Ferula tenuisecta - Unknown
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Internal ID UUID64401c40eff18662040594
Scientific name Ferula tenuisecta
Authority Korovin
First published in Monogr. Ferula : 60 (1947)

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Language Common/alternative name
Russian Ферула тонкорассечённая

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Distribution (via POWO/KEW) Top

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Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000686844
Tropicos 1702793
KEW urn:lsid:ipni.org:names:842527-1
The Plant List kew-2808684
Open Tree Of Life 1068062
Observations.org 147435
NCBI Taxonomy 82087
iNaturalist 985888
GBIF 3636263
Elurikkus 614803

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)!
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Title Authors Publication Released IDs
In Vitro Evaluation of Ferutinin Rich-Ferula communis L., ssp. glauca, Root Extract on Doxorubicin-Induced Cardiotoxicity: Antioxidant Properties and Cell Cycle Modulation Macrì R, Bava I, Scarano F, Mollace R, Musolino V, Gliozzi M, Greco M, Foti D, Tucci L, Maiuolo J, Carresi C, Tavernese A, Palma E, Muscoli C, Mollace V Int J Mol Sci 13-Aug-2023
PMCID:PMC10454821
doi:10.3390/ijms241612735
PMID:37628916
Review of the traditional uses, phytochemistry, pharmacology and toxicology of giant fennel (Ferula communis L. subsp. communis) Akaberi M, Iranshahy M, Iranshahi M Iran J Basic Med Sci 01-Nov-2015
PMCID:PMC4764105
PMID:26949491
Phospholipids ofFerula tenuisecta seeds F. Yu. Gazizov, A. I. Glushenkova Springer Science and Business Media LLC 25-Jan-2006
doi:10.1007/BF02282522
Structure and stereochemistry of fertidin A. I. Saidkodzhaev, L. A. Golovina, V. M. Malikov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00629929
The structure of teferidin — A new ester from the fruit of Ferula tenuisecta A. I. Saidkhodzhaev, G. K. Nikonov Springer Science and Business Media LLC 10-Dec-2004
doi:10.1007/BF00570211
Investigation of natural compounds by the HPLC method I. Microcolumn HPLC separation of esters of carotane alcohols from the roots of Ferula tenuisecta M. R. Nuriddinova, A. I. Saidkhodzhaev, V. M. Malikov Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630426
Investigation of natural compounds by the HPLC method II. HPLC fingerprint method for the epigeal organs of Ferula kuhistanica and F. tenuisecta M. R. Nuriddinova, V. M. Malikov, A. Yu. Kushmuradov, A. I. Saidkhodzhaev Springer Science and Business Media LLC 26-Nov-2004
doi:10.1007/BF00630427
The structures of tenuferin, tenuferinin, and tenuferidin A. I. Saidkhodzhaev Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565876
Structure of teferin — A new ester from the roots of Ferula tenuisecta T. Kh. Khasanov, A. I. Saidkhodzhaev, G. K. Nikonov Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00563843

