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The future of pharmacological treatment. Anne Lingford-Hughes Professor of Addiction Biology, Imperial College.
The future of pharmacological treatment. Anne Lingford-Hughes Professor of Addiction Biology, Imperial College.

... Naltrexone significantly elevates activity during decisionmaking (immediate reward vs later reward) in the OFC: Same area previously shown to predict ‘later’ decisionmaking ...
PNB-0718
PNB-0718

... Require more nutrients, oxygen and removal of waste due to higher metabolic demand New blood vessels fulfill all these requirements ...
Drug Targets
Drug Targets

... • Not all small drug molecules act through specific receptors. • Some small drug molecules interacts non-specifically with lipopolysaccharides, carbohydrates and DNA For example: some group of compound used as narcotics or anaesthetics, the pharmacological effect is mainly related to physical rather ...
N receptors
N receptors

... types of subunits, two a subunits bind ACh for ligand gating • All other nAChRs, including those at the peripheral ganglia, have 2 a’s and 3 b’s ...
File - NorthStar Mental Wellness
File - NorthStar Mental Wellness

... North American Center for Continuing Medical Education, LLC (NACCME) is approved by the American Psychological Association to sponsor continuing education for psychologists. NACCME maintains responsibility for this program and its content. Physician assistants, nurse practitioners and nurses may par ...
1 Evaluation of Dual-Activity Opioid
1 Evaluation of Dual-Activity Opioid

... experiments determined that difluoroethyl is the superior flouro-ethyl substituents as its insertion as a side chain into the compound led to high activity, reduced basicity, and improved lipophilicity with minimal reduction in 5-HT5AR receptor affinity (Figure 6-2). Figure 6. ...
Terms and symbols - Guide to Pharmacology
Terms and symbols - Guide to Pharmacology

... pathways, it would be desirable to use a drug that acts only on the receptor or biological site of interest at all concentrations and doesn’t interact with others at any achievable concentration. Unfortunately, there are very few or no drugs with this ideal property. Fortunately, there are numerous ...


... critical motif for activity was the tripeptide WVG, tryptophan and valine represents a hydrophobic component next to an amide functionality of glutamine. A number of small molecules have been synthesised as potential drug candidates based on this structure. A caprolactam was used in place of the glu ...
Muscarinic AChR agonist
Muscarinic AChR agonist

...  Drugs targeting synthesis and release of NE and NA eg DBH inhibitors, reserpine - depletes stores  Drugs targeting reuptake at synapse eg cocaine, ...
Drug Intoxication and Withdrawal - CA
Drug Intoxication and Withdrawal - CA

... Chemically similar to stimulants Antidepressant, no wt gain or sexual dysfunction Abused intranasally; high similar to cocaine, but less intense • Seizure with high doses (>600 mg/d) • WD rare; anxiety, lethargy, irritability • Tx: gradual taper ...
The cannabinoids: An overview. Therapeutic implications in
The cannabinoids: An overview. Therapeutic implications in

... During the 1970s and early 1980s, it was generally assumed that the high lipophilicity of the cannabinoids was the cause of much of their pharmacological effects. The possibility that THC acts through specific receptors was dismissed due to the lack of stereospecificity of cannabinoid action (13,14) ...
OTC Drugs, Herbal Remedies and Other Stuff Chapter 14
OTC Drugs, Herbal Remedies and Other Stuff Chapter 14

... skin eruptions, heart palpitations, or postmenopausal uterine bleeding ...
SECONDARY METABOLITES ISOLATED FROM PEROVSKIA
SECONDARY METABOLITES ISOLATED FROM PEROVSKIA

... atom types, number of chiral centers, and number of rings and chains (Gao, 2010). Based on the results of this investigation, it was determined that natural products are significantly more diverse than combinatorial compounds (Gao, 2010). Furthermore, natural products have superior drug-like propert ...
drugs affecting the autonomic nervous system
drugs affecting the autonomic nervous system

... 2. the sympathetic fibers to the sweat gland and blood vessels of skeletal muscles are cholinergic. 3. all preganglionic synapses of the ans are cholinergic 4. these are also found in the pns and contols the voluntary skeletal muscle action. 5. they are also found in the cns. ...
PSYC 342: Psychopharmacology
PSYC 342: Psychopharmacology

