Scientific name	Authority	First published in
Pleione communis	Gagnep.	Bull. Soc. Bot. France 78: 25 (1931)
Pleione delavayi	Rolfe	Orchid Rev. 11: 291 (1903)
Pleione fargesii	Gagnep.	Bull. Soc. Bot. France 78: 26 (1931)
Pleione ganchuenensis	Gagnep.	Bull. Soc. Bot. France 78: 26 (1931)
Pleione henryi	Schltr.	Repert. Spec. Nov. Regni Veg. Beih. 4: 186 (1919)
Pleione mairei	Schltr.	Repert. Spec. Nov. Regni Veg. Beih. 4: 61 (1919)
Pleione pogonioides	Rolfe	Orchid Rev. 11: 291 (1903)
Pleione rhombilabia	Hand.-Mazz.	Symb. Sin. 7: 1348 (1936)
Pleione smithii	Schltr.	Acta Horti Gothob. 1: 149 (1924)
Coelogyne bulbocodioides	Franch.	Nouv. Arch. Mus. Hist. Nat. , sér. 2, 10: 84 (1887 publ. 1888)
Coelogyne delavayi	Rolfe	Bull. Misc. Inform. Kew 1896: 195 (1896)
Coelogyne henryi	Rolfe	Bull. Misc. Inform. Kew 1896: 195 (1896)
Coelogyne pogonioides	Rolfe	Bull. Misc. Inform. Kew 1896: 196 (1896)
Pleione communis var. subobtusum	Gagnep.	Bull. Soc. Bot. France 78: 25. 1931

Common names Top

Add a new one! Suggest a correction!

Filter by language:

Language	Common/alternative name
Chinese	山慈菇
Chinese	冰球子
Chinese	山慈姑叶
Chinese	山慈菇叶
Chinese	朱兰状独蒜兰
Chinese	独叶白芨
Chinese	独蒜兰
Chinese	臺灣一葉蘭
Chinese	一叶兰

Subspecies (abbr. subsp./ssp.) Top

Add a new one! Suggest a correction!

No subspecies added yet.

Varieties (abbr. var.) Top

Add a new one! Suggest a correction!

No variety added yet.

Subvarieties (abbr. subvar.) Top

Add a new one! Suggest a correction!

No subvariety added yet.

Forms (abbr. f.) Top

Add a new one! Suggest a correction!

No forms added yet.

Germination/Propagation Top

Suggest a correction or add new data!

Start at 20°C; if no germination occurs within 3 months, cool seeds to 4°C for 1-2 months, then return to 20°C.

grow in moist compost to which has been added soil from parent plant to provide symbiotic fungi

Distribution (via POWO/KEW) Top

Legend for the distribution data:

- Doubtful data

- Extinct

- Introduced

- Native

Asia-temperate click to expand
- China
  - China North-central
  - China South-central
  - China Southeast
  - Tibet

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000276360
UNII	576980937I
Tropicos	23507592
KEW	urn:lsid:ipni.org:names:652134-1
The Plant List	kew-159011
Open Tree Of Life	227365
NCBI Taxonomy	141752
IPNI	652134-1
iNaturalist	904993
GBIF	5321422
EOL	1134127
USDA GRIN	420123
CMAUP	NPO17553

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

Identification, Biological Function Profiling and Biosynthesis of Secondary Metabolites in Medicinal Orchids

Li K, Wu F, Chen M, Xiao Z, Xu Y, Xu M, Liu J, Xu D

Metabolites

07-Jul-2023

PMCID:	PMC10385179
doi:	10.3390/metabo13070829
PMID:	37512536

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

Comparative analyses and phylogenetic relationships of thirteen Pholidota species (Orchidaceae) inferred from complete chloroplast genomes

Li L, Wang W, Zhang G, Wu K, Fang L, Li M, Liu Z, Zeng S

BMC Plant Biol

20-May-2023

PMCID:	PMC10199590
doi:	10.1186/s12870-023-04233-8
PMID:	37210501

Lung protective effects of dietary malate esters derivatives from Bletilla striata against SiO2 nanoparticles through activation of Nrf2 pathway

Zhou D, Chang W, Qi J, Chen G, Li N

Chin Herb Med

04-Nov-2022

PMCID:	PMC9975635
doi:	10.1016/j.chmed.2022.11.001
PMID:	36875434

In-depth analysis of genomes and functional genomics of orchid using cutting-edge high-throughput sequencing

