Spring 2016 CHEM Handbook - Chemistry | Virginia Tech
... Minimum Grade Requirement: Chemistry majors must earn a grade of “C” (2.0) or better in CHEM 1055, 1056, and 2565. If a chemistry major fails to earn a “C” (2.0) or better in CHEM 1055, the student must either retake this class (and earn the minimum grade) or take CHEM 1035-1036, General Chemistr ...
... Minimum Grade Requirement: Chemistry majors must earn a grade of “C” (2.0) or better in CHEM 1055, 1056, and 2565. If a chemistry major fails to earn a “C” (2.0) or better in CHEM 1055, the student must either retake this class (and earn the minimum grade) or take CHEM 1035-1036, General Chemistr ...
Opioid Receptors and Legal Highs - The Salvia divinorum Research
... agonists, have discrete psychoactive effects that have contributed to their increasing popularity. Salvia divinorum contains the highly selective kappa- opioid receptor agonist salvinorin A; this compound produces visual hallucinations and synesthesia. Mitragynine, the major alkaloid identified from ...
... agonists, have discrete psychoactive effects that have contributed to their increasing popularity. Salvia divinorum contains the highly selective kappa- opioid receptor agonist salvinorin A; this compound produces visual hallucinations and synesthesia. Mitragynine, the major alkaloid identified from ...
Chemistry - Wheeling Jesuit University
... 4. Be proficient in oral and written communication. The BA chemistry major is designed to be combined with a minor or a program rather than as a stand-alone program.The flexible nature of this program allows students to take courses in biology, education, computer science, math, business, etc. to pr ...
... 4. Be proficient in oral and written communication. The BA chemistry major is designed to be combined with a minor or a program rather than as a stand-alone program.The flexible nature of this program allows students to take courses in biology, education, computer science, math, business, etc. to pr ...
THESIS FILESObesity is a medical condition in
... impact on the cholesterol profile and adverse effects. For example, some may lower the "bad cholesterol" low density lipoprotein (LDL) more so than others, while others may preferentially increase high density lipoprotein (HDL), "the good cholesterol". Clinically, the choice of an agent will depend ...
... impact on the cholesterol profile and adverse effects. For example, some may lower the "bad cholesterol" low density lipoprotein (LDL) more so than others, while others may preferentially increase high density lipoprotein (HDL), "the good cholesterol". Clinically, the choice of an agent will depend ...
The Medical History of Psychedelic Drugs
... and summarise the various ways that they have been used. By placing their medical use in this wider historical context, it is hoped that a broader sense of their properties will be appreciated. This section will describe the way in which psychedelics began to be used medically and show how researche ...
... and summarise the various ways that they have been used. By placing their medical use in this wider historical context, it is hoped that a broader sense of their properties will be appreciated. This section will describe the way in which psychedelics began to be used medically and show how researche ...
PART 3-ICHO 11-15
... solution and crystalline KI were added. Iodine produced as a result of the reaction was titrated with sodium thiosulphate solution in the presence of starch as an indicator. 18.46 cm3 of 0.1512 normal Na2S2O3 solution were required. The last metal contained in the precipitate as a sparingly soluble ...
... solution and crystalline KI were added. Iodine produced as a result of the reaction was titrated with sodium thiosulphate solution in the presence of starch as an indicator. 18.46 cm3 of 0.1512 normal Na2S2O3 solution were required. The last metal contained in the precipitate as a sparingly soluble ...
ERLN-TB expert opinion on the use of the rapid molecular assays
... Genotype MTBDR/MTBDRplus (GT/GTplus) and Genotype MTBDRsl (GTsl;Hain Lifescience, GmbH, Germany). INNOLIPA detects only RIF-resistance, GT/GTplus detect both RIF and isoniazid (INH) resistance, and the GTsl detects resistance to fluoroquinolones, injectable second line drugs and ethambutol. These te ...
... Genotype MTBDR/MTBDRplus (GT/GTplus) and Genotype MTBDRsl (GTsl;Hain Lifescience, GmbH, Germany). INNOLIPA detects only RIF-resistance, GT/GTplus detect both RIF and isoniazid (INH) resistance, and the GTsl detects resistance to fluoroquinolones, injectable second line drugs and ethambutol. These te ...
