The pathway with the name 2,4,5-Trichlorophenoxyacetic Acid
 has the following structure: 
Result: 
C(=C/C(=O)[O-])/C(=O)CC(=O)[O-]
 no rule associatedC(CC(=O)[O-])C(=O)CC(=O)[O-]
C1=C(C=C(C(=C1)O)O)O
 no rule associatedC(=C/C(=O)[O-])/C(=O)CC(=O)[O-]
C1=C(C(=CC(=C1Cl)O)O)O
 no rule associatedC1=CC(=O)C(=CC1=O)O
C1=C(C(=CC(=C1Cl)Cl)O)Cl
 no rule associatedC1=C(C(=CC(=C1Cl)O)Cl)O
C1=C(C(=CC(=C1Cl)Cl)OCC(=O)[O-])Cl
 no rule associatedC1=C(C(=CC(=C1Cl)Cl)O)Cl
C(=O)C(=O)[O-]
C1=C(C(=CC(=C1Cl)O)Cl)O
 no rule associatedC1=C(C(=CC(=C1Cl)O)O)O
C1=CC(=O)C(=CC1=O)O
 no rule associatedC1=C(C=C(C(=C1)O)O)O

Description: 2,4,5-Trichlorophenoxyacetic acid, more commonly known as 2,4,5-T, is a widely-used herbicide. For example, it is often used as a weed killer for home lawns. It is considered to be less readily biodegradable than the analogous herbicide 2,4-D. The greater resistance to microbial metabolism likely stems from the additional chlorine substituent on the aromatic ring. However, bacteria have been identified that are capable of metabolizing 2,4,5-T ([http://www.ncbi.nlm.nih.gov/pubmed/7538273|Daubaras et al., 1995]).
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