Song C, Wang Y, Manzoor MA, Mao D, Wei P, Cao Y, Zhu F

Front Plant Sci

23-Sep-2022

PMCID:	PMC9539832
doi:	10.3389/fpls.2022.1018029
PMID:	36212315

Progress in ICP-MS Analysis of Minerals and Heavy Metals in Traditional Medicine

Chen W, Yang Y, Fu K, Zhang D, Wang Z

Front Pharmacol

28-Jun-2022

PMCID:	PMC9274010
doi:	10.3389/fphar.2022.891273
PMID:	35837276

Herbal Medicine Intervention for the Treatment of COVID-19: A Living Systematic Review and Cumulative Meta-Analysis

Ang L, Song E, Hu XY, Lee HW, Chen Y, Lee MS

Front Pharmacol

20-Jun-2022

PMCID:	PMC9251500
doi:	10.3389/fphar.2022.906764
PMID:	35795550

Co-Targeting Tumor Angiogenesis and Immunosuppressive Tumor Microenvironment: A Perspective in Ethnopharmacology

Zhou J, Wang L, Peng C, Peng F

Front Pharmacol

15-Jun-2022

PMCID:	PMC9242535
doi:	10.3389/fphar.2022.886198
PMID:	35784750

Market survey on the traditional medicine of the Lijiang area in Yunnan Province, China

Zhang M, Li H, Wang J, Tang M, Zhang X, Yang S, Liu J, Li Y, Huang X, Li Z, Huang L

J Ethnobiol Ethnomed

23-May-2022

PMCID:	PMC9125852
doi:	10.1186/s13002-022-00532-w
PMID:	35606860

Vegetation Classification and Distribution Patterns in the South Slope of Yarlung Zangbo Grand Canyon National Nature Reserve, Eastern Himalayas

Wu PP, Wang Z, Jia NX, Dong SQ, Qu XY, Qiao XG, Liu CC, Guo K

Plants (Basel)

28-Apr-2022

PMCID:	PMC9105001
doi:	10.3390/plants11091194
PMID:	35567195

Comparative Chloroplast Genomics and Phylogenetic Analysis of Thuniopsis and Closely Related Genera within Coelogyninae (Orchidaceae)

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

Front Genet

24-Mar-2022

PMCID:	PMC8987740
doi:	10.3389/fgene.2022.850201
PMID:	35401668

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

Mycorrhizal Fungal Partners Remain Constant during a Root Lifecycle of Pleione bulbocodioides (Orchidaceae)

Qin J, Feng JQ, Zhang W, Zhang SB

J Fungi (Basel)

22-Nov-2021

PMCID:	PMC8621020
doi:	10.3390/jof7110994
PMID:	34829281

Effect of Fuzheng Qingdu Therapy for Metastatic Gastric Cancer is Associated With Improved Survival: A Multicenter Propensity-Matched Study

