ID: ALA1834501
Chembl Id: CHEMBL1834501
PubChem CID: 53484097
Max Phase: Preclinical
Molecular Formula: C19H16ClN3O3
Molecular Weight: 369.81
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCOC(=O)c1cc(-c2ccc(NC(=O)c3ccccc3Cl)cc2)[nH]n1
Standard InChI: InChI=1S/C19H16ClN3O3/c1-2-26-19(25)17-11-16(22-23-17)12-7-9-13(10-8-12)21-18(24)14-5-3-4-6-15(14)20/h3-11H,2H2,1H3,(H,21,24)(H,22,23)
Standard InChI Key: CZYXWJKMIUVPFX-UHFFFAOYSA-N
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
| 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 |
|---|
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
| Molecular Weight: 369.81 | Molecular Weight (Monoisotopic): 369.0880 | AlogP: 4.16 | #Rotatable Bonds: 5 |
| Polar Surface Area: 84.08 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 2 |
| #RO5 Violations: ┄ | HBA (Lipinski): 6 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): ┄ |
| CX Acidic pKa: 9.31 | CX Basic pKa: ┄ | CX LogP: 4.09 | CX LogD: 4.08 |
| Aromatic Rings: 3 | Heavy Atoms: 26 | QED Weighted: 0.66 | Np Likeness Score: -1.95 |
| 1. Qi J, Zhu J, Liu X, Ding L, Zheng C, Han G, Lv J, Zhou Y.. (2011) Synthesis and acrosin inhibitory activities of substituted ethyl 5-(4-aminophenyl)-1H-pyrazole-3-carboxylate derivatives., 21 (19): [PMID:21880490] [10.1016/j.bmcl.2011.07.110] |
| 2. Zhao J, Sun N, Gao Y, Lv D, Liu Y, Jiang Y, Dong G, Chen Q, Li W, Zhou Y, Zhu J, Sheng C, Lv J. (2014) Discovery of novel guanidinophenylpyrazole human acrosin inhibitors by molecular hybridization, 5 (10): [10.1039/C4MD00160E] |
Source(1):
