Search More · GCI-TPs

Graphs show a maximum of 100 compounds. Use downloads for complete results.

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

2 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

4 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

3 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

C(=O)(C(O)=O)O

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

9 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

9 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

6 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

C([N+](=O)[O-])([O-])=O

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

5 steps

Dead-End Product

LYGJENNIWJXYER-UHFFFAOYSA-N

Nitromethane

C[N+](=O)[O-]

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

9 steps

Dead-End Product

LXNSRSYDQMJXSI-KTAJNNJTSA-N

C(C(=O)O)=[N+](CC(=O)O)[O-]

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

4 steps

Dead-End Product

XLJMAIOERFSOGZ-UHFFFAOYSA-N

Cyanic acid

N#CO

Previewing top 10 entries. If you want the full results, please use the download button above.

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

PriorBiotransformation

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

Abiotic

Downstream Successor

QTBSBXVTEAMEQO-UHFFFAOYSA-N

Acetic Acid

CC(=O)O

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

PriorBiotransformation

Downstream Successor

QTBSBXVTEAMEQO-UHFFFAOYSA-N

Acetic Acid

CC(=O)O

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

Abiotic

Downstream Successor

IKHGUXGNUITLKF-UHFFFAOYSA-N

Acetaldehyde

C(C)=O

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

Abiotic

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

PriorBiotransformation

Downstream Successor

LFQSCWFLJHTTHZ-UHFFFAOYSA-N

Ethanol

C(C)O

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

Abiotic

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

PriorBiotransformation

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

KCFIDDRVZLDJEY-UHFFFAOYSA-N

2-(1,2,3,6-Tetrahydro-1,3-dimethyl-2,6-dioxo-7H-purin-7-yl)ethyl 4-(diethylamino)-4-oxobutyrate

CCN(CC)C(=O)CCC(=O)OCCN1C=NC2=C1C(=O)N(C(=O)N2C)C

Abiotic

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

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No Original Precursors

No entries were found for this section with the current query and depth.

No All Precursors

No entries were found for this section with the current query and depth.

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