ID: ALA3260895

Max Phase: Preclinical

Molecular Formula: C22H22N2O4

Molecular Weight: 378.43

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)C1=C(C)NC(c2ccc(C)cc2)=CC1c1ccccc1[N+](=O)[O-]

Standard InChI:  InChI=1S/C22H22N2O4/c1-4-28-22(25)21-15(3)23-19(16-11-9-14(2)10-12-16)13-18(21)17-7-5-6-8-20(17)24(26)27/h5-13,18,23H,4H2,1-3H3

Standard InChI Key:  GRIPLABMJDOAPW-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: 378.43Molecular Weight (Monoisotopic): 378.1580AlogP: 4.47#Rotatable Bonds: 5
Polar Surface Area: 81.47Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: CX LogP: 4.24CX LogD: 4.24
Aromatic Rings: 2Heavy Atoms: 28QED Weighted: 0.47Np Likeness Score: -0.75

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