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.

Among communities of Yunnan and Guangxi in southern China, dried bulbs of Nervilia fordii are prepared as decoctions for “removing heat” in fevers and easing respiratory “heat” that drives cough, according to Han and Ke, 1975, a pharmacognosy survey of regional medicinal orchids. The bulbs are also powdered for poulticing furuncles, abscesses, and bruises, commonly applied as a thick paste (for example, in Bosheng County, Yunnan) and moistened with a little water. Across northern Vietnam, fresh leaves are boiled in a little water to a soft pulp and applied topically as a poultice on swellings, skin infections, and inflamed gums, a practice noted in 2012 in an ethnobotanical study of Ha Giang province. In northern Laos, the same leaf preparations are used for treating wounds and mouth sores.

Active constituents that plausibly explain the activities include phenanthrene quinones such as nervilifordin C, iso Naparquinone, and other dihydrophenanthrenes that show antibacterial and anti-inflammatory effects in laboratory tests. The tubers also contain polysaccharides and flavonoids, including rutin and kaempferol glycosides, compounds with antioxidant and immunomodulatory properties documented for N. fordii (Nguyen et al., 2016; Cheng et al., 2012). These profiles align with the traditional use for fevers, coughs, and topical wound care.

A traditional yet practical preparation is a 1:5 ethanol tincture of dried Nervilia bulbs: weigh 20 grams of sliced or powdered dried bulb, place in a clean jar, and cover with 100 milliliters of 50% ethanol. Macerate in a dark place for 4–6 weeks, shaking the jar every 2–3 days. Strain through fine cloth and store in a dark bottle. Typical internal dose in folk practice is 3–5 milliliters of tincture in a small glass of warm water once or twice daily, or a corresponding decoction of 5–10 grams sliced bulb boiled for 15–20 minutes and cooled before use. Because of limited modern pharmacokinetic data and the presence of potentially irritating phenanthrene quinones, it is prudent to limit internal use to short periods of a few days, avoid during pregnancy and lactation, and stop use if digestive upset or rash occurs; topical pastes should be discontinued if irritation appears.

Modern relevance is active: ethanol extracts of N. fordii show antibacterial activity against Staphylococcus aureus and anti-inflammatory effects in animal models (Nguyen et al., 2016), while tuber polysaccharides have been studied for immunomodulatory effects (Chinese Journal of Natural Medicines, 2012). Dried bulbs are still sold as “Zhujie” in many South China herbal shops and marketed online as a traditional remedy.

General Uses Top

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Synonyms Top

Scientific name	Authority	First published in
Pogonia fordii	Hance	J. Bot. 23: 247 (1885)
Nervilia mekongensis	S.W.Gale, Schuit. & Suddee	Phytotaxa 247: 268 (2016)

Common names Top

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Language	Common/alternative name
Chinese	青天葵
Chinese	毛唇芋兰
Chinese	福氏芋兰
Chinese	毛唇芋蘭

Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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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
- Indo-China
  - Laos
  - Thailand
  - Vietnam

Links to other databases Top

Suggest others/fix!

Database	ID/link to page
World Flora Online	wfo-0000251670
Tropicos	50017478
KEW	urn:lsid:ipni.org:names:645477-1
The Plant List	kew-135285
Open Tree Of Life	562430
NCBI Taxonomy	1168071
IPNI	645477-1
iNaturalist	928125
GBIF	2836625
EOL	1137651
CMAUP	NPO5018

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

Alternative treatment of polycystic ovary syndrome: pre-clinical and clinical basis for using plant-based drugs

Malik S, Saeed S, Saleem A, Khan MI, Khan A, Akhtar MF

Front Endocrinol (Lausanne)

11-Jan-2024

PMCID:	PMC11081130
doi:	10.3389/fendo.2023.1294406
PMID:	38725974

Jiedu Fuzheng decoction improves the proliferation, migration, invasion and EMT of non-small cell lung cancer via the Wnt/β-catenin pathway

