ID: ALA2237183

Max Phase: Preclinical

Molecular Formula: C25H33N3O6

Molecular Weight: 471.55

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CCOC(=O)C1=C(C)NC(C)=C(C(=O)OC)C1c1ccc(OCC(=O)N2CCN(C)CC2)cc1

Standard InChI:  InChI=1S/C25H33N3O6/c1-6-33-25(31)22-17(3)26-16(2)21(24(30)32-5)23(22)18-7-9-19(10-8-18)34-15-20(29)28-13-11-27(4)12-14-28/h7-10,23,26H,6,11-15H2,1-5H3

Standard InChI Key:  FPCLEAUPADPOPL-UHFFFAOYSA-N

Associated Targets(non-human)

Voltage-gated L-type calcium channel 1164 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: 471.55Molecular Weight (Monoisotopic): 471.2369AlogP: 1.81#Rotatable Bonds: 7
Polar Surface Area: 97.41Molecular Species: NEUTRALHBA: 8HBD: 1
#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 1#RO5 Violations (Lipinski): 0
CX Acidic pKa: CX Basic pKa: 6.90CX LogP: 1.04CX LogD: 0.92
Aromatic Rings: 1Heavy Atoms: 34QED Weighted: 0.60Np Likeness Score: -0.95

References

1. Bansal R, Jain P, Calle C, Carron R, Pemberton K, Harvey AL.  (2012)  Synthesis of a New Series of 4-Aryl-1,4-Dihydropyridines with Calcium Channel Blocking and Vasodilatory Activity,  21  (6): [10.1007/s00044-011-9600-x]

Source