General Information of the Compound
Compound ID
CP0179673
Compound Name
[4-[[4-(ethylamino)-5-(trifluoromethyl)pyrimidin-2-yl]amino]-2-fluoro-5-methoxyphenyl]-morpholin-4-ylmethanone
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Synonyms
GNE 7915
GNE-7915
GNE7915
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Structure
Formula
C19H21F4N5O3
Molecular Weight
443.401
Canonical SMILES
CCNc1nc(Nc2cc(F)c(cc2OC)C(=O)N2CCOCC2)ncc1C(F)(F)F
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InChI
InChI=1S/C19H21F4N5O3/c1-3-24-16-12(19(21,22)23)10-25-18(27-16)26-14-9-13(20)11(8-15(14)30-2)17(29)28-4-6-31-7-5-28/h8-10H,3-7H2,1-2H3,(H2,24,25,26,27)
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InChIKey
XCFLWTZSJYBCPF-UHFFFAOYSA-N
Physicochemical Property
logP
3.2909
Rotatable Bonds
6
Heavy Atom Count
31
Polar Areas
88.61
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
7
Complexity
31

"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: 58539171
SID: 163502368
ChEMBL ID
CHEMBL2178134
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: PT01378, Leucine-rich repeat serine/threonine-protein kinase 2
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
IC50 = 9 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 97 nM
2 Ki = 1 nM
3 Ki = 2 nM
Clinical Information about the Compound
Drug 1 ( GNE-7915 )
Drug Name GNE-7915
Target(s)
Dual specificity protein kinase TTK (MPS1)
Inhibitor
Leucine-rich repeat kinase 2 (LRRK2)
Inhibitor