ID: ALA4086051

Max Phase: Preclinical

Molecular Formula: C28H29N7

Molecular Weight: 463.59

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  c1ccc(-c2ccccc2-n2cc(CCCCCCCn3cc(-c4cccnc4)nn3)nn2)cc1

Standard InChI:  InChI=1S/C28H29N7/c1(3-10-19-34-22-27(31-32-34)24-14-11-18-29-20-24)2-7-15-25-21-35(33-30-25)28-17-9-8-16-26(28)23-12-5-4-6-13-23/h4-6,8-9,11-14,16-18,20-22H,1-3,7,10,15,19H2

Standard InChI Key:  HDTNWBLZXIRJLG-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: 463.59Molecular Weight (Monoisotopic): 463.2484AlogP: 5.78#Rotatable Bonds: 11
Polar Surface Area: 74.31Molecular Species: NEUTRALHBA: 7HBD: 0
#RO5 Violations: 1HBA (Lipinski): 7HBD (Lipinski): 0#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 4.08CX LogP: 6.30CX LogD: 6.30
Aromatic Rings: 5Heavy Atoms: 35QED Weighted: 0.23Np Likeness Score: -1.22

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