General Information of the Compound
Compound ID
CP0084841
Compound Name
1-cyclopentyl-N-[(4,6-dimethyl-2-oxo-1H-pyridin-3-yl)methyl]-6-[4-(morpholin-4-ylmethyl)phenyl]indazole-4-carboxamide
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Synonyms
EPZ 005687
EPZ-005687
EPZ005687
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Structure
Formula
C32H37N5O3
Molecular Weight
539.68
Canonical SMILES
Cc1cc(C)c(CNC(=O)c2cc(cc3n(ncc23)C2CCCC2)-c2ccc(CN3CCOCC3)cc2)c(=O)[nH]1
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InChI
InChI=1S/C32H37N5O3/c1-21-15-22(2)35-32(39)28(21)18-33-31(38)27-16-25(17-30-29(27)19-34-37(30)26-5-3-4-6-26)24-9-7-23(8-10-24)20-36-11-13-40-14-12-36/h7-10,15-17,19,26H,3-6,11-14,18,20H2,1-2H3,(H,33,38)(H,35,39)
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InChIKey
ZOIBZSZLMJDVDQ-UHFFFAOYSA-N
Physicochemical Property
logP
4.88574
Rotatable Bonds
7
Heavy Atom Count
40
Polar Areas
92.25
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
6
Complexity
40

"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: 60160561
SID: 152143308
ChEMBL ID
CHEMBL3360855
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: PT03003, Histone-lysine N-methyltransferase EZH2
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000175 G-401 Homo sapiens (Human)  1
1
EC50 = 2900 nM
   TI
   LI
   LO
   TS
Biochemical Assays
1 IC50 = 54 nM
2 IC50 = 54000 nM
3 Ki = 24 nM
Clinical Information about the Compound
Drug 1 ( EPZ005687 )
Drug Name EPZ005687
Target(s)
Enhancer of zeste homolog 2 (EZH2)
Inhibitor