
(5aS,10aR)-4-[(1R,5S,6R)-6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-1,3,10a-trihydroxy-5a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 163103548 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C5C(=C(C=C4O)O)C(=O)C6(C(O5)(C7=CC=CC=C7O6)CC=C(C)C)O 692.70 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
(5aS,10aS)-4-[(1S,5S,6R)-6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-1,3,5a,8-tetrahydroxy-10a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 162989681 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C5C(=C(C=C4O)O)C(=O)C6(C(O5)(C7=C(O6)C=C(C=C7)O)O)CC=C(C)C 708.70 unknown https://doi.org/10.3987/COM-95-7310
2-[(1R,5S,6R)-6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-1,3,8,10a-tetrahydroxy-5a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 442459 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C5=C(C=C4O)OC6(C7=C(C=C(C=C7)O)OC6(C5=O)O)CC=C(C)C)O 708.70 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
2-[(1S,6R)-6-(2,4-dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-1,3,5a,8-tetrahydroxy-10a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 23641096 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C5=C(C=C4O)OC6(C7=C(C=C(C=C7)O)OC6(C5=O)CC=C(C)C)O)O 708.70 unknown via CMAUP database
4-[6-(2,4-Dihydroxybenzoyl)-5-(2,4-dihydroxyphenyl)-3-methylcyclohex-2-en-1-yl]-1,3,5a,8-tetrahydroxy-10a-(3-methylbut-2-enyl)-[1]benzofuro[3,2-b]chromen-11-one 14334685 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C5C(=C(C=C4O)O)C(=O)C6(C(O5)(C7=C(O6)C=C(C=C7)O)O)CC=C(C)C 708.70 unknown https://doi.org/10.3987/COM-95-7310
Cathayanon A 637411 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C5C(=C(C=C4O)O)C(=O)C6(C(O5)(C7=C(O6)C=C(C=C7)O)CC=C(C)C)O 708.70 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
Cathayanon B 10032722 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C5C(=C(C=C4O)O)C(=O)C6(C(O5)(C7=C(O6)C=C(C=C7)O)CC=C(C)C)O 708.70 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
CID 15479638 15479638 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C5=C(C=C4O)OC6(C7=C(C=C(C=C7)O)OC6(C5=O)O)CC=C(C)C)O 708.70 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
https://doi.org/10.1016/S0031-9422(01)00171-6
Sanggenon C 442458 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C5=C(C=C4O)OC6(C7=C(C=C(C=C7)O)OC6(C5=O)O)CC=C(C)C)O 708.70 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
https://doi.org/10.1016/S0031-9422(01)00171-6
sanggenon O 15479637 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C5=C(C=C4O)OC6(C7=C(C=C(C=C7)O)OC6(C5=O)O)CC=C(C)C)O 708.70 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
https://doi.org/10.3987/COM-00-S(I)106
Sanggenon-C 13824422 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C5=C(C=C4O)OC6(C7=C(C=C(C=C7)O)OC6(C5=O)CC=C(C)C)O)O 708.70 unknown https://doi.org/10.3987/COM-95-7310
Sanggenone C 3519902 Click to see CC1=CC(C(C(C1)C2=C(C=C(C=C2)O)O)C(=O)C3=C(C=C(C=C3)O)O)C4=C(C5=C(C=C4O)OC6(C7=C(C=C(C=C7)O)OC6(C5=O)O)CC=C(C)C)O 708.70 unknown https://doi.org/10.1016/S0031-9422(01)00171-6
https://doi.org/10.1021/NP000317C
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 3-prenylated flavans / 3-prenylated flavanones
(2R,3R)-2-[2,4-dihydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 46844950 Click to see CC(=CCC1=CC(=C(C(=C1O)CC=C(C)C)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)C 440.50 unknown https://doi.org/10.1080/10286020.2010.489817
(2R)-2-[3-(3,7-dimethylocta-2,6-dienyl)-2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 162948510 Click to see CC(=CCCC(=CCC1=C(C(=CC(=C1O)C2CC(=O)C3=C(C=C(C=C3O2)O)O)CC=C(C)C)O)C)C 492.60 unknown https://doi.org/10.1080/10286020.2010.489817
(2R)-2-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 46844951 Click to see CC(=CCCC(=CCC1=C(C(=CC(=C1O)C2CC(=O)C3=C(C=C(C=C3O2)O)O)CC=C(C)C)O)C)C 492.60 unknown https://doi.org/10.1080/10286020.2010.489817
