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Rhamnus pallasii

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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 UUID64404d5dcd3c0205841467
Scientific name Rhamnus pallasii
Authority Fisch. & C.A.Mey.
First published in Index Seminum (LE, Petropolitanus) 4: 46 (1838)

Description Top

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Synonyms Top

Scientific name Authority First published in
Rhamnus medwedewii Sachok. Zametki Sist. Geogr. Rast. 16: 67 (1951)

Common names Top

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Language Common/alternative name
Azerbaijani pallas murdarçası

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

No distribution data was extracted from POWO/KEW yet. We are constantly monitoring for new data.

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001131291
Tropicos 27500984
KEW urn:lsid:ipni.org:names:718540-1
The Plant List tro-27500984
Open Tree Of Life 7056831
Observations.org 137231
NCBI Taxonomy 1813065
IPNI 718540-1
iNaturalist 867961
GBIF 7273861
EPPO RHAPA
Elurikkus 6785
USDA GRIN 31047

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
Ethnopharmacological study of native medicinal plants and the impact of pastoralism on their loss in arid to semiarid ecosystems of southeastern Iran Sharafatmandrad M, Khosravi Mashizi A Sci Rep 23-Sep-2020
PMCID:PMC7511295
doi:10.1038/s41598-020-72536-z
PMID:32968162
Endozoochorous dispersal by herbivores and omnivores is mediated by germination conditions Karimi S, Hemami MR, Tarkesh Esfahani M, Baltzinger C BMC Ecol 31-Aug-2020
PMCID:PMC7457502
doi:10.1186/s12898-020-00317-3
PMID:32867734
Are endemic species necessarily ecological specialists? Functional variability and niche differentiation of two threatened Dianthus species in the montane steppes of northeastern Iran Behroozian M, Ejtehadi H, Memariani F, Pierce S, Mesdaghi M Sci Rep 16-Jul-2020
PMCID:PMC7366929
doi:10.1038/s41598-020-68618-7
PMID:32678159
Ethnobotanical Study of Medicinal Plants Used by Kurd Tribe in Dehloran and Abdanan Districts, Ilam Province, Iran Ghasemi Pirbalouti A, Momeni M, Bahmani M Afr J Tradit Complement Altern Med 31-Dec-2012
PMCID:PMC3746586
doi:10.4314/ajtcam.v10i2.24
PMID:24146463
Anthraquinones and flavonoids ofRhamnus pallasii V. A. Kompantsev, S. F. Dzhumyrko, A. V. Episheva Springer Science and Business Media LLC 21-Nov-2004
doi:10.1007/BF00574350
Flavonoids of the leaves of Rhamnus pallasii T. S. Zurabishvili, I. I. Moniava Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563641
Flavonoids from Rhamnus pallasii Akiyo Sakushima, Maksut Coşkun, Sueo Hisada, Sansei Nishibe Elsevier BV 25-Jul-2002
doi:10.1016/0031-9422(83)80110-1
An anthraquinone glycoside from Rhamnus pallasii Maksut Coşkun, Nevin Tanker, Akiyo Sakushima, Shizuka Kitagawa, Sansei Nishibe Elsevier BV 25-Jul-2002
doi:10.1016/S0031-9422(00)80491-4

