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Digitalis ciliata

Digitalis ciliata - 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 UUID644017091dce3727419725
Scientific name Digitalis ciliata
Authority Trautv.
First published in Bull. Acad. Imp. Sci. Saint-Pétersbourg , sér. 3, 10: 397 (1866)

Description Top

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Synonyms Top

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Common names Top

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Language Common/alternative name
Arabic قمعية مهدبة
Azerbaijani kirpikcikli üskükotu
azb کیرپیکجیکلی اۆسکوک اوْتو
os Уиззайы сæр
Russian Наперстянка реснитчатая

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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Sow seeds at 20°C, expecting germination within 3 months without further temperature treatment.

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-0000647270
Tropicos 29202392
KEW urn:lsid:ipni.org:names:801989-1
The Plant List kew-2767975
Open Tree Of Life 570858
Observations.org 117217
NCBI Taxonomy 285815
IPNI 801989-1
iNaturalist 743330
GBIF 7747863
Freebase /m/0jt1g2c
EOL 5669675
Elurikkus 618616
Wikipedia Digitalis_ciliata

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
Plants, Cells, Algae, and Cyanobacteria In Vitro and Cryobank Collections at the Institute of Plant Physiology, Russian Academy of Sciences—A Platform for Research and Production Center Yuorieva N, Sinetova M, Messineva E, Kulichenko I, Fomenkov A, Vysotskaya O, Osipova E, Baikalova A, Prudnikova O, Titova M, Nosov AV, Popova E Biology (Basel) 09-Jun-2023
PMCID:PMC10295647
doi:10.3390/biology12060838
PMID:37372123
Ethnobotanical survey of the medicinal flora of Harighal, Azad Jammu & Kashmir, Pakistan Amjad MS, Zahoor U, Bussmann RW, Altaf M, Gardazi SM, Abbasi AM J Ethnobiol Ethnomed 27-Oct-2020
PMCID:PMC7590686
doi:10.1186/s13002-020-00417-w
PMID:33109243
Gitaloxin fromDigitalis ciliata E. P. Kemertelidze, L. N. Gvazava Springer Science and Business Media LLC 09-Jul-2008
doi:10.1007/BF00564991
Dea cetyllanatoside a from the leaves of Digitalis ciliata L. N. Gvazava Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00563972
Cardiac glycosides from the seeds ofDigitalis ciliata Ts. P. Sulakvelidze, É. P. Kemertelidze Springer Science and Business Media LLC 22-Nov-2004
doi:10.1007/BF00579173
Flavonoids from the leaves ofDigitalis ciliata É. P. Kemertelidze Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00567716

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 / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives
Digitoxigenin 4369270 Click to see CC12CCC(CC1CCC3C2CCC4(C3(CCC4C5=CC(=O)OC5)O)C)O 374.50 unknown https://doi.org/10.1007/BF00579173
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Steroid lactones / Cardenolides and derivatives / Cardenolide glycosides and derivatives
[(2R,3R,4S,6S)-6-[(2R,3S,4S,6S)-4-hydroxy-6-[(2R,3S,4S,6R)-4-hydroxy-6-[[(3S,5S,8R,9R,10S,13R,14S,17R)-14-hydroxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]oxy]-2-methyloxan-3-yl]oxy-2-methyloxan-3-yl]oxy-2-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl] acetate 134688155 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)O)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC(=O)C)O 969.10 unknown https://doi.org/10.1007/BF00579173
3-{[2,6-Dideoxyhexopyranosyl-(1->4)-2,6-dideoxyhexopyranosyl-(1->4)-2,6-dideoxyhexopyranosyl]oxy}-16-(formyloxy)-14-hydroxycard-20(22)-enolide 71123 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3O)OC4CCC5(C(C4)CCC6C5CCC7(C6(CC(C7C8=CC(=O)OC8)OC=O)O)C)C)C)C)O)O 808.90 unknown https://doi.org/10.1007/BF00564991
Digilanid A 73383 Click to see CC1C(C(CC(O1)OC2CCC3(C(C2)CCC4C3CCC5(C4(CCC5C6=CC(=O)OC6)O)C)C)O)OC7CC(C(C(O7)C)OC8CC(C(C(O8)C)OC9C(C(C(C(O9)CO)O)O)O)OC(=O)C)O 969.10 unknown https://doi.org/10.1007/BF00579173
Digimed 3061 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3O)OC4CCC5(C(C4)CCC6C5CCC7(C6(CCC7C8=CC(=O)OC8)O)C)C)C)C)O)O 764.90 unknown https://doi.org/10.1007/BF00579173
Digitoxin 441207 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3O)OC4CCC5(C(C4)CCC6C5CCC7(C6(CCC7C8=CC(=O)OC8)O)C)C)C)C)O)O 764.90 unknown https://doi.org/10.1007/BF00564991
https://doi.org/10.1007/BF00579173
Gitaloxin 10440404 Click to see CC1C(C(CC(O1)OC2C(OC(CC2O)OC3C(OC(CC3O)OC4CCC5(C(C4)CCC6C5CCC7(C6(CC(C7C8=CC(=O)OC8)OC=O)O)C)C)C)C)O)O 808.90 unknown https://doi.org/10.1007/BF00564991
Purpurea glycoside A 197989 Click to see CC1C(C(CC(O1)OC2C(OC(CC2OC3CC(C(C(O3)C)O)OC4C(C(C(C(O4)CO)O)O)O)OC5CCC6(C(C5)CCC7C6CCC8(C7(CCC8C9=CC(=O)OC9)O)C)C)C)O)O 927.10 unknown https://doi.org/10.1007/BF00563972
> Phenylpropanoids and polyketides / Flavonoids / Flavones
Apigenin 5280443 Click to see C1=CC(=CC=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 270.24 unknown https://doi.org/10.1007/BF00567716
Luteolin 5280445 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00567716
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides
Luteolin 3'-glucoside 12309350 Click to see C1=CC(=C(C=C1C2=CC(=O)C3=C(C=C(C=C3O2)O)O)OC4C(C(C(C(O4)CO)O)O)O)O 448.40 unknown https://doi.org/10.1007/BF00567716

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