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Dendrobium densiflorum

Dendrobium densiflorum - Unknown
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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 UUID644037c987cb3200145838
Scientific name Dendrobium densiflorum
Authority Lindl. ex Wall.
First published in Pl. Asiat. Rar. 1: 34 (1830)

Description Top

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Synonyms Top

Scientific name Authority First published in
Callista densiflora Kuntze Revis. Gen. Pl. 2: 654 (1891)
Dendrobium schroederi B.S.Williams Nursery Cat. (B.S.Williams) 1869(Spring): 8 (1869)
Dendrobium clavatum Roxb. Fl. Ind. ed. 1832 , 3: 481 (1832)
Endeisa flava Raf. Fl. Tellur. 2: 51 (1837)
Epidendrum dumunsuttu Buch.-Ham. ex Lindl. Gen. Sp. Orchid. Pl. : 90 (1830)
Dendrobium densiflorum var. clavatum Rolfe Gard. Chron. , ser. 3, 11: 394 (1892)

Common names Top

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Language Common/alternative name
English densely flowered dendrobium
English pineapple orchid
Azerbaijani callista clavata
Azerbaijani callista densiflora
Azerbaijani callista guibertii
Azerbaijani dendrobium clavatum
Azerbaijani dendrobium guibertii
Azerbaijani dendrobium schroederi
Azerbaijani endeisa flava
Azerbaijani epidendrum dumunsuttu
mni ꯃꯦꯂꯩ ꯂꯩꯁꯅꯥ
Burmese ta hkaing lone shwe
Chinese 密花石斛
Chinese 粗黄草

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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Germination/Propagation Top

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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000938987
Tropicos 23500218
KEW urn:lsid:ipni.org:names:627283-1
The Plant List kew-57603
Open Tree Of Life 315561
NCBI Taxonomy 161866
IPNI 627282-1
iNaturalist 887416
GBIF 5316645
Freebase /m/065_0yw
EPPO DENDF
EOL 1100188
USDA GRIN 13497
Wikipedia Dendrobium_densiflorum
CMAUP NPO29285

