نتایج جستجو برای: cytotoxicity mechanism

تعداد نتایج: 605553  

Jalal Pourahmad

By discovering how chemical compounds/xenobiotics cytotoxicity is affected when their metabolic pathways are inhibited or activated, the metabolic pathways that activate versus detoxify chemical compound can be identified. Reactive metabolites contributing to cytotoxicity can also be identified. In this lecture, the pretreatment of inhibitors and activators of xenobiotic metabolizing enzymes as...

Journal: :asia pacific journal of medical toxicology 0
jalal pourahmad department of pharmacology and toxicology, faculty of pharmacy, shahid beheshti university of medical sciences, tehran, iranسازمان اصلی تایید شده: دانشگاه علوم پزشکی شهید بهشتی (shahid beheshti university of medical sciences)

by discovering how chemical compounds/xenobiotics cytotoxicity is affected when their metabolic pathways are inhibited or activated, the metabolic pathways that activate versus detoxify chemical compound can be identified. reactive metabolites contributing to cytotoxicity can also be identified. in this lecture, the pretreatment of inhibitors and activators of xenobiotic metabolizing enzymes as...

Journal: :The Journal of biological chemistry 1995
J S Kim J Soucek J Matousek R T Raines

Bovine seminal ribonuclease (BS-RNase), a dimeric homolog of bovine pancreatic ribonuclease A (RNase A), is toxic to mammalian cells. In contrast to dimeric BS-RNase, a monomeric BS-RNase and RNase A are not cytotoxic and are bound tightly by cytosolic ribonuclease inhibitor. To elucidate the mechanism of ribonuclease cytotoxicity, we constructed a series of hybrid and semisynthetic enzymes and...

Journal: :Environmental Health and Preventive Medicine 2002

Journal: :cell journal 0

objective: immunotoxins (its) have been developed for the treatment of cancer, and comprise of antibodies linked to toxins. also vascular endothelial growth factor (vegf) plays a key role in tumor angiogenesis, and the blockade of vegf receptor-2 (vegfr2) inhibits angiogenesis and tumor growth. the aim of this study was to produce anti-vegfr2/rpe (pseudomonas exotoxin) 38 it to test its cytotox...

Journal: :iranian journal of pharmaceutical sciences 0
jalal pourahma faculty of pharmacy and pharmaceutical sciences research center, shaheed beheshti medical university, tehran farzad kobarfard faculty of pharmacy and pharmaceutical sciences research center, shaheed beheshti medical university, tehran marzieh amirmostofian faculty of pharmacy and pharmaceutical sciences research center, shaheed beheshti medical university, tehran

dacarbazine (dtic) is a synthetic chemical antitumor agent which is used to treat malignant melanoma and hodgkin’s disease. dtic is a prodrug which is converted to an active form undergoing demethylation by liver enzymes. the active form prevents the progress of disease via alkylation of dna strand. in the structure of this drug, the imidazole ring, a triazen chain and carboxamide group exist. ...

Journal: :Journal of Drug Metabolism & Toxicology 2017

Journal: :iranian journal of pharmaceutical research 0
a shakoori

it has already been reported that muscle necrosis induced by various phenylenediamine derivatives are correlated with their autoxidation rate. now in a more detailed investigation of the cytotoxic mechanism using a model system of isolated hepatocytes and ring-methylated structural isomer durenediamine (dd) we have shown that under aerobic conditions, phenylenediamine induced cytotoxicity and r...

Farzad Kobarfard Jalal Pourahma, Marzieh Amirmostofian

     Dacarbazine (DTIC) is a synthetic chemical antitumor agent which is used to treat malignant melanoma and Hodgkin’s disease. DTIC is a prodrug which is converted to an active form undergoing demethylation by liver enzymes. The active form prevents the progress of disease via alkylation of DNA strand. In the structure of this drug, the imidazole ring, a triazen chain and carboxamide group ex...

Journal: :iranian journal of pharmaceutical sciences 0
ahmad salimi department of pharmacology and toxicology, faculty of pharmacy, shahid beheshti university of medical sciences, tehran, iran. department of pharmacology and toxicology, school of pharmacy, ardabil university of medical science, ardabil, iran. students research committee, school of pharmacy, shahid beheshti university of medical sciences, tehran, iran. melina ramandoost department of pharmacology and toxicology, faculty of pharmacy, shahid beheshti university of medical sciences, tehran, iran jalal pourahmad jaktaji department of pharmacology and toxicology, faculty of pharmacy, shahid beheshti university of medical sciences, tehran, iran

6- mercaptopurine (6-mp) is widely used in clinic as an immunosuppressive for treatment of acute lymphocytic leukemia, crohn's disease, and ulcerative colitis with documented unpredictable hepatotoxicity. the potential molecular cytotoxic mechanisms of 6-mp against isolated rat hepatocytes were searched in this study using “accelerated cytotoxicity mechanism screening (acms)” techniques. t...

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