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ID: ALA4126406
Max Phase: Preclinical
Molecular Formula: C22H26INO3
Molecular Weight: 352.45
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Cc1oc2ccccc2c1C(=O)c1ccc(OCCC[N+](C)(C)C)cc1.[I-]
Standard InChI: InChI=1S/C22H26NO3.HI/c1-16-21(19-8-5-6-9-20(19)26-16)22(24)17-10-12-18(13-11-17)25-15-7-14-23(2,3)4;/h5-6,8-13H,7,14-15H2,1-4H3;1H/q+1;/p-1
Standard InChI Key: VIZAXRZXZDYDFX-UHFFFAOYSA-M
Associated Targets(Human)
KDM5A Tchem Lysine-specific demethylase 5A (893 Activities)
KDM7A Tchem Lysine-specific demethylase 7 (35 Activities)
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PHF8 Tchem Histone lysine demethylase PHF8 (151 Activities)
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PHF2 Tbio Lysine-specific demethylase PHF2 (16 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: 352.45 | Molecular Weight (Monoisotopic): 352.1907 | AlogP: 4.45 | #Rotatable Bonds: 7 |
| Polar Surface Area: 39.44 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 0 |
| #RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: | CX Basic pKa: | CX LogP: -0.45 | CX LogD: -0.45 |
| Aromatic Rings: 3 | Heavy Atoms: 26 | QED Weighted: 0.36 | Np Likeness Score: -0.20 |
References
| 1. Bhushan B, Erdmann A, Zhang Y, Belle R, Johannson C, Oppermann U, Hopkinson RJ, Schofield CJ, Kawamura A.. (2018) Investigations on small molecule inhibitors targeting the histone H3K4 tri-methyllysine binding PHD-finger of JmjC histone demethylases., 26 (11): [PMID:29764755] [10.1016/j.bmc.2018.03.030] |
Source
Source(1):