ID: ALA553233

Max Phase: Preclinical

Molecular Formula: C19H23ClFNS

Molecular Weight: 315.46

Molecule Type: Small molecule

Representations

Canonical SMILES:  CN(C/C=C/C#CC(C)(C)C)Cc1cccc2c(F)csc12.Cl

Standard InChI:  InChI=1S/C19H22FNS.ClH/c1-19(2,3)11-6-5-7-12-21(4)13-15-9-8-10-16-17(20)14-22-18(15)16;/h5,7-10,14H,12-13H2,1-4H3;1H/b7-5+;

Standard InChI Key:  HAUQHSHQXAZERS-GZOLSCHFSA-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: 315.46

Molecular Weight (Monoisotopic): 315.1457

AlogP: 5.08

#Rotatable Bonds: 4

Polar Surface Area: 3.24

Molecular Species: BASE

HBA: 2

HBD: 0

#RO5 Violations: 1

HBA (Lipinski): 1

HBD (Lipinski): 0

#RO5 Violations (Lipinski): 1

CX Acidic pKa:

CX Basic pKa: 8.71

CX LogP: 5.56

CX LogD: 4.23

Aromatic Rings: 2

Heavy Atoms: 22

QED Weighted: 0.71

Np Likeness Score: -0.42

References

1. Nussbaumer P, Petranyi G, Stütz A..  (1991)  Synthesis and structure-activity relationships of benzo[b]thienylallylamine antimycotics.,  34  (1): [PMID:1992153] [10.1021/jm00105a011]

Source

Source(1):

• Scientific Literature