ID: ALA4174137

Max Phase: Preclinical

Molecular Formula: C23H28N2O6

Molecular Weight: 428.49

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  CC1=C(C(=O)OCC(C)C)C(c2cc([N+](=O)[O-])ccc2O)C2=C(CCC(C)(C)C2=O)N1

Standard InChI:  InChI=1S/C23H28N2O6/c1-12(2)11-31-22(28)18-13(3)24-16-8-9-23(4,5)21(27)20(16)19(18)15-10-14(25(29)30)6-7-17(15)26/h6-7,10,12,19,24,26H,8-9,11H2,1-5H3

Standard InChI Key:  APYNWJCVABYGBT-UHFFFAOYSA-N

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: 428.49Molecular Weight (Monoisotopic): 428.1947AlogP: 4.10#Rotatable Bonds: 5
Polar Surface Area: 118.77Molecular Species: NEUTRALHBA: 7HBD: 2
#RO5 Violations: 0HBA (Lipinski): 8HBD (Lipinski): 2#RO5 Violations (Lipinski): 0
CX Acidic pKa: 6.80CX Basic pKa: CX LogP: 4.12CX LogD: 3.44
Aromatic Rings: 1Heavy Atoms: 31QED Weighted: 0.41Np Likeness Score: -0.37

References

1. Schaller D, Gündüz MG, Zhang FX, Zamponi GW, Wolber G..  (2018)  Binding mechanism investigations guiding the synthesis of novel condensed 1,4-dihydropyridine derivatives with L-/T-type calcium channel blocking activity.,  155  [PMID:29843108] [10.1016/j.ejmech.2018.05.032]

Source