@
Home
Compounds
Reactions
Pathways
About
Login
Register
Admin
EAWAG-BBD Pathways
Total Pathways:
219
Draw Structure
Search
💡
Tip:
The "Draw Structure" button allows you to search for pathways whose starting compound contains your drawn structure as a
substructure
.
(+)-Camphor
(+)-Camphor
Starting Compound:
(+)-Camphor
CC1(C)C2CCC1(C)C(=O)C2
View Pathway Details →
1,1,1-Trichloro-2,2-bis-(4`-chlorophenyl)ethane (DDT)
1,1,1-Trichloro-2,2-bis-(4`-chlorophenyl)ethane (DDT)
Starting Compound:
1,1,1-Trichloro-2,2-bis-(4`-chlorophenyl)ethane (DDT)
C1=C(C=CC(=C1)Cl)C(C2=CC=C(C=C2)Cl)C(Cl)(Cl)Cl
View Pathway Details →
1,1,1-Trichloro-2,2-bis-(4`-chlorophenyl)ethane (DDT)
1,1,1-Trichloro-2,2-bis-(4`-chlorophenyl)ethane (DDT) (anaerobic)
Starting Compound:
1,1,1-Trichloro-2,2-bis-(4`-chlorophenyl)ethane (DDT)
C1=C(C=CC(=C1)Cl)C(C2=CC=C(C=C2)Cl)C(Cl)(Cl)Cl
View Pathway Details →
1,1,1-Trichloroethane
1,1,1-Trichloroethane (an/aerobic)
Starting Compound:
1,1,1-Trichloroethane
CC(Cl)(Cl)Cl
View Pathway Details →
1,2,3-Tribromopropane
1,2,3-Tribromopropane
Starting Compound:
1,2,3-Tribromopropane
C(C(CBr)Br)Br
View Pathway Details →
1,2,4-Trichlorobenzene
1,2,4-Trichlorobenzene (an/aerobic)
Starting Compound:
1,2,4-Trichlorobenzene
C1=C(C=C(C(=C1)Cl)Cl)Cl
View Pathway Details →
1,2-Dichloroethane
1,2-Dichloroethane
Starting Compound:
1,2-Dichloroethane
C(CCl)Cl
View Pathway Details →
1,3-Dichloro-2-propanol
1,3-Dichloro-2-propanol
Starting Compound:
1,3-Dichloro-2-propanol
C(C(CCl)O)Cl
View Pathway Details →
cis-1,3-Dichloropropene
1,3-Dichloropropene
Starting Compound:
cis-1,3-Dichloropropene
ClC=CCCl
View Pathway Details →
1,4-Dichlorobenzene
1,4-Dichlorobenzene
Starting Compound:
1,4-Dichlorobenzene
C1=C(C=CC(=C1)Cl)Cl
View Pathway Details →
1,4-Dioxane
1,4-Dioxane
Starting Compound:
1,4-Dioxane
C1COCCO1
View Pathway Details →
1,5-Anhydro-D-fructose
1,5-Anhydro-D-fructose (Fungal)
Starting Compound:
1,5-Anhydro-D-fructose
C([C@@H]1[C@H]([C@@H](C(=O)CO1)O)O)O
View Pathway Details →
1-Aminocyclopropane-1-carboxylate
1-Aminocyclopropane-1-carboxylate
Starting Compound:
1-Aminocyclopropane-1-carboxylate
C1CC1(C(=O)[O-])N
View Pathway Details →
1-Methylnaphthalene
1-Methylnaphthalene
Starting Compound:
1-Methylnaphthalene
CC1=CC=CC2=C1C=CC=C2
View Pathway Details →
1-Naphthoic acid
1-Naphthoic Acid
Starting Compound:
1-Naphthoic acid
C1=CC2=C(C=C1)C(=CC=C2)C(=O)[O-]
View Pathway Details →
2,4,5-Trichlorophenoxyacetic acid
2,4,5-Trichlorophenoxyacetic Acid
Starting Compound:
2,4,5-Trichlorophenoxyacetic acid
C1=C(C(=CC(=C1Cl)Cl)OCC(=O)[O-])Cl
View Pathway Details →
2,4,6-Trinitrotoluene
2,4,6-Trinitrotoluene (anaerobic)
Starting Compound:
2,4,6-Trinitrotoluene
CC1=C(C=C(C=C1[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-]
View Pathway Details →
2,4-Dichloroaniline
2,4-Dichloroaniline
Starting Compound:
2,4-Dichloroaniline
C1=C(C=C(C(=C1)N)Cl)Cl
View Pathway Details →
2,4-Dichlorobenzoate
2,4-Dichlorobenzoate
Starting Compound:
2,4-Dichlorobenzoate
C1=C(C=C(C(=C1)C(=O)[O-])Cl)Cl
View Pathway Details →
2,4-Dichlorophenoxyacetic acid
2,4-Dichlorophenoxyacetic Acid
Starting Compound:
2,4-Dichlorophenoxyacetic acid
C1=C(C=C(C(=C1)OCC(=O)[O-])Cl)Cl
View Pathway Details →
2,4-Dichlorotoluene
2,4-Dichlorotoluene
Starting Compound:
2,4-Dichlorotoluene
CC1=CC=C(C=C1Cl)Cl
View Pathway Details →
