Standard InChI: InChI=1S/C14H15F3N4OS/c1-7(5-14(15,16)17)12(22)21-13-20-8(2)11(23-13)9-3-4-10(18)19-6-9/h3-4,6-7H,5H2,1-2H3,(H2,18,19)(H,20,21,22)
Standard InChI Key: IIFUCWPNUMIYRT-UHFFFAOYSA-N
Associated Targets(Human)
PI4-kinase beta subunit 1593 Activities
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Cytochrome P450 3A4 53859 Activities
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Liver microsomes 16955 Activities
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Caco-2 12174 Activities
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Associated Targets(non-human)
Rattus norvegicus 775804 Activities
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rhinovirus B5 56 Activities
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rhinovirus A45 17 Activities
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rhinovirus A89 34 Activities
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rhinovirus A2 409 Activities
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Human rhinovirus 1A 153 Activities
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rhinovirus A16 69 Activities
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rhinovirus B14 1052 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
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Properties
Molecular Weight: 344.36
Molecular Weight (Monoisotopic): 344.0919
AlogP: 3.62
#Rotatable Bonds: 4
Polar Surface Area: 80.90
Molecular Species: NEUTRAL
HBA: 5
HBD: 2
#RO5 Violations: 0
HBA (Lipinski): 5
HBD (Lipinski): 3
#RO5 Violations (Lipinski): 0
CX Acidic pKa: 7.97
CX Basic pKa: 5.97
CX LogP: 2.67
CX LogD: 2.64
Aromatic Rings: 2
Heavy Atoms: 23
QED Weighted: 0.89
Np Likeness Score: -1.07
References
1.Décor A, Grand-Maître C, Hucke O, O'Meara J, Kuhn C, Constantineau-Forget L, Brochu C, Malenfant E, Bertrand-Laperle M, Bordeleau J, Ghiro E, Pesant M, Fazal G, Gorys V, Little M, Boucher C, Bordeleau S, Turcotte P, Guo T, Garneau M, Spickler C, Gauthier A.. (2013) Design, synthesis and biological evaluation of novel aminothiazoles as antiviral compounds acting against human rhinovirus., 23 (13):[PMID:23726345][10.1016/j.bmcl.2013.04.077]