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ID: ALA2086891
Max Phase: Preclinical
Molecular Formula: C18H24ClN3O5S
Molecular Weight: 429.93
Molecule Type: Small molecule
Associated Items:
ID: ALA2086891
Max Phase: Preclinical
Molecular Formula: C18H24ClN3O5S
Molecular Weight: 429.93
Molecule Type: Small molecule
Associated Items:
Canonical SMILES: C=CC(=O)Nc1ccc(S(=O)(=O)N2CCN(C(=O)OC(C)(C)C)CC2)c(Cl)c1
Standard InChI: InChI=1S/C18H24ClN3O5S/c1-5-16(23)20-13-6-7-15(14(19)12-13)28(25,26)22-10-8-21(9-11-22)17(24)27-18(2,3)4/h5-7,12H,1,8-11H2,2-4H3,(H,20,23)
Standard InChI Key: AUAPVOQGBUKHMB-UHFFFAOYSA-N
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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: 429.93 | Molecular Weight (Monoisotopic): 429.1125 | AlogP: 2.71 | #Rotatable Bonds: 4 |
Polar Surface Area: 96.02 | Molecular Species: NEUTRAL | HBA: 5 | HBD: 1 |
#RO5 Violations: 0 | HBA (Lipinski): 8 | HBD (Lipinski): 1 | #RO5 Violations (Lipinski): 0 |
CX Acidic pKa: 13.53 | CX Basic pKa: | CX LogP: 2.37 | CX LogD: 2.37 |
Aromatic Rings: 1 | Heavy Atoms: 28 | QED Weighted: 0.74 | Np Likeness Score: -1.85 |
1. Prime ME, Andersen OA, Barker JJ, Brooks MA, Cheng RK, Toogood-Johnson I, Courtney SM, Brookfield FA, Yarnold CJ, Marston RW, Johnson PD, Johnsen SF, Palfrey JJ, Vaidya D, Erfan S, Ichihara O, Felicetti B, Palan S, Pedret-Dunn A, Schaertl S, Sternberger I, Ebneth A, Scheel A, Winkler D, Toledo-Sherman L, Beconi M, Macdonald D, Muñoz-Sanjuan I, Dominguez C, Wityak J.. (2012) Discovery and structure-activity relationship of potent and selective covalent inhibitors of transglutaminase 2 for Huntington's disease., 55 (3): [PMID:22224594] [10.1021/jm201310y] |
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