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Verbascum sinaiticum

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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 UUID643ffa69f4024352349870
Scientific name Verbascum sinaiticum
Authority Benth.
First published in Prodr. 10: 236 (1846)

Description Top

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Synonyms Top

Scientific name Authority First published in
Verbascum somaliense Baker Bull. Misc. Inform. Kew 1895: 222 (1895)
Verbascum capusii Franch. Ann. Sci. Nat., Bot. , sér. 6, 18: 222 (1884)
Verbascum barradense Boiss. Fl. Orient. 4: 318 (1879)
Verbascum nubicum Murb. Acta Univ. Lund., 2 , 29(2): 293 (1933)
Verbascum fasciculatum Ehrenb. ex Sweet Hort. Brit. , ed. 2: 381 (1830)

Common names Top

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Language Common/alternative name
Amharic ቀጠጥና
Amharic ጉራ ሃሬ
Arabic بوصير سينائي
Polish dziewanna synajska

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
  • Africa
    • East Tropical Africa
      • Kenya
    • Northeast Tropical Africa
      • Eritrea
      • Ethiopia
      • Somalia
      • Sudan
  • Asia-temperate
    • Arabian Peninsula
      • Gulf States
      • Oman
      • Saudi Arabia
      • Yemen
    • Western Asia
      • Afghanistan
      • Iran
      • Iraq
      • Lebanon-Syria
      • Palestine
      • Sinai

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000418921
Tropicos 29202472
KEW urn:lsid:ipni.org:names:770131-1
The Plant List kew-2453128
Open Tree Of Life 7053975
NCBI Taxonomy 2072606
IPNI 770131-1
iNaturalist 502443
GBIF 3736050
EOL 5663445

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
Traditional ethnobotanical knowledge and ethnomedicinal use of plants in the Tropical Rift Valley of Ethiopia Wendimu A, Tekalign W, Bojago E, Abrham Y Heliyon 13-Mar-2024
PMCID:PMC10955238
doi:10.1016/j.heliyon.2024.e27528
PMID:38515698
Ethnoveterinary medicinal plants and their utilization by indigenous and local communities of Dugda District, Central Rift Valley, Ethiopia Oda BK, Lulekal E, Warkineh B, Asfaw Z, Debella A J Ethnobiol Ethnomed 09-Mar-2024
PMCID:PMC10924356
doi:10.1186/s13002-024-00665-0
PMID:38461267
Ethnobotanical study of traditional medicinal plants used by the local Gamo people in Boreda Abaya District, Gamo Zone, southern Ethiopia Zemede J, Mekuria T, Ochieng CO, Onjalalaina GE, Hu GW J Ethnobiol Ethnomed 28-Feb-2024
PMCID:PMC10900619
doi:10.1186/s13002-024-00666-z
PMID:38419092
Ethnoveterinary medicinal plants and their utilization by the people of Soro District, Hadiya Zone, southern Ethiopia Hankiso M, Asfaw Z, Warkineh B, Abebe A, Sisay B, Debella A J Ethnobiol Ethnomed 22-Feb-2024
PMCID:PMC10885532
doi:10.1186/s13002-024-00651-6
PMID:38389077
Exploring the benefits of wild plants in dietary nutrition: investigating perspectives, choices, health impacts and sustainable practices Anwar T, Qureshi H, Shahzadi S, Siddiqi EH, Ali HM, Abdelhamid MM, Nazim M BMC Complement Med Ther 14-Feb-2024
