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ID: ALA4210646
Max Phase: Preclinical
Molecular Formula: C15H13Cl2N3OS
Molecular Weight: 354.26
Molecule Type: Small molecule
Associated Items:
Representations
Canonical SMILES: NC(=S)N/N=C/c1ccc(OCc2ccc(Cl)c(Cl)c2)cc1
Standard InChI: InChI=1S/C15H13Cl2N3OS/c16-13-6-3-11(7-14(13)17)9-21-12-4-1-10(2-5-12)8-19-20-15(18)22/h1-8H,9H2,(H3,18,20,22)/b19-8+
Standard InChI Key: PRIZDNPCWVBWPG-UFWORHAWSA-N
Associated Targets(Human)
Associated Targets(non-human)
Molecule Features
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 |
Drug Indications
MESH ID | MESH Heading | EFO IDs | EFO Terms | Max Phase for Indication | References |
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Mechanisms of Action
Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
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Properties
Molecular Weight: 354.26 | Molecular Weight (Monoisotopic): 353.0156 | AlogP: 3.74 | #Rotatable Bonds: 5 |
Polar Surface Area: 59.64 | Molecular Species: NEUTRAL | HBA: 3 | HBD: 2 |
#RO5 Violations: 0 | HBA (Lipinski): 4 | HBD (Lipinski): 3 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 11.71 | CX Basic pKa: 2.20 | CX LogP: 4.44 | CX LogD: 4.44 |
Aromatic Rings: 2 | Heavy Atoms: 22 | QED Weighted: 0.49 | Np Likeness Score: -1.80 |
References
1. Linciano P, Moraes CB, Alcantara LM, Franco CH, Pascoalino B, Freitas-Junior LH, Macedo S, Santarem N, Cordeiro-da-Silva A, Gul S, Witt G, Kuzikov M, Ellinger B, Ferrari S, Luciani R, Quotadamo A, Costantino L, Costi MP.. (2018) Aryl thiosemicarbazones for the treatment of trypanosomatidic infections., 146 [PMID:29407968] [10.1016/j.ejmech.2018.01.043] |