Search More · GCI-TPs

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Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

1 step

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

7 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

7 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

9 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

15 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

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

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

10 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

c1(c(c(=O)c(c(c1=O)O)O)=O)=O

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

7 steps

Dead-End Product

XEDSRSOTDZKLMT-UHFFFAOYSA-N

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

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

Upstream Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

Abiotic

Product

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

Upstream Precursor

JOXOFRIHOFKJCG-UHFFFAOYSA-N

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[N+]2(CC=C)[O-])S(=O)(=O)N

Environmental

Product

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

Previewing top 2 entries. If you want the full results, please use the download button above.

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

Environmental

Downstream Successor

HGINCPLSRVDWNT-UHFFFAOYSA-N

Acrolein

C(C=C)=O

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

Environmental

Downstream Successor

DLVHCNKXFJLECF-UHFFFAOYSA-N

3-Chlorolactaldehyde

C(C(O)CCl)=O

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

Environmental

Downstream Successor

AUKXFNABVHIUAC-UHFFFAOYSA-N

2-Pyrrolidinemethanamine

NCC1CCCN1

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

Abiotic

Downstream Successor

AUKXFNABVHIUAC-UHFFFAOYSA-N

2-Pyrrolidinemethanamine

NCC1CCCN1

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

Abiotic

Downstream Successor

HTGKTSVPJJNEMQ-UHFFFAOYSA-N

1-(Allyl)pyrrolidine-2-methylamine

NCC1CCCN1CC=C

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

Environmental

Downstream Successor

HTGKTSVPJJNEMQ-UHFFFAOYSA-N

1-(Allyl)pyrrolidine-2-methylamine

NCC1CCCN1CC=C

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

Environmental

Downstream Successor

KNHVARJOHSBMHG-UHFFFAOYSA-N

(1-Allyl-pyrrolidin-2-yl)-methanol

C(C1CCCN1CC=C)O

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

Abiotic

Downstream Successor

YEVQOPOKMKTXMD-UHFFFAOYSA-N

2,3-Dimethoxy-5-sulphamoylbenzoic acid

C(=O)(C1=C(C(=CC(=C1)S(=O)(=O)N)OC)OC)O

Precursor

RYJXBGGBZJGVQF-UHFFFAOYSA-O

2,3-dimethoxy-N-[(1-prop-2-enylpyrrolidin-2-yl)methyl]-5-sulfamoylbenzamide;hydron

COC1=CC(=CC(=C1OC)C(=O)NCC2CCC[NH+]2CC=C)S(=O)(=O)N

Environmental

Downstream Successor

YEVQOPOKMKTXMD-UHFFFAOYSA-N

2,3-Dimethoxy-5-sulphamoylbenzoic acid

C(=O)(C1=C(C(=CC(=C1)S(=O)(=O)N)OC)OC)O

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

No Original Precursors

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