ID: ALA5195906

Max Phase: Preclinical

Molecular Formula: C28H31N5S

Molecular Weight: 469.66

Representations

Canonical SMILES:  c1ccc2sc(-c3ccnc(Nc4ccc(CN5CCC(N6CCCC6)CC5)cc4)n3)cc2c1

Standard InChI:  InChI=1S/C28H31N5S/c1-2-6-26-22(5-1)19-27(34-26)25-11-14-29-28(31-25)30-23-9-7-21(8-10-23)20-32-17-12-24(13-18-32)33-15-3-4-16-33/h1-2,5-11,14,19,24H,3-4,12-13,15-18,20H2,(H,29,30,31)

Standard InChI Key:  QCRCLCQGMMCOIX-UHFFFAOYSA-N

Molecule Features

Natural Product: No

Oral: No

Chemical Probe: No

Parenteral: No

Molecule Type:

Topical: No

First In Class: No

Black Box: No

Chirality: No

Availability: No

Prodrug: No

Properties

Molecular Weight: 469.66

Molecular Weight (Monoisotopic): 469.2300

AlogP: 6.16

#Rotatable Bonds: 6

Polar Surface Area: 44.29

Molecular Species: BASE

HBA: 6

HBD: 1

#RO5 Violations: 1

HBA (Lipinski): 5

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 1

CX Acidic pKa: 13.19

CX Basic pKa: 10.20

CX LogP: 5.45

CX LogD: 2.65

Aromatic Rings: 4

Heavy Atoms: 34

QED Weighted: 0.37

Np Likeness Score: -1.52

References

1. Galal KA, Truong A, Kwarcinski F, de Silva C, Avalani K, Havener TM, Chirgwin ME, Merten E, Ong HW, Willis C, Abdelwaly A, Helal MA, Derbyshire ER, Zutshi R, Drewry DH..  (2022)  Identification of Novel 2,4,5-Trisubstituted Pyrimidines as Potent Dual Inhibitors of Plasmodial PfGSK3/PfPK6 with Activity against Blood Stage Parasites In Vitro.,  65  (19.0): [PMID:36166733] [10.1021/acs.jmedchem.2c00996]

Source

Source(1):

• Scientific Literature