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Phosphodiesterase 4-targeted treatments for autoimmune diseases R E V I E W
Phosphodiesterase 4-targeted treatments for autoimmune diseases R E V I E W

... studied as an antidepressant several years before the discovery of its potent PDE4 inhibitory activity [24,25]. Despite its potent anti-inflammatory effects in vitro, clinical trials were associated with unacceptably high rates of adverse events, specifically nausea and vomiting [26]. Roflumilast ...
coagulation final 2
coagulation final 2

... residues of factors II, VII, IX, X ...
View/Open - University of Khartoum
View/Open - University of Khartoum

... (Human Intestinal Absorption), Caco-2 cell permeability and AMES test were calculated. The results obtained for BBB penetrability greatly agreed with structures of the studied compounds. Only Parthenolide, a less polar sesquiterpene lactone, was predicted to cross BBB. It was also found that all tes ...
张纬萍_Caner chemotherapy
张纬萍_Caner chemotherapy

... of estrogen receptor), for early-stage and metastatic breast cancer. Chemopreventive for women at high risk for breast cancer. - Flutamide(氟他米特) and bicalutamide(比卡 鲁胺), nonsteroidal antiandrogen agents, for early-stage prostate cancer and in the setting of metastatic prostate cancer. ...
Respiratory Drugs 2 - Suny-perfusion
Respiratory Drugs 2 - Suny-perfusion

... • Headache is the most frequently reported adverse effect. There are also a few reports of liver toxicity (elevated liver enzymes) with this drug. ...
Suggestion from clinicians
Suggestion from clinicians

... ACE inhibitors. When the different ACE inhibitors are compared, there is a remarkable similarity in their BP lowering effects at trough. When the best estimate of the BP lowering efficacy of these 14 drugs is compared, they range from -6/-4 mm Hg to -9/-5 mm Hg. The data are most consistent with the ...
NEW ANTICOAGULANTS
NEW ANTICOAGULANTS

... drug, but may be slightly prolonged. Low bleeding incidence. Has not been shown to cause HIT No direct inhibitor for Arixtra which can reverse it’s anticoagulant effect. May be monitored by an Anti-Xa method using the drug as a calibrator. ...
iPPI small molecule inhibitor of Protein
iPPI small molecule inhibitor of Protein

... orally available are known at this time) or can be allosteric inhibitors, thereby binding at, near or far away from the interface in cavities with recognition characteristics that could be highly similar to enzyme active sites. It would seem logical to explore and attempt to rationalize the propert ...
Growth Factor Receptor inhibitors
Growth Factor Receptor inhibitors

... (cisplatin most toxic), renal toxicity (cisplatin), myelosuppression, peripheral neuropathy (oxaliplatin) ...
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Antipsychotics Antimanics Antidepressants

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New TKI toward highly targeted therapies

... •Pan Bcr-Abl inhibitor (WT+ t315i + other mutated forms •Binding to the inactive form + ethinyl linkage (C≡C) •FDA-approved dec. 2012 ; Ariad ...
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Final Presentation

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COX 2 Inhibitors: New Non-Steroidal Anti

... efficacy studies rather than specifically designed toxicity studies.6,13,14 Of the peerreviewed studies published to date, the rate of ulceration with celecoxib was similar to that found with placebo. It remains to be seen whether the reduction in endoscopic ulcer rate observed with celecoxib will t ...
Nonsteroidal Anti-inflammatory Drugs
Nonsteroidal Anti-inflammatory Drugs

... thrombotic events with some of them as rofecoxib. ...
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Antileishmanial activity of HIV protease inhibitors

... The effects of the two PI, indinavir (Merck; a kind gift of S. Vella, Rome, Italy) and saquinavir (BS 00120083; a kind gift of Roche, Basel, Switzerland), on promastigotes of L. major and L. infantum were assessed by a method similar to that previously described [17]. Promastigotes were counted usin ...
Inhibitors of Microbial Protein Synthesis
Inhibitors of Microbial Protein Synthesis

... - Food, Mg++, AL+++ and Ca++ (milk) form complexes with tetracyclines ↓ absorption of tetracyclines ...
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503 paper

... doses less than 600 mg/day and diarrhea and rash were the most common. There was antitumor activity at all levels of dosing, but at 250 mg/day there is the best balance between anticancer activity and ill effects.5 Also, they found that the mean half-life of the drug was 30.5 hours, which confirms t ...
Drugs used to treat anxiety BENZODIAZEPINE DOSE
Drugs used to treat anxiety BENZODIAZEPINE DOSE

... disadvantages between classes ...
Drugs used to Treat Depression
Drugs used to Treat Depression

... • Developed in the late 1970’s and 1980’s • Maprotiline – one of the first clinically available antidepressants, has a long half life and blocks NE reuptake • Amoxapine – primarily a NE reuptake inhibitor • Trazodone – not a potent blocker of NE or 5-HT, its active metabolite blocks a subclass of 5- ...
Slajd 1 - Zakład Farmakologii Klinicznej w Poznaniu
Slajd 1 - Zakład Farmakologii Klinicznej w Poznaniu

... Recommendation: the use of low-dose ASA for cardioprophylaxis is associated with a 2-4 – fold increase in UGIE. Enteric-coated preparations do not reduce the risk of bleeding. For patients at risk of adverse events, gastroprotection should be prescribed. The risk of UGIE increases with dose of ASA; ...
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Hypertensive patients with concomitant diseases

... The loop diuretics act promptly, even in patients with poor renal function or who have not responded to thiazides or other diuretics. Loop diuretics cause decreased renal vascular resistance and increased renal blood flow. \[Note:Loop diuretics increase the Ca2+ content of urine, whereas thiazide di ...
Medical Pressure
Medical Pressure

... • Enalapril , ramipril are prodrugs, converted to the active metabolite in the liver • Have a long half-life & given once daily • Enalaprilat is the active metabolite of enalapril given by i.v. route in hypertensive emergency. ...
Protein Synthesis Inhibitors
Protein Synthesis Inhibitors

... Intraperitoneal/intrapleural high dose; myasthenia gravis patients at risk ...
MONOAMINE OXIDASE INHIBITORS: CLINICAL PROFILE OF
MONOAMINE OXIDASE INHIBITORS: CLINICAL PROFILE OF

... defensive medicine precludes its use. Recent studies in U. K. and Canada have shown that patients with phobic anxiety, atypical depression, panic attacks, and phobiai. do respond well to MAOI treatment if used in appropriate dosages (e.g., phenelzine 60 mg/day). The following three case histories il ...
Protein Synthesis Inhibitors
Protein Synthesis Inhibitors

... Intraperitoneal/intrapleural high dose; myasthenia gravis patients at risk ...
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Metalloprotease inhibitor

Metalloprotease inhibitors are cellular inhibitors of the matrix metalloprotease (or metalloproteinase) family of proteins (MMP).Several other proteins have similar inhibitory effects, however none as effective (netrins, procollagen C-terminal proteinase enhancer (PCPE), reversion-inducing cysteine-rich protein with Kazal motifs (RECK) and tissue factor pathway inhibitor (TFPI-2)). They might have other biological activities which have yet been fully characterised.There are three classes of commonly used inhibitors for metalloproteinases. In vitro, EDTA, 1,10-phenanthroline and other chelating compounds lower the concentration of metal to the point where the metal is removed from the enzyme active site. Classical lock and key inhibitors such as phosphoramidon and bestatin bind tightly by approximating the transition state of the hydrolysis of the peptide, preventing it from acting on other substrates. Protein inhibitors such as α2-macroglobulin are known to work with metalloproteinases.↑
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