The pathway with the name Atropine
 has the following structure: 
Result: 
C1=CC=C(C=C1)CC=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]) C1=CC=C(C=C1)CC(=O)[O-]
C1=CC=C(C=C1)C(CO)C(=O)[O-]
 no rule associatedC1=CC=C(C=C1)CC=O
CN1[C@H]2CC[C@@H]1CC(C2)O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/edaada18-7db8-4a5a-a481-4188338bc87b, SMIRKS = [#1,#6:6][#7;X3;!$(NC1CC1)!$([N][C]=O)!$([!#8]CNC=O):1]([#1,#6:7])[#6;A;X4:2][H:3]>>[#1,#6:6][#7;X3:1]([#1,#6:7])[H:3].[#6;A:2]=O) C=O
C1CC2CC(CC1N2)O
CC(=O)CC(=O)CCC(=O)[O-]
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/9bdcc525-2cb5-4d14-bf00-193dd44b9585, SMIRKS = [#6:6]-[#6:2](=[O:7])-[#6;X4:1]-[#6:5]([#6,#16;A:4])=[O:8]>>[#6:1]-[#6:5]([#6,#16;A:4])=[O:8].[#6:6]-[#6:2](-[#8-])=[O:7]) CC(=O)C
C(CC(=O)[O-])C(=O)[O-]
CN1[C@H]2CC[C@@H]1CC(C2)OC(=O)C(CO)C3=CC=CC=C3
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/57d978b5-f55f-462e-a9dc-c5908d165973, SMIRKS = [#6:2]-[#8:1]-[#6:6](-[#1,#6:3])=[O:7]>>[H][#8]-[#6:2].[#8-:1]-[#6:6](-[#1,#6:3])=[O:7]) C1=CC=C(C=C1)C(CO)C(=O)[O-]
CN1[C@H]2CC[C@@H]1CC(C2)O
C1CC2CC(CC1N2)O
 no rule associatedC1CC(=O)CC(CC1=O)O
C1CC(=O)CC(CC1=O)O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/a6b0b86b-ffb1-4446-ab9f-a85284c24747, SMIRKS = [H][#8:1][#6;A;!$(CCC(O)[O-]):2]([H])([#6:5])[#6,#8:6]>>[#6:5]-[#6:2](-[#6,#8:6])=[O:1]) C1CC(=O)CC(=O)CC1=O
C1CC(=O)CC(=O)CC1=O
 SimpleRule(uri = https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/simple-rule/9bdcc525-2cb5-4d14-bf00-193dd44b9585, SMIRKS = [#6:6]-[#6:2](=[O:7])-[#6;X4:1]-[#6:5]([#6,#16;A:4])=[O:8]>>[#6:1]-[#6:5]([#6,#16;A:4])=[O:8].[#6:6]-[#6:2](-[#8-])=[O:7]) CC(=O)CC(=O)CCC(=O)[O-]

Description: Atropine is a tropane alkaloid plant natural product. It is used medically as an anti-arrhythmic drug, broncodilator, pupil dilator, and muscarinic antagonist (PubChem, 2011). Pseudomonas sp. AT3 can grow on atropine as its sole carbon and nitrogen source. The initial step in the degradation is hydrolysis of the atropine ester bond to form tropine and tropate. Tropine is converted to nortropine, which is degraded through oxidative cleavage of the bridging N-C bonds to 6-hydroxycyclohepta-1,4-dione. This is oxidized to cyclohepta-1,3,5-trione. This latter compound is hydrolytically cleaved to 4,6-dioxoheptanoate, which is hydrolyzed to succinate and acetone ([http://www.ncbi.nlm.nih.gov/pubmed/16535398|Bartholomew et al., 1996]). Tropate is oxidized to phenylacetate through phenylmalonate semialdehyde (proposed) and phenylacetaldehyde ([http://www.ncbi.nlm.nih.gov/pubmed/9023182|Long et al., 1997]). Pseudomonas putida L can convert tropate to phenylacetate, possibly by the same mechanism ([http://www.ncbi.nlm.nih.gov/pubmed/9023182|Stevens and Roersch, 1971]).
Your Options:
Update the Pathway Information: POST with (required) pathwayName and (optional) pathwayDescription.
Delete the Pathway: DELETE.
Show nodes: GET on https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/pathway/8a650dac-691c-41cd-8690-5f160fd2a536/node
Show edges: GET on https://envipath.org/package/32de3cf4-e3e6-4168-956e-32fa5ddb0ce1/pathway/8a650dac-691c-41cd-8690-5f160fd2a536/edge