Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA3342992
Max Phase: Preclinical
Molecular Formula: C23H15ClFN3O4
Molecular Weight: 451.84
Molecule Type: Small molecule
Associated Items:
ID: ALA3342992
Max Phase: Preclinical
Molecular Formula: C23H15ClFN3O4
Molecular Weight: 451.84
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: N#Cc1ccc2c(Oc3ccc(Cl)cc3OCCn3ccc(=O)[nH]c3=O)cc(F)cc2c1
Standard InChI: InChI=1S/C23H15ClFN3O4/c24-16-2-4-19(21(11-16)31-8-7-28-6-5-22(29)27-23(28)30)32-20-12-17(25)10-15-9-14(13-26)1-3-18(15)20/h1-6,9-12H,7-8H2,(H,27,29,30)
Standard InChI Key: RIFJCVWQHKENRB-UHFFFAOYSA-N
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Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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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: 451.84 | Molecular Weight (Monoisotopic): 451.0735 | AlogP: 4.23 | #Rotatable Bonds: 6 |
Polar Surface Area: 97.11 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 7 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 9.91 | CX Basic pKa: | CX LogP: 4.11 | CX LogD: 4.10 |
Aromatic Rings: 4 | Heavy Atoms: 32 | QED Weighted: 0.47 | Np Likeness Score: -1.36 |
1. Lee WG, Frey KM, Gallardo-Macias R, Spasov KA, Bollini M, Anderson KS, Jorgensen WL.. (2014) Picomolar Inhibitors of HIV-1 Reverse Transcriptase: Design and Crystallography of Naphthyl Phenyl Ethers., 5 (11): [PMID:25408842] [10.1021/ml5003713] |
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