Scientific and community resources:
The species is recognized as an accepted name in the Kew Plants of the World Online (POWO) database. De-identified herbarium specimens are accessible via the Global Biodiversity Information Facility (GBIF), supporting taxonomy and biogeography but not serving as a model organism for laboratory protocols.

Properties relevant to use:
No commercially relevant material is reported; the plant has no documented use in timber, fiber, colorants, resins, fragrance, food or beverage production. Reported uses are limited to scientific and community resources.

Standards and regulation:
No specific standards or regulatory frameworks are applicable to this orchid.

Sustainability and sourcing:
As an epiphytic forest orchid, the species is not targeted for harvest. Conservation relies on ex situ cultivation in botanical collections and avoidance of wild collection. No production scale is documented, and the plant is not traded as a commercial commodity.

Synonyms Top

Scientific name	Authority	First published in
Pholidota annamensis	Gagnep.	Bull. Mus. Natl. Hist. Nat. , sér. 2, 3: 145 (1931)
Pleione corniculata	Kuntze	Revis. Gen. Pl. 2: 680 (1891)
Coelogyne corniculata	Rchb.f.	Gard. Chron. 1865: 746 (1865)
Coelogyne pholas	Rchb.f.	Ann. Bot. Syst. 6: 237 (1862)
Pholidota chinensis var. cylindracea	Tang & F.T.Wang	Acta Phytotax. Sin. 1: 77. 1951
Pholidota chinensis	Lindl.	J. Hort. Soc. London 2: 308 (1847)
Pholidota corniculata	(Rchb.f.) Pfitzer & Kraenzl.	Pflanzenr. , IV, 50(32): 159 (1907)
Pholidota pholas	(Rchb.f.) God.-Leb.	Ill. Hort. 18: 161 (1871)

Common names Top

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Filter by language:

Language	Common/alternative name
Japanese	フォリドタ・キネンシス
Chinese	石仙桃
Chinese	石橄榄

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

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
Tropicos	50023150
KEW	urn:lsid:ipni.org:names:650641-1
The Plant List	kew-152755
Open Tree Of Life	3991955
IPNI	650641-1
GBIF	5323492
EOL	1135058
Tropicos	23513264
KEW	urn:lsid:ipni.org:names:650636-1
The Plant List	kew-152749
Open Tree Of Life	916003
IUCN Red List	44393483
IPNI	650636-1
iNaturalist	140396
GBIF	5323489
EOL	1135061
USDA GRIN	423494
Tropicos	50025173
KEW	urn:lsid:ipni.org:names:650676-1
The Plant List	kew-152802
Open Tree Of Life	3991961
IPNI	650676-1
iNaturalist	1153175
GBIF	5323519
EOL	1135038
World Flora Online	wfo-0000907176
KEW	urn:lsid:ipni.org:names:623804-1
NCBI Taxonomy	180499
IPNI	623804-1
GBIF	2838684

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

Identifying potential monkeypox virus inhibitors: an in silico study targeting the A42R protein

Ashley CN, Broni E, Wood CM, Okuneye T, Ojukwu MP, Dong Q, Gallagher C, Miller WA III

Front Cell Infect Microbiol

04-Mar-2024

PMCID:	PMC10945028
doi:	10.3389/fcimb.2024.1351737
PMID:	38500508

Ethnobotanical study of medicinal plants used by the Yi people in Mile, Yunnan, China

Li H, Huang C, Li Y, Wang P, Sun J, Bi Z, Xia S, Xiong Y, Bai X, Huang X

J Ethnobiol Ethnomed

23-Feb-2024

PMCID:	PMC10893717
doi:	10.1186/s13002-024-00656-1
PMID:	38395900

Comparative chloroplast genomics of 24 species shed light on the genome evolution and phylogeny of subtribe Coelogyninae (Orchidaceae)

Li L, Wu Q, Zhai J, Wu K, Fang L, Li M, Zeng S, Li S

BMC Plant Biol

05-Jan-2024

PMCID:	PMC10768429
doi:	10.1186/s12870-023-04665-2
PMID:	38182989

Editorial: Omics data-based identification of plant specialized metabolic genes

Wang P, Fan P, Bao Y, Li W, Wang L

Front Plant Sci

09-Jun-2023

PMCID:	PMC10289223
doi:	10.3389/fpls.2023.1209334
PMID:	37360719

Diversity and traditional knowledge of medicinal plants used by Shui people in Southwest China

