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5-(4-(4-hydroxyphenylamino)phthalazin-1-yl)-2-methylbenzenesulfonamide ID: ALA5199666
Chembl Id: CHEMBL5199666
PubChem CID: 2893711
Max Phase: Preclinical
Molecular Formula: C21H18N4O3S
Molecular Weight: 406.47
Associated Items:
Names and Identifiers Canonical SMILES: Cc1ccc(-c2nnc(Nc3ccc(O)cc3)c3ccccc23)cc1S(N)(=O)=O
Standard InChI: InChI=1S/C21H18N4O3S/c1-13-6-7-14(12-19(13)29(22,27)28)20-17-4-2-3-5-18(17)21(25-24-20)23-15-8-10-16(26)11-9-15/h2-12,26H,1H3,(H,23,25)(H2,22,27,28)
Standard InChI Key: CDAWMQZSOPLPRB-UHFFFAOYSA-N
Associated Targets(Human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: Topical: 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: 406.47Molecular Weight (Monoisotopic): 406.1100AlogP: 3.70#Rotatable Bonds: 4Polar Surface Area: 118.20Molecular Species: NEUTRALHBA: 6HBD: 3#RO5 Violations: ┄HBA (Lipinski): 7HBD (Lipinski): 4#RO5 Violations (Lipinski): ┄CX Acidic pKa: 9.98CX Basic pKa: 3.33CX LogP: 3.65CX LogD: 3.65Aromatic Rings: 4Heavy Atoms: 29QED Weighted: 0.44Np Likeness Score: -1.31
References 1. Lee SY, Namasivayam V, Boshta NM, Perotti A, Mirza S, Bua S, Supuran CT, Müller CE.. (2021) Discovery of potent nucleotide pyrophosphatase/phosphodiesterase3 (NPP3) inhibitors with ancillary carbonic anhydrase inhibition for cancer (immuno)therapy., 12 (7.0): [PMID:34355184 ] [10.1039/D1MD00117E ]