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    <title>Szlater's New Writeups</title>
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    <updated>2002-12-09T13:12:45Z</updated>
<entry><title>Urinary tract infection (thing)</title><link rel="alternate" type="text/html" href="http://everything2.com/user/Szlater/writeups/Urinary+tract+infection"/><id>http://everything2.com/user/Szlater/writeups/Urinary+tract+infection</id><author><name>Szlater</name><uri>http://everything2.com/user/Szlater</uri></author><published>2002-12-09T13:12:45Z</published><updated>2002-12-09T13:12:45Z</updated>
<content type="html">&lt;h4&gt;Introduction&lt;/h4&gt;
&lt;p&gt;&lt;a href=&quot;/title/the+human+urinary+system&quot;&gt;The urinary tract&lt;/a&gt; is one of the most common sites for &lt;a href=&quot;/title/infection&quot;&gt;infection&lt;/a&gt; particularly in women. Between 10 and 20 percent of women will, at some point in their life, suffer from a urinary tract infection  &lt;a href=&quot;/title/UTI&quot;&gt;UTI&lt;/a&gt; and a significant number suffer from recurrent infections.  Most infections are short-lived, and cause little more than discomfort, however, severe infections can result in the loss of kidney function and have serious long term effects.  In females a distinction is made between &lt;a href=&quot;/title/cystitis&quot;&gt;cystitis&lt;/a&gt;, infection of the bladder, &lt;a href=&quot;/title/urethritis&quot;&gt;urethritis&lt;/a&gt;, infection of the urethra and &lt;a href=&quot;/title/vaginitis&quot;&gt;vaginitis&lt;/a&gt;, infection of the &lt;a href=&quot;/title/vagina&quot;&gt;vagina&lt;/a&gt; although symptoms may overlap.&lt;/p&gt;

&lt;h4&gt;What causes it?&lt;/h4&gt;
&lt;p&gt;UTI are most often caused by bacteria, but they can be caused by &lt;a href=&quot;/title/bacteria&quot;&gt;bacteria&lt;/a&gt;, &lt;a href=&quot;/title/virus&quot;&gt;viruses&lt;/a&gt;, &lt;a href=&quot;/title/fungi&quot;&gt;fungi&lt;/a&gt; or &lt;a href=&quot;/title/protozoa&quot;&gt;protozoa&lt;/a&gt;. &lt;/p&gt;
&lt;h5&gt;Organisms responsible for UTI:&lt;/h5&gt;
&lt;ul&gt;
&lt;li&gt;Bacteria
&lt;ul&gt;&lt;i&gt;
&lt;li&gt;&lt;a href=&quot;/title/Escherichia+coli&quot;&gt;Escherichia coli&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href=&quot;/title/Proteus+mirabilis&quot;&gt;Proteus mirabilis&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;&lt;a href=&quot;/title/Klebsiella&quot;&gt;Klebsiella&lt;/a&gt;&lt;/li&gt;
&lt;li&gt;&lt;/li&gt;&lt;/i&gt;&lt;/ul&gt;&lt;/li&gt;&lt;/ul&gt;&amp;hellip;</content>
</entry><entry><title>opioid (thing)</title><link rel="alternate" type="text/html" href="http://everything2.com/user/Szlater/writeups/opioid"/><id>http://everything2.com/user/Szlater/writeups/opioid</id><author><name>Szlater</name><uri>http://everything2.com/user/Szlater</uri></author><published>2002-12-09T13:06:53Z</published><updated>2002-12-09T13:06:53Z</updated>
<content type="html">&lt;p&gt;The structure of morphine was worked out in 1925 by &lt;a href=&quot;/title/English&quot;&gt;English&lt;/a&gt; &lt;a href=&quot;/title/chemist&quot;&gt;chemist&lt;/a&gt; &lt;a href=&quot;/title/Sir+Robert+Robinson&quot;&gt;Sir Robert Robinson&lt;/a&gt;.  He was also responsible for working out the structure of &lt;a href=&quot;/title/strychnine&quot;&gt;strychnine&lt;/a&gt; in 1946.

