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ID: ALA4873799
Max Phase: Preclinical
Molecular Formula: C17H14FN5
Molecular Weight: 307.33
Molecule Type: Unknown
Associated Items:
Representations
Canonical SMILES: Fc1cc2[nH]ncc2c2c3c(c(-c4cn[nH]c4)nc12)CCCC3
Standard InChI: InChI=1S/C17H14FN5/c18-13-5-14-12(8-21-23-14)15-10-3-1-2-4-11(10)16(22-17(13)15)9-6-19-20-7-9/h5-8H,1-4H2,(H,19,20)(H,21,23)
Standard InChI Key: QAWBPBLABQUSRL-UHFFFAOYSA-N
Associated Targets(Human)
CDK2/Cyclin A1 171 Activities
Tyrosine-protein kinase receptor FLT3 13481 Activities
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K562 73714 Activities
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MV4-11 7307 Activities
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Cyclin-dependent kinase 1/cyclin B1 1887 Activities
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Cyclin-dependent kinase 2/cyclin E1 1877 Activities
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CDK2/Cyclin A2 2260 Activities
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Cyclin-dependent kinase 4/cyclin D1 2340 Activities
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CDK9/cyclin T1 2643 Activities
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MOLM-13 2241 Activities
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MOLM-14 399 Activities
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SEM 217 Activities
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CCRF-CEM 65223 Activities
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THP-1 11052 Activities
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U-937 7138 Activities
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Associated Targets(non-human)
BaF3 4657 Activities
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Molecule Features
| Natural Product: No | Oral: No | Chemical Probe: No | Parenteral: No |
| Molecule Type: Unknown | 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: 307.33 | Molecular Weight (Monoisotopic): 307.1233 | AlogP: 3.52 | #Rotatable Bonds: 1 |
| Polar Surface Area: 70.25 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 2 |
| #RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
| CX Acidic pKa: 11.66 | CX Basic pKa: 2.19 | CX LogP: 3.39 | CX LogD: 3.39 |
| Aromatic Rings: 4 | Heavy Atoms: 23 | QED Weighted: 0.57 | Np Likeness Score: -1.35 |
References
| 1. Dayal N, Řezníčková E, Hernandez DE, Peřina M, Torregrosa-Allen S, Elzey BD, Škerlová J, Ajani H, Djukic S, Vojáčková V, Lepšík M, Řezáčová P, Kryštof V, Jorda R, Sintim HO.. (2021) 3H-Pyrazolo[4,3-f]quinoline-Based Kinase Inhibitors Inhibit the Proliferation of Acute Myeloid Leukemia Cells In Vivo., 64 (15.0): [PMID:34288692] [10.1021/acs.jmedchem.1c00330] |
Source
Source(1):