ID: ALA4794323

Max Phase: Preclinical

Molecular Formula: C23H20N4O2S

Molecular Weight: 416.51

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  COc1cc(-c2cnc3c(-c4cccc(NC(=O)C5CC5)c4)snc3c2)ccc1N

Standard InChI:  InChI=1S/C23H20N4O2S/c1-29-20-11-14(7-8-18(20)24)16-10-19-21(25-12-16)22(30-27-19)15-3-2-4-17(9-15)26-23(28)13-5-6-13/h2-4,7-13H,5-6,24H2,1H3,(H,26,28)

Standard InChI Key:  USWHRHQETHBPEE-UHFFFAOYSA-N

Associated Targets(Human)

Serine/threonine-protein kinase GAK 1150 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

dengue virus type 2 2400 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: 416.51Molecular Weight (Monoisotopic): 416.1307AlogP: 4.96#Rotatable Bonds: 5
Polar Surface Area: 90.13Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.80CX Basic pKa: 3.86CX LogP: 3.81CX LogD: 3.81
Aromatic Rings: 4Heavy Atoms: 30QED Weighted: 0.45Np Likeness Score: -1.34

References

1. Martinez-Gualda B,Saul S,Froeyen M,Schols D,Herdewijn P,Einav S,De Jonghe S.  (2021)  Discovery of 3-phenyl- and 3-N-piperidinyl-isothiazolo[4,3-b]pyridines as highly potent inhibitors of cyclin G-associated kinase.,  213  [PMID:33497888] [10.1016/j.ejmech.2021.113158]

Source