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Anoectochilus formosanus

Anoectochilus formosanus - Unknown
Part: Unknown
Author: Public Domain - WikiMedia
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Table of Contents

Details
Description
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Biological Material
Contributors
Collections

Details Top

Internal ID UUID643fdf65168d0359815886
Scientific name Anoectochilus formosanus
Authority Hayata
First published in Icon. Pl. Formosan. 4: 101 (1914)

Description Top

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Synonyms Top

Scientific name Authority First published in
Anoectochilus tetsuoi Ohwi ex Hatus. & T.Amano Fl. Okinawa : 148 (1958)

Common names Top

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Language Common/alternative name
Chinese 台灣金線連
Chinese 臺灣金線蓮
Chinese 金线兰
Chinese 金线莲
Chinese 台湾金线莲
Chinese 台湾银线兰

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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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
    • China
      • China Southeast
    • Eastern Asia
      • Nansei-shoto
      • Taiwan

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000216658
Tropicos 23514259
KEW urn:lsid:ipni.org:names:616574-1
The Plant List kew-10177
Open Tree Of Life 320868
NCBI Taxonomy 173437
IPNI 616574-1
iNaturalist 702338
GBIF 5308604
EOL 1142739
USDA GRIN 451725

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
Immunomodulatory Effects of Sodium Hyaluronate Health Drink on Immunosuppressed Mice Peng X, Yao X, Liu Y, Peng B Foods 09-Mar-2024
PMCID:PMC10969082
doi:10.3390/foods13060842
PMID:38540831
Corrigendum to “Polysaccharide and ethanol extracts of Anoectochilus formosanus Hayata: Antioxidant, wound-healing, antibacterial, and cytotoxic activities” Nguyen TP, Phan HN, Do TD, Do GD, Ngo LH, Khoa Do HD, Nguyen KT Heliyon 15-Dec-2023
PMCID:PMC10851288
doi:10.1016/j.heliyon.2023.e23881
PMID:38332880
Contribution of endophytes towards improving plant bioactive metabolites: a rescue option against red-taping of medicinal plants Tsipinana S, Husseiny S, Alayande KA, Raslan M, Amoo S, Adeleke R Front Plant Sci 12-Sep-2023
PMCID:PMC10522919
doi:10.3389/fpls.2023.1248319
PMID:37771494
Drug Development from Natural Products Based on the Pathogenic Mechanism of Asthma Kim MH, Bae CS, Bok SH, Choi HS, Ahn T, Cho SS, Park DH Int J Mol Sci 05-Aug-2023
PMCID:PMC10419019
doi:10.3390/ijms241512469
PMID:37569846
Therapeutic Effects of Plant Extracts of Anoectochilus roxburghii on Side Effects of Chemotherapy in BALB/c Breast Cancer Mice Cheng CF, Lu CW, Wu WJ, Su LY, Nguyen TK, Shen SC, Lien CY, Chuang WC, Lee MC, Wu CH Plants (Basel) 29-Jun-2023
PMCID:PMC10346958
doi:10.3390/plants12132494
PMID:37447055
Protective Effect of Anoectochilus formosanus Polysaccharide against Cyclophosphamide-Induced Immunosuppression in BALB/c Mice Xie A, Wan H, Feng L, Yang B, Wan Y Foods 07-May-2023
PMCID:PMC10178248
doi:10.3390/foods12091910
PMID:37174447
Redox Signaling Modulates Activity of Immune Checkpoint Inhibitors in Cancer Patients Allegra A, Murdaca G, Mirabile G, Gangemi S Biomedicines 29-Apr-2023
PMCID:PMC10215686
doi:10.3390/biomedicines11051325
PMID:37238995
Antidiabetic Properties of Plant Secondary Metabolites Sukhikh S, Babich O, Prosekov A, Kalashnikova O, Noskova S, Bakhtiyarova A, Krol O, Tsvetkova E, Ivanova S Metabolites 03-Apr-2023
PMCID:PMC10144365
doi:10.3390/metabo13040513
PMID:37110171
Beneficial effects of endophytic fungi inoculation on tanshinones and phenolic compounds of Salvia abrotanoides Masoudi Khorasani F, Ganjeali A, Asili J, Cheniany M Iran J Basic Med Sci 01-Apr-2023
PMCID:PMC10008390
doi:10.22038/IJBMS.2023.67730.14828
PMID:37009009
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
Bio-Derived Furanic Compounds with Natural Metabolism: New Sustainable Possibilities for Selective Organic Synthesis Romashov LV, Kucherov FA, Kozlov KS, Ananikov VP Int J Mol Sci 16-Feb-2023
PMCID:PMC9966152
doi:10.3390/ijms24043997
PMID:36835429
Polysaccharide and ethanol extracts of Anoectochilus formosanus Hayata: Antioxidant, wound-healing, antibacterial, and cytotoxic activities Nguyen TP, Phan HN, Do TD, Do GD, Ngo LH, Do HD, Nguyen KT Heliyon 14-Feb-2023
PMCID:PMC9981919
doi:10.1016/j.heliyon.2023.e13559
PMID:36873493
Environmental Factors Regulate Plant Secondary Metabolites Qaderi MM, Martel AB, Strugnell CA Plants (Basel) 18-Jan-2023
PMCID:PMC9920071
doi:10.3390/plants12030447
PMID:36771531
Biosynthesis of α-Bisabolol by Farnesyl Diphosphate Synthase and α-Bisabolol Synthase and Their Related Transcription Factors in Matricaria recutita L. Tai Y, Wang H, Yao P, Sun J, Guo C, Jin Y, Yang L, Chen Y, Shi F, Yu L, Li S, Yuan Y Int J Mol Sci 15-Jan-2023
PMCID:PMC9864331
doi:10.3390/ijms24021730
PMID:36675248
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

