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ID: ALA4582511
Max Phase: Preclinical
Molecular Formula: C15H15N3O2S
Molecular Weight: 301.37
Molecule Type: Unknown
Associated Items:
ID: ALA4582511
Max Phase: Preclinical
Molecular Formula: C15H15N3O2S
Molecular Weight: 301.37
Molecule Type: Unknown
Associated Items:
Canonical SMILES: Cc1cnc(NC(=O)CCCOc2cccc(C#N)c2)s1
Standard InChI: InChI=1S/C15H15N3O2S/c1-11-10-17-15(21-11)18-14(19)6-3-7-20-13-5-2-4-12(8-13)9-16/h2,4-5,8,10H,3,6-7H2,1H3,(H,17,18,19)
Standard InChI Key: AGGFXGBQARTACI-UHFFFAOYSA-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: 301.37 | Molecular Weight (Monoisotopic): 301.0885 | AlogP: 3.12 | #Rotatable Bonds: 6 |
Polar Surface Area: 75.01 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 8.08 | CX Basic pKa: 0.52 | CX LogP: 3.10 | CX LogD: 3.02 |
Aromatic Rings: 2 | Heavy Atoms: 21 | QED Weighted: 0.83 | Np Likeness Score: -2.46 |
1. Nguyen W, Jacobson J, Jarman KE, Jousset Sabroux H, Harty L, McMahon J, Lewin SR, Purcell DF, Sleebs BE.. (2019) Identification of 5-Substituted 2-Acylaminothiazoles That Activate Tat-Mediated Transcription in HIV-1 Latency Models., 62 (10): [PMID:30973727] [10.1021/acs.jmedchem.9b00462] |
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