2,4-Dinitrotoluene
2,4-Dinitrotoluene
Starting Compound:
2,4-Dinitrotoluene
CC1=CC=C(C=C1[N+](=O)[O-])[N+](=O)[O-]
View Pathway Details →
2-Aminobenzenesulfonate
2-Aminobenzenesulfonate
Starting Compound:
2-Aminobenzenesulfonate
C1=CC(=C(C=C1)S(=O)(=O)[O-])N
View Pathway Details →
2-Aminobenzoate
2-Aminobenzoate
Starting Compound:
2-Aminobenzoate
C1=CC(=C(C=C1)N)C(=O)[O-]
View Pathway Details →
2-Aminobenzoate
2-Aminobenzoate (anaerobic)
Starting Compound:
2-Aminobenzoate
C1=CC(=C(C=C1)N)C(=O)[O-]
View Pathway Details →
2-Chloro-N-isopropylacetanilide
2-Chloro-N-isopropylacetanilide
Starting Compound:
2-Chloro-N-isopropylacetanilide
CC(C)N(C1=CC=CC=C1)C(=O)CCl
View Pathway Details →
2-Mercaptobenzothiazole
2-Mercaptobenzothiazole
Starting Compound:
2-Mercaptobenzothiazole
SC1=NC=2C=CC=CC2S1
View Pathway Details →
2-Methylnaphthalene
2-Methylnaphthalene
Starting Compound:
2-Methylnaphthalene
C=1C=CC=2C=C(C=CC2C1)C
View Pathway Details →
2-Methylnaphthalene
2-Methylnaphthalene (anaerobic)
Starting Compound:
2-Methylnaphthalene
C=1C=CC=2C=C(C=CC2C1)C
View Pathway Details →
2-Nitropropane
2-Nitropropane
Starting Compound:
2-Nitropropane
O=[N+]([O-])C(C)C
View Pathway Details →
3,3`-Dithiodipropionate
3,3`-Dithiodipropionate
Starting Compound:
3,3`-Dithiodipropionate
O=C([O-])CCSSCCC(=O)[O-]
View Pathway Details →
3-(4-Sulfophenyl)butyrate
3-(4-Sulfophenyl)butyrate
Starting Compound:
3-(4-Sulfophenyl)butyrate
O=C([O-])CC(C1=CC=C(C=C1)S(=O)(=O)[O-])C
View Pathway Details →
cis-3-Chloroacrylic acid
3-Chloroacrylic Acid
Starting Compound:
cis-3-Chloroacrylic acid
O=C([O-])C=CCl
View Pathway Details →
3-Fluorobenzoate
3-Fluorobenzoate
Starting Compound:
3-Fluorobenzoate
O=C([O-])C=1C=CC=C(F)C1
View Pathway Details →
3-Methylquinoline
3-Methylquinoline
Starting Compound:
3-Methylquinoline
N=1C=C(C=C2C=CC=CC12)C
View Pathway Details →
3-Nitrotyrosine
3-Nitrotyrosine Family
Starting Compound:
3-Nitrotyrosine
O=C([O-])C(N)CC1=CC=C(O)C(=C1)[N+](=O)[O-]
View Pathway Details →
3-Phenylpropionate
3-Phenylpropionate
Starting Compound:
3-Phenylpropionate
O=C([O-])CCC=1C=CC=CC1
View Pathway Details →
4-(1-Ethyl-1,4-dimethyl-pentyl)phenol
4-(1-Ethyl-1,4-dimethyl-pentyl)phenol
Starting Compound:
4-(1-Ethyl-1,4-dimethyl-pentyl)phenol
OC1=CC=C(C=C1)C(C)(CC)CCC(C)C
View Pathway Details →
4-Carboxy-4`-sulfoazobenzene
4-Carboxy-4`-Sulfoazobenzene
Starting Compound:
4-Carboxy-4`-sulfoazobenzene
O=C([O-])C1=CC=C(N=NC2=CC=C(C=C2)S(=O)(=O)[O-])C=C1
View Pathway Details →
4-Chlorobiphenyl
4-Chlorobiphenyl
Starting Compound:
4-Chlorobiphenyl
ClC=1C=CC(=CC1)C=2C=CC=CC2
View Pathway Details →
4-Fluorobenzoate
4-Fluorobenzoate (an/aerobic)
Starting Compound:
4-Fluorobenzoate
O=C([O-])C1=CC=C(F)C=C1
View Pathway Details →
4-Hydroxyacetophenone
4-Hydroxyacetophenone
Starting Compound:
4-Hydroxyacetophenone
O=C(C1=CC=C(O)C=C1)C
View Pathway Details →
4-Hydroxypyridine
4-Hydroxypyridine
Starting Compound:
4-Hydroxypyridine
OC=1C=CN=CC1
View Pathway Details →
5-Nitroanthranilate
5-Nitroanthanilate
Starting Compound:
5-Nitroanthranilate
O=C([O-])C1=CC(=CC=C1N)[N+](=O)[O-]
View Pathway Details →
Acenaphthylene
Acenaphthylene
Starting Compound:
Acenaphthylene
C=1C=C2C=CC=C3C=CC(C1)=C23
View Pathway Details →
Acetylene
Acetylene
Starting Compound:
Acetylene
C#C
View Pathway Details →
Acrylonitrile
Acrylonitrile
Starting Compound:
