• Study Resource
  • Explore Categories
    • Arts & Humanities
    • Business
    • Engineering & Technology
    • Foreign Language
    • History
    • Math
    • Science
    • Social Science

    Top subcategories

    • Advanced Math
    • Algebra
    • Basic Math
    • Calculus
    • Geometry
    • Linear Algebra
    • Pre-Algebra
    • Pre-Calculus
    • Statistics And Probability
    • Trigonometry
    • other →

    Top subcategories

    • Astronomy
    • Astrophysics
    • Biology
    • Chemistry
    • Earth Science
    • Environmental Science
    • Health Science
    • Physics
    • other →

    Top subcategories

    • Anthropology
    • Law
    • Political Science
    • Psychology
    • Sociology
    • other →

    Top subcategories

    • Accounting
    • Economics
    • Finance
    • Management
    • other →

    Top subcategories

    • Aerospace Engineering
    • Bioengineering
    • Chemical Engineering
    • Civil Engineering
    • Computer Science
    • Electrical Engineering
    • Industrial Engineering
    • Mechanical Engineering
    • Web Design
    • other →

    Top subcategories

    • Architecture
    • Communications
    • English
    • Gender Studies
    • Music
    • Performing Arts
    • Philosophy
    • Religious Studies
    • Writing
    • other →

    Top subcategories

    • Ancient History
    • European History
    • US History
    • World History
    • other →

    Top subcategories

    • Croatian
    • Czech
    • Finnish
    • Greek
    • Hindi
    • Japanese
    • Korean
    • Persian
    • Swedish
    • Turkish
    • other →
 
Profile Documents Logout
Upload
St. Michael`s/U of T Presentation Template
St. Michael`s/U of T Presentation Template

... • UF is an alternative to diuretics for removing fluid • Well tolerated with respect to renal function, although can remove fluid too quickly/too much • No known effects on drug concentrations determined to date ...
Phyto Lec 16
Phyto Lec 16

... 2 types of compounds; either semi-synthetic from morphine structure by 1)replacing OHs on the 3&6 positions most properly get morphine agonist "with similar activity, lower side effects, more potent than morphine" or 2)substituting on N most properly get morphine antagonist. Here we have new termino ...
The Major Narcotics
The Major Narcotics

... Most effective IV (heroin 100 times more potent IV than orally) ...
Neuromuscular Blockers Joanne Leung
Neuromuscular Blockers Joanne Leung

... Isoquinoline derivatives - d-tubocurarine Steroid derivatives - pancuronium ...
Delirium - Canadian Society of Hospital Pharmacists
Delirium - Canadian Society of Hospital Pharmacists

Drug-like properties and the causes of poor solubility
Drug-like properties and the causes of poor solubility

... the completion of human Phase I clinical trials. Compounds that survive through Phase I and into Phase II clinical efficacy studies are conveniently identified by the presence of a United States Adopted Name (USAN), International Non-Proprietary Name (INN). Some of these may be New Chemical Entities ...
First Dose in Humans
First Dose in Humans

... Position paper on the non-clinical safety studies to support clinical trials with a single micro dose (2003, R1 2004) Strategies to identify and mitigate risks for first-in-human clinical trials with investigational medical products (2007) Non-clinical studies required before first clinical use of g ...
here - National Medicinal Chemistry Symposium
here - National Medicinal Chemistry Symposium

... Volume  of  distribution  is  the  pharmacokinetic  parameter  that  relates  concentrations  in  blood/plasma  to  the  amount  of  drug  in  the  body  at  any  given  time  after  dosing.  It  is  an  important  parameter  because  in  combination  with  clearance,  it  drives  half‐life  and  co ...
GI Drugs
GI Drugs

...  Uses: antiemesis associated with anesthesia and motion sickness; pre/post-op sedation  Side effects: sedation is prominent side effect  Contraindications: children <2, due to fatal respiratory depression and sleep apnea Other anti-emetics used during chemotherapy and surgery o Aprepitant  MOA: ...
Targeting the androgen receptor in the
Targeting the androgen receptor in the

... not necessarily signify significant disease progression and argues for a consideration of maintenance or continuation of therapy in future trials. Future development plans for aa focus on assessing the drug in combination with a wide range of chemotherapeutic, biologic, immunologic, and hormonal age ...
Is there a role for EGFR Tyrosine Kinase Inhibitors in recurrent
Is there a role for EGFR Tyrosine Kinase Inhibitors in recurrent