Clarithromycin increases linezolid exposure in multidrug-resistant tuberculosis patients
... using the common toxicity criteria (CTC) and were scored grades 0–4 [22]. Routine testing of neurotoxic adverse events through electromyogram or vibration sense monitoring were not carried out during the 6-week study, since these effects have been reported to occur after a median (range) of 16 weeks ...
... using the common toxicity criteria (CTC) and were scored grades 0–4 [22]. Routine testing of neurotoxic adverse events through electromyogram or vibration sense monitoring were not carried out during the 6-week study, since these effects have been reported to occur after a median (range) of 16 weeks ...
Actavis v ICOS
... as low as 5mg and the advantages it provides in terms of efficacy and low side effects were not obvious. Even if the skilled team embarked on a clinical research project into tadalafil starting from Daugan, they would have no reasonable prospect of success as to the outcome and no reasonable basis f ...
... as low as 5mg and the advantages it provides in terms of efficacy and low side effects were not obvious. Even if the skilled team embarked on a clinical research project into tadalafil starting from Daugan, they would have no reasonable prospect of success as to the outcome and no reasonable basis f ...
Activity and Enzyme Kinetics of Human UDP
... Human UDP-glucuronosyltransferases (UGTs) are important in the metabolic elimination of xenobiotics and endogenous compounds from the body. These enzymes transfer glucuronic acid moiety from the cosubstrate, UDP-glucuronic acid (UDPGA), to nucleophilic groups of small organic molecules, such as hydr ...
... Human UDP-glucuronosyltransferases (UGTs) are important in the metabolic elimination of xenobiotics and endogenous compounds from the body. These enzymes transfer glucuronic acid moiety from the cosubstrate, UDP-glucuronic acid (UDPGA), to nucleophilic groups of small organic molecules, such as hydr ...
quantitative analysis of loperamide hydrochloride in the presence its
... Loperamide hydrochloride (4-(p-chlorophenyl)-4-hydroxy-N,N-dimethyl-diphenyl-1-piperidine butyramide hydrochloride), is an opiate agonist widely used as an effective drug for the control and symptomatic relief of acute non-specific diarrhea [1]. More recently, it has also been reported that loperami ...
... Loperamide hydrochloride (4-(p-chlorophenyl)-4-hydroxy-N,N-dimethyl-diphenyl-1-piperidine butyramide hydrochloride), is an opiate agonist widely used as an effective drug for the control and symptomatic relief of acute non-specific diarrhea [1]. More recently, it has also been reported that loperami ...
NCPDP Recommendations for Improved Prescription Container Labels for Medicines Containing Acetaminophen
... provide the public with education on the safe use of acetaminophen and provide support to healthcare professionals in their attempts to educate their patients. All of these programs provide tools for the public and encourage the public to read their medicine labels and take action to make sure they ...
... provide the public with education on the safe use of acetaminophen and provide support to healthcare professionals in their attempts to educate their patients. All of these programs provide tools for the public and encourage the public to read their medicine labels and take action to make sure they ...
Warfarin – INR – Antibiotic Interactions
... increase INR and the effects of warfarin ***S-warfarin is 2-5 times more active than the R-enantiomer Related Information: A challenging aspect of warfarin management has always been keeping patients’ INR within the therapeutic window. Once on a stable dose of warfarin, numerous factors can affect I ...
... increase INR and the effects of warfarin ***S-warfarin is 2-5 times more active than the R-enantiomer Related Information: A challenging aspect of warfarin management has always been keeping patients’ INR within the therapeutic window. Once on a stable dose of warfarin, numerous factors can affect I ...
amyotrophic lateral sclerosis (als) – opportunity analysis and
... Amyotrophic Lateral Sclerosis (ALS) – Opportunity Analysis and Forecasts to 2018 © GlobalData. This report is a licensed product and is not to be copied, reproduced, shared or resold in any form. ...
... Amyotrophic Lateral Sclerosis (ALS) – Opportunity Analysis and Forecasts to 2018 © GlobalData. This report is a licensed product and is not to be copied, reproduced, shared or resold in any form. ...
