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ID: ALA97695
Max Phase: Preclinical
Molecular Formula: C24H28O4
Molecular Weight: 380.48
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: C[C@@H](OC(=O)c1ccc(C(=O)O)cc1)c1ccc2c(c1)C(C)(C)CCC2(C)C
Standard InChI: InChI=1S/C24H28O4/c1-15(28-22(27)17-8-6-16(7-9-17)21(25)26)18-10-11-19-20(14-18)24(4,5)13-12-23(19,2)3/h6-11,14-15H,12-13H2,1-5H3,(H,25,26)/t15-/m1/s1
Standard InChI Key: QHMOPZIZOBBDJY-OAHLLOKOSA-N
Associated Targets(non-human)
F9 (77 Activities)
Rattus norvegicus (775804 Activities)
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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: 380.48 | Molecular Weight (Monoisotopic): 380.1988 | AlogP: 5.65 | #Rotatable Bonds: 4 |
| Polar Surface Area: 63.60 | Molecular Species: ACID | HBA: 3 | HBD: 1 |
| #RO5 Violations: 1 | HBA (Lipinski): 4 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 1 |
| CX Acidic pKa: 3.61 | CX Basic pKa: | CX LogP: 6.40 | CX LogD: 3.06 |
| Aromatic Rings: 2 | Heavy Atoms: 28 | QED Weighted: 0.70 | Np Likeness Score: 0.11 |
References
| 1. Charpentier B, Bernardon J, Diaz P, Vion M, Millois C, Bernard B, Shroot B. (1995) Chemoenzymatic synthesis of enantiomers of a new retinoid to investigate the role of chirality in the biological response, 5 (23): [10.1016/0960-894X(95)00489-G] |
Source
Source(1):