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  1. Article

    Open Access

    Synthesis and cytotoxic activity evaluation of novel imidazopyridine carbohydrazide derivatives

    Two series of novel imidazo[1,2-a]pyridine-2-carbohydrazide derivatives have been designed, synthesized, and evaluated for cytotoxic activity. Target compounds were designed in two series: aryl hydrazone deriv...

    Maryam Firouzi, Zahra Haghighijoo, Masoomeh Eskandari, Maryam Mohabbati in BMC Chemistry (2024)

  2. No Access

    Article

    5-Oxo-hexahydroquinoline and 5-oxo-tetrahydrocyclopentapyridine derivatives as promising antiproliferative agents with potential apoptosis-inducing capacity

    Discovery of novel anticancer agents is of crucial importance to expand the therapeutic options for cancer patients. In this study, a series of 49 5-oxo-hexahydroquinoline and 5-oxo-tetrahydrocyclopentapyridin...

    Sara Ranjbar, Mehdi Khoshneviszadeh, Marjan Tavakkoli, Ramin Miri in Molecular Diversity (2022)

  3. Article

    Open Access

    Synthesis, biological evaluation and molecular docking analysis of vaniline–benzylidenehydrazine hybrids as potent tyrosinase inhibitors

    In this work, 11 novel compounds based on vaniline and benzylidenehydrazine structure were synthesized with various substituents on phenyl aromatic ring of the molecule and evaluated as tyrosinase inhibitors. ...

    Aida Iraji, Tina Adelpour, Najmeh Edraki, Mahsima Khoshneviszadeh in BMC Chemistry (2020)

  4. No Access

    Article

    The Effect of Platanus orientalis L. Distillate on Mouse Model of Allergic Rhinitis

    Platanus orientalis L. has been used in traditional Persian medicine to treat allergic rhinitis. In this study, the therapeutic effects of P. orientalis L. distillate on allergic rhinitis mouse model were assesse...

    Soheila Alyasin, Behjat Maneshian in Iranian Journal of Science and Technology,… (2020)

  5. No Access

    Article

    5-Oxo-hexahydroquinoline: an attractive scaffold with diverse biological activities

    5-Oxo-hexahydroquinoline (5-oxo-HHQ) represents a biologically attractive fused heterocyclic core. Various synthetic analogs of 5-oxo-HHQ have been synthesized and assessed for different biological activities....

    Sara Ranjbar, Najmeh Edraki, Omidreza Firuzi, Mehdi Khoshneviszadeh in Molecular Diversity (2019)

  6. No Access

    Article

    Structural Insight into Binding Mode of 9-Hydroxy Aristolochic Acid, Diclofenac and Indomethacin to PLA2

    Phospholipase A2 (PLA2) catalyzes the hydrolysis of phospholipids into arachidonic acid and lysophospholipids. Arachidonic acid is modified by cyclooxygenases into active compounds called eicosanoids that act as ...

    Mohsen Ebrahimi, Omidreza Firuzi, Ramin Miri in Interdisciplinary Sciences: Computational … (2018)

  7. No Access

    Article

    Virtual screening of some heterocyclic structures toward novel antibacterial agents

    Infectious diseases and their treatment are among the most important issues in global health and economy. Moreover, increasing prevalence of antibiotic-resistant pathogenic bacteria necessitates the considera...

    Zahra S. Hosseini, Mohammad Reza Housaindokht in Journal of the Iranian Chemical Society (2018)

  8. No Access

    Article

    The antileishmanial effects of Lowsonia inermis and Cedrus libani on Leishmania major promastigotes: an in vitro study

    Leishmaniasis is a parasitic disease caused by different species of protozoan parasites belonging to the genus Leishmania. In this study, Leishmania major (MRHO/IR/75/ER) promastigotes were cultured at 23–25 °C i...

    Mohammad Hossein Motazedian, Fattaneh Mikaeili in Journal of Parasitic Diseases (2017)

  9. No Access

    Article

    2-Imino 2H-chromene and 2-(phenylimino) 2H-chromene 3-aryl carboxamide derivatives as novel cytotoxic agents: synthesis, biological assay, and molecular docking study

    The inhibition of AKR1B10 has been recognized as a potential therapeutic approach to the treatment of various types of cancers. A novel series of compounds with imino-2H-chromen and phenylimino-2H-chromen scaffol...

    Najmeh Edraki, Aida Iraji, Omidreza Firuzi in Journal of the Iranian Chemical Society (2016)

  10. No Access

    Article

    In vitro efficacy of ethanolic extract of Artemisia absinthium (Asteraceae) against Leishmania major L. using cell sensitivity and flow cytometry assays

    Leishmaniasis is one of the most neglected human diseases with an estimated global burden ranking second in mortality and fourth in morbidity among the tropical infections. Chemotherapy involving the use of d...

