(2Z)-4,4,4-Trifluoro-2-[2-(4-methylphenyl)hydrazinylidene]-3-oxobutanoic acid

ID: ALA4475685

Chembl Id: CHEMBL4475685

PubChem CID: 155538094

Max Phase: Preclinical

Molecular Formula: C11H9F3N2O3

Molecular Weight: 274.20

Molecule Type: Unknown

Associated Items:

Names and Identifiers

Canonical SMILES:  Cc1ccc(N/N=C(\C(=O)O)C(=O)C(F)(F)F)cc1

Standard InChI:  InChI=1S/C11H9F3N2O3/c1-6-2-4-7(5-3-6)15-16-8(10(18)19)9(17)11(12,13)14/h2-5,15H,1H3,(H,18,19)/b16-8-

Standard InChI Key:  RJFITWNAPYZYNY-PXNMLYILSA-N

Alternative Forms

  1. Parent:

    ALA4475685

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Associated Targets(Human)

ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Carboxylesterase (379 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Cholinesterase (8742 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Calculated Properties

Molecular Weight: 274.20Molecular Weight (Monoisotopic): 274.0565AlogP: 1.98#Rotatable Bonds: 4
Polar Surface Area: 78.76Molecular Species: ACIDHBA: 4HBD: 2
#RO5 Violations: HBA (Lipinski): 5HBD (Lipinski): 2#RO5 Violations (Lipinski):
CX Acidic pKa: 1.32CX Basic pKa: CX LogP: 4.12CX LogD: -0.58
Aromatic Rings: 1Heavy Atoms: 19QED Weighted: 0.50Np Likeness Score: -0.96

References

1. Khudina OG, Makhaeva GF, Elkina NA, Boltneva NP, Serebryakova OG, Shchegolkov EV, Rudakova EV, Lushchekina SV, Burgart YV, Bachurin SO, Richardson RJ, Saloutin VI..  (2019)  Synthesis of 2-arylhydrazinylidene-3-oxo-4,4,4-trifluorobutanoic acids as new selective carboxylesterase inhibitors and radical scavengers.,  29  (23): [PMID:31640885] [10.1016/j.bmcl.2019.126716]

Source