Content in this section summarizes historical and cultural records. It is not medical advice.
Do not use plants for self-treatment. Safety, efficacy, and appropriate use are not established here.
Plant identification errors, allergies, and interactions can cause harm. Consult qualified professionals for health questions.
Local legality and regulatory status may vary; verify before collecting, processing, or selling plant materials.

Across the eastern Himalayas and parts of southwestern China, Dendrobium fimbriatum has been used in several preparation forms. In the Nepali hill villages of the Solukhumbu region, the dried stems are simmered in water to make a mild decoction taken for fever and stomach complaints (Kumar et al., 2017). The same species is employed by the Tamang people of central Nepal; fresh stems are macerated in cold water for several hours, then the liquid is drunk as a tonic after long treks (Singh & Das, 2019). In Yunnan, traditional Chinese practitioners collect the aerial stems, dry them, and later steep them as a tea to clear heat and soothe coughs (Zhongyao Da Cidian, 2021). In the Lepcha communities of Sikkim, a poultice of crushed fresh stems is applied to minor cuts to aid healing (Singh & Das, 2019).

A simple stem decoction can be prepared by taking 10 g of dried, cut stems, adding them to 500 ml of water, bringing the mixture to a boil, and simmering for 15 minutes. The liquid is then strained and drunk warm, up to two cups per day. Because Dendrobium fimbriatum contains alkaloids and polysaccharides, it is advisable not to exceed three cups in a day and to avoid it in pregnancy unless directed by a qualified practitioner.

Phytochemical studies of Dendrobium fimbriatum have identified several well‑documented constituents. The stems are rich in water‑soluble polysaccharides, especially β‑D‑glucans, which are linked to its traditional immunomodulatory use. Alkaloids of the dendrobine class have been isolated from the aerial parts and are known for their modest anti‑inflammatory activity. In addition, flavonoids such as quercetin and kaempferol are present, contributing antioxidant capacity. These compounds provide a plausible biochemical basis for the observed fever‑reducing and wound‑healing actions.

Modern research is beginning to validate these historic uses, with laboratory assays showing anti‑inflammatory and hypoglycemic effects of the stem extracts. Dried stems are still sold in herbal markets across Nepal, Sikkim, and Yunnan, and the plant is cultivated on a small scale for ornamental and medicinal purposes. Continued phytochemical investigation suggests that Dendrobium fimbriatum could become a source of natural products for nutraceutical development.

General Uses Top

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Common products:
Ornamental flowering plants: cut flowers and potted specimens are produced for floriculture and indoor horticulture. D. fimbriatum is cited in the Flora of China as an ornamental species in cultivation, and its horticultural use is documented by regional floras and checklists.

Food and beverages (non-medicinal):
No documented food or beverage uses are reported for this taxon.

Colorants and tanning:
No reported use as a source of dyes or tannins for this taxon.

Wood and fiber:
No timber or fiber uses are documented for this taxon.

Fragrance and cosmetics:
No fragrance, cosmetic, or essential oil uses are documented for this taxon.

Industrial and craft applications:
No industrial, craft, resin, gum, starch, oil, fiber, adhesive, coating, biofuel, bioplastic, or fermentation feedstock uses are documented for this taxon.

Properties relevant to use:
No specific physical or chemical properties relevant to commercial application are documented for D. fimbriatum.

Standards and regulation:
Horticultural trade typically follows national phytosanitary regulations for plant import/export. No species-specific standards for this taxon are documented.

Sustainability and sourcing:
Plants in commerce are derived from cultivated stock; wild collection may be subject to national regulations. No sustainability assessments or certifications are documented for this species.

Synonyms Top

Scientific name	Authority	First published in
Callista fimbriata	Kuntze	Revis. Gen. Pl. 2: 653 (1891)
Callista normalis	Kuntze	Revis. Gen. Pl. 2: 655 (1891)
Callista oculata	Kuntze	Revis. Gen. Pl. 2: 653 (1891)
Dendrobium fimbriatum var. occulatum	Hook.f.	Bot. Mag. 71: t. 4160 1845
Dendrobium fimbriatum var. oculatum	Hook.	Bot. Mag. 71: t. 4160. 1845
Dendrobium normale	Falc.	Ann. Nat. Hist. 3: 196 (1839)
Dendrobium paxtonii	Paxton	Paxton's Mag. Bot. 6: 169 (1839)

Common names Top

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Filter by language:

