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)

Common names Top

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Filter by language:

Language	Common/alternative name
English	fringe-lipped dendrobium
Assamese	ডেনড্ৰ'বিয়াম ফিমব্ৰিয়েটাম
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

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

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

Research progress in traditional Chinese medicine in the treatment of Alzheimer’s disease and related dementias

Tan W, Qi L, Hu X, Tan Z

Front Pharmacol

24-Nov-2022

PMCID:	PMC9729772
doi:	10.3389/fphar.2022.921794
PMID:	36506569

Polysaccharide from Atractylodes macrocephala Koidz. ameliorates DSS-induced colitis in mice by regulating the Th17/Treg cell balance

Yang M, Zhang Q, Taha R, Abdelmotalab MI, Wen Q, Yuan Y, Zhao Y, Li Q, Liao C, Huang X, Jiang Z, Chu C, Jiao C, Sun L

Front Immunol

20-Oct-2022

PMCID:	PMC9630481
doi:	10.3389/fimmu.2022.1021695
PMID:	36341374

Combined metabolomics and proteomics to reveal beneficial mechanisms of Dendrobium fimbriatum against gastric mucosal injury

Sun J, Liu PF, Liu JN, Lu C, Tong LT, Wang YQ, Liu JM, Fan B, Wang FZ

Front Pharmacol

30-Aug-2022

PMCID:	PMC9468276
doi:	10.3389/fphar.2022.948987
PMID:	36110550

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 C1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)C(=O)O	284.22	unknown	via CMAUP database
> Benzenoids / Anthracenes / Anthraquinones
Physcione	10639	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)OC	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
3,4-Dihydroxybenzoic acid	72	Click to see C1=CC(=C(C=C1C(=O)O)O)O	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 COC1=CC(=CC(=C1O)OC)C(=O)O	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 COC1=CC2=C(C=C1)C3=C(C(=C(C=C3C=C2)OC)OC)OC	298.30	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
2,4,7-Trihydroxy-9,10-dihydrophenanthrene	21678577	Click to see C1CC2=C(C3=C1C=C(C=C3)O)C(=CC(=C2)O)O	228.24	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
1,5,6-Trimethoxyphenanthrene-2,7-diol	11983285	Click to see COC1=C(C=CC2=C1C=CC3=CC(=C(C(=C32)OC)OC)O)O	300.30	unknown	via CMAUP database
2,4-Dimethoxyphenanthrene-3,5-diol	44445443	Click to see COC1=C(C(=C2C(=C1)C=CC3=C2C(=CC=C3)O)OC)O	270.28	unknown	via CMAUP database
2,7-Phenanthrenediol, 3,4-dimethoxy-	158975	Click to see COC1=C(C=C2C=CC3=C(C2=C1OC)C=CC(=C3)O)O	270.28	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 COC1=C2C(=C3C=CC(=CC3=C1)O)C(=CC4=C2C5(CC(=O)C6=C7C=CC(=CC7=CC(=C65)OC)O)C(=O)O4)O	508.50	unknown	via CMAUP database
> Hydrocarbons / Saturated hydrocarbons / Alkanes
Hentriacontane	12410	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC	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 COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	418.40	unknown	via CMAUP database
Syringaresinol, (+)-	443023	Click to see COC1=CC(=CC(=C1O)OC)C2C3COC(C3CO2)C4=CC(=C(C(=C4)OC)O)OC	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 CCCCCCCCCCCCCCCCC(=O)O	270.50	unknown	via CMAUP database
Palmitic Acid	985	Click to see CCCCCCCCCCCCCCCC(=O)O	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
1-Heptadecanoyl-rac-glycerol	107036	Click to see CCCCCCCCCCCCCCCCC(=O)OCC(CO)O	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 CC1CCC2(C(C3(C4(CCC5C(C4CC3(O2)O)CC=C6C5(CCC(C6)O)C)C)O)C)OC1	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 CC1CCC2(C(C3(C4(CCC5C(C4CC3(O2)O)CC=C6C5(CCC(C6)O)C)C)O)C)OC1	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 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
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(-)-beta-Sitosterol	6432744	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	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
Beta-Sitosterol	222284	Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C	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 C1=NC2=C(N1C3C(C(C(O3)CO)O)O)NC(=NC2=O)N	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 C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)O	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-en-1-yl)-1H-indol-3-yl]methyl}piperazine-2,5-dione	12309532	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
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
alpha-D-Glucopyranoside, beta-D-fructofuranosyl	91692850	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
Sucrose	5988	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	342.30	unknown	via CMAUP database
Sucrose NF	46782954	Click to see C(C1C(C(C(C(O1)OC2(C(C(C(O2)CO)O)O)CO)O)O)O)O	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 CC1(CC(CC2(C1=CC(=O)O2)C)O)C	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
Aduncin	101316879	Click to see CC(C)C1(C2C3CC4C5(C3(C(C1OC2=O)OC5=O)C)O4)O	294.30	unknown	via CMAUP database
> Organoheterocyclic compounds / Indoles and derivatives
(-)-Dendrobin	15558892	Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C	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 CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C	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 CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C	263.37	unknown	via CMAUP database
From Dendrobium nobile	355017	Click to see CC(C)C1C2C3CCC4C3(C(C1OC2=O)N(C4)C)C	263.37	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acid esters / Coumaric acid esters
3-(4-Hydroxyphenyl)acrylic acid triacontyl ester	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
Triacontyl 3-(4-hydroxyphenyl)prop-2-enoate	71344737	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 C1OC2=C(O1)C=C3C(=C2)C=CC(=O)O3	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 COC1=CC(=C(C(=C1)O)CC2=C(C=C(C=C2OC)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
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
(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
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	via CMAUP database
Naringenin	439246	Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC=C(C=C3)O	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 COC1=CC(=C(C(=C1)O)CC2=C(C=C(C=C2O)OC)CCC3=CC(=C(C=C3)O)OC)CCC4=CC(=C(C=C4)O)OC	560.60	unknown	https://doi.org/10.1016/J.BMCL.2014.09.052
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 COC1=CC(=C(C(=C1)O)CC2=C(C=C(C=C2OC)O)CCC3=CC(=C(C=C3)O)OC)CCC4=CC(=C(C=C4)O)OC	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 COC1=CC(=CC(=C1CC2=C(C=C(C=C2OC)O)CCC3=CC(=C(C=C3)O)OC)CCC4=CC(=C(C=C4)O)OC)O	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 COC1=C(C=C(C=C1)CCC2=CC(=C(C(=C2)OC)O)OC)O	304.34	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 COC1=C(C=C(C=C1)CCC2=CC(=C(C(=C2)OC)OC)OC)OC	332.40	unknown	https://doi.org/10.5530/PJ.2014.3.6
Crepidatin	14353469	Click to see COC1=CC(=CC(=C1OC)OC)CCC2=CC(=C(C=C2)O)OC	318.40	unknown	via CMAUP database
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
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/J.BMCL.2014.09.052
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 COC1=C(C=CC(=C1)CCC2=CC(=CC(=C2)O)O)O	260.28	unknown	https://doi.org/10.1016/J.BMCL.2014.09.052

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Dendrobium fimbriatum

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