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Details Top

Internal ID UUID643fe4701d174055226624
Scientific name Nervilia fordii
Authority Schltr.
First published in Bot. Jahrb. Syst. 45: 403 (1911)

Description 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

Subspecies (abbr. subsp./ssp.) Top

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No subspecies added yet.

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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No germination or propagation data was added yet.

Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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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
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
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
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
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
Rhamnocitrin Attenuates Ovarian Fibrosis in Rats with Letrozole-Induced Experimental Polycystic Ovary Syndrome Zhou Y, Lan H, Dong Z, Li W, Qian B, Zeng Z, He W, Song JL Oxid Med Cell Longev 26-May-2022
PMCID:PMC9162838
doi:10.1155/2022/5558599
PMID:35663203
Qingfei Litan Decoction Against Acute Lung Injury/Acute Respiratory Distress Syndrome: The Potential Roles of Anti-Inflammatory and Anti-Oxidative Effects Diao Y, Ding Q, Xu G, Li Y, Li Z, Zhu H, Zhu W, Wang P, Shi Y Front Pharmacol 23-May-2022
PMCID:PMC9168533
doi:10.3389/fphar.2022.857502
PMID:35677439
Calcium–Permeable Channels and Endothelial Dysfunction in Acute Lung Injury Hao Y, Wang Z, Frimpong F, Chen X Curr Issues Mol Biol 16-May-2022
PMCID:PMC9164020
doi:10.3390/cimb44050150
PMID:35678679
Preparation of Novel Nanomaterial and Its Application in Food Industry Wu H, Zhang H Foods 11-May-2022
PMCID:PMC9141088
doi:10.3390/foods11101382
PMID:35626952
Flavonoids as Potential Anti-Inflammatory Molecules: A Review Al-Khayri JM, Sahana GR, Nagella P, Joseph BV, Alessa FM, Al-Mssallem MQ Molecules 02-May-2022
PMCID:PMC9100260
doi:10.3390/molecules27092901
PMID:35566252

