ID: ALA4079201

Max Phase: Preclinical

Molecular Formula: C28H29N3OS

Molecular Weight: 455.63

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(CCCCCCCc1cnc(-c2cccnc2)s1)Nc1ccccc1-c1ccccc1

Standard InChI:  InChI=1S/C28H29N3OS/c32-27(31-26-17-10-9-16-25(26)22-12-5-4-6-13-22)18-8-3-1-2-7-15-24-21-30-28(33-24)23-14-11-19-29-20-23/h4-6,9-14,16-17,19-21H,1-3,7-8,15,18H2,(H,31,32)

Standard InChI Key:  PIAFFRRLNJFHIB-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: 455.63Molecular Weight (Monoisotopic): 455.2031AlogP: 7.39#Rotatable Bonds: 11
Polar Surface Area: 54.88Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 1HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: 13.52CX Basic pKa: 4.04CX LogP: 6.96CX LogD: 6.96
Aromatic Rings: 4Heavy Atoms: 33QED Weighted: 0.24Np Likeness Score: -1.18

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