ID: ALA4528964

Max Phase: Preclinical

Molecular Formula: C15H18N4O2S2

Molecular Weight: 350.47

Molecule Type: Unknown

Associated Items:

Representations

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

Standard InChI:  InChI=1S/C15H18N4O2S2/c1-8(2)5-6-12(21)19-14-18-11(7-22-14)13-9(3)16-15(23-13)17-10(4)20/h5-8H,1-4H3,(H,16,17,20)(H,18,19,21)/b6-5+

Standard InChI Key:  BHNLPHFGIMIKBX-AATRIKPKSA-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: 350.47Molecular Weight (Monoisotopic): 350.0871AlogP: 3.68#Rotatable Bonds: 5
Polar Surface Area: 83.98Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.72CX Basic pKa: CX LogP: 3.17CX LogD: 2.99
Aromatic Rings: 2Heavy Atoms: 23QED Weighted: 0.81Np Likeness Score: -1.41

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