Fang F, Jin X, Meng J, He J, Wang J, Wang C, Xie S, Shi W

Cell Div

16-Dec-2023

PMCID:	PMC10725601
doi:	10.1186/s13008-023-00105-7
PMID:	38104091

Aquaporins: Potential Targets in Inflammatory Diseases

Bozkurt A, Halici H, Yayla M

Eurasian J Med

01-Dec-2023

PMCID:	PMC11075024
doi:	10.5152/eurasianjmed.2023.23357
PMID:	39128069

Engineering of PVA/PVP Hydrogels for Agricultural Applications

Malka E, Margel S

Gels

12-Nov-2023

PMCID:	PMC10671072
doi:	10.3390/gels9110895
PMID:	37998985

Signaling pathways and targeted therapeutic strategies for polycystic ovary syndrome

Wang K, Li Y

Front Endocrinol (Lausanne)

19-Oct-2023

PMCID:	PMC10622806
doi:	10.3389/fendo.2023.1191759
PMID:	37929034

A systematic review of the research progress of traditional Chinese medicine against pulmonary fibrosis: from a pharmacological perspective

Qin S, Tan P, Xie J, Zhou Y, Zhao J

Chin Med

03-Aug-2023

PMCID:	PMC10398979
doi:	10.1186/s13020-023-00797-7
PMID:	37537605

PI3K/Akt/Nrf2 mediated cellular signaling and virus-host interactions: latest updates on the potential therapeutic management of SARS-CoV-2 infection

Lekshmi VS, Asha K, Sanicas M, Asi A, Arya UM, Kumar B

Front Mol Biosci

01-Jun-2023

PMCID:	PMC10267462
doi:	10.3389/fmolb.2023.1158133
PMID:	37325475

Which Factors Influence Healthy Aging? A Lesson from the Longevity Village of Bama in China

Zhang W, Huang Q, Kang Y, Li H, Tan G

Aging Dis

01-Jun-2023

PMCID:	PMC10187713
doi:	10.14336/AD.2022.1108
PMID:	37191421

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

Recent Progress of Electrospun Herbal Medicine Nanofibers

Liu H, Bai Y, Huang C, Wang Y, Ji Y, Du Y, Xu L, Yu DG, Bligh SW

Biomolecules

16-Jan-2023

PMCID:	PMC9855805
doi:	10.3390/biom13010184
PMID:	36671570

Cultivable endophytic fungal community associated with the karst endemic plant Nervilia fordii and their antimicrobial activity

Zhou YQ, Yao SC, Wang J, Xie XY, Tan XM, Huang RS, Yang XF, Tan Y, Yu LY, Fu P

Front Microbiol

24-Nov-2022

PMCID:	PMC9730403
doi:	10.3389/fmicb.2022.1063897
PMID:	36504825

Recent Advances on Natural Aryl-C-glycoside Scaffolds: Structure, Bioactivities, and Synthesis—A Comprehensive Review

Liu CF

Molecules

01-Nov-2022

PMCID:	PMC9654268
doi:	10.3390/molecules27217439
PMID:	36364266

The extremely reduced, diverged and reconfigured plastomes of the largest mycoheterotrophic orchid lineage

Wen Y, Qin Y, Shao B, Li J, Ma C, Liu Y, Yang B, Jin X

BMC Plant Biol

20-Sep-2022

PMCID:	PMC9487142
doi:	10.1186/s12870-022-03836-x
PMID:	36123622

Rhamnocitrin decreases fibrosis of ovarian granulosa cells by regulating the activation of the PPARγ/NF-κB/TGF-β1/Smad2/3 signaling pathway mediated by Wisp2

Zhou YY, He CH, Lan H, Dong ZW, Wu YQ, Song JL

Ann Transl Med

01-Jul-2022

PMCID:	PMC9372664
doi:	10.21037/atm-22-2496
PMID:	35965823

Ethnobotany of medicinal plants used by the Yao people in Gongcheng County, Guangxi, China