Hou C, Yang D, Zhang Y, Li Y, He Z, Dai X, Lu Q, Wang S, Zhang X, Liu Y

Integr Cancer Ther

15-Nov-2021

PMCID:	PMC8600555
doi:	10.1177/15347354211058464
PMID:	34781754

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

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 / Anthraquinones
Chrysophanic acid	10208	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=CC=C3O	254.24	unknown	via CMAUP database
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 / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin	3220	Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O	270.24	unknown	via CMAUP database
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Hydroxybenzoic acid derivatives
3-Hydroxybenzoic acid	7420	Click to see C1=CC(=CC(=C1)O)C(=O)O	138.12	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 / Xylenes / m-Xylenes
Secocrispiolide	90475612	Click to see CC1=C(C(=CC=C1)C)CC2CCOC(=O)C2=C	230.30	unknown	via CMAUP database
> Benzenoids / Dibenzocycloheptenes
(2R)-2-(4-hydroxy-3-methoxyphenyl)-4-methoxytricyclo[9.4.0.03,8]pentadeca-1(11),3(8),4,6,12,14-hexaene-6,13-diol	163081557	Click to see COC1=CC(=CC2=C1C(C3=C(CC2)C=C(C=C3)O)C4=CC(=C(C=C4)O)OC)O	378.40	unknown	https://doi.org/10.1016/S0031-9422(97)00785-1
Pleionol	102316537	Click to see COC1=CC(=CC2=C1C(C3=C(CC2)C=C(C=C3)O)C4=CC(=C(C=C4)O)OC)O	378.40	unknown	https://doi.org/10.1016/S0031-9422(97)00785-1
> Benzenoids / Phenanthrenes and derivatives / Hydrophenanthrenes
1-(4-Hydroxybenzyl)-2-methoxy-9,10-dihydrophenanthrene-4,7-diol	44392570	Click to see COC1=C(C2=C(C3=C(CC2)C=C(C=C3)O)C(=C1)O)CC4=CC=C(C=C4)O	348.40	unknown	https://doi.org/10.1016/0031-9422(95)00068-2
1-(4-Hydroxybenzyl)-4-methoxy-9,10-dihydrophenanthrene-2,7-diol	11163864	Click to see COC1=C2C(=C(C(=C1)O)CC3=CC=C(C=C3)O)CCC4=C2C=CC(=C4)O	348.40	unknown	https://doi.org/10.1016/0031-9422(95)00068-2
7-Methoxy-9,10-dihydrophenanthrene-2,4-diol	11615663	Click to see COC1=CC2=C(C=C1)C3=C(CC2)C=C(C=C3O)O	242.27	unknown	https://doi.org/10.1016/0031-9422(95)00068-2
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/10.1016/0031-9422(95)00068-2
8-[(4-Hydroxyphenyl)methyl]-9,10-dihydrophenanthrene-2,5-diol	101995285	Click to see C1CC2=C(C=CC(=C2C3=C1C=C(C=C3)O)O)CC4=CC=C(C=C4)O	318.40	unknown	https://doi.org/10.1016/0031-9422(95)00068-2
Coelonin	11390848	Click to see COC1=CC(=CC2=C1C3=C(CC2)C=C(C=C3)O)O	242.27	unknown	https://doi.org/10.1016/0031-9422(95)00068-2
Hircinol	442705	Click to see COC1=CC(=CC2=C1C3=C(CC2)C=CC=C3O)O	242.27	unknown	via CMAUP database
> Benzenoids / Phenanthrenes and derivatives / Phenanthrols
Blestriarene B	442695	Click to see COC1=C2C(=C(C(=C1)O)C3=C4C=CC5=C(C4=C(C=C3O)OC)C=CC(=C5)O)CCC6=C2C=CC(=C6)O	480.50	unknown	via CMAUP database
Flavanthrinin	14777892	Click to see COC1=C2C(=CC(=C1)O)C=CC3=C2C=CC(=C3)O	240.25	unknown	via CMAUP database
> Benzenoids / Phenols / Benzenediols / Hydroquinones
Hydroquinone	785	Click to see C1=CC(=CC=C1O)O	110.11	unknown	via CMAUP database
> Benzenoids / Phenols / Methoxyphenols
Homovanillyl alcohol	16928	Click to see COC1=C(C=CC(=C1)CCO)O	168.19	unknown	via CMAUP database
Vanillin	1183	Click to see COC1=C(C=CC(=C1)C=O)O	152.15	unknown	via CMAUP database
> Benzenoids / Phenols / Tyrosols and derivatives / Tyrosols
Tyrosol	10393	Click to see C1=CC(=CC=C1CCO)O	138.16	unknown	via CMAUP database
> Lignans, neolignans and related compounds
Shancilin	101995284	Click to see COC1=CC2=C(C3=C(CC2)C=C(C=C3)OC4=C(C=C(C=C4OC)CCC5=CC(=CC=C5)O)O)C(=C1)O	484.50	unknown	https://doi.org/10.1016/0031-9422(95)00068-2
> 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
