Search More · GCI-TPs

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

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

1 step

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

2 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

6 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

C(CC(C(O)O)O)O

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

But-1-ene-1,1,4-triol

C(CC=C(O)O)O

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

9 steps

Dead-End Product

WCJLIWFWHPOTAC-UHFFFAOYSA-N

Rhodizonic acid

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

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

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

Environmental

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

Environmental

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

Abiotic

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

Environmental

Downstream Successor

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

Environmental

Downstream Successor

JBEBGTMCZIGUTK-UHFFFAOYSA-N

2-Hydroxyhexa-2,4-diendioic acid

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

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

Environmental

Downstream Successor

NLARCUDOUOQRPB-UHFFFAOYSA-N

2-(2-Aminothiazole-4-yl)-2-methoxyiminoacetic acid

OC(=O)C(=NOC)C1=CSC(=N1)N

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

Abiotic

Downstream Successor

NLARCUDOUOQRPB-UHFFFAOYSA-N

2-(2-Aminothiazole-4-yl)-2-methoxyiminoacetic acid

OC(=O)C(=NOC)C1=CSC(=N1)N

Precursor

PKPGSMOHYWOGJR-SLMZUGIISA-N

(Z)-2-methoxymino-2-(2-(tritylamino)thiazol-4-yl)acetic acid

CO/N=C(/C1=CSC(=N1)NC(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)\C(=O)O

Abiotic

Downstream Successor

NLARCUDOUOQRPB-UHFFFAOYSA-N

2-(2-Aminothiazole-4-yl)-2-methoxyiminoacetic acid

OC(=O)C(=NOC)C1=CSC(=N1)N

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 All Precursors

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