Search More · GCI-TPs

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

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

3 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

14 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

14 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

4 steps

Dead-End Product

LJDZFAPLPVPTBD-UHFFFAOYSA-M

CID 22568690

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

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

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

Abiotic

Downstream Successor

KXDHJXZQYSOELW-UHFFFAOYSA-N

Carbamic Acid

OC(=O)N

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

Environmental

Downstream Successor

KXDHJXZQYSOELW-UHFFFAOYSA-N

Carbamic Acid

OC(=O)N

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

Environmental

Downstream Successor

JJYPMNFTHPTTDI-UHFFFAOYSA-N

m-Toluidine

CC1=CC=CC(=C1)N

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

Abiotic

Downstream Successor

JJYPMNFTHPTTDI-UHFFFAOYSA-N

m-Toluidine

CC1=CC=CC(=C1)N

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

Abiotic

Downstream Successor

JJYPMNFTHPTTDI-UHFFFAOYSA-N

m-Toluidine

CC1=CC=CC(=C1)N

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

Abiotic

Downstream Successor

HDGMAACKJSBLMW-UHFFFAOYSA-N

5-Amino-2-hydroxytoluene

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

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

Abiotic

Downstream Successor

AGPKZVBTJJNPAG-UHFFFAOYSA-N

2-Amino-3-methylpentanoic acid

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

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

Environmental

Downstream Successor

AGPKZVBTJJNPAG-UHFFFAOYSA-N

2-Amino-3-methylpentanoic acid

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

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

Abiotic

Downstream Successor

FEZGEJXYMLVCRV-UHFFFAOYSA-N

C1=CC(C(=CC1C)N)=O

Precursor

OQEXHCZNOQFFEZ-UHFFFAOYSA-N

N-[5-(3-bromophenyl)-1,3,4-thiadiazol-2-yl]-3-methyl-2-[(3-methylphenyl)carbamoylamino]pentanamide

CCC(C)C(C(=O)NC1=NN=C(S1)C2=CC(=CC=C2)Br)NC(=O)NC3=CC=CC(=C3)C

Abiotic

Downstream Successor

ALQKEYVDQYGZDN-UHFFFAOYSA-N

6-Amino-o-cresol

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

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

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

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