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(=CC(=C1Cl)O)Cl)O
 no rule associatedC1=C(C(=CC(=C1Cl)O)O)O
C1=C(C(=CC(=C1Cl)Cl)O)Cl
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/10b20b9f-e9b0-41ba-94d4-d422247a0ac5, SMIRKS = [#9,#17,#35,#53]-[c:1]1[c:7][c:6][c:5](-[$(O[H]),$([C](-[O-])=O):4])[c:9][c:8]1>>[#8]-[c:1]1[c:7][c:6][c:5](-[$(O[H]),$([C](-[O-])=O):4])[c:9][c:8]1) C1=C(C(=CC(=C1Cl)O)Cl)O
C1=CC(=O)C(=CC1=O)O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/acdf7b98-dbbd-4599-8675-ce4505553101, SMIRKS = [O:8]=[#6:1]-1-[#6:2]=[#6:3]-[#6:4](=[O:7])-[#6:5]=[#6:6]-1>>[#8:7]-[#6:4]1-[#6:3]=[#6:2]-[#6:1](-[#8:8])=[#6:6]-[#6:5]=1) C1=C(C=C(C(=C1)O)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)OCC(=O)[O-])Cl
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/cf2bc731-6b0c-4f1d-b192-8e859d9505aa, SMIRKS = [H][#6;A;!$([#6]=[#8]):3]!@-[#8:2]!@-[#6;!$([#6]=[#8]):1]>>[#6:1]-[#8:2].[#6;A:3]=O) C(=O)C(=O)[O-]
C1=C(C(=CC(=C1Cl)Cl)O)Cl

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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