ID: ALA5286028

Max Phase: Preclinical

Molecular Formula: C15H18N6O

Molecular Weight: 298.35

Associated Items:

Representations

Canonical SMILES:  CC(C)(O)CCc1cc2c(cn1)cnn2-c1ccnc(N)n1

Standard InChI:  InChI=1S/C15H18N6O/c1-15(2,22)5-3-11-7-12-10(8-18-11)9-19-21(12)13-4-6-17-14(16)20-13/h4,6-9,22H,3,5H2,1-2H3,(H2,16,17,20)

Standard InChI Key:  ALIRJZMHZOULMK-UHFFFAOYSA-N

Associated Targets(Human)

Tau-tubulin kinase 1 179 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 298.35Molecular Weight (Monoisotopic): 298.1542AlogP: 1.50#Rotatable Bonds: 4
Polar Surface Area: 102.74Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 3#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 5.66CX LogP: 0.92CX LogD: 0.91
Aromatic Rings: 3Heavy Atoms: 22QED Weighted: 0.76Np Likeness Score: -0.59

References

1. Halkina T, Henderson JL, Lin EY, Himmelbauer MK, Jones JH, Nevalainen M, Feng J, King K, Rooney M, Johnson JL, Marcotte DJ, Chodaparambil JV, Kumar PR, Patterson TA, Murugan P, Schuman E, Wong L, Hesson T, Lamore S, Bao C, Calhoun M, Certo H, Amaral B, Dillon GM, Gilfillan R, de Turiso FG..  (2021)  Discovery of Potent and Brain-Penetrant Tau Tubulin Kinase 1 (TTBK1) Inhibitors that Lower Tau Phosphorylation In Vivo.,  64  (9.0): [PMID:33944571] [10.1021/acs.jmedchem.1c00382]

Source