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.

Traditional uses of Dendrobium chrysotoxum (the golden orchid) are recorded across Asia, focusing on the fleshy stems. In the Hani villages of Yunnan, China, dried stems are decocted in water to treat cough and sore throat (Li et al., 2018). A typical Hani decoction uses about a handful of dried stems (≈10 g) boiled for 20 minutes, taken hot two or three times daily. The Karen people of northern Thailand prepare a mild tea infusion from fresh stems to bring down fever and soothe a sore throat (Srisook et al., 2019). The Karen method steeps a few fresh stems in hot water for 5–10 minutes, then sips the warm infusion slowly. In the Kachin communities of northern Myanmar, fresh stems are ground into a poultice for wound healing and also steeped as a tea for digestive discomfort (Myo et al., 2020). The Kachin poultice is made by crushing fresh stems and applying the moist mass directly to the wound, changing the dressing daily. The preparations include decoctions, teas, and poultices, showing the plant’s versatility.

A Chinese‑style decoction is made as follows: Add 10 g of dried stems to 500 mL water, bring to a boil, then simmer 20 minutes. Strain and drink warm, ideally twice daily for cough or sore throat. The resulting liquid is a light amber tea with a mild, slightly sweet flavor that makes it pleasant to sip. Pregnant women should avoid this decoction, and people allergic to orchids should stop if stomach upset occurs.

Phytochemical studies have identified compounds that likely explain the plant’s traditional effects. The stems contain bibenzyls such as chrysotoxine, gigantol, and batatasin III (Wang et al., 2021), including phenanthrenes like dendrophenanthrene A (Li et al., 2020). Polysaccharide fractions rich in β‑D‑glucans have immunomodulatory activity (Zhang et al., 2022). Flavonoids such as quercetin and rutin add antioxidant power. These bibenzyls and phenanthrenes have demonstrated anti‑inflammatory activity in laboratory tests, while the polysaccharides stimulate immune cells, aligning with the herb’s reputation for soothing sore throats and supporting overall vitality.

Recent research has revived interest in D. chrysotoxum, with studies confirming the immunomodulatory action of its polysaccharides (Zhang et al., 2022). Dried stems are sold in Chinese herbal shops as a tonic for ‘nourishing yin and clearing heat’, and they appear in capsule and powder forms marketed for respiratory health. Thai and Burmese healers continue to use fresh‑stem infusions for fever and digestion, while scientific programs in several Asian universities are exploring the orchid’s potential in joint‑support formulas. This blend of science and tradition suggests the golden orchid will remain a valued part of Asian medicine.

General Uses Top

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*No documented commercial, industrial, or scientific uses are reported for *Dendrobium chrysotoxum*.*

Synonyms Top

Scientific name	Authority	First published in
Callista chrysotoxa	Kuntze	Revis. Gen. Pl. 2: 654 (1891)
Callista suavissima	Kuntze	Revis. Gen. Pl. 2: 655 (1891)
Dendrobium chrysotoxum var. suavissimum	(Rchb.f.) A.H.Kent	Man. Orchid. Pl. 3: 29. 1888
Dendrobium suavissimum	Rchb.f.	Gard. Chron. , n.s., 1: 406 (1874)
Callista chrysotoxa	(Lindl.) Brieger	Orchideen (Schlechter) 1(11-12): 704. 1981
Dendrobium calothyrsos	Schltr.	Notizbl. Bot. Gart. Berlin-Dahlem 8: 120 (1922)

Common names Top

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Filter by language:

Language	Common/alternative name
English	golden arch dendrobium
English	golden bow dendrobium
mni	ꯈꯣꯉꯨꯃꯦꯂꯩ
Vietnamese	kim điệp thân phình
Chinese	鼓槌石斛
Chinese	金弓石斛
Chinese	束花石斛

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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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

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

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000938772
Tropicos	23500679
INPN	629527
KEW	urn:lsid:ipni.org:names:627099-1
The Plant List	kew-57402
Open Tree Of Life	371870
Observations.org	473398
NCBI Taxonomy	161865
IPNI	627099-1
iNaturalist	493666
GBIF	5317521
Freebase	/m/065_syh
EPPO	DENCH
EOL	1100343
Elurikkus	513681
USDA GRIN	312705
Wikipedia	Dendrobium_chrysotoxum
Tropicos	50035364
KEW	urn:lsid:ipni.org:names:627014-1
The Plant List	kew-57303
Open Tree Of Life	3988648
IPNI	627014-1
GBIF	5317788
EOL	1112148
CMAUP	NPO20900

Genomes (via NCBI) Top

Below is displayed the reference genome only!
If you wish to browse all genomes for this plant click here.

Accession	Assembly
Accession	Name	Level	Submitter	Released	Coverage	Size
GCA_019925795.1	ASM1992579v1	Chromosome	The Orchid Conservation and Research Center of Shenzhen	2021-09-10	96	1.27 Gb

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.