Acrylonitrile
N#CC=C
View Pathway Details →
Adamantanone
Adamantanone
Starting Compound:
Adamantanone
O=C1C2CC3CC1CC(C2)C3
View Pathway Details →
Alachlor
Alachlor
Starting Compound:
Alachlor
O=C(N(C=1C(=CC=CC1CC)CC)COC)CCl
View Pathway Details →
Anthracene
Anthracene
Starting Compound:
Anthracene
C=1C=CC=2C=C3C=CC=CC3=CC2C1
View Pathway Details →
Anthracene
Anthracene (fungal)
Starting Compound:
Anthracene
C=1C=CC=2C=C3C=CC=CC3=CC2C1
View Pathway Details →
Arsonoacetate
Arsonoacetate
Starting Compound:
Arsonoacetate
O=C([O-])C[As](=O)(O)O
View Pathway Details →
Asulam
Asulam
Starting Compound:
Asulam
O=C(OC)NS(=O)(=O)C1=CC=C(N)C=C1
View Pathway Details →
Atenolol
Atenolol
Starting Compound:
Atenolol
O=C(N)CC1=CC=C(OCC(O)CNC(C)C)C=C1
View Pathway Details →
Atrazine
Atrazine
Starting Compound:
Atrazine
ClC=1N=C(N=C(N1)NC(C)C)NCC
View Pathway Details →
Atropine
Atropine
Starting Compound:
Atropine
O=C(OC1CC2N(C)C(CC2)C1)C(C=3C=CC=CC3)CO
View Pathway Details →
Benomyl
Benomyl
Starting Compound:
Benomyl
O=C(OC)NC1=NC=2C=CC=CC2N1C(=O)NCCCC
View Pathway Details →
Benzo(a)pyrene
Benzo[a]pyrene
Starting Compound:
Benzo(a)pyrene
C=1C=CC2=C(C1)C=C3C=CC4=CC=CC=5C=CC2=C3C45
View Pathway Details →
Benzoate
Benzoate
Starting Compound:
Benzoate
O=C([O-])C=1C=CC=CC1
View Pathway Details →
Terephthalate
Benzoate (anaerobic)
Starting Compound:
Terephthalate
O=C([O-])C1=CC=C(C=C1)C(=O)[O-]
View Pathway Details →
Benzonitrile
Benzonitrile
Starting Compound:
Benzonitrile
N#CC=1C=CC=CC1
View Pathway Details →
Benzothiophene
Benzothiophene Desulfurization
Starting Compound:
Benzothiophene
S1C=CC=2C=CC=CC12
View Pathway Details →
Benzyl sulfide
Benzyl Sulfide
Starting Compound:
Benzyl sulfide
S(CC=1C=CC=CC1)CC=2C=CC=CC2
View Pathway Details →
Biphenyl
Biphenyl
Starting Compound:
Biphenyl
C=1C=CC(=CC1)C=2C=CC=CC2
View Pathway Details →
Bisphenol A
Bisphenol A
Starting Compound:
Bisphenol A
OC1=CC=C(C=C1)C(C2=CC=C(O)C=C2)(C)C
View Pathway Details →
Bisphenol F
Bisphenol F
Starting Compound:
Bisphenol F
OC1=CC=C(C=C1)CC2=CC=C(O)C=C2
View Pathway Details →
Branched-chain dodecylbenzene sulfonate
Branched Chain Dodecylbenzene Sulfonate
Starting Compound:
Branched-chain dodecylbenzene sulfonate
O=S(=O)([O-])C1=CC=C(C=C1)CCCCCCCCCCCC
View Pathway Details →
Bromoxynil
Bromoxynil (an/aerobic)
Starting Compound:
Bromoxynil
N#CC1=CC(Br)=C(O)C(Br)=C1
View Pathway Details →
Methane
C1 Metabolic Cycle
Starting Compound:
Methane
C
View Pathway Details →
Caffeine
Caffeine
Starting Compound:
Caffeine
O=C1C2=C(N=CN2C)N(C(=O)N1C)C
View Pathway Details →
Caffeine
Caffeine (fungal)
Starting Compound:
Caffeine
O=C1C2=C(N=CN2C)N(C(=O)N1C)C
View Pathway Details →
epsilon-Caprolactam
Caprolactam
Starting Compound:
epsilon-Caprolactam
O=C1NCCCCC1
View Pathway Details →
Carbaryl
Carbaryl
Starting Compound:
Carbaryl
O=C(OC1=CC=CC=2C=CC=CC12)NC
View Pathway Details →
Carbazole
Carbazole
Starting Compound:
Carbazole
C=1C=CC2=C(C1)NC=3C=CC=CC32
View Pathway Details →
Carbofuran
Carbofuran
Starting Compound:
Carbofuran
O=C(OC1=CC=CC2=C1OC(C)(C)C2)NC
View Pathway Details →
Carbon Tetrachloride
Carbon Tetrachloride (anaerobic)
Starting Compound:
Carbon Tetrachloride
ClC(Cl)(Cl)Cl
View Pathway Details →
Chlorobenzene
Chlorobenzene
Starting Compound:
Chlorobenzene
ClC=1C=CC=CC1
View Pathway Details →
Chromate
Chromium (VI)
Starting Compound:
