ID: ALA5266382

Max Phase: Preclinical

Molecular Formula: C16H19NOS

Molecular Weight: 273.40

Associated Items:

Representations

Canonical SMILES:  O=C(NC1CCCCCC1)c1cc2ccccc2s1

Standard InChI:  InChI=1S/C16H19NOS/c18-16(17-13-8-3-1-2-4-9-13)15-11-12-7-5-6-10-14(12)19-15/h5-7,10-11,13H,1-4,8-9H2,(H,17,18)

Standard InChI Key:  GQTPFDDQSROTBS-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: 273.40Molecular Weight (Monoisotopic): 273.1187AlogP: 4.35#Rotatable Bonds: 2
Polar Surface Area: 29.10Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 2HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.30CX LogD: 4.30
Aromatic Rings: 2Heavy Atoms: 19QED Weighted: 0.81Np Likeness Score: -1.52

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