2-[3-(3,7-Dimethylocta-2,6-dienyl)-2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 162905942 Click to see CC(=CCCC(=CCC1=C(C(=CC(=C1O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)CC=C(C)C)O)C)C 508.60 unknown https://doi.org/10.3987/COM-95-7310
2-[3-(3,7-Dimethylocta-2,6-dienyl)-2,4-dihydroxyphenyl]-5,7-dihydroxy-2,3-dihydrochromen-4-one 73189755 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O)C)C 424.50 unknown https://doi.org/10.3987/COM-95-7310
3,5,7-Trihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]-2,3-dihydrochromen-4-one 75219223 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)C 424.50 unknown https://doi.org/10.1080/10286020.2010.489817
Cathayanon H 46844949 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)C 424.50 unknown https://doi.org/10.1080/10286020.2010.489817
Cathayanon I 75219224 Click to see CC(=CCC1=CC(=C(C(=C1O)CC=C(C)C)O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)C 440.50 unknown https://doi.org/10.1080/10286020.2010.489817
Sanggenol A 15233693 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O)C)C 424.50 unknown https://doi.org/10.3987/COM-95-7310
Sanggenol D 15233695 Click to see CC(=CCCC(=CCC1=C(C(=CC(=C1O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)CC=C(C)C)O)C)C 508.60 unknown https://doi.org/10.3987/COM-95-7310
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans
(1S,6R,14S,20R,28S,32R)-20-(2,4-dihydroxyphenyl)-3,6,10,24-tetrahydroxy-30-methyl-14-(3-methylbut-2-enyl)-7,15,19,21-tetraoxaoctacyclo[18.11.1.02,18.04,16.06,14.08,13.022,27.028,32]dotriaconta-2,4(16),8(13),9,11,17,22(27),23,25,30-decaen-5-one 162974056 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC6=C(C(=C25)O)C(=O)C7(C(O6)(C8=C(O7)C=C(C=C8)O)CC=C(C)C)O)C9=C(C=C(C=C9)O)O 690.70 unknown https://doi.org/10.1080/10286020.2010.489817
(1S,6S,14R,20R,28S,32R)-20-(2,4-dihydroxyphenyl)-3,6,10,24-tetrahydroxy-30-methyl-14-(3-methylbut-2-enyl)-7,15,19,21-tetraoxaoctacyclo[18.11.1.02,18.04,16.06,14.08,13.022,27.028,32]dotriaconta-2,4(16),8(13),9,11,17,22(27),23,25,30-decaen-5-one 162974055 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC6=C(C(=C25)O)C(=O)C7(C(O6)(C8=C(O7)C=C(C=C8)O)CC=C(C)C)O)C9=C(C=C(C=C9)O)O 690.70 unknown https://doi.org/10.1080/10286020.2010.489817
20-(2,4-Dihydroxyphenyl)-3,6,10,24-tetrahydroxy-30-methyl-14-(3-methylbut-2-enyl)-7,15,19,21-tetraoxaoctacyclo[18.11.1.02,18.04,16.06,14.08,13.022,27.028,32]dotriaconta-2,4(16),8(13),9,11,17,22(27),23,25,30-decaen-5-one 162974054 Click to see CC1=CC2C3C(C1)C4=C(C=C(C=C4)O)OC3(OC5=CC6=C(C(=C25)O)C(=O)C7(C(O6)(C8=C(O7)C=C(C=C8)O)CC=C(C)C)O)C9=C(C=C(C=C9)O)O 690.70 unknown https://doi.org/10.1080/10286020.2010.489817
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 6-prenylated flavans / 6-prenylated flavanones
(2R,3R)-2-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxyphenyl]-3,5,7-trihydroxy-6-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 101938901 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1O)C2C(C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)O)C)C 508.60 unknown https://doi.org/10.1016/S0031-9422(97)00564-5
> Phenylpropanoids and polyketides / Flavonoids / Flavans / 8-prenylated flavans / 8-prenylated flavanones
(2S,3S)-2-[3-[(2E)-3,7-dimethylocta-2,6-dienyl]-2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-3,5,7-trihydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162883775 Click to see CC(=CCCC(=CCC1=C(C(=CC(=C1O)C2C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)CC=C(C)C)O)C)C 576.70 unknown https://doi.org/10.3987/COM-95-7310
2-[3-(3,7-Dimethylocta-2,6-dienyl)-2,4-dihydroxy-5-(3-methylbut-2-enyl)phenyl]-3,5,7-trihydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 162883774 Click to see CC(=CCCC(=CCC1=C(C(=CC(=C1O)C2C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)CC=C(C)C)O)C)C 576.70 unknown https://doi.org/10.3987/COM-95-7310
