General Information of the Compound
Compound ID
CP0103780
Compound Name
1-(4-Dimethylaminomethyl-phenyl)-8,9-dihydro-7H-2,7,9a-triaza-benzo[cd]azulen-6-one
    Show/Hide
Synonyms
Nucleoside analogue
1-(4-((dimethylamino)methyl)phenyl)-8,9-dihydro-2,7,9a-triazabenzo[cd]azulen-6(7H)-one
2-[4-[(Dimethylamino)methyl]phenyl]-5,6-dihydroimidazo[4,5,1-jk][1,4]benzodiazepin-7(4H)-one
328543-09-5
48N0U0K50I
AG 14361
AG-014361
AG-14361
AG14361
CC-486
CHEMBL65892
Imidazo(4,5,1-jk)(1,4)benzodiazepin-7(4H)-one, 2-(4-((dimethylamino)methyl)phenyl)-5,6-dihydro-
Imidazo[4,5,1-jk][1,4]benzodiazepin-7(4H)-one, 2-[4-[(dimethylamino)methyl]phenyl]-5,6-dihydro-
MLS001065917
MLS006011157
SMR000486393
UNII-48N0U0K50I
    Show/Hide
Structure
Formula
C19H20N4O
Molecular Weight
320.396
Canonical SMILES
CN(C)Cc1ccc(cc1)-c1nc2cccc3C(=O)NCCn1c23
    Show/Hide
InChI
InChI=1S/C19H20N4O/c1-22(2)12-13-6-8-14(9-7-13)18-21-16-5-3-4-15-17(16)23(18)11-10-20-19(15)24/h3-9H,10-12H2,1-2H3,(H,20,24)
    Show/Hide
InChIKey
SEKJSSBJKFLZIT-UHFFFAOYSA-N
Physicochemical Property
logP
2.5083
Rotatable Bonds
3
Heavy Atom Count
24
Polar Areas
50.16
Hydrogen Bond Donor Count
1
Hydrogen Bond Acceptor Count
4
Complexity
24

"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: 9840076
SID: 14801398
ChEMBL ID
CHEMBL65892
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: PT06109, Geminin
Cell-based Assay
Cell Line ID Cell Line Name Cell Line Organism
CL000015 SW480 Homo sapiens (Human)  1
1
Potency ~ 23109.3 nM
   TI
   LI
   LO
   TS
Clinical Information about the Compound
Drug 1 ( CC-486 )
Drug Name CC-486
Company Celgene
Indication
Myelodysplastic syndrome
Phase 3
Acute myeloid leukaemia
Phase 3
Myelodysplastic syndrome
Phase 3
Diffuse large B-cell lymphoma
Phase 1
Target(s)
Poly [ADP-ribose] polymerase 1 (PARP1)
Inhibitor
DNA [cytosine-5]-methyltransferase 1 (DNMT1)
Inhibitor