1. Medicinal Chemistry

2. But First – Some Flowers

3. 15 th Century Turkish Tulip

4. Semper Augustus Tulip

5. Triumph Tulips

6. Queen of the Night Tulip

7. Rosa alba – White Rose of York – England pre-16 th Century

8. Madame Hardy Rose – bred 1832

9. Modern Hybrid Tea Rose

10. Medicinal Chemistry Medicinal chemistry is the chemical study of chemical substances useful in medical treatments

11. Diospyros lycioides – source of chewing sticks in Namibia

12. Ceanothus americanus – Native American chewing stick

13. Modern Chewing Sticks Most chewing stick plants have a wide range of antibacterial activity against a number of odontopathic bacterial species, and many also contained healing and/or analgesic compounds

14. Bloodroot – Sanguinaria canadensis

15. Rhizome of Bloodroot

16. Bloodroot extracts to treat dental plaque Bloodroot extracts have been identified as potentially valuable in controlling plaque Blood root has many alkaloids, known as sanguinaria alkaloids, and sanguinarine in particular, is thought to be a potential problem limiting the usefulness of blood root as a dental medicine There is an indication that sanguinarine may provoke glaucoma in predisposed humans and cats.

17. Double Blind Testing A key component of western testing is to do double-blind testing, so neither healer nor patient knows what the patient is receiving. Such tests often involve the use of a real substance and a placebo. The test for the placebo effect assumes that patients are not expecting the substance to have certain effects. If patients do expect certain effects, it renders placebo testing difficult or impossible.

18. Dwarf ginseng – Panax trifolium

19. Medicinal properties of Ginseng There are many claims that ginseng (Panax sp. – F. Araliaceae – the arums) increases sexual functioning, has anti-cancer properties, boosts the immune system, and even increases ability to perform in stressful situations. Difficult to test because ginseng preparations differ in their composition. Many of the chemicals produced by ginseng have counteractive effects. Isolated compounds work well in vitro, but simple ginseng preparations in vivo do not seem to have the benefits originally claimed. How ginsenosides are absorped, transported, degraded, and excreted is poorly known in humans.

20. Opium poppy – Papaver somniferum

21. Plant chemical composition changes with development The opium poppy Papaver somniferum is a good example of changes in metabolites during development. The seeds are free of alkaloids. After germination, the plant produces narcotine within 3 days. When the seedling is about 7 cm tall, the plant begins to produce codeine, morphine, and papaverine. Total alkaloid content slowly increases until flowering and then there is a sharp increase in alkaloids until the floral leaves fall off the plant.

22. Poison hemlock – Conium maculatum

23. Poison hemlock in the wild

24. Water hemlock – Cicuta virosa

25. Poison Hemlocks Poison hemlock and the water hemlocks are the most poisonous plants in North America. The active ingredient in poison hemlock is the alkaloid coniine. It is a central nervous system stimulant that affects the body like a nicotine overdose; paralysis creeps from the lower limbs upward. Death is due to the paralysis of the diaphragm and subsequent respiratory failure. Water hemlocks are toxic due to an alcohol, cicutoxin. It produces violent convulsions and death.

26. Alkaloid content varies during the day In poison hemlock, the amount of coniine varies during the day. The fruits are very high in coniine at 4 a.m. (226 micrograms) and low in coniine by 4 p.m. (8 micrograms). The amount of coniine varies with amount of sun as well. Another relative, wild parsnip (Pastinaca sativa) is toxic to the skin and is more toxic during bright sun than in cloudy weather or at night.

27. Wild parsnip – Pastinaca sativa

28. Wild parsnip in the field

29. Teonanacatl – The Flesh of the Gods

30. Psilocybe mushrooms

31. Dr. Albert Hoffman – Swiss Chemist

32. Conocybe – also produces psilocin

33. Panaeolus – also produces psilocin, may be toxic

34. Stropharia – also produces psilocin, may be toxic

35. Chemical structures of several hallucinogenic substances

36. Drug Similarities Interestingly, the drug Visken, used to treat hypertension was developed as an analog to 4- hydroxyindole, the phenolic nucleus of psilocybin and psilocin, from chemicals in Albert Hoffman’s lab.