Chromate
O=[Cr](=O)([O-])[O-]
View Pathway Details →
Cinnamate
Cinnamate
Starting Compound:
Cinnamate
O=C([O-])C=CC=1C=CC=CC1
View Pathway Details →
Citronellol
Citronellol
Starting Compound:
Citronellol
OCCC(C)CCC=C(C)C
View Pathway Details →
Cocaine
Cocaine
Starting Compound:
Cocaine
O=C(OC1C(C(=O)OC)C(O)CC2N(C)C1C2)C=3C=CC=CC3
View Pathway Details →
Cyanamide
Cyanamide
Starting Compound:
Cyanamide
N#CN
View Pathway Details →
Cyanuric acid
Cyanuric Acid
Starting Compound:
Cyanuric acid
OC=1N=C(O)N=C(O)N1
View Pathway Details →
Cyclohexane
Cyclohexane
Starting Compound:
Cyclohexane
C1CCCCC1
View Pathway Details →
Cyclohexylsulfamate
Cyclohexylsulfamate
Starting Compound:
Cyclohexylsulfamate
O=S(=O)([O-])NC1CCCCC1
View Pathway Details →
Cyclopropanecarboxylate
Cyclopropanecarboxylate
Starting Compound:
Cyclopropanecarboxylate
O=C([O-])C1CC1
View Pathway Details →
Cypermethrin
Cypermethrin
Starting Compound:
Cypermethrin
N#CC(OC(=O)C1C(C=C(Cl)Cl)C1(C)C)C=2C=CC=C(OC=3C=CC=CC3)C2
View Pathway Details →
Diazepam
Diazepam
Starting Compound:
Diazepam
O=C1N(C=2C=CC(Cl)=CC2C(=NC1)C=3C=CC=CC3)C
View Pathway Details →
Dibenzo-p-dioxin
Dibenzo-p-dioxin
Starting Compound:
Dibenzo-p-dioxin
O1C=2C=CC=CC2OC=3C=CC=CC13
View Pathway Details →
Dibenzofuran
Dibenzofuran
Starting Compound:
Dibenzofuran
O1C=2C=CC=CC2C=3C=CC=CC13
View Pathway Details →
Dibenzothiophene
Dibenzothiophene Degradation
Starting Compound:
Dibenzothiophene
S1C=2C=CC=CC2C=3C=CC=CC13
View Pathway Details →
Dibenzothiophene
Dibenzothiophene Desulfurization
Starting Compound:
Dibenzothiophene
S1C=2C=CC=CC2C=3C=CC=CC13
View Pathway Details →
2,6-Dichlorobenzonitrile
Dichlobenil
Starting Compound:
2,6-Dichlorobenzonitrile
C1=CC(=C(C#N)C(=C1)Cl)Cl
View Pathway Details →
Dichloromethane
Dichloromethane
Starting Compound:
Dichloromethane
ClCCl
View Pathway Details →
Dimethyl Sulfoxide
Dimethyl Sulfoxide & Organosulfide Cycle
Starting Compound:
Dimethyl Sulfoxide
O=S(C)C
View Pathway Details →
Dimethyl ether
Dimethyl ether
Starting Compound:
Dimethyl ether
O(C)C
View Pathway Details →
Dimethyl isophthalate
Dimethylisophthalate
Starting Compound:
Dimethyl isophthalate
O=C(OC)C1=CC=CC(=C1)C(=O)OC
View Pathway Details →
Dimethylphosphinate
Dimethylphosphinate
Starting Compound:
Dimethylphosphinate
O=P([O-])(C)C
View Pathway Details →
Dodecyl sulfate
Dodecyl sulfate
Starting Compound:
Dodecyl sulfate
O=S(=O)([O-])OCCCCCCCCCCCC
View Pathway Details →
Endosulfan
Endosulfan
Starting Compound:
Endosulfan
O=S1OCC2C(CO1)C3(Cl)C(Cl)=C(Cl)C2(Cl)C3(Cl)Cl
View Pathway Details →
Ethylbenzene
Ethylbenzene
Starting Compound:
Ethylbenzene
C=1C=CC(=CC1)CC
View Pathway Details →
Ethylbenzene
Ethylbenzene (anaerobic)
Starting Compound:
Ethylbenzene
C=1C=CC(=CC1)CC
View Pathway Details →
Fluorene
Fluorene
Starting Compound:
Fluorene
C=1C=CC2=C(C1)C=3C=CC=CC3C2
View Pathway Details →
Hydrogen (2R,3S)-3-methyloxiran-2-ylphosphonic acid
Fosfomycin
Starting Compound:
Hydrogen (2R,3S)-3-methyloxiran-2-ylphosphonic acid
O=P(O)(O)C1OC1C
View Pathway Details →
Furfural
Furfural
Starting Compound:
Furfural
O=CC=1OC=CC1
View Pathway Details →
Gallate
Gallate (anaerobic)
Starting Compound:
Gallate
O=C([O-])C1=CC(O)=C(O)C(O)=C1
View Pathway Details →
Geraniol
Geraniol
Starting Compound:
Geraniol
OCC=C(C)CCC=C(C)C
View Pathway Details →
Glyphosate
Glyphosate
