| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
ID: ALA2381020
Max Phase: Preclinical
Molecular Formula: C20H25ClN2O3
Molecular Weight: 376.88
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C[C@H](C1CCCCC1)N1C(=O)CC(=O)N(CCc2cccc(Cl)c2)C1=O
Standard InChI: InChI=1S/C20H25ClN2O3/c1-14(16-7-3-2-4-8-16)23-19(25)13-18(24)22(20(23)26)11-10-15-6-5-9-17(21)12-15/h5-6,9,12,14,16H,2-4,7-8,10-11,13H2,1H3/t14-/m1/s1
Standard InChI Key: YDLHMUFCKVDRIE-CQSZACIVSA-N
Associated Targets(non-human)
CACNA1C Voltage-gated L-type calcium channel alpha-1C subunit (335 Activities)
Cacna1d Voltage-gated L-type calcium channel alpha-1D subunit (336 Activities)
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
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: 376.88 | Molecular Weight (Monoisotopic): 376.1554 | AlogP: 4.03 | #Rotatable Bonds: 5 |
| Polar Surface Area: 57.69 | Molecular Species: ACID | HBA: 3 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 5.00 | CX Basic pKa: | CX LogP: 4.32 | CX LogD: 1.99 |
| Aromatic Rings: 1 | Heavy Atoms: 26 | QED Weighted: 0.73 | Np Likeness Score: -0.96 |
References
| 1. Kang S, Cooper G, Dunne SF, Luan CH, Surmeier DJ, Silverman RB.. (2013) Structure-activity relationship of N,N'-disubstituted pyrimidinetriones as Ca(V)1.3 calcium channel-selective antagonists for Parkinson's disease., 56 (11): [PMID:23651412] [10.1021/jm4005048] |
Source
Source(1):