ID: ALA4556068

Max Phase: Preclinical

Molecular Formula: C11H14N4O2S2

Molecular Weight: 298.39

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  CC(=O)Nc1nc(C)c(-c2csc(NCCO)n2)s1

Standard InChI:  InChI=1S/C11H14N4O2S2/c1-6-9(19-11(13-6)14-7(2)17)8-5-18-10(15-8)12-3-4-16/h5,16H,3-4H2,1-2H3,(H,12,15)(H,13,14,17)

Standard InChI Key:  PGPPITSUVBAOTE-UHFFFAOYSA-N

Associated Targets(Human)

PI4-kinase beta subunit 1593 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

RD 1212 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Enterovirus A71 1246 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: 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: 298.39Molecular Weight (Monoisotopic): 298.0558AlogP: 1.94#Rotatable Bonds: 5
Polar Surface Area: 87.14Molecular Species: NEUTRALHBA: 7HBD: 3
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.98CX Basic pKa: 2.59CX LogP: 0.84CX LogD: 0.74
Aromatic Rings: 2Heavy Atoms: 19QED Weighted: 0.78Np Likeness Score: -2.01

References

1. Tassini S, Langron E, Delang L, Mirabelli C, Lanko K, Crespan E, Kissova M, Tagliavini G, Fontò G, Bertoni S, Palese S, Giorgio C, Ravanetti F, Ragionieri L, Zamperini C, Mancini A, Dreassi E, Maga G, Vergani P, Neyts J, Radi M..  (2019)  Multitarget CFTR Modulators Endowed with Multiple Beneficial Side Effects for Cystic Fibrosis Patients: Toward a Simplified Therapeutic Approach †.,  62  (23): [PMID:31729878] [10.1021/acs.jmedchem.9b01416]

Source