N-(4-(4-aminopiperidin-1-yl)-5-(3,5-dichlorophenyl)pyridin-3-yl)-1,3-dimethyl-1H-pyrazole-5-carboxamide

ID: ALA4870834

PubChem CID: 164624692

Max Phase: Preclinical

Molecular Formula: C22H24Cl2N6O

Molecular Weight: 459.38

Molecule Type: Unknown

Names and Identifiers

Canonical SMILES:  Cc1cc(C(=O)Nc2cncc(-c3cc(Cl)cc(Cl)c3)c2N2CCC(N)CC2)n(C)n1

Standard InChI:  InChI=1S/C22H24Cl2N6O/c1-13-7-20(29(2)28-13)22(31)27-19-12-26-11-18(14-8-15(23)10-16(24)9-14)21(19)30-5-3-17(25)4-6-30/h7-12,17H,3-6,25H2,1-2H3,(H,27,31)

Standard InChI Key:  NTRKYUHADCVHCH-UHFFFAOYSA-N

Molfile:  

 
     RDKit          2D

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    6.7413  -28.2326    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4494  -28.6415    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.1590  -28.2321    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1562  -27.4094    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4476  -27.0042    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8593  -26.9994    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5689  -27.4071    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2746  -26.9965    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
   10.2719  -26.1784    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    9.5577  -25.7727    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.8549  -26.1856    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4436  -26.1926    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    8.1519  -25.7831    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    8.1514  -24.9695    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4443  -24.5592    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7360  -24.9687    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    6.7348  -25.7885    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    7.4449  -23.7420    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    9.5517  -24.9555    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
   10.9836  -27.4028    0.0000 Cl  0  0  0  0  0  0  0  0  0  0  0  0
    6.0347  -27.0046    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    5.3271  -27.4134    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    4.6193  -27.0049    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    5.3273  -28.2305    0.0000 O   0  0  0  0  0  0  0  0  0  0  0  0
    4.5332  -26.1933    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7338  -26.0236    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.3254  -26.7314    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.8724  -27.3385    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
    3.4013  -25.2771    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.7032  -28.1380    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
  1  2  2  0
  2  3  1  0
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  9 10  2  0
 10 11  1  0
 11 12  2  0
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  5  7  1  0
 13 14  1  0
 13 18  1  0
 14 15  1  0
 15 16  1  0
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 17 18  1  0
  6 13  1  0
 16 19  1  0
 11 20  1  0
  9 21  1  0
  1 22  1  0
 22 23  1  0
 23 24  1  0
 23 25  2  0
 24 26  2  0
 26 27  1  0
 27 28  2  0
 28 29  1  0
 29 24  1  0
 27 30  1  0
 29 31  1  0
M  END

Alternative Forms

1. Parent:

   

   ALA4870834

   ---

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type: Unknown

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Calculated Properties

Molecular Weight: 459.38

Molecular Weight (Monoisotopic): 458.1389

AlogP: 4.28

#Rotatable Bonds: 4

Polar Surface Area: 89.07

Molecular Species: BASE

HBA: 6

HBD: 2

#RO5 Violations: ┄

HBA (Lipinski): 7

HBD (Lipinski): 3

#RO5 Violations (Lipinski): ┄

CX Acidic pKa: ┄

CX Basic pKa: 10.03

CX LogP: 2.50

CX LogD: -0.38

Aromatic Rings: 3

Heavy Atoms: 31

QED Weighted: 0.61

Np Likeness Score: -1.45

References

1. Ishida A, Okabe Y, Matsushita T, Sekiguchi T, Nishio T, Komagata T, Iwaki M, Miyata H, Katagi J, Naganawa A, Maruyama T, Imagawa A..  (2021)  Design, synthesis, and biological evaluation of novel somatostatin receptor subtype-2 agonists: Optimization for potency and risk mitigation of hERG and phospholipidosis.,  49  [PMID:34626901] [10.1016/j.bmc.2021.116424]

Source

Source(1):

• Scientific Literature