Search More · GCI-TPs

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

Upstream Precursor

BTNNPSLJPBRMLZ-UHFFFAOYSA-O

CC1=NC=C(C(=N1)N)C[NH+](C=O)C(=C(CCOP(=O)(O)O)SC(=O)C2=CC=CC=C2)C

Abiotic

Product

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Upstream Precursor

BTNNPSLJPBRMLZ-UHFFFAOYSA-O

CC1=NC=C(C(=N1)N)C[NH+](C=O)C(=C(CCOP(=O)(O)O)SC(=O)C2=CC=CC=C2)C

Environmental

Product

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Upstream Precursor

BTNNPSLJPBRMLZ-UHFFFAOYSA-O

CC1=NC=C(C(=N1)N)C[NH+](C=O)C(=C(CCOP(=O)(O)O)SC(=O)C2=CC=CC=C2)C

Environmental

Product

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Upstream Precursor

AZJUFRDUYTYIHV-UHFFFAOYSA-N

C26H26N4O4S

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCOC(=O)C2=CC=CC=C2)SC(=O)C3=CC=…

Abiotic

Product

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Upstream Precursor

AZJUFRDUYTYIHV-UHFFFAOYSA-N

C26H26N4O4S

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCOC(=O)C2=CC=CC=C2)SC(=O)C3=CC=…

PriorBiotransformation

Product

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Upstream Precursor

AZJUFRDUYTYIHV-UHFFFAOYSA-N

C26H26N4O4S

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCOC(=O)C2=CC=CC=C2)SC(=O)C3=CC=…

Abiotic

Product

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Upstream Precursor

AZJUFRDUYTYIHV-UHFFFAOYSA-N

C26H26N4O4S

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCOC(=O)C2=CC=CC=C2)SC(=O)C3=CC=…

Abiotic

Product

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Upstream Precursor

AZJUFRDUYTYIHV-UHFFFAOYSA-N

C26H26N4O4S

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCOC(=O)C2=CC=CC=C2)SC(=O)C3=CC=…

PriorBiotransformation

Product

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Upstream Precursor

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Abiotic

Product

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Upstream Precursor

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Environmental

Product

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

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

Precursor

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Environmental

Downstream Successor

WPYMKLBDIGXBTP-UHFFFAOYSA-N

Benzoic Acid

C1=CC(=CC=C1)C(O)=O

Precursor

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Environmental

Downstream Successor

ISWSIDIOOBJBQZ-UHFFFAOYSA-N

Phenol

Oc1ccccc1

Precursor

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Environmental

Downstream Successor

FJKROLUGYXJWQN-UHFFFAOYSA-N

4-Hydroxybenzoic Acid

C(=O)(C1=CC=C(O)C=C1)O

Precursor

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Abiotic

Downstream Successor

FJKROLUGYXJWQN-UHFFFAOYSA-N

4-Hydroxybenzoic Acid

C(=O)(C1=CC=C(O)C=C1)O

Precursor

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Environmental

Downstream Successor

FRJCLFVLGNIIPX-UHFFFAOYSA-N

4-Oxocyclohex-2,5-dienecarboxylate

OC(=O)C1C=CC(=O)C=C1

Precursor

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Abiotic

Downstream Successor

FRJCLFVLGNIIPX-UHFFFAOYSA-N

4-Oxocyclohex-2,5-dienecarboxylate

OC(=O)C1C=CC(=O)C=C1

Precursor

KAIJJYZTDMVKOW-UHFFFAOYSA-N

S-[2-[(4-amino-2-methylpyrimidin-5-yl)methyl-formylamino]-5-hydroxypent-2-en-3-yl] benzenecarbothioate

CC1=NC=C(C(=N1)N)CN(C=O)C(=C(CCO)SC(=O)C2=CC=CC=C2)C

Environmental

Downstream Successor

GLDQAMYCGOIJDV-UHFFFAOYSA-N

2,3-Dihydroxybenzoic Acid

C1=CC(=C(C(=C1)C(O)=O)O)O

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

No Original Precursors

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

No Dead-Ends

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

Search with another depth

Depth:

or Explore another compound

Higher depth reveals distant relationships but increases loading time.