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
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
(3r)-3-(beta-d-Glucopyranosyloxy)-4-hydroxybutanoic acid 91047195 Click to see C(C1C(C(C(C(O1)OC(CC(=O)O)CO)O)O)O)O 282.24 unknown https://doi.org/10.1016/S0031-9422(98)00388-4
https://doi.org/10.1007/S11418-007-0169-0
https://doi.org/10.1248/CPB.48.1803
(4R)-4-hydroxy-3,5,5-trimethyl-4-[(E,3R)-3-[(2S,3S,4R,5R,6S)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one 133561811 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1248/CPB.48.1803
3,5,5-Trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one 73815024 Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 370.40 unknown https://doi.org/10.1248/CPB.48.1803
3Eec4Q65S4 21630888 Click to see CC1=CC(=O)CC(C1C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)(C)C 370.40 unknown https://doi.org/10.1248/CPB.48.1803
4-Hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybutanoic acid 85126754 Click to see C(C1C(C(C(C(O1)OC(CC(=O)O)CO)O)O)O)O 282.24 unknown https://doi.org/10.1248/CPB.48.1803
https://doi.org/10.1016/S0031-9422(98)00388-4
4-Hydroxy-3,5,5-trimethyl-4-[3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxybut-1-enyl]cyclohex-2-en-1-one 73815023 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1248/CPB.48.1803
Corchoionoside C 10317980 Click to see CC1=CC(=O)CC(C1(C=CC(C)OC2C(C(C(C(O2)CO)O)O)O)O)(C)C 386.40 unknown https://doi.org/10.1248/CPB.48.1803
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / O-glycosyl compounds
(2R,3R,4S,5S,6R)-2-[(5-hydroxyfuran-2-yl)methoxy]-6-(hydroxymethyl)oxane-3,4,5-triol 163191259 Click to see C1=C(OC(=C1)O)COC2C(C(C(C(O2)CO)O)O)O 276.24 unknown https://doi.org/10.1248/CPB.48.1803
(4R)-4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxolan-2-one 125181694 Click to see C1C(COC1=O)OC2C(C(C(C(O2)CO)O)O)O 264.23 unknown https://doi.org/10.1007/S11418-007-0169-0
2-(Hydroxymethyl)-6-(propan-2-yloxy)oxane-3,4,5-triol 15613266 Click to see CC(C)OC1C(C(C(C(O1)CO)O)O)O 222.24 unknown https://doi.org/10.1248/CPB.48.1803
https://doi.org/10.1016/S0031-9422(98)00388-4
2-(Hydroxymethyl)-6-[[5-(hydroxymethyl)furan-2-yl]methoxy]oxane-3,4,5-triol 19758192 Click to see C1=C(OC(=C1)COC2C(C(C(C(O2)CO)O)O)O)CO 290.27 unknown https://doi.org/10.1248/CPB.48.1803
2-[(beta-d-Glucopyranosyloxy)methyl]-5-hydroxymethylfuran 10708602 Click to see C1=C(OC(=C1)COC2C(C(C(C(O2)CO)O)O)O)CO 290.27 unknown https://doi.org/10.1007/S11418-007-0169-0
https://doi.org/10.1248/CPB.48.1803
3-Hydroxy-4-butanolide 72569818 Click to see C1C(COC1=O)OC2C(C(C(C(O2)CO)O)O)O 264.23 unknown https://doi.org/10.1016/S0031-9422(98)00388-4
https://doi.org/10.1248/CPB.48.1803
Isopropyl beta-D-glucopyranoside 21572943 Click to see CC(C)OC1C(C(C(C(O1)CO)O)O)O 222.24 unknown https://doi.org/10.1248/CPB.48.1803