Liu S, Zhang B, Lei Q, Zhou J, Ali M, Long C

J Ethnobiol Ethnomed

30-May-2023

PMCID:	PMC10230803
doi:	10.1186/s13002-023-00594-4
PMID:	37254191

Ethnobotanical study on herbal tea drinks in Guangxi, China

Long T, Hu R, Cheng Z, Xu C, Hu Q, Liu Q, Gu R, Huang Y, Long C

J Ethnobiol Ethnomed

31-Mar-2023

PMCID:	PMC10064729
doi:	10.1186/s13002-023-00579-3
PMID:	37004116

The gastrodin biosynthetic pathway in Pholidota chinensis Lindl. revealed by transcriptome and metabolome profiling

Liu B, Chen J, Zhang W, Huang Y, Zhao Y, Juneidi S, Dekebo A, Wang M, Shi L, Hu X

Front Plant Sci

03-Nov-2022

PMCID:	PMC9673822
doi:	10.3389/fpls.2022.1024239
PMID:	36407583

Editorial: Emerging and old viral diseases: Antiviral drug discovery from medicinal plants

Rahmatullah M, Jahan R, Nissapatorn V, Pereira MD, Wiart C

Front Pharmacol

19-Aug-2022

PMCID:	PMC9437638
doi:	10.3389/fphar.2022.976592
PMID:	36059941

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

Hearty recipes for health: the Hakka medicinal soup in Guangdong, China

Ding M, Shi S, Luo B

J Ethnobiol Ethnomed

25-Jan-2022

PMCID:	PMC8787035
doi:	10.1186/s13002-022-00502-2
PMID:	35078485

Dihydrophenanthrenes from a Sicilian Accession of Himantoglossum robertianum (Loisel.) P. Delforge Showed Antioxidant, Antimicrobial, and Antiproliferative Activities

Badalamenti N, Russi S, Bruno M, Maresca V, Vaglica A, Ilardi V, Zanfardino A, Di Napoli M, Varcamonti M, Cianciullo P, Calice G, Laurino S, Falco G, Basile A

Plants (Basel)

15-Dec-2021

PMCID:	PMC8708532
doi:	10.3390/plants10122776
PMID:	34961247

Allometry Between Vegetative and Reproductive Traits in Orchids

Feng JQ, Zhang FP, Huang JL, Hu H, Zhang SB

Front Plant Sci

13-Oct-2021

PMCID:	PMC8548613
doi:	10.3389/fpls.2021.728843
PMID:	34721458

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

Antimicrobial Activity of Necklace Orchids is Phylogenetically Clustered and can be Predicted With a Biological Response Method

