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Neuromuscular Blocking Agents
Neuromuscular Blocking Agents

... Non-classical Blockade • Some drugs interfere without agonist or antagonist properties – Include inhaled anesthetic, local anesthetic or ketamine – Interfere with normal functioning of ach binding site and/or opening and closing of receptor channel – Closed channel blockade – Open channel blockade ...
28.2 Hormones and the Endocrine System
28.2 Hormones and the Endocrine System

... Homeostasis is as important to the study of living things as atomic structure is to the study of chemistry. Conditions such as body temperature, the availability of chemical compounds that supply energy, and the disposal of waste products must remain within specific limits for an organism to functio ...
Immune Functions of B Cells
Immune Functions of B Cells

... “ Let us […] imagine the despair of the mouse experimentalist when we suggest that he or she randomly allocate treatments to animals of different genetic backgrounds and immunized with different disease triggers.” ….[This is essentially how we treat RA in 2006] ...
PHAR 303 PHARMACEUTICAL CHEMISTRY I
PHAR 303 PHARMACEUTICAL CHEMISTRY I

... g/mol and a dose of 20 mg, this leads to a solution concentration of approximately 2 × 10−6 M (2 mM). When considering the solution behavior of a drug within the body, we are dealing with a dilute solution, for which the BrönstedLowry (8) acid–base theory is most appropriate to explain and predict a ...
Opioids OD fact sheet
Opioids OD fact sheet

... Pethidine: stronger kappa; some 5-HT (can cause SS); 50% BA; 60% protein bound; DOA 3hrs; more euphoria and addiction, seizures Fentanyl: rapid onset of action; DOA 30-40mins; serotonin syndrome Remifentanyl: rapid onset; assoc with muscle rigidity; HL 3-10mins; DOA 5-10mins Codeine: 66% BA Methadon ...
5-Hydroxytryptamine2C Receptor Contribution to m
5-Hydroxytryptamine2C Receptor Contribution to m

... implicated in mood and anxiety disorders and is a target for development of novel anxiolytic drugs (Wood, 2003). Selective and nonselective 5-HT2C receptor antagonists reduce anxiety-like behavior in several animal models of anxiety (Stutzmann et al., 1991; Kennett et al., 1995; Griebel et al., 1997 ...
Application of drugs based on release-active
Application of drugs based on release-active

... 2. the assessment of vital functions: 3.the assessment of main laboratory rangers: clinical blood analysis clinical urine analysis biochemical markers Data from regulatory bodies of countries where the drugs have been registered (15 countries) on adverse events associated with the drug use ...
Opioids and Sucrose: An Overview
Opioids and Sucrose: An Overview

... ► The existence of these receptors and the fact that opioid antagonists exert effects on opiate-naieve subjects lead to discovery of endogenous (naturally occurring in the brain) opioids. ► Beta-endorphin, enkephalins, dynorphins, more ...
Cannabis—A Valuable Drug That Deserves Better Treatment
Cannabis—A Valuable Drug That Deserves Better Treatment

... Hyperemesis is not an acute effect of cannabis smoking. In the case series reported by Simonetto et al,10 hyperemesis appeared in most patients after more than 2 years of smoking at least once a week. Surprisingly, most patients (83%) had lost weight (median loss, 12 kg), and 23% had diarrhea. These ...
Pharmacophore Approach in Drug Discovery
Pharmacophore Approach in Drug Discovery

... SOSA = Selective Optimization of Side Activities 1 – Start screening with a limited set of carefully chosen, structurally diverse, drug molecules (a smart library of about 1000 compounds). Already bioavailability and toxicity studies have been performed and as they have proven usefulness in human th ...
American Society of Clinical Oncology Guideline for Antiemetics in
American Society of Clinical Oncology Guideline for Antiemetics in

... dolasetron, and granisetron6; and from the Oregon Evidence-Based Practice Center’s recent systematic review of the range of available 5-HT3 serotonin receptor antagonists.9 Intravenous palonosetron became available in 2003. This agent was developed because of its longer serum half-life (about five t ...
Topic 1 Organic Structures and Interactions of Drugs
Topic 1 Organic Structures and Interactions of Drugs

... Orientation is beneficial if other binding groups are positioned correctly with respect to the corresponding binding regions Orientation is detrimental if the binding groups are not positioned correctly with respect to corresponding binding regions The strength of the interaction decreases with dist ...
Pharmacological Evidence of Hypotensive Activity of Somina
Pharmacological Evidence of Hypotensive Activity of Somina

... intravenous administration of Ach 10-4 M produced a 45 % fall in SBP, DBP and MAP as shown in Table 1 which remained for 35 ± 2.43 s. Intravenous administration of somina at the different doses of 5, 10, 15, 20, and 35 mg/kg was found to reduce the systolic, diastolic and mean arterial blood pressur ...
Slide Deck
Slide Deck

