ID: ALA5268651

Max Phase: Preclinical

Molecular Formula: C17H23ClN2

Molecular Weight: 290.84

Associated Items:

Representations

Canonical SMILES:  Clc1ccc2cc(CNC3CCCCCCC3)[nH]c2c1

Standard InChI:  InChI=1S/C17H23ClN2/c18-14-9-8-13-10-16(20-17(13)11-14)12-19-15-6-4-2-1-3-5-7-15/h8-11,15,19-20H,1-7,12H2

Standard InChI Key:  KTFNDLOQGICVEV-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: 290.84Molecular Weight (Monoisotopic): 290.1550AlogP: 5.02#Rotatable Bonds: 3
Polar Surface Area: 27.82Molecular Species: BASEHBA: 1HBD: 2
#RO5 Violations: 1HBA (Lipinski): 2HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 9.87CX LogP: 4.84CX LogD: 2.44
Aromatic Rings: 2Heavy Atoms: 20QED Weighted: 0.82Np Likeness Score: -0.88

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