> Lignans, neolignans and related compounds / Furanoid lignans / Tetrahydrofuran lignans / 9,9-epoxylignans
[(R)-[(3R,4R)-4-[(S)-acetyloxy-(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]-(4-hydroxy-3-methoxyphenyl)methyl] acetate	162885522	Click to see CC(=O)OC(C1COCC1C(C2=CC(=C(C=C2)O)OC)OC(=O)C)C3=CC(=C(C=C3)O)OC	460.50	unknown	https://doi.org/10.1016/S0031-9422(96)00549-3
[(S)-[(3R,4S)-4-[(R)-acetyloxy-(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]-(4-hydroxy-3-methoxyphenyl)methyl] acetate	162885524	Click to see CC(=O)OC(C1COCC1C(C2=CC(=C(C=C2)O)OC)OC(=O)C)C3=CC(=C(C=C3)O)OC	460.50	unknown	https://doi.org/10.1016/S0031-9422(96)00549-3
[[(3R,4S)-4-[acetyloxy-(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]-(4-hydroxy-3-methoxyphenyl)methyl] acetate	102062195	Click to see CC(=O)OC(C1COCC1C(C2=CC(=C(C=C2)O)OC)OC(=O)C)C3=CC(=C(C=C3)O)OC	460.50	unknown	https://doi.org/10.1016/S0031-9422(96)00549-3
[[(3S,4S)-4-[acetyloxy-(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]-(4-hydroxy-3-methoxyphenyl)methyl] acetate	102062196	Click to see CC(=O)OC(C1COCC1C(C2=CC(=C(C=C2)O)OC)OC(=O)C)C3=CC(=C(C=C3)O)OC	460.50	unknown	https://doi.org/10.1016/S0031-9422(96)00549-3
[[4-[Acetyloxy-(4-hydroxy-3-methoxyphenyl)methyl]oxolan-3-yl]-(4-hydroxy-3-methoxyphenyl)methyl] acetate	162885520	Click to see CC(=O)OC(C1COCC1C(C2=CC(=C(C=C2)O)OC)OC(=O)C)C3=CC(=C(C=C3)O)OC	460.50	unknown	https://doi.org/10.1016/S0031-9422(96)00549-3
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acids and conjugates / Long-chain fatty acids
2-Dodecyl-3-methylbutanedioic acid	99891	Click to see CCCCCCCCCCCCC(C(C)C(=O)O)C(=O)O	300.40	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Ambrosanolides and secoambrosanolides
(3aR)-alpha-Methylene-3-oxo-3abeta,8alpha-dimethyl-6alpha-hydroxy-1,2,3,3a,4,5,6,7,8,8abeta-decahydroazulene-5alpha-acetic acid 5,6-lactone	24893981	Click to see CC1CC2C(CC3(C1CCC3=O)C)C(=C)C(=O)O2	248.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
(3S,4aS,6aR,6bS,8aR,12aR,14aS,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol	40469639	Click to see CC1(CCC2(CCC3(C(=CCC4C3(CCC5C4(CCC(C5(C)C)O)C)C)C2C1)C)C)C	426.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
Pholidotin	13970951	Click to see CC(C)C(=C)CCC(C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)OC(=O)C=CC6=CC=C(C=C6)O)C)C	586.90	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Ergostane steroids / Ergosterols and derivatives
Ergosta-4,6,8(14),22-tetraen-3-one	6441416	Click to see CC(C)C(C)C=CC(C)C1CCC2=C3C=CC4=CC(=O)CCC4(C3CCC12C)C	392.60	unknown	via CMAUP database
> 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
(3S,8R,9R,10R,13R,14R,17R)-17-[(2R,5R)-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	11870456	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	via CMAUP database
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
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
> Organic acids and derivatives / Carboxylic acids and derivatives / Amino acids, peptides, and analogues / Alpha amino acids and derivatives
L-Pyroglutamic acid	7405	Click to see C1CC(=O)NC1C(=O)O	129.11	unknown	via CMAUP database
> Organic acids and derivatives / Carboxylic acids and derivatives / Dicarboxylic acids and derivatives
(E)-but-2-enedioate;hydron	21883788	Click to see [H+].[H+].C(=CC(=O)[O-])C(=O)[O-]	116.07	unknown	via CMAUP database
Butanedioate;hydron	21952380	Click to see [H+].[H+].C(CC(=O)[O-])C(=O)[O-]	118.09	unknown	via CMAUP database
> Organic acids and derivatives / Keto acids and derivatives / Gamma-keto acids and derivatives
