How does MDMA inhibit cytochrome P450 ?
1a.) Drug C goes through the cytochrome P450 enzyme. Drug D is anti-inducer of cytochrome P450. A patient has been using Drug C with good results. The patient has now started therapy with Drug D. What will happen to the concentrations of Drug C? (Choices: Increase, Decrease, Stay the same, Not enough info given) 1b.) Drug C goes through the cytochrome P450 enzyme. Drug D is an inhibitor of cytochrome P450. A patient has been using Drug D with good...
(9) What is the difference in the proximal ligand between myoglobin and cytochrome P450? (10) In the cytochrome P450 reaction mechanism, what has to happen after the oxygen (O2) binds to the iron, before it can form one of the transient and highly reactive species (iron(lI)-peroxo, iron(lIlI)-hydroperoxo or high valent iron-oxo)? (9) What is the difference in the proximal ligand between myoglobin and cytochrome P450? (10) In the cytochrome P450 reaction mechanism, what has to happen after the oxygen (O2)...
Which of the statements about Cytochrome P450 biotransfomations of xenobiotics are true (select all that apply)? A. The highest tissue levels of CYP450 enzymes is in the small intestines B. Dietary intake can induce the activity of CYP450 enzymes C. Poor biotransformation of a xenobiotic can be due to a mutation in a cytochrome P450 enzyme D. CYP450 enzymes catalyze the glucoronidation of xenobiotics E. Cytochrome P450 enzymes can be inhibited by xenobioticsCYP450
Cyclophosphamide (CPA) is an anticancer prodrug that requires activation in the liver by cytochrome P450 2B enzymes for production of cytotoxic metabolites. Site-specific mutagenesis is used to alter the amino acid sequence of P450 2B1 The results are as follows. an attempt to improve the kinetics of CPA activation. The rate of reaction of CPA is studied using rat P450 2B1 and a site-specific variant of P450 2B1 produced using Escherichia coli. Initial Reaction Velocity (mol min mol1 P450) Initial...
Sodium azide is known to inhibit Cytochrome c Oxidase. Using sodium azide at a concentration of 2 µM, you run an enzyme assay. After careful data analysis, you determine the following values. Vmax = 50 µM/sec Vmax(app) = 50 µM/sec Km = 6 µM Km (app) = 18 µM Determine the type of inhibition present. Calculate the associated Ki(a), and (or) Ki(b), if applicable. Show your work.
does unc-76 gene promote or inhibit axon outgrowth?
12. (1.5) Azides are used as propellants in airbags, but they can inhibit the function of the heme group found within cytochrome oxidase (complex IV) of the ETC. There have been some repo azide intoxication in car crash victims, and the victims often have increased lactic acid levels in their brains. Explain why the increased lactate is observed, including all the products of all the relevant pathways rted cases of
How many moles of the protein cytochrome C (MW = 13,000) are there in 10 ngs of the substance?
antidiuretic hormone does not increase thirst cause water to shift out of the icf inhibit water intake increase ecf sodium concentration increase ecf volume
Aspirin & Vioxx are both NSAIDs. They inhibit which enzyme? How are they different?