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Depiction
Upstream Precursor
UIAGMCDKSXEBJQ-UHFFFAOYSA-N
Nimodipine
CC1=C(C(C(=C(N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCOC
Depth 2
Depiction
Product
PWPBMCUBOQNEJD-UHFFFAOYSA-N
3-(2-Hydroxyethyl) 5-isopropyl 2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
CC1=C(C(=C(C(=N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCO
Depiction
Upstream Precursor
SJJUCKCPGPCJQM-UHFFFAOYSA-N
Dehydro nimodipine
CC1=C(C(=C(C(=N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCOC
Depth 1
Depiction
Product
PWPBMCUBOQNEJD-UHFFFAOYSA-N
3-(2-Hydroxyethyl) 5-isopropyl 2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
CC1=C(C(=C(C(=N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCO
Depiction
Upstream Precursor
RNXRFRBWBFBZCQ-UHFFFAOYSA-N
2-Hydroxyethyl isopropyl 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
CC1=C(C(C(=C(N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCO
Depth 1
Depiction
Product
PWPBMCUBOQNEJD-UHFFFAOYSA-N
3-(2-Hydroxyethyl) 5-isopropyl 2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
CC1=C(C(=C(C(=N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCO

Previewing top 3 entries. If you want the full results, please use the download button above.

Depiction
Precursor
PWPBMCUBOQNEJD-UHFFFAOYSA-N
3-(2-Hydroxyethyl) 5-isopropyl 2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
CC1=C(C(=C(C(=N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCO
Depth 3
Depiction
Downstream Successor
AEMRFAOFKBGASW-UHFFFAOYSA-N
Glycolic Acid
C(=O)(CO)O
Depiction
Precursor
PWPBMCUBOQNEJD-UHFFFAOYSA-N
3-(2-Hydroxyethyl) 5-isopropyl 2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
CC1=C(C(=C(C(=N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCO
Depth 2
Depiction
Downstream Successor
WGCNASOHLSPBMP-UHFFFAOYSA-N
Glycolaldehyde
C(C=O)O
Depiction
Precursor
PWPBMCUBOQNEJD-UHFFFAOYSA-N
3-(2-Hydroxyethyl) 5-isopropyl 2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
CC1=C(C(=C(C(=N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCO
Depth 1
Depiction
Downstream Successor
LYCAIKOWRPUZTN-UHFFFAOYSA-N
Ethylene Glycol
C(CO)O
Depiction
Precursor
PWPBMCUBOQNEJD-UHFFFAOYSA-N
3-(2-Hydroxyethyl) 5-isopropyl 2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
CC1=C(C(=C(C(=N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCO
Depth 1
Depiction
Downstream Successor
KFZMGEQAYNKOFK-UHFFFAOYSA-N
Isopropanol
C(C)(C)O
Depiction
Precursor
PWPBMCUBOQNEJD-UHFFFAOYSA-N
3-(2-Hydroxyethyl) 5-isopropyl 2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
CC1=C(C(=C(C(=N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCO
Depth 3
Depiction
Downstream Successor
XLSMFKSTNGKWQX-UHFFFAOYSA-N
Hydroxyacetone
CC(CO)=O
Depiction
Precursor
PWPBMCUBOQNEJD-UHFFFAOYSA-N
3-(2-Hydroxyethyl) 5-isopropyl 2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
CC1=C(C(=C(C(=N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCO
Depth 3
Depiction
Downstream Successor
BULLHNJGPPOUOX-UHFFFAOYSA-N
Chloroacetone
C(CCl)(C)=O
Depiction
Precursor
PWPBMCUBOQNEJD-UHFFFAOYSA-N
3-(2-Hydroxyethyl) 5-isopropyl 2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
CC1=C(C(=C(C(=N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCO
Depth 2
Depiction
Downstream Successor
QLKWNZOBTJKSCW-UHFFFAOYSA-N
2,6-Dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylic acid
CC1=C(C(=C(C(=N1)C)C(=O)O)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)O
Depiction
Precursor
PWPBMCUBOQNEJD-UHFFFAOYSA-N
3-(2-Hydroxyethyl) 5-isopropyl 2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
CC1=C(C(=C(C(=N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCO
Depth 1
Depiction
Downstream Successor
QHTXAYAFRQRYOP-UHFFFAOYSA-N
2,6-Dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylic acid monoisopropyl ester
OC(=O)C1=C(N=C(C(=C1C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OC(C)C)C)C
Depiction
Precursor
PWPBMCUBOQNEJD-UHFFFAOYSA-N
3-(2-Hydroxyethyl) 5-isopropyl 2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5-dicarboxylate
CC1=C(C(=C(C(=N1)C)C(=O)OC(C)C)C2=CC(=CC=C2)[N+](=O)[O-])C(=O)OCCO
Depth 3
Depiction
Downstream Successor
IJAVOCQFNMLMEX-UHFFFAOYSA-N
2,6-Dimethyl-4-(3-nitrophenyl)nicotinic acid
CC1=CC(=C(C(=N1)C)C(=O)O)C2=CC(=CC=C2)[N+](=O)[O-]

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

No Original Precursors

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No Dead-Ends

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