&lt;pre&gt;


                     
                         
             C == C    C - N - CH&lt;sub&gt;3&lt;/sub&gt;
            /      \   &lt;b&gt;:&lt;/b&gt;  /
      HO - C        C -&lt;b&gt;:&lt;/b&gt;-C
            \      /   &lt;b&gt;:&lt;/b&gt;  \
             C -- C ...C   C
             |     \      /
             |      C == C
             |     /      \
             O -- C       C
                   \\    //
                    C -- C
                   /
                 HO

                &lt;a href=&quot;/title/Morphine&quot;&gt;Morphine&lt;/a&gt;

&lt;/pre&gt;
&lt;p&gt;The C&lt;sub&gt;5&lt;/sub&gt;-N-CH&lt;sub&gt;3&lt;/sub&gt; ring structure in morphine is called a &lt;a href=&quot;/title/piperidine&quot;&gt;piperidine&lt;/a&gt;.  The ring formed by &lt;a href=&quot;/title/oxygen&quot;&gt;oxygen&lt;/a&gt;  and the four &lt;a href=&quot;/title/carbon&quot;&gt;carbons&lt;/a&gt; is called a &lt;a href=&quot;/title/furan&quot;&gt;furan&lt;/a&gt;.

&lt;pre&gt;


   OH                  
   |                      
   C = O     C == C    C - N - CH&lt;sub&gt;3&lt;/sub&gt;
   |        /      \   &lt;b&gt;:&lt;/b&gt;  /
   CH&lt;sub&gt;2&lt;/sub&gt;-O -&lt;/pre&gt;&amp;hellip;</content>
</entry><entry><title>Beta-lactam (thing)</title><link rel="alternate" type="text/html" href="http://everything2.com/user/Szlater/writeups/Beta-lactam"/><id>http://everything2.com/user/Szlater/writeups/Beta-lactam</id><author><name>Szlater</name><uri>http://everything2.com/user/Szlater</uri></author><published>2002-10-01T11:38:54Z</published><updated>2002-10-01T11:38:54Z</updated>
<content type="html">&lt;p&gt;&amp;beta;-lactam &lt;a href=&quot;/title/antibiotic&quot;&gt;antibiotics&lt;/a&gt; are some of the most important weapons in the clinical fight against bacterial &lt;a href=&quot;/title/infection&quot;&gt;infection&lt;/a&gt;.  &lt;a href=&quot;/title/Alexander+Fleming&quot;&gt;Alexander Fleming&lt;/a&gt;'s 1928 discovery, &lt;a href=&quot;/title/Penicillin&quot;&gt;Penicillin&lt;/a&gt;, is a classic example of a &amp;beta;-lactam antibiotic.

&lt;pre&gt;
       R - C = O     
           | 
           N - H
           |   
       H - C - C = O
           |   |
       H - C - N
          /    |
         S     |
          \    |
         H&lt;sub&gt;2&lt;/sub&gt;C - C - H
               |
           O = C - OH
             
    The general structure of penicillins        &lt;/pre&gt;
&lt;pre&gt;
          R
          |
      H - C - C = O
          |   |
      H - C - N 
          |   |
          R'  R&quot;

  &amp;beta;-lactam ring structure
&lt;/pre&gt;

&lt;h5&gt;What do &amp;beta;-lactam antibiotics do?&lt;/h5&gt;
&lt;p&gt;&amp;beta;-lactam antibiotics act by inhibiting the action of bacterial &lt;a href=&quot;/title/transpeptidase&quot;&gt;transpeptidases&lt;/a&gt;, these &lt;a href=&quot;/title/enzyme&quot;&gt;enzymes&lt;/a&gt; &lt;a href=&quot;/title/catalyse&quot;&gt;catalyse&lt;/a&gt; the final cross linking step in the synthesis of the &lt;a href=&quot;/title/peptidoglycan&quot;&gt;peptidoglycan&lt;/a&gt; layer of the&amp;hellip;</content>
</entry><entry><title>cold remedies (idea)</title><link rel="alternate" type="text/html" href="http://everything2.com/user/Szlater/writeups/cold+remedies"/><id>http://everything2.com/user/Szlater/writeups/cold+remedies</id><author><name>Szlater</name><uri>http://everything2.com/user/Szlater</uri></author><published>2002-09-30T12:29:17Z</published><updated>2002-09-30T12:29:17Z</updated>
<content type="html">&lt;p&gt;There really is nothing you can take to cure a cold, it's just that simple.

&lt;p&gt;The so-called &quot;cold and flu remedies&quot; available from pharmacists do nothing but alleviate the symptoms and this in itself &lt;i&gt;can&lt;/i&gt; prolong the time you spend feeling ill.