Levulinic acid	11579	Click to see CC(=O)CCC(=O)O	116.11	unknown	via CMAUP database
> 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 / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
Dactylorhin A	10819499	Click to see CC(C)CC(CC(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O	888.90	unknown	via CMAUP database
Gastrodin	115067	Click to see C1=CC(=CC=C1CO)OC2C(C(C(C(O2)CO)O)O)O	286.28	unknown	via CMAUP database
Loroglossin	185907	Click to see CC(C)CC(C(C(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)O)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O	742.70	unknown	via CMAUP database
Militarine	171638	Click to see CC(C)CC(CC(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)(C(=O)OCC3=CC=C(C=C3)OC4C(C(C(C(O4)CO)O)O)O)O	726.70	unknown	via CMAUP database
Vanilloloside	44577222	Click to see COC1=C(C=CC(=C1)CO)OC2C(C(C(C(O2)CO)O)O)O	316.30	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Benzaldehydes / Hydroxybenzaldehydes
4-Hydroxybenzaldehyde	126	Click to see C1=CC(=CC=C1C=O)O	122.12	unknown	via CMAUP database
> Organoheterocyclic compounds / Benzopyrans / 1-benzopyrans
(3R,4R)-3-[(3R,4R)-6-hydroxy-4-methoxy-3,4-dihydro-2H-chromen-3-yl]-4-methoxy-3,4-dihydro-2H-chromen-6-ol	162922821	Click to see COC1C(COC2=C1C=C(C=C2)O)C3COC4=C(C3OC)C=C(C=C4)O	358.40	unknown	https://doi.org/10.1016/S0031-9422(96)00549-3
3-(6-hydroxy-4-methoxy-3,4-dihydro-2H-chromen-3-yl)-4-methoxy-3,4-dihydro-2H-chromen-6-ol	162922819	Click to see COC1C(COC2=C1C=C(C=C2)O)C3COC4=C(C3OC)C=C(C=C4)O	358.40	unknown	https://doi.org/10.1016/S0031-9422(96)00549-3
Pleionin A	102062197	Click to see COC1C(COC2=C1C=C(C=C2)O)C3COC4=C(C3OC)C=C(C=C4)O	358.40	unknown	https://doi.org/10.1016/S0031-9422(96)00549-3
> Organoheterocyclic compounds / Furans / Furoic acid and derivatives / Furoic acids
2-Furoic acid	6919	Click to see C1=COC(=C1)C(=O)O	112.08	unknown	via CMAUP database
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(1S)-alpha-Methylene-1beta,3beta,6alpha-trihydroxy-3,8alpha-dimethyl-1,2,3,4,5,6,7,8-octahydroazulene-5alpha-acetic acid 5,6-lactone	102408121	Click to see CC1CC2C(CC3=C1C(CC3(C)O)O)C(=C)C(=O)O2	264.32	unknown	via CMAUP database
> Organoheterocyclic compounds / Tetrahydroisoquinolines
(7S,9aR)-6-hydroxy-5-methoxy-1-methylspiro[3,8,9,9a-tetrahydro-2H-benzo[de]quinoline-7,4'-cyclohex-2-ene]-1'-one	101278288	Click to see CN1CCC2=CC(=C(C3=C2C1CCC34CCC(=O)C=C4)O)OC	313.40	unknown	https://doi.org/10.1016/S0031-9422(97)00785-1
> Phenylpropanoids and polyketides / 2-arylbenzofuran flavonoids
Shanciol H	102097660	Click to see CC(=O)OCC1C(OC2=C1C=C3C(=C2)CCC4=C3C(=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC	462.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Coumaric acids and derivatives
Hexacosyl (E)-ferulate	5318033	Click to see CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=CC1=CC(=C(C=C1)O)OC	558.90	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Cinnamic acids and derivatives / Hydroxycinnamic acids and derivatives / Hydroxycinnamic acids
4-Hydroxycinnamic acid	322	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
cis-p-Coumaric acid	1549106	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
Ferulic acid	445858	Click to see COC1=C(C=CC(=C1)C=CC(=O)O)O	194.18	unknown	via CMAUP database
p-Coumaric acid	637542	Click to see C1=CC(=CC=C1C=CC(=O)O)O	164.16	unknown	via CMAUP database
> 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	via CMAUP database
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids
2-(4-hydroxy-3-methoxyphenyl)-5-[2-(3-hydroxyphenyl)ethyl]-7-methoxy-3,4-dihydro-2H-chromen-3-ol	154791004	Click to see COC1=CC(=C2CC(C(OC2=C1)C3=CC(=C(C=C3)O)OC)O)CCC4=CC(=CC=C4)O	422.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
