General Information of the Compound
Compound ID
CP0097523
Compound Name
US9315520, 1
    Show/Hide
Synonyms
1818339-66-0
1Y0Y126GUG
BDBM223395
CHEMBL3952064
CS-0043501
HY-112157
N-(2-((4aR,6S,8aR)-2-Amino-6-methyl-4a,5,6,8-tetrahydro-4H-pyrano(3,4-d)(1,3)thiazin-8a-yl)thiazol-4-yl)-5-(difluoromethoxy)pyridine-2-carboxamide
N-{2-[(4aR,6S,8aR)-2-Amino-6-methyl-4,4a,5,6-tetrahydropyrano[3,4-d][1,3]thiazin-8a(8H)-yl]-1,3-thiazol-4-yl}-5-(difluoromethoxy)pyridine-2-carb
PF-06751979
SCHEMBL17162186
UNII-1Y0Y126GUG
US9315520, 1
US9315520, Comparator 1
US9315520, Example 1
US9315520, Example 2
ZLZUHACSRMOLLV-RAALSFIWSA-N
    Show/Hide
Structure
Formula
C18H19F2N5O3S2
Molecular Weight
455.512
Canonical SMILES
C[C@H]1C[C@H]2CSC(N)=N[C@]2(CO1)c1nc(NC(=O)c2ccc(OC(F)F)cn2)cs1
    Show/Hide
InChI
InChI=1S/C18H19F2N5O3S2/c1-9-4-10-6-30-17(21)25-18(10,8-27-9)15-24-13(7-29-15)23-14(26)12-3-2-11(5-22-12)28-16(19)20/h2-3,5,7,9-10,16H,4,6,8H2,1H3,(H2,21,25)(H,23,26)/t9-,10-,18-/m0/s1
    Show/Hide
InChIKey
ZLZUHACSRMOLLV-RAALSFIWSA-N
Physicochemical Property
logP
3.0736
Rotatable Bonds
5
Heavy Atom Count
30
Polar Areas
111.72
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
9
Complexity
30

"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: 118435360
ChEMBL ID
CHEMBL3952064
DrugBank ID
DB15105
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: PT01020, Beta-secretase 1
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000008 H4 Homo sapiens (Human)  1
1
IC50 = 5.1 nM
   TI
   LI
   LO
   TS
CL000006 HEK293 Homo sapiens (Human)  1
1
IC50 = 7.3 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 36.9 nM
Protein ID: PT01134, Beta-secretase 2
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000006 HEK293 Homo sapiens (Human)  1
1
IC50 = 194 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 Activity = 2860 nM
2 IC50 = 238 nM
Protein ID: PT00897, Potassium voltage-gated channel subfamily H member 2
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000026 CHO-K1 Cricetulus griseus (Chinese hamster)  1
1
IC50 = 9900 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( PF-06751979 )
Drug Name PF-06751979
Company Pfizer New York, NY
Indication
Alzheimer disease
Phase 1