General Information of the Compound
Compound ID
CP0043977
Compound Name
14-[[[(2R)-1,4-dioxan-2-yl]methyl-methylsulfamoyl]amino]-5-(1-methylpyrazol-4-yl)-2-oxo-7-azatricyclo[9.4.0.03,8]pentadeca-1(11),3(8),4,6,9,12,14-heptaene
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Synonyms
MK 2461
MK-2461
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Structure
Formula
C24H25N5O5S
Molecular Weight
495.561
Canonical SMILES
CN(C[C@@H]1COCCO1)S(=O)(=O)Nc1ccc2ccc3ncc(cc3c(=O)c2c1)-c1cnn(C)c1
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InChI
InChI=1S/C24H25N5O5S/c1-28-13-18(12-26-28)17-9-22-23(25-11-17)6-4-16-3-5-19(10-21(16)24(22)30)27-35(31,32)29(2)14-20-15-33-7-8-34-20/h3-6,9-13,20,27H,7-8,14-15H2,1-2H3/t20-/m1/s1
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InChIKey
JGEBLDKNWBUGRZ-HXUWFJFHSA-N
CAS
917879-39-1
Physicochemical Property
logP
2.1526
Rotatable Bonds
6
Heavy Atom Count
35
Polar Areas
115.65
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
8
Complexity
35

"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: 44137946
SID: 99311589
ChEMBL ID
CHEMBL1822792
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: PT01201, Hepatocyte growth factor receptor
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000282 GTL-16 Homo sapiens (Human)  3
1
IC50 = 50 nM
   TI
   LI
   LO
   TS
2
IC50 = 56 nM
   TI
   LI
   LO
   TS
3
IC50 > 2500 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 0.4 nM
2 IC50 = 2 nM
3 IC50 = 26 nM
4 IC50 = 100 nM
5 IC50 = 900 nM
6 Kd = 4 nM
7 Kd = 4.4 nM
8 Kd = 25 nM
9 Kd = 27.2 nM
Clinical Information about the Compound
Drug 1 ( MK-2461 )
Drug Name MK-2461
Indication
Alzheimer disease
Phase 1/2
Target(s)
Vascular endothelial growth factor receptor 3 (FLT-4)
Inhibitor
Tyrosine-protein kinase Mer (MERTK)
Inhibitor
Fms-like tyrosine kinase 3 (FLT-3)
Inhibitor
Proto-oncogene c-Met (MET)
Inhibitor
Fibroblast growth factor receptor 1 (FGFR1)
Inhibitor
Platelet-derived growth factor receptor beta (PDGFRB)
Inhibitor
Vascular endothelial growth factor receptor 2 (KDR)
Inhibitor
VEGFR1 messenger RNA (VEGFR1 mRNA)
Inhibitor
Fibroblast growth factor receptor 3 (FGFR3)
Inhibitor
NT-3 growth factor receptor (TrkC)
Inhibitor
BDNF/NT-3 growth factors receptor (TrkB)
Inhibitor
Fibroblast growth factor receptor 2 (FGFR2)
Inhibitor
Macrophage-stimulating protein receptor (RON)
Inhibitor