The pathway with the name 2-Chloro-N-isopropylacetanilide
 has the following structure: 
Result: 
CC(=O)NC1=CC=CC=C1
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/42add347-d29c-4ac9-9b35-89308c3b1bd6, SMIRKS = [H][c:2](:[c:7]):[c:1](:[c:6])-[#7;!$(NC(N)=O)!$(N(C=O)c1ccccc1C):5](-[#1,#6:9])-[#1,#6:10]>>[#8]-[c:1](:[c:6]):[c:2](-[#8]):[c:7].[#1,#6:10]-[#7:5]-[#1,#6:9]) C1=CC(=C(C=C1)O)O
CC(C)N(C1=CC=CC=C1)C(=O)CCl
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/42add347-d29c-4ac9-9b35-89308c3b1bd6, SMIRKS = [H][c:2](:[c:7]):[c:1](:[c:6])-[#7;!$(NC(N)=O)!$(N(C=O)c1ccccc1C):5](-[#1,#6:9])-[#1,#6:10]>>[#8]-[c:1](:[c:6]):[c:2](-[#8]):[c:7].[#1,#6:10]-[#7:5]-[#1,#6:9]) CC(C)NC(=O)CCl
C1=CC(=C(C=C1)O)O
CC(C)N(C1=CC=CC=C1)C(=O)CCl
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/ffd47aaf-234b-432c-bf01-02e34c79672f, SMIRKS = [#6:1]-[#17,#35,#53]>>[#6:1][H]) CC(C)N(C(=O)C)C1=CC=CC=C1
CC(C)N
 no rule associatedC
CC=O
CC(C)N(C(=O)C)C1=CC=CC=C1
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/bf030393-4fc7-40f1-aa21-e3a853ba26c8, SMIRKS = [#6,#7:6][#6:7](=[O:8])[#7;!$(N(CC)C(=O)C(O)C(C)(C)COP(O)(=O)OP(O)(=O)OCC1OC(C(O)C1OP(O)(O)=O)n1cnc2c(N)ncnc12)!$(NC(CCC(=O)NC(CS)C(=O)NCC([O-])=O)C([O-])=O):1]!@-[#6;A:2][H:3]>>[#6,#7:6][#6:7](=[O:8])[#7:1][H:3].[#6;A:2]=O) CC(=O)NC1=CC=CC=C1
CC(=O)C
CC(C)N(C(=O)C)C1=CC=CC=C1
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/1d57e800-f2e2-43a4-911a-2ef2ccc1b06b, SMIRKS = [#6:5]-[#7:1](-[#6:7])-[#6:3](-[#1,#6:6])=[O:4]>>[#8-]-[#6:3](-[#1,#6:6])=[O:4].[#6:5]-[#7:1]-[#6:7]) CC(C)NC1=CC=CC=C1
CC(=O)[O-]
CC(C)NC(=O)CCl
 no rule associatedC(=O)=O
CC(C)NC1=CC=CC=C1
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/42add347-d29c-4ac9-9b35-89308c3b1bd6, SMIRKS = [H][c:2](:[c:7]):[c:1](:[c:6])-[#7;!$(NC(N)=O)!$(N(C=O)c1ccccc1C):5](-[#1,#6:9])-[#1,#6:10]>>[#8]-[c:1](:[c:6]):[c:2](-[#8]):[c:7].[#1,#6:10]-[#7:5]-[#1,#6:9]) C1=CC(=C(C=C1)O)O

Description: 2-Chloro-N-isopropylacetanilide (Propachlor) is an acetamide herbicide widely used to protect corn, onion, cabbage, rose bushes, and ornamental plants. This chemical dissipates primarily by biodegradation in the soil ([http://www.ncbi.nlm.nih.gov/pubmed/9925619|Martin et al., 1999]), or in water ([http://www.ncbi.nlm.nih.gov/pubmed/2604396|Steen and Colette, 1989]). Two of the pathways share the same first step ([http://www.ncbi.nlm.nih.gov/pubmed/9925619|Martin et al., 1999]), and are intiated by Pseudomonas sp. PEM1, Acinetobacter sp. BEM2, and Pseudomonas sp. GH1 ([http://www.ncbi.nlm.nih.gov/pubmed/10698790|Martin et al., 2000]). The other pathway is begun by Moraxella sp. DAK3 and continued by Xanthobacter sp. MAB2, ATCC 49876 ([http://www.ncbi.nlm.nih.gov/pubmed/1768085|Villarreal et al. 1991]).
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