PMCID:PMC10865668
doi:10.1186/s12906-024-04379-4
PMID:38355544
Medicinal herbs and their metabolites with biological potential to protect and combat liver toxicity and its disorders: A review Islam Shawon S, Nargis Reyda R, Qais N Heliyon 01-Feb-2024
PMCID:PMC10864916
doi:10.1016/j.heliyon.2024.e25340
PMID:38356556
Ethnobotanical study of traditional medicinal plants used by the local people in Habru District, North Wollo Zone, Ethiopia Alemu M, Asfaw Z, Lulekal E, Warkineh B, Debella A, Sisay B, Debebe E J Ethnobiol Ethnomed 04-Jan-2024
PMCID:PMC10768247
doi:10.1186/s13002-023-00644-x
PMID:38178202
Antimicrobial Potential of Different Isolates of Chaetomium globosum Combined with Liquid Chromatography Tandem Mass Spectrometry Chemical Profiling Goda MS, El-Kattan N, Abdel-Azeem MA, Allam KA, Badr JM, Nassar NA, Almalki AJ, Alharbi M, Elhady SS, Eltamany EE Biomolecules 21-Nov-2023
PMCID:PMC10742071
doi:10.3390/biom13121683
PMID:38136556
Ethnobotanical Study of Medicinal Plants Used against Human Diseases in Zuway Dugda District, Ethiopia Megersa M, Nedi T, Belachew S Evid Based Complement Alternat Med 18-Oct-2023
PMCID:PMC10599937
doi:10.1155/2023/5545294
PMID:37886427
Antioxidant Potential of Ethiopian Medicinal Plants and Their Phytochemicals: A Review of Pharmacological Evaluation Nigussie G, Siyadatpanah A, Norouzi R, Debebe E, Alemayehu M, Dekebo A Evid Based Complement Alternat Med 12-Oct-2023
PMCID:PMC10586904
doi:10.1155/2023/1901529
PMID:37868204
Impact of Diverse Parameters on the Physicochemical Characteristics of Green-Synthesized Zinc Oxide–Copper Oxide Nanocomposites Derived from an Aqueous Extract of Garcinia mangostana L. Leaf Chan YB, Aminuzzaman M, Tey LH, Win YF, Watanabe A, Djearamame S, Akhtaruzzaman M Materials (Basel) 02-Aug-2023
PMCID:PMC10419950
doi:10.3390/ma16155421
PMID:37570124
Antidiarrheal activities of methanolic crude extract and solvent fractions of the root of Verbascum sinaiticum Benth. (Scrophularaceae) in mice Worku SA, Tadesse SA, Abdelwuhab M, Asrie AB Heliyon 25-May-2023
PMCID:PMC10241862
doi:10.1016/j.heliyon.2023.e16386
PMID:37287619
An ethnomedicinal study in tulo district, west hararghe zone, oromia region, Ethiopia Bogale M, Sasikumar JM, Egigu MC Heliyon 07-Apr-2023
PMCID:PMC10106503
doi:10.1016/j.heliyon.2023.e15361
PMID:37077674
Traditional Herbal Remedies in the Management of Metabolic Disorders in Ethiopia: A Systematic Review of Ethnobotanical Studies and Pharmacological Activities Tola MA, Ibrahim F, Melak H, Tafesse T, Alemayehu M, Nigussie G Evid Based Complement Alternat Med 12-Jan-2023
PMCID:PMC9851791
doi:10.1155/2023/1413038
PMID:36686979
An Assessment of the In Vitro Models and Clinical Trials Related to the Antimicrobial Activities of Phytochemicals Kopel J, McDonald J, Hamood A Antibiotics (Basel) 17-Dec-2022
PMCID:PMC9774156
doi:10.3390/antibiotics11121838
PMID:36551494

