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ID: ALA3752616
Max Phase: Preclinical
Molecular Formula: C14H13N3O3
Molecular Weight: 271.28
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: Cn1c(=O)c2c(-c3ccc(O)cc3)c[nH]c2n(C)c1=O
Standard InChI: InChI=1S/C14H13N3O3/c1-16-12-11(13(19)17(2)14(16)20)10(7-15-12)8-3-5-9(18)6-4-8/h3-7,15,18H,1-2H3
Standard InChI Key: JMZCWPHSDMRELZ-UHFFFAOYSA-N
Associated Targets(non-human)
Bacillus mycoides 84 Activities
Bacillus subtilis 32866 Activities
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Escherichia coli 133304 Activities
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Pseudomonas aeruginosa 123386 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
| MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanisms of Action
| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
| Molecular Weight: 271.28 | Molecular Weight (Monoisotopic): 271.0957 | AlogP: 0.94 | #Rotatable Bonds: 1 |
| Polar Surface Area: 80.02 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 9.66 | CX Basic pKa: | CX LogP: 1.35 | CX LogD: 1.35 |
| Aromatic Rings: 3 | Heavy Atoms: 20 | QED Weighted: 0.69 | Np Likeness Score: -0.12 |
References
| 1. Saikia L, Roudragouda P, Thakur AJ.. (2016) A one pot, two-step synthesis of 5-arylpyrrolo[2,3-d]pyrimidines and screening of their preliminary antibacterial properties., 26 (3): [PMID:26739778] [10.1016/j.bmcl.2015.12.047] |
Source
Source(1):