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14. Davies, M.E.B. and Davies, T.S.: Lyseggic Acid in Mental Deficiency. Lancet, 269, p. 1090, 1955. 15. DeShon, H.J., Rinkel, K. and Solomon, H.C.: Mental Changes Experimentally Produced by LSD; Psychiat. Quart., 26, p. 33, 1952. 16. Eisner, B.G. and Cohen, S.: Psychotherapy with Lysefgic Acid Diethylamide Press. 17. Evarts, E.V.: A Review of the Neurophysiological Effects of Lyse5gic Acid Diethylamide LSD ; and other Psychotomimetic Agents. Ann. New York Acad. Sc., 66, p. 479, 1957. 18. Frederking, W.: Intoxicant Drugs LSD-25 and Mescaline ; in Psychotherapy. J. Mer. And Ment. Dis., 121, p. 263-266, 1955. 19. Guttman, E.: Artificial Psychoses Produced by Mescaline, J. of Ment. Sc., 82, p. 203, 1936. 20. Gibran, K. : The Prophet, New York, N.Y., Knopff, 1956. 21. Green, R.F. and Nowlis, V. : A factor Analytic Study of the Domain of Mood with Independent Experimental Validation of the Factors. Paper given at the 65th Annual Convention of the American Psychological Association, New York, Spet. 1957. 22. Hoffer, A. & Agnew, N. Nicotinic acid modified LSD-25 psychosis. J. of Mental Sci., 101, p. 12-27, 1955. 23. Omitted in manuscript. 24. Hubbard, A.L.: Personal communication, 1958. 25. Huxley, A. : Letter to H. Osmond, 1957. 26. Huxley, F. : Personal communication, 1958. 27. James, W. : Varieties of Religious Experience. Twelfth Impression ; . Longman's, Green, London, England, 1906. 28. Jarvik, M.E., Abramson, H.A. and Hirsch, M.W. : Lyse4gic Acid Diethylamide LSD25 ; . VI.- Effect upon Recall and Recognition of Various Stimuli. J. of Psychology, 39, p. 443-454, 1955.

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Reference Books: 1. 2. 3. Wagner, J.G. Biopharmaceutics and Relevant Pharmacokinetics, Drug Intelligence Pub. Hamilton. Swarbick, J: Current Concepts in the Pharmaceutical Sciences: Biopharmaceutics. Lea and Febiger, Philadelphia. Wagner, J.G., Fundamentals of Clinical Pharmacokinetics. Drug Intelligence Publications, Hamilton. Swarbick, J: Current Concepts in the Pharmaceutical Sciences: Dosage Form Design and Bioavailability. Lea & Febiger, Philadelphia. Gibaldi, M: Biopharmaceutics and Clinical Pharmacokinetics. Lea & Febiger, Philadelphia. Rowland, M, and Tozer, T. N. Clinical pharmacokinetic: Concepts and Applications. Lea & Febiger, Philadelphia. Notari, R.E., Biopharmaceutics and Clinical Pharmacokinetics, Marcel Dekker. Gibaldi, M and Perrier, D: Pharmacokinetics, Marcel Dekker. Leon Shargel and Andrew B.C. Yu., Applied Biopharmaceutics and Pharmacokinetics Appleton Century - Crofts and medroxyprogesterone, for example, synthesis of lysergic acid.

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Possess an immediate precursor chemical with intent to manufacture a controlled substance; or 2 ; Possess or distribute an immediate precursor chemical knowing, or having reasonable cause to believe, that the immediate precursor chemical will be used to manufacture a controlled substance. Any person who violates this subsection shall be punished as a Class H felon. d2 ; The immediate precursor chemicals to which subsection d1 ; of this section applies are those immediate precursor chemicals designated by the Commission pursuant to its authority under G.S. 90-88, and the following until otherwise specified by the Commission ; : 1 ; Anthranilic acid. 1 ; Anhydrous ammonia. 1a ; Anthranilic acid. 2 ; Benzyl cyanide. 3 ; Chloroephedrine. 4 ; Chloropseudoephedrine. 5 ; D-lysergic acid. 6 ; Ephedrine. 7 ; Ergonovine maleate. 8 ; Ergotamine tartrate. 9 ; Ethyl Malonate. 10 ; Ethylamine. 10a ; Iodine. 11 ; Isosafrole. 11a ; Lithium. 12 ; Malonic acid. 13 ; Methylamine. 14 ; N-acetylanthranilic acid. 15 ; N-ethylephedrine. 16 ; N-ethylepseudoephedrine. 17 ; N-methylephedrine. 18 ; N-methylpseudoephedrine. 19 ; Norpseudoephedrine. 20 ; Phenyl-2-propane. 21 ; Phenylacetic acid. 22 ; Phenylpropanolamine. 23 ; Piperidine. 24 ; Piperonal. 25 ; Propionic anhydride. 26 ; Pseudoephedrine. 27 ; Pyrrolidine. 27a ; Red phosphorous. 28 ; Safrole. SENATE BILL 888 version 2 Page 3 and mescaline.

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18. De Mayo, The chemistry of Natural Products, 2-3, Interscience New York. 19. Export potential of selected medicinal plants, prepared by basic chemicals, pharmaceuticals and cosmeticexport promotion council, Bombay, and other reports. 20. Fabn A, Plant anatomy, 3rd Ed. Pergamon press, Oxford. 21. Faulkner D. J. and Fenical W. H. , Marine Natural Product Chemistry NATO conference series 4 ; plenum press, New York. 22. Kokate C. K., Cultivation of Medicinal Plants. 23. Pulok Mukharji, Quality control of Herbal drugs. Infectious Diseases 32, p. 492, 2001 ; indicates that more and more HIV-infected patients are dying from liver disease. The increase in death from this cause may be explained by the fact that liver disease may be accelerated in patients with both hepatitis C and HIV. In the study, the researchers looked at the causes of death for patients at the Lemuel Shattuck Hospital in Massachusetts during 3 time periods. w w w 1991 only 11.5% of patients died from liver disease; In 1996 after drug "cocktails" were introduced ; the rate of death from liver disease was 13.9%; From 1998 to 1999 liver disease accounted for 50% of the deaths. The researchers conclude that patients should be screened on their first visit for both HIV and hepatitis C. When appropriate, patients should receive vaccines for other forms of hepatitis or have liver biopsies. There is no cure or vaccine for hepatitis C and morphine.

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