ID: ALA3632693

Max Phase: Preclinical

Molecular Formula: C24H27F3N2O4

Molecular Weight: 464.48

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  COc1cc(C(F)(F)F)ccc1OCC(O)CN1CCC(N2Cc3ccccc3C2=O)CC1

Standard InChI:  InChI=1S/C24H27F3N2O4/c1-32-22-12-17(24(25,26)27)6-7-21(22)33-15-19(30)14-28-10-8-18(9-11-28)29-13-16-4-2-3-5-20(16)23(29)31/h2-7,12,18-19,30H,8-11,13-15H2,1H3

Standard InChI Key:  YALYZRWQAGAROS-UHFFFAOYSA-N

Associated Targets(Human)

Sodium channel protein type IX alpha subunit 8393 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Sodium channel protein type I alpha subunit 483 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Sodium channel protein type V alpha subunit 3462 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Sodium channel protein type 9 subunit alpha 111 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: 464.48Molecular Weight (Monoisotopic): 464.1923AlogP: 3.57#Rotatable Bonds: 7
Polar Surface Area: 62.24Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: 13.82CX Basic pKa: 8.03CX LogP: 2.78CX LogD: 2.06
Aromatic Rings: 2Heavy Atoms: 33QED Weighted: 0.68Np Likeness Score: -0.93

References

1. Suzuki S, Kuroda T, Kimoto H, Domon Y, Kubota K, Kitano Y, Yokoyama T, Shimizugawa A, Sugita R, Koishi R, Asano D, Tamaki K, Shinozuka T, Kobayashi H..  (2015)  Discovery of (phenoxy-2-hydroxypropyl)piperidines as a novel class of voltage-gated sodium channel 1.7 inhibitors.,  25  (22): [PMID:26358159] [10.1016/j.bmcl.2015.09.005]

Source