The pathway with the name o-Xylene
 has the following structure: 
Result: 
CC1=C(C)C=CC=C1
 no rule associatedCC1=C(C=CC=C1)CO
CC1=C(C=CC=C1)C=O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/737ec046-645e-46ec-af34-c44500fe5899, SMIRKS = [H][#6:1](-[#6:5])=[O:4]>>[#6:5]-[#6:1](-[#8-])=[O:4]) CC1=C(C=CC=C1)C(=O)[O-]
CC1=C(C)C=C(C(=C1)O)O
 no rule associatedC/C(=C(\C)/C=O)/C=C(\C(=O)[O-])/O
C/C(=C/C=C(\C(=O)[O-])/O)/C(=O)C
 no rule associatedC(=O)=O
CC1=CC=C(C(=C1C)O)O
 no rule associatedC/C(=C/C=C(\C(=O)[O-])/O)/C(=O)C
C/C(=C(\C)/C=O)/C=C(\C(=O)[O-])/O
 no rule associatedC(=O)=O
CC1=C(C)C=CC=C1
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/333e9050-8a30-4af0-9f64-881ab5bd4598, SMIRKS = [H][c:1]1[c:7][c:10][c:9][#6,#7;a:8][c:2]1[H]>>[#8]-[c:1]1[c:7][c:10][c:9][#6,#7;a:8][c:2]1-[#8]) CC1=CC=C(C(=C1C)O)O
CC1=CC=C[C@@H]([C@]1(C(=O)[O-])O)O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/1b7001bb-4b19-4cd3-b46b-18623c3012b4, SMIRKS = [H][#8:10][C@@:2]1([H])[#6:3]=,:[#6:4]-,:[#6:5]=,:[#6:6][C@:1]1([#8:11][H])[#6](-[#8-])=O>>[H][#8:10]-[#6:2]-1=[#6:1](-[#8:11][H])-[#6:6]=[#6:5]-[#6:4]=[#6:3]-1) CC1=CC=CC(=C1O)O
CC1=C(C)C=CC=C1
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/333e9050-8a30-4af0-9f64-881ab5bd4598, SMIRKS = [H][c:1]1[c:7][c:10][c:9][#6,#7;a:8][c:2]1[H]>>[#8]-[c:1]1[c:7][c:10][c:9][#6,#7;a:8][c:2]1-[#8]) CC1=C(C)C=C(C(=C1)O)O
CC1=C(C=CC=C1)CO
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/24d3215b-aefa-4538-b345-16e2a5e042b1, SMIRKS = [H][#8:2][C:1]([H:5])([H])[#1,#6:6]>>[H:5][#6:1](-[#1,#6:6])=[O:2]) CC1=C(C=CC=C1)C=O
CC1=C(C=CC=C1)C(=O)[O-]
 no rule associatedCC1=CC=C[C@@H]([C@]1(C(=O)[O-])O)O

Description: o-Xylene is a member of the BTEX class of aromatic compounds (benzene, toluene, ethylbenzene, and XYLENES). The major use of o-xylene is in the manufacture of phthalic anhydride. A small amount is also used in solvent applications and to make bactericides, soybean herbicides and lubricating oils. [http://www.ncbi.nlm.nih.gov/pubmed/7772940|Jorgensen et al. (1995)] report, "The oxidation of o-xylene proceeded through o-methylbenzyl alcohol, o-methylbenzaldehyde, and o-methylbenzoate." o-Xylene removal depended on the simultaneous degradation of toluene. [http://www.ncbi.nlm.nih.gov/pubmed/1371658|Higson and Focht (1992)] reported that the degradation of 2-Methylbenzoate was utilized by Burkholderia cepacia MB2. The metabolism from 2-Methylbenzoate to 3-methylcatechol is through a proposed carboxy-hydrodiol compound by dioxygenation. Rhodococcus sp. strain YU6 is able to metabolize o-xylene via direct ring oxidation and meta-cleavage ([http://www.ncbi.nlm.nih.gov/pubmed/16145546|Jang et al., 2005]). The related m-Xylene and p-Xylene degradation pathways are also included in the EAWAG-BBD.
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