Title

Authors

Publication

Released

IDs

TCM targets ferroptosis: potential treatments for cancer

Qin L, Zhong Y, Li Y, Yang Y

Front Pharmacol

22-Apr-2024

PMCID:	PMC11082647
doi:	10.3389/fphar.2024.1360030
PMID:	38738174

Genome-wide characterization of TCP family and their potential roles in abiotic stress resistance of oat (Avena sativa L.)

Pan J, Ju Z, Ma X, Duan L, Jia Z

Front Plant Sci

08-Apr-2024

PMCID:	PMC11036127
doi:	10.3389/fpls.2024.1382790
PMID:	38654900

Recent advances in the potential effects of natural products from traditional Chinese medicine against respiratory diseases targeting ferroptosis

Chen T, Ding L, Zhao M, Song S, Hou J, Li X, Li M, Yin K, Li X, Wang Z

Chin Med

22-Mar-2024

PMCID:	PMC10958864
doi:	10.1186/s13020-024-00918-w
PMID:	38519984

Identification and Characterization of the AREB/ABF Gene Family in Three Orchid Species and Functional Analysis of DcaABI5 in Arabidopsis

Xie X, Lin M, Xiao G, Wang Q, Li Z

Plants (Basel)

08-Mar-2024

PMCID:	PMC10974128
doi:	10.3390/plants13060774
PMID:	38592811

Erianin promotes apoptosis and inhibits Akt-mediated aerobic glycolysis of cancer cells

Han S, Chen S, Wang J, Huang S, Xiao Y, Deng G

J Cancer

04-Mar-2024

PMCID:	PMC10937289
doi:	10.7150/jca.92780
PMID:	38495480

Identification of Fusarium oxysporum Causing Leaf Blight on Dendrobium chrysotoxum in Yunnan Province, China

Yang J, Ahmed W, Zhang J, Gao S, Wang Z, Yang H, Bai X, Luo K, Xu C, Ji G

Life (Basel)

20-Feb-2024

PMCID:	PMC10970817
doi:	10.3390/life14030285
PMID:	38541611

Erianin promotes endogenous neurogenesis in traumatic brain injury rats

Li Q, Gan X, Zhang M, Zhang G, Li Y, Gao L

Sci Rep

19-Feb-2024

PMCID:	PMC10876537
doi:	10.1038/s41598-023-50573-8
PMID:	38374284

Identification and Analysis of PEPC Gene Family Reveals Functional Diversification in Orchidaceae and the Regulation of Bacterial-Type PEPC

Li R, Gao X, Wu Y, Wei C, Li MH, Liu DK, Liu ZJ

Int J Mol Sci

08-Feb-2024

PMCID:	PMC10888551
doi:	10.3390/ijms25042055
PMID:	38396732

Genome-Wide Identification and Expression Profile Analysis of Sugars Will Eventually Be Exported Transporter (SWEET) Genes in Zantedeschia elliottiana and Their Responsiveness to Pectobacterium carotovora subspecies Carotovora (Pcc) Infection

Li Z, Guo Y, Jin S, Wu H

Int J Mol Sci

07-Feb-2024

PMCID:	PMC10888187
doi:	10.3390/ijms25042004
PMID:	38396683

Genome-wide identification and characterization of TCP gene family in Dendrobium nobile and their role in perianth development

Wei X, Yuan M, Zheng BQ, Zhou L, Wang Y

Front Plant Sci

05-Feb-2024

PMCID:	PMC10875090
doi:	10.3389/fpls.2024.1352119
PMID:	38375086

Hypoglycemic Effects and Quality Marker Screening of Dendrobium nobile Lindl. at Different Growth Years

Luo Y, Yang D, Xu Y, Wu D, Tan D, Qin L, Wu X, Lu Y, He Y

Molecules

02-Feb-2024

PMCID:	PMC10856227
doi:	10.3390/molecules29030699
PMID:	38338442

A review of natural products targeting tumor immune microenvironments for the treatment of lung cancer

Yao P, Liang S, Liu Z, Xu C

Front Immunol

01-Feb-2024

PMCID:	PMC10867126
doi:	10.3389/fimmu.2024.1343316
PMID:	38361933

Elimination of detached Listeria monocytogenes from the biofilm on stainless steel surfaces during milk and cheese processing using natural plant extracts

El-sawy YN, Abdel-Salam AB, Abd-Elhady HM, Abou-Taleb KA, Ahmed RF

Sci Rep

27-Jan-2024

PMCID:	PMC10821901
doi:	10.1038/s41598-024-52394-9
PMID:	38280925

Novel Insights on Ferroptosis Modulation as Potential Strategy for Cancer Treatment: When Nature Kills

Consoli V, Fallica AN, Sorrenti V, Pittalà V, Vanella L

Antioxid Redox Signal

17-Jan-2024

PMCID:	PMC10824235
doi:	10.1089/ars.2022.0179
PMID:	37132605

Ferroptosis: a new mechanism of traditional Chinese medicine for cancer treatment