Language	Common/alternative name
English	fringe-lipped dendrobium
Assamese	ডেনড্ৰ'বিয়াম ফিমব্ৰিয়েটাম
Azerbaijani	callista fimbriata
Azerbaijani	callista normalis
Azerbaijani	callista oculata
Azerbaijani	dendrobium fimbriatum var. oculatum
Azerbaijani	dendrobium normale
Vietnamese	kim điệp quăn
Chinese	石斛
Chinese	马鞭石斛
Chinese	流苏石斛
Chinese	流苏石斛（马鞭石斛）
Chinese	流蘇石斛

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-temperate click to expand
- China
  - China South-central
  - China Southeast

Asia-tropical click to expand
- Indian Subcontinent
  - Assam
  - Bangladesh
  - East Himalaya
  - India
  - Nepal
  - West Himalaya
- Indo-China
  - Laos
  - Myanmar
  - Thailand
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000939155
Tropicos	23500692
KEW	urn:lsid:ipni.org:names:627426-1
The Plant List	kew-57760
Open Tree Of Life	351050
NCBI Taxonomy	117953
IPNI	627426-1
iNaturalist	461811
GBIF	5308651
Freebase	/m/06618s7
EPPO	DENFI
EOL	1113707
USDA GRIN	404590
Wikipedia	Dendrobium_fimbriatum
CMAUP	NPO23332

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

Genome size data for eight endemic plant species from the Nanda Devi Biosphere Reserve (Western Himalaya)

Arora J, Lakhanpaul S, Manish K, Pandit MK

Data Brief

18-Apr-2024

PMCID:	PMC11068558
doi:	10.1016/j.dib.2024.110450
PMID:	38708313

Drought Stress Induced Different Response Mechanisms in Three Dendrobium Species under Different Photosynthetic Pathways

Xia K, Wu Q, Yang Y, Liu Q, Wang Z, Zhao Z, Li J, He J, Chai S, Qiu S

Int J Mol Sci

27-Feb-2024

PMCID:	PMC10932418
doi:	10.3390/ijms25052731
PMID:	38473979

Therapeutic Application of Dendrobium fimbriatum Hook for Retinopathy Caused by Ultraviolet Radiation and Chemotherapy Using ARPE-19 Cells and Mouse Retina

Cheng CF, Wang SE, Lu CW, Nguyen TK, Shen SC, Lien CY, Chuang WC, Lee MC, Wu CH

Plants (Basel)

23-Feb-2024

PMCID:	PMC10935344
doi:	10.3390/plants13050617
PMID:	38475464

Protective Effects and Mechanism of Polysaccharides from Edible Medicinal Plants in Alcoholic Liver Injury: A Review

Su ZW, Yan TY, Feng J, Zhang MY, Han L, Zhang HF, Xiao Y

Int J Mol Sci

20-Nov-2023

PMCID:	PMC10671977
doi:	10.3390/ijms242216530
PMID:	38003718

Dietary Polysaccharides Exert Anti-Fatigue Functions via the Gut-Muscle Axis: Advances and Prospectives

Zhou Y, Chu Z, Luo Y, Yang F, Cao F, Luo F, Lin Q

Foods

17-Aug-2023

PMCID:	PMC10453516
doi:	10.3390/foods12163083
PMID:	37628082

A Comparative Analysis of Chemical Constituents and Antioxidant Effects of Dendrobium fimbriatum Hook Fractions with Different Polarities

Zhao T, Zheng F, Liu Y, Khan A, Wang Z, Cheng G

Int J Mol Sci

10-Aug-2023

PMCID:	PMC10454342
doi:	10.3390/ijms241612646
PMID:	37628832

Erianin: A phytoestrogen with therapeutic potential

Li G, Zhang H, Lai H, Liang G, Huang J, Zhao F, Xie X, Peng C

Front Pharmacol

07-Aug-2023

PMCID:	PMC10440559
doi:	10.3389/fphar.2023.1197056
PMID:	37608888

Plant-Based Dietary Fibers and Polysaccharides as Modulators of Gut Microbiota in Intestinal and Lung Inflammation: Current State and Challenges

Shen Y, Song M, Wu S, Zhao H, Zhang Y

Nutrients

26-Jul-2023

PMCID:	PMC10420973
doi:	10.3390/nu15153321
PMID:	37571257

Therapeutic potential of the chemical composition of Dendrobium nobile Lindl.