Starting Compound:
Glyphosate
O=C([O-])CNCP(=O)([O-])[O-]
View Pathway Details →
Hexadecyltrimethylammonium chloride
Hexadecyltrimethylammonium Chloride
Starting Compound:
Hexadecyltrimethylammonium chloride
CCCCCCCCCCCCCCCC[N+](C)(C)C
View Pathway Details →
Hexahydro-1,3,5-trinitro-1,3,5-triazine
Hexahydro-1,3,5-Trinitro-1,3,5-Triazine (anaerobic)
Starting Compound:
Hexahydro-1,3,5-trinitro-1,3,5-triazine
O=[N+]([O-])N1CN([N+](=O)[O-])CN([N+](=O)[O-])C1
View Pathway Details →
Hexahydro-1,3,5-trinitro-1,3,5-triazine
Hexahydro-1,3,5-trinitro-1,3,5-triazine
Starting Compound:
Hexahydro-1,3,5-trinitro-1,3,5-triazine
O=[N+]([O-])N1CN([N+](=O)[O-])CN([N+](=O)[O-])C1
View Pathway Details →
Hypophosphite
Hypophosphite
Starting Compound:
Hypophosphite
O=PO
View Pathway Details →
Ibuprofen
Ibuprofen
Starting Compound:
Ibuprofen
O=C([O-])C(C1=CC=C(C=C1)CC(C)C)C
View Pathway Details →
(R,R)-Iminodisuccinate
Imidosuccinate
Starting Compound:
(R,R)-Iminodisuccinate
C([C@H](C(=O)[O-])NC(CC(=O)[O-])C(=O)[O-])C(=O)[O-]
View Pathway Details →
Iprodione
Iprodione
Starting Compound:
Iprodione
O=C(NC(C)C)N1C(=O)N(C(=O)C1)C=2C=C(Cl)C=C(Cl)C2
View Pathway Details →
Isocarbophos
Isocarbophos
Starting Compound:
Isocarbophos
O=C(OC(C)C)C=1C=CC=CC1OP(=S)(OC)N
View Pathway Details →
Isoniazid
Isoniazid
Starting Compound:
Isoniazid
O=C(NN)C=1C=CN=CC1
View Pathway Details →
Isooctane
Isooctane
Starting Compound:
Isooctane
CC(C)CC(C)(C)C
View Pathway Details →
Isoproturon
Isoproturon
Starting Compound:
Isoproturon
O=C(NC1=CC=C(C=C1)C(C)C)N(C)C
View Pathway Details →
Ketoprofen
Ketoprofen
Starting Compound:
Ketoprofen
O=C([O-])C(C=1C=CC=C(C1)C(=O)C=2C=CC=CC2)C
View Pathway Details →
Limonene
Limonene
Starting Compound:
Limonene
C=C(C)C1CC=C(C)CC1
View Pathway Details →
Malathion
Malathion
Starting Compound:
Malathion
O=C(OCC)CC(SP(=S)(OC)OC)C(=O)OCC
View Pathway Details →
(R)-Mandelate
Mandelate
Starting Compound:
(R)-Mandelate
C1=CC=C(C=C1)[C@H](C(=O)[O-])O
View Pathway Details →
(-)-(1R,2S,5R)-Menthol
Menthol (anaerobic)
Starting Compound:
(-)-(1R,2S,5R)-Menthol
CC(C)[C@@H]1CC[C@@H](C)CC1O
View Pathway Details →
Metamitron
Metamitron
Starting Compound:
Metamitron
O=C1C(=NN=C(N1N)C)C=2C=CC=CC2
View Pathway Details →
Methamidophos
Methamidophos
Starting Compound:
Methamidophos
O=P(OC)(SC)N
View Pathway Details →
Methanesulfonate
Methanesulfonic Acid
Starting Compound:
Methanesulfonate
O=S(=O)([O-])C
View Pathway Details →
Carbon Dioxide
Methanogenesis
Starting Compound:
Carbon Dioxide
O=C=O
View Pathway Details →
Methionine
Methionine and Threonine
Starting Compound:
Methionine
O=C([O-])C(N)CCSC
View Pathway Details →
Methyl ethyl ketone
Methyl ethyl ketone
Starting Compound:
Methyl ethyl ketone
O=C(C)CC
View Pathway Details →
Methyl fluoride
Methyl fluoride
Starting Compound:
Methyl fluoride
FC
View Pathway Details →
Methyl tert-butyl ether
Methyl tert-butyl ether
Starting Compound:
Methyl tert-butyl ether
O(C)C(C)(C)C
View Pathway Details →
Methylarsonate
Methylarsonate
Starting Compound:
Methylarsonate
O=[As]([O-])([O-])C
View Pathway Details →
Mordant Yellow 3
Mordant Yellow 3
Starting Compound:
Mordant Yellow 3
O=C([O-])C1=CC(N=NC=2C=CC3=CC(=CC=C3C2)S(=O)(=O)[O-])=CC=C1O
View Pathway Details →
Morpholine
Morpholine
Starting Compound:
Morpholine
O1CCNCC1
View Pathway Details →
N,N-Diethyl-m-toluamide
