ID: ALA2268732

Max Phase: Preclinical

Molecular Formula: C12H6Cl2FN3OS2

Molecular Weight: 362.24

Molecule Type: Small molecule

Representations

Canonical SMILES:  N=C1SCC(=O)N1c1nc(-c2cc(F)c(Cl)cc2Cl)cs1

Standard InChI:  InChI=1S/C12H6Cl2FN3OS2/c13-6-2-7(14)8(15)1-5(6)9-3-21-12(17-9)18-10(19)4-20-11(18)16/h1-3,16H,4H2

Standard InChI Key:  LEOHGOYQSRJGOL-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: 362.24

Molecular Weight (Monoisotopic): 360.9313

AlogP: 4.27

#Rotatable Bonds: 2

Polar Surface Area: 57.05

Molecular Species: NEUTRAL

HBA: 5

HBD: 1

#RO5 Violations: 0

HBA (Lipinski): 4

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 0

CX Acidic pKa:

CX Basic pKa:

CX LogP: 4.34

CX LogD: 4.34

Aromatic Rings: 2

Heavy Atoms: 21

QED Weighted: 0.81

Np Likeness Score: -1.95

References

1. Liu H, Lieberzeit Z, Anthonsen T.  (2000)  Synthesis and Fungicidal Activity of 2-Imino-3-(4-arylthiazol-2-yl)-thiazolidin-4-ones and Their 5-Arylidene Derivatives,  5  (9): [10.3390/50901055]

Source

Source(1):

• Scientific Literature