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Prescribing information Lortab® (USA)September-2014
Prescribing information Lortab® (USA)September-2014

... and toxic epidermal necrolysis (TEN), which can be fatal. Patients should be informed about the signs of serious skin reactions, and use of the drug should be discontinued at the first appearance of skin rash or any other sign of hypersensitivity. Hypersensitivity/anaphylaxis: There have been post-m ...
Antihistamines - Take Control of your Health
Antihistamines - Take Control of your Health

... the American Academy of Allergy Asthma and Immunology (AAAAI). Hives are usually harmless and disappear on their own, but if they become severe, an antihistamine might be appropriate. Hay fever is a type of allergic rhinitis, an allergic reaction triggered when a person breathes in something they ar ...
Amidine: Structure, Reactivity and Complexation Behaviour
Amidine: Structure, Reactivity and Complexation Behaviour

... inhibiting effects on arginine specific cystein proteinases of P. gingivalis[19]. In vitro effects of the synthetic inhibitors of cystein proteinases on virulence of P. gingivalis were observed further in vitro tests concerning immunomodulatory effects should be done before these substances are used ...
Lortab® (hydrocodone bitartrate and acetaminophen tablets
Lortab® (hydrocodone bitartrate and acetaminophen tablets

... and toxic epidermal necrolysis (TEN), which can be fatal. Patients should be informed about the signs of serious skin reactions, and use of the drug should be discontinued at the first appearance of skin rash or any other sign of hypersensitivity. Hypersensitivity/anaphylaxis: There have been post-m ...
PROTECTIVE EFFECT OF NIGELLA SATIVA AGAINST ASPIRIN INDUCED GASTRIC DAMAGE IN RATS  Original Article
PROTECTIVE EFFECT OF NIGELLA SATIVA AGAINST ASPIRIN INDUCED GASTRIC DAMAGE IN RATS Original Article

... million prescriptions are issued annually, at an approximate cost of $4.8 billion [1]. NSAIDs are used very commonly in long term basis like in rheumatoid arthritis, post myocardial infarction etc. In spite of this they have significant adverse effects related burden to the community. For the averag ...
- Ontario.ca
- Ontario.ca

... 7. (1) This section sets out additional conditions to be met in order for a strength and dosage form of a product to be designated as interchangeable. O. Reg. 299/95, s. 1. (2) A strength and dosage form of a product shall not be designated as interchangeable with other products unless it meets the ...
Full-Text  - Tropical Journal of Pharmaceutical Research
Full-Text - Tropical Journal of Pharmaceutical Research

... be attributable to the erratic absorption of suppositories generally. This type of profile may be beneficial during malaria treatment because it can provide a more sustained plasma drug concentration leading to prolonged effect of the drug. QN is known to exhibit wide inter- and intra- individual va ...
Report of the International Narcotics Control Board for 2015
Report of the International Narcotics Control Board for 2015

... However, INCB is convinced that these challenges can be met by fully implementing the conventions and the principles of the political declarations. The drug control system is a balanced system, driving towards improving public health and welfare, based on the underlying principles of proportionalit ...
Is there an interaction between erythromycin and statins?
Is there an interaction between erythromycin and statins?

... Simvastatin is contra-indicted in patients taking erythromycin and should be withdrawn if the antibiotic is required [8, 13, 15, 16. 26, 27]. Atorvastatin and erythromycin should be used together with caution. It may be prudent to withhold atorvastatin if erythromycin treatment is required to avoid ...
in-vitro determination of fine particle dose (fine respirable fraction)
in-vitro determination of fine particle dose (fine respirable fraction)

... However, the effect of the slightly reduced dead space associated with the currently available FSI on values of FPF<4.7 μm was so small that it may be acceptable as a systematic deviation between the two techniques. Substantially equivalent measures of fine particle fraction were obtained for most o ...
Calculations on the equations reaction
Calculations on the equations reaction

... 6. To equalize the oxidation-reduction reaction by electron balance method Cu + HNO3 → Cu(NO3)2 + NO2 + H2O Determine the degree of oxidation of elements. Write the oxidant and reductant. 7. To equalize the oxidation-reduction reaction by electron balance method Cl2 + KOH → KCl + KClO3 + H2O Determi ...
Bulletin PST 206
Bulletin PST 206