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
Targeting Cell Signaling Pathways in Lung Cancer by Bioactive Phytocompounds Choudhary N, Bawari S, Burcher JT, Sinha D, Tewari D, Bishayee A Cancers (Basel) 05-Aug-2023
PMCID:PMC10417502
doi:10.3390/cancers15153980
PMID:37568796
Genomic evidence reveals high genetic diversity in a narrowly distributed species and natural hybridization risk with a widespread species in the genus Geodorum Zhu X, Tang J, Jiang H, Yang Y, Chen Z, Zou R, Xu A, Luo Y, Deng Z, Wei X, Chai S BMC Plant Biol 14-Jun-2023
PMCID:PMC10265804
doi:10.1186/s12870-023-04285-w
PMID:37316828
Orchid Micropropagation Using Conventional Semi-Solid and Temporary Immersion Systems: A Review Nongdam P, Beleski DG, Tikendra L, Dey A, Varte V, EL Merzougui S, Pereira VM, Barros PR, Vendrame WA Plants (Basel) 02-Mar-2023
PMCID:PMC10005664
doi:10.3390/plants12051136
PMID:36904000
Therapeutic Potential of Phenolic Compounds in Medicinal Plants—Natural Health Products for Human Health Sun W, Shahrajabian MH Molecules 15-Feb-2023
PMCID:PMC9960276
doi:10.3390/molecules28041845
PMID:36838831
Phylogenetic affiliation of endophytic actinobacteria associated with selected orchid species and their role in growth promotion and suppression of phytopathogens Saikia J, Mazumdar R, Thakur D Front Plant Sci 07-Dec-2022
PMCID:PMC9769409
doi:10.3389/fpls.2022.1058867
PMID:36570961
Orchidaceae-Derived Anticancer Agents: A Review Śliwiński T, Kowalczyk T, Sitarek P, Kolanowska M Cancers (Basel) 31-Jan-2022
PMCID:PMC8833831
doi:10.3390/cancers14030754
PMID:35159021
Effects of Different Molecular Weight Polysaccharides From Dendrobium officinale Kimura & Migo on Human Colorectal Cancer and Transcriptome Analysis of Differentially Expressed Genes Tao S, Ren Z, Yang Z, Duan S, Wan Z, Huang J, Liu C, Wei G Front Pharmacol 03-Dec-2021
PMCID:PMC8678483
doi:10.3389/fphar.2021.704486
PMID:34925000
Dihydrophenanthrenes from medicinal plants of Orchidaceae: A review Qi JX, Zhou D, Jiang WR, Chen G, Li W, Li N Chin Herb Med 07-Oct-2021
PMCID:PMC9476782
doi:10.1016/j.chmed.2021.10.004
PMID:36119366
Scoparone Induces Expression of Pluripotency Transcription Factors SOX2 and NANOG in Dermal Papilla Cells SUWANPRAKORN N, CHANVORACHOTE P, TONGYEN T, SRITULARAK B, SUVANPRAKORN P In Vivo 03-Sep-2021
PMCID:PMC8408723
doi:10.21873/invivo.12541
PMID:34410946
Targeting the PI3K/AKT/mTOR Signaling Pathway in Lung Cancer: An Update Regarding Potential Drugs and Natural Products Iksen, Pothongsrisit S, Pongrakhananon V Molecules 05-Jul-2021
PMCID:PMC8271933
doi:10.3390/molecules26134100
PMID:34279440
Development, Identification, and Application of a Germplasm Specific SCAR Marker for Dendrobium officinale Kimura et Migo Zheng K, Cai Y, Chen W, Gao Y, Jin J, Wang H, Feng S, Lu J Front Plant Sci 14-May-2021
PMCID:PMC8160518
doi:10.3389/fpls.2021.669458
PMID:34054907
Combined Analysis of Volatile Terpenoid Metabolism and Transcriptome Reveals Transcription Factors Related to Terpene Synthase in Two Cultivars of Dendrobium officinale Flowers Li N, Dong Y, Lv M, Qian L, Sun X, Liu L, Cai Y, Fan H Front Genet 22-Apr-2021
PMCID:PMC8101708
doi:10.3389/fgene.2021.661296
PMID:33968137
Traditional Uses and Pharmacologically Active Constituents of Dendrobium Plants for Dermatological Disorders: A Review Wang YH Nat Prod Bioprospect 20-Apr-2021
PMCID:PMC8390561
doi:10.1007/s13659-021-00305-0
PMID:33880726
Paphiopedilum insigne Morphological and Physiological Features during In Vitro Rooting and Ex Vitro Acclimatization Depending on the Types of Auxin and Substrate Poniewozik M, Parzymies M, Szot P, Rubinowska K Plants (Basel) 19-Mar-2021
PMCID:PMC8003477
doi:10.3390/plants10030582
PMID:33808606
RAPD, ISSR, and SCoT markers based genetic stability assessment of micropropagated Dendrobium fimbriatum Lindl. var. oculatum Hk. f.- an important endangered orchid Tikendra L, Potshangbam AM, Dey A, Devi TR, Sahoo MR, Nongdam P Physiol Mol Biol Plants 16-Feb-2021
PMCID:PMC7907394
doi:10.1007/s12298-021-00939-x
PMID:33707873

