The pathway with the name Orcinol
 has the following structure: 
Result: 
CC1=C(C(=CC(=C1)O)O)O
 no rule associatedCC(=O)CC(=O)CC(=O)C(=O)[O-]
CC1=CC(=CC(=C1)O)O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/f2d84038-66a1-44cb-a73e-946a9d7c9115, SMIRKS = [H:10][#8:9]-[c:4]1[c;R1:5][c;R1:6][c:1]([H])[c;R1:7][c;R1:8]1>>[H:10][#8:9]-[c:4]1[c;R1:5][c;R1:6][c:1](-[#8])[c;R1:7][c;R1:8]1) CC1=C(C(=CC(=C1)O)O)O
CC(=O)CC(=O)C(=O)[O-]
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/e4bfe962-cfa8-47cb-beb9-d0c38efec095, SMIRKS = [#8:4]=[#6;D3,D4H1;R0:1](-[#6:2])!@-[#6:3]-[#6:8](=[O:10])-[#6:7](-[#8-:6])=[O:9]>>[#6:3]-[#6:8](=[O:10])-[#6:7](-[#8-:6])=[O:9].[#6:2]-[#6:1](-[#8-])=[O:4]) CC(=O)C(=O)[O-]
CC(=O)[O-]
CC(=O)CC(=O)CC(=O)C(=O)[O-]
 no rule associatedCC(=O)CC(=O)C(=O)[O-]

Description: Benzene compounds with dihydroxylated rings, e.g. catechol (1,2-benzenediol) and hydroquinone (1,4-benzenediol), are important intermediates in bacterial catabolism of aromatic compounds. The bacterial catabolism of orcinol (5-methyl-1,3-benzenediol) can be used as a model for the metabolism of other members of the resorcinol (1,3-benzenediol) compound family. This family includes many commercially-important compounds; for example, 4-hexylresorcinol is used medicinally as a topical antiseptic. This pathway is based on [http://www.ncbi.nlm.nih.gov/pubmed/1254564|Chapman and Ribbons (1976)].
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