... Ring binders Rulers School art portfolios Work books ...
Bulletin PST 206, Grocery and Drug Stores
Bulletin PST 206, Grocery and Drug Stores

... Ring binders Rulers School art portfolios Work books ...
For effective and well-tolerated treatment
For effective and well-tolerated treatment

... drugs is currently an integral part of routine clinical practice for solid organ transplant patients.”1 Immunosuppressive therapies The development of potent immunosuppressive drugs (ISDs, ­summarized in Table 1) has greatly improved the short-term ­survival of transplant recipients during the last ...
Drug Treatments for Metastasis of the Lewis Lung Carcinoma: Lack
Drug Treatments for Metastasis of the Lewis Lung Carcinoma: Lack

... aggregation inhibitors have been examined as antimetastatic agents. The results of these numerous studies have been con flicting. Some investigators found an inhibition of metastasis, others an increase, and still others found no effect. Part of the controversy, especially in the older investigation ...
BioAssay Systems Kinase
BioAssay Systems Kinase

... interfere with this assay and should be avoided. Kinase Activity Assay in 384-well Plate 1. Kinase Reaction. Users should provide their own enzyme, ultra-pure ATP (e.g. Sigma # A7699) and substrate. Set up 20 µL reaction mixture containing the kinase, ATP and substrate in the provided Assay Buffer ( ...
Mechanism-based Inhibition: Deriving KI and kinact
Mechanism-based Inhibition: Deriving KI and kinact

... even without the need of additional pre-incubation experiments. The application of this approach is illustrated using a fluorimetric assay to access the drug-drug interaction potential associated with new chemical entities. The approach can easily be implemented using standard software tools (e.g., ...
Micelle-enhanced spectrofluorimetric determination of amlexanox in
Micelle-enhanced spectrofluorimetric determination of amlexanox in

... rigid microenvironment capable of restricting the freedom of fluorophores, and so diminish the probabilities of non-radiative processes and provide relatively high viscous microenvironments that can inhibit quenching by molecular oxygen. These factors might increase the fluorescence quantum yield and ...
Understanding Stimulant Drugs
Understanding Stimulant Drugs

... circulation- an effect that historically has made cocaine the preferred local anesthetic agent for eye surgery and other delicate procedures. The local anesthetic effects of cocaine are most pronounced when it is applied to the skin or mucous membranes. Thus, when cocaine is “snorted” it temporarily ...
Bactericidal Activity and Resistance
Bactericidal Activity and Resistance

... phenotype, all strains exhibited a ⱖ3-log10 decrease in viable counts and, in most cases, exhibited about a 5-log10 decrease when they were exposed to ⱖ1 ␮g/ml of dalbavancin for 24 h. Two strains (one MSSA strain and one MRSA strain) were also killed to that extent by the lowest dalbavancin concent ...
DUinventory_October2..
DUinventory_October2..

... This report shows the results of one of the goals set by the PROTECT project: to build up an inventory on national drug consumption databases across Europe. The interest behind this inventory is to collect information on sources of drug utilisation data across Europe from a researcher’s point of vie ...
Wrath Thor UNSIN
Wrath Thor UNSIN

... side effects would occur as a result of dispersed ligand binding throughout the brain. Furthermore, literature indicates that 5-HT1B receptors can elicit contrasting behavioural effects depending on their location. For example, in the prefrontal cortex, they function as terminal receptors that inhib ...
Antibiotics
Antibiotics

... – wasn't able to find the "magic bullet” ...
Cocaine Addiction
Cocaine Addiction

... sending a signal to that neuron. Drugs of abuse are able to interfere effects. Regularly snorting cocaine, for example, can lead to loss of with this normal communication process. For example, scientists have sense of smell, nosebleeds, problems with swallowing, hoarseness, and discovered that cocai ...
Molly: The Not So Convincing Truth of MDMA
Molly: The Not So Convincing Truth of MDMA

... have lurked in the shadows, scaring off anyone who has a ‘decent’ amount of common sense. However, these rumors are just that- rumors. The truth is, the long held stigmas about MDMA have little support through scientific evidence and the opposite may in fact be true- MDMA should not be a schedule 1 ...
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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.
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