Search More · GCI-TPs

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

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

11 steps

Dead-End Product

OKKJLVBELUTLKV-UHFFFAOYSA-N

Methanol

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

5 steps

Dead-End Product

BDAGIHXWWSANSR-UHFFFAOYSA-N

Formic Acid

OC=O

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

6 steps

Dead-End Product

BVKZGUZCCUSVTD-UHFFFAOYSA-N

Carbonic Acid

C(=O)(O)O

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

5 steps

Dead-End Product

MUBZPKHOEPUJKR-UHFFFAOYSA-N

Oxalic Acid

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

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

11 steps

Dead-End Product

CKFGINPQOCXMAZ-UHFFFAOYSA-N

Methanediol

C(O)O

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

11 steps

Dead-End Product

VNWKTOKETHGBQD-UHFFFAOYSA-N

Methane

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

8 steps

Dead-End Product

HEPCJCVNHBXRBO-UHFFFAOYSA-N

Succinyl-carboxylic acid

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

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

13 steps

Dead-End Product

RBBOAWUPWQANPY-UHFFFAOYSA-N

1,2,4-Butantriol Alkohol

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

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

13 steps

Dead-End Product

YPOPNBBFFROUGR-UHFFFAOYSA-N

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

C(CC=C(O)O)O

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

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

RYWJPLGWOMDLNH-UHFFFAOYSA-N

1H-Indole, 1,1'-(3,7-dimethyl-6-octen-1-ylidene)bis-

CC(=CCCC(CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43)C)C

Environmental

Product

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Upstream Precursor

XSHXVCYGTIAJFF-XUTLUUPISA-N

1,1'-(3,7-Dimethylocta-2,6-dienylidene)bis(1H-indole)

CC(=CCC/C(=C/C(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43)/C)C

Environmental

Product

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Upstream Precursor

NSZDWXJCTHRIIL-UHFFFAOYSA-N

CC(CCCC(CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43)C)C

Environmental

Product

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Upstream Precursor

MVYWISPDTAXXGR-UHFFFAOYSA-N

CC(CCCC(=CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43)C)C

Environmental

Product

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Upstream Precursor

JNOSKSCHXKVMKF-UHFFFAOYSA-N

CC(CCCC(=CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43)C)(C)O

Environmental

Product

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Previewing top 5 entries. If you want the full results, please use the download button above.

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Environmental

Downstream Successor

SIKJAQJRHWYJAI-UHFFFAOYSA-N

Indole

c1ccc2cc[nH]c2c1

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Environmental

Downstream Successor

SIKJAQJRHWYJAI-UHFFFAOYSA-N

Indole

c1ccc2cc[nH]c2c1

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Environmental

Downstream Successor

AQULTZMTCLLZBM-UHFFFAOYSA-N

2-(2,3-Dihydroxyphenyl)-2-hydroxyacetic acid

C(=O)(C(C1=CC=CC(=C1O)O)O)O

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Environmental

Downstream Successor

SGNZYJXNUURYCH-UHFFFAOYSA-N

5,6-Dihydroxyindole

OC1=CC2=C(C=C1O)C=CN2

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Environmental

Downstream Successor

RTTHZDANMGTYSE-UHFFFAOYSA-N

1H-Indole-4,5-diol

OC1=C(C=CC2=C1C=CN2)O

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Environmental

Downstream Successor

NLCITBUDQXHLLX-UHFFFAOYSA-N

1H-Indole-6,7-diol

OC1=C(C2=C(C=C1)C=CN2)O

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Environmental

Downstream Successor

MLCFNGQWWKZFBD-UHFFFAOYSA-N

2,3-Dioxy-2,3-dihydroindole

C1=CC2=C(C(C(N2)O)O)C=C1

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Environmental

Downstream Successor

LBBSPQOXZLKDOD-UHFFFAOYSA-N

7-Hydroxycitronellic acid

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

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Environmental

Downstream Successor

CTYSDKAOIQAQAD-UHFFFAOYSA-N

C=1(C=CNC1C=C(O)C(=O)O)C(O)=O

Precursor

YKLKFIPZNHLBMW-UHFFFAOYSA-N

1H-Indole-1-heptanol, eta-1H-indol-1-yl-alpha,alpha,epsilon-trimethyl-

CC(CCCC(C)(C)O)CC(N1C=CC2=CC=CC=C21)N3C=CC4=CC=CC=C43

Environmental

Downstream Successor

DZNZQVKZLOMGIU-UHFFFAOYSA-N

C1=CC=C2C(=C1)C(C(N2O)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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