Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4176952
Max Phase: Preclinical
Molecular Formula: C16H17NS3
Molecular Weight: 319.52
Molecule Type: Small molecule
Associated Items:
ID: ALA4176952
Max Phase: Preclinical
Molecular Formula: C16H17NS3
Molecular Weight: 319.52
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: S=C(SSc1cccc2ccccc12)N1CCCCC1
Standard InChI: InChI=1S/C16H17NS3/c18-16(17-11-4-1-5-12-17)20-19-15-10-6-8-13-7-2-3-9-14(13)15/h2-3,6-10H,1,4-5,11-12H2
Standard InChI Key: FMASKSLFLLUQDD-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: 319.52 | Molecular Weight (Monoisotopic): 319.0523 | AlogP: 5.35 | #Rotatable Bonds: 2 |
Polar Surface Area: 3.24 | Molecular Species: | HBA: 3 | HBD: 0 |
#RO5 Violations: 1 | HBA (Lipinski): 1 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: | CX LogP: 5.49 | CX LogD: 5.49 |
Aromatic Rings: 2 | Heavy Atoms: 20 | QED Weighted: 0.54 | Np Likeness Score: -0.84 |
1. Gucchait A, Joardar N, Parida PK, Roy P, Mukherjee N, Dutta A, Yesuvadian R, SinhaBabu SP, Jana K, Misra AK.. (2018) Development of novel anti-filarial agents using carbamo(dithioperoxo)thioate derivatives., 143 [PMID:29207343] [10.1016/j.ejmech.2017.11.047] |
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