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Curcuma comosa

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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 UUID643ff4c12d86f420734667
Scientific name Curcuma comosa
Authority Roxb.
First published in Asiat. Res. 11:336. (1810)

Description Top

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Curcuma comosa is a species of flowering plant in the ginger family native to much of Asia, including Thailand, Indonesia, and Malaysia. It is widely used as a traditional herbal remedy for its anti-inflammatory properties and to treat postpartum uterine bleeding, uterine inflammation, vaginal dryness, hot flashes, excessive white and yellow vaginal discharge, bad odor, and irregular, excessive, or absent menstrual cycles. Research has shown that it can reduce blood cholesterol, increase the thickness of epithelial cells lining the vagina, and decrease uterine smooth muscle contraction. It has also been found to have an estrogenic effect, and is used in Thai luxury spas to lift sagging muscles, promote circulation, and provide good health and glowing skin.

Synonyms Top

No known synonyms.

Common names Top

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Language Common/alternative name
Thai ว่านทรหด
Chinese 多毛姜黄

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

Varieties (abbr. var.) Top

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No variety added yet.

Subvarieties (abbr. subvar.) Top

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No subvariety added yet.

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
      • Myanmar
      • Thailand
    • Malesia
      • Malaya

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000365517
Tropicos 50179129
KEW urn:lsid:ipni.org:names:796436-1
The Plant List kew-235211
Open Tree Of Life 1053721
NCBI Taxonomy 199633
IPNI 796436-1
GBIF 2757575
Freebase /m/0gg99l8
EOL 1122332
USDA GRIN 468573
Wikipedia Curcuma_comosa