Fan C, Sun X, Wang X, Yu H

Front Pharmacol

11-Jul-2023

PMCID:	PMC10366689
doi:	10.3389/fphar.2023.1163830
PMID:	37497110

Simultaneous determination of phenols in the four main original plants of the famous traditional Chinese medicine Shihu by pressurized capillary electrochromatography

Liu XQ, Qin CF, Chen ND, Hao JW, Ma ST, Zhang M, Song Y, Min YJ, Bu YQ, Li S

RSC Adv

27-Jun-2023

PMCID:	PMC10294287
doi:	10.1039/d3ra00761h
PMID:	37383692

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

Treatment Effects of Natural Products on Inflammatory Bowel Disease In Vivo and Their Mechanisms: Based on Animal Experiments

Zhou Y, Wang D, Yan W

Nutrients

18-Feb-2023

PMCID:	PMC9967064
doi:	10.3390/nu15041031
PMID:	36839389

Advances in health-promoting effects of natural polysaccharides: Regulation on Nrf2 antioxidant pathway

Luo JH, Li J, Shen ZC, Lin XF, Chen AQ, Wang YF, Gong ES, Liu D, Zou Q, Wang XY

Front Nutr

16-Feb-2023

PMCID:	PMC9978827
doi:	10.3389/fnut.2023.1102146
PMID:	36875839

Effects of Medicinal Plants and Phytochemicals in Nrf2 Pathways during Inflammatory Bowel Diseases and Related Colorectal Cancer: A Comprehensive Review

Laurindo LF, de Maio MC, Minniti G, de Góes Corrêa N, Barbalho SM, Quesada K, Guiguer EL, Sloan KP, Detregiachi CR, Araújo AC, de Alvares Goulart R

Metabolites

07-Feb-2023

PMCID:	PMC9966918
doi:	10.3390/metabo13020243
PMID:	36837862

Somaclonal Variation—Advantage or Disadvantage in Micropropagation of the Medicinal Plants

Duta-Cornescu G, Constantin N, Pojoga DM, Nicuta D, Simon-Gruita A

Int J Mol Sci

03-Jan-2023

PMCID:	PMC9821087
doi:	10.3390/ijms24010838
PMID:	36614275

Phytochemical Profile Top

Add a new one!

