Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA5206385
Max Phase: Preclinical
Molecular Formula: C19H24Cl2N2S
Molecular Weight: 383.39
Associated Items:
ID: ALA5206385
Max Phase: Preclinical
Molecular Formula: C19H24Cl2N2S
Molecular Weight: 383.39
Associated Items:
Canonical SMILES: CN(Cc1ccsc1)CC1CCN(Cc2ccc(Cl)c(Cl)c2)CC1
Standard InChI: InChI=1S/C19H24Cl2N2S/c1-22(12-17-6-9-24-14-17)11-15-4-7-23(8-5-15)13-16-2-3-18(20)19(21)10-16/h2-3,6,9-10,14-15H,4-5,7-8,11-13H2,1H3
Standard InChI Key: APGPIGPXEVBIPX-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: | 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: 383.39 | Molecular Weight (Monoisotopic): 382.1037 | AlogP: 5.40 | #Rotatable Bonds: 6 |
Polar Surface Area: 6.48 | Molecular Species: BASE | HBA: 3 | HBD: 0 |
#RO5 Violations: 1 | HBA (Lipinski): 2 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: 9.14 | CX LogP: 5.12 | CX LogD: 3.07 |
Aromatic Rings: 2 | Heavy Atoms: 24 | QED Weighted: 0.66 | Np Likeness Score: -2.48 |
1. Woolard KJ, Sandala JL, Melander RJ, Gunn JS, Melander C.. (2022) Development of small molecules that work cooperatively with ciprofloxacin to clear salmonella biofilms in a chronic gallbladder carriage model., 232 [PMID:35219950] [10.1016/j.ejmech.2022.114203] |
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