Graphs show a maximum of 100 compounds. Use downloads for complete results.
Depiction
Upstream Precursor
{4-[3-(3,4,5-Trimethoxyphenyl)prop-2-enoyl]piperazin-1-YL}acetic acid
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
Abiotic
Depiction
Product
{4-[3-(3,4,5-Trimethoxyphenyl)prop-2-enoyl]piperazin-1-YL}acetic acid
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
Depiction
Upstream Precursor
COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CCN(CC2)CC(=O)[NH+]3CCCC3
Abiotic
Depiction
Product
{4-[3-(3,4,5-Trimethoxyphenyl)prop-2-enoyl]piperazin-1-YL}acetic acid
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
Depiction
Upstream Precursor
COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CCN(CC2)CC(=O)[NH+]3CCCC3
Abiotic
Depiction
Product
{4-[3-(3,4,5-Trimethoxyphenyl)prop-2-enoyl]piperazin-1-YL}acetic acid
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
Depiction
Upstream Precursor
COC1=CC(=CC(=C1OC)OC)C=CC(=O)N2CCN(CC2)CC(=O)[NH+]3CCCC3
Environmental
Depiction
Product
{4-[3-(3,4,5-Trimethoxyphenyl)prop-2-enoyl]piperazin-1-YL}acetic acid
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
Depiction
Upstream Precursor
CC(C)NC(=O)CN1CC[NH+](CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC
Environmental
Depiction
Product
{4-[3-(3,4,5-Trimethoxyphenyl)prop-2-enoyl]piperazin-1-YL}acetic acid
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
Depiction
Upstream Precursor
CC(C)NC(=O)CN1CC[NH+](CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC
Abiotic
Depiction
Product
{4-[3-(3,4,5-Trimethoxyphenyl)prop-2-enoyl]piperazin-1-YL}acetic acid
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
Depiction
Upstream Precursor
CC(C)NC(=O)CN1CC[NH+](CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC
Environmental
Depiction
Product
{4-[3-(3,4,5-Trimethoxyphenyl)prop-2-enoyl]piperazin-1-YL}acetic acid
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
Depiction
Upstream Precursor
C(=O)(CN1CC[N+](CC1)(C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)[O-])O
Environmental
Depiction
Product
{4-[3-(3,4,5-Trimethoxyphenyl)prop-2-enoyl]piperazin-1-YL}acetic acid
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
Depiction
Upstream Precursor
C(=O)(CN1CC[N+](CC1)(C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)[O-])O
Environmental
Depiction
Product
{4-[3-(3,4,5-Trimethoxyphenyl)prop-2-enoyl]piperazin-1-YL}acetic acid
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
Depiction
Precursor
{4-[3-(3,4,5-Trimethoxyphenyl)prop-2-enoyl]piperazin-1-YL}acetic acid
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
Environmental
Depiction
Downstream Successor
Cinepazide Impurity G
OC(=O)C=CC1=CC(=C(C(=C1)OC)OC)OC
Depiction
Precursor
{4-[3-(3,4,5-Trimethoxyphenyl)prop-2-enoyl]piperazin-1-YL}acetic acid
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
Abiotic
Depiction
Downstream Successor
Cinepazide Impurity G
OC(=O)C=CC1=CC(=C(C(=C1)OC)OC)OC
Depiction
Precursor
{4-[3-(3,4,5-Trimethoxyphenyl)prop-2-enoyl]piperazin-1-YL}acetic acid
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)OC)OC)OC)O
Environmental
Depiction
Downstream Successor
C(=O)(CN1CCN(CC1)C(=O)C=CC2=CC(=C(C(=C2)O)OC)OC)O
No Original Precursors

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

No Dead-Ends

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

Search with another depth
or Explore another compound
Higher depth reveals distant relationships but increases loading time.