N,N-Diethyl-m-toluamide
Starting Compound:
N,N-Diethyl-m-toluamide
O=C(C1=CC=CC(=C1)C)N(CC)CC
View Pathway Details →
N-Cyclohexylisocyanide
N-Cyclohexylisocyanide
Starting Compound:
N-Cyclohexylisocyanide
C#[N+]C1CCCCC1
View Pathway Details →
Cyromazine
N-Cyclopropylmelamine
Starting Compound:
Cyromazine
N=1C(=NC(=NC1N)NC2CC2)N
View Pathway Details →
N-Methylmorpholine-N-oxide
N-Methylmorpholine-N-oxide
Starting Compound:
N-Methylmorpholine-N-oxide
[O-][N+]1(C)CCOCC1
View Pathway Details →
N-Nitrosodimethylamine
N-Nitrosodimethylamine
Starting Compound:
N-Nitrosodimethylamine
O=NN(C)C
View Pathway Details →
N-Oleoyl-N-methyltaurine
N-Oleoyl-N-methyltaurine
Starting Compound:
N-Oleoyl-N-methyltaurine
O=C(N(C)CCS(=O)(=O)[O-])CCCCCCCC=CCCCCCCCC
View Pathway Details →
Naphthalene
Naphthalene
Starting Compound:
Naphthalene
C=1C=CC=2C=CC=CC2C1
View Pathway Details →
Naphthalene-2-sulfonate
Naphthalenesulfonate Family
Starting Compound:
Naphthalene-2-sulfonate
O=S(=O)([O-])C=1C=CC=2C=CC=CC2C1
View Pathway Details →
(RS)-Nicotine
Nicotine
Starting Compound:
(RS)-Nicotine
CN1CCCC1C2=CC=CN=C2
View Pathway Details →
Nitrate
Nitrate (anaerobic)
Starting Compound:
Nitrate
O=[N+]([O-])[O-]
View Pathway Details →
Nitrilotriacetate
Nitrilotriacetate (an/aerobic)
Starting Compound:
Nitrilotriacetate
O=C([O-])CN(CC(=O)[O-])CC(=O)[O-]
View Pathway Details →
Nitrobenzene
Nitrobenzene
Starting Compound:
Nitrobenzene
O=[N+]([O-])C=1C=CC=CC1
View Pathway Details →
Nitrofen
Nitrofen
Starting Compound:
Nitrofen
O=[N+]([O-])C1=CC=C(OC2=CC=C(Cl)C=C2Cl)C=C1
View Pathway Details →
Nitroglycerin (NG)
Nitroglycerin
Starting Compound:
Nitroglycerin (NG)
O=[N+]([O-])OCC(O[N+](=O)[O-])CO[N+](=O)[O-]
View Pathway Details →
p-Nitrophenol
Nitrophenol Family (an/aerobic)
Starting Compound:
p-Nitrophenol
O=[N+]([O-])C1=CC=C(O)C=C1
View Pathway Details →
6-Aminohexanoate Cyclic Dimer
Nylon Oligomer
Starting Compound:
6-Aminohexanoate Cyclic Dimer
O=C1NCCCCCC(=O)NCCCCC1
View Pathway Details →
Orcinol
Orcinol
Starting Compound:
Orcinol
OC=1C=C(O)C=C(C1)C
View Pathway Details →
Phenylmercury acetate
Organomercury
Starting Compound:
Phenylmercury acetate
O=C(O[Hg]C=1C=CC=CC1)C
View Pathway Details →
Octamethylcyclotetrasiloxane
Organosilicone (an/aerobic)
Starting Compound:
Octamethylcyclotetrasiloxane
O1[Si](O[Si](O[Si](O[Si]1(C)C)(C)C)(C)C)(C)C
View Pathway Details →
Osmium dioxide
Osmium Reduction
Starting Compound:
Osmium dioxide
O=[Os]=O
View Pathway Details →
Parathion
Parathion (an/aerobic)
Starting Compound:
Parathion
O=[N+]([O-])C1=CC=C(OP(=S)(OCC)OCC)C=C1
View Pathway Details →
Pentachlorophenol
Pentachlorophenol Family
Starting Compound:
Pentachlorophenol
ClC=1C(Cl)=C(Cl)C(O)=C(Cl)C1Cl
View Pathway Details →
Pentaerythritol tetranitrate
Pentaerythritol tetranitrate
Starting Compound:
Pentaerythritol tetranitrate
O=[N+]([O-])OCC(CO[N+](=O)[O-])(CO[N+](=O)[O-])CO[N+](=O)[O-]
View Pathway Details →
Perchlorate
Perchlorate (anaerobic)
Starting Compound:
Perchlorate
O=Cl(=O)(=O)[O-]
View Pathway Details →
Permethrin
Permethrin
Starting Compound:
Permethrin
O=C(OCC=1C=CC=C(OC=2C=CC=CC2)C1)C3C(C=C(Cl)Cl)C3(C)C
View Pathway Details →
Phenanthrene
Phenanthrene
Starting Compound:
Phenanthrene
C=1C=CC2=C(C1)C=CC=3C=CC=CC32
View Pathway Details →
Phenanthrene
Phenanthrene (fungal 9R,10R)
Starting Compound:
Phenanthrene