Revisiting `The Hidden Epidemic` - Local Consultative Groups in
... users - simply because they are drug users - not only continues but is being increased and strengthened. This is despite the fact that there is mounting evidence from the Asian region, confirming what has been known in the west for some time, that incarceration not only does not help drug dependent ...
... users - simply because they are drug users - not only continues but is being increased and strengthened. This is despite the fact that there is mounting evidence from the Asian region, confirming what has been known in the west for some time, that incarceration not only does not help drug dependent ...
HIV Drug Therapy - Immunodeficiency Clinic
... within this book does not constitute endorsement by the authors, Toronto General Hospital, or the Northern Alberta Program. ...
... within this book does not constitute endorsement by the authors, Toronto General Hospital, or the Northern Alberta Program. ...
Nasal Drug Delivery
... an in vitro model, and glucose, insulin, lidocaine, mannitol, melagatran, nicotine, PEG 4000, propranolol, sumatriptan, verapamil, vinblastine and an aminodiether were used as model compounds. The pharmacokinetics of melagatran and propiomazine were investigated in absorption studies in rats, and th ...
... an in vitro model, and glucose, insulin, lidocaine, mannitol, melagatran, nicotine, PEG 4000, propranolol, sumatriptan, verapamil, vinblastine and an aminodiether were used as model compounds. The pharmacokinetics of melagatran and propiomazine were investigated in absorption studies in rats, and th ...
Dextromethorphan abuse: Clinical effects
... recognized as an effective antitussant.3,6 The drug is the dextro-isomer of levorphanol and acts centrally within the medulla oblongata to raise the cough threshold.1 Its specific actions are modulated by central sigma receptor binding.1,3,6 Unlike most opioids, the drug is devoid of activity at mu a ...
... recognized as an effective antitussant.3,6 The drug is the dextro-isomer of levorphanol and acts centrally within the medulla oblongata to raise the cough threshold.1 Its specific actions are modulated by central sigma receptor binding.1,3,6 Unlike most opioids, the drug is devoid of activity at mu a ...
APPROACHES TO CARBOHYDRATE-BASED CHEMICAL LIBRARIES: THE
... superior new leads in drug discovery". This would entail the discovery of more lead structures, possessing higher affinities, significant conformational restraints, greater potential for optimization, easier synthesis, better pharmacokinetic properties, etc. Given * The alternative, parallel synthes ...
... superior new leads in drug discovery". This would entail the discovery of more lead structures, possessing higher affinities, significant conformational restraints, greater potential for optimization, easier synthesis, better pharmacokinetic properties, etc. Given * The alternative, parallel synthes ...
Product Information - Therapeutic Goods Administration
... Tenofovir disoproxil fumarate: HIV-1 isolates with reduced susceptibility to tenofovir have been selected in vitro. These viruses expressed a K65R mutation in reverse transcriptase and showed a 2 to 4 fold reduction in susceptibility to tenofovir. Emtricitabine: Emtricitabine-resistant isolates of H ...
... Tenofovir disoproxil fumarate: HIV-1 isolates with reduced susceptibility to tenofovir have been selected in vitro. These viruses expressed a K65R mutation in reverse transcriptase and showed a 2 to 4 fold reduction in susceptibility to tenofovir. Emtricitabine: Emtricitabine-resistant isolates of H ...
Synthesis and in vitro activities of a new antiviral duplex drug linking
... The chemical synthesis of AZT–lipid–PFA is practicable on a preparative scale and the yield of the single reaction steps, which are not yet optimized are in the range of 70–83%. This fulfills an important prerequisite, namely that the new antiviral duplex drug can be synthesized at sufficiently large ...
... The chemical synthesis of AZT–lipid–PFA is practicable on a preparative scale and the yield of the single reaction steps, which are not yet optimized are in the range of 70–83%. This fulfills an important prerequisite, namely that the new antiviral duplex drug can be synthesized at sufficiently large ...
S0735109711027628_mmc1
... Drug treatment efficacies, in terms of Relative Risks (RR) were obtained from meta analyses and considered the relative risk in incidence of CHD (any of the following outcomes: non-fatal myocardial infarction, CABG, PCI, and CHD mortality) or stroke (ischemic, hemorrhagic or unspecified) compared to ...
