Search More · GCI-TPs

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

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

1 step

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

3 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

5 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

4 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

12 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

12 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

7 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

12 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

12 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

8 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

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Abiotic

Product

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Upstream Precursor

YUUSIWGGZJJALB-UHFFFAOYSA-N

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[N+](CC3)(C4=CC=CC=C4)[O-]

Abiotic

Product

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Upstream Precursor

YUUSIWGGZJJALB-UHFFFAOYSA-N

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[N+](CC3)(C4=CC=CC=C4)[O-]

Environmental

Product

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Upstream Precursor

YUUSIWGGZJJALB-UHFFFAOYSA-N

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[N+](CC3)(C4=CC=CC=C4)[O-]

Environmental

Product

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Upstream Precursor

IISWCMXRCFIUEB-UHFFFAOYSA-N

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CC[N+]3(CCN(CC3)C4=CC=CC=C4)[O-]

Abiotic

Product

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Upstream Precursor

IISWCMXRCFIUEB-UHFFFAOYSA-N

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CC[N+]3(CCN(CC3)C4=CC=CC=C4)[O-]

Environmental

Product

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Upstream Precursor

IISWCMXRCFIUEB-UHFFFAOYSA-N

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CC[N+]3(CCN(CC3)C4=CC=CC=C4)[O-]

Environmental

Product

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Upstream Precursor

VMYXYAKWRWTRJW-UHFFFAOYSA-N

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CC[N+]3(CC[N+](CC3)(C4=CC=CC=C4)[…

Environmental

Product

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Previewing top 8 entries. If you want the full results, please use the download button above.

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Environmental

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Abiotic

Downstream Successor

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Environmental

Downstream Successor

GLUUGHFHXGJENI-UHFFFAOYSA-N

Piperazine

C1CNCCN1

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Abiotic

Downstream Successor

GLUUGHFHXGJENI-UHFFFAOYSA-N

Piperazine

C1CNCCN1

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Environmental

Downstream Successor

YZTJYBJCZXZGCT-UHFFFAOYSA-O

1-Phenylpiperazin-4-ium

C1C[NH+](CCN1)c2ccccc2

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Environmental

Downstream Successor

GOXGEQNLELAGME-UHFFFAOYSA-N

3-(Piperazin-1-yl)benzene-1,2-diol

OC1=C(C=CC=C1N2CCNCC2)O

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Environmental

Downstream Successor

HINNJCVZQJDZMT-UHFFFAOYSA-N

4-(1-Piperazinyl)-1,2-benzenediol

N1CCN(CC1)C2=CC=C(C(=C2)O)O

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Environmental

Downstream Successor

CDVPQTNUJIAOCZ-UHFFFAOYSA-N

1-Oxido-1-phenylpiperazin-1-ium

C1C[N+](CCN1)(c2ccccc2)[O-]

Precursor

XCWPUUGSGHNIDZ-UHFFFAOYSA-O

5,6-dimethoxy-2-methyl-3-[2-(4-phenylpiperazin-1-yl)ethyl]-1H-indole;hydron

CC1=C(C2=CC(=C(C=C2N1)OC)OC)CCN3CC[NH+](CC3)C4=CC=CC=C4

Abiotic

Downstream Successor

CDVPQTNUJIAOCZ-UHFFFAOYSA-N

1-Oxido-1-phenylpiperazin-1-ium

C1C[N+](CCN1)(c2ccccc2)[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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