C=1C=CC2=C(C1)C=CC=3C=CC=CC32
View Pathway Details →
Phenanthrene
Phenanthrene (fungal 9S,10S)
Starting Compound:
Phenanthrene
C=1C=CC2=C(C1)C=CC=3C=CC=CC32
View Pathway Details →
Phenol
Phenol (anaerobic)
Starting Compound:
Phenol
OC=1C=CC=CC1
View Pathway Details →
Diphenyl ether
Phenol Family
Starting Compound:
Diphenyl ether
O(C=1C=CC=CC1)C=2C=CC=CC2
View Pathway Details →
Phenylacetate
Phenylacetate
Starting Compound:
Phenylacetate
O=C([O-])CC=1C=CC=CC1
View Pathway Details →
Phorate
Phorate
Starting Compound:
Phorate
S=P(OCC)(OCC)SCSCC
View Pathway Details →
4-Hydroxyphthalate
Phthalate Family
Starting Compound:
4-Hydroxyphthalate
O=C([O-])C1=CC=C(O)C=C1C(=O)[O-]
View Pathway Details →
2,4,6-Trinitrophenol
Picric Acid Family
Starting Compound:
2,4,6-Trinitrophenol
C1=C(C(=C(C=C1[N+](=O)[O-])[N+](=O)[O-])[O-])[N+](=O)[O-]
View Pathway Details →
Pivalate
Pivalic Acid (anaerobic)
Starting Compound:
Pivalate
O=C([O-])C(C)(C)C
View Pathway Details →
Propylene
Propylene
Starting Compound:
Propylene
C=CC
View Pathway Details →
Pyrene
Pyrene
Starting Compound:
Pyrene
C=1C=C2C=CC3=CC=CC=4C=CC(C1)=C2C34
View Pathway Details →
Pyridoxine
Pyridoxine
Starting Compound:
Pyridoxine
OC=1C(=NC=C(C1CO)CO)C
View Pathway Details →
Pyrrole-2-carboxylate
Pyrrole-2-carboxylate
Starting Compound:
Pyrrole-2-carboxylate
O=C([O-])C1=CC=CN1
View Pathway Details →
Quercetin
Quercetin
Starting Compound:
Quercetin
O=C1C(O)=C(OC=2C=C(O)C=C(O)C12)C=3C=CC(O)=C(O)C3
View Pathway Details →
Quinaldine
Quinaldine
Starting Compound:
Quinaldine
N=1C=2C=CC=CC2C=CC1C
View Pathway Details →
Selenate
Selenate
Starting Compound:
Selenate
O=[Se](=O)([O-])[O-]
View Pathway Details →
Maltotriose
Starch Oligomer
Starting Compound:
Maltotriose
OCC1OC(OC2C(O)C(O)C(OC2CO)OC3C(O)C(O)C(O)OC3CO)C(O)C(O)C1O
View Pathway Details →
Styrene
Styrene
Starting Compound:
Styrene
C=CC=1C=CC=CC1
View Pathway Details →
Syringate
Syringate
Starting Compound:
Syringate
O=C([O-])C1=CC(OC)=C(O)C(OC)=C1
View Pathway Details →
Pertechnetate ion
Technetium Immobilization
Starting Compound:
Pertechnetate ion
O=[Tc](=O)(=O)[O-]
View Pathway Details →
Testosterone
Testosterone
Starting Compound:
Testosterone
O=C1C=C2CCC3C(CCC4(C)C(O)CCC34)C2(C)CC1
View Pathway Details →
3,3`,5,5`-Tetrabromobisphenol A
Tetrabromobisphenol A
Starting Compound:
3,3`,5,5`-Tetrabromobisphenol A
BrC=1C=C(C=C(Br)C1O)C(C2=CC(Br)=C(O)C(Br)=C2)(C)C
View Pathway Details →
1,2,3,4-Tetrachlorobenzene
Tetrachlorobenzene
Starting Compound:
1,2,3,4-Tetrachlorobenzene
C1=C(C(=C(C(=C1)Cl)Cl)Cl)Cl
View Pathway Details →
Tetrachloroethene
Tetrachloroethene (anaerobic)
Starting Compound:
Tetrachloroethene
ClC(Cl)=C(Cl)Cl
View Pathway Details →
Tetrahydrofuran
Tetrahydrofuran
Starting Compound:
Tetrahydrofuran
O1CCCC1
View Pathway Details →
Tetralin
Tetralin
Starting Compound:
Tetralin
C=1C=CC2=C(C1)CCCC2
View Pathway Details →
Thiamin
Thiamin
Starting Compound:
Thiamin
OCCC=1SC=[N+](C1C)CC2=CN=C(N=C2N)C
View Pathway Details →
Thioacetamide
Thioacetamide
Starting Compound:
Thioacetamide
S=C(N)C
View Pathway Details →
Thiobenzamide
Thiobenzamide
Starting Compound:
Thiobenzamide
S=C(N)C=1C=CC=CC1
View Pathway Details →
Thiocyanate
Thiocyanate
Starting Compound:
Thiocyanate
N#C[S-]
View Pathway Details →
Thiophene-2-carboxylate
Thiophene-2-carboxylate
Starting Compound:
Thiophene-2-carboxylate