Wati RK, de Graaf EF, Bogarín D, Heijungs R, van Vugt R, Smets EF, Gravendeel B

Front Pharmacol

12-Mar-2021

PMCID:	PMC7994927
doi:	10.3389/fphar.2020.586345
PMID:	33776752

Ethnobotanical study on medicinal plants used by Mulam people in Guangxi, China

Hu R, Lin C, Xu W, Liu Y, Long C

J Ethnobiol Ethnomed

02-Jul-2020

PMCID:	PMC7333293
doi:	10.1186/s13002-020-00387-z
PMID:	32616044

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 / Naphthalenes / Phenylnaphthalenes
3-[4-Hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl]-7-methoxy-9,10-dihydrophenanthrene-2,5-diol	102477415	Click to see	484.50	unknown	https://doi.org/10.1016/J.TETASY.2008.08.013
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
1-[(7-Hydroxy-4-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-4-methoxy-9,10-dihydrophenanthrene-2,7-diol	14583570	Click to see COC1=CC(=CC2=C1C3=C(CC2)C=C(C=C3)O)OC4=C5CCC6=C(C5=C(C=C4O)OC)C=CC(=C6)O	482.50	unknown	https://doi.org/10.1002/HLCA.200890228
2-Methoxy-9,10-dihydrophenanthrene-4,5-diol	11506999	Click to see COC1=CC2=C(C(=C1)O)C3=C(CC2)C=CC=C3O	242.27	unknown	https://doi.org/10.1007/S11418-007-0162-7
2,4,7-Trihydroxy-9,10-dihydrophenanthrene	21678577	Click to see	228.24	unknown	https://doi.org/10.1007/S11418-007-0162-7
3-(2,7-Dihydroxy-4-methoxy-9,10-dihydrophenanthren-1-yl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol	14863073	Click to see	482.50	unknown	https://doi.org/10.1016/J.TETASY.2008.08.013
3-(4,7-Dihydroxy-3-methoxy-9,10-dihydrophenanthren-1-yl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol	102026933	Click to see	482.50	unknown	https://doi.org/10.1002/HLCA.200890228
4-Methoxy-9,10-Dihydrophenanthrene-2,7-Diol	11390848	Click to see	242.27	unknown	https://doi.org/10.1007/S11418-007-0162-7 https://doi.org/10.1002/HLCA.200890228
6-(4,7-Dihydroxy-3-methoxy-9,10-dihydrophenanthren-1-yl)-7-methoxy-9,10-dihydrophenanthrene-2,5-diol	102477414	Click to see	482.50	unknown	https://doi.org/10.1016/J.TETASY.2008.08.013
7-[4-Hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenoxy]-2-methoxy-9,10-dihydrophenanthren-4-ol	11705759	Click to see COC1=CC2=C(C3=C(CC2)C=C(C=C3)OC4=C(C=C(C=C4OC)O)CCC5=CC(=CC=C5)O)C(=C1)O	484.50	unknown	https://doi.org/10.1002/HLCA.200890228
8-[(5-Hydroxy-7-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol	102026936	Click to see COC1=CC2=C(C3=C(CC2)C=C(C=C3)OC4=CC(=C(C5=C4CCC6=C5C=CC(=C6)O)O)OC)C(=C1)O	482.50	unknown	https://doi.org/10.1002/HLCA.200890228
8-[(7-Hydroxy-4-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol	102026937	Click to see	482.50	unknown	https://doi.org/10.1002/HLCA.200890228
8-[(7-Hydroxy-5-methoxy-9,10-dihydrophenanthren-2-yl)oxy]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol	102026935	Click to see	482.50	unknown	https://doi.org/10.1002/HLCA.200890228
8-[2-hydroxy-6-[(E)-2-(3-hydroxyphenyl)ethenyl]-4-methoxyphenyl]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol	102477418	Click to see	482.50	unknown	https://doi.org/10.1016/J.TETASY.2008.08.013
8-[2-Hydroxy-6-[2-(3-hydroxyphenyl)ethenyl]-4-methoxyphenyl]-6-methoxy-9,10-dihydrophenanthrene-2,5-diol	163084801	Click to see	482.50	unknown	https://doi.org/10.1016/J.TETASY.2008.08.013
8-[4-Hydroxy-2-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl]-7-methoxy-9,10-dihydrophenanthrene-2,5-diol	102477417	Click to see	484.50	unknown	https://doi.org/10.1016/J.TETASY.2008.08.013
Blestriarene A	11317652	Click to see	482.50	unknown	https://doi.org/10.1002/HLCA.200890228 https://doi.org/10.1016/J.TETASY.2008.08.013
Cannithrene 1	53438738	Click to see COC1=CC2=C(C(=C1)O)C3=C(CC2)C=CC(=C3)O	242.27	unknown	https://doi.org/10.1007/S11418-007-0162-7
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/S11418-007-0162-7
Eulophiol	25261830	Click to see	272.29	unknown	https://doi.org/10.1007/S11418-007-0162-7
Gymconopin C	11465808	Click to see COC1=CC(=CC2=C1C3=CC(=C(C=C3CC2)O)C4=C5CCC6=C(C5=C(C=C4O)OC)C=CC(=C6)O)O	482.50	unknown	https://doi.org/10.1016/J.TETASY.2008.08.013
Hircinol	442705	Click to see	242.27	unknown	https://doi.org/10.1007/S11418-007-0162-7
