Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4208988
Max Phase: Preclinical
Molecular Formula: C20H23FN2O3S
Molecular Weight: 390.48
Molecule Type: Small molecule
Associated Items:
ID: ALA4208988
Max Phase: Preclinical
Molecular Formula: C20H23FN2O3S
Molecular Weight: 390.48
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: CC(C)(C)OC(=O)Cn1c(SCc2ccc(F)cc2)nc(=O)c2c1CCC2
Standard InChI: InChI=1S/C20H23FN2O3S/c1-20(2,3)26-17(24)11-23-16-6-4-5-15(16)18(25)22-19(23)27-12-13-7-9-14(21)10-8-13/h7-10H,4-6,11-12H2,1-3H3
Standard InChI Key: AAOZOLSYGYWFGV-UHFFFAOYSA-N
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: 390.48 | Molecular Weight (Monoisotopic): 390.1413 | AlogP: 3.51 | #Rotatable Bonds: 5 |
Polar Surface Area: 61.19 | Molecular Species: NEUTRAL | HBA: 6 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 5 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 3.88 | CX LogD: 3.88 |
Aromatic Rings: 2 | Heavy Atoms: 27 | QED Weighted: 0.44 | Np Likeness Score: -1.78 |
1. Guibbal F, Bénard S, Patché J, Meneyrol V, Couprie J, Yong-Sang J, Meilhac O, Jestin E.. (2018) Regioselectivity of thiouracil alkylation: Application to optimization of Darapladib synthesis., 28 (4): [PMID:29336874] [10.1016/j.bmcl.2017.12.052] |
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