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ID: ALA2235685
Max Phase: Preclinical
Molecular Formula: C19H16Cl2N4O2
Molecular Weight: 403.27
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: CN(C)c1ccc(C2C(Cl)C(=O)N2/N=C2\C(=O)Nc3ccc(Cl)cc32)cc1
Standard InChI: InChI=1S/C19H16Cl2N4O2/c1-24(2)12-6-3-10(4-7-12)17-15(21)19(27)25(17)23-16-13-9-11(20)5-8-14(13)22-18(16)26/h3-9,15,17H,1-2H3,(H,22,23,26)
Standard InChI Key: LJRABRXGTKKZDK-UHFFFAOYSA-N
Associated Targets(non-human)
Aspergillus flavus 8875 Activities
Trichoderma viride 1263 Activities
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Fusarium solani 1274 Activities
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Trichophyton longifusum 101 Activities
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Rhizoctonia solani 2251 Activities
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Microsporum canis 872 Activities
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Alternaria alternata 757 Activities
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Candida albicans 78123 Activities
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Aspergillus awamori 40 Activities
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Aspergillus niger 16508 Activities
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Pseudomonas aeruginosa 123386 Activities
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Escherichia coli 133304 Activities
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Klebsiella pneumoniae 43867 Activities
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Salmonella typhi 4293 Activities
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Proteus mirabilis 3894 Activities
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Proteus vulgaris 5823 Activities
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Bacillus cereus 7522 Activities
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Bacillus pumilus 984 Activities
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Staphylococcus hominis 482 Activities
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Staphylococcus aureus 210822 Activities
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Micrococcus luteus 7463 Activities
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Staphylococcus epidermidis 22802 Activities
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Bacillus spizizenii 1898 Activities
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Aspergillus fumigatus 16427 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: 403.27 | Molecular Weight (Monoisotopic): 402.0650 | AlogP: 3.25 | #Rotatable Bonds: 3 |
| Polar Surface Area: 65.01 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 1 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 9.91 | CX Basic pKa: 4.82 | CX LogP: 3.67 | CX LogD: 3.67 |
| Aromatic Rings: 2 | Heavy Atoms: 27 | QED Weighted: 0.63 | Np Likeness Score: -0.73 |
References
| 1. Shingade SG, Bari SB, Waghmare UB. (2012) Synthesis and antimicrobial activity of 5-chloroindoline-2,3-dione derivatives, 21 (7): [10.1007/s00044-011-9644-y] |
Source
Source(1):