Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4169355
Max Phase: Preclinical
Molecular Formula: C20H17Cl2FN2O4S2
Molecular Weight: 503.40
Molecule Type: Small molecule
Associated Items:
ID: ALA4169355
Max Phase: Preclinical
Molecular Formula: C20H17Cl2FN2O4S2
Molecular Weight: 503.40
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: Cc1ccc(S(=O)(=O)Nc2ccc(F)cc2NS(=O)(=O)c2ccc(C)c(Cl)c2)cc1Cl
Standard InChI: InChI=1S/C20H17Cl2FN2O4S2/c1-12-3-6-15(10-17(12)21)30(26,27)24-19-8-5-14(23)9-20(19)25-31(28,29)16-7-4-13(2)18(22)11-16/h3-11,24-25H,1-2H3
Standard InChI Key: NNDDIRBOPLDCAZ-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: 503.40 | Molecular Weight (Monoisotopic): 501.9991 | AlogP: 5.35 | #Rotatable Bonds: 6 |
Polar Surface Area: 92.34 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 2 |
#RO5 Violations: 2 | HBA (Lipinski): 6 | HBD (Lipinski): 2 | #RO5 Violations (Lipinski): 2 |
CX Acidic pKa: 7.10 | CX Basic pKa: | CX LogP: 5.33 | CX LogD: 4.76 |
Aromatic Rings: 3 | Heavy Atoms: 31 | QED Weighted: 0.47 | Np Likeness Score: -1.58 |
1. Lorenz DA, Kaur T, Kerk SA, Gallagher EE, Sandoval J, Garner AL.. (2018) Expansion of cat-ELCCA for the Discovery of Small Molecule Inhibitors of the Pre-let-7-Lin28 RNA-Protein Interaction., 9 (6): [PMID:29937975] [10.1021/acsmedchemlett.8b00126] |
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