(3Z)-3-(1-(1H-imidazol-5-yl)-ethylidene)-N-(3,4-dimethoxybenzyl)-2-oxoindoline-5-sulfonamide

ID: ALA3734965

PubChem CID: 127034946

Max Phase: Preclinical

Molecular Formula: C21H20N4O5S

Molecular Weight: 440.48

Molecule Type: Small molecule

Associated Items:

This compound is not in our inventory system

Names and Identifiers

Canonical SMILES:  COc1ccc(CNS(=O)(=O)c2ccc3c(c2)/C(=C/c2cnc[nH]2)C(=O)N3)cc1OC

Standard InChI:  InChI=1S/C21H20N4O5S/c1-29-19-6-3-13(7-20(19)30-2)10-24-31(27,28)15-4-5-18-16(9-15)17(21(26)25-18)8-14-11-22-12-23-14/h3-9,11-12,24H,10H2,1-2H3,(H,22,23)(H,25,26)/b17-8-

Standard InChI Key:  ZGOCJQADASOZEP-IUXPMGMMSA-N

Molfile:  

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M  END

Alternative Forms

  1. Parent:

    ALA3734965

    ---

Associated Targets(Human)

ASPC1 (1310 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Small moleculeTopical: 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: 440.48Molecular Weight (Monoisotopic): 440.1154AlogP: 2.40#Rotatable Bonds: 7
Polar Surface Area: 122.41Molecular Species: NEUTRALHBA: 6HBD: 3
#RO5 Violations: HBA (Lipinski): 9HBD (Lipinski): 3#RO5 Violations (Lipinski):
CX Acidic pKa: 9.99CX Basic pKa: 6.64CX LogP: 1.31CX LogD: 1.25
Aromatic Rings: 3Heavy Atoms: 31QED Weighted: 0.49Np Likeness Score: -0.90

References

1. Sestito S, Nesi G, Daniele S, Martelli A, Digiacomo M, Borghini A, Pietra D, Calderone V, Lapucci A, Falasca M, Parrella P, Notarangelo A, Breschi MC, Macchia M, Martini C, Rapposelli S..  (2015)  Design and synthesis of 2-oxindole based multi-targeted inhibitors of PDK1/Akt signaling pathway for the treatment of glioblastoma multiforme.,  105  [PMID:26498573] [10.1016/j.ejmech.2015.10.020]

Source