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Ferula diversivittata

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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 UUID64401c30b74ce614154457
Scientific name Ferula diversivittata
Authority Regel & Schmalh.
First published in Trudy Imp. S.-Peterburgsk. Bot. Sada 5: 593 (1877)

Description Top

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Synonyms Top

Scientific name Authority First published in
Ferula sintenisii H.Wolff Repert. Spec. Nov. Regni Veg. 19: 311 (1924)
Ferula suaveolens Aitch. & Hemsl. Trans. Linn. Soc. London, Bot. 3: 69 (1886)

Common names Top

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Language Common/alternative name
French ferula sintenisii
French ferula suaveolens

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
    • Middle Asia
      • Kazakhstan
      • Kirgizstan
      • Tadzhikistan
      • Turkmenistan
      • Uzbekistan
    • Western Asia
      • Afghanistan
      • Iran

Links to other databases Top

Suggest others/fix!
Database ID/link to page
World Flora Online wfo-0000686530
UNII 6AUK63DV8J
Tropicos 1700091
KEW urn:lsid:ipni.org:names:842252-1
The Plant List kew-2808393
Open Tree Of Life 634398
Observations.org 123672
NCBI Taxonomy 371338
IPNI 842252-1
GBIF 3638866
EOL 5045643
Elurikkus 388606
USDA GRIN 16607

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
Antibacterial and Antifungal Terpenes from the Medicinal Angiosperms of Asia and the Pacific: Haystacks and Gold Needles Wiart C, Kathirvalu G, Raju CS, Nissapatorn V, Rahmatullah M, Paul AK, Rajagopal M, Sathiya Seelan JS, Rusdi NA, Lanting S, Sulaiman M Molecules 04-May-2023
PMCID:PMC10180233
doi:10.3390/molecules28093873
PMID:37175283
Ethnobotanical knowledge of Apiaceae family in Iran: A review Amiri MS, Joharchi MR Avicenna J Phytomed 01-Nov-2016
PMCID:PMC5206921
PMID:28078243
Bioassay-Guided Isolation of Sesquiterpene Coumarins from Ferula narthex Bioss: A New Anticancer Agent Alam M, Khan A, Wadood A, Khan A, Bashir S, Aman A, Jan AK, Rauf A, Ahmad B, Khan AR, Farooq U Front Pharmacol 16-Feb-2016
PMCID:PMC4754424
doi:10.3389/fphar.2016.00026
PMID:26909039
Antioxidant and antitumor effects of ferula sinkiangensis K. M. Shen Zhang H, Lu J, Zhou L, Jiang L, Zhou M Int J Clin Exp Med 15-Nov-2015
PMCID:PMC4723854
PMID:26885009
Annual Meeting Abstracts N/A J Med Toxicol 26-May-2012
PMCID:PMC3550232
doi:10.1007/s13181-012-0237-z
Antifungal Activity of Extracts and Prenylated Coumarins Isolated from Baccharis darwinii Hook & Arn. (Asteraceae) Kurdelas RR, Lima B, Tapia A, Egly Feresin G, Gonzalez Sierra M, Rodríguez MV, Zacchino S, Enriz RD, Freile ML Molecules 13-Jul-2010
PMCID:PMC6257657
doi:10.3390/molecules15074898
PMID:20657398
Diversolides A-G, guaianolides from the roots of Ferula diversivittata. Iranshahi M, Hosseini ST, Shahverdi AR, Molazade K, Khan SS, Ahmad VU Phytochemistry 01-Nov-2008
doi:10.1016/J.PHYTOCHEM.2008.08.009
PMID:18804823
Diversoside — A new coumarin from the roots of Ferula diversivitata Kh. M. Kamilov, V. V. Kiseleva, G. K. Nikonov Springer Science and Business Media LLC 07-Jul-2008
doi:10.1007/BF00564004
Coumarins ofFerula diversivittata A. A. Nabiev, T. Kh. Khasanov, S. Melibaev Springer Science and Business Media LLC 20-Nov-2004
doi:10.1007/BF00565258

