General Information of the Compound
Compound ID
CP0018039
Compound Name
N-[4-[4-(4-methylpiperazin-1-yl)-6-[(5-methyl-1H-pyrazol-3-yl)amino]pyrimidin-2-yl]sulfanylphenyl]cyclopropanecarboxamide
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Synonyms
Cyclopropane carboxylic acid{4-[4-(4-methyl-piperazin-1-yl)-6-(5-methyl-2H-pyrazol-3-ylamino)-pyrimidin-2-ylsulphanyl]-phenyl}-amide
Cyclopropanecarboxylic Acid {4-[4-(4-Methyl-Piperazin-1-Yl)-6-(5-Methyl-2h-Pyrazol-3-Ylamino)-Pyrimidin-2-Ylsulfanyl]-Phenyl}-Amide
Cyclopropanecarboxylic acid N-(4-((4-(4-methylpiperazin-1-yl)-6-(5-methyl-2H-pyrazol-3-ylamino)pyrimidin-2-yl)sulfanyl)phenyl)amide
L-001281814
MK 0457
MK-045
MK-0457
MK-0457, Tozasertib, VX680, VX-680
N-(4-(4-(3-methyl-1H-pyrazol-5-ylamino)-6-(4-methylpiperazin-1-yl)pyrimidin-2-ylthio)phenyl)cyclopropanecarboxamide
N-[4-[4-(4-methylpiperazin-1-yl)-6-[(5-methyl-1H-pyrazol-3-yl)amino]pyrimidin-2-yl]sulfanylphenyl]cyclopropanecarboxamide
Tozasertib
Tozasertib (USAN)
VX 680
VX-68
VX-680
VX6
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Structure
Formula
C23H28N8OS
Molecular Weight
464.599
Canonical SMILES
CN1CCN(CC1)c1cc(Nc2cc(C)n[nH]2)nc(Sc2ccc(NC(=O)C3CC3)cc2)n1
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InChI
InChI=1S/C23H28N8OS/c1-15-13-20(29-28-15)25-19-14-21(31-11-9-30(2)10-12-31)27-23(26-19)33-18-7-5-17(6-8-18)24-22(32)16-3-4-16/h5-8,13-14,16H,3-4,9-12H2,1-2H3,(H,24,32)(H2,25,26,27,28,29)
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InChIKey
GCIKSSRWRFVXBI-UHFFFAOYSA-N
CAS
639089-54-6
Physicochemical Property
logP
3.50322
Rotatable Bonds
7
Heavy Atom Count
33
Polar Areas
102.07
Hydrogen Bond Donor Count
3
Hydrogen Bond Acceptor Count
8
Complexity
33

"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: 5494449
SID: 26683796
ChEMBL ID
CHEMBL572878
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: PT00980, Aurora kinase A
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000013 Sf9 Spodoptera frugiperda (Fall armyworm)  2
1
IC50 = 20 nM
   TI
   LI
   LO
   TS
2
IC50 = 23 nM
   TI
   LI
   LO
   TS
CL000017 HeLa Homo sapiens (Human)  1
1
Ki = 2 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 0.24 nM
2 IC50 = 0.6 nM
3 IC50 = 0.7 nM
4 IC50 = 0.95 nM
5 IC50 = 1.05 nM
6 IC50 = 1.4 nM
7 IC50 = 1.9 nM
8 IC50 = 2.8 nM
9 IC50 = 6 nM
10 IC50 = 15 nM
11 IC50 = 20 nM
12 IC50 = 30 nM
13 IC50 = 31.62 nM
14 IC50 = 127 nM
15 IC50 = 130 nM
16 Kd = 0.3333 nM
17 Kd = 0.645 nM
18 Kd = 3.9 nM
19 Kd = 4 nM
20 Kd = 4.1 nM
21 Kd = 17 nM
22 Ki = 0.37 nM
23 Ki = 0.6 nM
24 Ki = 0.65 nM
25 Ki = 1 nM
Protein ID: PT01223, Aurora kinase B
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000067 HCT 116 Homo sapiens (Human)  1
1
IC50 = 55 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 14.7 nM
2 IC50 = 15.7 nM
3 IC50 = 17 nM
4 IC50 = 18 nM
5 IC50 = 18.6 nM
6 IC50 = 30 nM
7 IC50 = 40 nM
8 IC50 = 43 nM
9 IC50 = 68 nM
10 Kd = 7 nM
11 Kd = 7.4 nM
12 Ki = 1.8 nM
13 Ki = 3.36 nM
14 Ki = 18 nM
Protein ID: PT06109, Geminin
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000015 SW480 Homo sapiens (Human)  1
1
Potency ~ 259.3 nM
   TI
   LI
   LO
   TS
Cell Viability or Cytotoxicity Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000017 HeLa Homo sapiens (Human)  1
1
GI50 = 46200 nM
   TI
   LI
   LO
   TS
CL000067 HCT 116 Homo sapiens (Human)  1
1
IC50 = 28 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( VX-680 )
Drug Name VX-680
Company Vertex; Merck
Indication
Solid tumour/cancer
Phase 2
Target(s)
Aurora kinase A (AURKA)
Inhibitor
LCK tyrosine protein kinase (LCK)
Inhibitor
Aurora kinase B (AURKB)
Inhibitor