ID: ALA5173069

Max Phase: Preclinical

Molecular Formula: C12H8Cl2OS

Molecular Weight: 271.17

Associated Items:

Representations

Canonical SMILES:  Oc1ccccc1Sc1cc(Cl)cc(Cl)c1

Standard InChI:  InChI=1S/C12H8Cl2OS/c13-8-5-9(14)7-10(6-8)16-12-4-2-1-3-11(12)15/h1-7,15H

Standard InChI Key:  BGLNTEMWXTXCEG-UHFFFAOYSA-N

Associated Targets(non-human)

Pup--protein ligase 18 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: 271.17Molecular Weight (Monoisotopic): 269.9673AlogP: 4.85#Rotatable Bonds: 2
Polar Surface Area: 20.23Molecular Species: NEUTRALHBA: 2HBD: 1
#RO5 Violations: 0HBA (Lipinski): 1HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 8.72CX Basic pKa: CX LogP: 5.07CX LogD: 5.05
Aromatic Rings: 2Heavy Atoms: 16QED Weighted: 0.84Np Likeness Score: -0.87

References

1. Li C, Liu S, Dong B, Li C, Jian L, He J, Zeng J, Zhou Q, Jia D, Luo Y, Sun Q..  (2022)  Discovery and Mechanistic Study of Mycobacterium tuberculosis PafA Inhibitors.,  65  (16.0): [PMID:35926511] [10.1021/acs.jmedchem.2c00289]

Source