ID: ALA5270432

Max Phase: Preclinical

Molecular Formula: C15H19NS

Molecular Weight: 245.39

Associated Items:

Representations

Canonical SMILES:  c1ccc2sc(CNC3CCCCC3)cc2c1

Standard InChI:  InChI=1S/C15H19NS/c1-2-7-13(8-3-1)16-11-14-10-12-6-4-5-9-15(12)17-14/h4-6,9-10,13,16H,1-3,7-8,11H2

Standard InChI Key:  NKHZKPMJADMXLQ-UHFFFAOYSA-N

Associated Targets(non-human)

Mycobacterium tuberculosis variant bovis 1746 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 245.39Molecular Weight (Monoisotopic): 245.1238AlogP: 4.32#Rotatable Bonds: 3
Polar Surface Area: 12.03Molecular Species: BASEHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 1HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 9.97CX LogP: 4.34CX LogD: 1.85
Aromatic Rings: 2Heavy Atoms: 17QED Weighted: 0.85Np Likeness Score: -1.24

References

1. Tan YJ, Li M, Gunawan GA, Nyantakyi SA, Dick T, Go ML, Lam Y..  (2021)  Amide-Amine Replacement in Indole-2-carboxamides Yields Potent Mycobactericidal Agents with Improved Water Solubility.,  12  (5.0): [PMID:34055215] [10.1021/acsmedchemlett.0c00588]

Source