2-(4-hydroxy-3,5-dimethoxyphenyl)-5-[2-(3-hydroxyphenyl)ethyl]-7-methoxy-3,4-dihydro-2H-chromen-3-ol	162855753	Click to see COC1=CC(=C2CC(C(OC2=C1)C3=CC(=C(C(=C3)OC)O)OC)O)CCC4=CC(=CC=C4)O	452.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
5-[(2R,3S)-3-hydroxy-5-[2-(3-hydroxyphenyl)ethyl]-7-methoxy-3,4-dihydro-2H-chromen-2-yl]-3-methoxybenzene-1,2-diol	102121475	Click to see COC1=CC(=C2CC(C(OC2=C1)C3=CC(=C(C(=C3)OC)O)O)O)CCC4=CC(=CC=C4)O	438.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
Arundinin	102316541	Click to see COC1=CC(=CC(=C1CC2=CC=C(C=C2)O)O)CCC3=CC(=CC=C3)O	350.40	unknown	https://doi.org/10.1016/S0031-9422(97)00785-1
Bulbocodin C	102316583	Click to see COC1=C(C(=CC(=C1CC2=CC=C(C=C2)O)O)CCC3=CC(=CC=C3)O)CC4=CC=C(C=C4)O	456.50	unknown	https://doi.org/10.1016/S0031-9422(97)01110-2
Bulbocodin D	102316584	Click to see COC1=C(C(=C(C(=C1)CCC2=CC(=CC=C2)O)CC3=CC=C(C=C3)O)O)CC4=CC=C(C=C4)O	456.50	unknown	https://doi.org/10.1016/S0031-9422(97)01110-2
Shanciol A	15834310	Click to see COC1=CC(=C2CC(C(OC2=C1)C3=CC(=C(C(=C3)OC)O)OC)O)CCC4=CC(=CC=C4)O	452.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
Shanciol B	15834311	Click to see COC1=CC(=C2CC(C(OC2=C1)C3=CC(=C(C=C3)O)OC)O)CCC4=CC(=CC=C4)O	422.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
> Phenylpropanoids and polyketides / Diarylheptanoids / Linear diarylheptanoids / Curcuminoids
Bulbocodin[bibenzyl]	102316538	Click to see COC1=C(C(=C(C(=C1)O)CC2=CC=C(C=C2)O)CCC3=C(C=CC(=C3)CC4=CC=C(C=C4)O)O)CC5=CC=C(C=C5)O	562.60	unknown	https://doi.org/10.1016/S0031-9422(97)00785-1
Shanciguol	101995286	Click to see C1=CC(=CC(=C1)O)CCC2=C(C(=CC(=C2CC3=CC=C(C=C3)O)O)O)CC4=CC=C(C=C4)O	442.50	unknown	https://doi.org/10.1016/0031-9422(95)00068-2
> 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
Kayaflavone	9894522	Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(O2)C(=C(C=C3O)OC)C4=C(C=CC(=C4)C5=CC(=O)C6=C(C=C(C=C6O5)O)O)OC	580.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
6-Methoxykaempferol	5377945	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O	316.26	unknown	via CMAUP database
Quercetin	5280343	Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O	302.23	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-3-methoxy-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]oxan-2-yl]oxychromen-4-one	11520194	Click to see COC1=C(OC2=C(C1=O)C(=C(C(=C2)O)OC3C(C(C(C(O3)COC4C(C(C(C(O4)CO)O)O)O)O)O)O)O)C5=CC=C(C=C5)O	640.50	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
(2R,3R)-5,7-dihydroxy-2-(4-hydroxyphenyl)-6-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3-dihydrochromen-4-one	11634368	Click to see COC1=C(C2=C(C=C1O)OC(C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O)O	480.40	unknown	via CMAUP database
6-Methoxykaempferol 3-O-glucoside	5319460	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC=C(C=C4)O)O	478.40	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 6-O-methylated flavonoids
Axillarin	5281603	Click to see COC1=C(C2=C(C=C1O)OC(=C(C2=O)OC)C3=CC(=C(C=C3)O)O)O	346.30	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 7-O-methylated flavonoids
2-(4-hydroxy-3-methoxyphenyl)-11-methoxy-3,4,5,6-tetrahydro-2H-naphtho[2,1-f]chromene-3,8-diol	74977157	Click to see COC1=C(C=CC(=C1)C2C(CC3=C4CCC5=C(C4=C(C=C3O2)OC)C=CC(=C5)O)O)O	420.50	unknown	https://doi.org/10.1016/0031-9422(95)00642-7
2-(4-hydroxy-3,5-dimethoxyphenyl)-11-methoxy-3,4,5,6-tetrahydro-2H-naphtho[2,1-f]chromene-3,8-diol	163007344	Click to see COC1=CC(=CC(=C1O)OC)C2C(CC3=C4CCC5=C(C4=C(C=C3O2)OC)C=CC(=C5)O)O	450.50	unknown	https://doi.org/10.1016/S0031-9422(97)01110-2