... Drug treatment efficacies, in terms of Relative Risks (RR) were obtained from meta analyses and considered the relative risk in incidence of CHD (any of the following outcomes: non-fatal myocardial infarction, CABG, PCI, and CHD mortality) or stroke (ischemic, hemorrhagic or unspecified) compared to ...
Antipsychotic Use in the Elderly
... antipsychotic agents (namely: risperidone, quetiapine, olanzapine, aripiprazole) when compared to placebo among patients with dementia and BPSD. Additionally, in elderly patients with dementia and BPSD, none of the atypical antipsychotics showed significant symptom improvements when compared to each ...
... antipsychotic agents (namely: risperidone, quetiapine, olanzapine, aripiprazole) when compared to placebo among patients with dementia and BPSD. Additionally, in elderly patients with dementia and BPSD, none of the atypical antipsychotics showed significant symptom improvements when compared to each ...
pharmacology basic principles
... PHARMACOLOGY BASIC PRINCIPLES Drug: a molecule that when introduced into body alters body’s functions by interaction at molecular level; most are molecular weight 100-1000, which allows efficient absorption and distribution; 25% of drugs are chiral (stereoisomeric) Xenobiotics: chemicals not synthes ...
... PHARMACOLOGY BASIC PRINCIPLES Drug: a molecule that when introduced into body alters body’s functions by interaction at molecular level; most are molecular weight 100-1000, which allows efficient absorption and distribution; 25% of drugs are chiral (stereoisomeric) Xenobiotics: chemicals not synthes ...
Review Advances in nucleoside monophosphate prodrugs as anti
... the majority of infections progress to chronic infection. In addition, >20% of chronically infected individuals will eventually develop more serious liver problems, such as cirrhosis, hepatocellular carcinoma or liver ...
... the majority of infections progress to chronic infection. In addition, >20% of chronically infected individuals will eventually develop more serious liver problems, such as cirrhosis, hepatocellular carcinoma or liver ...
Drug discovery
In the fields of medicine, biotechnology and pharmacology, drug discovery is the process by which new candidate medications are discovered. Historically, drugs were discovered through identifying the active ingredient from traditional remedies or by serendipitous discovery. Later chemical libraries of synthetic small molecules, natural products or extracts were screened in intact cells or whole organisms to identify substances that have a desirable therapeutic effect in a process known as classical pharmacology. Since sequencing of the human genome which allowed rapid cloning and synthesis of large quantities of purified proteins, it has become common practice to use high throughput screening of large compounds libraries against isolated biological targets which are hypothesized to be disease modifying in a process known as reverse pharmacology. Hits from these screens are then tested in cells and then in animals for efficacy.Modern drug discovery involves the identification of screening hits, medicinal chemistry and optimization of those hits to increase the affinity, selectivity (to reduce the potential of side effects), efficacy/potency, metabolic stability (to increase the half-life), and oral bioavailability. Once a compound that fulfills all of these requirements has been identified, it will begin the process of drug development prior to clinical trials. One or more of these steps may, but not necessarily, involve computer-aided drug design. Modern drug discovery is thus usually a capital-intensive process that involves large investments by pharmaceutical industry corporations as well as national governments (who provide grants and loan guarantees). Despite advances in technology and understanding of biological systems, drug discovery is still a lengthy, ""expensive, difficult, and inefficient process"" with low rate of new therapeutic discovery. In 2010, the research and development cost of each new molecular entity (NME) was approximately US$1.8 billion. Drug discovery is done by pharmaceutical companies, with research assistance from universities. The ""final product"" of drug discovery is a patent on the potential drug. The drug requires very expensive Phase I, II and III clinical trials, and most of them fail. Small companies have a critical role, often then selling the rights to larger companies that have the resources to run the clinical trials.Discovering drugs that may be a commercial success, or a public health success, involves a complex interaction between investors, industry, academia, patent laws, regulatory exclusivity, marketing and the need to balance secrecy with communication. Meanwhile, for disorders whose rarity means that no large commercial success or public health effect can be expected, the orphan drug funding process ensures that people who experience those disorders can have some hope of pharmacotherapeutic advances.