PhytoHub: Showing entry for Guarana

Guarana

Group:: Beverages, Non-alcoholic

Identification

Name: Guarana
ID: 336
Food group: Beverages, Non-alcoholic

Synonyms

No Synonyms

External Links

ITIS: 506078
FooDB (Foods): FOOD00915
Wikipedia: Guarana
Wikidata: Q209089

Compounds

Name	Structure	Monoisotopic mass	Formula	Family	Class
Caffeine	CN1C=NC2=C1C(=O)N(C)C(=O)N2C	194.080375578	C₈H₁₀N₄O₂	N-containing compounds	Alkaloids	Publications	Show
Theobromine	CN1C=NC2=C1C(=O)NC(=O)N2C	180.064725514	C₇H₈N₄O₂	N-containing compounds	Alkaloids	Publications	Show
Theophylline	CN1C2=C(NC=N2)C(=O)N(C)C1=O	180.064725514	C₇H₈N₄O₂	N-containing compounds	Alkaloids	Publications	Show

Related Metabolites

Name	Structure	Monoisotopic mass	Formula	Family	Class
Theobromine	CN1C=NC2=C1C(=O)NC(=O)N2C	180.064725514	C₇H₈N₄O₂	N-containing compounds	Alkaloids	Show
4-Amino-(5-formylmethyl- amino) 1,3-dimethyluracil	CN1C(=O)N(C)C(=O)C(NC=O)=C1N	198.075290198	C₇H₁₀N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
6-Amino-5(N-methylformylamino)-1-methyluracil	CN(C=O)C1=C(N)N(C)C(=O)NC1=O	198.075290198	C₇H₁₀N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
3-Methyluric acid	CN1C2=C(NC(=O)N2)C(=O)NC1=O	182.043990069	C₆H₆N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
7-methyluric acid	CN1C(=O)NC2=C1C(=O)NC(=O)N2	182.043990069	C₆H₆N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
7-methylxanthine	CN1C=NC2=C1C(=O)NC(=O)N2	166.049075449	C₆H₆N₄O₂	N-containing compound metabolites	Alkaloid metabolites	Show
3-methylxanthine	CN1C2=C(NC=N2)C(=O)NC1=O	166.049075449	C₆H₆N₄O₂	N-containing compound metabolites	Alkaloid metabolites	Show
1,7-dimethyluricacid	CN1C(=O)NC2=C1C(=O)N(C)C(=O)N2	196.059640134	C₇H₈N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
1-methyluric acid	CN1C(=O)NC2=C(NC(=O)N2)C1=O	182.043990069	C₆H₆N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
5-acetylamino-6-formylamino-3-methyluracil	CN1C(=O)NC(NC=O)=C(NC(C)=O)C1=O	226.070204818	C₈H₁₀N₄O₄	N-containing compound metabolites	Alkaloid metabolites	Show
5-acetyl-amino-6-amino-3-methyluracil	CN1C(=O)NC(N)=C(NC(C)=O)C1=O	198.075290198	C₇H₁₀N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
1-methylxanthine	CN1C(=O)NC2=C(NC=N2)C1=O	166.049075449	C₆H₆N₄O₂	N-containing compound metabolites	Alkaloid metabolites	Show
1,3,7-Trimethyluric acid	CN1C(=O)NC2=C1C(=O)N(C)C(=O)N2C	210.075290198	C₈H₁₀N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
1,3-dimethyluric acid	CN1C2=C(NC(=O)N2)C(=O)N(C)C1=O	196.059640134	C₇H₈N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
Theophylline	CN1C2=C(NC=N2)C(=O)N(C)C1=O	180.064725514	C₇H₈N₄O₂	N-containing compounds	Alkaloids	Show
Caffeine	CN1C=NC2=C1C(=O)N(C)C(=O)N2C	194.080375578	C₈H₁₀N₄O₂	N-containing compounds	Alkaloids	Show
Paraxanthine	CN1C=NC2=C1C(=O)N(C)C(=O)N2	180.064725514	C₇H₈N₄O₂	N-containing compounds	Alkaloids	Show
Paraxanthine	CN1C=NC2=C1C(=O)N(C)C(=O)N2	180.064725514	C₇H₈N₄O₂	N-containing compounds	Alkaloids	Show
6-Amino-5(N-methylformylamino)-1-methyluracil	CN(C=O)C1=C(N)N(C)C(=O)NC1=O	198.075290198	C₇H₁₀N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
7-methyluric acid	CN1C(=O)NC2=C1C(=O)NC(=O)N2	182.043990069	C₆H₆N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
7-methylxanthine	CN1C=NC2=C1C(=O)NC(=O)N2	166.049075449	C₆H₆N₄O₂	N-containing compound metabolites	Alkaloid metabolites	Show
3-methylxanthine	CN1C2=C(NC=N2)C(=O)NC1=O	166.049075449	C₆H₆N₄O₂	N-containing compound metabolites	Alkaloid metabolites	Show
1,7-dimethyluricacid	CN1C(=O)NC2=C1C(=O)N(C)C(=O)N2	196.059640134	C₇H₈N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
3,7 dimethyluric acid	CN1C(=O)NC2=C1C(=O)NC(=O)N2C	196.059640134	C₇H₈N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
1-methylxanthine	CN1C(=O)NC2=C(NC=N2)C1=O	166.049075449	C₆H₆N₄O₂	N-containing compound metabolites	Alkaloid metabolites	Show
Theobromine	CN1C=NC2=C1C(=O)NC(=O)N2C	180.064725514	C₇H₈N₄O₂	N-containing compounds	Alkaloids	Show
Caffeine	CN1C=NC2=C1C(=O)N(C)C(=O)N2C	194.080375578	C₈H₁₀N₄O₂	N-containing compounds	Alkaloids	Show
Theophylline	CN1C2=C(NC=N2)C(=O)N(C)C1=O	180.064725514	C₇H₈N₄O₂	N-containing compounds	Alkaloids	Show
1,3-dimethyluric acid	CN1C2=C(NC(=O)N2)C(=O)N(C)C1=O	196.059640134	C₇H₈N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
1-methylxanthine	CN1C(=O)NC2=C(NC=N2)C1=O	166.049075449	C₆H₆N₄O₂	N-containing compound metabolites	Alkaloid metabolites	Show
Paraxanthine	CN1C=NC2=C1C(=O)N(C)C(=O)N2	180.064725514	C₇H₈N₄O₂	N-containing compounds	Alkaloids	Show
1-methyluric acid	CN1C(=O)NC2=C(NC(=O)N2)C1=O	182.043990069	C₆H₆N₄O₃	N-containing compound metabolites	Alkaloid metabolites	Show
3-methylxanthine	CN1C2=C(NC=N2)C(=O)NC1=O	166.049075449	C₆H₆N₄O₂	N-containing compound metabolites	Alkaloid metabolites	Show

Biomarkers of intake

No Biomarkers of intake found

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