(R)-1-(4-(3-amino-1H-pyrazolo[3,4-d]pyrimidin-6-ylamino)phenyl)-3-(1-phenylethyl)urea

ID: ALA2089216

PubChem CID: 70684935

Max Phase: Preclinical

Molecular Formula: C20H20N8O

Molecular Weight: 388.44

Molecule Type: Small molecule

Names and Identifiers

Canonical SMILES:  C[C@@H](NC(=O)Nc1ccc(Nc2ncc3c(N)n[nH]c3n2)cc1)c1ccccc1

Standard InChI:  InChI=1S/C20H20N8O/c1-12(13-5-3-2-4-6-13)23-20(29)25-15-9-7-14(8-10-15)24-19-22-11-16-17(21)27-28-18(16)26-19/h2-12H,1H3,(H2,23,25,29)(H4,21,22,24,26,27,28)/t12-/m1/s1

Standard InChI Key:  XUUHPPLVUFQCHZ-GFCCVEGCSA-N

Molfile:  

     RDKit          2D

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    8.8266  -13.7898    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5414  -14.2027    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.5396  -12.5497    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2550  -12.9588    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2598  -13.7853    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.0473  -14.0361    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.5292  -13.3646    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
   11.0395  -12.6989    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   11.2898  -11.9128    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.1118  -14.2018    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.1111  -15.0268    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3962  -15.4371    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.3952  -16.2614    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1099  -16.6753    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8271  -16.2589    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8245  -15.4360    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1103  -17.5003    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3961  -17.9131    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.6814  -17.5010    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    7.3965  -18.7381    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    5.9672  -17.9139    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2525  -17.5018    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.9676  -18.7389    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.2573  -16.6775    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5434  -16.2655    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8282  -16.6784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.8313  -17.5077    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.5457  -17.9160    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
 13 14  1  0
  1  2  2  0
 14 15  2  0
  5  4  2  0
 15 16  1  0
  6  7  1  0
 16 17  2  0
 17 12  1  0
  7  8  1  0
 15 18  1  0
  8  9  2  0
 18 19  1  0
  9  5  1  0
 19 20  1  0
  4  1  1  0
 19 21  2  0
  9 10  1  0
 20 22  1  0
  5  6  1  0
 22 23  1  0
  2 11  1  0
 22 24  1  6
 23 25  2  0
 11 12  1  0
 25 26  1  0
  2  3  1  0
 26 27  2  0
 12 13  2  0
 27 28  1  0
  3  6  2  0
 28 29  2  0
 29 23  1  0
M  END

Alternative Forms

1. Parent:

   

   ALA2089216

   1-[4-[(3-amino-2H-pyrazolo[3,4-d]pyrimidin-6-yl)amino]phenyl]-3-[(1R)-1-phenylethyl]urea

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Small molecule

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 388.44

Molecular Weight (Monoisotopic): 388.1760

AlogP: 3.56

#Rotatable Bonds: 5

Polar Surface Area: 133.64

Molecular Species: NEUTRAL

HBA: 6

HBD: 5

#RO5 Violations: ┄

HBA (Lipinski): 9

HBD (Lipinski): 6

#RO5 Violations (Lipinski): 1

CX Acidic pKa: 12.27

CX Basic pKa: 3.43

CX LogP: 2.89

CX LogD: 2.89

Aromatic Rings: 4

Heavy Atoms: 29

QED Weighted: 0.35

Np Likeness Score: -1.56

References

1. Yang LL, Li GB, Yan HX, Sun QZ, Ma S, Ji P, Wang ZR, Feng S, Zou J, Yang SY..  (2012)  Discovery of N6-phenyl-1H-pyrazolo[3,4-d]pyrimidine-3,6-diamine derivatives as novel CK1 inhibitors using common-feature pharmacophore model based virtual screening and hit-to-lead optimization.,  56  [PMID:22944772] [10.1016/j.ejmech.2012.08.007]

Source

Source(1):

• Scientific Literature