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ID: ALA4860579
Max Phase: Preclinical
Molecular Formula: C23H23Cl2N3O3
Molecular Weight: 460.36
Molecule Type: Unknown
Associated Items:
ID: ALA4860579
Max Phase: Preclinical
Molecular Formula: C23H23Cl2N3O3
Molecular Weight: 460.36
Molecule Type: Unknown
Associated Items:
Canonical SMILES: Cc1cn(C2CCN(Cc3cccc(Oc4ccc(Cl)c(Cl)c4)c3)CC2)c(=O)[nH]c1=O
Standard InChI: InChI=1S/C23H23Cl2N3O3/c1-15-13-28(23(30)26-22(15)29)17-7-9-27(10-8-17)14-16-3-2-4-18(11-16)31-19-5-6-20(24)21(25)12-19/h2-6,11-13,17H,7-10,14H2,1H3,(H,26,29,30)
Standard InChI Key: QTVDJUHVCWKGDB-UHFFFAOYSA-N
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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 |
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Molecular Weight: 460.36 | Molecular Weight (Monoisotopic): 459.1116 | AlogP: 4.78 | #Rotatable Bonds: 5 |
Polar Surface Area: 67.33 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 6 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 10.32 | CX Basic pKa: 8.02 | CX LogP: 4.22 | CX LogD: 3.51 |
Aromatic Rings: 3 | Heavy Atoms: 31 | QED Weighted: 0.60 | Np Likeness Score: -1.16 |
1. Song L, Merceron R, Hulpia F, Lucía A, Gracia B, Jian Y, Risseeuw MDP, Verstraelen T, Cos P, Aínsa JA, Boshoff HI, Munier-Lehmann H, Savvides SN, Van Calenbergh S.. (2021) Structure-aided optimization of non-nucleoside M. tuberculosis thymidylate kinase inhibitors., 225 [PMID:34450493] [10.1016/j.ejmech.2021.113784] |
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