CHEMBL5583940
General
Type : Piperidine, Carbamate
Chemical_Nomenclature : [3-[(1~{S})-1-oxidanyl-2-piperidin-1-yl-ethyl]-5-piperidin-1-ylcarbonyloxy-phenyl] piperidine-1-carboxylate
Canonical SMILES : O[CH](CN1CCCCC1)c2cc(OC(=O)N3CCCCC3)cc(OC(=O)N4CCCCC4)c2
InChI : InChI=1S\/C25H37N3O5\/c29-23(19-26-10-4-1-5-11-26)20-16-21(32-24(30)27-12-6-2-7-13-27)18-22(17-20)33-25(31)28-14-8-3-9-15-28\/h16-18,23,29H,1-15,19H2
InChIKey : BWDDGVMFEKGIRS-UHFFFAOYSA-N
Other name(s) : A1I0F
MW : 459.578
Formula : C25H37N3O5
CAS_number :
PubChem : 177377881
UniChem : BWDDGVMFEKGIRS-UHFFFAOYSA-N
Target
Structure :
9I4W
References (1)
| Title : Integrative Structural and Kinetic Analysis of the Molecular Basis for Reduced Carbamate Inhibition in Atypical Butyrylcholinesterase - Matosevic_2026_Chem.Biol.Interact__112134 |
| Author(s) : Matosevic A , Marakovic N , Baric D , Igert A , Brazzolotto X , Kovarik Z , Bosak A |
| Ref : Chemico-Biological Interactions , :112134 , 2026 |
| Abstract : |
| PubMedSearch : Matosevic_2026_Chem.Biol.Interact__112134 |
| PubMedID: 42097478 |
| Gene_locus related to this paper: human-BCHE |