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
Improving hematopoietic differentiation from human induced pluripotent stem cells by the modulation of Hippo signaling with a diarylheptanoid derivative Thongsa-ad U, Wongpan A, Wongkummool W, Chaiwijit P, Uppakara K, Chaiyakitpattana G, Singpant P, Tong-ngam P, Chukhan A, Pabuprappap W, Wongniam S, Suksamrarn A, Hongeng S, Anurathapan U, Kulkeaw K, Tubsuwan A, Bhukhai K Stem Cell Res Ther 03-Mar-2024
PMCID:PMC10910864
doi:10.1186/s13287-024-03686-4
PMID:38433217
Targeted Isolation of Antibiofilm Compounds from Halophytic Endophyte Bacillus velezensis 7NPB-3B Using LC-HR-MS-Based Metabolomics Singh S, Nwagwu E, Young L, Kumar P, Shinde PB, Edrada-Ebel R Microorganisms 19-Feb-2024
PMCID:PMC10891937
doi:10.3390/microorganisms12020413
PMID:38399817
Fabrication and Optimization of Electrospun Shellac Fibers Loaded with Senna alata Leaf Extract Aung WW, Krongrawa W, Limmatvapirat S, Kulpicheswanich P, Okonogi S, Limmatvapirat C Polymers (Basel) 08-Jan-2024
PMCID:PMC10819501
doi:10.3390/polym16020183
PMID:38256981
Mechanisms of action and synergetic formulas of plant-based natural compounds from traditional Chinese medicine for managing osteoporosis: a literature review Zhou C, Shen S, Zhang M, Luo H, Zhang Y, Wu C, Zeng L, Ruan H Front Med (Lausanne) 28-Aug-2023
PMCID:PMC10493415
doi:10.3389/fmed.2023.1235081
PMID:37700771
Advances in Natural Product Extraction Techniques, Electrospun Fiber Fabrication, and the Integration of Experimental Design: A Comprehensive Review Ponphaiboon J, Krongrawa W, Aung WW, Chinatangkul N, Limmatvapirat S, Limmatvapirat C Molecules 02-Jul-2023
PMCID:PMC10343563
doi:10.3390/molecules28135163
PMID:37446825
Endogenous and Exogenous Regulation of Redox Homeostasis in Retinal Pigment Epithelium Cells: An Updated Antioxidant Perspective Markitantova Y, Simirskii V Int J Mol Sci 28-Jun-2023
PMCID:PMC10341664
doi:10.3390/ijms241310776
PMID:37445953
Formerly bile-farmed bears as a model of accelerated ageing Kalogeropoulu SK, Rauch-Schmücking H, Lloyd EJ, Stenvinkel P, Shiels PG, Johnson RJ, Fröbert O, Redtenbacher I, Burgener IA, Painer-Gigler J Sci Rep 15-Jun-2023
PMCID:PMC10272202
doi:10.1038/s41598-023-36447-z
PMID:37322151
Potential therapeutic effects of Chinese meteria medica in mitigating drug-induced acute kidney injury Li J, Li T, Li Z, Song Z, Gong X Front Pharmacol 03-Apr-2023
PMCID:PMC10106589
doi:10.3389/fphar.2023.1153297
PMID:37077810
A systematic review of mucoadhesive vaginal tablet testing Abidin IZ, Murphy EJ, Fehrenbach GW, Rezoagli E, Gately N, Major I Drug Target Insights 16-Jan-2023
PMCID:PMC9851603
doi:10.33393/dti.2023.2477
PMID:36687797
Formulation and In Vitro Evaluation of Mucoadhesive Sustained Release Gels of Phytoestrogen Diarylheptanoids from Curcuma comosa for Vaginal Delivery Limpongsa E, Tabboon P, Tuntiyasawasdikul S, Sripanidkulchai B, Pongjanyakul T, Jaipakdee N Pharmaceutics 12-Jan-2023
PMCID:PMC9862155
doi:10.3390/pharmaceutics15010264
PMID:36678892
Characterization of the produced electrospun fish gelatin nanofiber containing fucoxanthin Azarshah A, Moosavi-Nasab M, Khorram M, Babaei S, Oliyaei N Food Sci Biotechnol 05-Nov-2022
PMCID:PMC9905401
doi:10.1007/s10068-022-01197-7
PMID:36778089
A pure compound from Curcuma comosa Roxb. protects neurons against hydrogen peroxide-induced neurotoxicity via the activation of Nrf-2 Khin Aung ZM, Jantaratnotai N, Piyachaturawat P, Sanvarinda P Heliyon 25-Oct-2022
PMCID:PMC9626547
doi:10.1016/j.heliyon.2022.e11228
PMID:36339760
A Novel Drug Modulator Diarylheptanoid (trans-1,7-Diphenyl-5-hydroxy-1-heptene) from Curcuma comosa Rhizomes for P-glycoprotein Function and Apoptosis Induction in K652/ADR Leukemic Cells Viriyaadhammaa N, Duangmano S, Saiai A, Tungjai M, Dejkriengkraikul P, Tima S, Chiampanichayakul S, Krise J, Anuchapreeda S Int J Mol Sci 12-Aug-2022
PMCID:PMC9409401
doi:10.3390/ijms23168989
PMID:36012254
Enhancing Erythropoiesis by a Phytoestrogen Diarylheptanoid from Curcuma comosa Bhukhai K, Fouquet G, Rittavee Y, Tanhuad N, Lakmuang C, Borwornpinyo S, Anurathapan U, Suksamrarn A, Piyachaturawat P, Chairoungdua A, Hermine O, Hongeng S Biomedicines 16-Jun-2022
PMCID:PMC9219836
doi:10.3390/biomedicines10061427
PMID:35740448
Advances in Fingerprint Analysis for Standardization and Quality Control of Herbal Medicines Noviana E, Indrayanto G, Rohman A Front Pharmacol 02-Jun-2022
PMCID:PMC9201489
doi:10.3389/fphar.2022.853023
PMID:35721184

