Green/roasted coffee
- Group:
- Coffee and coffee products
Showing entry for Green/roasted coffee
Identification
- Name
- Green/roasted coffee
- ID
- 409
- Food group
- Coffee and coffee products
Synonyms
No Synonyms
External Links
No external links
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 | |
Coffee purines | 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 | ||
7-methylxanthine | CN1C=NC2=C1C(=O)NC(=O)N2 | 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 | ||
Paraxanthine | CN1C=NC2=C1C(=O)N(C)C(=O)N2 | 180.064725514 | C7H8N4O2 | N-containing compounds | Alkaloids | Show | ||
1-methylxanthine | CN1C(=O)NC2=C(NC=N2)C1=O | 166.049075449 | C6H6N4O2 | 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 | ||
3-methylxanthine | CN1C2=C(NC=N2)C(=O)NC1=O | 166.049075449 | C6H6N4O2 | 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 | ||
7-methyluric acid | CN1C(=O)NC2=C1C(=O)NC(=O)N2 | 182.043990069 | C6H6N4O3 | 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 | ||
1,7-dimethyluricacid | CN1C(=O)NC2=C1C(=O)N(C)C(=O)N2 | 196.059640134 | C7H8N4O3 | 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 | ||
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 |
Biomarkers of intake
No Biomarkers of intake found