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(E)-4-(2-(3,5-Dichloro-2-hydroxybenzylidene)hydrazinecarbonyl)-N-(5-methylisoxazol-3-yl)-benzenesulfonamide ID: ALA3613060
Chembl Id: CHEMBL3613060
PubChem CID: 137133408
Max Phase: Preclinical
Molecular Formula: C18H14Cl2N4O5S
Molecular Weight: 469.31
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: Cc1cc(NS(=O)(=O)c2ccc(C(=O)N/N=C/c3cc(Cl)cc(Cl)c3O)cc2)no1
Standard InChI: InChI=1S/C18H14Cl2N4O5S/c1-10-6-16(23-29-10)24-30(27,28)14-4-2-11(3-5-14)18(26)22-21-9-12-7-13(19)8-15(20)17(12)25/h2-9,25H,1H3,(H,22,26)(H,23,24)/b21-9+
Standard InChI Key: BSBXQIZAPMLUEL-ZVBGSRNCSA-N
Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Small moleculeTopical: NoFirst In Class: NoBlack Box: NoChirality: NoAvailability: NoProdrug: No
Drug Indications MESH ID MESH Heading EFO IDs EFO Terms Max Phase for Indication References
Mechanisms of Action Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References
Calculated Properties Molecular Weight: 469.31Molecular Weight (Monoisotopic): 468.0062AlogP: 3.56#Rotatable Bonds: 6Polar Surface Area: 133.89Molecular Species: ACIDHBA: 7HBD: 3#RO5 Violations: 0HBA (Lipinski): 9HBD (Lipinski): 3#RO5 Violations (Lipinski): 0CX Acidic pKa: 5.69CX Basic pKa: 0.44CX LogP: 3.51CX LogD: 1.91Aromatic Rings: 3Heavy Atoms: 30QED Weighted: 0.37Np Likeness Score: -2.26
References 1. Sunduru N, Salin O, Gylfe Å, Elofsson M.. (2015) Design, synthesis and evaluation of novel polypharmacological antichlamydial agents., 101 [PMID:26204507 ] [10.1016/j.ejmech.2015.07.019 ]