The pathway with the name Bisphenol F
 has the following structure: 
Result: 
C1=C(C=CC(=C1)O)CC2=CC=C(C=C2)O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/5adea520-8b47-48be-bcae-8d31e35087f8, SMIRKS = [H][#6;A;!$(CCNC(=O)C(O)C(C)(C)COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP(O)(O)=O)n1cnc2c(N)ncnc12)!$(CCC(=O)NC(CS)C(=O)NCC([O-])=O)!$(CC(=O)NC(CS)C(=O)NCC([O-])=O)!$(C(C!@-,!@=[#7,#8])([H])([H])[C]):3]([H:2])([#6;X3:5])[#6:6]>>[H:2][C:3]([#6;X3:5])([#6:6])[#8]) C1=C(C=CC(=C1)O)C(C2=CC=C(C=C2)O)O
C1=C(C=CC(=C1)O)C(=O)OC2=CC=C(C=C2)O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/57d978b5-f55f-462e-a9dc-c5908d165973, SMIRKS = [#6:2]-[#8:1]-[#6:6](-[#1,#6:3])=[O:7]>>[H][#8]-[#6:2].[#8-:1]-[#6:6](-[#1,#6:3])=[O:7]) C1=C(C=CC(=C1)O)C(=O)[O-]
C1=C(C=CC(=C1)O)O
C1=C(C=CC(=C1)O)C(C2=CC=C(C=C2)O)O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/a6b0b86b-ffb1-4446-ab9f-a85284c24747, SMIRKS = [H][#8:1][#6;A;!$(CCC(O)[O-]):2]([H])([#6:5])[#6,#8:6]>>[#6:5]-[#6:2](-[#6,#8:6])=[O:1]) C1=C(C=CC(=C1)O)C(=O)C2=CC=C(C=C2)O
C1=C(C=CC(=C1)O)C(=O)C2=CC=C(C=C2)O
 no rule associatedC1=C(C=CC(=C1)O)C(=O)OC2=CC=C(C=C2)O

Description: Bisphenol F (BPF) consists of two phenolic rings joined together through a bridging carbon. It belongs to the bisphenol group which are important raw materials used in the production of polycarbonate and epoxy resins. Considerable amounts of bisphenols have been discharged into a broad range of aquatic and terrestrial environments as a result of its widespread use. Sphingobium yanoikuyae strain FM-2 can degrade BPF by attack on the bridging carbon, forming first the alcohol and then the ketone. Next Baeyer-Villiger oxidation forms 4-hydroxyphenyl 4-hydroxybenzoate, which is hydrolyzed to form 4-hydroxybenzoate and 1,4-hydroquinone ([http://www.ncbi.nlm.nih.gov/pubmed/18024680|Inoue et al., 2008]).
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