ID: ALA2271143
Max Phase: Preclinical
Molecular Formula: C13H16O2
Molecular Weight: 204.27
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CC(=O)c1ccc2c(c1)C[C@H](C(C)C)O2
Standard InChI: InChI=1S/C13H16O2/c1-8(2)13-7-11-6-10(9(3)14)4-5-12(11)15-13/h4-6,8,13H,7H2,1-3H3/t13-/m1/s1
Standard InChI Key: SJSDMYAMNRSNKZ-CYBMUJFWSA-N
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| Natural Product: Yes | 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: 204.27 | Molecular Weight (Monoisotopic): 204.1150 | AlogP: 2.85 | #Rotatable Bonds: 2 |
| Polar Surface Area: 26.30 | Molecular Species: NEUTRAL | HBA: 2 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 2 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: 2.72 | CX LogD: 2.72 |
| Aromatic Rings: 1 | Heavy Atoms: 15 | QED Weighted: 0.69 | Np Likeness Score: 0.69 |
| 1. Céspedes CL, Uchoa A, Salazar JR, Perich F, Pardo F.. (2002) Plant growth inhibitory activity of p-hydroxyacetophenones and tremetones from Chilean endemic Baccharis species and some analogous: a comparative study., 50 (8): [PMID:11929285] [10.1021/jf011108g] |
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