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shell vs. # orbitals vs. # electrons s p d f |
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s, 1, 2 p, 3, 6 d, 5, 10 f, 7, 14 |
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the hybridization for Carbons of Acetylene is___ the bonds consist of 1___ 2___ 3___ |
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the hybridization is sp 1 pair e- in σ orbital 1 pair e- in π_z 1 pair e- in π_y |
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The geometry for H2O is____ and the angle is ___ |
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tetrahedral structure 104.5 degrees two lone pairs and two H-bonds |
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Ammonia and Trimethyl Amine have ___ structure and consist of ___ |
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pyramidal 5 valenc-shell electrons shares 3 bonds w/ H or CH3 (respectively) one lone pair |
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Explain the structure of Ammonium |
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Four H bonds one electron short: has positive charge N+ electron density surrounds N tetrahedral |
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Ammonium vs. Hydronium which is more dominate when in aq solns |
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Ammonium, since Hydronium is more electronegative and Nitrogen atom tolerates additional proton more readily. |
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Sulfoxide structure Sulfone structure |
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One oxygen double bond, two methyl, one lone pair. tetrahedral Two oxygen double bonds, two methyl. tetrahedral |
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definition: effect on disease state, which is proven in clinic that molecular target could be used for something useful. Target is at the molecular-level. |
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The Hybridization of ethylene is ___ |
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sp2 one sigma pair e- one pi pair e- two planes of bonds |
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disease cause of defective chloride membrane transporter |
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What are methods of target modulation? |
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methods: agonism antagonism potentiation (make enzyme more potent) inhibition |
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broad meaning of receptor |
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molecular level target, any molecule that has specific binding site for ligand (latin word for "link"), includes agonists, antagonists, substrates, inhibitors, any smaller molecule that binds to specific site on micromolecule |
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Narrow meaning of receptor (more commonly encountered use) |
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enzymes and binding sites, micromolecule embedded in membrane or cytoplasm that has binding site htat has specific ligand but will be filled with drug |
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Definition ligand that can activate a signal transuction process |
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Definition: can not "flip the switch" as long as it is bound. nothing can be activated |
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Definition: behaves like agonist: binds and can activate transduction, but not with full efficacy can also behave like antagonist: as long as it is bound an agonist can not come in and activate it with full efficacy; very few drugs like the this but have potential here |
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Definition: Includes any ligand that regulates the activity of any molecule. common sitiuation: two proteins binding to create acitve or inactive situation Includes: agonists, antagonists, and enzyme inhibitor competitive, noncompetitive, uncompetitive |
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Definition: ligand binds to binding state other than catalytic site or agonist binding site; have multiple protein subunits |
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Allosteric Modulator "allo" means "other" Steric denotes space and volume |
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Define Competitive Inhibition |
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The inhibitor does not necessarily have to bind to the same active site that the substrate would bind to. As long as the binding of the inhibitor prevents the binding of the substrate (before it has done so), the inhibition mechanism is competitive |
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Definine non-competitive inhibition |
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Inhibition by binding to allosteric site (site other than substrate binding site); reduces the maximum rate of chemical rxn w/o changing binding affinity of catalyst for substrate |
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Define uncompetitve inhibition |
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takes place when an enzyme inhibitor binds only to the complex formed between the enzyme and the substrate reduces the effective concentration of the E-S decreases the maximum enzyme activity (Vmax), as it takes longer for the substrate or product to leave the active site |
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Receptors on the cell surface of the cell that the neuron is acting on respond specifically to that _______ |
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Neurotransmitters on responding cell generate ____ or a ____ |
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EPSP (cell will become more postive) or IPSP terminate response by uptake of NT by enzymatic degradation |
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True or False In regards to selectivity, "potency" is most important. |
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False selectivity of action is most important |
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enzymes with different amino acid sequence but catalyze same chemical rxn |
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