Phytochemical Profile Top

Add a new one!
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 / 1-hydroxy-2-unsubstituted benzenoids
(+)-Rhododendrol 919204 Click to see CC(CCC1=CC=C(C=C1)O)O 166.22 unknown https://doi.org/10.1248/CPB.56.1604
4-(3-Hydroxybutyl)phenol 97790 Click to see CC(CCC1=CC=C(C=C1)O)O 166.22 unknown https://doi.org/10.1248/CPB.56.1604
4-(4-Hydroxyphenyl)-2-butanone 21648 Click to see CC(=O)CCC1=CC=C(C=C1)O 164.20 unknown https://doi.org/10.1248/CPB.56.1604
> Benzenoids / Phenols / Methoxyphenols
Vanillin 1183 Click to see COC1=C(C=CC(=C1)C=O)O 152.15 unknown https://doi.org/10.1248/CPB.56.1604
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Colensane and clerodane diterpenoids
3-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethenyl]furan 85079076 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=COC=C3)C)C 284.40 unknown https://doi.org/10.1021/NP900568K
Coronarin E 9971144 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=COC=C3)C)C 284.40 unknown https://doi.org/10.1021/NP900568K
> Lipids and lipid-like molecules / Prenol lipids / Monoterpenoids / Menthane monoterpenoids
(1S)-1-(2-hydroxypropan-2-yl)-4-methylcyclohex-3-en-1-ol 101630055 Click to see CC1=CCC(CC1)(C(C)(C)O)O 170.25 unknown https://doi.org/10.1248/CPB.56.1604
(6S)-6-hydroxy-3-(2-hydroxypropan-2-yl)-6-methylcyclohex-2-en-1-one 162909242 Click to see CC1(CCC(=CC1=O)C(C)(C)O)O 184.23 unknown https://doi.org/10.1248/CPB.56.1604
1,8-Dihydroxy-p-menth-3-en-2-one 60151497 Click to see CC1(CCC(=CC1=O)C(C)(C)O)O 184.23 unknown https://doi.org/10.1248/CPB.56.1604
3-Cyclohexene-1-methanol, 1-hydroxy-alpha,alpha,4-trimethyl- 179652 Click to see CC1=CCC(CC1)(C(C)(C)O)O 170.25 unknown https://doi.org/10.1248/CPB.56.1604
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Diterpene lactones
12-Hydroxy-8(17),13-labdadien-16,15-olide 16081507 Click to see CC1(CCCC2(C1CCC(=C)C2CC(C3=CCOC3=O)O)C)C 318.40 unknown https://doi.org/10.1021/NP900568K
4-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethenyl]-2H-furan-5-one 73315303 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=CCOC3=O)C)C 300.40 unknown https://doi.org/10.1021/NP900568K
4-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethenyl]-3-hydroxy-2H-furan-5-one 76213530 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=C(COC3=O)O)C)C 316.40 unknown https://doi.org/10.1021/NP900568K
4-[2-(5,5,8a-trimethyl-2-methylidene-6-oxo-1,3,4,4a,7,8-hexahydronaphthalen-1-yl)ethenyl]-2H-furan-5-one 75148999 Click to see CC1(C2CCC(=C)C(C2(CCC1=O)C)C=CC3=CCOC3=O)C 314.40 unknown https://doi.org/10.1021/NP900568K
4-[2-(6-hydroxy-5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethenyl]-2H-furan-5-one 75149000 Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)C=CC3=CCOC3=O)C 316.40 unknown https://doi.org/10.1021/NP900568K