Lu Z, Chen H, Lin C, Ou G, Li J, Xu W

J Ethnobiol Ethnomed

21-Jun-2022

PMCID:	PMC9210605
doi:	10.1186/s13002-022-00544-6
PMID:	35729593

Phytochemical Profile Top

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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 / Benzene and substituted derivatives / Benzoyl derivatives
Capillin	10321	Click to see	168.19	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(+)-Epi-alpha-bisabolol	1201551	Click to see CC1=CCC(CC1)C(C)(CCC=C(C)C)O	222.37	unknown	via CMAUP database
(1R,4S,6R,10S)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane	9991037	Click to see	220.35	unknown	via CMAUP database
Caryophylla-4,8-dien-5-ol	14524924	Click to see CC1(CC2C1CCC(=C)C(CCC2=C)O)C	220.35	unknown	via CMAUP database
Caryophyllene	5281515	Click to see CC1=CCCC(=C)C2CC(C2CC1)(C)C	204.35	unknown	via CMAUP database
Fgpdtarjoxrwjd-rrfjbimhsa-	11435962	Click to see	220.35	unknown	via CMAUP database
Oplopanone	10466745	Click to see	238.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
Spathulenol	92231	Click to see	220.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S,2S,3S,6S)-3-ethenyl-3-methyl-6-propan-2-yl-2-prop-1-en-2-ylcyclohexan-1-ol	102012174	Click to see	222.37	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
(1R,2R,4aR,5R,8aS)-2-(2-hydroxypropan-2-yl)-4a-methyl-8-methylidene-1,2,3,4,5,6,7,8a-octahydronaphthalene-1,5-diol	10729639	Click to see CC12CCC(C(C1C(=C)CCC2O)O)C(C)(C)O	254.36	unknown	via CMAUP database
2-[(2R,4aR)-4a,8-dimethyl-3,4,5,6-tetrahydro-2H-naphthalen-2-yl]propan-2-ol	10632752	Click to see CC1=CCCC2(C1=CC(CC2)C(C)(C)O)C	220.35	unknown	via CMAUP database
Beta-Eudesmol	91457	Click to see	222.37	unknown	via CMAUP database
Pygmol	14167388	Click to see	256.38	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Germacrane sesquiterpenoids
(1E,7S)-4beta,5alpha-Epoxygermacr-1(10)-en-2beta,6beta-diol	101014201	Click to see CC1=CC(CC2(C(O2)C(C(CC1)C(C)C)O)C)O	254.36	unknown	via CMAUP database
(1R,2E,6E,10S)-3,7-dimethyl-10-propan-2-ylcyclodeca-2,6-dien-1-ol	71608919	Click to see CC1=CCCC(=CC(C(CC1)C(C)C)O)C	222.37	unknown	via CMAUP database
(1R,2E,6R,10R)-10-(2-hydroxypropan-2-yl)-3-methyl-7-methylidenecyclodec-2-ene-1,6-diol	15479893	Click to see CC1=CC(C(CCC(=C)C(CC1)O)C(C)(C)O)O	254.36	unknown	via CMAUP database
(1R,2E,6S,10R)-10-(2-hydroxypropan-2-yl)-3-methyl-7-methylidenecyclodec-2-ene-1,6-diol	15479892	Click to see	254.36	unknown	via CMAUP database
(1R,2E,6S,10S)-3-methyl-7-methylidene-10-propan-2-ylcyclodec-2-ene-1,6-diol	100982187	Click to see	238.37	unknown	via CMAUP database
(1R,2R,3S,6E,10S)-6,10-dimethyl-3-propan-2-yl-11-oxabicyclo[8.1.0]undec-6-en-2-ol	14109689	Click to see	238.37	unknown	via CMAUP database
(1R,2R,3S,7R,10S)-10-methyl-6-methylidene-3-propan-2-yl-11-oxabicyclo[8.1.0]undecane-2,7-diol	10610977	Click to see	254.36	unknown	via CMAUP database
(1R,4S,5E,7S)-4-methyl-10-methylidene-7-propan-2-ylcyclodec-5-ene-1,4-diol	9991811	Click to see	238.37	unknown	via CMAUP database
(1S,2R,3S,6E)-6-methyl-10-methylidene-3-propan-2-ylcyclodec-6-ene-1,2-diol	100982186	Click to see CC1=CCCC(=C)C(C(C(CC1)C(C)C)O)O	238.37	unknown	via CMAUP database
(4aR,11E,12aR)-2,2,4,4,11-pentamethyl-7-methylidene-4a,5,6,9,10,12a-hexahydrocyclodeca[d][1,3]dioxin-8-one	10732427	Click to see	292.40	unknown	via CMAUP database
(4E,6R,7R)-6-hydroxy-7-(2-hydroxypropan-2-yl)-4-methyl-10-methylidenecyclodec-4-en-1-one	10729506	Click to see	252.35	unknown	via CMAUP database
