ID: ALA2420070

Max Phase: Preclinical

Molecular Formula: C17H17N3O3S

Molecular Weight: 343.41

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cc(C)c2c(OCCOC(=O)Nc3ccccc3)nsc2n1

Standard InChI:  InChI=1S/C17H17N3O3S/c1-11-10-12(2)18-16-14(11)15(20-24-16)22-8-9-23-17(21)19-13-6-4-3-5-7-13/h3-7,10H,8-9H2,1-2H3,(H,19,21)

Standard InChI Key:  JUGODKRFWVHPOB-UHFFFAOYSA-N

Associated Targets(non-human)

Cutibacterium acnes 887 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mycolicibacterium fortuitum 1335 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mycobacterium tuberculosis 203094 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 343.41Molecular Weight (Monoisotopic): 343.0991AlogP: 3.94#Rotatable Bonds: 5
Polar Surface Area: 73.34Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.04CX Basic pKa: CX LogP: 3.93CX LogD: 3.93
Aromatic Rings: 3Heavy Atoms: 24QED Weighted: 0.71Np Likeness Score: -1.66

References

1. Malinka W, Swiątek P, Sliwińska M, Szponar B, Gamian A, Karczmarzyk Z, Fruziński A..  (2013)  Synthesis of novel isothiazolopyridines and their in vitro evaluation against Mycobacterium and Propionibacterium acnes.,  21  (17): [PMID:23850103] [10.1016/j.bmc.2013.06.027]

Source