ID: ALA4173466

Max Phase: Preclinical

Molecular Formula: C27H29ClF3N5O2

Molecular Weight: 548.01

Molecule Type: Small molecule

Representations

Canonical SMILES:  CC(Oc1ccnc(NN2CCN(C)CC2)c1)c1cccc(C(=O)NCc2ccc(Cl)c(C(F)(F)F)c2)c1

Standard InChI:  InChI=1S/C27H29ClF3N5O2/c1-18(38-22-8-9-32-25(16-22)34-36-12-10-35(2)11-13-36)20-4-3-5-21(15-20)26(37)33-17-19-6-7-24(28)23(14-19)27(29,30)31/h3-9,14-16,18H,10-13,17H2,1-2H3,(H,32,34)(H,33,37)

Standard InChI Key:  VWINXVFVVLWUGN-UHFFFAOYSA-N

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

Properties

Molecular Weight: 548.01

Molecular Weight (Monoisotopic): 547.1962

AlogP: 5.40

#Rotatable Bonds: 8

Polar Surface Area: 69.73

Molecular Species: BASE

HBA: 6

HBD: 2

#RO5 Violations: 2

HBA (Lipinski): 7

HBD (Lipinski): 2

#RO5 Violations (Lipinski): 2

CX Acidic pKa:

CX Basic pKa: 12.80

CX LogP: 4.94

CX LogD: 3.45

Aromatic Rings: 3

Heavy Atoms: 38

QED Weighted: 0.39

Np Likeness Score: -1.45

References

1. Tian Y, Zhang T, Long L, Li Z, Wan S, Wang G, Yu Y, Hou J, Wu X, Zhang J..  (2018)  Design, synthesis, biological evaluation and molecular modeling of novel 2-amino-4-(1-phenylethoxy) pyridine derivatives as potential ROS1 inhibitors.,  143  [PMID:29174814] [10.1016/j.ejmech.2017.11.002]

Source

Source(1):

• Scientific Literature