Curcucomosin A 46209660 Click to see CC1(C2CCC(=C)C(C2(CCC1=O)C)C=CC3=CCOC3=O)C 314.40 unknown https://doi.org/10.1021/NP900568K
Curcucomosin B 46209661 Click to see CC1(C2CCC(=C)C(C2(CCC1O)C)C=CC3=CCOC3=O)C 316.40 unknown https://doi.org/10.1021/NP900568K
Villosin 16733738 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=CCOC3=O)C)C 300.40 unknown https://doi.org/10.1021/NP900568K
Vitexolide D 73235937 Click to see CC1(CCCC2(C1CCC(=C)C2CC(C3=CCOC3=O)O)C)C 318.40 unknown https://doi.org/10.1021/NP900568K
Zerumin 54734314 Click to see CC1(CCCC2(C1CCC(=C)C2C=CC3=C(COC3=O)O)C)C 316.40 unknown https://doi.org/10.1021/NP900568K
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(3R,6R)-2,2,6-trimethyl-1-oxaspiro[2.5]oct-4-en-6-ol 25130461 Click to see CC1(C2(O1)CCC(C=C2)(C)O)C 168.23 unknown https://doi.org/10.1248/CPB.56.1604
2-(6-Methyl-7-oxabicyclo[4.1.0]hept-2-en-3-yl)propan-2-ol 74390185 Click to see CC12CCC(=CC1O2)C(C)(C)O 168.23 unknown https://doi.org/10.1248/CPB.56.1604
2-[(1R,6S)-6-methyl-7-oxabicyclo[4.1.0]hept-2-en-3-yl]propan-2-ol 162949977 Click to see CC12CCC(=CC1O2)C(C)(C)O 168.23 unknown https://doi.org/10.1248/CPB.56.1604
2,2,6-Trimethyl-1-oxaspiro[2.5]oct-4-en-6-ol 74390184 Click to see CC1(C2(O1)CCC(C=C2)(C)O)C 168.23 unknown https://doi.org/10.1248/CPB.56.1604
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(1S,2S,4R)-1,8-Epoxy-p-menthan-2-ol glucoside 73815050 Click to see CC1(C2CCC(O1)(C(C2)OC3C(C(C(C(O3)CO)O)O)O)C)C 332.39 unknown https://doi.org/10.1248/CPB.56.1604
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[[(1S,4R,6S)-1,3,3-trimethyl-2-oxabicyclo[2.2.2]octan-6-yl]oxy]oxane-3,4,5-triol 21630948 Click to see CC1(C2CCC(O1)(C(C2)OC3C(C(C(C(O3)CO)O)O)O)C)C 332.39 unknown https://doi.org/10.1248/CPB.56.1604
(2S)-6-hydroxy-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-1,4-benzoxazin-3-one 641761 Click to see C1=CC2=C(C=C1O)NC(=O)C(O2)OC3C(C(C(C(O3)CO)O)O)O 343.29 unknown https://doi.org/10.1016/J.BMC.2008.05.051
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
1-[2,4-dihydroxy-6-[(2R,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone 10042250 Click to see CC(=O)C1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)O)O 330.29 unknown https://doi.org/10.1016/J.BMC.2008.05.051
1-[2,4-Dihydroxy-6-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]ethanone 14655247 Click to see CC(=O)C1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(96)00778-9
https://doi.org/10.1016/J.BMC.2008.05.051
2-(Hydroxymethyl)-6-[5-(2-hydroxypropan-2-yl)-2-methylphenoxy]oxane-3,4,5-triol 74390186 Click to see CC1=C(C=C(C=C1)C(C)(C)O)OC2C(C(C(C(O2)CO)O)O)O 328.36 unknown https://doi.org/10.1248/CPB.56.1604
Comososide 25130463 Click to see CC1=C(C=C(C=C1)C(C)(C)O)OC2C(C(C(C(O2)CO)O)O)O 328.36 unknown https://doi.org/10.1248/CPB.56.1604
