ID: ALA4078160

Max Phase: Preclinical

Molecular Formula: C28H32N6O

Molecular Weight: 468.61

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(NCCCCCCCCn1cc(-c2cccnc2)nn1)Nc1ccccc1-c1ccccc1

Standard InChI:  InChI=1S/C28H32N6O/c35-28(31-26-17-9-8-16-25(26)23-13-6-5-7-14-23)30-19-10-3-1-2-4-11-20-34-22-27(32-33-34)24-15-12-18-29-21-24/h5-9,12-18,21-22H,1-4,10-11,19-20H2,(H2,30,31,35)

Standard InChI Key:  AVMWWZXTZQYQMD-UHFFFAOYSA-N

Associated Targets(Human)

SH-SY5Y 11521 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Nicotinamide phosphoribosyltransferase 67 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: 468.61Molecular Weight (Monoisotopic): 468.2638AlogP: 6.17#Rotatable Bonds: 12
Polar Surface Area: 84.73Molecular Species: NEUTRALHBA: 5HBD: 2
#RO5 Violations: 1HBA (Lipinski): 7HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: 12.93CX Basic pKa: 4.08CX LogP: 5.77CX LogD: 5.77
Aromatic Rings: 4Heavy Atoms: 35QED Weighted: 0.24Np Likeness Score: -1.59

References

1. Travelli C, Aprile S, Rahimian R, Grolla AA, Rogati F, Bertolotti M, Malagnino F, di Paola R, Impellizzeri D, Fusco R, Mercalli V, Massarotti A, Stortini G, Terrazzino S, Del Grosso E, Fakhfouri G, Troiani MP, Alisi MA, Grosa G, Sorba G, Canonico PL, Orsomando G, Cuzzocrea S, Genazzani AA, Galli U, Tron GC..  (2017)  Identification of Novel Triazole-Based Nicotinamide Phosphoribosyltransferase (NAMPT) Inhibitors Endowed with Antiproliferative and Antiinflammatory Activity.,  60  (5): [PMID:28165742] [10.1021/acs.jmedchem.6b01392]

Source