    Kourosh Azizi, Fatemeh Shahidi-Hakak, Qasem Asgari in Journal of Parasitic Diseases (2016)

  11. No Access

    Article

    Detailed atomistic molecular modeling of a potent type ΙΙ p38α inhibitor

    The active site conservation among protein kinases makes it a real challenge to design selective inhibitors. In this regard, detailed understanding of structural features responsible for functional behavior of...

    Seyed Ahmad Ebadi, Nima Razzaghi-Asl, Mehdi Khoshneviszadeh in Structural Chemistry (2015)

  12. No Access

    Article

    Inhibition of Alzheimer’s BACE-1 by 2,6-dialkyl-4-chromon-3-yl-1,4-dihydropyridine-3,5-dicarboxylates

    Alzheimer’s disease is the most common cause of dementia in the elderly, and no disease-modifying therapy is yet available for this devastating pathology. Deposition of different physicochemical forms of amylo...

    Nima Razzaghi-Asl, Neha Aggarwal, Smriti Srivastava in Medicinal Chemistry Research (2015)

  13. No Access

    Article

    Synthesis and cytotoxic activity of novel poly-substituted imidazo[2,1- \(c\) ][1,2,4]triazin-6-amines

    A novel series of 3,4-diphenyl-7-(hetero)arylimidazo[2,1- \(c\) c ...

    Tahmineh Akbarzadeh, Saeedeh Noushini, Somayeh Taban in Molecular Diversity (2015)

  14. No Access

    Article

    A validated dispersive liquid-liquid microextraction method for extraction of ochratoxin A from raisin samples

    A method based on dispersive liquid-liquid microextraction (DLLME) was developed for the quantitative extraction of Ochratoxin A (OTA) from raisin samples. The influence of various parameters on the recovery o...

    Rouhollah Karami-Osboo, Ramin Miri in Journal of Food Science and Technology (2015)

  15. No Access

    Article

    Inhibitors of Alzheimer’s BACE-1 with 3,5-bis-N-(aryl/heteroaryl) carbamoyl-4-aryl-1,4-dihydropyridine structure

    β-site amyloid precursor protein cleaving enzyme (BACE-1) is a validated target for Alzheimer therapy due to its distinctive role in pathogenesis of AD. In the present contribution, a series of new 3,5-bis-N-(ary...

    Ramin Miri, Omidreza Firuzi, Nima Razzaghi-Asl in Archives of Pharmacal Research (2015)

  16. No Access

    Article

    Molecular docking and quantum mechanical studies on biflavonoid structures as BACE-1 inhibitors

    Beta-site amyloid precursor protein cleaving enzyme (BACE-1) is a well-known therapeutic target for Alzheimer disease (AD) due to its characteristic role in the pathogenesis of AD. Numerous researches have bee...

    Nima Razzaghi-Asl, Saghi Sepehri, Ahmad Ebadi, Ramin Miri in Structural Chemistry (2015)

  17. No Access

    Article

    Cytotoxic activity assessment and c-Src tyrosine kinase docking simulation of thieno[2,3-b] pyridine-based derivatives

    Thienopyridine derivatives possess various promising biological properties and particularly cytotoxic effect. In vitro cytotoxic activities of some thienopyridine analogous were evaluated by MTT reduction assa...

    Ali Reza Nikkhoo, Ramin Miri, Nahid Arianpour in Medicinal Chemistry Research (2014)

  18. Article

    Open Access

    Novel 9-(alkylthio)-Acenaphtho[1,2-e]-1,2,4-triazine derivatives: synthesis, cytotoxic activity and molecular docking studies on B-cell lymphoma 2 (Bcl-2)

    Acenaphtho derivatives have been reported as antitumor agents. Due to this fact and also with the aim of develo** the chemistry of potentially bioactive heterocyclic compounds via efficient reactions, a faci...

    Mohammad K Mohammadi, Omidreza Firuzi in DARU Journal of Pharmaceutical Sciences (2014)

  19. No Access

    Article

    Comparative hydrodistillation and headspace SPME-GC-MS analysis of volatile constituents of roots and shoots of Artemisia annua and Artemisia sieberi

    Amir Reza Jassbi, Ramin Miri, Ian T. Baldwin in Chemistry of Natural Compounds (2014)

  20. No Access

    Article

    Reversal of multidrug resistance in cancer cells by novel asymmetrical 1,4-dihydropyridines

    Multidrug resistance (MDR) is an important obstacle that limits the efficacy of chemotherapy in many types of cancer. In this study, 14 novel asymmetrical DHPs possessing pyridyl alkyl carboxylate substitution...

    Omidreza Firuzi, Katayoun Javidnia, Elham Mansourabadi in Archives of Pharmacal Research (2013)

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