ID: ALA2419956

Max Phase: Preclinical

Molecular Formula: C25H25N5O2S2

Molecular Weight: 491.64

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1cc(C)c2c(=O)n(CN(Cc3ccccc3)Cn3sc4nc(C)cc(C)c4c3=O)sc2n1

Standard InChI:  InChI=1S/C25H25N5O2S2/c1-15-10-17(3)26-22-20(15)24(31)29(33-22)13-28(12-19-8-6-5-7-9-19)14-30-25(32)21-16(2)11-18(4)27-23(21)34-30/h5-11H,12-14H2,1-4H3

Standard InChI Key:  RKVALZPPPGCAGX-UHFFFAOYSA-N

Associated Targets(non-human)

Cutibacterium acnes 887 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: 491.64Molecular Weight (Monoisotopic): 491.1450AlogP: 4.58#Rotatable Bonds: 6
Polar Surface Area: 73.02Molecular Species: NEUTRALHBA: 9HBD: 0
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 3.24CX LogP: 5.00CX LogD: 5.00
Aromatic Rings: 5Heavy Atoms: 34QED Weighted: 0.35Np Likeness Score: -0.80

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