ID: ALA4100482

Max Phase: Preclinical

Molecular Formula: C23H27N5O2S

Molecular Weight: 437.57

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Cc1ccccc1S(=O)(=O)N1CCN(c2ccc(CNCc3ccccc3)nn2)CC1

Standard InChI:  InChI=1S/C23H27N5O2S/c1-19-7-5-6-10-22(19)31(29,30)28-15-13-27(14-16-28)23-12-11-21(25-26-23)18-24-17-20-8-3-2-4-9-20/h2-12,24H,13-18H2,1H3

Standard InChI Key:  GVMUJFXKKPIMRM-UHFFFAOYSA-N

Associated Targets(Human)

dCTP pyrophosphatase 1 562 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 437.57Molecular Weight (Monoisotopic): 437.1885AlogP: 2.59#Rotatable Bonds: 7
Polar Surface Area: 78.43Molecular Species: NEUTRALHBA: 6HBD: 1
#RO5 Violations: 0HBA (Lipinski): 7HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 7.56CX LogP: 3.04CX LogD: 2.65
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.61Np Likeness Score: -2.04

References

1. Llona-Minguez S, Höglund A, Ghassemian A, Desroses M, Calderón-Montaño JM, Burgos Morón E, Valerie NCK, Wiita E, Almlöf I, Koolmeister T, Mateus A, Cazares-Körner C, Sanjiv K, Homan E, Loseva O, Baranczewski P, Darabi M, Mehdizadeh A, Fayezi S, Jemth AS, Warpman Berglund U, Sigmundsson K, Lundbäck T, Jenmalm Jensen A, Artursson P, Scobie M, Helleday T..  (2017)  Piperazin-1-ylpyridazine Derivatives Are a Novel Class of Human dCTP Pyrophosphatase 1 Inhibitors.,  60  (10): [PMID:28508636] [10.1021/acs.jmedchem.7b00182]

Source