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
> Benzenoids / Fluorenes
1,4,7-trihydroxy-5-methoxy-9H-fluoren-9-one 44418788 Click to see COC1=CC(=CC2=C1C3=C(C=CC(=C3C2=O)O)O)O 258.23 unknown https://doi.org/10.1080/10286020008041369
https://doi.org/10.1016/S0031-9422(01)00168-6
2,5-Dihydroxy-4-methoxy-9H-fluoren-9-one 10879298 Click to see COC1=CC(=CC2=C1C3=C(C2=O)C=CC=C3O)O 242.23 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
https://doi.org/10.1080/10286020008041369
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
7-Methoxy-9,10-dihydrophenanthrene-2,5-diol 442702 Click to see COC1=CC2=C(C3=C(CC2)C=C(C=C3)O)C(=C1)O 242.27 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
2,6-Phenanthrenediol, 1,5,7-trimethoxy- 11779542 Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C=CC(=C3OC)O)OC)O 300.30 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
7-Hydroxy-2-methoxyphenanthrene-1,4-dione 637413 Click to see COC1=CC(=O)C2=C(C1=O)C=CC3=C2C=CC(=C3)O 254.24 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
Cypripedin 174864 Click to see COC1=CC(=O)C2=C(C1=O)C=CC3=C2C=CC(=C3OC)O 284.26 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
Moscatin 194774 Click to see COC1=C2C(=CC(=C1)O)C=CC3=C2C(=CC=C3)O 240.25 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids
(1S,4abeta,10aalpha)-1beta-Isopropenyl-3abeta,5,8aalpha-trimethyltetradecahydrobenzo[f]azulene-5alpha,8alpha-diol 24862125 Click to see CC(=C)C1CCC2(C1CCC3(C(CCC(C3C2)(C)O)O)C)C 306.50 unknown via CMAUP database
(1S,4abeta,10aalpha)-1beta-Isopropenyl-3abeta,5,8aalpha-trimethyltetradecahydrobenzo[f]azulene-5beta,8alpha-diol 24829354 Click to see CC(=C)C1CCC2(C1CCC3(C(CCC(C3C2)(C)O)O)C)C 306.50 unknown via CMAUP database
(1S,4abeta,10aalpha)-1beta-Isopropenyl-3abeta,8aalpha-dimethyl-5-methylenetetradecahydrobenzo[f]azulene-8alpha-ol 24862181 Click to see CC(=C)C1CCC2(C1CCC3(C(CCC(=C)C3C2)O)C)C 288.50 unknown via CMAUP database
(1S)-1beta-Isopropenyl-3abeta,5,8aalpha-trimethyl-1,2,3,3a,4,4abeta,7,8,8a,9,10,10aalpha-dodecahydrobenzo[f]azulene-8alpha-ol 24829355 Click to see CC1=CCC(C2(C1CC3(CCC(C3CC2)C(=C)C)C)C)O 288.50 unknown via CMAUP database
(1S)-1beta-Isopropenyl-3abeta,5,8aalpha-trimethyl-1,2,3,3a,4,6,7,8,8a,9,10,10aalpha-dodecahydrobenzo[f]azulene-8alpha-ol 101847584 Click to see CC1=C2CC3(CCC(C3CCC2(C(CC1)O)C)C(=C)C)C 288.50 unknown via CMAUP database
(5E)-9alpha-Acetoxy-1beta-isopropenyl-3abeta,6-dimethyl-10-methylene-1,2,3,3a,4,7,8,9,10,11,12,12aalpha-dodecahydrocyclopentacycloundecene-3-one 70676027 Click to see CC1=CCC2(C(CCC(=C)C(CC1)OC(=O)C)C(CC2=O)C(=C)C)C 344.50 unknown via CMAUP database
(5E)-9alpha,11alpha-Dihydroxy-1beta-isopropenyl-3abeta,6-dimethyl-10-methylene-1,2,3,3a,4,7,8,9,10,11,12,12aalpha-dodecahydrocyclopentacycloundecene-3-one 70676028 Click to see CC1=CCC2(C(CC(C(=C)C(CC1)O)O)C(CC2=O)C(=C)C)C 318.40 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Acyclic diterpenoids
Phytol 5280435 Click to see CC(C)CCCC(C)CCCC(C)CCCC(=CCO)C 296.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Dolabellane and neodolabellane diterpenoids
(1R,3E,7E,11S,12S,14S)-14-Acetoxy-3,7,18-dolabellatriene 51040051 Click to see CC1=CCCC(=CCC2(C(CC1)C(CC2OC(=O)C)C(=C)C)C)C 330.50 unknown via CMAUP database
(1R,3E,7E,11S,12S,14S)-14-Hydroxy-3,7,18-dolabellatriene 51040050 Click to see CC1=CCCC(=CCC2(C(CC1)C(CC2O)C(=C)C)C)C 288.50 unknown via CMAUP database
(1R,3E,7E,11S,12S)-3,7,18-Dolabellatriene 51039832 Click to see CC1=CCCC(=CCC2(CCC(C2CC1)C(=C)C)C)C 272.50 unknown via CMAUP database
(1R,3E,7S,8S,11S,12S)-7,8-Epoxy-14-oxo-3,18-dolabelladiene 51040055 Click to see CC1=CCC2(C(CCC3(C(O3)CC1)C)C(CC2=O)C(=C)C)C 302.50 unknown via CMAUP database
