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In one embodiment, the term “substituted tetracycline compound” does not include unsubstituted tetracycline compounds such as minocycline, doxycycline, tetracycline, anhydrotetracycline, doxycycline, chlorotetracycline, oxytetracycline and others disclosed by Hlavka and Boothe, “The Tetracyclines,” in Handbook of Experimental Pharmacology 78, R. Taxonomy Description This compound belongs to the class of organic compounds known as tetracyclines?
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Examples of such classifications, some of which overlap include, nonpolar (ie, hydrophobic) amino acid residues can include alanine (Ala or A), leucine (Leu or L), isoleucine (Ile or I), valine (Val or V), proline (Pro or P), phenylalanine (Phe or F), tryptophan (Trp or W) and methionine (Met or M); polar neutral amino acid residues can include glycine (Gly or G), serine (Ser or S), threonine (Thr or T), cysteine (Cys or C), tyrosine (Tyr or Y), asparagine (Asn or N) and glutamine (Gln or Q); small amino acids include glycine (Gly or G), and alanine (Ala or A); hydrophobic amino acid residues can include valine (Val or V), leucine (Leu or L), isoleucine (Ile or I), methionine (Met or M), and proline (Pro or P); nucleophilic amino acids can include serine (Ser or S), threonine (Thr or T), and cysteine (Cys or C); aromatic amino acids can include phenylalanine (Phe or F), tyrosine (Tyr or Y), and tryptophan (Trp or W); amide amino acids can include asparagine (Asn or N), and glutamine (Gln or Q); positively charged (ie, basic) amino acid residues can include arginine (Arg or R), lysine (Lys or K) and histidine (His or H); and negatively charged (ie, acidic) amino acid residues can include aspartic acid (Asp or D) and glutamic acid (Glu or E). If you want information about a specific disease, you can access the Merck Manual of Disease.
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