Lusianthridin	442702	Click to see	242.27	unknown	https://doi.org/10.1002/HLCA.200890228 https://doi.org/10.1007/S11418-007-0162-7
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
8-(4,7-Dihydroxy-3-methoxy-9,10-dihydrophenanthren-1-yl)-6-methoxyphenanthrene-2,5-diol	102026934	Click to see	480.50	unknown	https://doi.org/10.1002/HLCA.200890228
> Lignans, neolignans and related compounds
3-[2-Hydroxy-4-[2-(3-hydroxyphenyl)ethyl]-6-methoxyphenyl]-7-methoxy-9,10-dihydrophenanthrene-2,5-diol	102477416	Click to see	484.50	unknown	https://doi.org/10.1016/J.TETASY.2008.08.013
Phochinenin G	102477413	Click to see	482.50	unknown	https://doi.org/10.1016/J.TETASY.2008.08.013
> Lipids and lipid-like molecules / Fatty Acyls / Fatty alcohols
Dotriacontanol	96117	Click to see	466.90	unknown	https://doi.org/10.1055/S-2007-969052
> Organoheterocyclic compounds / Benzoxepines / Dibenzoxepines
13-Methoxy-2,15,17-trioxatetracyclo[9.7.0.03,8.014,18]octadeca-1(18),3(8),4,6,11,13-hexaen-6-ol	11818504	Click to see	286.28	unknown	https://doi.org/10.1007/S11418-007-0162-7
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
(2S,3S)-3-(3-hydroxy-5-methoxyphenyl)-2-(4-hydroxy-3-methoxyphenyl)-10-methoxy-2,3,4,5-tetrahydronaphtho[2,1-e][1]benzofuran-7-ol	102026938	Click to see	512.50	unknown	https://doi.org/10.1002/HLCA.200890228
3-(3-Hydroxy-5-methoxyphenyl)-2-(4-hydroxy-3-methoxyphenyl)-10-methoxy-2,3,4,5-tetrahydronaphtho[2,1-e][1]benzofuran-7-ol	163049256	Click to see	512.50	unknown	https://doi.org/10.1002/HLCA.200890228
> Phenylpropanoids and polyketides / Stilbenes
(z)-3,3'-Dihydroxy-5-methoxystilbene	11622859	Click to see	242.27	unknown	https://doi.org/10.1007/S11418-007-0162-7
1,3-Benzodioxol-4-ol, 5-[2-(1,3-benzodioxol-5-yl)ethyl]-7-methoxy-	11544204	Click to see COC1=C2C(=C(C(=C1)CCC3=CC4=C(C=C3)OCO4)O)OCO2	316.30	unknown	https://doi.org/10.1248/CPB.54.1216
3-[2-(2,3-Dimethoxyphenyl)ethenyl]-5-methoxyphenol	73025850	Click to see	286.32	unknown	https://doi.org/10.1248/CPB.54.1216
3-[2-(3-Hydroxy-5-methoxyphenyl)ethenyl]-2-methoxyphenol	72988360	Click to see	272.29	unknown	https://doi.org/10.1248/CPB.54.1216
3-[2-(3-Hydroxy-5-methoxyphenyl)ethenyl]benzene-1,2-diol	73316039	Click to see	258.27	unknown	https://doi.org/10.1007/S11418-007-0162-7
3,3'-Dihydroxy-5-methoxystilbene	73032981	Click to see	242.27	unknown	https://doi.org/10.1002/HLCA.200890228 https://doi.org/10.1248/CPB.54.1216
5-(2-(4-Hydroxyphenyl)Ethenyl)Benzene-1,3-Diol	5056	Click to see	228.24	unknown	https://doi.org/10.1248/CPB.54.1216
5-[2-(4-Hydroxyphenyl)ethyl]-2-methoxyphenol	71372825	Click to see	244.28	unknown	https://doi.org/10.1248/CPB.54.1216
batatasin III	10466989	Click to see COC1=CC(=CC(=C1)O)CCC2=CC(=CC=C2)O	244.28	unknown	https://doi.org/10.1002/HLCA.200890228
Phenol, 3-[2-(4-hydroxyphenyl)ethyl]-5-methoxy-	10014709	Click to see COC1=CC(=CC(=C1)O)CCC2=CC=C(C=C2)O	244.28	unknown	https://doi.org/10.1248/CPB.54.1216
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/10.1002/HLCA.200890228
Pholidotol A	11701981	Click to see	288.29	unknown	https://doi.org/10.1248/CPB.54.1216
Pholidotol C	16735893	Click to see	258.27	unknown	https://doi.org/10.1007/S11418-007-0162-7
Phoyunbene C	11507326	Click to see	272.29	unknown	https://doi.org/10.1248/CPB.54.1216
Phoyunbene D	11601663	Click to see COC1=CC=CC(=C1OC)C=CC2=CC(=CC(=C2)OC)O	286.32	unknown	https://doi.org/10.1248/CPB.54.1216
Resveratrol	445154	Click to see	228.24	unknown	https://doi.org/10.1248/CPB.54.1216
Thunalbene	25756094	Click to see	242.27	unknown	https://doi.org/10.1248/CPB.54.1216 https://doi.org/10.1002/HLCA.200890228

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Coelogyne chinensis

Table of Contents

Details Top

Ethnobotanical Use Top

General Uses Top

Synonyms Top

Common names Top

Subspecies (abbr. subsp./ssp.) Top

Varieties (abbr. var.) Top

Subvarieties (abbr. subvar.) Top

Forms (abbr. f.) Top

Germination/Propagation Top

Distribution (via POWO/KEW) Top

Links to other databases Top

Genomes (via NCBI) Top

Scientific Literature Top

Phytochemical Profile Top

Gallery Top

Contributors Top

Collections Top