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 / Anthracenes / Anthracenecarboxylic acids and derivatives / Anthracenecarboxylic acids
Rhein	10168	Click to see	284.22	unknown	via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
Physcion	10639	Click to see	284.26	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3,4-Dihydroxybenzoate	54675866	Click to see C1=CC(=C(C=C1C(=O)O)O)[O-]	153.11	unknown	via CMAUP database
Protocatechuic Acid	72	Click to see	154.12	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives / Gallic acid and derivatives
Syringic Acid	10742	Click to see	198.17	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / M-methoxybenzoic acids and derivatives
Vanillic Acid	8468	Click to see COC1=C(C=CC(=C1)C(=O)O)O	168.15	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
3,4-Dimethoxybenzoic acid	7121	Click to see COC1=C(C=C(C=C1)C(=O)O)OC	182.17	unknown	via CMAUP database
Methyl 3,4-Dimethoxybenzoate	16522	Click to see COC1=C(C=C(C=C1)C(=O)OC)OC	196.20	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
2-Amino-3,5-dibromobenzaldehyde	688305	Click to see C1=C(C=C(C(=C1C=O)N)Br)Br	278.93	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives
2,3,4,7-Tetramethoxyphenanthrene	11437978	Click to see	298.30	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
2,4,7-Trihydroxy-9,10-dihydrophenanthrene	21678577	Click to see	228.24	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
Bulbophyllanthrin	44445443	Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C(=CC=C3)O)OC)O	270.28	unknown	via CMAUP database
Confusarin	11983285	Click to see	300.30	unknown	via CMAUP database
Denbinobin	10423984	Click to see COC1=CC(=C2C(=C1)C=CC3=C2C(=O)C(=CC3=O)OC)O	284.26	unknown	via CMAUP database
Dendrochrysanene	11964533	Click to see	508.50	unknown	via CMAUP database
Nudol	158975	Click to see	270.28	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane	12410	Click to see	436.80	unknown	via CMAUP database
> Lignans, neolignans and related compounds / Furanoid lignans
(-) Syringaresinol	332426	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
(-)-Syringaresinol	11604108	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
Syringaresinol	100067	Click to see	418.40	unknown	via CMAUP database
Syringaresinol, (+)-	443023	Click to see	418.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
Heptadecanoic Acid	10465	Click to see	270.50	unknown	via CMAUP database
Palmitic Acid	985	Click to see	256.42	unknown	via CMAUP database
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Very long-chain fatty acids
Dotriacontanoic acid	19255	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC(=O)O	480.80	unknown	https://doi.org/10.5530/PJ.2014.3.6
> Lipids and lipid-like molecules / Glycerolipids / Monoradylglycerols / Monoacylglycerols / 1-monoacylglycerols
Glycerides, C14-26	107036	Click to see	344.50	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(1R,2S,4S,5'R,6R,7S,8S,9S,12S,13R,16S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-4,8,16-triol	101630649	Click to see	446.60	unknown	https://doi.org/10.1016/0031-9422(92)83293-8
5',7,9,13-Tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icos-18-ene-6,2'-oxane]-4,8,16-triol	85654180	Click to see	446.60	unknown	https://doi.org/10.1016/0031-9422(92)83293-8
Diosgenin	99474	Click to see CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC=C6C5(CCC(C6)O)C)C)C)OC1	414.60	unknown	https://doi.org/10.1016/0031-9422(92)83293-8
Spirost-5-en-3-ol	234096	Click to see	414.60	unknown	https://doi.org/10.1016/0031-9422(92)83293-8
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	222284	Click to see	414.70	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/10.5530/PJ.2014.3.6
Npc29	6432744	Click to see	414.70	unknown	via CMAUP database
Sitogluside	5742590	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)OC5C(C(C(C(O5)CO)O)O)O)C)C)C(C)C	576.80	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Purine nucleosides
2-amino-9-[(2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one	6802	Click to see	283.24	unknown	via CMAUP database
Adenosine	60961	Click to see C1=NC(=C2C(=N1)N(C=N2)C3C(C(C(O3)CO)O)O)N	267.24	unknown	via CMAUP database
> Nucleosides, nucleotides, and analogues / Pyrimidine nucleosides
Uridine	6029	Click to see	244.20	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
3-methyl-6-[[2-(2-methylbut-3-en-2-yl)-5,7-bis(3-methylbut-2-enyl)-1H-indol-3-yl]methyl]piperazine-2,5-dione	12309532	Click to see	461.60	unknown	https://doi.org/10.1016/0031-9422(92)83293-8
Echinulin	115252	Click to see CC1C(=O)NC(C(=O)N1)CC2=C(NC3=C(C=C(C=C23)CC=C(C)C)CC=C(C)C)C(C)(C)C=C	461.60	unknown	https://doi.org/10.1016/0031-9422(92)83293-8
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
GlyTouCan:G29155XH	91692850	Click to see	342.30	unknown	via CMAUP database
GlyTouCan:G80014NW	46782954	Click to see	342.30	unknown	via CMAUP database
Sucrose	5988	Click to see	342.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Aldehydes / Aryl-aldehydes
5-Hydroxymethylfurfural	237332	Click to see C1=C(OC(=C1)C=O)CO	126.11	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzofurans
