Smyrniopsis aucheri - Unknown
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Internal ID UUID644046efd5582984113664
Scientific name Smyrniopsis aucheri
Authority Boiss.
First published in Ann. Sci. Nat., Bot. , sér. 3, 2: 72 (1844)

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Synonyms Top

Scientific name Authority First published in
Smyrniopsis armena Schischk. Ref. Nauchno-Issl. Rabot, Otdelenie Biol. Nauk 1945: 10 (1947)

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Language Common/alternative name
Armenian Սմիրնիոպսիս հայկական

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native
  • Asia-temperate
    • Caucasus
      • Transcaucasus
    • Western Asia
      • Iran
      • Iraq
      • Turkey

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0001067716
Tropicos 1700244
The Plant List tro-1700244
Open Tree Of Life 671425 122443
NCBI Taxonomy 52572
IPNI 849085-1
iNaturalist 1106284
GBIF 3639116

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
Volatile Oils Discrepancy between Male and Female Ochradenus arabicus and Their Allelopathic Activity on Dactyloctenium aegyptium Abd-ElGawad AM, Assaeed AM, El Gendy AE, Dar BA, Elshamy AI Plants (Basel) 26-Dec-2022
Overview on Adjunct Ingredients Used in Hydroxyapatite-Based Oral Care Products Enax J, Amaechi BT, Schulze zur Wiesche E, Meyer F Biomimetics (Basel) 19-Dec-2022
Bioactivity study and metabolic profiling of Colletotrichum alatae LCS1, an endophyte of club moss Lycopodium clavatum L. Santra HK, Banerjee D PLoS One 28-Apr-2022
Possible Use of Phytochemicals for Recovery from COVID-19-Induced Anosmia and Ageusia Koyama S, Kondo K, Ueha R, Kashiwadani H, Heinbockel T Int J Mol Sci 18-Aug-2021
Asymmetric organocatalyzed synthesis of coumarin derivatives Moreira NM, Martelli LS, Corrêa AG Beilstein J Org Chem 03-Aug-2021
Analgesic and Anti-Inflammatory Effects of Hydroalcoholic and Hexane Extracts of Smyrniopsis aucheri in Animal Models Hajhashemi V, Sajjadi SE, Hasani M Int J Prev Med 15-May-2021
Unraveling the importance of molecules of natural origin in antifungal drug development through targeting ergosterol biosynthesis pathway Jamzivar F, Shams-Ghahfarokhi M, Khoramizadeh M, Yousefi N, Gholami-Shabani M, Razzaghi-Abyaneh M Iran J Microbiol 01-Dec-2019
Iran supports a great share of biodiversity and floristic endemism for Fritillaria spp. (Liliaceae): A review Kiani M, Mohammadi S, Babaei A, Sefidkon F, Naghavi MR, Ranjbar M, Razavi SA, Saeidi K, Jafari H, Asgari D, Potter D Plant Divers 13-Sep-2017
Cytotoxic Activity of Some Medicinal Plants from Hamedan District of Iran Behzad S, Pirani A, Mosaddegh M Iran J Pharm Res 01-Jan-2014
Asymmetric total synthesis of smyrindiol employing an organocatalytic aldol key step Enders D, Fronert J, Bisschops T, Boeck F Beilstein J Org Chem 18-Jul-2012
A new dihydrofurocoumarin from Smyrniopsis aucheri Z. R. Dzhafarov, A. A. Kuliev, Z. A. Kuliev, V. M. Malikov, N. M. Ismailov Springer Science and Business Media LLC 26-Nov-2004
Crystal and molecular structures of two polymorphs of a furanocoumarin — Smyrindiol from Smyrniopsis aucheri B. Tashkhodzhaev, Z. A. Kuliev, Z. R. Dzhafarov Springer Science and Business Media LLC 26-Nov-2004
Coumarins of Smyrniopsis aucheri Z. R. Dzhafarov, Z. A. Kuliev, A. D. Vdovin, A. A. Kuliev, V. M. Malikov, N. M. Ismailov Springer Science and Business Media LLC 26-Nov-2004

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
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
3-hydroxy-2-propan-2-ylidene-3H-furo[3,2-g]chromen-7-one 14185724 Click to see CC(=C1C(C2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)C 244.24 unknown
Smyrindiol 92261439 Click to see CC(C)(C1C(C2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)O 262.26 unknown
Smyrindioloside 10836072 Click to see CC(C)(C1C(C2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)OC4C(C(C(C(O4)CO)O)O)O 424.40 unknown
> Phenylpropanoids and polyketides / Coumarins and derivatives / Pyranocoumarins / Linear pyranocoumarins
Decursinol 442127 Click to see CC1(C(CC2=C(O1)C=C3C(=C2)C=CC(=O)O3)O)C 246.26 unknown

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