3-(4-chlorophenyl)-N-[(4-cyanophenyl)methyl]-4-oxo-3,4-dihydrophthalazine-1-carboxamide

ID: ALA5172522

PubChem CID: 168271113

Max Phase: Preclinical

Molecular Formula: C23H15ClN4O2

Molecular Weight: 414.85

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  N#Cc1ccc(CNC(=O)c2nn(-c3ccc(Cl)cc3)c(=O)c3ccccc23)cc1

Standard InChI:  InChI=1S/C23H15ClN4O2/c24-17-9-11-18(12-10-17)28-23(30)20-4-2-1-3-19(20)21(27-28)22(29)26-14-16-7-5-15(13-25)6-8-16/h1-12H,14H2,(H,26,29)

Standard InChI Key:  RYXPSMVJXCUXHW-UHFFFAOYSA-N

Molfile:  

 
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    0.3583    2.6837    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
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    1.0758    1.4441    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5007    3.0942    0.0000 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.2153    3.5068    0.0000 N   0  0  0  0  0  0  0  0  0  0  0  0
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M  END

Alternative Forms

  1. Parent:

    ALA5172522

    ---

Associated Targets(Human)

A549 (127892 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
K562 (73714 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
K562/A02 (383 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ABCB1 Tchem P-glycoprotein 1 (14716 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

MDCK (10148 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: Topical: 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: 414.85Molecular Weight (Monoisotopic): 414.0884AlogP: 3.84#Rotatable Bonds: 4
Polar Surface Area: 87.78Molecular Species: NEUTRALHBA: 5HBD: 1
#RO5 Violations: HBA (Lipinski): 6HBD (Lipinski): 1#RO5 Violations (Lipinski):
CX Acidic pKa: 12.45CX Basic pKa: CX LogP: 4.28CX LogD: 4.28
Aromatic Rings: 4Heavy Atoms: 30QED Weighted: 0.55Np Likeness Score: -1.98

References

1. Shi W, Zhang P, Zou F, Zhou J, Yin Z, Cai Z, Ghaleb H, Jiang Y, Huang W, Liu Y, Qiu Q, Qian H..  (2022)  Exploration of novel phthalazinone derivatives as potential efflux transporter inhibitors for reversing multidrug resistance and improving the oral absorption of paclitaxel.,  233  [PMID:35247755] [10.1016/j.ejmech.2022.114231]

Source