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 / Glycerophospholipids / Glycerophosphates / Diacylglycerophosphates / 1,2-diacylglycerol-3-phosphates
(1r)-2-(Phosphonooxy)-1-[(Tridecanoyloxy)methyl]ethyl Pentadecanoate 447791 Click to see CCCCCCCCCCCCCCC(=O)OC(COC(=O)CCCCCCCCCCCC)COP(=O)(O)O 592.80 unknown https://doi.org/10.1007/BF02282522
2-(Hexadecanoyloxy)-1-[(phosphonooxy)methyl]ethyl hexadecanoate 446066 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)O)OC(=O)CCCCCCCCCCCCCCC 648.90 unknown https://doi.org/10.1007/BF02282522
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphocholines / Lysophosphatidylcholines / 1-acyl-sn-glycero-3-phosphocholines
Lysophosphatidylcholine 5311264 Click to see CC(=O)OCC(COP(=O)([O-])OCC[N+](C)(C)C)O 299.26 unknown https://doi.org/10.1007/BF02282522
> Lipids and lipid-like molecules / Glycerophospholipids / Glycerophosphoglycerols / Phosphatidylglycerols
Phosphatidyl Glycerol 44566653 Click to see CCCCCCCCCCCCCCCC(=O)OCC(COP(=O)(O)OCC(CO)O)OC(=O)CCCCCCCC=CCC=CCCCCC 747.00 unknown https://doi.org/10.1007/BF02282522
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids
(3-Hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl) 3-hydroxy-4-methoxybenzoate 4524229 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC(=C(C=C3)OC)O)(C(C)C)O)C 388.50 unknown https://doi.org/10.1007/BF00630427
https://doi.org/10.1007/BF00570211
[(3R,3aS,4S,8aS)-3-hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl] 4-hydroxybenzoate 91747167 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=C(C=C3)O)(C(C)C)O)C 358.50 unknown https://doi.org/10.1007/BF00630426
https://doi.org/10.1007/BF00570211
[(3S,8aR)-3-hydroxy-6,8a-dimethyl-3-propan-2-yl-1,2,3a,4,5,8-hexahydroazulen-4-yl] 4-hydroxy-3-methoxybenzoate 389016 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC(=C(C=C3)O)OC)(C(C)C)O)C 388.50 unknown https://doi.org/10.1007/BF00630427
https://doi.org/10.1007/BF00563843
Ferutidin 10172562 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=C(C=C3)OC)(C(C)C)O)C 372.50 unknown https://doi.org/10.1007/BF00629929
Ferutinine 354654 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=C(C=C3)O)(C(C)C)O)C 358.50 unknown https://doi.org/10.1007/BF00630427
https://doi.org/10.1007/BF00630426
https://doi.org/10.1007/BF00570211
Teferidine 91747169 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC=CC=C3)(C(C)C)O)C 342.50 unknown https://doi.org/10.1007/BF00570211
Teferin 10271607 Click to see CC1=CCC2(CCC(C2C(C1)OC(=O)C3=CC(=C(C=C3)O)OC)(C(C)C)O)C 388.50 unknown https://doi.org/10.1007/BF00563843
https://doi.org/10.1007/BF00630427
> Lipids and lipid-like molecules / Prenol lipids / Sesquiterpenoids / Guaianes
(6-Hydroxy-1a,6-dimethyl-3-propan-2-yl-1b,2,3,4,5,6a,7,7a-octahydroazuleno[1,2-b]oxiren-4-yl) 3-hydroxy-4-methoxybenzoate 162991120 Click to see CC(C)C1CC2C(CC3C2(O3)C)C(CC1OC(=O)C4=CC(=C(C=C4)OC)O)(C)O 404.50 unknown https://doi.org/10.1007/BF00565876
(6-Hydroxy-1a,6-dimethyl-3-propan-2-yl-1b,2,3,4,5,6a,7,7a-octahydroazuleno[1,2-b]oxiren-4-yl) 4-hydroxy-3-methoxybenzoate 162871605 Click to see CC(C)C1CC2C(CC3C2(O3)C)C(CC1OC(=O)C4=CC(=C(C=C4)O)OC)(C)O 404.50 unknown https://doi.org/10.1007/BF00565876
Tenuferidin 14391700 Click to see CC(C)C1CC2C(CC3C2(O3)C)C(CC1OC(=O)C4=CC=C(C=C4)O)(C)O 374.50 unknown https://doi.org/10.1007/BF00630426
https://doi.org/10.1007/BF00565876
> Phenylpropanoids and polyketides / Macrolactams
Desferrioxamine X5 85625752 Click to see C1CCCN(C(=O)CCC(=O)NCCCCCN(C(=O)CCC(=O)NCCCCCNC(=O)CCC(=O)NCC1)O)O 598.70 unknown https://doi.org/10.1007/BF02282522

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