ID: ALA3260892

Max Phase: Preclinical

Molecular Formula: C22H23NO2

Molecular Weight: 333.43

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)C1=C(C)NC(c2ccccc2)=CC1c1ccc(C)cc1

Standard InChI:  InChI=1S/C22H23NO2/c1-4-25-22(24)21-16(3)23-20(18-8-6-5-7-9-18)14-19(21)17-12-10-15(2)11-13-17/h5-14,19,23H,4H2,1-3H3

Standard InChI Key:  WVBSXFXYFWMWMR-UHFFFAOYSA-N

Associated Targets(Human)

Voltage-gated L-type calcium channel alpha-1D subunit 39 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

SH-SY5Y 11521 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Voltage-gated L-type calcium channel alpha-1C subunit 1321 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Hippocampus 432 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: 333.43Molecular Weight (Monoisotopic): 333.1729AlogP: 4.56#Rotatable Bonds: 4
Polar Surface Area: 38.33Molecular Species: NEUTRALHBA: 3HBD: 1
#RO5 Violations: 0HBA (Lipinski): 3HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.30CX LogD: 4.30
Aromatic Rings: 2Heavy Atoms: 25QED Weighted: 0.83Np Likeness Score: -0.37

References

1. Tenti G, Parada E, León R, Egea J, Martínez-Revelles S, Briones AM, Sridharan V, López MG, Ramos MT, Menéndez JC..  (2014)  New 5-unsubstituted dihydropyridines with improved CaV1.3 selectivity as potential neuroprotective agents against ischemic injury.,  57  (10): [PMID:24754640] [10.1021/jm500263v]

Source