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Benzenoids / Benzene and substituted derivatives / Benzoyl derivatives
Capillin 10321 Click to see CC#CC#CC(=O)C1=CC=CC=C1 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,5R,9S)-4,5-Epoxy-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undecane 9991037 Click to see CC1(CC2C1CCC3(C(O3)CCC2=C)C)C 220.35 unknown via CMAUP database
(1R,5S,9S)-4,8-Dimethylene-11,11-dimethylbicyclo[7.2.0]undecan-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 CC(C)C1=CCC2(C(CCC(=C)C2C1)O)C 220.35 unknown via CMAUP database
Oplopanone 10466745 Click to see CC(C)C1CCC(C2C1C(CC2)C(=O)C)(C)O 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 CC1(C2C1C3C(CCC3(C)O)C(=C)CC2)C 220.35 unknown via CMAUP database
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Elemane sesquiterpenoids
(1S)-3alpha-Vinyl-3-methyl-2beta-(1-methylvinyl)-6beta-isopropylcyclohexane-1alpha-ol 102012174 Click to see CC(C)C1CCC(C(C1O)C(=C)C)(C)C=C 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 CC12CCCC(=C)C1CC(CC2)C(C)(C)O 222.37 unknown via CMAUP database
Pygmol 14167388 Click to see CC12CCCC(C1C(C(CC2)C(C)(C)O)O)(C)O 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,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 CC1=CCCC2(C(O2)C(C(CC1)C(C)C)O)C 238.37 unknown via CMAUP database
(1R,2R,3S,7R,10S)-6-Methylene-10-methyl-3-isopropyl-11-oxabicyclo[8.1.0]undecane-2,7-diol 10610977 Click to see CC(C)C1CCC(=C)C(CCC2(C(C1O)O2)C)O 254.36 unknown via CMAUP database
(1R,2S,6E,10S)-3-Methylene-7-methyl-10-isopropyl-6-cyclodecene-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
(1R,4E,6R,7R)-4-Methyl-7-(1-hydroxy-1-methylethyl)-10-methylene-4-cyclodecene-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,4S,5E,7S)-4-methyl-10-methylidene-7-propan-2-ylcyclodec-5-ene-1,4-diol 9991811 Click to see CC(C)C1CCC(=C)C(CCC(C=C1)(C)O)O 238.37 unknown via CMAUP database
(1S,4E,6R,7R)-4-Methyl-7-(1-hydroxy-1-methylethyl)-10-methylene-4-cyclodecene-1,6-diol 15479892 Click to see CC1=CC(C(CCC(=C)C(CC1)O)C(C)(C)O)O 254.36 unknown via CMAUP database
(1S,4E,6R,7S)-4-Methyl-7-isopropyl-10-methylene-4-cyclodecene-1,6-diol 100982187 Click to see CC1=CC(C(CCC(=C)C(CC1)O)C(C)C)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 CC1=CC2C(CCC(=C)C(=O)CC1)C(OC(O2)(C)C)(C)C 292.40 unknown via CMAUP database
(4E,6R,7R)-4-Methyl-6-hydroxy-7-(1-hydroxy-1-methylethyl)-10-methylene-4-cyclodecene-1-one 10729506 Click to see CC1=CC(C(CCC(=C)C(=O)CC1)C(C)(C)O)O 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 CC1C2C3CCC4C5(CCC(C(C5CCC4(C3(CC(C2(CCC1=C)C)O)C)C)(C)C)O)C 442.70 unknown via CMAUP database
Calenduladiol 461835 Click to see CC(=C)C1CCC2(C1C3CCC4C5(CCC(C(C5CCC4(C3(CC2O)C)C)(C)C)O)C)C 442.70 unknown via CMAUP database
CID 14137680 14137680 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)OC(=O)C)C)C)C)C 468.80 unknown via CMAUP database
Dammaradienol 13893946 Click to see CC(=CCCC(=C)C1CCC2(C1CCC3C2(CCC4C3(CCC(C4(C)C)O)C)C)C)C 426.70 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 CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 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 CC(CC(C)(C)O)O 118.17 unknown via CMAUP database
> Organic oxygen compounds / Organooxygen compounds / Ethers / Acetals / Ketals
(5R)-2-[(E)-2,4-Hexadiyne-1-ylidene]-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
(5R)-2-[(Z)-2,4-Hexadiyne-1-ylidene]-1,6-dioxaspiro[4.4]nona-3,7-diene 44575223 Click to see CC#CC#CC=C1C=CC2(O1)CC=CO2 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 CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 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 CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 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 CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 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 CC#CC#CC=C1C=CC2(O1)C(C=CO2)OC(=O)C 256.25 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives
7,8-Methylenedioxy-6-methoxycoumarin 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 COC1=C(C=C2C=CC(=O)OC2=C1)O 192.17 unknown via CMAUP database
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 6,7-dihydroxycoumarins
Esculetin 5281416 Click to see C1=CC(=O)OC2=CC(=C(C=C21)O)O 178.14 unknown https://doi.org/10.1021/NP800760P
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Rhamnazin 5320945 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)OC)O 330.29 unknown https://doi.org/10.1021/NP800760P
Rhamnetin 5281691 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC(=C(C=C3)O)O)O 316.26 unknown https://doi.org/10.1021/NP800760P
Rhamnocitrin 5320946 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)O)C3=CC=C(C=C3)O)O 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-[(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-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]-8-(3,4,5-trihydroxyoxan-2-yl)chromen-4-one 3550102 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 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
> 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,5R)-3,4,5-trihydroxyoxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-2-(4-hydroxyphenyl)-7-methoxychromen-4-one 44179422 Click to see COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)OC4C(C(C(CO4)O)O)O)O)O)C5=CC=C(C=C5)O)O 594.50 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-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 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)O 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 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
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 COC1=CC(=C2C(=C1)OC(=C(C2=O)OC3C(C(C(C(O3)CO)OC4C(C(C(CO4)O)O)O)O)O)C5=CC=C(C=C5)O)O 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 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)O 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 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
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 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)O 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 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
5-hydroxy-7-methoxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2-[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]chromen-4-one 56677686 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)OC5C(C(C(C(O5)CO)O)O)O)O 624.50 unknown https://doi.org/10.1021/NP800760P
Complanatuside 5492406 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)OC5C(C(C(C(O5)CO)O)O)O)O 624.50 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 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)O 640.50 unknown https://doi.org/10.1021/NP800760P
Rhamnazin 3-glucoside 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
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-8-O-glycosides
Apigenin 6-C-beta-D-glucopyranoside 8-C-alpha-L-arabinopyranoside 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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