ID: ALA2437428

Max Phase: Preclinical

Molecular Formula: C31H41FN6O2

Molecular Weight: 548.71

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  Nc1cc(CN2CCC(C(=O)N3CCC(n4c(=O)n(CC5CCCCC5)c5cc(F)ccc54)CC3)CC2)ccn1

Standard InChI:  InChI=1S/C31H41FN6O2/c32-25-6-7-27-28(19-25)37(21-22-4-2-1-3-5-22)31(40)38(27)26-11-16-36(17-12-26)30(39)24-9-14-35(15-10-24)20-23-8-13-34-29(33)18-23/h6-8,13,18-19,22,24,26H,1-5,9-12,14-17,20-21H2,(H2,33,34)

Standard InChI Key:  USFZHGOWALHXMB-UHFFFAOYSA-N

Associated Targets(Human)

Cytochrome P450 2D6 33882 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Cytochrome P450 3A4 53859 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Histamine H3 receptor 1015 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: 548.71Molecular Weight (Monoisotopic): 548.3275AlogP: 4.58#Rotatable Bonds: 6
Polar Surface Area: 89.39Molecular Species: NEUTRALHBA: 7HBD: 1
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 8.13CX LogP: 3.51CX LogD: 2.70
Aromatic Rings: 3Heavy Atoms: 40QED Weighted: 0.49Np Likeness Score: -1.19

References

1. Zeng Q, Rosenblum SB, Yang Z, Jiang Y, McCormick KD, Aslanian RG, Duguma L, Kozlowski JA, Shih NY, Hey JA, West RE, Korfmacher WA, Berlin M, Boyce CW..  (2013)  Synthesis and SAR studies of benzimidazolone derivatives as histamine H3-receptor antagonists.,  23  (21): [PMID:24050887] [10.1016/j.bmcl.2013.08.012]

Source