Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4174137
Max Phase: Preclinical
Molecular Formula: C23H28N2O6
Molecular Weight: 428.49
Molecule Type: Small molecule
Associated Items:
ID: ALA4174137
Max Phase: Preclinical
Molecular Formula: C23H28N2O6
Molecular Weight: 428.49
Molecule Type: Small molecule
Associated Items:
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
Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 428.49 | Molecular Weight (Monoisotopic): 428.1947 | AlogP: 4.10 | #Rotatable Bonds: 5 |
Polar Surface Area: 118.77 | Molecular Species: NEUTRAL | HBA: 7 | HBD: 2 |
#RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 6.80 | CX Basic pKa: | CX LogP: 4.12 | CX LogD: 3.44 |
Aromatic Rings: 1 | Heavy Atoms: 31 | QED Weighted: 0.41 | Np Likeness Score: -0.37 |
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(1):