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ID: ALA4776685
Max Phase: Preclinical
Molecular Formula: C24H33N5O3
Molecular Weight: 439.56
Molecule Type: Unknown
Associated Items:
ID: ALA4776685
Max Phase: Preclinical
Molecular Formula: C24H33N5O3
Molecular Weight: 439.56
Molecule Type: Unknown
Associated Items:
Canonical SMILES: CCC(=O)CCCCC[C@H](NC(=O)C1CN(C)C1)c1[nH]c(-c2ccccc2)nc1C(N)=O
Standard InChI: InChI=1S/C24H33N5O3/c1-3-18(30)12-8-5-9-13-19(26-24(32)17-14-29(2)15-17)20-21(22(25)31)28-23(27-20)16-10-6-4-7-11-16/h4,6-7,10-11,17,19H,3,5,8-9,12-15H2,1-2H3,(H2,25,31)(H,26,32)(H,27,28)/t19-/m0/s1
Standard InChI Key: XGWNKDSIJSHVCT-IBGZPJMESA-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: 439.56 | Molecular Weight (Monoisotopic): 439.2583 | AlogP: 2.82 | #Rotatable Bonds: 12 |
Polar Surface Area: 121.18 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 3 |
#RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 4 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 9.32 | CX Basic pKa: 7.78 | CX LogP: 2.15 | CX LogD: 1.78 |
Aromatic Rings: 2 | Heavy Atoms: 32 | QED Weighted: 0.44 | Np Likeness Score: -0.28 |
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] |
2. Yu W, Fells J, Clausen D, Liu J, Klein DJ, Christine Chung C, Myers RW, Wu J, Wu G, Howell BJ, Barnard RJO, Kozlowski J.. (2021) Discovery of macrocyclic HDACs 1, 2, and 3 selective inhibitors for HIV latency reactivation., 47 [PMID:34091041] [10.1016/j.bmcl.2021.128168] |
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