General Information of the Compound
Compound ID
CP0285045
Compound Name
N,N-dimethyl-4-[pyridin-2-yl-[1-(1,3-thiazol-4-ylmethyl)piperidin-4-ylidene]methyl]benzamide
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Structure
Formula
C24H26N4OS
Molecular Weight
418.566
Canonical SMILES
CN(C)C(=O)c1ccc(cc1)C(=C1CCN(Cc2cscn2)CC1)c1ccccn1
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InChI
InChI=1S/C24H26N4OS/c1-27(2)24(29)20-8-6-18(7-9-20)23(22-5-3-4-12-25-22)19-10-13-28(14-11-19)15-21-16-30-17-26-21/h3-9,12,16-17H,10-11,13-15H2,1-2H3
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InChIKey
ARTNWBGMVYZVIZ-UHFFFAOYSA-N
Physicochemical Property
logP
4.3378
Rotatable Bonds
5
Heavy Atom Count
30
Polar Areas
49.33
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
5
Complexity
30

"RO5" indicates the cutoff set by lipinski's rule of five:

(1) Molecular weight less than 500 Dalton;

(2) xlogp less than 5;

(3) No more than 5 hbonddonor (Hydrogen Bond Donor Count);

(4) No more than 10 hbondacc (Hydrogen Bond Acceptor Count);

(5) No more than 10 rotbonds (Rotatable Bond Count).

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PubChem ID
CID: 46869046
SID: 99308177
ChEMBL ID
CHEMBL1946621
Map of Molecular Bioactivity Related to the Compound
Map of Molecular Bioactivity Related to the Compound

Compound
Cell Line
Protein

Bioactivity Value:

<= 0.1 μM
> 0.1 μM and <= 10 μM
> 10 μM
Imprecise Activity
Table of Molecular Bioactivities Related to the Compound
Protein ID: PT01200, Delta-type opioid receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
IC50 = 2.7 nM
   TI
   LI
   LO
   TS
Protein ID: PT01515, Mu-type opioid receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
IC50 = 5400 nM
   TI
   LI
   LO
   TS