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
> Lignans, neolignans and related compounds / Flavonolignans
5,7-Dihydroxy-2-[3-(hydroxymethyl)-2-(4-hydroxyphenyl)-2,3-dihydro-1,4-benzodioxin-6-yl]chromen-4-one 85141546 Click to see C1=CC(=CC=C1C2C(OC3=C(O2)C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO)O 434.40 unknown https://doi.org/10.1016/0031-9422(93)85369-3
Hydnocarpin 5489114 Click to see COC1=C(C=CC(=C1)C2C(OC3=C(O2)C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO)O 464.40 unknown https://doi.org/10.1016/0031-9422(93)85369-3
Sinaticin 10433042 Click to see C1=CC(=CC=C1C2C(OC3=C(O2)C=CC(=C3)C4=CC(=O)C5=C(C=C(C=C5O4)O)O)CO)O 434.40 unknown https://doi.org/10.1016/0031-9422(93)85369-3
> Lipids and lipid-like molecules / Prenol lipids / Terpene glycosides / Triterpene glycosides / Triterpene saponins
(2S,3R,4R,5R,6S)-2-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-[(2R,3R,4S,5S,6R)-5-hydroxy-2-[[(1S,2S,4S,5R,8R,9R,10S,13S,14R,17S,18R)-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 101933149 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3OC4C(C(C(C(O4)CO)O)O)O)OC5CCC6(C(C5(C)CO)CCC7(C6C=CC89C7(CC(C1(C8CC(CC1)(C)C)CO9)OC1C(C(C(C(O1)CO)O)O)O)C)C)C)C)O)CO)O)O)O 1251.40 unknown https://doi.org/10.1248/CPB.45.2029
(2S,3R,4R,5R,6S)-2-[(2R,3S,4R,5R,6S)-4,5-dihydroxy-6-[(2R,3R,4S,5S,6R)-5-hydroxy-2-[[9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-4-yl]oxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 11968772 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3OC4C(C(C(C(O4)CO)O)O)O)OC5CCC6(C(C5(C)CO)CCC7(C6C=CC89C7(CCC1(C8CC(CC1)(C)C)CO9)C)C)C)C)O)CO)O)O)O 1073.30 unknown https://doi.org/10.1248/CPB.45.2029
(2S,3R,4R,5R,6S)-2-[(2R,3S,4R,5R,6S)-6-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-2-[[(1S,2S,4S,5R,8R,9R,10S,13S,14R,17S,18R)-2-hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-methyloxan-4-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 101933145 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3O)OC4CCC5(C(C4(C)CO)CCC6(C5C=CC78C6(CC(C9(C7CC(CC9)(C)C)CO8)O)C)C)C)C)O)CO)O)O)O 927.10 unknown https://doi.org/10.1248/CPB.45.2029
(2S,3R,4R,5R,6S)-2-[(2R,3S,4R,5R,6S)-6-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-2-[[(1S,4S,5R,8R,9R,10S,13S,14R,17S,18R)-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-methyloxan-4-yl]oxy-4,5-dihydroxy-2-(hydroxymethyl)oxan-3-yl]oxy-6-methyloxane-3,4,5-triol 101933144 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3O)OC4CCC5(C(C4(C)CO)CCC6(C5C=CC78C6(CCC9(C7CC(CC9)(C)C)CO8)C)C)C)C)O)CO)O)O)O 911.10 unknown https://doi.org/10.1248/CPB.45.2029
(2S,3R,4S,5S,6R)-2-[(2R,3R,4S,5S,6R)-3,5-dihydroxy-2-[[(1S,4S,5R,8R,9R,10S,13S,14R,17S,18R)-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-methyloxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 101933143 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC56C4(CCC7(C5CC(CC7)(C)C)CO6)C)C)C)O)OC8C(C(C(C(O8)CO)O)O)O)O 765.00 unknown https://doi.org/10.1248/CPB.45.2029
(2S)-2-[(2R)-3,5-dihydroxy-2-[[(1S,4S,5R,8R,9R,13S,14R,17S,18R)-2-hydroxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-10-yl]oxy]-6-methyloxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol 138114182 Click to see CC1C(C(C(C(O1)OC2CCC3(C(C2(C)CO)CCC4(C3C=CC56C4(CC(C7(C5CC(CC7)(C)C)CO6)O)C)C)C)O)OC8C(C(C(C(O8)CO)O)O)O)O 781.00 unknown https://doi.org/10.1248/CPB.45.2029
[(1S,2S,4S,5R,8R,9R,10S,13S,14R,17S,18R)-10-[(2R,3R,4S,5S,6R)-4-[(2S,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-5-hydroxy-6-methyl-3-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyoxan-2-yl]oxy-9-(hydroxymethyl)-4,5,9,13,20,20-hexamethyl-24-oxahexacyclo[15.5.2.01,18.04,17.05,14.08,13]tetracos-15-en-2-yl] acetate 101933148 Click to see CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3OC4C(C(C(C(O4)CO)O)O)O)OC5CCC6(C(C5(C)CO)CCC7(C6C=CC89C7(CC(C1(C8CC(CC1)(C)C)CO9)OC(=O)C)C)C)C)C)O)CO)O)O)O 1131.30 unknown https://doi.org/10.1248/CPB.45.2029
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Oligosaccharides
[(2R,3R,4R,5R,6R)-6-[2-(3,4-dihydroxyphenyl)ethoxy]-5-hydroxy-4-[(3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxy-2-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate 44584310 Click to see CC1C(C(C(C(O1)OC2C(C(OC(C2OC(=O)C=CC3=CC(=C(C=C3)O)O)COC4C(C(C(CO4)O)O)O)OCCC5=CC(=C(C=C5)O)O)O)O)O)O 756.70 unknown https://doi.org/10.1016/0031-9422(93)85178-T
> Phenylpropanoids and polyketides / Flavonoids / Flavones
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/10.1016/0305-1978(94)90058-2
https://doi.org/10.1016/0031-9422(93)85369-3
> Phenylpropanoids and polyketides / Flavonoids / Flavonoid glycosides / Flavonoid O-glycosides / Flavonoid-7-O-glycosides
Thermopsoside 11294177 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O)O 462.40 unknown https://doi.org/10.1016/0305-1978(94)90058-2
Tilianin 5321954 Click to see COC1=CC=C(C=C1)C2=CC(=O)C3=C(C=C(C=C3O2)OC4C(C(C(C(O4)CO)O)O)O)O 446.40 unknown https://doi.org/10.1016/0305-1978(94)90058-2
> Phenylpropanoids and polyketides / Flavonoids / O-methylated flavonoids / 3-O-methylated flavonoids
Chryseriol 5280666 Click to see COC1=C(C=CC(=C1)C2=CC(=O)C3=C(C=C(C=C3O2)O)O)O 300.26 unknown https://doi.org/10.1016/0031-9422(93)85369-3

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