Title: Secondary
1Secondary Compounds
Coumarins, Lignin, Flavonoids, Tanins
Ashley Malinowski Emma McAllister Kelli Meyer
2Coumarins
- Phytochemicals are non-nutritive plant chemicals
that have protective or diseases-preventative
properties. - Plants produce these secondary compounds to
protect themselves. - Coumarin is an example of a phytochemical.
Coumarin C9H6O2
3Coumarins
- Coumarin has a vanilla like flavor, is an oxygen
heterocycle, and can occur either free or
combined with sugar glucose. - Coumarin is found in several plants such as tonka
beans, lavender, cinnamon, and sweet clover.
- It works as a pesticide in plants that produce
it. - Coumarin also protects humans against certain
diseases. It has blood thinning, anti-fungicidal,
and anti-tumor activities. However, it can be
toxic at high doses for a long period of time.
4Flavonoids
- Polyphenolic compounds with 15 C atoms, 2
benzene rings on linear 3 C chain - Over 4,000 flavonoids
- Easily recognized as flower pigments in most
angiosperm plants but are not always flower
pigments - In plants they repair damage and shield from
environmental toxins
5Flavonoids
- Act like antioxidants. How effective they are
depends on their molecular structural
characteristics - Some flavonoids in hops and beer have been
found to have better antioxidant effects than tea
or red wine most flavonoids are found in fruits,
vegetables, teas, and other drinks. - Flavonoids have been known to have antiviral,
anti-allergic, antiplatelet, anti-inflammatory,
antitumor and antioxidant activities
6Lignin
- Compounds are complex with 3D polymers that all
have a phenylpropane structure (1 benzene ring
with 3C tail - In natural form, so complex non has ever been
completely described. - Many compounds, not just one
- Key participant in forming organic material from
C in atmosphere - Molecular weights may reach 15,000
- Contain acid but are not acid themselves
- Very resistant to degradation
spruce wood lignin fragment comprising four
repeating units linked to four xylan
chains //www.lignin.fi/438.jpgimgrefurlhttp//
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7Lignin
- Found in all plants, mostly between the cells but
also within the cell walls. - Most important component in terrestrial plants
after cellulose - Gives vegetables their crunch and provides Fiber
- Nearly 1/3 of all plant tissues
- Grouped into several types from hardwoods,
softwoods, and grasses. Vary from species to
species. - Bonded very complexly to carbohydrates in wood
- Helps regulate the transport of liquid in plants
by keeping the cell walls from collapsing and
regulating the flow of the liquid
8Tannins
- Tannins are astringent, bitter tasting
polyphenols that bind and precipitate proteins - The term tannins refers to the source of tannins
used in tanning animal hides into leather - Located in various plant tissues such as bud,
leaf, root, seed, and stem tissues - Located mainly in the vacuoles or surface wax of
the plants
9Tannins
- Most tannins are water soluble, but some very
large condensed tannins are insoluble - Have molecular weight ranging from 500 to over
3,000 - If ingested in large quantities, tannins can
inhibit the absorption of minerals into the body - Tannins are usually divided into two groups
10Two Groups of Tannins
- Hydrolyzable tannins
- Molecules with a polyol core (often glucose)
- Hydrolyzed by mild acids or mild bases to yield
carbohydrate and phenolic acids - Proantocyanindins (condensed tannins)
- Condensed chemical structure
- Can contain 2-50 flavonoid units
- Responsible for the pink, scarlet, red, mauve,
violet, and blue colors in flowers, leaves, and
fruits - Responsible for the astringent taste of fruits
and wines
11Tannins
- Tea
- Wine
- Pomegranates
- Persimmons
- Most berries (cranberries, strawberries, and
blueberries have both types of tannins)
12Works Cited
http//www.cgu.edu.tw/DMI/lavendar.jpg http//www.
phytochemicals.info/phytochemicals/coumarin.php
http//lpi.oregonstate.edu/f-w00/flavonoid.html ht
tp//www.friedli.com/herbs/phytochem/flavonoids.ht
ml http//www.clevelandclinic.org/heartcenter/pub/
guide/prevention/nutrition/chocolate.htm
http//palimpsest.stanford.edu/byorg/abbey/ap/ap04
/ap04-4/ap04-402.html http//www.kolumbus.fi/kaj.f
orss/lignin.html
http//www.ansci.cornell.edu/plants/toxicagents/ta
nnin/index.html