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Pharmacology 3a – Cholinomimetics
Pharmacology 3a – Cholinomimetics

... A cholinomimetic drug is one that mimics the action of acetylcholine. They are clinically important because they act on post-ganglionic muscarinic receptors. s NB:  ACh is of no therapeutic use as it does not differentiate between nicotinic and muscarinic receptors and is rapidly degraded  Nicotin ...
Print
Print

... th aspirin than ii Orally, not much potential for abuse Opioid--like at high doses, intravenous Opioid ...
hypertension
hypertension

... antioxidant/free radical scavenging properties. Carvedilol is a frequently selected drug for long-term treatment of CHF, and is approved as an antihypertensive as well. ...
The serotonin RECEPTOR antagonists NAN
The serotonin RECEPTOR antagonists NAN

... indicate that methamphetamine increased central serotonin (5-HT) levels more markedly than other psychomotor stimulants such as amphetamine or cocaine. However, several studies indicate that 5-HT agonists and uptake inhibitors did not produce any methamphetamine-like stimulus effects when administra ...
PDF - National Alliance for Medication Assisted Recovery
PDF - National Alliance for Medication Assisted Recovery

... is a long acting narcotic antagonist which is used for maintenance treatment. It works by binding to the receptor over a 24 hour period thus making any injection or administration of an opioid agonist ineffective. It must be emphasized that naltrexone does not have agonist properties it merely block ...
Immunosuppressants 2
Immunosuppressants 2

... • Hypertension; hyperlipedemia; Hyperkalemia; D.M; Osteoporosis Hirsutism and gum hyperplacia (So What) ...
New and Emerging Treatments in Pemphigus and Bullous
New and Emerging Treatments in Pemphigus and Bullous

... •  60  –  70%  of  BP  pts  have  elevated  serum  IgE •  25%  of  patientss  have  linear  deposits  of  IgE  at  the   epidermal  BM  on  DIF •  Omalizumab  is  a  humanized  monoclonal  AB  that  blocks   binding  of  IgE  to  its  receptors   •  Omalizumab  is  FDA  approved  for  treatmen ...
IVG. Well-established Second Messengers Ca++
IVG. Well-established Second Messengers Ca++

... can reduce heart rate without preventing the sympathetic nervous system from inducing vasoconstriction (because it acts at beta-adrenergic and not alpha) (alpha mediates vasoconstriction) ...
Psychopharmacology - the Peninsula MRCPsych Course
Psychopharmacology - the Peninsula MRCPsych Course

... Typical antipsychotics such as loxapine and chlorpromazine show equally high 5HT2A occupancy. Amisulpride is an effective atypical antipsychotic drugs but doesn’t have 5HT2A affinity. ...
Biosteres and You
Biosteres and You

...  “A lead compound with a desired pharmacological activity may have ...
Synaptic transmission & antipsychotic drugs
Synaptic transmission & antipsychotic drugs

... As effective as typical drugs on positive symptoms; better for negative symptoms (Bilder et al, 2002) More effective with treatment-resistant patients (DeNayer et al, 2003) Less risk of EPS, but other side effects may occur (e.g. blood disorders) ...
Norepinephrine
Norepinephrine

... bulkiness than agonist, so they said if we change the hydroxyls in catechol to something more hydrophobic then we make it antagonist. We extended the alkyl chain by one atom and we try to put many other atoms than carbon, the only atom that gives us the antagonist effect is O (ether linkage) . ...
The Use of iCell Cardiomyocytes with Cell-by
The Use of iCell Cardiomyocytes with Cell-by

... outcomes. An extensive literature search was performed to identify clinical studies that reported both the free plasma concentration of the test compound and the effects on QT interval prolongation. A.) Of the 35 QT prolonging compounds identified correctly by the assay we were able to collect data ...
Frank Vocci - Consumer Demand
Frank Vocci - Consumer Demand

... Quit Rate % ...
SCHIZOPHRENIA2001
SCHIZOPHRENIA2001

... SCHIZOPHRENIA has a genetic component. Genetics, however, is not the whole story. Concordance rate far less than 100%. Genetics may predispose an individual to developing SCHIZOPHRENIA. Environmental factors may interact with genetics to increase susceptibility. Therefore, there must be “unexpr ...
View Announcement  - Chi-Med
View Announcement - Chi-Med

... Sulfatinib clinical results and fruquintinib-savolitinib combination preclinical results to be presented at the 2015 AACR-NCI-EORTC Molecular Targets and Cancer Therapeutics conference London: Friday, 30 October 2015: Hutchison China MediTech Limited (“Chi-Med”) (AIM: HCM) today announces that Hutch ...
Adrenergic Agonists
Adrenergic Agonists

... Dopamine dilates renal and splanchnic arterioles by activating dopaminergic receptors, thus increasing blood flow to the kidneys and other viscera (see Figure 6.12). These receptors are not affected by α or β-blocking drugs. Therefore, dopamine is clinically useful in the treatment of shock, in whic ...
The use of cannabinoids in animals and therapeutic implications for
The use of cannabinoids in animals and therapeutic implications for

... precursors of the neutral cannabinoids, such as THC and cannabidiol) for veterinary purposes in Czechoslovakia already in the 1950s because of their antibiotic properties. The use of cannabinoids as antibiotic drugs, however, was not further investigated, although it has been shown that cannabinoids ...
Lecture 9 - Abercrombie 10/27 Notes
Lecture 9 - Abercrombie 10/27 Notes

... regions, sites for bond formation on some side chains, side chain group components as sites for protein phosphorylation. Secondary structure of protein determined by hydrogen bonds (transmembrane domains of proteins often have secondary structure of alpha-helices formed by runs of hydrophobic residu ...
Biacore™ concentration and ligand-binding analyses in late
Biacore™ concentration and ligand-binding analyses in late

... concentration with high precision Concentration analysis is vital in several process development steps: to determine the yield in cell cultures over time; for identification of suitable chromatography conditions; for monitoring of final purification processes; and in formulation studies. Concentrati ...
What is a “zebrafish”? - Charles R. Drew University of Medicine and
What is a “zebrafish”? - Charles R. Drew University of Medicine and

... placed into single wells of a multi well plate • Multi-plate illuminated from below with a 15w lightbox • Larvae given 5 minutes to ...
HU 210: A Potent Tool for Investigations of the Cannabinoid System
HU 210: A Potent Tool for Investigations of the Cannabinoid System

... The cloning of CB1 (26) and CB2 (101) receptors clearly established the molecular determinants of ligand binding and selectivity, as well as of their activation. CB receptors, which belong to the class of pertussis toxin-sensitive and G protein-coupled receptors, activate multiple intracellular sign ...
Activation instead of blocking mesolimbic dopaminergic reward
Activation instead of blocking mesolimbic dopaminergic reward

... prone individuals. While in vivo experiments using a typical D2 receptor agonist induce down regulation, experiments in vitro have shown that constant stimulation of the DA receptor system via a known D2 agonist results in significant proliferation of D2 receptors in spite of genetic antecedents. In ...
Benzodiazepine Metabolism and Pharmacokinetics
Benzodiazepine Metabolism and Pharmacokinetics

rhEGF-NLC
rhEGF-NLC

... Chronic wounds represent a major clinical challenge for the health care systems due to their increasing incidence. Currently, the risk of suffering from chronic wounds has increased alarmingly, resulting in about the 2 % of the total European Health budgets [1]. Therefore, the development of advance ...
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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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