ID: ALA4793216
Max Phase: Preclinical
Molecular Formula: C18H24O3
Molecular Weight: 288.39
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: CCCCCCC1=CC(C)(C)c2c(O)ccc(O)c2C1=O
Standard InChI: InChI=1S/C18H24O3/c1-4-5-6-7-8-12-11-18(2,3)16-14(20)10-9-13(19)15(16)17(12)21/h9-11,19-20H,4-8H2,1-3H3
Standard InChI Key: YTEYODKXUDLMMX-UHFFFAOYSA-N
Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Unknown | 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 |
|---|
Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
Properties
| Molecular Weight: 288.39 | Molecular Weight (Monoisotopic): 288.1725 | AlogP: 4.47 | #Rotatable Bonds: 5 |
| Polar Surface Area: 57.53 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 3 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 8.87 | CX Basic pKa: | CX LogP: 5.53 | CX LogD: 5.51 |
| Aromatic Rings: 1 | Heavy Atoms: 21 | QED Weighted: 0.62 | Np Likeness Score: 1.49 |
References
| 1. Méndez D,Urra FA,Millas-Vargas JP,Alarcón M,Rodríguez-Lavado J,Palomo I,Trostchansky A,Araya-Maturana R,Fuentes E. (2020) Synthesis of antiplatelet ortho-carbonyl hydroquinones with differential action on platelet aggregation stimulated by collagen or TRAP-6., 192 [PMID:32155530] [10.1016/j.ejmech.2020.112187] |
Source
Source(1):