The pathway with the name 2-Chloro-N-isopropylacetanilide
 has the following structure: 
Result: 
CC(C)N(C(=O)C)C1=CC=CC=C1
 no rule associatedCC(=O)[O-]
CC(C)NC1=CC=CC=C1
CC(C)NC(=O)CCl
 no rule associatedC(=O)=O
CC(C)NC1=CC=CC=C1
 no rule associatedC1=CC(=C(C=C1)O)O
CC(C)N(C(=O)C)C1=CC=CC=C1
 no rule associatedCC(=O)C
CC(=O)NC1=CC=CC=C1
CC(=O)NC1=CC=CC=C1
 no rule associatedC1=CC(=C(C=C1)O)O
CC(C)N(C1=CC=CC=C1)C(=O)CCl
 no rule associatedCC(C)N(C(=O)C)C1=CC=CC=C1
CC(C)N
 no rule associatedCC=O
C
CC(C)N(C1=CC=CC=C1)C(=O)CCl
 no rule associatedCC(C)NC(=O)CCl
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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