ID: ALA3260891

Max Phase: Preclinical

Molecular Formula: C22H22ClNO3

Molecular Weight: 383.88

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)C1=C(C)NC(c2ccc(Cl)cc2)=CC1c1cccc(OC)c1

Standard InChI:  InChI=1S/C22H22ClNO3/c1-4-27-22(25)21-14(2)24-20(15-8-10-17(23)11-9-15)13-19(21)16-6-5-7-18(12-16)26-3/h5-13,19,24H,4H2,1-3H3

Standard InChI Key:  AFNXKZTXBIZKJA-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

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: 383.88Molecular Weight (Monoisotopic): 383.1288AlogP: 4.91#Rotatable Bonds: 5
Polar Surface Area: 47.56Molecular Species: NEUTRALHBA: 4HBD: 1
#RO5 Violations: 0HBA (Lipinski): 4HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.23CX LogD: 4.23
Aromatic Rings: 2Heavy Atoms: 27QED Weighted: 0.74Np Likeness Score: -0.60

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