(E)-6-((3-(diethylamino)propyl)amino)-7-fluoro-3-(3,4,5-trimethoxybenzylidene)-2,3-dihydropyrrolo[2,1-b]quinazolin-9(1H)-one

ID: ALA4071264

PubChem CID: 137638213

Max Phase: Preclinical

Molecular Formula: C28H35FN4O4

Molecular Weight: 510.61

Molecule Type: Small molecule

This compound is available for customization.

Associated Items:

Names and Identifiers

Canonical SMILES:  CCN(CC)CCCNc1cc2nc3n(c(=O)c2cc1F)CC/C3=C\c1cc(OC)c(OC)c(OC)c1

Standard InChI:  InChI=1S/C28H35FN4O4/c1-6-32(7-2)11-8-10-30-23-17-22-20(16-21(23)29)28(34)33-12-9-19(27(33)31-22)13-18-14-24(35-3)26(37-5)25(15-18)36-4/h13-17,30H,6-12H2,1-5H3/b19-13+

Standard InChI Key:  AAIKBVZTWBPSRV-CPNJWEJPSA-N

Molfile:  

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M  END

Alternative Forms

  1. Parent:

    ALA4071264

    ---

Associated Targets(Human)

NME2 Tbio Nucleoside diphosphate kinase 2 (168 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: 510.61Molecular Weight (Monoisotopic): 510.2642AlogP: 4.65#Rotatable Bonds: 11
Polar Surface Area: 77.85Molecular Species: BASEHBA: 8HBD: 1
#RO5 Violations: 1HBA (Lipinski): 8HBD (Lipinski): 1#RO5 Violations (Lipinski): 1
CX Acidic pKa: CX Basic pKa: 9.94CX LogP: 3.21CX LogD: 0.72
Aromatic Rings: 3Heavy Atoms: 37QED Weighted: 0.38Np Likeness Score: -0.84

References

1. Wang YQ, Huang ZL, Chen SB, Wang CX, Shan C, Yin QK, Ou TM, Li D, Gu LQ, Tan JH, Huang ZS..  (2017)  Design, Synthesis, and Evaluation of New Selective NM23-H2 Binders as c-MYC Transcription Inhibitors via Disruption of the NM23-H2/G-Quadruplex Interaction.,  60  (16): [PMID:28714689] [10.1021/acs.jmedchem.7b00421]

Source