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Depiction
Upstream Precursor
COC1=CC=C(C=C1)CC2C3=C(CCCC3)CC[NH+]2C(=O)C4CCC4
Abiotic
Depiction
Product
cyclobutyl-[1-[(4-methoxyphenyl)methyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]methanone
COC1=CC=C(C=C1)CC2C3C(CCCC3)CCN2C(=O)C4CCC4
Depiction
Upstream Precursor
COC1=CC=C(C=C1)CC2C3=C(CCCC3)CC[NH+]2C(=O)C4CCC4
Environmental
Depiction
Product
cyclobutyl-[1-[(4-methoxyphenyl)methyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]methanone
COC1=CC=C(C=C1)CC2C3C(CCCC3)CCN2C(=O)C4CCC4
Depiction
Upstream Precursor
COC1=CC=C(C=C1)CC2C3=C(CCCC3)CC[NH+]2C(=O)C4CCC4
Environmental
Depiction
Product
cyclobutyl-[1-[(4-methoxyphenyl)methyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]methanone
COC1=CC=C(C=C1)CC2C3C(CCCC3)CCN2C(=O)C4CCC4
Depiction
Upstream Precursor
cyclobutyl-[1-[(4-methoxyphenyl)methyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]methanone
COC1=CC=C(C=C1)CC2C3C(CCCC3)CCN2C(=O)C4CCC4
Abiotic
Depiction
Product
cyclobutyl-[1-[(4-methoxyphenyl)methyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]methanone
COC1=CC=C(C=C1)CC2C3C(CCCC3)CCN2C(=O)C4CCC4
Depiction
Upstream Precursor
COC1=CC=C(C=C1)CC2C3C(CCCC3)CC[N+]2(C(=O)C4CCC4)[O-]
Environmental
Depiction
Product
cyclobutyl-[1-[(4-methoxyphenyl)methyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]methanone
COC1=CC=C(C=C1)CC2C3C(CCCC3)CCN2C(=O)C4CCC4
Depiction
Upstream Precursor
COC1=CC=C(C=C1)CC2C3=C(CCCC3)CC[N+]2(C(=O)C4CCC4)[O-]
Environmental
Depiction
Product
cyclobutyl-[1-[(4-methoxyphenyl)methyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]methanone
COC1=CC=C(C=C1)CC2C3C(CCCC3)CCN2C(=O)C4CCC4
Depiction
Precursor
cyclobutyl-[1-[(4-methoxyphenyl)methyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]methanone
COC1=CC=C(C=C1)CC2C3C(CCCC3)CCN2C(=O)C4CCC4
Environmental
Depiction
Downstream Successor
Glutaric Acid
OC(=O)CCCC(O)=O
Depiction
Precursor
cyclobutyl-[1-[(4-methoxyphenyl)methyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]methanone
COC1=CC=C(C=C1)CC2C3C(CCCC3)CCN2C(=O)C4CCC4
Environmental
Depiction
Downstream Successor
Cyclobutanecarboxylic acid
OC(=O)C1CCC1
Depiction
Precursor
cyclobutyl-[1-[(4-methoxyphenyl)methyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]methanone
COC1=CC=C(C=C1)CC2C3C(CCCC3)CCN2C(=O)C4CCC4
Abiotic
Depiction
Downstream Successor
Cyclobutanecarboxylic acid
OC(=O)C1CCC1
Depiction
Precursor
cyclobutyl-[1-[(4-methoxyphenyl)methyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]methanone
COC1=CC=C(C=C1)CC2C3C(CCCC3)CCN2C(=O)C4CCC4
Environmental
Depiction
Downstream Successor
Cyclobutanecarboxylic acid
OC(=O)C1CCC1
Depiction
Precursor
cyclobutyl-[1-[(4-methoxyphenyl)methyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]methanone
COC1=CC=C(C=C1)CC2C3C(CCCC3)CCN2C(=O)C4CCC4
Abiotic
Depiction
Downstream Successor
Cyclobutanecarboxylic acid
OC(=O)C1CCC1
Depiction
Precursor
cyclobutyl-[1-[(4-methoxyphenyl)methyl]-3,4,4a,5,6,7,8,8a-octahydro-1H-isoquinolin-2-yl]methanone
COC1=CC=C(C=C1)CC2C3C(CCCC3)CCN2C(=O)C4CCC4
Environmental
Depiction
Downstream Successor
C1(=CC=C(C=C1)CC2C3C(CCCC3)CCN2)O
No Original Precursors

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No Dead-Ends

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