https://doi.org/10.1007/S11418-007-0169-0
https://doi.org/10.1016/S0031-9422(98)00388-4
Kinsenoside 10422896 Click to see C1C(COC1=O)OC2C(C(C(C(O2)CO)O)O)O 264.23 unknown https://doi.org/10.1248/CPB.48.1803
https://doi.org/10.1016/S0031-9422(98)00388-4
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 https://doi.org/10.1248/CPB.48.1803
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
(2R,3R,4S,5R,6S)-2-(hydroxymethyl)-6-[4-(hydroxymethyl)phenoxy]oxane-3,4,5-triol 154496023 Click to see C1=CC(=CC=C1CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown https://doi.org/10.1007/S11418-007-0169-0
2-(Hydroxymethyl)-6-[4-(hydroxymethyl)phenoxy]oxane-3,4,5-triol 3645183 Click to see C1=CC(=CC=C1CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown https://doi.org/10.1248/CPB.48.1803
Gastrodin 115067 Click to see C1=CC(=CC=C1CO)OC2C(C(C(C(O2)CO)O)O)O 286.28 unknown https://doi.org/10.1248/CPB.48.1803
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Monosaccharides / Hexoses
(2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal 107526 Click to see C(C(C(C(C(C=O)O)O)O)O)O 180.16 unknown https://doi.org/10.1248/CPB.48.1803
D-Glucose 5793 Click to see C(C1C(C(C(C(O1)O)O)O)O)O 180.16 unknown https://doi.org/10.1248/CPB.48.1803
> Organoheterocyclic compounds / Lactones / Gamma butyrolactones
(R)-4-Hydroxydihydrofuran-2(3H)-one 7060520 Click to see C1C(COC1=O)O 102.09 unknown https://doi.org/10.1007/S11418-007-0169-0
https://doi.org/10.1248/CPB.48.1803
2(3H)-Furanone, dihydro-4-hydroxy- 95652 Click to see C1C(COC1=O)O 102.09 unknown https://doi.org/10.1248/CPB.48.1803
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-3-O-glycosides
5,7-dihydroxy-2-[4-hydroxy-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 91264059 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 626.50 unknown https://doi.org/10.1021/JF0113575
5,7-Dihydroxy-2-[4-hydroxy-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]-3-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one 74978162 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O)O 626.50 unknown https://doi.org/10.1021/JF0113575
Dactylin 5901757 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 640.50 unknown https://doi.org/10.1021/JF0113575
Isorhamnetin 3-galactoside 13245586 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1021/JF0113575
isorhamnetin 3-O-glucoside 5318645 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 478.40 unknown https://doi.org/10.1021/JF0113575
Isorhamnetin 3,4'-diglucoside 11802256 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)OC5C(C(C(C(O5)CO)O)O)O 640.50 unknown https://doi.org/10.1021/JF0113575

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