Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
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ID: ALA4794602
Max Phase: Preclinical
Molecular Formula: C20H16Cl2N4S
Molecular Weight: 415.35
Molecule Type: Unknown
Associated Items:
ID: ALA4794602
Max Phase: Preclinical
Molecular Formula: C20H16Cl2N4S
Molecular Weight: 415.35
Molecule Type: Unknown
Associated Items:
Canonical SMILES: Clc1cccc(CCSc2ncnc3c2ncn3Cc2cccc(Cl)c2)c1
Standard InChI: InChI=1S/C20H16Cl2N4S/c21-16-5-1-3-14(9-16)7-8-27-20-18-19(23-12-24-20)26(13-25-18)11-15-4-2-6-17(22)10-15/h1-6,9-10,12-13H,7-8,11H2
Standard InChI Key: ALCANKFHLDKOSQ-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: Unknown | 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: 415.35 | Molecular Weight (Monoisotopic): 414.0473 | AlogP: 5.52 | #Rotatable Bonds: 6 |
Polar Surface Area: 43.60 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 0 |
#RO5 Violations: 1 | HBA (Lipinski): 4 | HBD (Lipinski): 0 | #RO5 Violations (Lipinski): 1 |
CX Acidic pKa: | CX Basic pKa: 3.05 | CX LogP: 5.99 | CX LogD: 5.99 |
Aromatic Rings: 4 | Heavy Atoms: 27 | QED Weighted: 0.31 | Np Likeness Score: -1.53 |
1. Rojas-Prats E,Martinez-Gonzalez L,Gonzalo-Consuegra C,Liachko NF,Perez C,Ramírez D,Kraemer BC,Martin-Requero Á,Perez DI,Gil C,de Lago E,Martinez A. (2021) Targeting nuclear protein TDP-43 by cell division cycle kinase 7 inhibitors: A new therapeutic approach for amyotrophic lateral sclerosis., 210 [PMID:33139113] [10.1016/j.ejmech.2020.112968] |
Source(1):