Search More · GCI-TPs

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

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

2 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

6 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

6 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

9 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.

Upstream Precursor

JICJBGPOMZQUBB-UHFFFAOYSA-N

Tianeptine

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)NCCCCCCC(=O)O

Environmental

Product

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Upstream Precursor

JICJBGPOMZQUBB-UHFFFAOYSA-N

Tianeptine

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)NCCCCCCC(=O)O

Environmental

Product

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Upstream Precursor

JICJBGPOMZQUBB-UHFFFAOYSA-N

Tianeptine

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)NCCCCCCC(=O)O

Environmental

Product

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Upstream Precursor

BYPYVXCZPZLHBO-UHFFFAOYSA-N

Tianeptine Metabolite MC5

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)NCCCCC(O)=O

Environmental

Product

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Upstream Precursor

BYPYVXCZPZLHBO-UHFFFAOYSA-N

Tianeptine Metabolite MC5

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)NCCCCC(O)=O

Environmental

Product

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Upstream Precursor

DNCDZUCGWZZQMV-UHFFFAOYSA-N

N-(3-Chloro-6,11-dihydro-6-methyl-5,5-dioxidodibenzo[c,f][1,2]thiazepin-11-yl)-Beta-alanine

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)NCCC(O)=O

Environmental

Product

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Previewing top 6 entries. If you want the full results, please use the download button above.

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Environmental

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Abiotic

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Environmental

Downstream Successor

BAVYZALUXZFZLV-UHFFFAOYSA-N

Methylamine

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Environmental

Downstream Successor

RGOFXWXKWORKIP-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyl-5,5,11-trioxodibenzo(c,f)(1,2)thiazepine

CN1C2=CC=CC=C2C(=O)C3=C(S1(=O)=O)C=C(C=C3)Cl

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Environmental

Downstream Successor

HYSUCZDIWZXITO-UHFFFAOYSA-M

CNC1=CC(=C(C=C1C(C2=C(S(=O)(=O)[O-])C=C(C=C2)Cl)N)O)O

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Environmental

Downstream Successor

QWHIBFIFUAUOHQ-UHFFFAOYSA-M

CNC1=C(C(=CC=C1C(C2=C(S(=O)(=O)[O-])C=C(C=C2)Cl)N)O)O

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Environmental

Downstream Successor

XIHKHAMAHLSENZ-UHFFFAOYSA-N

CNC1=CC=CC=C1C(=O)C2=C(S(=O)(=O)O)C=C(C=C2)Cl

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Abiotic

Downstream Successor

XIHKHAMAHLSENZ-UHFFFAOYSA-N

CNC1=CC=CC=C1C(=O)C2=C(S(=O)(=O)O)C=C(C=C2)Cl

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Environmental

Downstream Successor

DNYMONIDGFACKY-UHFFFAOYSA-M

CNC1=CC=C(C(=C1C(C2=C(S(=O)(=O)[O-])C=C(C=C2)Cl)N)O)O

Precursor

IGSJOGMOHGCKOZ-UHFFFAOYSA-N

3-Chloro-6,11-dihydro-6-methyldibenzo(c,f)(1,2)thiazepin-11-amine 5,5-dioxide

CN1C2=CC=CC=C2C(C3=C(S1(=O)=O)C=C(C=C3)Cl)N

Abiotic

Downstream Successor

KMWVRBIPSRORON-UHFFFAOYSA-N

C1(=C(C=CC=C1C(C2=C(S(=O)(=O)O)C=C(C=C2)Cl)N)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.

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