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ID: ALA4741834
Max Phase: Preclinical
Molecular Formula: C16H14Cl2N2O4
Molecular Weight: 369.20
Molecule Type: Unknown
Associated Items:
Representations Canonical SMILES: O=C(/C=C/c1ccc(Cl)cc1Cl)N(O)CCCN1C(=O)C=CC1=O
Standard InChI: InChI=1S/C16H14Cl2N2O4/c17-12-4-2-11(13(18)10-12)3-5-16(23)20(24)9-1-8-19-14(21)6-7-15(19)22/h2-7,10,24H,1,8-9H2/b5-3+
Standard InChI Key: DWCGMXOBKNVKQD-HWKANZROSA-N
Associated Targets(Human) Associated Targets(non-human) Molecule Features Natural Product: NoOral: NoChemical Probe: NoParenteral: NoMolecule Type: UnknownTopical: 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
Properties Molecular Weight: 369.20Molecular Weight (Monoisotopic): 368.0331AlogP: 2.54#Rotatable Bonds: 6Polar Surface Area: 77.92Molecular Species: NEUTRALHBA: 4HBD: 1#RO5 Violations: 0HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski): 0CX Acidic pKa: 8.77CX Basic pKa: CX LogP: 2.23CX LogD: 2.22Aromatic Rings: 1Heavy Atoms: 24QED Weighted: 0.36Np Likeness Score: -0.55
References 1. Turner, Lewis D., Nielsen, Alexander L., Lin, Lucy, Pellett, Sabine, Sugane, Takashi, Olson, Margaret E., Johnson, Eric A., Janda, Kim D.. (2021) Irreversible inhibition of BoNT/A protease: proximity-driven reactivity contingent upon a bifunctional approach, 12 (6.0): [PMID:34223161 ] [10.1039/d1md00089f ] 2. Patel EN, Turner LD, Hixon MS, Janda KD.. (2022) Identification of Slow-Binding Inhibitors of the BoNT/A Protease., 13 (4.0): [PMID:35450355 ] [10.1021/acsmedchemlett.2c00028 ]