Myrciaphenone A 179470 Click to see CC(=O)C1=C(C=C(C=C1OC2C(C(C(C(O2)CO)O)O)O)O)O 330.29 unknown https://doi.org/10.1016/S0031-9422(96)00778-9
> 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/10.1248/CPB.56.1604
> Organoheterocyclic compounds / Isoquinolines and derivatives / Benzylisoquinolines
Lindoldhamine (R,R) 10370752 Click to see COC1=C(C=C2C(NCCC2=C1)CC3=CC=C(C=C3)OC4=C(C=CC(=C4)CC5C6=CC(=C(C=C6CCN5)OC)O)O)O 568.70 unknown https://doi.org/10.1016/J.BMC.2008.05.051
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
3-[2-(5,5,8a-trimethyl-2-methylidene-3,4,4a,6,7,8-hexahydro-1H-naphthalen-1-yl)ethylidene]-4-hydroxyoxolan-2-one 75238669 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C3C(COC3=O)O)C)C 318.40 unknown https://doi.org/10.1021/NP900568K
isocoronarin D 46871816 Click to see CC1(CCCC2(C1CCC(=C)C2CC=C3C(COC3=O)O)C)C 318.40 unknown https://doi.org/10.1021/NP900568K
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
(-)-(3S)-1-(3,4-dihydroxyphenyl)-7-phenyl-(6E)-6-hepten-3-ol 44560893 Click to see C1=CC=C(C=C1)C=CCCC(CCC2=CC(=C(C=C2)O)O)O 298.40 unknown https://doi.org/10.1016/J.BMC.2008.05.051
(+)-(3R)-1-(3,4-dihydroxyphenyl)-7-phenyl-(6E)-6-hepten-3-ol 49831860 Click to see C1=CC=C(C=C1)C=CCCC(CCC2=CC(=C(C=C2)O)O)O 298.40 unknown https://doi.org/10.1016/S0031-9422(96)00778-9
(+)-(3R)-1,7-bis(4-hydroxyphenyl)-(6E)-6-hepten-3-ol 38362130 Click to see C1=CC(=CC=C1CCC(CCC=CC2=CC=C(C=C2)O)O)O 298.40 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
(3R,5R)-1,7-Bis(3,4-dihydroxyphenyl)-5-hydroxyheptan-3-ylacetate 54577120 Click to see CC(=O)OC(CCC1=CC(=C(C=C1)O)O)CC(CCC2=CC(=C(C=C2)O)O)O 390.40 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
(3r)-1,7-Diphenyl-(4e,6e)-4,6-heptadien-3-ol 44560847 Click to see C1=CC=C(C=C1)CCC(C=CC=CC2=CC=CC=C2)O 264.40 unknown https://doi.org/10.1021/JF802702C
https://doi.org/10.1016/J.BMC.2008.05.051
(4E,6E)-1-(4-hydroxyphenyl)-7-phenylhepta-4,6-dien-3-one 641618 Click to see C1=CC=C(C=C1)C=CC=CC(=O)CCC2=CC=C(C=C2)O 278.30 unknown https://doi.org/10.1021/JF802702C
https://doi.org/10.1016/J.BMC.2008.05.051
(4E,6E)-1,7-diphenylhepta-4,6-dien-3-ol 13347322 Click to see C1=CC=C(C=C1)CCC(C=CC=CC2=CC=CC=C2)O 264.40 unknown https://doi.org/10.1021/NP50104A006
(4E,6E)-7-(3,4-dihydroxyphenyl)-1-(4-hydroxyphenyl)hepta-4,6-dien-3-one 72164688 Click to see C1=CC(=CC=C1CCC(=O)C=CC=CC2=CC(=C(C=C2)O)O)O 310.30 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
(6e)-1,7-Diphenylhept-6-en-3-ol 5316931 Click to see C1=CC=C(C=C1)CCC(CCC=CC2=CC=CC=C2)O 266.40 unknown https://doi.org/10.1021/NP50104A006
(alphaS)-4-Hydroxy-alpha-[(3E)-4-phenyl-3-buten-1-yl]benzenepropanol 44560892 Click to see C1=CC=C(C=C1)C=CCCC(CCC2=CC=C(C=C2)O)O 282.40 unknown https://doi.org/10.1016/J.BMC.2008.05.051
(E,3R)-1,7-diphenylhept-6-en-3-ol 102294797 Click to see C1=CC=C(C=C1)CCC(CCC=CC2=CC=CC=C2)O 266.40 unknown https://doi.org/10.1016/S0031-9422(96)00778-9