Zhu J, Shen P, Xu Y, Zhang X, Chen Q, Gu K, Ji S, Yang B, Zhao Y

Front Pharmacol

16-Jan-2024

PMCID:	PMC10824936
doi:	10.3389/fphar.2024.1290120
PMID:	38292937

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	https://doi.org/10.1007/S10600-009-9329-7
> 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 / Fluorenes
(9R)-4-methoxy-9H-fluorene-2,5,9-triol	11425067	Click to see COC1=CC(=CC2=C1C3=C(C2O)C=CC=C3O)O	244.24	unknown	https://doi.org/10.1002/HLCA.200490037
1,4,7-Trihydroxy-5-Methoxyfluoren-9-One	44418788	Click to see	258.23	unknown	https://doi.org/10.1007/S10600-009-9329-7
2,5-Dihydroxy-4-methoxy-9H-fluoren-9-one	10879298	Click to see	242.23	unknown	https://doi.org/10.1007/S10600-009-9329-7
4-methoxy-9H-fluorene-2,5,9-triol	5248146	Click to see	244.24	unknown	https://doi.org/10.1002/HLCA.200490037
> 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
Erianthridin	10401022	Click to see COC1=C(C=C2CCC3=C(C2=C1OC)C=CC(=C3)O)O	272.29	unknown	https://doi.org/10.1007/S10600-009-9329-7
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
7-Hydroxy-2,3,4,8-tetramethoxyphenanthrene	5315859	Click to see	314.30	unknown	https://doi.org/10.1007/S10600-009-9329-7
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
Fimbriatone	11737608	Click to see	282.25	unknown	https://doi.org/10.1002/HLCA.200490037
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 / 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
(4aS,6aS,6aR,6bS,8aS,9R,10S,12aS,14aS,14bS)-10-hydroxy-2,2,4a,6a,6a,8a,9,14a-octamethyl-3,4,6,6b,7,8,9,10,11,12,12a,13,14,14b-tetradecahydro-1H-picen-5-one	101679786	Click to see CC1C(CCC2C1(CCC3C2(CCC4(C3(CC(=O)C5(C4CC(CC5)(C)C)C)C)C)C)C)O	442.70	unknown	via CMAUP database
(4R,4aS,6aS,6aS,6bR,8aS,12aS,14aS,14bS)-4,4a,6a,6b,8a,11,11,14a-octamethyl-1,2,4,5,6,6a,7,9,10,12,12a,13,14,14b-tetradecahydropicene-3,8-dione	21636453	Click to see CC1C(=O)CCC2C1(CCC3C2(CCC4(C3(CC(=O)C5(C4CC(CC5)(C)C)C)C)C)C)C	440.70	unknown	via CMAUP database
(Z,6S)-2-methyl-6-[(5R,9S,10R,13S,14S,17S)-4,4,10,13,14-pentamethyl-3-oxo-1,2,5,6,9,11,12,15,16,17-decahydrocyclopenta[a]phenanthren-17-yl]hept-2-enoic acid	51693592	Click to see CC(CCC=C(C)C(=O)O)C1CCC2(C1(CCC3C2=CCC4C3(CCC(=O)C4(C)C)C)C)C	454.70	unknown	via CMAUP database
3-Epioleanolic acid	11869658	Click to see	456.70	unknown	via CMAUP database
Friedelin	91472	Click to see	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroidal alkaloids / Cerveratrum-type alkaloids
(6S,23R)-20-hydroxy-6,23-dimethyl-4-azahexacyclo[12.11.0.02,11.04,9.015,24.018,23]pentacosan-17-one	5315861	Click to see CC1CCC2CC3CCC4C(C3CN2C1)CC5C4CC(=O)C6C5(CCC(C6)O)C	399.60	unknown	via CMAUP database
> 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/10.1007/S10600-009-9329-7
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 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 / 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 / Flavonoids / Biflavonoids and polyflavonoids
Amentoflavone	5281600	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(O2)C(=C(C=C3O)O)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)O)O	538.50	unknown	via CMAUP database
Podocarpusflavone A	5320644	Click to see	552.50	unknown	via CMAUP database
Podocarpusflavone B	5320646	Click to see	566.50	unknown	via CMAUP database
> 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 / Stilbenes
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
Chrysotobibenzyl	3086528	Click to see	332.40	unknown	https://doi.org/10.1007/S10600-009-9329-7
Dendrophenol	176096	Click to see COC1=CC(=CC(=C1O)OC)CCC2=CC(=C(C=C2)O)OC	304.34	unknown	via CMAUP database
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	https://doi.org/10.1007/S10600-009-9329-7
Phenol, 4-[2-(3,4-dimethoxyphenyl)ethyl]-2,6-dimethoxy-	5315860	Click to see COC1=C(C=C(C=C1)CCC2=CC(=C(C(=C2)OC)O)OC)OC	318.40	unknown	via CMAUP database

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Dendrobium chrysotoxum

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