Graphs show a maximum of 100 compounds. Use downloads for complete results.
Depiction
Upstream Precursor
FNPXMHRZILFCKX-KAJVQRHHSA-N
Prednicarbate
CCC(=O)OCC(=O)[C@]1(CC[C@@H]2[C@@]1(C[C@@H]([C@H]3[C@H]2CCC4=…
Environmental
Depiction
Product
BPAMAIXNRIHJGN-UHFFFAOYSA-N
[2-(17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl] propanoate
CCC(=O)OCC(=O)C1(CCC2C1(CC(C3C2CCC4=CC(=O)CCC34C)O)C)OC(=O)OCC

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Depiction
Precursor
BPAMAIXNRIHJGN-UHFFFAOYSA-N
[2-(17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl] propanoate
CCC(=O)OCC(=O)C1(CCC2C1(CC(C3C2CCC4=CC(=O)CCC34C)O)C)OC(=O)OCC
Environmental
Depiction
Downstream Successor
QTBSBXVTEAMEQO-UHFFFAOYSA-N
Acetic Acid
CC(=O)O
Depiction
Precursor
BPAMAIXNRIHJGN-UHFFFAOYSA-N
[2-(17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl] propanoate
CCC(=O)OCC(=O)C1(CCC2C1(CC(C3C2CCC4=CC(=O)CCC34C)O)C)OC(=O)OCC
Environmental
Depiction
Downstream Successor
IKHGUXGNUITLKF-UHFFFAOYSA-N
Acetaldehyde
C(C)=O
Depiction
Precursor
BPAMAIXNRIHJGN-UHFFFAOYSA-N
[2-(17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl] propanoate
CCC(=O)OCC(=O)C1(CCC2C1(CC(C3C2CCC4=CC(=O)CCC34C)O)C)OC(=O)OCC
Abiotic
Depiction
Downstream Successor
IKHGUXGNUITLKF-UHFFFAOYSA-N
Acetaldehyde
C(C)=O
Depiction
Precursor
BPAMAIXNRIHJGN-UHFFFAOYSA-N
[2-(17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl] propanoate
CCC(=O)OCC(=O)C1(CCC2C1(CC(C3C2CCC4=CC(=O)CCC34C)O)C)OC(=O)OCC
Environmental
Depiction
Downstream Successor
IKHGUXGNUITLKF-UHFFFAOYSA-N
Acetaldehyde
C(C)=O
Depiction
Precursor
BPAMAIXNRIHJGN-UHFFFAOYSA-N
[2-(17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl] propanoate
CCC(=O)OCC(=O)C1(CCC2C1(CC(C3C2CCC4=CC(=O)CCC34C)O)C)OC(=O)OCC
Environmental
Depiction
Downstream Successor
BDAGIHXWWSANSR-UHFFFAOYSA-N
Formic Acid
OC=O
Depiction
Precursor
BPAMAIXNRIHJGN-UHFFFAOYSA-N
[2-(17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl] propanoate
CCC(=O)OCC(=O)C1(CCC2C1(CC(C3C2CCC4=CC(=O)CCC34C)O)C)OC(=O)OCC
Environmental
Depiction
Downstream Successor
LFQSCWFLJHTTHZ-UHFFFAOYSA-N
Ethanol
C(C)O
Depiction
Precursor
BPAMAIXNRIHJGN-UHFFFAOYSA-N
[2-(17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl] propanoate
CCC(=O)OCC(=O)C1(CCC2C1(CC(C3C2CCC4=CC(=O)CCC34C)O)C)OC(=O)OCC
Abiotic
Depiction
Downstream Successor
LFQSCWFLJHTTHZ-UHFFFAOYSA-N
Ethanol
C(C)O
Depiction
Precursor
BPAMAIXNRIHJGN-UHFFFAOYSA-N
[2-(17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl] propanoate
CCC(=O)OCC(=O)C1(CCC2C1(CC(C3C2CCC4=CC(=O)CCC34C)O)C)OC(=O)OCC
Abiotic
Depiction
Downstream Successor
LFQSCWFLJHTTHZ-UHFFFAOYSA-N
Ethanol
C(C)O
Depiction
Precursor
BPAMAIXNRIHJGN-UHFFFAOYSA-N
[2-(17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl] propanoate
CCC(=O)OCC(=O)C1(CCC2C1(CC(C3C2CCC4=CC(=O)CCC34C)O)C)OC(=O)OCC
Environmental
Depiction
Downstream Successor
LFQSCWFLJHTTHZ-UHFFFAOYSA-N
Ethanol
C(C)O
Depiction
Precursor
BPAMAIXNRIHJGN-UHFFFAOYSA-N
[2-(17-ethoxycarbonyloxy-11-hydroxy-10,13-dimethyl-3-oxo-2,6,7,8,9,11,12,14,15,16-decahydro-1H-cyclopenta[a]phenanthren-17-yl)-2-oxoethyl] propanoate
CCC(=O)OCC(=O)C1(CCC2C1(CC(C3C2CCC4=CC(=O)CCC34C)O)C)OC(=O)OCC
Environmental
Depiction
Downstream Successor
XBDQKXXYIPTUBI-UHFFFAOYSA-N
Propionic Acid
C(=O)(CC)O

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No Original Precursors

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No Dead-Ends

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