ID: ALA194143

Max Phase: Preclinical

Molecular Formula: C28H21ClN4O

Molecular Weight: 464.96

Molecule Type: Small molecule

Representations

Canonical SMILES:  Cn1c(=O)cc(-c2cccc(Cl)c2)c2cc(Cn3cncc3Cc3ccc(C#N)cc3)ccc21

Standard InChI:  InChI=1S/C28H21ClN4O/c1-32-27-10-9-21(12-26(27)25(14-28(32)34)22-3-2-4-23(29)13-22)17-33-18-31-16-24(33)11-19-5-7-20(15-30)8-6-19/h2-10,12-14,16,18H,11,17H2,1H3

Standard InChI Key:  PHPWMLQIAMSLPU-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: 464.96

Molecular Weight (Monoisotopic): 464.1404

AlogP: 5.57

#Rotatable Bonds: 5

Polar Surface Area: 63.61

Molecular Species: NEUTRAL

HBA: 5

HBD: 0

#RO5 Violations: 1

HBA (Lipinski): 5

HBD (Lipinski): 0

#RO5 Violations (Lipinski): 1

CX Acidic pKa:

CX Basic pKa: 6.67

CX LogP: 5.04

CX LogD: 4.99

Aromatic Rings: 5

Heavy Atoms: 34

QED Weighted: 0.34

Np Likeness Score: -1.06

References

1. Li Q, Woods KW, Wang W, Lin NH, Claiborne A, Gu WZ, Cohen J, Stoll VS, Hutchins C, Frost D, Rosenberg SH, Sham HL..  (2005)  Design, synthesis, and activity of achiral analogs of 2-quinolones and indoles as non-thiol farnesyltransferase inhibitors.,  15  (8): [PMID:15808463] [10.1016/j.bmcl.2005.02.062]

Source

Source(1):

• Scientific Literature