Germacrene D	5317570	Click to see CC1=CCCC(=C)C=CC(CC1)C(C)C	204.35	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones
tatridin B	14191260	Click to see CC1=CC(C2C(CC(=C)C(CC1)O)OC(=O)C2=C)O	264.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Terpene lactones / Sesquiterpene lactones / Germacranolides and derivatives
(3aR,4S,6E,10E,11aR)-4-hydroxy-6,10-dimethyl-3-methylidene-3a,4,5,8,9,11a-hexahydrocyclodeca[b]furan-2-one	12299961	Click to see CC1=CC2C(C(CC(=CCC1)C)O)C(=C)C(=O)O2	248.32	unknown	via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Triterpenoids
Arnidiol	10478550	Click to see	442.70	unknown	via CMAUP database
Calenduladiol	461835	Click to see	442.70	unknown	via CMAUP database
Dammaradienol	13893946	Click to see	426.70	unknown	via CMAUP database
Dammaradienyl acetate	14137680	Click to see	468.80	unknown	via CMAUP database
Faradiol	9846222	Click to see CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CC(C2(CC=C1C)C)O)C)C)(C)C)O)C	442.70	unknown	via CMAUP database
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Cycloartanols and derivatives
Cycloartenol	92110	Click to see CC(CCC=C(C)C)C1CCC2(C1(CCC34C2CCC5C3(C4)CCC(C5(C)C)O)C)C	426.70	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
> Organic oxygen compounds / Organooxygen compounds / Alcohols and polyols / Tertiary alcohols
(4S)-2-Methyl-2,4-pentanediol	5288834	Click to see	118.17	unknown	via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(2E,5R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-diene	44575221	Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2	198.22	unknown	via CMAUP database
(2Z,5R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-diene	44575223	Click to see	198.22	unknown	via CMAUP database
[(2E,5R,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate	92269932	Click to see	256.25	unknown	via CMAUP database
[(2E,5S,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate	92269933	Click to see	256.25	unknown	via CMAUP database
[(2Z,5R,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate	92973365	Click to see	256.25	unknown	via CMAUP database
[(2Z,5S,9R)-2-hexa-2,4-diynylidene-1,6-dioxaspiro[4.4]nona-3,7-dien-9-yl] acetate	92973366	Click to see	256.25	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
Dracunculin	5319474	Click to see COC1=C2C(=C3C(=C1)C=CC(=O)O3)OCO2	220.18	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins
Isoscopoletin	69894	Click to see	192.17	unknown	via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin	5281416	Click to see	178.14	unknown	https://doi.org/10.1021/NP800760P
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnazin	5320945	Click to see	330.29	unknown	https://doi.org/10.1021/NP800760P
Rhamnetin	5281691	Click to see	316.26	unknown	https://doi.org/10.1021/NP800760P
Rhamnocitrin	5320946	Click to see	300.26	unknown	https://doi.org/10.1021/NP800760P
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid C-glycosides / Flavonoid 8-C-glycosides
5,7-Dihydroxy-2-(4-Hydroxyphenyl)-6-(3,4,5-Trihydroxy-6-(Hydroxymethyl)Oxan-2-Yl)-8-(3,4,5-Trihydroxyoxan-2-Yl)Chromen-4-One	3550102	Click to see	564.50	unknown	https://doi.org/10.1021/NP800760P
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(3R,4R,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]chromen-4-one	138454316	Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O	564.50	unknown	https://doi.org/10.1021/NP800760P
