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ID: ALA217408
Max Phase: Preclinical
Molecular Formula: C23H14Cl2N2O5
Molecular Weight: 469.28
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: O=C(O)c1ccc(C(O)=C2C(=O)N(c3ccc(Cl)cc3)N(c3ccc(Cl)cc3)C2=O)cc1
Standard InChI: InChI=1S/C23H14Cl2N2O5/c24-15-5-9-17(10-6-15)26-21(29)19(20(28)13-1-3-14(4-2-13)23(31)32)22(30)27(26)18-11-7-16(25)8-12-18/h1-12,28H,(H,31,32)
Standard InChI Key: RHCZTOVMZMUOCW-UHFFFAOYSA-N
Associated Targets(non-human)
murB UDP-N-acetylmuramate dehydrogenase (113 Activities)
Staphylococcus aureus (210822 Activities)
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Enterococcus faecalis (29875 Activities)
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Streptococcus pneumoniae (31063 Activities)
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Escherichia coli (133304 Activities)
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Candida albicans (78123 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: 469.28 | Molecular Weight (Monoisotopic): 468.0280 | AlogP: 4.96 | #Rotatable Bonds: 4 |
| Polar Surface Area: 98.15 | Molecular Species: ACID | HBA: 4 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 3.87 | CX Basic pKa: | CX LogP: 4.43 | CX LogD: -0.37 |
| Aromatic Rings: 3 | Heavy Atoms: 32 | QED Weighted: 0.32 | Np Likeness Score: -0.36 |
References
| 1. Gilbert AM, Failli A, Shumsky J, Yang Y, Severin A, Singh G, Hu W, Keeney D, Petersen PJ, Katz AH.. (2006) Pyrazolidine-3,5-diones and 5-hydroxy-1H-pyrazol-3(2H)-ones, inhibitors of UDP-N-acetylenolpyruvyl glucosamine reductase., 49 (20): [PMID:17004716] [10.1021/jm060499t] |
Source
Source(1):