(Z)-(2,4-dinitrophenoxy)imino-[4-[2-fluoro-5-[(4-oxo-3H-phthalazin-1-yl)methyl]benzoyl]piperazin-1-yl]-oxidoazanium

ID: ALA3237591

Max Phase: Preclinical

Molecular Formula: C26H21FN8O8

Molecular Weight: 592.50

Molecule Type: Small molecule

Associated Items:

Representations

Canonical SMILES:  O=C(c1cc(Cc2n[nH]c(=O)c3ccccc23)ccc1F)N1CCN(/[N+]([O-])=N/Oc2ccc([N+](=O)[O-])cc2[N+](=O)[O-])CC1

Standard InChI:  InChI=1S/C26H21FN8O8/c27-21-7-5-16(14-22-18-3-1-2-4-19(18)25(36)29-28-22)13-20(21)26(37)31-9-11-32(12-10-31)35(42)30-43-24-8-6-17(33(38)39)15-23(24)34(40)41/h1-8,13,15H,9-12,14H2,(H,29,36)/b35-30-

Standard InChI Key:  ZTILXVUHIIMORJ-GXVXDJONSA-N

Associated Targets(Human)

PARP1 Tclin Poly [ADP-ribose] polymerase-1 (6206 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H1703 (410 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H1693 (116 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H2122 (340 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H322M (45589 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H1355 (159 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H2030 (117 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NCI-H1792 (313 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GSTP1 Tchem Glutathione S-transferase Pi (449 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GSTA1 Tchem Glutathione S-transferase A1 (120 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Tumor (97 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

Properties

Molecular Weight: 592.50Molecular Weight (Monoisotopic): 592.1466AlogP: 3.10#Rotatable Bonds: 8
Polar Surface Area: 203.24Molecular Species: ACIDHBA: 10HBD: 1
#RO5 Violations: 1HBA (Lipinski): 16HBD (Lipinski): 1#RO5 Violations (Lipinski): 2
CX Acidic pKa: 2.60CX Basic pKa: CX LogP: 0.31CX LogD: 2.33
Aromatic Rings: 4Heavy Atoms: 43QED Weighted: 0.14Np Likeness Score: -1.35

References

1. Maciag AE, Holland RJ, Kim Y, Kumari V, Luthers CE, Sehareen WS, Biswas D, Morris NL, Ji X, Anderson LM, Saavedra JE, Keefer LK..  (2014)  Nitric oxide (NO) releasing poly ADP-ribose polymerase 1 (PARP-1) inhibitors targeted to glutathione S-transferase P1-overexpressing cancer cells.,  57  (6): [PMID:24521039] [10.1021/jm401550d]

Source