&lt;h5&gt;How can relieving the symptoms prolong the infection?&lt;/h5&gt; 

&lt;p&gt;Symptoms such as &lt;a href=&quot;/title/fever&quot;&gt;fever&lt;/a&gt; and &lt;a href=&quot;/title/catarrh&quot;&gt;catarrh&lt;/a&gt; are the body's natural mechanisms for fighting infection.  

&lt;p&gt;Many of the microbes that cause sickness in humans are very sensitive to temperature, and cannot grow at temperatures above the body's normal 37.5&amp;deg;C (98.6&amp;deg;F) .  By raising the temperature of the body, as in a fever (&lt;a href=&quot;/title/pyrexia&quot;&gt;pyrexia&lt;/a&gt;), the body is attempting to inhibit microbial growth, thereby giving the immune system a chance to react to the invading organism.  Paracetamol can be used to bring down mild fevers, to allow you to get a good night's sleep, but generally the fever should be allowed to run it's course.  However, excessively high temperatures in adults or fevers in&amp;hellip;</content>
</entry><entry><title>Phencyclidine (thing)</title><link rel="alternate" type="text/html" href="http://everything2.com/user/Szlater/writeups/Phencyclidine"/><id>http://everything2.com/user/Szlater/writeups/Phencyclidine</id><author><name>Szlater</name><uri>http://everything2.com/user/Szlater</uri></author><published>2002-09-15T16:20:18Z</published><updated>2002-09-15T16:20:18Z</updated>
<content type="html">&lt;p&gt;See also: &lt;a href=&quot;/title/PCP&quot;&gt;PCP&lt;/a&gt;&lt;/p&gt;

&lt;p&gt;&lt;a href=&quot;/title/IUPAC&quot;&gt;IUPAC&lt;/a&gt; name: &lt;b&gt;1-(1-phenylcyclohexyl)piperidine&lt;/b&gt;&lt;br&gt;
&lt;a href=&quot;/title/Synonyms&quot;&gt;Synonyms&lt;/a&gt;: &lt;b&gt;Phencylcidine, &lt;a href=&quot;/title/PCP&quot;&gt;PCP&lt;/a&gt;, Sernyl, Sernylan, 1-phenylcyclohexylamine, &lt;a href=&quot;/title/Angel+Dust&quot;&gt;Angel Dust&lt;/a&gt;, Killer Weed, Embalming Fluid, Rocket Fuel, Crystal, Wet, Water, Wack, Fry, Amp, Zoot, Hog&lt;/b&gt;&lt;br&gt;
&lt;a href=&quot;/title/Molecular+Formula&quot;&gt;Molecular Formula&lt;/a&gt;: &lt;b&gt;&lt;a href=&quot;/title/carbon&quot;&gt;C&lt;/a&gt;&lt;sub&gt;17&lt;/sub&gt;&lt;a href=&quot;/title/hydrogen&quot;&gt;H&lt;/a&gt;&lt;sub&gt;25&lt;/sub&gt;&lt;a href=&quot;/title/Nitrogen&quot;&gt;N&lt;/a&gt;&lt;/b&gt;&lt;br&gt;
&lt;a href=&quot;/title/Structural+Formula&quot;&gt;Structural Formula&lt;/a&gt;:&lt;br&gt;&lt;pre&gt;



          
           C -- C
          /      \
         C        C = O
          \      /   
           C -- C    C - C
                | \ /     \ 
           C == C  N       C
          /      \  \     /
         C        C  C - C
          \\    //
           C -- C



&lt;/pre&gt;
 &lt;br&gt;
&lt;a href=&quot;/title/Molecular+Mass&quot;&gt;Molecular Mass&lt;/a&gt;: &lt;b&gt;243.38&lt;/b&gt;&lt;br&gt;
&lt;a href=&quot;/title/CAS&quot;&gt;CAS&lt;/a&gt; number: &lt;b&gt;956-90-1&lt;/b&gt;&lt;br&gt;
&lt;a href=&quot;/title/Melting+point&quot;&gt;Melting point&lt;/a&gt; (Hydrochloride): &lt;b&gt; 117&amp;deg;C&lt;/b&gt;&lt;br&gt;
Appearance: &lt;b&gt;White crystalline powder&lt;/b&gt;&lt;br&gt;

&lt;p&gt;&lt;b&gt;&lt;a href=&quot;/title/Toxicology&quot;&gt;Toxicology&lt;/a&gt;&lt;/b&gt; data:

&lt;p&gt;RAT&lt;sub&gt;Oral&lt;/sub&gt; &lt;a href=&quot;/title/LD50&quot;&gt;LD50&lt;/a&gt;:&lt;b&gt;135mg kg&lt;sup&gt;-1&lt;/sup&gt;&lt;/b&gt;&lt;br&gt; 

&lt;p&gt;&lt;b&gt;Synthesis&lt;/b&gt;:&lt;br&gt;
&lt;ol&gt;&lt;/ol&gt;&amp;hellip;</content>
</entry><entry><title>Piperidine (thing)</title><link rel="alternate" type="text/html" href="http://everything2.com/user/Szlater/writeups/Piperidine"/><id>http://everything2.com/user/Szlater/writeups/Piperidine</id><author><name>Szlater</name><uri>http://everything2.com/user/Szlater</uri></author><published>2002-09-14T15:40:06Z</published><updated>2002-09-14T15:40:06Z</updated>
<content type="html">&lt;p&gt;&lt;a href=&quot;/title/IUPAC&quot;&gt;IUPAC&lt;/a&gt; name: &lt;b&gt;Piperidine&lt;/b&gt;&lt;br&gt;
&lt;a href=&quot;/title/Synonyms&quot;&gt;Synonyms&lt;/a&gt;: &lt;b&gt;Azacyclohexane, Cyclopentimine, Cypentil, Hexahydropyridine, Hexazane, Pentamethseneimine&lt;/b&gt;&lt;br&gt;
&lt;a href=&quot;/title/Molecular+Formula&quot;&gt;Molecular Formula&lt;/a&gt;: &lt;b&gt;&lt;a href=&quot;/title/carbon&quot;&gt;C&lt;/a&gt;&lt;sub&gt;5&lt;/sub&gt;&lt;a href=&quot;/title/hydrogen&quot;&gt;H&lt;/a&gt;&lt;sub&gt;11&lt;/sub&gt;&lt;a href=&quot;/title/Nitrogen&quot;&gt;N&lt;/a&gt;&lt;/b&gt;&lt;br&gt;
&lt;a href=&quot;/title/Structural+Formula&quot;&gt;Structural Formula&lt;/a&gt;:&lt;br&gt;&lt;pre&gt;

                    C -- C
                   /      \
                  C       :N - H
                   \      /
                    C -- C
                   
                  Piperidine
&lt;/pre&gt;
 &lt;br&gt;
&lt;a href=&quot;/title/Molecular+Mass&quot;&gt;Molecular Mass&lt;/a&gt;: &lt;b&gt;85.2&lt;/b&gt;&lt;br&gt;
&lt;a href=&quot;/title/CAS&quot;&gt;CAS&lt;/a&gt; number: &lt;b&gt;110-89-4&lt;/b&gt;&lt;br&gt;
&lt;a href=&quot;/title/Melting+point&quot;&gt;Melting point&lt;/a&gt;: &lt;b&gt;-8 C&lt;/b&gt;&lt;br&gt;
&lt;a href=&quot;/title/Boiling+point&quot;&gt;Boiling point&lt;/a&gt;: &lt;b&gt;106 C&lt;/b&gt;&lt;br&gt;
&lt;a href=&quot;/title/Flash+point&quot;&gt;Flash point&lt;/a&gt;: &lt;b&gt;4 C&lt;/b&gt;&lt;br&gt;
Appearance: &lt;b&gt;Clear oily liquid with a pungent peppary ammoniacal odour&lt;/b&gt;&lt;br&gt;

&lt;p&gt;&lt;a href=&quot;/title/Toxicology&quot;&gt;Toxicology&lt;/a&gt; data:

&lt;p&gt;MOUSE&lt;sub&gt;Oral&lt;/sub&gt; &lt;a href=&quot;/title/LD50&quot;&gt;LD50&lt;/a&gt;:&lt;b&gt;30mg kg&lt;sup&gt;-1&lt;/sup&gt;&lt;/b&gt;&lt;br&gt; 
RABBIT&lt;sub&gt;Dermal&lt;/sub&gt; &lt;a href=&quot;/title/LD50&quot;&gt;LD50&lt;/a&gt;:&lt;b&gt;320mg kg&lt;sup&gt;-1&lt;/sup&gt;&lt;/b&gt;&lt;br&gt; 

&lt;p&gt;Skin contact may cause severe irritation or burns. Contact with the eyes may lead to permanent damage. 

&lt;p&gt;Pipe&amp;hellip;</content>
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