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 / Anthracenes / Anthraquinones
1-Hydroxy-3-methyl-6-methoxy-8-(6-O-beta-D-xylopyranosyl-beta-D-glucopyranosyloxy)-9,10-anthraquinone 101870821 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC 578.50 unknown https://doi.org/10.1016/S0031-9422(00)80491-4
1-Hydroxy-6-methoxy-3-methyl-8-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxyanthracene-9,10-dione 163013208 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O)OC 578.50 unknown https://doi.org/10.1016/S0031-9422(00)80491-4
> Benzenoids / Anthracenes / Anthraquinones / Hydroxyanthraquinones
Emodin 3220 Click to see CC1=CC2=C(C(=C1)O)C(=O)C3=C(C2=O)C=C(C=C3O)O 270.24 unknown https://doi.org/10.1007/BF00574350
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Aromadendrane sesquiterpenoids / 5,10-cycloaromadendrane sesquiterpenoids
(1aR,4R,4aS,7R,7aR,7bS)-1,1,4,7-tetramethyl-1a,2,3,4,4a,5,6,7,7a,7b-decahydrocyclopropa[e]azulene 162976506 Click to see CC1CCC2C(C2(C)C)C3C1CCC3C 206.37 unknown https://doi.org/10.1016/0031-9422(83)80110-1
1H-Cycloprop[e]azulene, decahydro-1,1,4,7-tetramethyl- 520381 Click to see CC1CCC2C(C2(C)C)C3C1CCC3C 206.37 unknown https://doi.org/10.1016/0031-9422(83)80110-1
> Organic oxygen compounds / Organooxygen compounds / Carbohydrates and carbohydrate conjugates / Glycosyl compounds / Phenolic glycosides
9-hydroxy-6-methoxy-8-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(2S,3R,4S,5R)-3,4,5-trihydroxyoxan-2-yl]oxymethyl]oxan-2-yl]oxy-3H-benzo[f][2]benzofuran-1-one 16216015 Click to see COC1=CC(=C2C(=C1)C=C3COC(=O)C3=C2O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 540.50 unknown https://doi.org/10.1016/S0031-9422(00)80491-4
9-hydroxy-6-methoxy-8-[3,4,5-trihydroxy-6-[(3,4,5-trihydroxyoxan-2-yl)oxymethyl]oxan-2-yl]oxy-3H-benzo[f][2]benzofuran-1-one 162868600 Click to see COC1=CC(=C2C(=C1)C=C3COC(=O)C3=C2O)OC4C(C(C(C(O4)COC5C(C(C(CO5)O)O)O)O)O)O 540.50 unknown https://doi.org/10.1016/S0031-9422(00)80491-4
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Catechins / Epigallocatechins
(2S,3R)-2-(3,5-dihydroxy-4-methoxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 162971222 Click to see COC1=C(C=C(C=C1O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 334.28 unknown https://doi.org/10.1016/0031-9422(83)80110-1
2-(3,5-Dihydroxy-4-methoxyphenyl)-3,5,7-trihydroxy-2,3-dihydrochromen-4-one 72766774 Click to see COC1=C(C=C(C=C1O)C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 334.28 unknown https://doi.org/10.1016/0031-9422(83)80110-1
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones
(+/-)-Eriodictyol 11095 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(83)80110-1
Eriodictyol 440735 Click to see C1C(OC2=CC(=CC(=C2C1=O)O)O)C3=CC(=C(C=C3)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(83)80110-1
> Phenylpropanoids and polyketides / Flavonoids / Flavans / Flavanones / Flavanonols
(+/-)-Taxifolin 471 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/0031-9422(83)80110-1
3,5,7-Trihydroxy-2-(4-hydroxyphenyl)-2,3-dihydrochromen-4-one 662 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(83)80110-1
Aromadendrin 122850 Click to see C1=CC(=CC=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 288.25 unknown https://doi.org/10.1016/0031-9422(83)80110-1
Taxifolin 439533 Click to see C1=CC(=C(C=C1C2C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 304.25 unknown https://doi.org/10.1016/0031-9422(83)80110-1
> Phenylpropanoids and polyketides / Flavonoids / Flavones / Flavonols
Isorhamnetin 5281654 Click to see COC1=C(C=CC(=C1)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 316.26 unknown https://doi.org/10.1016/0031-9422(83)80110-1
https://doi.org/10.1007/BF00563641
Kaempferol 5280863 Click to see C1=CC(=CC=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 286.24 unknown https://doi.org/10.1007/BF00563641
https://doi.org/10.1016/0031-9422(83)80110-1
Mearnsetin 10359384 Click to see COC1=C(C=C(C=C1O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O 332.26 unknown https://doi.org/10.1016/0031-9422(83)80110-1
Quercetin 5280343 Click to see C1=CC(=C(C=C1C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)O)O)O 302.23 unknown https://doi.org/10.1016/0031-9422(83)80110-1
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/10.1007/BF00574350
> Phenylpropanoids and polyketides / Isoflavonoids / Coumestans
1,3-Dihydroxy-8,9-dimethoxy-[1]benzofuro[3,2-c]chromen-6-one 11602329 Click to see COC1=C(C=C2C(=C1)C3=C(O2)C4=C(C=C(C=C4OC3=O)O)O)OC 328.27 unknown https://doi.org/10.1007/BF00574350

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