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ID: ALA4173973
Max Phase: Preclinical
Molecular Formula: C24H28N4O3S
Molecular Weight: 452.58
Molecule Type: Small molecule
Associated Items:
ID: ALA4173973
Max Phase: Preclinical
Molecular Formula: C24H28N4O3S
Molecular Weight: 452.58
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CCOC(=O)c1cnc2ccc(OCc3ccc(N[C@@H]4CCNC4)nc3)cc2c1SCC
Standard InChI: InChI=1S/C24H28N4O3S/c1-3-30-24(29)20-14-26-21-7-6-18(11-19(21)23(20)32-4-2)31-15-16-5-8-22(27-12-16)28-17-9-10-25-13-17/h5-8,11-12,14,17,25H,3-4,9-10,13,15H2,1-2H3,(H,27,28)/t17-/m1/s1
Standard InChI Key: MQRALJYJKNFYFY-QGZVFWFLSA-N
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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 |
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: 452.58 | Molecular Weight (Monoisotopic): 452.1882 | AlogP: 4.27 | #Rotatable Bonds: 9 |
Polar Surface Area: 85.37 | Molecular Species: BASE | HBA: 8 | HBD: 2 |
#RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 10.38 | CX LogP: 3.37 | CX LogD: 0.58 |
Aromatic Rings: 3 | Heavy Atoms: 32 | QED Weighted: 0.37 | Np Likeness Score: -1.16 |
1. Goncalves V, Brannigan JA, Laporte A, Bell AS, Roberts SM, Wilkinson AJ, Leatherbarrow RJ, Tate EW.. (2017) Structure-guided optimization of quinoline inhibitors of Plasmodium N-myristoyltransferase., 8 (1): [PMID:28626547] [10.1039/C6MD00531D] |
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