N-(3-(6-(4-amino-3-methoxyphenyl)isothiazolo[4,3-b]pyridin-3-yl)phenyl)pyrrolidine-1-carboxamide

ID: ALA4740761

PubChem CID: 162645177

Max Phase: Preclinical

Molecular Formula: C24H23N5O2S

Molecular Weight: 445.55

Molecule Type: Unknown

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  COc1cc(-c2cnc3c(-c4cccc(NC(=O)N5CCCC5)c4)snc3c2)ccc1N

Standard InChI:  InChI=1S/C24H23N5O2S/c1-31-21-13-15(7-8-19(21)25)17-12-20-22(26-14-17)23(32-28-20)16-5-4-6-18(11-16)27-24(30)29-9-2-3-10-29/h4-8,11-14H,2-3,9-10,25H2,1H3,(H,27,30)

Standard InChI Key:  JJUIKKILUHSIRW-UHFFFAOYSA-N

Molfile:  

 
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M  END

Alternative Forms

  1. Parent:

    ALA4740761

    ---

Associated Targets(Human)

GAK Tchem 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

Calculated Properties

Molecular Weight: 445.55Molecular Weight (Monoisotopic): 445.1572AlogP: 5.24#Rotatable Bonds: 4
Polar Surface Area: 93.37Molecular Species: NEUTRALHBA: 6HBD: 2
#RO5 Violations: 1HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.20CX Basic pKa: 3.86CX LogP: 3.55CX LogD: 3.55
Aromatic Rings: 4Heavy Atoms: 32QED Weighted: 0.42Np Likeness Score: -1.38

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