... – Note CATIE and Cutlass studies reported in text • Claims for superior efficacy over 1st gens (for increased tolerability, superior performance with negative symptoms and in treatment refractory) not entirely supported. • Tolerability - similarly lousy compliance rates ...
Agents to Treat Gastric Acidity and Gastroesophageal Reflux (GERD)
Agents to Treat Gastric Acidity and Gastroesophageal Reflux (GERD)

... Omeprazole (Prilosec) Omeprazole/sodium bicarbonate (Zegerid) ...
ACh
ACh

... It directly combines with freeorganophosphates , prevents them further combine with AChE It has marked action on neuromuscular junctions and promptly inhibits fasciculation. Improves CNS symptoms  It can’t directly antagonize the accumulated ACh, therefore, it should be used with atropine ...
The Influence of Conformational Isomerism on Drug
The Influence of Conformational Isomerism on Drug

... specific agonists and/or antagonists for these receptors. By locking the molecule in either conformation A or B, it should be possible to elicit only the desired beneficial effect without the side effect or any other unnecessary effects. This knowledge could then be used to make affinity labels spec ...
DIABETIC ENTEROPATHY: TWO DIFFICULT PROBLEMS
DIABETIC ENTEROPATHY: TWO DIFFICULT PROBLEMS

... Domperidone p ...
Mainly 15-45 age range, but increasing in kids!
Mainly 15-45 age range, but increasing in kids!

... antagonist for many different postsynaptic receptors: dopamine receptors (subtypes D1, D2, D3 and D4): account for antipsychotic properties serotonin receptors (5-HT1 and 5-HT2): antiaggressive properties but also leading to weight gain, fall in blood pressure, sedation histamine receptors (H1 recep ...
JWH018, a common constituent of Spice herbal blends, is a potent
JWH018, a common constituent of Spice herbal blends, is a potent

... The cannabinoid receptor 1 (CB1) cannabinoid receptor (nomenclature follows Alexander et al., 2008) has been identified as the receptor that mediates the behavioural effects of THC in animals (Monory et al., 2007) and likely does so in humans (Huestis et al., 2001). The CB1 receptor is predominately ...
NON-INFECTIOUS DISEASES
NON-INFECTIOUS DISEASES

... Leukotriene antagonists (e.g. montelukast, zafirlukast) Glucocorticosteroids Many available for oral or aeorosol use (AEROSOL: beclamethasone, budesonide. fluticasone, triamcinolone, mometasone, ciclesonide – ORAL: prednisone, methylprednisolone, cortisone) ...
Drugs That Act in the Central Nervous System
Drugs That Act in the Central Nervous System

... schizophrenia and hospitalized. Haloperidol was started at a dose of 10 mg/d. On the second day, he was found to develop a “seizure”. His neck was strained backward with his face turned upward toward the ceiling. He was having difficulty speaking but was quite conscious of his surroundings. The atte ...
Under-Investigated Indications in Cannabis Therapeutics
Under-Investigated Indications in Cannabis Therapeutics

... Fig. 3. High-magnification view of different types of CB1 positive cells in the cochlear nucleus. A group of granule cells in the molecular layer of the dorsal cochlear nucleus (DCN) (A); a stellate cell (B), a cartwheel cell (C), a giant cell (D), a fusiform cell (E) and a corn cell (F) in the DCN; a ...
Caffeine
Caffeine

... Alkaloid found in the leaves of Erythroxylon coca. A shrub endogenous to the Andes. For more than 100 years it has been used a local anesthetic & to dilate the pupil in ophthalmology. Mechanism of action Blocks the uptake of DA, NE & 5HT. The reward effect of cocaine is due to the increase of DA con ...
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Cannabinoid receptor antagonist



The discovery of the endogenous cannabinoid system led to the development of CB1 receptor antagonists. The first cannabinoid receptor antagonist, rimonabant, was described in 1994. Rimonabant blocks the CB1 receptor selectively and it has been shown to decrease food intake and regulate body-weight gain. The prevalence of obesity worldwide is increasing dramatically and has a great impact on public health. The lack of efficient and well-tolerated drugs to cure obesity has led to an increased interest in research and development of cannabinoid antagonists. Cannabidiol, a naturally occurring cannabinoid, is a non-competitive CB1/2 antagonist.
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