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ID: ALA2420192
Max Phase: Preclinical
Molecular Formula: C8H12BrN3O2
Molecular Weight: 262.11
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CC(C)(O)Cc1nc(N)[nH]c(=O)c1Br
Standard InChI: InChI=1S/C8H12BrN3O2/c1-8(2,14)3-4-5(9)6(13)12-7(10)11-4/h14H,3H2,1-2H3,(H3,10,11,12,13)
Standard InChI Key: YLESACYPDCUJLP-UHFFFAOYSA-N
Associated Targets(Human)
HeLa 62764 Activities
HEL 6614 Activities
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Associated Targets(non-human)
Human alphaherpesvirus 3 4092 Activities
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Cytomegalovirus 1023 Activities
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Vesicular stomatitis virus 4460 Activities
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Influenza B virus 2113 Activities
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Influenza A virus 11224 Activities
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Punta Toro virus 1491 Activities
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Coxsackievirus B4 2249 Activities
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Sindbis virus 1599 Activities
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Mammalian orthoreovirus 1 1523 Activities
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Human respirovirus 3 1674 Activities
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Respiratory syncytial virus 3434 Activities
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Human alphaherpesvirus 1 11089 Activities
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Vaccinia virus 4609 Activities
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Human alphaherpesvirus 2 4932 Activities
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Felid alphaherpesvirus 1 460 Activities
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Feline coronavirus 624 Activities
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MDCK 10148 Activities
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Vero 26788 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 |
Drug Indications
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Mechanisms of Action
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Properties
| Molecular Weight: 262.11 | Molecular Weight (Monoisotopic): 261.0113 | AlogP: 0.43 | #Rotatable Bonds: 2 |
| Polar Surface Area: 92.00 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 3 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 4 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 7.18 | CX Basic pKa: 1.72 | CX LogP: -0.05 | CX LogD: -0.40 |
| Aromatic Rings: 1 | Heavy Atoms: 14 | QED Weighted: 0.72 | Np Likeness Score: 0.32 |
References
| 1. Singh K, Singh K, Balzarini J.. (2013) Regioselective synthesis of 6-substituted-2-amino-5-bromo-4(3H)-pyrimidinones and evaluation of their antiviral activity., 67 [PMID:23911856] [10.1016/j.ejmech.2013.06.036] |
Source
Source(1):