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ID: ALA4522149
Max Phase: Preclinical
Molecular Formula: C27H30N4O4
Molecular Weight: 474.56
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: Cc1ccc(NC(=O)CCN(Cc2ccc(C(=O)NO)cc2)C(=O)c2ccc(N(C)C)cc2)cc1
Standard InChI: InChI=1S/C27H30N4O4/c1-19-4-12-23(13-5-19)28-25(32)16-17-31(18-20-6-8-21(9-7-20)26(33)29-35)27(34)22-10-14-24(15-11-22)30(2)3/h4-15,35H,16-18H2,1-3H3,(H,28,32)(H,29,33)
Standard InChI Key: SBSXFASFHOVIDA-UHFFFAOYSA-N
Associated Targets(Human)
HDAC1 Tclin Histone deacetylase 1 (10854 Activities)
HDAC6 Tclin Histone deacetylase 6 (20808 Activities)
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CHP-134 (45 Activities)
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IMR-32 (1082 Activities)
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SK-N-AS (237 Activities)
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NB1 (136 Activities)
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G55T2 (24 Activities)
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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 |
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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: 474.56 | Molecular Weight (Monoisotopic): 474.2267 | AlogP: 3.85 | #Rotatable Bonds: 9 |
| Polar Surface Area: 101.98 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 3 |
| #RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 9.05 | CX Basic pKa: 3.46 | CX LogP: 3.61 | CX LogD: 3.60 |
| Aromatic Rings: 3 | Heavy Atoms: 35 | QED Weighted: 0.32 | Np Likeness Score: -1.55 |
References
| 1. Reßing N, Marquardt V, Gertzen CGW, Schöler A, Schramm A, Kurz T, Gohlke H, Aigner A, Remke M, Hansen FK.. (2019) Design, synthesis and biological evaluation of β-peptoid-capped HDAC inhibitors with anti-neuroblastoma and anti-glioblastoma activity., 10 (7): [PMID:31391882] [10.1039/C8MD00454D] |
Source
Source(1):