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ID: ALA4788911
Max Phase: Preclinical
Molecular Formula: C28H36FN5O2
Molecular Weight: 493.63
Molecule Type: Unknown
Associated Items:
ID: ALA4788911
Max Phase: Preclinical
Molecular Formula: C28H36FN5O2
Molecular Weight: 493.63
Molecule Type: Unknown
Associated Items:
Canonical SMILES: CCC(=O)CCCCC[C@H](NC(=O)[C@H]1CC12CCN(C)CC2)c1[nH]c(-c2ccc(F)cc2)nc1C#N
Standard InChI: InChI=1S/C28H36FN5O2/c1-3-21(35)7-5-4-6-8-23(32-27(36)22-17-28(22)13-15-34(2)16-14-28)25-24(18-30)31-26(33-25)19-9-11-20(29)12-10-19/h9-12,22-23H,3-8,13-17H2,1-2H3,(H,31,33)(H,32,36)/t22-,23+/m1/s1
Standard InChI Key: KTUYYMOKNXBOLX-PKTZIBPZSA-N
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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 |
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: 493.63 | Molecular Weight (Monoisotopic): 493.2853 | AlogP: 4.91 | #Rotatable Bonds: 11 |
Polar Surface Area: 101.88 | Molecular Species: BASE | HBA: 5 | HBD: 2 |
#RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 10.02 | CX Basic pKa: 8.83 | CX LogP: 3.89 | CX LogD: 2.70 |
Aromatic Rings: 2 | Heavy Atoms: 36 | QED Weighted: 0.43 | Np Likeness Score: -0.42 |
1. Clausen DJ,Liu J,Yu W,Duffy JL,Chung CC,Myers RW,Klein DJ,Fells J,Holloway K,Wu J,Wu G,Howell BJ,Barnard RJO,Kozlowski J. (2020) Development of a selective HDAC inhibitor aimed at reactivating the HIV latent reservoir., 30 (17.0): [PMID:32738976] [10.1016/j.bmcl.2020.127367] |
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