| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA3612978
Max Phase: Preclinical
Molecular Formula: C11H10Cl2N2S
Molecular Weight: 273.19
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CC1=CC(c2ccc(Cl)cc2Cl)NC(=S)N1
Standard InChI: InChI=1S/C11H10Cl2N2S/c1-6-4-10(15-11(16)14-6)8-3-2-7(12)5-9(8)13/h2-5,10H,1H3,(H2,14,15,16)
Standard InChI Key: RCBDSJFNNVDGRI-UHFFFAOYSA-N
Associated Targets(non-human)
Cyclooxygenase-1 1373 Activities
Cyclooxygenase-2 1953 Activities
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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 |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 273.19 | Molecular Weight (Monoisotopic): 271.9942 | AlogP: 3.42 | #Rotatable Bonds: 1 |
| Polar Surface Area: 24.06 | Molecular Species: NEUTRAL | HBA: 1 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 2 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 11.25 | CX Basic pKa: | CX LogP: 3.17 | CX LogD: 3.17 |
| Aromatic Rings: 1 | Heavy Atoms: 16 | QED Weighted: 0.77 | Np Likeness Score: -0.80 |
References
| 1. Seebacher W, Faist J, Presser A, Weis R, Saf R, Kaserer T, Temml V, Schuster D, Ortmann S, Otto N, Bauer R.. (2015) Synthesis of new 4-phenylpyrimidine-2(1H)-thiones and their potency to inhibit COX-1 and COX-2., 101 [PMID:26197159] [10.1016/j.ejmech.2015.07.003] |
Source
Source(1):