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ID: ALA216361
Max Phase: Preclinical
Molecular Formula: C23H30N4O3S2
Molecular Weight: 474.65
Molecule Type: Small molecule
Associated Items:
ID: ALA216361
Max Phase: Preclinical
Molecular Formula: C23H30N4O3S2
Molecular Weight: 474.65
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCCCNC(=O)NS(=O)(=O)c1sc(CC(C)C)cc1-c1ccc(Cn2ccnc2)cc1
Standard InChI: InChI=1S/C23H30N4O3S2/c1-4-5-10-25-23(28)26-32(29,30)22-21(14-20(31-22)13-17(2)3)19-8-6-18(7-9-19)15-27-12-11-24-16-27/h6-9,11-12,14,16-17H,4-5,10,13,15H2,1-3H3,(H2,25,26,28)
Standard InChI Key: QMKDXFGVHANNCT-UHFFFAOYSA-N
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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: 474.65 | Molecular Weight (Monoisotopic): 474.1759 | AlogP: 4.65 | #Rotatable Bonds: 10 |
Polar Surface Area: 93.09 | Molecular Species: ACID | HBA: 6 | HBD: 2 |
#RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 5.73 | CX Basic pKa: 6.55 | CX LogP: 4.35 | CX LogD: 4.13 |
Aromatic Rings: 3 | Heavy Atoms: 32 | QED Weighted: 0.42 | Np Likeness Score: -1.16 |
1. Wu X, Wan Y, Mahalingam AK, Murugaiah AM, Plouffe B, Botros M, Karlén A, Hallberg M, Gallo-Payet N, Alterman M.. (2006) Selective angiotensin II AT2 receptor agonists: arylbenzylimidazole structure-activity relationships., 49 (24): [PMID:17125268] [10.1021/jm0606185] |
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