(S)-1,7-Diphenyl-6(E)-hepten-3-ol 44560846 Click to see C1=CC=C(C=C1)CCC(CCC=CC2=CC=CC=C2)O 266.40 unknown https://doi.org/10.1016/J.BMC.2008.05.051
https://doi.org/10.1021/NP900568K
https://doi.org/10.1021/JF802702C
[(3R,5R)-1-(3,4-dihydroxyphenyl)-5-hydroxy-7-(4-hydroxyphenyl)heptan-3-yl] acetate 54577123 Click to see CC(=O)OC(CCC1=CC(=C(C=C1)O)O)CC(CCC2=CC=C(C=C2)O)O 374.40 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
[(E)-1,7-diphenylhept-6-en-3-yl] acetate 10380587 Click to see CC(=O)OC(CCC=CC1=CC=CC=C1)CCC2=CC=CC=C2 308.40 unknown https://doi.org/10.1021/NP50104A006
1-(4-hydroxyphenyl)-7-phenyl-(6E)-hept-6-en-3-one 44560848 Click to see C1=CC=C(C=C1)C=CCCC(=O)CCC2=CC=C(C=C2)O 280.40 unknown https://doi.org/10.1021/JF802702C
https://doi.org/10.1016/J.BMC.2008.05.051
1-(4-Hydroxyphenyl)-7-phenylhept-6-en-3-one 75070101 Click to see C1=CC=C(C=C1)C=CCCC(=O)CCC2=CC=C(C=C2)O 280.40 unknown https://doi.org/10.1021/JF802702C
https://doi.org/10.1016/J.BMC.2008.05.051
1-(4-Hydroxyphenyl)-7-phenylhepta-4,6-dien-3-one 78201074 Click to see C1=CC=C(C=C1)C=CC=CC(=O)CCC2=CC=C(C=C2)O 278.30 unknown https://doi.org/10.1016/J.BMC.2008.05.051
https://doi.org/10.1021/JF802702C
1,2-Benzenediol, 4-[(3R,5R)-3,5-bis(acetyloxy)-7-(4-hydroxyphenyl)heptyl]- 54577121 Click to see CC(=O)OC(CCC1=CC=C(C=C1)O)CC(CCC2=CC(=C(C=C2)O)O)OC(=O)C 416.50 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
1,7-Bis(4-hydroxyphenyl)hept-6-en-3-one 49831652 Click to see C1=CC(=CC=C1CCC(=O)CCC=CC2=CC=C(C=C2)O)O 296.40 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
1,7-Bis(4-hydroxyphenyl)hepta-4,6-dien-3-one 10613719 Click to see C1=CC(=CC=C1CCC(=O)C=CC=CC2=CC=C(C=C2)O)O 294.30 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
1,7-Diphenyl-(6e)-6-hepten-3-one 44593373 Click to see C1=CC=C(C=C1)CCC(=O)CCC=CC2=CC=CC=C2 264.40 unknown https://doi.org/10.1021/NP50104A006
https://doi.org/10.1021/JF802702C
https://doi.org/10.1016/J.BMC.2008.05.051
1,7-Diphenyl-1,3,5-heptratriene 44560845 Click to see C1=CC=C(C=C1)CC=CC=CC=CC2=CC=CC=C2 246.30 unknown https://doi.org/10.1016/J.BMC.2008.05.051
1,7-Diphenyl-4,6-heptadien-3-one 342344 Click to see C1=CC=C(C=C1)CCC(=O)C=CC=CC2=CC=CC=C2 262.30 unknown https://doi.org/10.1016/J.BMC.2008.05.051
1,7-Diphenyl-6-hepten-3-one 73123116 Click to see C1=CC=C(C=C1)CCC(=O)CCC=CC2=CC=CC=C2 264.40 unknown https://doi.org/10.1021/JF802702C
1,7-Diphenylhept-6-EN-3-OL 57354969 Click to see C1=CC=C(C=C1)CCC(CCC=CC2=CC=CC=C2)O 266.40 unknown https://doi.org/10.1021/JF802702C
https://doi.org/10.1016/S0031-9422(96)00778-9
https://doi.org/10.1016/J.BMC.2008.05.051
https://doi.org/10.1021/NP900568K
1,7-Diphenylhepta-4,6-dien-3-ol 641642 Click to see C1=CC=C(C=C1)CCC(C=CC=CC2=CC=CC=C2)O 264.40 unknown https://doi.org/10.1016/J.BMC.2008.05.051
