General Information of the Compound
Compound ID
CP0481346
Compound Name
N-butyl-4-chloro-N-[5-(3-fluorophenyl)-1,3,4-thiadiazol-2-yl]benzamide
    Show/Hide
Structure
Formula
C19H17ClFN3OS
Molecular Weight
389.883
Canonical SMILES
CCCCN(C(=O)c1ccc(Cl)cc1)c1nnc(s1)-c1cccc(F)c1
    Show/Hide
InChI
InChI=1S/C19H17ClFN3OS/c1-2-3-11-24(18(25)13-7-9-15(20)10-8-13)19-23-22-17(26-19)14-5-4-6-16(21)12-14/h4-10,12H,2-3,11H2,1H3
    Show/Hide
InChIKey
QIPZYKFTFMNIBT-UHFFFAOYSA-N
Physicochemical Property
logP
5.4445
Rotatable Bonds
6
Heavy Atom Count
26
Polar Areas
46.09
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
4
Complexity
26

"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).

    Show/Hide
Click to Show/Hide the External Link(s) of This Compound
PubChem ID
CID: 70693634
ChEMBL ID
CHEMBL2011728
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: PT01688, Sphingosine 1-phosphate receptor 1
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000043 U2OS Homo sapiens (Human)  1
1
EC50 = 125.89 nM
   TI
   LI
   LO
   TS
Protein ID: PT01838, Sphingosine 1-phosphate receptor 3
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000025 HEK-293T Homo sapiens (Human)  1
1
EC50 > 10000 nM
   TI
   LI
   LO
   TS