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
Image result for Tannic acid

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
Image result for Catechin
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
Image result for gallic acid
170.12 g/mol
Antioxidant and potential hepatoprotective effects
Cinnamic acid
trans-3-Phenylacrylic acid
C9H8O2
Image result for Cinnamic acid
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
    Image result for p-Coumaric acid
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
Image result for gallocatechin gallate
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
Image result for Ferulic acid
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

 C40H56
Image result for Trans-α carotene

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
Image result for Trans-β carotene'
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
Image result for Violaxanthin

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
Image result for Cryptoxanthin
552.85 g/mol
Food colourant might reduce the risk of lung cancer
Serotonin
3-(2-aminoethyl)-1H-indol-5-ol
C10H12N2O
Image result for Serotonin
176.21 g/mol
Might contribute to feelings of well-being and happiness
Dopamine
4-(2-aminoethyl)benzene-1,2-diol
C8H11NO2
Image result for Dopamine

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
Image result for Catecholamines
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
Image result for β-Sitosterol
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
Image result for Campesterol
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
Image result for stigmasterol

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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