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Asthma
Asthma

... Zileuton: potential drug interactions • Zileuton decreases clearance of theophylline and increases AUC and Cmax. More adverse reactions to theophylline with zileuton. • Zileuton decreases clearance of propranolol and increases AUC and Cmax. There is increased beta-blockade and a greater decrease in ...
Benzodiazepines (not including sedative/hypnotics*)
Benzodiazepines (not including sedative/hypnotics*)

... comorbid depression and/or bipolar disorder in patients with panic disorder. Benzodiazepines are less effective than other available agents when panic disorder coexists with other mood disorders. Therefore, patients with panic disorder and other psychiatric comorbidities may benefit from short-term ...
Dr. Amani A. Noory Khartoum, Sudan
Dr. Amani A. Noory Khartoum, Sudan

... Cough is rare – no interference with bradykinin and other ACE substrates  Complete inhibition of AT1 – alternative remains with ACEs  Result in indirect activation of AT2 – vasodilatation (additional benefit)  Clinical benefit of ARBs over ACEIs – not known  However, losartan decreases BP in hyp ...
(HMG-CoA) REDUCTASE INHIBITORS ON THE CYP3A4
(HMG-CoA) REDUCTASE INHIBITORS ON THE CYP3A4

... values of itraconazole using human liver microsomes and applied them to a pharmacokinetic model (Ito et al., 1998), together with pharmacokinetic parameters for itraconazole. As a result, we have found that the predicted increase in plasma levels of simvastatin by concomitant administration of itrac ...
PHL 424 5th S
PHL 424 5th S

...  Lincomycin, although structurally distinct, resembles erythromycin in activity, but it is toxic and no longer used ...
Potential Part D Drug-Drug Interactions
Potential Part D Drug-Drug Interactions

... muscle movement, psychosis, hypotension, coma and death have been associated with combination. CoAdministration is contraindicated. Sympathomimetic drugs with indirect activity can release large quantities of norepinephrine, which accumulates during monoamine oxidase inhibition and produces excessiv ...
Coagulation
Coagulation

... Haemostasis ...
Chemotherapy regimen: Hyper CVAD
Chemotherapy regimen: Hyper CVAD

... One study evaluated the clinical impact of co-administration of cART with CHOP (cyclophosphamide 750 mg/m2, doxorubicin 50 mg/m2, vincristine 1.4 mg/m2 [max 2 mg], prednisone 100 mg/m2) in the context of treatment for non-Hodgkin’s lymphoma. In comparison to hyper CVAD, vincristine and cyclophospham ...
Overview of Tenofovir`s Anticipated Adverse Events and Resistance
Overview of Tenofovir`s Anticipated Adverse Events and Resistance

... Monkey studies: virus initially transmitted is usually not drug-resistant, but resistance is more likely with time if the PrEP ARV is continued Mothers who took single dose nevirapine for pMTCT and developed nevirapine resistance: no decrease in response to ARV treatment if initiated after 6 months ...
Discovery of PF-04457845: A Highly Potent
Discovery of PF-04457845: A Highly Potent

... central tissues, an irreversible inhibitor may be beneficial because the nonequilibrium binding mechanism limits the competition with high endogenous substrate concentrations leading to increased biochemical efficiency.24 Furthermore, the pharmacodynamic effect resulting from covalent inhibition oft ...
Test Set - Focus Synthesis LLC
Test Set - Focus Synthesis LLC

... the ability of TIDEA to identify active kinase inhibitors in collaboration with Focus Synthesis. He designed and screened a diverse, 181-molecule subset of a 3186-molecule kinase-targeted library using Src, Abl, and Hck kinases and identified 27 hits (>20% inhibition for 1 or more kinases). The TIDE ...
March 08, 2012 Meeting Summary - Posted 04/11/2012
March 08, 2012 Meeting Summary - Posted 04/11/2012

... was provided with a general overview of the drug class including the indications and clinical considerations, clinical guidelines for the use in asthma treatment, and current NYS prospective and retrospective utilization review system edits. The Board was also provided with the NYS Medicaid informat ...
Cylene Builds on Success, Presents Second CK2 Inhibitor at AACR
Cylene Builds on Success, Presents Second CK2 Inhibitor at AACR

