(S)-hexyl 2-(benzyloxycarbonylamino)-5-(2-(1-benzylpiperidin-4-yl)ethylamino)-5-oxopentanoate

Modify Date: 2025-08-27 11:38:08

(S)-hexyl 2-(benzyloxycarbonylamino)-5-(2-(1-benzylpiperidin-4-yl)ethylamino)-5-oxopentanoate Structure
(S)-hexyl 2-(benzyloxycarbonylamino)-5-(2-(1-benzylpiperidin-4-yl)ethylamino)-5-oxopentanoate structure
Common Name (S)-hexyl 2-(benzyloxycarbonylamino)-5-(2-(1-benzylpiperidin-4-yl)ethylamino)-5-oxopentanoate
CAS Number 1161426-64-7 Molecular Weight 565.7
Density N/A Boiling Point N/A
Molecular Formula C33H47N3O5 Melting Point N/A
MSDS N/A Flash Point N/A

 Names

Name (S)-hexyl 2-(benzyloxycarbonylamino)-5-(2-(1-benzylpiperidin-4-yl)ethylamino)-5-oxopentanoate

 Chemical & Physical Properties

Molecular Formula C33H47N3O5
Molecular Weight 565.7
InChIKey MHODVJVESFLWQL-PMERELPUSA-N
SMILES CCCCCCOC(=O)C(CCC(=O)NCCC1CCN(Cc2ccccc2)CC1)NC(=O)OCc1ccccc1

 Bioassay

View more

Name: Neuroprotective activity against H2O2-induced human SH-SY5Y cells assessed as cell vi...
Source: ChEMBL
Target: SH-SY5Y
External Id: CHEMBL1105056
Name: Selectivity ratio of IC50 for human AChE to IC50 for human BuChE
Source: ChEMBL
Target: N/A
External Id: CHEMBL1105047
Name: Inhibition of human BuChE in serum
Source: ChEMBL
Target: Cholinesterase
External Id: CHEMBL1105046
Name: Inhibition of human AChE in erythrocyte
Source: ChEMBL
Target: Acetylcholinesterase
External Id: CHEMBL1105045
Name: Inhibition of BuChE in horse serum by Ellman method
Source: ChEMBL
Target: Cholinesterase
External Id: CHEMBL1105044
Name: Inhibition of AChE in bovine erythrocyte by Ellman method
Source: ChEMBL
Target: Acetylcholinesterase
External Id: CHEMBL1116696
Name: Neuroprotective activity against human SH-SY5Y cells assessed as protection reduction...
Source: ChEMBL
Target: SH-SY5Y
External Id: CHEMBL1105055
Name: Neuroprotective activity against human SH-SY5Y cells assessed as protection reduction...
Source: ChEMBL
Target: SH-SY5Y
External Id: CHEMBL1105054
Name: Neuroprotective activity against human SH-SY5Y cells assessed as protection reduction...
Source: ChEMBL
Target: SH-SY5Y
External Id: CHEMBL1105053
Name: Neuroprotective activity against human SH-SY5Y cells assessed as protection reduction...
Source: ChEMBL
Target: SH-SY5Y
External Id: CHEMBL1105052
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