General Information of the Compound
Compound ID
CP0575835
Compound Name
6-(4-((5-(Furan-3-yl)pyridin-3-yl)methoxy)-6-methoxybenzofuran-2-yl)-2-methoxyimidazo[2,1-b][1,3,4]thiadiazole
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Structure
Formula
C24H18N4O5S
Molecular Weight
474.498
Canonical SMILES
COc1nn2cc(nc2s1)-c1cc2c(OCc3cncc(c3)-c3ccoc3)cc(OC)cc2o1
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InChI
InChI=1S/C24H18N4O5S/c1-29-17-6-20(32-12-14-5-16(10-25-9-14)15-3-4-31-13-15)18-8-22(33-21(18)7-17)19-11-28-23(26-19)34-24(27-28)30-2/h3-11,13H,12H2,1-2H3
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InChIKey
HKIGWTJZBHDXHZ-UHFFFAOYSA-N
Physicochemical Property
logP
5.4552
Rotatable Bonds
7
Heavy Atom Count
34
Polar Areas
97.05
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
10
Complexity
34

"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: 72190264
ChEMBL ID
CHEMBL3717838
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: PT04808, Proteinase-activated receptor 4
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
IC50 = 1.08 nM
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