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ID: ALA5178616
Max Phase: Preclinical
Molecular Formula: C23H25ClN2O3S
Molecular Weight: 444.98
Associated Items:
Representations
Canonical SMILES: Cc1ccc(OCCC2CCN(c3nc4ccc(Cl)cc4s3)CC2)cc1CC(=O)O
Standard InChI: InChI=1S/C23H25ClN2O3S/c1-15-2-4-19(12-17(15)13-22(27)28)29-11-8-16-6-9-26(10-7-16)23-25-20-5-3-18(24)14-21(20)30-23/h2-5,12,14,16H,6-11,13H2,1H3,(H,27,28)
Standard InChI Key: ACXVPJWIBMHZAF-UHFFFAOYSA-N
Associated Targets(Human)
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
PPARD Tchem Peroxisome proliferator-activated receptor delta (6293 Activities)
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Associated Targets(non-human)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
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Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: | 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: 444.98 | Molecular Weight (Monoisotopic): 444.1274 | AlogP: 5.57 | #Rotatable Bonds: 7 |
| Polar Surface Area: 62.66 | Molecular Species: ACID | HBA: 5 | HBD: 1 |
| #RO5 Violations: 1 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: 4.16 | CX Basic pKa: 2.47 | CX LogP: 6.00 | CX LogD: 3.07 |
| Aromatic Rings: 3 | Heavy Atoms: 30 | QED Weighted: 0.52 | Np Likeness Score: -1.62 |
References
| 1. Kato T, Ohara T, Suzuki N, Muto S, Tokuyama R, Mizutani M, Fukasawa H, Matsumura KI, Itai A.. (2022) Discovery and structure-based design of a new series of potent and selective PPARδ agonists utilizing a virtual screening method., 59 [PMID:35063634] [10.1016/j.bmcl.2022.128567] |
Source
Source(1):