ID: ALA3928561

Max Phase: Preclinical

Molecular Formula: C17H21N3O2S2

Molecular Weight: 363.51

Molecule Type: Small molecule

Representations

Canonical SMILES:  CC(C)CC(=O)NN1C(=O)/C(=C/c2ccc(N(C)C)cc2)SC1=S

Standard InChI:  InChI=1S/C17H21N3O2S2/c1-11(2)9-15(21)18-20-16(22)14(24-17(20)23)10-12-5-7-13(8-6-12)19(3)4/h5-8,10-11H,9H2,1-4H3,(H,18,21)/b14-10-

Standard InChI Key:  OFZXPAXAILJVJO-UVTDQMKNSA-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: 363.51

Molecular Weight (Monoisotopic): 363.1075

AlogP: 3.03

#Rotatable Bonds: 5

Polar Surface Area: 52.65

Molecular Species: NEUTRAL

HBA: 5

HBD: 1

#RO5 Violations: 0

HBA (Lipinski): 5

HBD (Lipinski): 1

#RO5 Violations (Lipinski): 0

CX Acidic pKa: 10.05

CX Basic pKa: 4.55

CX LogP: 3.69

CX LogD: 3.69

Aromatic Rings: 1

Heavy Atoms: 24

QED Weighted: 0.64

Np Likeness Score: -1.71

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