Search More · GCI-TPs

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

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

10 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

4 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

5 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

10 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

10 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

10 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

10 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

7 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

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Abiotic

Product

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Upstream Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Abiotic

Product

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Upstream Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Environmental

Product

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Upstream Precursor

LNEABKIOUMIBER-UHFFFAOYSA-N

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4S(C5=CC=CC=C53)=O

Abiotic

Product

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Upstream Precursor

LNEABKIOUMIBER-UHFFFAOYSA-N

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4S(C5=CC=CC=C53)=O

Environmental

Product

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Upstream Precursor

LNEABKIOUMIBER-UHFFFAOYSA-N

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4S(C5=CC=CC=C53)=O

Abiotic

Product

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Upstream Precursor

OIIMTAJTLRSHSP-UHFFFAOYSA-N

C1=CC=C2C(=C1)N=CN2CCNCCC[N+]3(C4=CC=CC=C4SC5=CC=CC=C53)[O-]

Environmental

Product

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Upstream Precursor

OIIMTAJTLRSHSP-UHFFFAOYSA-N

C1=CC=C2C(=C1)N=CN2CCNCCC[N+]3(C4=CC=CC=C4SC5=CC=CC=C53)[O-]

Abiotic

Product

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Upstream Precursor

WUYSDGOKQDMLNS-UHFFFAOYSA-N

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4[S+](C5=CC=CC=C53)Cl

Abiotic

Product

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Upstream Precursor

OIIMTAJTLRSHSP-UHFFFAOYSA-N

C1=CC=C2C(=C1)N=CN2CCNCCC[N+]3(C4=CC=CC=C4SC5=CC=CC=C53)[O-]

Environmental

Product

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

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

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Environmental

Downstream Successor

TXXHDPDFNKHHGW-UHFFFAOYSA-N

2,4-Hexadienedioic acid, (2Z,4Z)-

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

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Environmental

Downstream Successor

LYIIBVSRGJSHAV-UHFFFAOYSA-N

Aminoacetaldehyde

NCC=O

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Environmental

Downstream Successor

PCXDJQZLDDHMGX-UHFFFAOYSA-N

Propanal, 3-amino-

NCCC=O

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Environmental

Downstream Successor

WJFKNYWRSNBZNX-UHFFFAOYSA-N

Phenothiazine

N1C2=CC=CC=C2SC3=C1C=CC=C3

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Abiotic

Downstream Successor

HYZJCKYKOHLVJF-UHFFFAOYSA-N

Benzimidazole

C1=NC2=CC=CC=C2N1

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Environmental

Downstream Successor

HYZJCKYKOHLVJF-UHFFFAOYSA-N

Benzimidazole

C1=NC2=CC=CC=C2N1

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Environmental

Downstream Successor

HYZJCKYKOHLVJF-UHFFFAOYSA-N

Benzimidazole

C1=NC2=CC=CC=C2N1

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Environmental

Downstream Successor

DSAFSORWJPSMQS-UHFFFAOYSA-N

Phenothiazine-5-oxide

N1C2=CC=CC=C2S(=O)C3=C1C=CC=C3

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Abiotic

Downstream Successor

DSAFSORWJPSMQS-UHFFFAOYSA-N

Phenothiazine-5-oxide

N1C2=CC=CC=C2S(=O)C3=C1C=CC=C3

Precursor

IOYXESKZORVKOR-UHFFFAOYSA-N

N-[2-(benzimidazol-1-yl)ethyl]-3-phenothiazin-10-ylpropan-1-amine

C1=CC=C2C(=C1)N=CN2CCNCCCN3C4=CC=CC=C4SC5=CC=CC=C53

Abiotic

Downstream Successor

FEWXSEQPMYYWOQ-UHFFFAOYSA-N

N1C2=CC=CC=C2[S+](C3=CC=CC=C31)Cl

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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