Drug General Information |
Drug ID |
D0D0BI
|
Former ID |
DNC005438
|
Drug Name |
CHLORANIL
|
Drug Type |
Small molecular drug
|
Indication |
Discovery agent
|
Investigative |
[1]
|
Structure |
|
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2D MOL
3D MOL
|
Formula |
C6Cl4O2
|
Canonical SMILES |
C1(=C(C(=O)C(=C(C1=O)Cl)Cl)Cl)Cl
|
InChI |
1S/C6Cl4O2/c7-1-2(8)6(12)4(10)3(9)5(1)11
|
InChIKey |
UGNWTBMOAKPKBL-UHFFFAOYSA-N
|
PubChem Compound ID |
|
Target and Pathway |
Target(s) |
Liver carboxylesterase |
Target Info |
Inhibitor |
[1]
|
Acetylcholinesterase |
Target Info |
Inhibitor |
[1]
|
Cholinesterase |
Target Info |
Inhibitor |
[1]
|
KEGG Pathway
|
Drug metabolism - other enzymes
|
Metabolic pathwayshsa00564:Glycerophospholipid metabolism
|
Cholinergic synapse
|
PANTHER Pathway
|
Muscarinic acetylcholine receptor 1 and 3 signaling pathway
|
Muscarinic acetylcholine receptor 2 and 4 signaling pathway
|
Nicotinic acetylcholine receptor signaling pathwayP00042:Muscarinic acetylcholine receptor 1 and 3 signaling pathway
|
Nicotinic acetylcholine receptor signaling pathway
|
Pathway Interaction Database
|
E2F transcription factor networkatf2_pathway:ATF-2 transcription factor network
|
PathWhiz Pathway
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Phospholipid Biosynthesis
|
WikiPathways
|
NRF2 pathway
|
Nuclear Receptors Meta-Pathway
|
Heroin metabolism
|
Irinotecan Pathway
|
Fluoropyrimidine Activity
|
Phase I biotransformations, non P450WP727:Monoamine Transport
|
Biogenic Amine Synthesis
|
Acetylcholine Synthesis
|
Integrated Pancreatic Cancer PathwayWP229:Irinotecan Pathway
|
References |
REF 1 | J Med Chem. 2005 Apr 21;48(8):2906-15.Identification and characterization of novel benzil (diphenylethane-1,2-dione) analogues as inhibitors of mammalian carboxylesterases. |