General Information of the Compound
Compound ID
CP0012254
Compound Name
BX-795
    Show/Hide
Synonyms
BX 795
BX-795
BX795
    Show/Hide
Structure
Formula
C23H26IN7O2S
Molecular Weight
591.479
Canonical SMILES
Ic1cnc(Nc2cccc(NC(=O)N3CCCC3)c2)nc1NCCCNC(=O)c1cccs1
    Show/Hide
InChI
InChI=1S/C23H26IN7O2S/c24-18-15-27-22(30-20(18)25-9-5-10-26-21(32)19-8-4-13-34-19)28-16-6-3-7-17(14-16)29-23(33)31-11-1-2-12-31/h3-4,6-8,13-15H,1-2,5,9-12H2,(H,26,32)(H,29,33)(H2,25,27,28,30)
    Show/Hide
InChIKey
VAVXGGRQQJZYBL-UHFFFAOYSA-N
Physicochemical Property
logP
4.746
Rotatable Bonds
9
Heavy Atom Count
34
Polar Areas
111.28
Hydrogen Bond Donor Count
4
Hydrogen Bond Acceptor Count
7
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).

    Show/Hide
Click to Show/Hide the External Link(s) of This Compound
PubChem ID
CID: 10077147
SID: 15062621
ChEMBL ID
CHEMBL577784
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: PT05581, Cyclic GMP-AMP synthase
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000040 THP-1 Homo sapiens (Human)  1
1
IC50 = 60 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( BX-795 )
Drug Name BX-795
Target(s)
Checkpoint kinase-1 (CHK1)
Inhibitor
Cyclin-dependent kinase 2 (CDK2)
Inhibitor
Vascular endothelial growth factor receptor 2 (KDR)
Inhibitor
Phosphoinositide dependent protein kinase-1 (PDPK1)
Inhibitor
Glycogen synthase kinase-3 beta (GSK-3B)
Inhibitor