(1S,4S,5S,12R,15S)-15-Isopropenyl-4,9,12-trimethyl-5-oxa-tricyclo[10.3.0.0(4,6)]pentadec-9-ene 51040057 Click to see CC1=CCC2(CCC(C2CCC3(C(O3)CC1)C)C(=C)C)C 288.50 unknown via CMAUP database
(3S,3aS,6E,10E,12aR)-6,10,12a-trimethyl-3-(prop-1-en-2-yl)-3,3a,4,5,8,9,12,12a-octahydrocyclopenta[11]annulen-1(2H)-one 51039830 Click to see CC1=CCCC(=CCC2(C(CC1)C(CC2=O)C(=C)C)C)C 286.50 unknown via CMAUP database
2-((1S,3aR,5E,9E,12aS)-3a,6,10-trimethyl-1,2,3,3a,4,7,8,11,12,12a-decahydrocyclopenta[11]annulen-1-yl)propan-2-ol 51040257 Click to see CC1=CCCC(=CCC2(CCC(C2CC1)C(C)(C)O)C)C 290.50 unknown via CMAUP database
rel-(1R,3E,7E,11R,12R)-12-Hydroxy-3,7-dolabelladiene 51040258 Click to see CC1=CCCC(=CCC2(CCC(C2CC1)(C(C)C)O)C)C 290.50 unknown via CMAUP database
rel-(1R,3E,7E,11S,12R)-14-Oxo-3,7,18-dolabellatriene 51039829 Click to see CC1=CCCC(=CCC2(C(CC1)C(CC2=O)C(=C)C)C)C 286.50 unknown via CMAUP database
rel-(1R,3Z,7E,11S,12S)-14-Oxo-3,7,18-dolabellatriene 51039831 Click to see CC1=CCCC(=CCC2(C(CC1)C(CC2=O)C(=C)C)C)C 286.50 unknown via CMAUP database
rel-(1R,3Z,7S,8S,11S,12S)-7,8-Epoxy-14-oxo-3,18-dolabelladiene 51040056 Click to see CC1=CCC2(C(CCC3(C(O3)CC1)C)C(CC2=O)C(=C)C)C 302.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Diterpenoids / Pachydictyane and cneorubin diterpenoids
(3aR,5R)-3,8-dimethyl-5-[(2R)-6-methylhept-5-en-2-yl]-1,3a,4,5,6,7-hexahydroazulene 23426828 Click to see CC1=C2CC=C(C2CC(CC1)C(C)CCC=C(C)C)C 272.50 unknown via CMAUP database
Isopachydictyol A 21583475 Click to see CC1=CCC(C(C2C1CC=C2C)O)C(C)CCC=C(C)C 288.50 unknown via CMAUP database
Pachydictyol A 122837 Click to see CC1=CCC2C1C(C(CCC2=C)C(C)CCC=C(C)C)O 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(R)-4-(1beta-Isopropenyl-3abeta,6-dimethyl-1,2,3,3a,4,7,8,8aalpha-octahydroazulene-5-yl)pentanal 53359310 Click to see CC1=C(CC2(CCC(C2CC1)C(=C)C)C)C(C)CCC=O 288.50 unknown via CMAUP database
Dictyoxide 21726361 Click to see CC1=CCC2C1C3C(CCC2(O3)C)C(C)CCC=C(C)C 288.50 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Tetraterpenoids / Carotenoids / Xanthophylls
CID 20054917 20054917 Click to see CC(=CC=CC=C(C)C=CC=C(C)C(=O)CC1(C(CC(CC1(C)O)O)(C)C)O)C=CC=C(C)C=C=C2C(CC(CC2(C)O)OC(=O)C)(C)C 676.90 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Friedelin 91472 Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CCC5(C4CC(CC5)(C)C)C)C)C)C)C 426.70 unknown https://doi.org/10.1080/10286020008041369
Oleanolic Acid 10494 Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C(=O)O)C 456.70 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(24E)-24-N-Propylidenecholesterol 5281328 Click to see CC=C(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown via CMAUP database
17-(5-ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 86821 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
24-Ethylcholest-5-en-3beta-ol 22012 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Organic acids and derivatives / Carboxylic acids and derivatives / Carboxylic acid derivatives / Carboxylic acid esters
(1R,3S,4S,7E,11S,12S,14S)-14-Acetoxy-3,4-epoxy-7,18-dolabelladiene 51040054 Click to see CC1=CCCC2(C(O2)CC3(C(CC1)C(CC3OC(=O)C)C(=C)C)C)C 346.50 unknown via CMAUP database
[(1R,3S,5S,8S,12S,13S,15S)-8-hydroxy-1,5-dimethyl-9-methylidene-13-prop-1-en-2-yl-4-oxatricyclo[10.3.0.03,5]pentadecan-15-yl] acetate 70676030 Click to see CC(=C)C1CC(C2(C1CCC(=C)C(CCC3(C(C2)O3)C)O)C)OC(=O)C 362.50 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Secondary alcohols
(1R,3S,5S,8S,12S,13S)-8-hydroxy-1,5-dimethyl-9-methylidene-13-prop-1-en-2-yl-4-oxatricyclo[10.3.0.03,5]pentadecan-15-one 70676029 Click to see CC(=C)C1CC(=O)C2(C1CCC(=C)C(CCC3(C(C2)O3)C)O)C 318.40 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Ketones
