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1% - ISpatula
1% - ISpatula

Incretin based therapy in type 2 diabetes
Incretin based therapy in type 2 diabetes

АНАЛГЕЗИВНІ ЗАСОБИ
АНАЛГЕЗИВНІ ЗАСОБИ

Structure-based drug design strategies in medicinal
Structure-based drug design strategies in medicinal

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6-作用于神经系统的药物

Smoking Cessation chapter from CPhA`s Therapeutic Choices
Smoking Cessation chapter from CPhA`s Therapeutic Choices

Anti Histamin H 1 receptor antagonists
Anti Histamin H 1 receptor antagonists

... • Beneficial effects of capsaicin have been reported in chronic, localized pruritic disorders, particularly those of neuropathic origin, • Initial application causes an intense transient burning sensation at the application site which may lead to poor compliance or premature cessation of treatment; ...
D-Cycloserine in Neuropsychiatric Diseases: A
D-Cycloserine in Neuropsychiatric Diseases: A

... meaning that in vivo, it acts like an agonist at low doses but has antagonistic features with high doses. This seems to be due to its different receptor subtype selectivity and intrinsic action, which depends on various NR2 subunits (NR2A, NR2B, NR2C), the location of glutamate binding (Dravid et al ...
St. Michael`s/U of T Presentation Template
St. Michael`s/U of T Presentation Template

... Can have pacing capabilities Can be combined with ICD Impact on drug therapy – Implantation – holding of anticoagulation – Post – improvement in symptoms – decrease in furosemide ...
The Health Effect of Psychostimulants: A Literature Review
The Health Effect of Psychostimulants: A Literature Review

... specific societies in east-Africa for its psychostimulant properties. Psychostimulants (e.g. sibutramine) can be prescribed to lower appetite in obesity. This can be considered the pharmacologic part of the treatment of a huge epidemic of obesity (BMI > 30) which increased from 23% of the population ...
Analgesics, Opioid Antagonists, and Nonopioid Centrally Acting
Analgesics, Opioid Antagonists, and Nonopioid Centrally Acting

... Preparations, dosage, and administration • Usually oral (formulated alone or with aspirin or ...
benzoyl benzoic acid based 1,3,4-oxadiazole analogues
benzoyl benzoic acid based 1,3,4-oxadiazole analogues

... therapeutic agents due to their anti-inflammatory, analgesic and antipyretic effects. The biological activity of NSAIDs is associated to suppression of prostaglandin biosynthesis by inhibiting the enzyme cyclooxygenase (COX).COX is an endogenous enzyme which catalyzes the conversion of arachidonic a ...
Levodopa
Levodopa

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Curr.Med. Chem._Martínez, A._2015 - digital

... Many different compounds have been designed and synthesized following this strategy [33]. In general, the pattern shows in Fig.3 is followed for the design of bitopic inhibitors. The design contains three different chemical features: a known and small AChE inhibitor to interact with the catalytic si ...
tobacco smoking.
tobacco smoking.

... on the health of infants and children. Disease risks from smoking by women have risen over the last 50 years and for many tobacco-related diseases are now equal to ...
6 State of New Product Development (as of May 8, 2012)
6 State of New Product Development (as of May 8, 2012)

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Hypertension

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Bioassays

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Opioids - David Kan, MD

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... A Powerful Drug Teens who use tobacco are at a greater risk for forming an addiction to tobacco. Some of the behaviors that indicate a person may be addicted to tobacco use include the following: • Needing tobacco at certain times of the day, such as after a meal • Becoming irritable or restless if ...
Desensitization of Cannabinoid-Mediated Presynaptic Inhibition of
Desensitization of Cannabinoid-Mediated Presynaptic Inhibition of

... degree of desensitization was dependent on the level of receptor activation. Treatment with Win55,212-2 for 24 h Markedly Desensitizes Inhibition of Excitatory Synaptic Transmission by Cannabimimetic Drugs. Acute treatment with Win55,212-2 (100 nM) completely inhibited 0.1 mM [Mg2⫹]oinduced [Ca2⫹]i ...
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Chemosensory organs

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DISCUSSION  197
DISCUSSION 197

... alpha-2 decreasing properties found in the present study. Early pharmaco-EEG research on LSD had also shown decreases in alpha activity after acute drug administration (Itil and Fink, 1966). Amphetamine, on the other hand, is known to enhance alpha in addition to its slow wave dampening effects, a f ...
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Nicotinic agonist



A nicotinic agonist is a drug that mimics the action of acetylcholine (ACh) at nicotinic acetylcholine receptors (nAChRs). The nAChR is named for its affinity for nicotine.Examples include nicotine (by definition), acetylcholine (the endogenous agonist of nAChRs), choline, epibatidine, lobeline, varenicline and cytisine.
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