... [email protected] ...
Vitex agnus
Vitex agnus

... Vitex agnus-castus has a long tradition as a herbal remedy and was used in ancient times not only as an anaphrodisiac and for preserving chastity but also against diverse disturbances of the female genital system. In actual clinical trials, the fruit Agni casti fructus was shown to relieve premenstr ...
Quantum Molecular Design of Drugs
Quantum Molecular Design of Drugs

... optimized property. QM/MM calculations are performed on all of the conformers from the ligands chosen by the algorithm. The parameterized binding equation is used to get a binding score that will determine the direction along the property surface. In total, five runs with different initial starting ...
Pharmacology II - 3-14
Pharmacology II - 3-14

... Rate of ingress and egress from CNS b. Half-life c. Presence of active metabolites and their half-lives d. Frequency and chronicity of dosing a. ...
Is there a difference between an angiotensin
Is there a difference between an angiotensin

... trials with 958 000 people with hypertension mainly, but other cardiac conditions were also included in this meta-analysis.3 They concluded that the five major classes of blood pressure (BP)-lowering drugs had a similar effect in reducing coronary heart disease events and strokes for a given reducti ...
BALANCING ANTI-AMYLOID AND ANTI-CHOLINESTERASE CAPACITY IN A SINGLE CHEMICAL INSILICO Research Article
BALANCING ANTI-AMYLOID AND ANTI-CHOLINESTERASE CAPACITY IN A SINGLE CHEMICAL INSILICO Research Article

... prevent the challenge of administering multiple single-drug entities that could have different bioavailability, pharmacokinetics, and metabolism. Furthermore, in terms of pharmacokinetic and toxicological optimization, the clinical development of a drug able to hit multiple targets should not, in pr ...
Cannabinoid CB1 Receptor Antagonists as Promising New
Cannabinoid CB1 Receptor Antagonists as Promising New

... blocks the subjective effects of ⌬9-THC in humans and prevents relapse to smoking in exsmokers. Findings from both clinical and preclinical studies suggest that ligands blocking CB1 receptors offer a novel approach for patients suffering from drug dependence that may be efficacious across different ...
RT101 Basic Therapeutics
RT101 Basic Therapeutics

... Tolerance: A condition in which the dose of a drug must be increased (over time) to obtain the desired effect -or- a decreasing intensity of responsiveness to a drug over time Tachyphylaxis: Rapidly developing tolerance to a drug -or- a rapid decrease in responsiveness to a drug. Additive effects: T ...
Possible Endogenous Ligand of the Sigma
Possible Endogenous Ligand of the Sigma

... compounds activate the sigma-1 receptor. It was later shown in clinical trials that the hallucinogenic effects of the benzomorphans are prevented by naloxone [36,37], which blocks opiate receptors but not sigma-1 receptors. Thus, it is currently accepted [38] that the hallucinogenic effects of the b ...
drug treatment of gastric diseases of dogs and cats
drug treatment of gastric diseases of dogs and cats

... age. Dosage for motion sickness is 8 mg/kg PO q 24H. Dosage for acute vomiting is 1 mg/kg SC q 24 H for up to 5 days. The drug is metabolized via hepatic P450 enzymes. Safe drug and side effects are similar to placebo. It was more effective than metoclopramide in a European clinical study in reducin ...
Chapter 16 Cholinesterase Inhibitors
Chapter 16 Cholinesterase Inhibitors

... • Dark room with ice pack to neck ...
Delta-Opioid Ligands Reverse Alfentanil
Delta-Opioid Ligands Reverse Alfentanil

... colleagues also found stimulatory effects of opioids on respiration; the fetal breathing movement of lamb was stimulated by lower doses of DPDPE and deltrophin I (Cheng et al., 1992, 1993a, b). The involvement of the kappa receptor in respiratory control seems to be minimal (Pfeiffer et al., 1983; B ...
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NK1 receptor antagonist

Neurokinin 1 (NK1) antagonists are a novel class of medications that possesses unique antidepressant, anxiolytic, and antiemetic properties. The discovery of neurokinin 1 (NK1) receptor antagonists was a turning point in the prevention of nausea and vomiting associated with cancer chemotherapy.An example of a drug in this class is aprepitant. Chemotherapy-induced emesis appears to consist of acute and delayed phases. So far, the acute phase emesis responds to 5-HT3 antagonists while the delayed phase remains difficult to control. The discovery and development of NK1 receptor antagonists have elicited antiemetic effect in both acute and especially in delayed phases of emesis.The first registered clinical use of NK1 receptor antagonists was the treatment of emesis, associated with cancer chemotherapy.
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