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 / Benzene and substituted derivatives / Benzoic acids and derivatives / Benzoic acid esters
[(3S,3aR,4S,9aR,9bS)-3-acetyloxy-3,6,9-trimethyl-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-4-yl] benzoate 25149680 Click to see CC1=C2C(C3C(C(C1)OC(=O)C4=CC=CC=C4)C(C(=O)O3)(C)OC(=O)C)C(=CC2=O)C 424.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.009
[(3S,3aR,4S,9aR,9bS)-3,6,9-trimethyl-3-(3-methylbut-2-enoyloxy)-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-4-yl] benzoate 101591269 Click to see CC1=C2C(C3C(C(C1)OC(=O)C4=CC=CC=C4)C(C(=O)O3)(C)OC(=O)C=C(C)C)C(=CC2=O)C 464.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.009
> Benzenoids / Benzene and substituted derivatives / Benzoic acids and derivatives / Methoxybenzoic acids and derivatives / P-methoxybenzoic acids and derivatives
[(3S,3aR,4S,9aR,9bS)-3-acetyloxy-3,6,9-trimethyl-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-4-yl] 3,4-dimethoxybenzoate 25149678 Click to see CC1=C2C(C3C(C(C1)OC(=O)C4=CC(=C(C=C4)OC)OC)C(C(=O)O3)(C)OC(=O)C)C(=CC2=O)C 484.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.009
[(3S,3aR,4S,9aR,9bS)-3,6,9-trimethyl-3-(3-methylbut-2-enoyloxy)-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-4-yl] 3,4-dimethoxybenzoate 25149784 Click to see CC1=C2C(C3C(C(C1)OC(=O)C4=CC(=C(C=C4)OC)OC)C(C(=O)O3)(C)OC(=O)C=C(C)C)C(=CC2=O)C 524.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.009
[(3S,3aR,4S,9aR,9bS)-3,6,9-trimethyl-3-[(Z)-2-methylbut-2-enoyl]oxy-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-4-yl] 3,4-dimethoxybenzoate 102026089 Click to see CC=C(C)C(=O)OC1(C2C(CC(=C3C(C2OC1=O)C(=CC3=O)C)C)OC(=O)C4=CC(=C(C=C4)OC)OC)C 524.60 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.009
> Lipids and lipid-like molecules / Fatty Acyls / Fatty acyl glycosides / Fatty acyl glycosides of mono- and disaccharides
Diversoside 134714934 Click to see CC(=CCOC1=CC2=C(C=C1)C=CC(=O)O2)CCC(C(C)(C)O)OC3C(C(C(C(O3)CO)O)O)O 494.50 unknown https://doi.org/10.1007/BF00564004
> Lipids and lipid-like molecules / Steroids and steroid derivatives / Stigmastanes and derivatives
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2S,5S)-5-Ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol 12314479 Click to see CCC(C=CC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 412.70 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.009
Beta-Sitosterol 222284 Click to see CCC(CCC(C)C1CCC2C1(CCC3C2CC=C4C3(CCC(C4)O)C)C)C(C)C 414.70 unknown https://doi.org/10.1007/BF00565258
> Organic acids and derivatives / Carboxylic acids and derivatives / Tricarboxylic acids and derivatives
[(3S,3aR,4S,9aR,9bS)-3,6,9-trimethyl-3-[(Z)-2-methylbut-2-enoyl]oxy-2,7-dioxo-4,5,9a,9b-tetrahydro-3aH-azuleno[4,5-b]furan-4-yl] (Z)-2-methylbut-2-enoate 25149679 Click to see CC=C(C)C(=O)OC1CC(=C2C(C3C1C(C(=O)O3)(C)OC(=O)C(=CC)C)C(=CC2=O)C)C 442.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.009
Diversolide B 102026088 Click to see CC=C(C)C(=O)OC1CC(=C2C(C3C1C(C(=O)O3)(C)OC(=O)C=C(C)C)C(=CC2=O)C)C 442.50 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.009
> Phenylpropanoids and polyketides / Coumarins and derivatives
Diversin 13800313 Click to see CC(=C)CC(=O)C=C(C)CCOC1=CC2=C(C=C1)C=CC(=O)O2 312.40 unknown https://doi.org/10.1016/J.PHYTOCHEM.2008.08.009
Feselol 179577 Click to see CC1=CCC2C(C(CCC2(C1COC3=CC4=C(C=C3)C=CC(=O)O4)C)O)(C)C 382.50 unknown https://doi.org/10.1007/BF00565258
> Phenylpropanoids and polyketides / Coumarins and derivatives / Hydroxycoumarins / 7-hydroxycoumarins
Umbelliferone 5281426 Click to see C1=CC(=CC2=C1C=CC(=O)O2)O 162.14 unknown https://doi.org/10.1007/BF00565258

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