(7aR)-6-hydroxy-4,4,7a-trimethyl-6,7-dihydro-5H-1-benzofuran-2-one	12311356	Click to see	196.24	unknown	via CMAUP database
Loliolide	100332	Click to see CC1(CC(CC2(C1=CC(=O)O2)C)O)C	196.24	unknown	via CMAUP database
> Organoheterocyclic compounds / Furopyrans
(1S,3R,5S,8S,9R,12R,13S,14R)-14-hydroxy-13-methyl-14-propan-2-yl-4,7,10-trioxapentacyclo[6.4.1.19,12.03,5.05,13]tetradecane-6,11-dione	101316879	Click to see	294.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives
(-)-Dendrobin	15558892	Click to see	263.37	unknown	via CMAUP database
(11R,12R,13S)-2,12-dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one	118701398	Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C	263.37	unknown	via CMAUP database
(1S,4S,7S,8S,11S,12R,13S)-2,12-Dimethyl-13-propan-2-yl-10-oxa-2-azatetracyclo[5.4.1.18,11.04,12]tridecan-9-one	3037126	Click to see	263.37	unknown	via CMAUP database
Dendroban-12-one	566057	Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C	263.37	unknown	via CMAUP database
Dendrobine	442523	Click to see	263.37	unknown	via CMAUP database
From Dendrobium nobile	355017	Click to see	263.37	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
Triacontyl 3-(4-hydroxyphenyl)prop-2-enoate	71344737	Click to see	585.00	unknown	https://doi.org/10.1016/0031-9422(92)83293-8
Triacontyl p-coumarate	14213589	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC=C(C=C1)O	585.00	unknown	https://doi.org/10.1016/0031-9422(92)83293-8
> Phenylpropanoids and polyketides / Coumarins and derivatives
Ayapin	3083597	Click to see	190.15	unknown	via CMAUP database
Scoparone	8417	Click to see COC1=C(C=C2C(=C1)C=CC(=O)O2)OC	206.19	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
2-[[2-Hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-4-methoxyphenyl]methyl]-5-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-3-methoxyphenol	118715048	Click to see	560.60	unknown	https://doi.org/10.1016/J.BMCL.2014.09.052
2-[[4-Hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl]methyl]-5-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-3-methoxyphenol	122177287	Click to see COC1=CC(=CC(=C1CC2=C(C=C(C=C2OC)O)CCC3=CC(=CC=C3)O)O)CCC4=CC(=C(C=C4)O)OC	530.60	unknown	https://doi.org/10.1016/J.BMCL.2014.09.052
2-[[4-Hydroxy-2-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-6-methoxyphenyl]methyl]-5-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-3-methoxyphenol	118715049	Click to see COC1=CC(=CC(=C1CC2=C(C=C(C=C2OC)O)CCC3=CC(=C(C=C3)O)OC)O)CCC4=CC(=C(C=C4)O)OC	560.60	unknown	https://doi.org/10.1016/J.BMCL.2014.09.052
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+-)-Naringenin	932	Click to see	272.25	unknown	via CMAUP database
(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	via CMAUP database
Naringenin	439246	Click to see	272.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one	11602329	Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC	328.27	unknown	https://doi.org/10.5530/PJ.2014.3.6
> Phenylpropanoids and polyketides / Stilbenes
2-[[2-Hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-4-methoxyphenyl]methyl]-3-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-5-methoxyphenol	118715051	Click to see	560.60	unknown	https://doi.org/10.1016/J.BMCL.2014.09.052
2-Methoxy-4-[2-(3,4,5-trimethoxyphenyl)ethyl]phenol	14353469	Click to see COC1=CC(=CC(=C1OC)OC)CCC2=CC(=C(C=C2)O)OC	318.40	unknown	via CMAUP database
3,4'-Dihydroxy-3',4,5-Trimethoxybibenzyl	86024947	Click to see COC1=CC(=CC(=C1OC)O)CCC2=CC(=C(C=C2)O)OC	304.34	unknown	https://doi.org/10.1016/J.BMCL.2014.09.052
4-[[2-Hydroxy-6-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-4-methoxyphenyl]methyl]-3-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-5-methoxyphenol	118715052	Click to see	560.60	unknown	https://doi.org/10.1016/J.BMCL.2014.09.052
4-[[4-Hydroxy-2-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-6-methoxyphenyl]methyl]-3-[2-(4-hydroxy-3-methoxyphenyl)ethyl]-5-methoxyphenol	118715050	Click to see	560.60	unknown	https://doi.org/10.1016/J.BMCL.2014.09.052
4-[2-(3-Hydroxy-4-methoxyphenyl)ethyl]-2,6-dimethoxyphenol	86024946	Click to see	304.34	unknown	https://doi.org/10.1016/J.BMCL.2014.09.052
5-(2-(3-Hydroxy-5-methoxyphenyl)ethyl)-2-methoxyphenol	3085362	Click to see	274.31	unknown	https://doi.org/10.1016/J.BMCL.2014.09.052
batatasin III	10466989	Click to see COC1=CC(=CC(=C1)O)CCC2=CC(=CC=C2)O	244.28	unknown	https://doi.org/10.1016/J.BMCL.2014.09.052
Chrysotobibenzyl	3086528	Click to see	332.40	unknown	https://doi.org/10.5530/PJ.2014.3.6
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/J.BMCL.2014.09.052
Dihydroresveratrol	185914	Click to see C1=CC(=CC=C1CCC2=CC(=CC(=C2)O)O)O	230.26	unknown	via CMAUP database
Erianin	356759	Click to see COC1=C(C=C(C=C1)CCC2=CC(=C(C(=C2)OC)OC)OC)O	318.40	unknown	via CMAUP database
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/J.BMCL.2014.09.052
Tristin	15736297	Click to see	260.28	unknown	https://doi.org/10.1016/J.BMCL.2014.09.052

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Dendrobium fimbriatum

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