Bioactive compounds I
Bioactive
compound
|
IUPAC
NAME
|
ChemicalFormula
|
Structure
|
Molar
Mass
|
Uses
|
Tannic acid
|
[2,3-dihydroxy-5-[[(2R,3R,4S,5R,6S)-3,4,5,6-tetrakis[[3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoyl]oxy]oxan-2-yl]methoxycarbonyl]phenyl]
3,4,5-trihydroxybenzoate
|
C76H52O46
|
1701.2 g/mol |
Applied as medicinal agents for the treatment of burns
|
|
Catechin
|
(2R,3S)-2-(3,4-dihydroxyphenyl)-3,4-dihydro-2H-chromene-3,5,7-triol
|
C15H14O6
|
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290.26 g/mol
|
Resistance of LDL to oxidation, brachial artery dilation increased
plasma antioxidant activity, and fat oxidation
|
Gallic acid
|
3,4,5-trihydroxybenzoic acid
|
C6H2(OH)3COOH
|
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170.12 g/mol
|
Antioxidant and potential hepatoprotective effects
|
Cinnamic acid
|
trans-3-Phenylacrylic acid
|
C9H8O2
|
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148.1586 g/mol
|
Is a precursor to the sweetener aspartame by the means of enzyme
catalysed amination to phenylalanine
|
p-Coumaric acid
|
4-Hydroxycinnamic acid.
|
C9H8O3
|
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164.0473 g/mol
|
Antioxidant properties and potentially reduce the risk of stomach cancer
|
Gallocatechin gallate
|
(2R,3R)-5,7-Dihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-3-yl
3,4,5-trihydroxybenzoate
|
C22H18O11
|
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458.372 g/mol
|
Cholesterol reduction
|
Quercetin
|
2-(3,4-dihydroxyphenyl)-3,5,7-trihydroxy-4H-chromen-4-one
|
C15H10O7
|
302.236 g/mol
|
Promotes overall cardiovascular health by encouraging blood flow
|
|
Ferulic acid
|
3-(4-Hydroxy-3-methoxyphenyl)acrylic
acid
|
C10H10O4
|
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194.18 g/mol
|
Antioxidant, antimicrobial, anti-inflammatory, antiallergic,
anticarcinogenic, modulation of enzyme activity, antiviral and vasodilatory
actions
|
Trans-α carotene
|
1,3,3-Trimethyl-2-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethyl-2-cyclohexen-1-yl)-1,3,5,7,9,11,13,15,17-octadecanonaen-1-yl]cyclohexen
|
536.9 g/mol
|
Precursor to vitamin A
|
||
Trans-β carotene
|
1,3,3-trimethyl-2-[3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohexene
|
C40H56
|
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536.9 g/mol
|
Reduce the risk of CVD and cancer
|
Violaxanthin
|
(1R,3S,6S)-6-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-18-[(1S,4S,6R)-4-hydroxy-2,2,6-trimethyl-7-oxabicyclo[4.1.0]heptan-1-yl]-3,7,12,16-tetramethyloctadeca-1,3,5,7,9,11,13,15,17-nonaenyl]-1,5,5-trimethyl-7-oxabicyclo[4.1.0]heptan-3-ol
|
C40H56O4
|
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600.9 g/mol |
Used as a food dye
|
Cryptoxanthin
|
(1R)-3,5,5-trimethyl-4-[(1E,3E,5E,7E,9E,11E,13E,15E,17E)-3,7,12,16-tetramethyl-18-(2,6,6-trimethylcyclohexen-1-yl)octadeca-1,3,5,7,9,11,13,15,17-nonaenyl]cyclohex-3-en-1-ol
|
C40H56O
|
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552.85 g/mol
|
Food colourant might reduce the risk of lung cancer
|
Serotonin
|
3-(2-aminoethyl)-1H-indol-5-ol
|
C10H12N2O
|
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176.21 g/mol
|
Might contribute to feelings of well-being and happiness
|
Dopamine
|
4-(2-aminoethyl)benzene-1,2-diol
|
C8H11NO2
|
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153.18 g/mol
|
Reduce the plasma oxidative stress and enhance the resistance to
oxidative modification of LDL
|
Catecholamines
|
4-(2-Aminoethyl)pyrocatechol
[4-(2-aminoethyl)benzene-1,2-diol]
|
C8H9NO2R2
|
151.163g/mol
|
Increases blood pressure, glucose levels, and heart beat rate
|
|
β-Sitosterol
|
17-(5-Ethyl-6-methylheptan-2-yl)-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
|
C29H50O
|
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414.71 g/mol
|
Potential to reduce blood cholesterol levels and benign prostatic
hyperplasia (BPH)
|
Campesterol
|
(3S,8S,9S,10R,13R,14S,17R)-17-[(2R,5R)-5,6-dimethylheptan-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
|
C28H48O
|
400.7 g/mol
|
Reduces the absorption of cholesterol in the human intestines
|
|
stigmasterol
|
(3S,8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,3,4,7,8,9,11,12,14,15,16,17-dodecahydro-1H-cyclopenta[a]phenanthren-3-ol
|
C29H48O
|
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412.7 g/mol
|
Reduces the absorption of cholesterol in the human intestines
|
References:
Rinah K. Netshiheni, A. O. (n.d.). Banana
Bioactives: Absorption,Utilisation and Health Benefits. IntechOpen.
Zafar, J. S. (2018). Bioactive compounds in banana
fruits and their. Food Quality and Safety, 183–188.
Maharani Laillyza Apriasari, I. a. (2014). Bioactive
Compound and Antioxidant Activity of Methanol Extract Mauli Bananas (Musa sp)
Stem . International Journal of Bioscience, Biochemistry and Bioinformatics,
4(2)110-115.
Maraschin, A. P. (2015). Banana (Musa spp) from Peel
to Pulp: Ethnopharmacology, Source of Bioactive Compounds and its Relevance for
Human Health. Journal of Ethnopharmacology, 149-163.
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