2-[3-(3,7-Dimethylocta-2,6-dienyl)-4-hydroxyphenyl]-3,5,7-trihydroxy-8-(3-methylbut-2-enyl)-2,3-dihydrochromen-4-one 78412020 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1)C2C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)O)C)C 492.60 unknown https://doi.org/10.3987/COM-95-7310
Sanggenol C 6475725 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1)C2C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)O)C)C 492.60 unknown https://doi.org/10.3987/COM-95-7310
Sanggenol E 15233696 Click to see CC(=CCCC(=CCC1=C(C(=CC(=C1O)C2C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)CC=C(C)C)O)C)C 576.70 unknown https://doi.org/10.3987/COM-95-7310
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2S)-2-(2,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydrochromen-4-one 15233699 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=C(C=C(C=C3)O)O 272.25 unknown https://doi.org/10.3987/COM-95-7310
2',4',7-Trihydroxy-flavanone 91557562 Click to see C1C(OC2=C(C1=O)C=CC(=C2)O)C3=C(C=C(C=C3)O)O 272.25 unknown https://doi.org/10.3987/COM-95-7310
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 3-prenylated flavones
3,5,7-Trihydroxy-2-[4-hydroxy-3,5-bis(3-methylbut-2-enyl)phenyl]chromen-4-one 46844821 Click to see CC(=CCC1=CC(=CC(=C1O)CC=C(C)C)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)C 422.50 unknown https://doi.org/10.1080/10286020.2010.489817
> Phenylpropanoids and polyketides / Flavonoids / Flavones / 8-prenylated flavones
2-[3-(3,7-Dimethylocta-2,6-dienyl)-4-hydroxyphenyl]-3,5,7-trihydroxy-8-(3-methylbut-2-enyl)chromen-4-one 73189756 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)O)C)C 490.60 unknown https://doi.org/10.3987/COM-95-7310
Sanggenol B 15233694 Click to see CC(=CCCC(=CCC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C(=C3O2)CC=C(C)C)O)O)O)O)C)C 490.60 unknown https://doi.org/10.3987/COM-95-7310
> Phenylpropanoids and polyketides / Isocoumarins and derivatives
(1R)-7,8,9-trihydroxy-3,5-dioxo-1,2-dihydrocyclopenta[c]isochromene-1-carboxylic acid 102004656 Click to see C1C(C2=C(C1=O)OC(=O)C3=CC(=C(C(=C32)O)O)O)C(=O)O 292.20 unknown via CMAUP database
Brevifolin[Geranium] 10131135 Click to see C1CC(=O)C2=C1C3=C(C(=C(C=C3C(=O)O2)O)O)O 248.19 unknown via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Isoflavans / Isoflavanones
(3R)-5,7-dihydroxy-3-(4-hydroxyphenyl)-6-[(1R,6R)-3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-yl]-2,3-dihydrochromen-4-one 46844820 Click to see CC1=CC(C(CC1)C(=C)C)C2=C(C3=C(C=C2O)OCC(C3=O)C4=CC=C(C=C4)O)O 406.50 unknown https://doi.org/10.1080/10286020.2010.489817
5,7-Dihydroxy-3-(4-hydroxyphenyl)-6-(3-methyl-6-prop-1-en-2-ylcyclohex-2-en-1-yl)-2,3-dihydrochromen-4-one 75219161 Click to see CC1=CC(C(CC1)C(=C)C)C2=C(C3=C(C=C2O)OCC(C3=O)C4=CC=C(C=C4)O)O 406.50 unknown https://doi.org/10.1080/10286020.2010.489817
> 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/10.3987/COM-95-7310
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/10.3987/COM-95-7310
> Phenylpropanoids and polyketides / Linear 1,3-diarylpropanoids / Chalcones and dihydrochalcones / 3-prenylated chalcones
Isobavachalcone 5281255 Click to see CC(=CCC1=C(C=CC(=C1O)C(=O)C=CC2=CC=C(C=C2)O)O)C 324.40 unknown https://doi.org/10.3987/COM-95-7310
> Phenylpropanoids and polyketides / Tannins
1,3,4,6-Tetragalloylglucose 471531 Click to see C1=C(C=C(C(=C1O)O)O)C(=O)OCC2C(C(C(C(O2)OC(=O)C3=CC(=C(C(=C3)O)O)O)O)OC(=O)C4=CC(=C(C(=C4)O)O)O)OC(=O)C5=CC(=C(C(=C5)O)O)O 788.60 unknown via CMAUP database
> Phenylpropanoids and polyketides / Tannins / Hydrolyzable tannins
Ellagic Acid 5281855 Click to see C1=C2C3=C(C(=C1O)O)OC(=O)C4=CC(=C(C(=C43)OC2=O)O)O 302.19 unknown via CMAUP database

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