Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4165671
Max Phase: Preclinical
Molecular Formula: C11H14N2S3
Molecular Weight: 270.45
Molecule Type: Small molecule
Associated Items:
ID: ALA4165671
Max Phase: Preclinical
Molecular Formula: C11H14N2S3
Molecular Weight: 270.45
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: S=C(SSc1ccccn1)N1CCCCC1
Standard InChI: InChI=1S/C11H14N2S3/c14-11(13-8-4-1-5-9-13)16-15-10-6-2-3-7-12-10/h2-3,6-7H,1,4-5,8-9H2
Standard InChI Key: GKQSSJMVOCJKGV-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: 270.45 | Molecular Weight (Monoisotopic): 270.0319 | AlogP: 3.59 | #Rotatable Bonds: 2 |
Polar Surface Area: 16.13 | Molecular Species: NEUTRAL | HBA: 4 | HBD: 0 |
#RO5 Violations: 0 | HBA (Lipinski): 2 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: | CX Basic pKa: 2.32 | CX LogP: 3.88 | CX LogD: 3.88 |
Aromatic Rings: 1 | Heavy Atoms: 16 | QED Weighted: 0.60 | Np Likeness Score: -1.20 |
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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