... profile the small molecule CK2 inhibitor, CX-8184, at the 2012 American Association for Cancer Research (AACR) annual meeting, held from March 31 to April 4 in Chicago, IL. The presentation will highlight the agent’s potent and sustained suppression of protein kinase CK2, its impact on multiple key ...
Materials(PDF 3.8 MB)
Materials(PDF 3.8 MB)

...  EPHA2 is known to be highly expressed in multiple tumors ...
Pharmacy_Lecture_08_..
Pharmacy_Lecture_08_..

... acidic, but not carboxylic acid-containing (salicylic acid) structurally novel compounds. • Measurement of a physical property (pKa) as well as serum half-life in dogs was the guide for the synthesis program. • Several generations of leads were refined and ultimately led to a successful structure wi ...
Print this article - Journal of Applied Pharmaceutical Research
Print this article - Journal of Applied Pharmaceutical Research

... Carbohydrate digestion Starch is composed of amylose, which is a linear alpha-1,4linked glucose polymer, and highly branched amylopectin consisting of linear alpha-1,4-linked glucose chains with alpha1,6-linked branch chains. Salivary and pancreatic alphaamylases catalyze the endo-hydrolysis of alph ...
Tutorial - 3: Diuretics
Tutorial - 3: Diuretics

... 22. Diuretic drug/s ________________ can also be used for the treatment of anion overdose, hyperkalemia and hypercalcemia. 23. Compounds ________________ can block Na+ / K+ / 2Cl- cotransporter at site ________ in the _____________________________________________ of the nephron. 24. The diuretics dr ...
Cardiovascular Drugs and Therapies HMG CoAa REDUCTASE
Cardiovascular Drugs and Therapies HMG CoAa REDUCTASE

... bedtime evening meal ...
ISOLATION AND IDENTIFICATION OF α-GLUCOSIDASE, α-AMYLASE AND LIPASE INHIBITORS
ISOLATION AND IDENTIFICATION OF α-GLUCOSIDASE, α-AMYLASE AND LIPASE INHIBITORS

... those reported to the cinnamic acid derivative known as integrifoliodiol [14]. The other compounds were identified as limonin (3) [10], scopoletin (5) [18] and skimmianine (6) [13] by comparing their 1H and 13C NMR data with those reported previously. Effects of the compounds on α-amylase, α-glucosi ...
Diuretic - e
Diuretic - e

... spironolactone (synthesis steriod),  eplerenone (spironolactone analog) ...
Syncope secondary to second-degree atrioventricular block with
Syncope secondary to second-degree atrioventricular block with

... Aneley Hundae, MD, Aasim Afzal, MD, Manish D. Assar, MD, and Jeffrey M. Schussler, MD ...
Generic Name - UHN Research
Generic Name - UHN Research

... bedtime evening meal ...
CAFERGOT
CAFERGOT

... described as 62% in a study of elderly subjects. However, there appears to be extensive first pass metabolism. A study using rectal suppositories revealed low and variable plasma levels of ergotamine. Bioavailability is < 5% from both oral and rectal formulations. It has been suggested that the ther ...
O-13928 DD Combining Targeted Agents Poster Handouts 2nd
O-13928 DD Combining Targeted Agents Poster Handouts 2nd

... • Kinase inhibitors as well as RNAi were used for validation of the pathway, and to analyze possible combinatorial effects when used in tandem. • Small molecule kinase inhibitors tested against components of the EGFR pathway show potency at the receptor level (e.g. AG1478, PD153035) as well as cytoso ...
Hydrogen Bonding: The Last Mystery in Drug Design?
Hydrogen Bonding: The Last Mystery in Drug Design?

... hydrogen bond and a mutual repulsion of the two electronegative oxygen atoms. On the other hand, it has been predicted that –CH2– analogues should have about the same affinities as the –NH– analogues, which turned out to be true – one of the rare cases of a correct quantitative prediction from molec ...
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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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