(3S,4S,7E,11alpha)-1beta,4,8-Trimethyl-12beta-(1-methylethenyl)-3,4-epoxybicyclo[9.3.0]tetradeca-7-ene-14-one 51040052 Click to see CC1=CCCC2(C(O2)CC3(C(CC1)C(CC3=O)C(=C)C)C)C 302.50 unknown via CMAUP database
4-[2aalpha,7abeta-Dimethyl-5alpha-isopropenyl-1aalpha,2,2a,3,4,5,5abeta,6,7,7a-decahydro-1H-cyclopropa[f]azulene-1beta-yl]-2-butanone 53359311 Click to see CC(=C)C1CCC2(C1CCC3(C(C2)C3CCC(=O)C)C)C 288.50 unknown via CMAUP database
4-[2abeta,7aalpha-Dimethyl-5beta-isopropenyl-1abeta,2,2a,3,4,5,5aalpha,6,7,7a-decahydro-1H-cyclopropa[f]azulene-1alpha-yl]-2-butanone 101805159 Click to see CC(=C)C1CCC2(C1CCC3(C(C2)C3CCC(=O)C)C)C 288.50 unknown via CMAUP database
> Organoheterocyclic compounds / Dihydrofurans / Furanones / Butenolides
(4S,7R,7aS,8aS)-4-[(1R)-1,5-Dimethyl-4-hexenyl]-7-methyl-1,4,5,6,7,7a,8,8a-octahydro-3H-cyclopropa[3,4]cycloocta[1,2-c]furan-3-one 23426901 Click to see CC1CCC(C2=C(COC2=O)C3C1C3)C(C)CCC=C(C)C 302.50 unknown via CMAUP database
> Organoheterocyclic compounds / Epoxides
(1R,3S,5S,8E,12S,13S)-1,5,9-trimethyl-13-prop-1-en-2-yl-4-oxatricyclo[10.3.0.03,5]pentadec-8-ene 51040053 Click to see CC1=CCCC2(C(O2)CC3(CCC(C3CC1)C(=C)C)C)C 288.50 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Ayapin 3083597 Click to see C1OC2=C(O1)C=C3C(=C2)C=CC(=O)O3 190.15 unknown https://doi.org/10.1080/10286020008041369
https://doi.org/10.1016/S0031-9422(01)00168-6
Scoparone 8417 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC 206.19 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
https://doi.org/10.1080/10286020008041369
> Phenylpropanoids and polyketides / Coumarins and derivatives / Coumarin glycosides
Scopolin 439514 Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC3C(C(C(C(O3)CO)O)O)O 354.31 unknown https://doi.org/10.1080/10286020008041369
> 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)00168-6
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(2R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-2,3-dihydro-4H-chromen-4-one 667495 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
5,7-Dihydroxy-2-(4-hydroxyphenyl)chroman-4-one 932 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
Naringenin 439246 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O 272.25 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
(2R)-7-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-4-oxo-2,3-dihydrochromen-5-olate 25200448 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)[O-])O 301.27 unknown via CMAUP database
Homoeriodictyol 73635 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
Homoeriodictyol (+/-)- 3512637 Click to see COC1=C(C=CC(=C1)C2CC(=O)C3=C(C=C(C=C3O2)O)O)O 302.28 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
Ayanin 5280682 Click to see COC1=C(C=C(C=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)OC)O)OC)O 344.30 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
> Phenylpropanoids and polyketides / Stilbenes
3-[2-(1,3-Benzodioxol-5-yl)ethyl]-5-methoxyphenol 637412 Click to see COC1=CC(=CC(=C1)O)CCC2=CC3=C(C=C2)OCO3 272.29 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
Dendrophenol 176096 Click to see COC1=CC(=CC(=C1O)OC)CCC2=CC(=C(C=C2)O)OC 304.34 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
Gigantol 3085362 Click to see COC1=C(C=C(C=C1)CCC2=CC(=CC(=C2)OC)O)O 274.31 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
Phenol, 4-[2-(3-hydroxy-5-methoxyphenyl)ethyl]-2-methoxy- 10221179 Click to see COC1=CC(=CC(=C1)O)CCC2=CC(=C(C=C2)O)OC 274.31 unknown https://doi.org/10.1016/S0031-9422(01)00168-6
Tristin 15736297 Click to see COC1=C(C=CC(=C1)CCC2=CC(=CC(=C2)O)O)O 260.28 unknown https://doi.org/10.1016/S0031-9422(01)00168-6

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