ID: ALA2419959

Max Phase: Preclinical

Molecular Formula: C26H27N5O3S2

Molecular Weight: 521.67

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1ccccc1CN(Cn1sc2nc(C)cc(C)c2c1=O)Cn1sc2nc(C)cc(C)c2c1=O

Standard InChI:  InChI=1S/C26H27N5O3S2/c1-15-10-17(3)27-23-21(15)25(32)30(35-23)13-29(12-19-8-6-7-9-20(19)34-5)14-31-26(33)22-16(2)11-18(4)28-24(22)36-31/h6-11H,12-14H2,1-5H3

Standard InChI Key:  CDNSDMJKJLJRPI-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

Mycolicibacterium fortuitum 1335 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: 521.67Molecular Weight (Monoisotopic): 521.1555AlogP: 4.59#Rotatable Bonds: 7
Polar Surface Area: 82.25Molecular Species: NEUTRALHBA: 10HBD: 0
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 2.95CX LogP: 4.84CX LogD: 4.84
Aromatic Rings: 5Heavy Atoms: 36QED Weighted: 0.31Np Likeness Score: -0.76

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