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5,7-Dichloro-1H-indole-2,3-dione 3-[N-(4-sulfamoylphenyl)thiosemicarbazone] ID: ALA4093328
Chembl Id: CHEMBL4093328
PubChem CID: 137196867
Max Phase: Preclinical
Molecular Formula: C15H11Cl2N5O3S2
Molecular Weight: 444.33
Molecule Type: Small molecule
Associated Items:
Names and Identifiers Canonical SMILES: NS(=O)(=O)c1ccc(NC(=S)N/N=C2\C(=O)Nc3c(Cl)cc(Cl)cc32)cc1
Standard InChI: InChI=1S/C15H11Cl2N5O3S2/c16-7-5-10-12(11(17)6-7)20-14(23)13(10)21-22-15(26)19-8-1-3-9(4-2-8)27(18,24)25/h1-6H,(H2,18,24,25)(H2,19,22,26)(H,20,21,23)
Standard InChI Key: ALRWEUNFASKTRZ-UHFFFAOYSA-N
Associated Targets(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: 444.33Molecular Weight (Monoisotopic): 442.9680AlogP: 2.28#Rotatable Bonds: 3Polar Surface Area: 125.68Molecular Species: NEUTRALHBA: 5HBD: 4#RO5 Violations: ┄HBA (Lipinski): 8HBD (Lipinski): 5#RO5 Violations (Lipinski): ┄CX Acidic pKa: 9.16CX Basic pKa: ┄CX LogP: 2.99CX LogD: 2.98Aromatic Rings: 2Heavy Atoms: 27QED Weighted: 0.43Np Likeness Score: -2.01
References 1. Karalı N, Akdemir A, Göktaş F, Eraslan Elma P, Angeli A, Kızılırmak M, Supuran CT.. (2017) Novel sulfonamide-containing 2-indolinones that selectively inhibit tumor-associated alpha carbonic anhydrases., 25 (14): [PMID:28545816 ] [10.1016/j.bmc.2017.05.029 ]