Genkwanin	5281617	Click to see COC1=CC(=C2C(=C1)OC(=CC2=O)C3=CC=C(C=C3)O)O	284.26	unknown	via CMAUP database
Shanciol	44257051	Click to see COC1=C(C=CC(=C1)C2C(CC3=C4CCC5=C(C4=C(C=C3O2)OC)C=CC(=C5)O)O)O	420.50	unknown	https://doi.org/10.1016/0031-9422(95)00642-7
Shanciol E	102316581	Click to see COC1=CC(=CC(=C1O)OC)C2C(CC3=C4CCC5=C(C4=C(C=C3O2)OC)C=CC(=C5)O)O	450.50	unknown	https://doi.org/10.1016/S0031-9422(97)01110-2
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 3-O-methylated isoflavonoids
(10S,11R)-10-(4-hydroxy-3-methoxyphenyl)-1-methoxy-6,9,10,11-tetrahydro-5H-naphtho[1,2-g]chromene-3,11-diol	102121476	Click to see COC1=CC(=CC2=C1C3=CC4=C(C=C3CC2)OCC(C4O)C5=CC(=C(C=C5)O)OC)O	420.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
(10S,11R)-10-(4-hydroxy-3,5-dimethoxyphenyl)-1-methoxy-6,9,10,11-tetrahydro-5H-naphtho[1,2-g]chromene-3,11-diol	15834313	Click to see COC1=CC(=CC(=C1O)OC)C2COC3=C(C2O)C=C4C(=C3)CCC5=C4C(=CC(=C5)O)OC	450.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
[(10R,11R)-3-hydroxy-10-(4-hydroxy-3-methoxyphenyl)-1-methoxy-6,9,10,11-tetrahydro-5H-naphtho[1,2-g]chromen-11-yl] acetate	163057784	Click to see CC(=O)OC1C(COC2=C1C=C3C(=C2)CCC4=C3C(=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC	462.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
[(10R,11S)-3-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-1-methoxy-6,9,10,11-tetrahydro-5H-naphtho[1,2-g]chromen-11-yl] acetate	163038791	Click to see CC(=O)OC1C(COC2=C1C=C3C(=C2)CCC4=C3C(=CC(=C4)O)OC)C5=CC(=C(C(=C5)OC)O)OC	492.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
[3-hydroxy-10-(4-hydroxy-3,5-dimethoxyphenyl)-1-methoxy-6,9,10,11-tetrahydro-5H-naphtho[1,2-g]chromen-11-yl] acetate	163038790	Click to see CC(=O)OC1C(COC2=C1C=C3C(=C2)CCC4=C3C(=CC(=C4)O)OC)C5=CC(=C(C(=C5)OC)O)OC	492.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
10-(4-hydroxy-3,5-dimethoxyphenyl)-1-methoxy-6,9,10,11-tetrahydro-5H-naphtho[1,2-g]chromene-3,11-diol	163031596	Click to see COC1=CC(=CC(=C1O)OC)C2COC3=C(C2O)C=C4C(=C3)CCC5=C4C(=CC(=C5)O)OC	450.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
Bletilol C	102121478	Click to see CC(=O)OC1C(COC2=C1C=C3C(=C2)CCC4=C3C(=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC	462.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
> Phenylpropanoids and polyketides / Isoflavonoids / O-methylated isoflavonoids / 7-O-methylated isoflavonoids
(3R,4S)-3-(4-hydroxy-3-methoxyphenyl)-11-methoxy-3,4,5,6-tetrahydro-2H-naphtho[2,1-f]chromene-4,8-diol	162843990	Click to see COC1=C(C=CC(=C1)C2COC3=CC(=C4C(=C3C2O)CCC5=C4C=CC(=C5)O)OC)O	420.50	unknown	https://doi.org/10.1016/S0031-9422(97)01110-2
(3R,4S)-3-(4-hydroxy-3,5-dimethoxyphenyl)-11-methoxy-3,4,5,6-tetrahydro-2H-naphtho[2,1-f]chromene-4,8-diol	162973508	Click to see COC1=CC(=CC(=C1O)OC)C2COC3=CC(=C4C(=C3C2O)CCC5=C4C=CC(=C5)O)OC	450.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
[8-hydroxy-3-(4-hydroxy-3-methoxyphenyl)-11-methoxy-3,4,5,6-tetrahydro-2H-naphtho[2,1-f]chromen-4-yl] acetate	162642271	Click to see CC(=O)OC1C(COC2=CC(=C3C(=C12)CCC4=C3C=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC	462.50	unknown	https://doi.org/10.1016/0031-9422(95)00642-7
[8-hydroxy-3-(4-hydroxy-3,5-dimethoxyphenyl)-11-methoxy-3,4,5,6-tetrahydro-2H-naphtho[2,1-f]chromen-4-yl] acetate	162938370	Click to see CC(=O)OC1C(COC2=CC(=C3C(=C12)CCC4=C3C=CC(=C4)O)OC)C5=CC(=C(C(=C5)OC)O)OC	492.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