5,7-dihydroxy-2-(4-hydroxyphenyl)-6,8-bis[(2S,4R,5S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]chromen-4-one	44257674	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O	594.50	unknown	https://doi.org/10.1021/NP800760P
Schaftoside	442658	Click to see C1C(C(C(C(O1)C2=C3C(=C(C(=C2O)C4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O	564.50	unknown	https://doi.org/10.1021/NP800760P
Vicenin 2	442664	Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C(=C(C(=C3O2)C4C(C(C(C(O4)CO)O)O)O)O)C5C(C(C(C(O5)CO)O)O)O)O)O	594.50	unknown	https://doi.org/10.1021/NP800760P
Vicenin 2	3084407	Click to see	594.50	unknown	https://doi.org/10.1021/NP800760P
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
3-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-[3-hydroxy-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-methoxychromen-4-one	44179500	Click to see	802.70	unknown	https://doi.org/10.1021/NP800760P
3-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-7-methoxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	44179499	Click to see	786.70	unknown	https://doi.org/10.1021/NP800760P
3-[3,4-Dihydroxy-6-(hydroxymethyl)-5-(3,4,5-trihydroxyoxan-2-yl)oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one	56656811	Click to see	594.50	unknown	https://doi.org/10.1021/NP800760P
3-[3,4-Dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-2-(3,4-dihydroxyphenyl)-5-hydroxy-7-methoxychromen-4-one	56664502	Click to see	640.50	unknown	https://doi.org/10.1021/NP800760P
3-[3,4-Dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one	56663900	Click to see	624.50	unknown	https://doi.org/10.1021/NP800760P
3-[3,4-Dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-[3-hydroxy-4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-7-methoxychromen-4-one	74941772	Click to see	802.70	unknown	https://doi.org/10.1021/NP800760P
3-[3,4-Dihydroxy-6-(hydroxymethyl)-5-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-7-methoxy-2-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	74941771	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)O)O)O)O)O)C5=CC=C(C=C5)OC6C(C(C(C(O6)CO)O)O)O)O	786.70	unknown	https://doi.org/10.1021/NP800760P
5-Hydroxy-2-(4-hydroxy-3-methoxyphenyl)-7-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one	15558601	Click to see	492.40	unknown	https://doi.org/10.1021/NP800760P
5-Hydroxy-7-methoxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[4-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one	56677686	Click to see	624.50	unknown	https://doi.org/10.1021/NP800760P
Complanatuside	5492406	Click to see	624.50	unknown	https://doi.org/10.1021/NP800760P
Flavoyadorinin A	5491385	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)O)O)O)C4=CC(=C(C=C4)O)OC)O	492.40	unknown	https://doi.org/10.1021/NP800760P
Nervilifordin A	44179422	Click to see	594.50	unknown	https://doi.org/10.1021/NP800760P
Nervilifordin B	44179423	Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)OC4C(C(C(C(O4)CO)O)O)O)O)O)C5=CC=C(C=C5)O)O	624.50	unknown	https://doi.org/10.1021/NP800760P
Nervilifordin C	44179424	Click to see	640.50	unknown	https://doi.org/10.1021/NP800760P
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
5,7-dihydroxy-2-(4-hydroxyphenyl)-6-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-8-[(2S,3R,4S,5S)-3,4,5-trihydroxyoxan-2-yl]oxychromen-4-one	45268176	Click to see C1C(C(C(C(O1)OC2=C3C(=C(C(=C2O)OC4C(C(C(C(O4)CO)O)O)O)O)C(=O)C=C(O3)C5=CC=C(C=C5)O)O)O)O	596.50	unknown	via CMAUP database

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Nervilia fordii

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