https://doi.org/10.1021/JF802702C
4-(3-Hydroxy-7-phenylhept-6-en-1-yl)benzene-1,2-diol 75070116 Click to see C1=CC=C(C=C1)C=CCCC(CCC2=CC(=C(C=C2)O)O)O 298.40 unknown https://doi.org/10.1016/J.BMC.2008.05.051
https://doi.org/10.1016/S0031-9422(96)00778-9
4-(3-Hydroxy-7-phenylhept-6-enyl)phenol 75070115 Click to see C1=CC=C(C=C1)C=CCCC(CCC2=CC=C(C=C2)O)O 282.40 unknown https://doi.org/10.1016/S0031-9422(96)00778-9
4-[(3R,5R)-3,5-dihydroxy-7-(4-hydroxyphenyl)heptyl]benzene-1,2-diol 636849 Click to see C1=CC(=CC=C1CCC(CC(CCC2=CC(=C(C=C2)O)O)O)O)O 332.40 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
4-[(E,3R)-3-hydroxy-7-phenylhept-6-enyl]phenol 102278940 Click to see C1=CC=C(C=C1)C=CCCC(CCC2=CC=C(C=C2)O)O 282.40 unknown https://doi.org/10.1016/S0031-9422(96)00778-9
4-[(E,3S)-3-hydroxy-7-(4-hydroxyphenyl)hept-6-enyl]-2-methoxyphenol 72164689 Click to see COC1=C(C=CC(=C1)CCC(CCC=CC2=CC=C(C=C2)O)O)O 328.40 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
5-Hydroxy-1,7-diphenyl-6-hepten-3-one 44559751 Click to see C1=CC=C(C=C1)CCC(=O)CC(C=CC2=CC=CC=C2)O 280.40 unknown https://doi.org/10.1021/NP50104A006
https://doi.org/10.1016/J.BMC.2008.05.051
7-Phenylhepta-1,3,5-trienylbenzene 53397073 Click to see C1=CC=C(C=C1)CC=CC=CC=CC2=CC=CC=C2 246.30 unknown https://doi.org/10.1016/J.BMC.2008.05.051
Alnustone 5317598 Click to see C1=CC=C(C=C1)CCC(=O)C=CC=CC2=CC=CC=C2 262.30 unknown https://doi.org/10.1016/J.BMC.2008.05.051
rel-4-((3R,5S)-3,5-Dihydroxy-7-(4-hydroxyphenyl)heptyl)benzene-1,2-diol 53387510 Click to see C1=CC(=CC=C1CCC(CC(CCC2=CC(=C(C=C2)O)O)O)O)O 332.40 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
(3R,5R)-1,7-Bis(4-hydroxyphenyl)-3,5-heptanediol 11034432 Click to see C1=CC(=CC=C1CCC(CC(CCC2=CC=C(C=C2)O)O)O)O 316.40 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
(3R,5S)-1-(4-hydroxy-3,5-dimethoxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)heptane-3,5-diol 21577371 Click to see COC1=CC(=CC(=C1O)OC)CCC(CC(CCC2=CC(=C(C=C2)O)OC)O)O 406.50 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
(5r)-5-Hydroxy-1-(4-hydroxyphenyl)-7-(4-hydroxy-3-methoxyphenyl)-3-heptanone 637003 Click to see COC1=C(C=CC(=C1)CCC(CC(=O)CCC2=CC=C(C=C2)O)O)O 344.40 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
(S)-1,7-Bis(4-hydroxyphenyl)-5-hydroxyheptan-3-one 13347313 Click to see C1=CC(=CC=C1CCC(CC(=O)CCC2=CC=C(C=C2)O)O)O 314.40 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
5-Hydroxy-1-(4-hydroxyphenyl)-7-(4-hydroxy-3-methoxylphenyl)-3-heptanone 21588208 Click to see COC1=C(C=CC(=C1)CCC(CC(=O)CCC2=CC=C(C=C2)O)O)O 344.40 unknown https://doi.org/10.1016/J.BMCL.2013.07.010
Diarylcomosol III 72164690 Click to see COC1=CC(=CC(=C1O)OC)CCC(CC(CCC2=CC=C(C=C2)O)O)O 376.40 unknown https://doi.org/10.1016/J.BMCL.2013.07.010

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