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ID: ALA432440
Max Phase: Preclinical
Molecular Formula: C21H21N3O5S
Molecular Weight: 427.48
Molecule Type: Small molecule
Associated Items:
ID: ALA432440
Max Phase: Preclinical
Molecular Formula: C21H21N3O5S
Molecular Weight: 427.48
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: COc1cc(OC)c(OC)cc1C[S+]([O-])c1ncccc1C(=O)Nc1ccncc1
Standard InChI: InChI=1S/C21H21N3O5S/c1-27-17-12-19(29-3)18(28-2)11-14(17)13-30(26)21-16(5-4-8-23-21)20(25)24-15-6-9-22-10-7-15/h4-12H,13H2,1-3H3,(H,22,24,25)
Standard InChI Key: QYPWHSRHSWAEJL-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: 427.48 | Molecular Weight (Monoisotopic): 427.1202 | AlogP: 3.06 | #Rotatable Bonds: 8 |
Polar Surface Area: 105.63 | Molecular Species: NEUTRAL | HBA: 7 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 13.90 | CX Basic pKa: 5.61 | CX LogP: 1.36 | CX LogD: 1.36 |
Aromatic Rings: 3 | Heavy Atoms: 30 | QED Weighted: 0.55 | Np Likeness Score: -0.76 |
1. Terauchi H, Tanitame A, Tada K, Nakamura K, Seto Y, Nishikawa Y.. (1997) Nicotinamide derivatives as a new class of gastric H+/K(+)-ATPase inhibitors. 1. Synthesis and structure-activity relationships of N-substituted 2-(benzhydryl- and benzylsulfinyl)nicotinamides., 40 (3): [PMID:9022797] [10.1021/jm9605593] |
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