ID: ALA3889620

Max Phase: Preclinical

Molecular Formula: C15H16N2O3S2

Molecular Weight: 336.44

Molecule Type: Small molecule

Representations

Canonical SMILES:  CN(C)c1ccc(/C=C2\SC(=S)N(CCC(=O)O)C2=O)cc1

Standard InChI:  InChI=1S/C15H16N2O3S2/c1-16(2)11-5-3-10(4-6-11)9-12-14(20)17(15(21)22-12)8-7-13(18)19/h3-6,9H,7-8H2,1-2H3,(H,18,19)/b12-9-

Standard InChI Key:  GKOFEHBEXPYGCD-XFXZXTDPSA-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: 336.44

Molecular Weight (Monoisotopic): 336.0602

AlogP: 2.43

#Rotatable Bonds: 5

Polar Surface Area: 60.85

Molecular Species: ACID

HBA: 5

HBD: 1

#RO5 Violations: 0

HBA (Lipinski): 5

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 4.01

CX Basic pKa: 4.70

CX LogP: 1.90

CX LogD: -0.28

Aromatic Rings: 1

Heavy Atoms: 22

QED Weighted: 0.66

Np Likeness Score: -1.72

References

1. Slepikas L, Chiriano G, Perozzo R, Tardy S, Kranjc A, Patthey-Vuadens O, Ouertatani-Sakouhi H, Kicka S, Harrison CF, Scrignari T, Perron K, Hilbi H, Soldati T, Cosson P, Tarasevicius E, Scapozza L..  (2016)  In Silico Driven Design and Synthesis of Rhodanine Derivatives as Novel Antibacterials Targeting the Enoyl Reductase InhA.,  59  (24): [PMID:26730986] [10.1021/acs.jmedchem.5b01620]

Source

Source(1):

• Scientific Literature