| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA4176115
Max Phase: Preclinical
Molecular Formula: C23H27BrN2O6
Molecular Weight: 507.38
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CC1=C(C(=O)OCC(C)C)C(c2cc([N+](=O)[O-])cc(Br)c2O)C2=C(CC(C)(C)CC2=O)N1
Standard InChI: InChI=1S/C23H27BrN2O6/c1-11(2)10-32-22(29)18-12(3)25-16-8-23(4,5)9-17(27)20(16)19(18)14-6-13(26(30)31)7-15(24)21(14)28/h6-7,11,19,25,28H,8-10H2,1-5H3
Standard InChI Key: ZVIUQSHRFZUVPW-UHFFFAOYSA-N
Associated Targets(non-human)
Voltage-gated L-type calcium channel alpha-1C subunit 1321 Activities
Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Small molecule | Topical: No | First In Class: No | Black Box: No |
| Chirality: No | Availability: No | Prodrug: No |
Drug Indications
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 507.38 | Molecular Weight (Monoisotopic): 506.1052 | AlogP: 4.87 | #Rotatable Bonds: 5 |
| Polar Surface Area: 118.77 | Molecular Species: ACID | HBA: 7 | HBD: 2 |
| #RO5 Violations: 1 | HBA (Lipinski): 8 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: 5.46 | CX Basic pKa: | CX LogP: 4.38 | CX LogD: 2.68 |
| Aromatic Rings: 1 | Heavy Atoms: 32 | QED Weighted: 0.33 | Np Likeness Score: -0.83 |
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
Source(1):