O=C([O-])C=1SC=CC1
View Pathway Details →
Toluene
Toluene
Starting Compound:
Toluene
C=1C=CC(=CC1)C
View Pathway Details →
Toluene
Toluene (anaerobic)
Starting Compound:
Toluene
C=1C=CC(=CC1)C
View Pathway Details →
Toluene-4-sulfonate
Toluene-4-sulfonate
Starting Compound:
Toluene-4-sulfonate
O=S(=O)([O-])C1=CC=C(C=C1)C
View Pathway Details →
Tri-n-butyltin (TBT)
Tri-n-butyltin
Starting Compound:
Tri-n-butyltin (TBT)
[Sn+](CCCC)(CCCC)CCCC
View Pathway Details →
Triazophos
Triazophos
Starting Compound:
Triazophos
S=P(OC=1N=CN(N1)C=2C=CC=CC2)(OCC)OCC
View Pathway Details →
1,1,2-Trichloroethylene
Trichloroethylene
Starting Compound:
1,1,2-Trichloroethylene
C(=C(Cl)Cl)Cl
View Pathway Details →
Triethanolamine
Triethanolamine
Starting Compound:
Triethanolamine
OCCN(CCO)CCO
View Pathway Details →
Trifluoroacetate
Trifluoroacetate (An/Aerobic)
Starting Compound:
Trifluoroacetate
O=C([O-])C(F)(F)F
View Pathway Details →
2,4,6-Trinitrotoluene
Trinitrotoluene
Starting Compound:
2,4,6-Trinitrotoluene
CC1=C(C=C(C=C1[N+](=O)[O-])[N+](=O)[O-])[N+](=O)[O-]
View Pathway Details →
Triphenyltin
Triphenyltin
Starting Compound:
Triphenyltin
C=1C=CC(=CC1)[SnH](C=2C=CC=CC2)C=3C=CC=CC3
View Pathway Details →
L-Tyrosine
Tyrosine
Starting Compound:
L-Tyrosine
O=C([O-])C(N)CC1=CC=C(O)C=C1
View Pathway Details →
Uranyl ion
Uranium
Starting Compound:
Uranyl ion
O=[U+2]=O
View Pathway Details →
L-Serine
Valanimycin Synthesis
Starting Compound:
L-Serine
O=C([O-])C([NH3+])CO
View Pathway Details →
Vanillin
Vanillin
Starting Compound:
Vanillin
O=CC1=CC=C(O)C(OC)=C1
View Pathway Details →
Z-Phenylacetaldoxime
Z-Phenylacetaldoxime
Starting Compound:
Z-Phenylacetaldoxime
ON=CCC=1C=CC=CC1
View Pathway Details →
alpha-Pinene
alpha-Pinene
Starting Compound:
alpha-Pinene
C1=C(C)C2CC(C1)C2(C)C
View Pathway Details →
beta-1,2,3,4,5,6-Hexachlorocyclohexane
beta-1,2,3,4,5,6-Hexachlorocyclohexane (an/aerobic)
Starting Compound:
beta-1,2,3,4,5,6-Hexachlorocyclohexane
ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl
View Pathway Details →
gamma-Hexachlorocyclohexane
gamma-1,2,3,4,5,6-Hexachlorocyclohexane
Starting Compound:
gamma-Hexachlorocyclohexane
ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl
View Pathway Details →
3-Hydroxytoluene
m-Cresol
Starting Compound:
3-Hydroxytoluene
OC1=CC=CC(=C1)C
View Pathway Details →
m-Xylene
m-Xylene
Starting Compound:
m-Xylene
C=1C=C(C=C(C1)C)C
View Pathway Details →
n-Hexane
n-Hexane (anaerobic)
Starting Compound:
n-Hexane
CCCCCC
View Pathway Details →
n-Octane
n-Octane
Starting Compound:
n-Octane
CCCCCCCC
View Pathway Details →
o-Nitrobenzoate
o-Nitrobenzoate
Starting Compound:
o-Nitrobenzoate
O=C([O-])C=1C=CC=CC1[N+](=O)[O-]
View Pathway Details →
o-Xylene
o-Xylene
Starting Compound:
o-Xylene
C=1C=CC(=C(C1)C)C
View Pathway Details →
p-Cymene
p-Cymene
Starting Compound:
p-Cymene
C=1C=C(C=CC1C)C(C)C
View Pathway Details →
p-Xylene
p-Xylene
Starting Compound:
p-Xylene
C=1C=C(C=CC1C)C
View Pathway Details →
No starting compound
s-Triazine Metabolism Metapathway
Starting Compound:
Not specified
View Pathway Details →
Draw Chemical Structure for Search
Close
Loading structure editor...
Instructions:
Draw your structure in the editor above. When finished, click "Search by Structure" to find pathways whose starting compound contains this substructure.
Search by Structure
Clear Editor