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ID: ALA5266539
Max Phase: Preclinical
Molecular Formula: C20H16Cl2N4O2
Molecular Weight: 378.82
Associated Items:
Representations
Canonical SMILES: Cc1ccc2oc(=O)c(-c3nc4cc(C5=NCCN5)ccc4[nH]3)c(Cl)c2c1.Cl
Standard InChI: InChI=1S/C20H15ClN4O2.ClH/c1-10-2-5-15-12(8-10)17(21)16(20(26)27-15)19-24-13-4-3-11(9-14(13)25-19)18-22-6-7-23-18;/h2-5,8-9H,6-7H2,1H3,(H,22,23)(H,24,25);1H
Standard InChI Key: DWBBQVKIFZYNLH-UHFFFAOYSA-N
Associated Targets(Human)
HEL 299 144 Activities
Huh-7 12904 Activities
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LN-229 376 Activities
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CAPAN-1 772 Activities
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HCT-116 91556 Activities
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NCI-H460 60772 Activities
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HL-60 67320 Activities
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K562 73714 Activities
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Z-138 387 Activities
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Associated Targets(non-human)
MDCK 10148 Activities
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Human coronavirus 229E 235 Activities
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Human coronavirus OC43 66 Activities
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Influenza A virus 11224 Activities
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Influenza B virus 2113 Activities
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Respiratory syncytial virus 3434 Activities
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Human alphaherpesvirus 1 11089 Activities
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Yellow fever virus 1530 Activities
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Zika virus 1028 Activities
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Sindbis virus 1599 Activities
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Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: | 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
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Properties
| Molecular Weight: 378.82 | Molecular Weight (Monoisotopic): 378.0884 | AlogP: 3.65 | #Rotatable Bonds: 2 |
| Polar Surface Area: 83.28 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 8.82 | CX Basic pKa: 8.36 | CX LogP: 2.42 | CX LogD: 1.61 |
| Aromatic Rings: 4 | Heavy Atoms: 27 | QED Weighted: 0.52 | Np Likeness Score: -0.66 |
References
| 1. Beč A, Racané L, Žonja L, Persoons L, Daelemans D, Starčević K, Vianello R, Hranjec M.. (2023) Biological evaluation of novel amidino substituted coumarin-benzazole hybrids as promising therapeutic agents., 14 (5): [PMID:37252100] [10.1039/d3md00055a] |
Source
Source(1):