3-(4-hydroxy-3-methoxyphenyl)-11-methoxy-3,4,5,6-tetrahydro-2H-naphtho[2,1-f]chromene-4,8-diol	162843989	Click to see COC1=C(C=CC(=C1)C2COC3=CC(=C4C(=C3C2O)CCC5=C4C=CC(=C5)O)OC)O	420.50	unknown	https://doi.org/10.1016/S0031-9422(97)01110-2
3-(4-hydroxy-3,5-dimethoxyphenyl)-11-methoxy-3,4,5,6-tetrahydro-2H-naphtho[2,1-f]chromene-4,8-diol	162973506	Click to see COC1=CC(=CC(=C1O)OC)C2COC3=CC(=C4C(=C3C2O)CCC5=C4C=CC(=C5)O)OC	450.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
Bletilol A	102121477	Click to see CC(=O)OC1C(COC2=CC(=C3C(=C12)CCC4=C3C=CC(=C4)O)OC)C5=CC(=C(C(=C5)OC)O)OC	492.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
Bletilol B	146075490	Click to see CC(=O)OC1C(COC2=CC(=C3C(=C12)CCC4=C3C=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC	462.50	unknown	https://doi.org/10.1016/0031-9422(95)00642-7
CID 101688453	101688453	Click to see CC(=O)OC1C(COC2=CC(=C3C(=C12)CCC4=C3C=CC(=C4)O)OC)C5=CC(=C(C=C5)O)OC	462.50	unknown	https://doi.org/10.1016/0031-9422(95)00642-7
Shanciol C	15834312	Click to see COC1=CC(=CC(=C1O)OC)C2COC3=CC(=C4C(=C3C2O)CCC5=C4C=CC(=C5)O)OC	450.50	unknown	https://doi.org/10.1016/S0031-9422(98)80084-8
Shanciol F	102316582	Click to see COC1=C(C=CC(=C1)C2COC3=CC(=C4C(=C3C2O)CCC5=C4C=CC(=C5)O)OC)O	420.50	unknown	https://doi.org/10.1016/S0031-9422(97)01110-2
> Phenylpropanoids and polyketides / Stilbenes
3-[2-(3-Methoxyphenyl)ethyl]phenol	163192622	Click to see COC1=CC=CC(=C1)CCC2=CC(=CC=C2)O	228.29	unknown	https://doi.org/10.1016/S0031-9422(96)00758-3
3'-O-Methylbatatasin III	442711	Click to see COC1=CC=CC(=C1)CCC2=CC(=CC(=C2)OC)O	258.31	unknown	https://doi.org/10.1016/S0031-9422(96)00758-3
3',5-Dihydroxy-2-(4-hydroxybenzyl)3-methoxybibenzyl	11187204	Click to see COC1=CC(=CC(=C1CC2=CC=C(C=C2)O)CCC3=CC(=CC=C3)O)O	350.40	unknown	https://doi.org/10.1016/S0031-9422(97)00785-1
batatasin III	10466989	Click to see COC1=CC(=CC(=C1)O)CCC2=CC(=CC=C2)O	244.28	unknown	https://doi.org/10.1016/S0031-9422(96)00758-3
Bulbocol	102316540	Click to see COC1=CC=CC(=C1)CCC2=C(C(=CC(=C2)O)OC)CC3=CC=C(C=C3)O	364.40	unknown	https://doi.org/10.1016/S0031-9422(97)00785-1
Isoarundinin II	91542987	Click to see COC1=CC(=C(C(=C1)O)CC2=CC=C(C=C2)O)CCC3=CC(=CC=C3)O	350.40	unknown	https://doi.org/10.1016/S0031-9422(97)00785-1
> Phenylpropanoids and polyketides / Stilbenes / Stilbene glycosides
(2R,3S,4S,5R,6S)-2-(hydroxymethyl)-6-[3-[2-(3-hydroxyphenyl)ethyl]-5-methoxyphenoxy]oxane-3,4,5-triol	102066459	Click to see COC1=CC(=CC(=C1)CCC2=CC(=CC=C2)O)OC3C(C(C(C(O3)CO)O)O)O	406.40	unknown	https://doi.org/10.1016/S0031-9422(96)00758-3
2-(Hydroxymethyl)-6-[3-[2-(3-hydroxyphenyl)ethyl]-5-methoxyphenoxy]oxane-3,4,5-triol	162915990	Click to see COC1=CC(=CC(=C1)CCC2=CC(=CC=C2)O)OC3C(C(C(C(O3)CO)O)O)O	406.40	unknown	https://doi.org/10.1016/S0031-9422(96)00758-3
2-(Hydroxymethyl)-6-[3-methoxy-5-[2-(3-methoxyphenyl)ethyl]phenoxy]oxane-3,4,5-triol	162968540	Click to see COC1=CC=CC(=C1)CCC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)OC	420.50	unknown	https://doi.org/10.1016/S0031-9422(96)00758-3
3-[2-(3-Methoxyphenyl)ethyl]-5-methoxyphenyl beta-D-glucopyranoside	102066460	Click to see COC1=CC=CC(=C1)CCC2=CC(=CC(=C2)OC3C(C(C(C(O3)CO)O)O)O)OC	420.50	unknown	https://doi.org/10.1016/S0031-9422(96)00758-3

Biological Material Top

Contributors Top

No known contributors. Be the first!

Collections Top

In private collections	0
In public collections	0

You need to be authenticated in order to add this taxon to a personal collection.

Pleione bulbocodioides

Table of Contents

Details Top

Description 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

Biological Material Top

Contributors Top

Collections Top