...  Cohort A will include 32 patients at first recurrence with EGFRVIII mutations.  Cohort B will include 32 patients at first recurrence with EGFR gene amplification but no EGFRVIII mutation ...
No Tolerance to Peripheral Morphine Analgesia in
No Tolerance to Peripheral Morphine Analgesia in

... and antiinflammatory actions in inflamed tissue of animals (reviewed in references 8, 9); intraarticular (i.a.) morphine produces potent clinical analgesia after surgery of the knee joint (reviewed in reference 10) and these effects are mediated by opioid receptors outside the CNS. Animal experiment ...
Shormones
Shormones

Effects of endocannabinoid neurotransmission modulators on brain
Effects of endocannabinoid neurotransmission modulators on brain

... release sites may result in a more selective pharmacological response than the stimulation of CB1 receptors by direct agonists, as mentioned above. This strategy would lead to enhanced levels of endocannabinoids only “on demand,” i.e., when their production and release is recruited. Several compound ...
Adreno-cortico-steroids, Inhibitors, and Antagonists
Adreno-cortico-steroids, Inhibitors, and Antagonists

... ➨ Explain the mechanism of the anti-inflammatory, immunosuppressive and antineoplastic action of glucocorticoids ➨ Describe the factors that regulate aldosterone secretion. ➨ Describe the main features of the pharmacokinetics of corticosteroids. ➨ List the routes of administration of corticosteroids ...
Morphine
Morphine

... opium poppy can be used to relieve pain and treat diarrhea.  In 1806, Morphine was first isolated from the juice of the opium poppy by German pharmacist Friedrich Sertürner.  During the 1950s, a series of morphine-like potent analgesics were synthesized, such as pethidine,methadone, etorphine,fent ...
Slide 1
Slide 1

... benchmarked against historical parameters — Absolute probability of approval as well as comparison to similar agents ...
Incretin based therapy in type 2 diabetes
Incretin based therapy in type 2 diabetes

Association study of 37 genes related to serotonin and dopamine
Association study of 37 genes related to serotonin and dopamine

... cocaine. Both environmental and genetic factors underlie this disorder. Although some studies have estimated a heritability of cocaine dependence around 60–70% (Kendler & Prescott 1998; Kendler et al . 2000), genetic susceptibility factors are not well understood. Several processes, such as reward a ...
An Introduction to Medicinal Chemistry
An Introduction to Medicinal Chemistry

... This text is aimed at undergraduates who have a basic grounding in chemistry and are interested in a future career in the pharmaceutical industry. It attempts to convey something of the fascination of working in a field which overlaps the disciplines of chemistry, biochemistry, cell biology, and pha ...
View Full Text-PDF
View Full Text-PDF

... today for the treatment of bacterial infections and those caused by other microorganisms, sulfa drugs achieve this bacteriostatic action by inhibiting the synthesis of folic acid in bacteria. The current study has the aim of Synthesis of some of sulfa drug compounds and Study the biological activity ...
15. Annie Smartt - California Cornflakes and Brown Sugar: The Genetic Predisposition to Heroin and Cocaine Addiction
15. Annie Smartt - California Cornflakes and Brown Sugar: The Genetic Predisposition to Heroin and Cocaine Addiction

... The 118G allele of A1186 single nucleotide polymorphism (SNP) mutation is positively associated with heroin abusers (Yuferov, V. et al 2010.) It is the most studied polymorphism of the OPRM1 gene. The variant 118AàG removes the N glycosylation site in OPRM1 extracellular domain. With this loss of a ...
PASS assisted search and evaluation of some azetidin-2
PASS assisted search and evaluation of some azetidin-2

... tremors induced by reserpine. It further supports the dopaminergic agonism by the test compound as reserpine induces oral dyskinetic features by depleting catecholamine (dopamine and nor- epinephrine). Conclusion: It was concluded that azetidinones possess considerable CNS activities and can be furt ...
Document
Document

... The augmented effects of drug are too strong to induce harm following increasing dose (normal dosage). ...
6- Diuretics
6- Diuretics

... 1- -SO2NH2 group hypersensitivity 2- Ototoxicity So care must be noticed when used with aminoglycosides. 3-NSAIDs may blunt the natriuresis produced by loop diuretics in patients with preexisting impaired renal function who are on diuretic therapy NSAIDs may increase the risk of renal ...
< 1 ... 31 32 33 34 35 36 37 38 39 ... 107 >

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.
  • studyres.com © 2026
  • DMCA
  • Privacy
  • Terms
  • Report